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Ottawa panel evidence-based clinical practice guidelines for electrotherapy and thermotherapy interventions in the management of rheumatoid arthritis in adults.


Introduction

Rheumatoid arthritis rheumatoid arthritis

Chronic, progressive autoimmune disease causing connective-tissue inflammation, mostly in synovial joints. It can occur at any age, is more common in women, and has an unpredictable course.
 (RA) affects a large proportion of the population. The Arthritis Foundation This article or section needs sources or references that appear in reliable, third-party publications. Alone, primary sources and sources affiliated with the subject of this article are not sufficient for an accurate encyclopedia article.  reported that more than 2.1 million Americans have the disease. (1) The prevalence of RA is increasing with the aging population in industrial countries. (2) Rheumatoid arthritis is recognized as an important source of disability and handicap, which leads to considerable socioeconomic so·ci·o·ec·o·nom·ic  
adj.
Of or involving both social and economic factors.


socioeconomic
Adjective

of or involving economic and social factors

Adj. 1.
 costs resulting from medical and surgical interventions and from frequent absences from work. (2,3)

A patient is said to have RA if he or she satisfies at least 4 of the following 7 American Rheumatism rheumatism (r`mətĭzəm), general term for a number of disorders that cause inflammation and pain in muscles, bones, joints, or nerves.  Association (ARA Ara or Arrah (both: ŭ`rə), city (1991 pop. 157,082), Bihar state, NE India, on the Son Canal. A major road and rail junction, it is the administrative center for a district that produces grain, sugarcane, and oilseed. ) criteria: (1) morning stiffness, (2) arthritis of 3 or more joints, (3) arthritis of the hand joints, (4) symmetric No difference in opposing modes. It typically refers to speed. For example, in symmetric operations, it takes the same time to compress and encrypt data as it does to decompress and decrypt it. Contrast with asymmetric.

(mathematics) symmetric - 1.
 arthritis, (5) rheumatoid nodules rheumatoid nodule
n.
A subcutaneous nodule occurring most commonly over bony prominences in some patients with rheumatoid arthritis.


rheumatoid nodule 
, (6) serum rheumatoid factor rheumatoid factor
n. Abbr. RF
Any of the immunoglobulins found in the serum of individuals with rheumatoid arthritis that enhance the agglutination of suspended particles that are coated with pooled human gamma globulin and that are used
, or (7) radiologic radiologic Radiological adjective Referring to radiology  changes. (4) A classification of functional capacity frequently used in patients with RA is described as: (I) complete functional capacity with ability to carry out all usual duties without handicaps, (II) functional capacity adequate to conduct normal activities despite handicap of discomfort or limited mobility of one or more .joints, (III) functional capacity adequate to perform only a few or none of the duties of usual occupation or of self-care, or (IV) largely or wholly incapacitated in·ca·pac·i·tate  
tr.v. in·ca·pac·i·tat·ed, in·ca·pac·i·tat·ing, in·ca·pac·i·tates
1. To deprive of strength or ability; disable.

2. To make legally ineligible; disqualify.
 with patient bedridden bed·rid·den or bed·rid
adj.
Confined to bed because of illness or infirmity.
 or wheelchair-bound, permitting little or no self-care. (5)

The rehabilitation rehabilitation: see physical therapy.  approach to the management of RA (5) has 9 goals: (1) to decrease pain, (2) to decrease effusion effusion /ef·fu·sion/ (e-fu´zhun)
1. escape of a fluid into a part; exudation or transudation.

2. effused material; an exudate or transudate.
 (joint swelling swelling /swell·ing/ (swel´ing)
1. transient abnormal enlargement of a body part or area not due to cell proliferation.

2. an eminence, or elevation.
), (3) to decrease stiffness, (4) to correct or prevent joint deformity Deformity
See also Lameness.

Calmady, Sir Richard

born without lower legs. [Br. Lit.: Sir Richard Calmady, Walsh Modern, 84]

Carey, Philip

embittered young man with club foot seeks fulfillment. [Br. Lit.
, (5) to increase range of motion (ROM), (6) to increase muscle force, or decrease weakness, (7) to improve mobility and walking, (8) to increase physical fitness or reduce fatigue, and (9) to increase functional status.

Electrotherapeutic modalities Modalities
The factors and circumstances that cause a patient's symptoms to improve or worsen, including weather, time of day, effects of food, and similar factors.
 and thermotherapy ther·mo·ther·a·py
n.
Medical therapy involving the application of heat.


thermotherapy
 physical agents are used as part of a rehabilitation program Noun 1. rehabilitation program - a program for restoring someone to good health
program, programme - a system of projects or services intended to meet a public need; "he proposed an elaborate program of public works"; "working mothers rely on the day care
 offered mainly for pain and inflammation inflammation, reaction of the body to injury or to infectious, allergic, or chemical irritation. The symptoms are redness, swelling, heat, and pain resulting from dilation of the blood vessels in the affected part with loss of plasma and leucocytes (white blood  relief in the management of various musculoskeletal musculoskeletal /mus·cu·lo·skel·e·tal/ (-skel´e-t'l) pertaining to or comprising the skeleton and muscles.

mus·cu·lo·skel·e·tal
adj.
Relating to or involving the muscles and the skeleton.
 conditions. (2,6,7) The electrotherapeutic modalities and thermal agents have been used primarily to reduce pain, effusion, and stiffness in RA. These therapeutic interventions also indirectly contribute to increased ROM, muscle force, mobility, walking ability, functional status, and physical fitness. Thus, electrotherapy electrotherapy /elec·tro·ther·a·py/ (-ther´ah-pe) treatment of disease by means of electricity.

e·lec·tro·ther·a·py
n.
Medical therapy using electric currents.
 and thermotherapy are promising interventions, especially for inflammatory polyarthritis such as RA, which could present subacute subacute /sub·acute/ (-ah-kut´) somewhat acute; between acute and chronic.

sub·a·cute
adj.
Between acute and chronic.
 and chronic inflammatory symptoms depending on the stage of the disease (eg, chronic stage >1 year).

Electrotherapy and thermotherapy offer several advantages. They are noninvasive non·in·va·sive
adj.
1. Not penetrating the body, as by incision. Used especially of a diagnostic procedure.

2. Not invading healthy tissue.
 interventions that present very few adverse side effects Side effects

Effects of a proposed project on other parts of the firm.
 and contraindications compared with a large number of pharmacologic pharmacologic /phar·ma·co·log·ic/ (-kah-loj´ik) pertaining to pharmacology or to the properties and reactions of drugs.

pharmacological, pharmacologic

pertaining to pharmacology.
 interventions. Electrotherapy and thermotherapy are rapid to administer and are convenient for community-based settings; the modalities and agents either can be found at home (eg, ice packs) or are portable (for instance, the electrotherapy devices for transcutaneous electrical nerve stimulation transcutaneous electrical nerve stimulation
n.
TENS.


Transcutaneous electrical nerve stimulation (TENS)
A method for relieving the muscle pain of TMJ by stimulating nerve endings that do not transmit pain.
 [TENS] or low-level laser therapy [LLLT LLLT Low Level Laser Therapy ]). The effectiveness of electrotherapy and thermotherapy in the management of RA has been reported in systematic or literature reviews. (8-18)

Trials on the efficacy of LLLT have been systematically reviewed for RA. (12,13) The experimental and placebo placebo (pləsē`bō), inert substance given instead of a potent drug. Placebo medications are sometimes prescribed when a drug is not really needed or when one would not be appropriate because they make patients feel well taken care of.  groups in the reviewed studies showed a significant difference (P<.05), suggesting that LLLT is effective for reducing pain and morning stiffness and increasing ROM. (12,13) However, other reviews (8,9) that were not conducted systematically did not yield reports of any effect of LLLT for musculoskeletal pain relief.

To our knowledge, only one systematic review (17) exists on the efficacy of therapeutic ultrasound Therapeutic ultrasound is a technique that uses high-frequency sound waves (ultrasound) to speed healing in injured joint or muscle tissue. The frequency used is typically 1-3 Mhz.  in the management of RA. The review, involving RA of the hand, found a significant difference (P<.05) between experimental and control groups on reduced number of painful and swollen joints. However, ultrasound ultrasound or sonography, in medicine, technique that uses sound waves to study and treat hard-to-reach body areas. In scanning with ultrasound, high-frequency sound waves are transmitted to the area of interest and the returning echoes recorded  combined with an exercise program was not effective for these outcome measures. Four other meta-analyses on the effects of therapeutic ultrasound (19-22) showed no evidence of clinically important or statistically significant results to support the effectiveness of therapeutic ultrasound in reducing musculoskeletal pain. However, these meta-analyses related to musculoskeletal or heel heel (hel) calx; the hindmost part of the foot.

cracked heels  pitted keratolysis.


heel
n.
1.
 pain and not specifically to RA. They also have not been updated.

For thermotherapy for RA, the results of a systematic Review (15) showed that the application of hot packs or ice packs had no effect on measures of disease activity, including joint swelling, pain, medication intake, ROM, grip force, and hand function compared with a control (no intervention). However, paraffin baths paraffin bath,
n dip treatment of hot paraffin wax; commonly used to encourage relaxation, relieve pain, and increase circulation in the hands and feet. See also thermotherapy.
 combined with therapeutic exercises for arthritic hands showed positive results on measures of pain on nonresisted motion, ROM, and stiffness, but not on grip force and pinch pinch,
n a small amount of chewing tobacco (snuff) an individual takes to use the substance for its desired effect. A “pinch” is called a
quid in Britain.
 function, compared with a control after 4 consecutive weeks of intervention. No beneficial effects were observed for an application of paraffin paraffin, white, more-or-less translucent, odorless, tasteless, waxy solid. It melts between 47°C; and 65°C; and is insoluble in water but soluble in ether, benzene, and certain esters.  alone compared with a control for any of these measures.

In a recent systematic review on the efficacy of TENS in the management of RA, (16) statistically significant results were observed for pain relief at rest for acupuncture-like (low frequency combined with high intensity) TENS compared with placebo. Conventional (high frequency combined with low intensity) TENS showed statistically significant benefit over a placebo for tenderness intensity. Similar results were obtained in previous review articles on pain management in musculoskeletal conditions (23,24) and in rheumatology rheumatology /rheu·ma·tol·o·gy/ (-tol´ah-je) the branch of medicine dealing with rheumatic disorders, their causes, pathology, diagnosis, treatment, etc.

rheu·ma·tol·o·gy
n.
 conditions. (16,25) A systematic review conducted by Pelland et aL (18) showed that electrical stimulation had effects on muscle force and endurance Endurance
See also Longevity.

Atalanta

feminine name denotes power of endurance. [Gk. Myth.: Jobes, 148]

Boston marathon

famous 26-mile race held annually for long-distance runners. [Am. Pop. Culture: Misc.
 of the first dorsal dorsal /dor·sal/ (dor´s'l)
1. pertaining to the back or to any dorsum.

2. denoting a position more toward the back surface than some other object of reference; a synonym of posterior
 interosseous interosseous /in·ter·os·se·ous/ (-os´e-us) between bones.

in·ter·os·se·ous or in·ter·os·se·al
adj.
Connecting or lying between bones.
 muscle when compared with a control group that received no intervention.

To our knowledge, only 4 evidence-based clinical practice guidelines clinical practice guidelines Clinical policies, practice guidelines, practice parameters, practice policies Medtalk Systematically developed statements to assist practitioner and Pt decisions about appropriate health care for specific clinical circumstances. See Psychology.  (EBCPGs) have been published specifically on electrotherapy and thermotherapy interventions for RA: The RA Management Protocol, (5) the American College American College is the name of:
  • American College Dublin, Dublin, Ireland
  • The American College in Madurai, Tamil Nadu, India
  • The American College of the Immaculate Conception, Leuven (also known as Louvain), Belgium
 of Rheumatology's guidelines guidelines,
n.pl a set of standards, criteria, or specifications to be used or followed in the performance of certain tasks.
, (26) the American Pain Society's guidelines, (27) and guidelines for occupational Therapists occupational therapist A person trained to help people manage daily activities of living–dressing, cooking, etc, and other activities that promote recovery and regaining vocational skills Salary $51K + 4% bonus. See ADL.  (28) (Appendix 1). Because it offers no specific recommendations for practitioners, the RA Management Protocol (5) can be categorized cat·e·go·rize  
tr.v. cat·e·go·rized, cat·e·go·riz·ing, cat·e·go·riz·es
To put into a category or categories; classify.



cat
 as somewhere between an exhaustive literature review and a guideline guideline Medtalk A series of recommendations by a body of experts in a particular discipline. See Cancer screening guidelines, Cardiac profile guidelines, Gatekeeper guidelines, Harvard guidelines, Transfusion guidelines.  for each specific physical agent mentioned in this article. Regardless, the 4 sets of guidelines have several drawbacks: (1) they were developed for limited clinical practice areas; (2) although the EBCPGs were based on the current scientific literature, a nonstandardized approach was used to synthesize To create a whole or complete unit from parts or components. See synthesis.  the scientific results, meaning that the evidence of intervention efficacy was not clear or precise, especially when conflicting results were present; (3) the raw data of each article were not analyzed an·a·lyze  
tr.v. an·a·lyzed, an·a·lyz·ing, an·a·lyz·es
1. To examine methodically by separating into parts and studying their interrelations.

2. Chemistry To make a chemical analysis of.

3.
 and synthesized syn·the·sized  
adj.
1. Relating to or being an instrument whose sound is modified or augmented by a synthesizer.

2. Relating to or being compositions or a composition performed on synthesizers or synthesized instruments.
 using Cochrane Collaboration The Cochrane Collaboration was developed in response to Archie Cochrane's call for up-to-date, systematic reviews of all relevant randomized controlled trials of health care.  systematic methods; (4) the studies reviewed were not based on a systematic literature search; (5) the scientific results of each study were reviewed, but no synthesis was carried out; (6) no rigorous grading system was used to assess the evidence; and (7) no recent updating has been completed for most of the guidelines.

The generally positive results from the recent meta-analyses and the lack of up-to-date and rigorously developed EBCPGs oil electrotherapy and thermotherapy suggest a need for the development of better-quality EBCPGs for these interventions. Evidence suggests that quality of care can be improved through the use of EBCPGs. (29-32) The aim of developing these guidelines was to promote appropriate use of electrotherapy and thermotherapy in the management of RA. These guidelines are aimed at various users, including physical therapists, physicians, and patients. This article discusses only LLLT, therapeutic ultrasound, TENS, electrical stimulation, and thermotherapy (including, for the purposes of this article, both cryotherapy Cryotherapy Definition

Cryotherapy is a technique that uses an extremely cold liquid or instrument to freeze and destroy abnormal skin cells that require removal.
 and heat therapy).

Methods

For this project, we used the same methods that were used in a previous study conducted by the Ottawa Panel on therapeutic exercises. (33) The methods have been explained in full in a previous article, (33) which discusses all relevant areas: population, trial designs, outcomes, theoretical framework, literature search, selection criteria, statistical analysis, and guideline review. Briefly, an a priori a priori

In epistemology, knowledge that is independent of all particular experiences, as opposed to a posteriori (or empirical) knowledge, which derives from experience.
 protocol was defined, and it guided separate systematic reviews for each intervention. Positive recommendations were sent to 5 practitioners--a physical therapist, an occupational therapist, a physiatrist physiatrist /phys·iat·rist/ (-trist) a physician who specializes in physiatry.

phys·i·at·rist
n.
1. A physician who specializes in physical medicine.

2.
, a family physician, and a rheumatologist--for comments.

Results of Literature Search

The literature search identified 14,111 potential RA-related articles for electrotherapy and thermotherapy. Of these, several publications were considered potentially relevant based on the selection criteria checklist: (1) for LLLT, 11 articles (34-44) (Tabs. 1 and 2) were initially considered relevant and 5 randomized controlled trials A randomized controlled trial (RCT) is a scientific procedure most commonly used in testing medicines or medical procedures. RCTs are considered the most reliable form of scientific evidence because it eliminates all forms of spurious causality.  (RCTs) involving 204 patients with RA (34-38) were ultimately included; (2) for therapeutic ultrasound, 8 studies (45-52) (Tabs. 3 and 4) were initially included and 1 RCT RCT Randomized Controlled Trial
RCT Regimental Combat Team (infantry regiment with their own artillery, engineers, medical and tanks)
RCT Rollercoaster Tycoon
RCT Randomized Clinical Trial
RCT Rhondda Cynon Taff
 involving 50 patients (45) was ultimately included; (3) for thermotherapy, 23 trials were initially included (47,49,53-74) (Tabs. 5 and 6) and 2 RCTs involving 76 patients (53,54) were ultimately included; and (4) for TENS, 9 articles were initially included (50,75-82) (Tabs. 7 and 8) and 3 RCTs involving 78 patients (75-77) were ultimately included (Appendixes 2-5).

Low-Level Laser Therapy (LLLT)

LLLT applied to the foot, knee, or hand versus a placebo, level I (RCT): grade A for pain at 3 months (clinically important benefit); grade C for function, tender joints, muscle force, and ROM at 3 and 6 months (no benefit). Patients with chronic RA.

Summary of trials. Five placebo-controlled RCTs were included (Tab. 1). (34-38) In these RCTs, the LLLT treatment schedule ranged from 2 to 3 sessions a week and from 4 to 10 consecutive weeks. The dosage dosage /dos·age/ (do´saj) the determination and regulation of the size, frequency, and number of doses.

dos·age
n.
1. Administration of a therapeutic agent in prescribed amounts.
 ranged between 2.7 and 8.1 J/[cm.sup.2]. All RCTs used a gallium gallium (găl`ēəm), metallic chemical element; symbol Ga; at. no. 31; at. wt. 69.72; m.p. 29.78°C;; b.p. 2,403°C;; sp. gr. 5.904 at 29.6°C; (solid), 6.095 at 29.8°C; (liquid); valence +2 or +3.  aluminum-arsenide laser medium, (34-37) except for that of Walker et al, (38) who used a helium-neon type of laser. Walker et al (38) also used LLLT to irradiate irradiate /ir·ra·di·ate/ (i-rad´e-at) to treat with radiant energy.

ir·ra·di·ate
v.
1. To expose to radiation, as for diagnostic or therapeutic purposes.

2.
 both painful RA joints and the appropriate superficial superficial /su·per·fi·cial/ (-fish´al) pertaining to or situated near the surface.

su·per·fi·cial
adj.
1. Of, affecting, or being on or near the surface.

2.
 nerve, whereas other investigators (34-37) treated only the RA joints (Appendix 2). Four trials (39-42) were excluded because of the lack of an appropriate control group, one trial (43) was excluded because the abstract did not provide enough statistical data to be analyzed, and one trial (44) was excluded because it was a duplicate DUPLICATE. The double of anything.
     2. It is usually applied to agreements, letters, receipts, and the like, when two originals are made of either of them. Each copy has the same effect.
 of an included study (Tab. 2).

Efficacy. A clinically important benefit was demonstrated for pain relief. Four RCTs (34-36,38) (n = 169) demonstrated a significant difference (weighted mean difference [WMD WMD

white muscle disease.
]=-1.05 cm on a 10-cm visual analog scale [VAS vas (vas) pl. va´ sa  [L.] vessel.va´sal

vas aber´rans 
1. a blind tubule sometimes connected with the epididymis; a vestigial mesonephric tubule.

2.
], 95% confidence interval confidence interval,
n a statistical device used to determine the range within which an acceptable datum would fall. Confidence intervals are usually expressed in percentages, typically 95% or 99%.
 [CI]=-1.58 to 0.53 cm) and percentage reductions in pain relative to a control group. Relative reductions in pain were -28% in patients with RA affecting 2 or more groups of joints, (34) -25% in patients at a chronic stage, (35) -19% in patients with RA according to according to
prep.
1. As stated or indicated by; on the authority of: according to historians.

2. In keeping with: according to instructions.

3.
 ARA criteria, (38) and -22% in patients with active RA (36) (Tab. 9, Fig. 1). For consistency in Figures 1 through 4, the results obtained for the intervention groups are presented on the left of the central vertical line representing no difference (value 0) between groups compared and the results obtained for the control or placebo groups are presented on the right of the central vertical line representing no difference (value=0) between groups compared. Two RCTs (36,37) (n=57) demonstrated a difference in favor of upon the side of; favorable to; for the advantage of.

See also: favor
 LLLT compared with a placebo (WMD=-1.26 cm, 95% CI=-1.72 to -0.85 cm) in increasing ROM in the band (-76% to -142% relative difference). The trial by Palmgren et al, (37) involved only patients with RA. However, the tip-to-palm distance measurement was not considered a valid outcome according to the American Society of Hand Therapists (83) (Tab. 10, Fig. 1). No clinically important benefit was shown for tender joints (Ritchie Articular articular /ar·tic·u·lar/ (ahr-tik´u-ler) pertaining to a joint.

ar·tic·u·lar
adj.
Of or relating to a joint or joints.



articular

pertaining to a joint.
 Index) or function (Fig. 1), and the results for grip force conflicted (Tab. 11, Fig. 1).

[FIGURE 1 OMITTED]

Strength of published evidence compared with other guidelines. The Ottawa Panel found good evidence (level I, RCT) suggesting that LLLT alone in the management of RA of the foot, knee, or hand is beneficial for pain relief The strength of evidence has not been assessed by other RA guidelines (Appendix 1).

Clinical recommendations compared with other guidelines. The Ottawa Panel believes that the evidence supports the inclusion of LLLT applied to the foot, knee, or hand as an intervention for the reduction of pain associated with RA (grade A for pain). Low-level laser therapy has not been assessed by other RA guidelines (Appendix 1).

Practitioners' response to Ottawa Panel guidelines. All surveyed practitioners found the Ottawa Panel's recommendation for LLLT clear. Two practitioners agreed with the recommendation, and 1 practitioner disagreed with the recommendation (although the Ottawa Methods Group sent the recommendations to 5 practitioners, only 3 practitioners responded in this case).

Therapeutic Ultrasound

Therapeutic ultrasound performed on the hand in water versus a placebo, level I (RCT): grade A for tender joints at 10 weeks (clinically important benefit); grade C for swollen joints and morning stiffness at 10 weeks (no benefit). Patients with RA involving the hand (functional class I or II, chronic stage).

Summary of trials. One placebo-controlled RCT of therapeutic ultrasound (45) (n=50) was included (Tab. 3, Appendix 3). One trial (47) was excluded because the sample contained both subjects with RA and subjects without known pathology pathology, study of the cause of disease and the modifications in cellular function and changes in cellular structure produced in any cell, organ, or part of the body by disease.  or impairments, one trial (46) was excluded because it contained subjects without known pathology or impairments, and the other trials (48-52) were excluded for various reasons (Tab. 4).

Continuous-wave ultrasound was applied in water to the dorsal and palmar aspects of the hand at 0.5 W/[cm.sup.2]. The therapeutic session lasted 10 minutes on alternate days for 3 weeks for a total of 10 sessions (Appendix 3).

Efficacy. Pain relief demonstrated a clinically important difference (-19% relative difference [Tab. 12]) and statistically significant benefits (WMD=1.20 for change in number of tender joints, 95% CI=0.45-1.95). (45) No clinically important difference was shown for swollen joints (-3% [Tab. 12]). A clinically important difference could not be calculated for grip force or ROM in patients with RA of the hand (functional class I or II, chronic stage). No clinically important difference was found for reduction of morning stiffness (-41% [Tab. 12], Fig. 2) because morning stiffness was not measured using a validated val·i·date  
tr.v. val·i·dat·ed, val·i·dat·ing, val·i·dates
1. To declare or make legally valid.

2. To mark with an indication of official sanction.

3.
 scale. (84,85)

Strength of published evidence compared with other guidelines. The Ottawa Panel found good evidence (level I, RCT) of the effects of therapeutic ultrasound for RA of the hand. The strength of evidence has not been graded in other guidelines (Appendix 1).

Clinical recommendations compared with other guidelines. The Ottawa Panel believes there is good evidence that therapeutic ultrasound alone performed on the hand in water should be included as an intervention for RA (grade A for tender joints, grade C for swollen joints and morning stiffness). To our knowledge, no EBCPGs in the scientific literature have dealt with therapeutic ultrasound (Appendix 1).

Practitioners' response to Ottawa Panel guidelines. All surveyed practitioners agreed with the Ottawa Panel's recommendation for therapeutic ultrasound and found it clear.

Thermotherapy

Cryotherapy applied to the knee joint versus a control, level I (RCT): grade C for thermographic index (measurement [in degrees Celsius] obtained using infrared An invisible band of radiation at the lower end of the visible light spectrum. With wavelengths from 750 nm to 1 mm, infrared starts at the end of the microwave spectrum and ends at the beginning of visible light.  thermography thermography (thûr'mŏg`rəfē), contact photocopying process that produces a direct positive image and in which infrared rays are used to expose the copy paper.  of the joint) at 5 days (no benefit). Patients with chronic RA, and with obvious effusion of joints.

Wax applied to the hand and wrist versus a control, level I (RCT): grade C for pain, ROM, muscle force, and function at 1 month (no benefit). Patients with functional class I or II with hands affected.

Wax applied to the hand or wrist and hand exercises versus a control, level I (RCT): grade A for ROM at 1 month (clinically important benefit), grade C+ for pain and stiffness at 1 month (clinical benefit), grade C for muscle force and function at 1 month (no benefit). Patients with functional class I or II with hands affected.

Summary of trials. Two RCTs (53,54) (n=76) evaluated controls versus 3 different types of thermotherapy for PA-affected upper- and lower-extremity joints: (1) cryotherapy (n=24), (2) wax (n=52), and (3) wax combined with exercise (n=52) (Tab. 5, Appendix 4). The treatment duration ranged from 5 consecutive days to 3 times a week for 4 weeks. The treatment session ranged from 10 to 20 minutes (Appendix 4).

Eight RCTs were excluded for the following reasons: the absence of a control group, (58,62) the inclusion of patients postsurgery, (70) the use of patients as their own controls, (67) or the use of individuals without known pathology or impairments as controls. (47,68,69,73) Two other studies (57,63) were excluded because they had no numerical data Numerical data (or quantitative data) is data measured or identified on a numerical scale. Numerical data can be analysed using statistical methods, and results can be displayed using tables, charts, histograms and graphs.  to be analyzed. Four head-to-head studies (involving comparison of 2 groups of subjects receiving active treatments; no placebo or control group) (49,65,66,74) were not accepted, and other studies (55,56,59-61,64,67,71,72) were excluded for various reasons (Tab. 6).

Efficacy. For cryotherapy versus a control (n=24), (53) no statistically significant difference or clinically important benefits were observed for thermographic index for patients with chronic RA and obvious effusion of joints (Tab. 13, Fig. 31). No other outcomes were reported.

No statistically significant difference or clinically important benefit was shown for patients with functional class I or II with hands affected for reducing pain or for improving ROM, muscle force, or function (Tab. 14) in wax versus a control (n=26). (54)

Wax combined with exercise versus a control (n=26) (54) demonstrated a clinically important benefit for improving ROM in finger flexion flexion /flex·ion/ (flek´shun) the act of bending or the condition of being bent.

flex·ion
n.
1. The act of bending a joint or limb in the body by the action of flexors.

2.
 (21% relative difference [Tab. 15]) in patients with pain resulting from the latter type of RA. Clinically important benefits without statistical significance were shown for pain and stiffness (44% and -23%, respectively [Tab. 15, Fig. 3b]). No clinically important benefit was shown for muscle force or the pinch function test. No statistical difference was observed in any outcome measured except for ROM in finger flexion (WMD=8.30[degrees], 95% CI-0.44[degrees]-16.16[degrees]).

Strength of published evidence compared with other guidelines. The Ottawa Panel found good evidence (level 1, RCT) showing that thermotherapy, especially wax combined with exercise, benefits ROM, pain, and stiffness in the management of RA. The strength of evidence has been either not graded by or not reported in other RA guidelines (Appendix 1).

Clinical recommendations compared with other guidelines. The Ottawa Panel found good evidence (grade A for ROM; grade C+ for pain and stiffness) that thermotherapy, especially wax combined with exercise for the hand and wrist, should be included as an intervention for patients with RA. This recommendation concurs with all existing guidelines (Appendix 1). (5,25,27)

Practitioners' response to Ottawa Panel guidelines. All practitioners surveyed agreed with the recommendations for thermotherapy and found them clear.

Transcutaneous Electrical Nerve Stimulation (TENS)

Low-frequency TENS applied to the hand and wrist versus no stimulation, level I (RCT): grade A for pain at 3 weeks (clinically important benefit), grade C+ for power at 3 weeks (clinical benefit), grade C for work at 3 weeks (no benefit). Patients with chronic RA.

High-frequency TENS applied to the hand and wrist versus placebo, level I (RCT): grade C for pain and joint tenderness, same day (no benefit). Patients with chronic RA.

High- versus low-frequency TENS applied to the hand and wrist, level I (RCT): grade C+ for global patient (patient's assessment of overall disease activity or improvement) (33) at 2 weeks (clinical benefit). Patients with chronic RA.

Summary of trials. Three placebo-controlled RCTs involving TENS (n=78) (75-77) were included (Tab. 7, Appendix 5). Three types of TENS were prescribed pre·scribe  
v. pre·scribed, pre·scrib·ing, pre·scribes

v.tr.
1. To set down as a rule or guide; enjoin. See Synonyms at dictate.

2. To order the use of (a medicine or other treatment).
: (1) low-frequency (0-70 Hz), acupuncture-like TENS versus no stimulation (n=26), (75) (2) high-frequency (70-100 Hz), conventional TENS versus a placebo (n=33), (76) and (3) high- versus low-frequency TENS (n=19). (77) Thus, both high-frequency TENS (76,77) and low-frequency TENS (75,77) were provided to patients with RA. The therapeutic application of TENS ranged from 5 to 20 minutes a session and from 1 to 15 consecutive sessions for up to 3 consecutive weeks (Appendix 5).

One trial (79) with a sample size of fewer than 5 patients per group was excluded. One trial (80) was excluded because the enrolled patients were the control, one trial (78) was excluded because it involved a sample of patients with total knee replacement who had preoperative pre·op·er·a·tive
adj.
Preceding a surgical operation.



preoperative

preceding an operation.


preoperative care
the preparation of a patient before operation.
 osteoarthritis osteoarthritis
 or osteoarthrosis or degenerative joint disease

Most common joint disorder, afflicting over 80% of those who reach age 70. It does not involve excessive inflammation and may have no symptoms, especially at first.
 or RA of the knee, another trial (82) was excluded because it offered no numerical data to be analyzed, and other trials (50, 81) were excluded for different reasons (Tab. 8).

Efficacy. For low-frequency TENS versus no stimulation, (75) a clinically important benefit was demonstrated for pain relief (-67% relative difference [Tab. 16]), and this outcome was statistically significant (WMD=-59.50 mm on a 100-mm VAS, 95% CI = -76.58 to -42.42 mm; Fig. 4a) for patients with chronic RA. Power (in watts) was improved by 55% compared with baseline. This outcome, however, was not statistically significant in TENS compared with a placebo at 3 weeks. Work (in joules) scores showed little difference between TENS and a control (Tab. 17, Fig. 4a).

Neither statistical significance nor a clinically important benefit was found in high-frequency TENS versus a placebo for pain relief in patients experiencing the aforementioned a·fore·men·tioned  
adj.
Mentioned previously.

n.
The one or ones mentioned previously.


aforementioned
Adjective

mentioned before

Adj. 1.
 type of RA (Fig. 4b). (76) A statistically significant result was obtained for the reduction of joint tenderness, but no clinically important benefit was found (Tab. 18, Fig. 4b). (76)

For high- versus low-frequency TENS, no statistically significant difference in patient assessment of overall disease improvement was determined, but a clinically important benefit (21% risk difference) was observed in patients with RA, in favor of high-frequency TENS (Tab. 19, Fig. 4C). (77)

Strength of published evidence compared with other guidelines. The Ottawa Panel found good evidence (level I, RCT) of the effects of TENS for management of RA in the hand and wrist. The strength of evidence has been graded by the American Pain Society, (26) which also reported good-quality evidence for TENS (Appendix 1).

Clinical recommendations compared with other guidelines. According to the Ottawa Panel, there is good evidence (grade A for pain, grade C+ for global patient and power) suggesting that TENS alone should be included as an intervention for management of RA in the hand and wrist. The Ottawa Panel partially agrees with The Arthritis Society, (5) which recommends the use of TENS for pain and joint swelling in patients with RA. The American Pain Society (26) gives TENS a fair recommendation for pain relief (Appendix 1).

Practitioners' response to Ottawa Panel guidelines. All practitioners surveyed agreed with the Ottawa Panel's TENS recommendations and found them clear.

Electrical Stimulation of Muscle

Evidence with acceptable research design, interventions, group comparisons, or outcomes could not be identified to guide the development of recommendations for electrical stimulation of muscle. To our knowledge, no EBCPGs exist on electrical stimulation for RA conditions.

Discussion

In the area of rehabilitation for RA, evidence-based practice is gaining popularity. (5,7,25-27,86,87) The Ottawa Panel's systematic review revealed that one or more controlled clinical trials controlled clinical trial,
n a research strategy that calls for two samples: an experimental sample of patients receiving a pharmaceutical, and a second sample of control patients receiving a placebo.
 (CCTs) demonstrated some clinically important benefits of electrotherapy and thermotherapy interventions for patients with RA. The Ottawa Panel developed several EBCPGs (n=8 with grade A, B, or C+ recommendations) for these interventions. However, other current clinical interventions for RA still need this evidence to prove their effectiveness (n=16 with grade C recommendations and n=4 with insufficient data).

Credibility of Guidelines

The Ottawa Panel's EBCPGs on electrotherapy and thermotherapy (grouped together in Appendix 6) for the management of RA are generally in accordance Accordance is Bible Study Software for Macintosh developed by OakTree Software, Inc.[]

As well as a standalone program, it is the base software packaged by Zondervan in their Bible Study suites for Macintosh.
 with other EBCPGs (Appendix 1). An earlier expert panel (the Philadelphia Panel) agreed on a systematic grading of the evidence for EBCPGs, and the Ottawa Panel's EBCPGs were based on this grading system. The evidence for the Ottawa Panel's EBCPGs came from systematic reviews and meta-analyses that used Cochrane Collaboration methods or similar methods. To ensure that the guidelines were applicable and easy for clinicians to use, several practitioners sat on the Ottawa Panel. Their involvement supports the credibility of the guidelines.

The development of the draft EBCPGs was done in accordance with Appraisal of Guidelines Research and Evaluation (AGREE) criteria. (88) On dimensions 1 (purpose), 2 (stakeholder stakeholder n. a person having in his/her possession (holding) money or property in which he/she has no interest, right or title, awaiting the outcome of a dispute between two or more claimants to the money or property.  involvement), 4 (clarity), and 6 (editorial independence), the guidelines received excellent scores. Dimensions 3 (rigor rigor /rig·or/ (rig´er) [L.] chill; rigidity.

rigor mor´tis  the stiffening of a dead body accompanying depletion of adenosine triphosphate in the muscle fibers.
 of development) and 5 (applicability) received lower scores. Inadequate reporting of side effects and risks, which were not reported in the primary trials and therefore not included in the guidelines, lowered the rigor of development score. In identifying cost implications, potential organizational barriers, and methods of applying and monitoring the guidelines, the EBCPGs' applicability was low. Exact scores and a decision aid tool are available on the University of Ottawa
The University of Ottawa or Université d'Ottawa in French (also known as uOttawa or nicknamed U of O or Ottawa U) is a bilingual [1], research-intensive, non-denominational, international university in Ottawa, Ontario.
 School of Rehabilitation Sciences' Web page (http://www.heafih.uottawa.ca/EBCpg/ english/main.htm).

LLLT

According to the Ottawa Panel, there is good evidence suggesting that LLLT should be included as an intervention for reducing RA-related pain. The use of this modality modality /mo·dal·i·ty/ (mo-dal´i-te)
1. a method of application of, or the employment of, any therapeutic agent, especially a physical agent.

2.
 fulfills one intervention goal of the RA Management Protocol. (5) The Ottawa Panel's position agrees with those of previous systematic reviews. (12, 13)

Several physiological physiological /phys·i·o·log·i·cal/ (-loj´i-kal) pertaining to physiology; normal; not pathologic.

phys·i·o·log·i·cal or phys·i·o·log·ic
adj. Abbr. phys.
1.
 studies confirm the pain relief observed among patients with RA managed with LLLT. Low-level laser therapy irradiation irradiation /ir·ra·di·a·tion/ (i-ra?de-a´shun)
1. radiotherapy.

2. the dispersion of nervous impulse beyond the normal path of conduction.

3.
 positively modifies the peripheral nerve activity and provides a reduction in the sensation of the pain, (7) particularly in long-standing pain such as that associated with RA. (89) One proposed animal model theory is that LLLT enhances the action of superoxide dismutase superoxide dismutase
n.
An enzyme that catalyzes the decomposition of a superoxide into hydrogen peroxide and oxygen.


superoxide dismutase
, which prevents the proliferation proliferation /pro·lif·er·a·tion/ (pro-lif?er-a´shun) the reproduction or multiplication of similar forms, especially of cells.prolif´erativeprolif´erous

pro·lif·er·a·tion
n.
 of prostaglandin E Prostaglandin E is a family of naturally occurring prostaglandins.

Types include:
  • Alprostadil (E1)
  • Dinoprostone (E2)
It is created from prostaglandin E synthase. External links
  • MeSH Prostaglandins+E
. (90) Other physiological studies in rats (91) and in humans (92-94) suggest a plausible mechanism of action for LLLT stimulation-produced analgesia analgesia /an·al·ge·sia/ (an?al-je´ze-ah)
1. absence of sensibility to pain.

2. the relief of pain without loss of consciousness.
. This beneficial physiological effect was observed in humans both at the end of intervention and at 1- and 3-month follow-up examinations. (94) Physiological studies concerned with the inflammatory process suggest that exposure to LLLT results in anti-inflammatory and analgesic analgesic (ăn'əljē`zĭk), any of a diverse group of drugs used to relieve pain. Analgesic drugs include the nonsteroidal anti-inflammatory drugs (NSAIDs) such as the salicylates, narcotic drugs such as morphine, and synthetic drugs  effects, (95) normalization In relational database management, a process that breaks down data into record groups for efficient processing. There are six stages. By the third stage (third normal form), data are identified only by the key field in their record.  of the permeability permeability /per·me·a·bil·i·ty/ (per?me-ah-bil´i-te) the property or state of being permeable.

per·me·a·bil·i·ty
n.
1. The property or condition of being permeable.

2.
 of the synovial membrane synovial membrane
n.
The connective-tissue membrane that lines the cavity of a synovial joint and produces the synovial fluid. Also called synovium.
, (95) enhancement of regional microcirculation microcirculation /mi·cro·cir·cu·la·tion/ (-sir?ku-la´shun) the flow of blood through the fine vessels (arterioles, capillaries, and venules).microcirculato´ry

mi·cro·cir·cu·la·tion
n.
, reduction of exudative exudative

of or pertaining to a process of exudation.


exudative diathesis
a disease of young pigs and chickens caused by a nutritional deficiency of vitamin E. Characterized by severe edema of the subcutaneous tissues.
 and infiltrative infiltrative /in·fil·tra·tive/ (in´fil-tra?tiv) pertaining to or characterized by infiltration.
Infiltrative 
 fluids, increased synovial membrane fibrosis fibrosis /fi·bro·sis/ (fi-bro´sis) formation of fibrous tissue.fibrot´ic

congenital hepatic fibrosis
, (96) and increased protein synthesis Protein synthesis is the creation of proteins using DNA and RNA. Biological and artificial methods for creation of proteins differ significantly.
  • For biological protein synthesis, see protein biosynthesis.
  • For artificial protein synthesis, see peptide synthesis.
 of synovial synovial /sy·no·vi·al/ (-al)
1. pertaining to a synovial membrane.

2. pertaining to or secreting synovia.


synovial

of, pertaining to, or secreting synovia.
 cells, a synthesis that indicates a regenerative re·gen·er·a·tive  
adj.
1. Of, relating to, or marked by regeneration.

2. Tending to regenerate.



re·gen
 process in the damaged synovial membrane. (97,98)

The evidence suggests that LLLT could be applied without the addition of other physical therapy interventions to solve a specific RA pain-related problem. Because LLLT is rapid to administer and portable devices are available, it offers advantages for community-based sex-vices such as the Arthritis Rehabilitation and Education Program of The Arthritis Society (Canada). Further studies are needed to determine the optimal LLLT wavelength, dosage, application techniques, and duration of intervention and to determine long-term effects in patients with RA. (99)

Therapeutic Ultrasound

According to the Ottawa Panel, therapeutic ultrasound without the addition of other physical therapy interventions is effective for reducing joint tenderness caused by RA. Our results do not seem to concur CONCUR - ["CONCUR, A Language for Continuous Concurrent Processes", R.M. Salter et al, Comp Langs 5(3):163-189 (1981)].  fully with those of previous systematic reviews (19-22) conducted for all musculoskeletal conditions. Perhaps continuous ultrasound (100) is more effective for patients with RA whose condition is chronic and marked by a medium level of disease activity (45) than for individuals with acute musculoskeletal conditions.

The use of continuous ultrasound is supported by its documented physiological effects. (7,100,101) The mechanical effect of both pulsed and continuous ultrasound increases skin permeability, thus decreasing inflammatory response, reducing pain, and facilitating the soft tissue healing Healing
See also Medicine.

Achilles’ spear

had power to heal whatever wound it made. [Gk. Lit.: Iliad]

Agamede

Augeas’ daughter; noted for skill in using herbs for healing. [Gk. Myth.
 process. Furthermore, both pulsed and continuous ultrasound reduce nerve conduction nerve conduction
n.
The transmission of an impulse along a nerve fiber.


Nerve conduction
The speed and strength of a signal being transmitted by nerve cells.
 velocity of pain nerve fibers nerve fiber
n.
A threadlike process of a neuron, especially the axon that conducts nerve impulses.
. Continuous ultrasound, however, has thermal effects that reduce muscle spasms muscle spasm
n.
Persistent increased tension and shortness in a muscle or group of muscles that cannot be released voluntarily.


muscle spasm,
n
 and pain. The thermal effects also cause vasodilation vasodilation /vaso·di·la·tion/ (-di-la´shun)
1. increase in caliber of blood vessels.

2. a state of increased caliber of blood vessels.
, which enhances the excretion excretion, process of eliminating from an organism waste products of metabolism and other materials that are of no use. It is an essential process in all forms of life. In one-celled organisms wastes are discharged through the surface of the cell.  of chronic inflammatory cells. (7,100)

Thermotherapy

The Ottawa Panel found good evidence that thermotherapy, especially paraffin baths combined with exercise, should be included as an intervention for patients with RA to improve ROM and decrease pain and hand stiffness. This recommendation agrees with all existing guidelines (5,25-27) on improving pain and is partially supported by Nicholas, (102) who concluded that the current literature in rheumatology does not provide clinicians with precise information on dosage or duration, or specific indications for heat or cold therapy in therapeutic application.

The Ottawa Panel found insufficient evidence insufficient evidence n. a finding (decision) by a trial judge or an appeals court that the prosecution in a criminal case or a plaintiff in a lawsuit has not proved the case because the attorney did not present enough convincing evidence.  on the efficacy of cryotherapy, although physiological studies have shown effects on circulatory circulatory /cir·cu·la·to·ry/ (ser´ku-lah-tor?e)
1. pertaining to circulation, particularly that of the blood.

2. containing blood.


cir·cu·la·to·ry
n.
1.
 and temperature responses, muscle spasms, and inflamed tissue. (9,103) Cryotherapy's mechanism of action has not yet been fully elucidated. (103) Whether these physiological effects translate to important clinical outcomes (such as pain and functional status) is unknown.

The beneficial effects observed for paraffin baths combined with therapeutic exercises for arthritic hands-effects on measures of ROM, stiffness, and pain on nonresisted motion--concur with the physiological and therapeutic effects such as facilitation Facilitation

The process of providing a market for a security. Normally, this refers to bids and offers made for large blocks of securities, such as those traded by institutions.
 of soft tissue healing, decrease of pain by reducing muscle spasms, and reduction of joint stiffness Joint stiffness may be either the symptom of pain on moving a joint, the symptom of loss of range of motion or the physical sign of reduced range of motion. Doctors prefer the latter two uses but patients often use the first meaning. . (7) Thermotherapy using paraffin baths combined with exercise for RA is more effective as an adjunct adjunct (aj´ungkt),
n a drug or other substance that serves a supplemental purpose in therapy.

adjunct 
 therapy than it is alone. The combination of several concurrent therapies within the same treatment session reflects current physical therapist practice (6) where heat therapy is used for its reflex vasodilative effect, which increases cell metabolism Cell metabolism

The sum of chemical reactions which transpire within cells. The cell performs chemical, osmotic, mechanical, and electrical work, for which it needs energy.
 and blood flow (7) for an optimal muscle preparation before hand exercises. The combination of wax and exercises can introduce confounders. Indeed, endorphin endorphin

Any of a group of proteins occurring in the brain and having pain-relieving properties typical of opium and related opiates. Discovered in the 1970s, they include enkephalin, beta-endorphin, and dynorphin.
 and enkephalin enkephalin (ĕnkĕf`əlĭn), one of several naturally occurring morphinelike substances (endorphins) released from nerve endings of the central nervous system and the adrenal medulla.  production is stimulated by exercise. (104) The reduction of arthritic pain also could be observed when exercise is combined with a thermotherapy modality. (15)

TENS

According to the Ottawa Panel, there is good evidence showing that acupuncture-like TENS alone should be included as an intervention for RA to decrease pain and improve power. However, patients with RA seem to prefer conventional TENS application compared with acupuncture-like TENS. (77) The Ottawa Panel partly agrees with The Arthritis Society, (5) which views TENS as beneficial for pain and joint swelling in patients with RA. Our results concur with the conclusions of several descriptive literature reviews. (16,23,24,102)

The neuroregulatoly peripheral and central effects (89,105-107) of TENS have been proposed to be more effective with higher-intensity applications. (75) This effect was observed in the study involving acupuncture-like (higher-intensity) application compared with a placebo. (75) However, both conventional and acupuncture-like TENS excite (Excite.com, Irvington, NY, www.excite.com) One of the major search engines on the Web founded in 1995 and part of IAC Search & Media. Excite was acquired by Ask Jeeves, Inc. in 2004, which was acquired by IAC in 2005. See Web search engines.  afferent fibers afferent fiber
n.
Any of the nerve fibers that convey impulses to a ganglion or to a nerve center in the brain or spinal cord.
 in the A-alpha-beta range. (108) The plausible effect is explained by the activation activation /ac·ti·va·tion/ (ak?ti-va´shun)
1. the act or process of rendering active.

2. the transformation of a proenzyme into an active enzyme by the action of a kinase or another enzyme.

3.
 of intrinsic pain-suppressive systems (109,110) and the concomitant concomitant /con·com·i·tant/ (kon-kom´i-tant) accompanying; accessory; joined with another.
concomitant adjective Accompanying, accessory, joined with another
 release of opiate opiate /opi·ate/ (o´pe-it)
1. any drug derived from opium.

2. hypnotic (2).


o·pi·ate
n.
1.
 observed in both animals (111) and humans. (105) The importance of the stimulation parameters in TENS analgesia is shown in animal and human research. Changes in frequency recruit different opioid receptors Opioid receptors
Receptors located in the brain and various organs that bind opiates or opioid substances.

Mentioned in: Methadone

opioid receptors,
n.pl any of the several receptors to which opiates bind.
, for example, and therefore an awareness of the parameters used during TENS treatments is essential. (112,113) Several investigators (114-116) have recommended that vibrator vibrator /vi·bra·tor/ (vi´bra-tor) an instrument for producing vibrations.

vibrator

an apparatus used in vibratory treatment.
 stimulation be part of TENS application, especially when TENS is being applied for relief of chronic pain.

Electrical Stimulation of Muscle

Electrical stimulation of muscle is one of the therapeutic interventions available to minimize the loss of joint mobility and function by enhancing muscle performance in patients with RA. (18,117) However, despite the potential benefits of electrical stimulation in RA management, only one CCT CCT Circuit
CCT Commission Canadienne du Tourisme (Canadian Tourism Commission)
CCT Correlated Color Temperature
CCT Common Customs Tariff (EU)
CCT Certificate of Completion of Training
 (117) was identified for this intervention, and the study was ultimately rejected because the control group included fewer than 5 patients, indicating a very low statistical power. This CCT (117) is also considered a head-to-head study because 2 methods of stimulation were compared. Clinically, electrical stimulation is used to facilitate effective muscle force and endurance in situations involving a decrease in the voluntary recruitment of the muscle. Electrical stimulation helps to increase this recruitment in subjects without known pathology, or impairments. However, patients with RA are not able to voluntarily recruit motor units to the level required for the performance of high-intensity exercises needed to enhance muscle function, (18) and electrical stimulation does not help these patients, who have chronic muscle weakness. Furthermore, the Ottawa Panel does not recommend high-intensity exercises for patients with RA. (33) Musculoskeletal dysfunction dysfunction /dys·func·tion/ (dis-funk´shun) disturbance, impairment, or abnormality of functioning of an organ.dysfunc´tional

erectile dysfunction  impotence (2).
, including pain and muscle disuse atrophy disuse atrophy A generic term encompassing the degenerative changes that tissues undergo when they are functioning at suboptimal levels; involvement of the musculoskeletal unit is characterized by atrophy of muscles, contraction of tendons and osteoporosis;  that are observed in patients with RA, may cause decreased voluntary recruitment. Although the biophysical actions of many physical therapy interventions are partially understood, further investigation needs to be undertaken in several areas of physical therapy research, particularly that involving rheumatology: the mechanism of action; the differential effects of dose, of wavelength, and of treatment duration (99); disease staging and treatment combinations; and the relationship of pain, impairment Impairment

1. A reduction in a company's stated capital.

2. The total capital that is less than the par value of the company's capital stock.

Notes:
1. This is usually reduced because of poorly estimated losses or gains.

2.
, and disability. To reproduce re·pro·duce
v.
1. To produce a counterpart, an image, or a copy of something.

2. To bring something to mind again.

3. To generate offspring by sexual or asexual means.
 the results of published RCTs, it is crucial that details on various kinds of characteristics be systematically reported. Characteristics include those of the device (eg, size of the ultrasound head or temperature of the paraffin); those of the therapeutic application (eg, specific area of application or mode of application); duration of the intervention; and schedule of intervention. Characteristics of the population such as age, sex, concurrent interventions, and disease status (cg, acuity acuity /acu·i·ty/ (ah-ku´i-te) clarity or clearness, especially of vision.

a·cu·i·ty
n.
Sharpness, clearness, and distinctness of perception or vision.
 and joint involvement) also must be reported.

Conclusion

Despite the fact that the scientific literature is limited in quantity, good-quality evidence exists to recommend and support the use of LLLT, ultrasound, thermotherapy, and TENS for the management of RA. Conversely con·verse 1  
intr.v. con·versed, con·vers·ing, con·vers·es
1. To engage in a spoken exchange of thoughts, ideas, or feelings; talk. See Synonyms at speak.

2.
, evidence is lacking as to whether the use of electrical stimulation should be included or excluded in physical rehabilitation physical rehabilitation See Physical therapy.  for RA management.

The main difficulty in determining the effectiveness of rehabilitation interventions is the lack of well-designed prospective RCTs. Future research in physical therapy should adopt rigorous methods such as the use of an appropriate placebo (and double-blind procedure Noun 1. double-blind procedure - an experimental procedure in which neither the subjects of the experiment nor the persons administering the experiment know the critical aspects of the experiment; "a double-blind procedure is used to guard against both experimenter ), adequate randomization randomization (ranˈ·d·m , a homogeneous The same. Contrast with heterogeneous.

homogeneous - (Or "homogenous") Of uniform nature, similar in kind.

1. In the context of distributed systems, middleware makes heterogeneous systems appear as a homogeneous entity. For example see: interoperable network.
 sample of patients based on rigorous selection and diagnostic criteria, and an adequate sample size to detect clinically important differences with confidence.

Unfortunately, at present, there is insufficient evidence to recommend or not recommend the use of several modalities and physical agents in certain clinical circumstances CIRCUMSTANCES, evidence. The particulars which accompany a fact.
     2. The facts proved are either possible or impossible, ordinary and probable, or extraordinary and improbable, recent or ancient; they may have happened near us, or afar off; they are public or
. The main difficulty is the lack of studies available and the methodological weaknesses in those studies: the variation in the quality of the included trials (sometimes because the randomization procedure is not described properly), the difficulty of masking mask·ing
n.
1. The concealment or the screening of one sensory process or sensation by another.

2. An opaque covering used to camouflage the metal parts of a prosthesis.
 patients to a physical agent or modality, (118) and the lack of standardized standardized

pertaining to data that have been submitted to standardization procedures.


standardized morbidity rate
see morbidity rate.

standardized mortality rate
see mortality rate.
 outcomes. (2,99)
Appendix 1.

Previous Clinical Practice Guidelines for Rheumatoid Arthritis (a)

                              Quality of
                              Scientific
Intervention    Author        Evidence       Clinical Recommendations

LLLT            ACR (26)      N/C            N/C
                APS (27)      N/C            N/C
                Yasuda (28)   N/C            N/C
Therapeutic     ACR (26)      N/C            N/C
  ultrasound    APS (27)      N/C            N/C
                Yasuda (28)   N/C            N/C
Thermotherapy   ACR (26)      N/R            Heat is recommended,
                                               especially just prior to
                                               exercise
                APS (27)      N/C            N/C
                Yasuda (28)   N/R            Physical agents, including
                                               paraffin bath, hot
                                               packs, and pain
                                               management techniques,
                                               are recommended
TENS            ACR (26)      N/C            N/C
                APS (27)      Good-quality   TENS is given a fair
                                evidence       recommendation for pain
                                               relief
                Yasuda (28)   N/C            N/C
Electrical      ACR (26)      N/C            N/C
  stimulation   APS (27)      N/C            N/C
                Yasuda (28)   N/C            N/C

(a) LLLT=low-level laser therapy, ACR=American College of Rheumatology,
N/C=not considered, APS=American Pain Society, N/R=not reported,
TENS=transcutaneous electrical nerve simulation.

Appendix 2.

Included Trials for LLLT (a)

                        Sample
Author/Year             Size        Population Details

Goats et al, (34)       RCT         Inclusion criteria: patients who
  1996                  Total: 35     were aged 16 y or over
                        Gr1 : 25      and had RA affecting 2 or
                        Gr2: 10       more of the following
                                      groups of joints:
                                      tibiofemoral, talocrural,
                                      subtalar, midtarsol, or
                                      metatarsophalangeal
                                    Exclusion criteria: patients
                                      receiving medication that
                                      might distort the planned
                                      assessments
Hall et al, (35)        RCT         Inclusion criteria: patients with
  1994                  Total: 40     definite RA and active
                        Gr1: 20       synovitis of all or some
                        Gr2: 20       MCP or PIP joints
                                    Exclusion criteria: patients
                                      who had had a recent drug
                                      change (<30 d earlier) and
                                      were incapable of joint
                                      response (bony ankylosis,
                                      joint replacement, or
                                      tendon rupture)
Johannsen et al, (36)   RCT         Inclusion criteria: patients who
  1994                  Total: 22     were aged 18-85 y, had
                        Gr1: 10       active Steinbrocker
                        Gr2: 12       functional class I or II RA,
                                      and had symmetrical
                                      involvement of the MCP
                                      joints
                                    Exclusion criteria: patients
                                      who had bony erosions or
                                      osteoarthritis of the MCP or
                                      PIP joints, were pregnant, or
                                      had an inflammatory
                                      rheumatic disease other
                                      than RA
Palmgren et al, (37)    RCT         Inclusion criteria: patients with
  1989                  Total: 35     classical RA
                        Gr1: 19
                        Gr2: 16
Walker et al, (38)      RCT         Inclusion criteria: patients with
  1987                  Total: 72     RA (according to ARA
                        Gr1: 34       criteria)
                        Gr2: 38

                        Symptom
Author/Year             Duration               Age

Goats et al, (34)       Gr1: [bar.X]=7.54 y,   Gr1: [bar.X]=57 y,
  1996                    SD=6.86 y              SD=14 y
                        Gr2: [bar.X]=9.8 y,    Gr2 [bar.X]=64 y,
                          SD=10.11 y             SD=8 y
Hall et al, (35)        Gr1: [bar.X]=12.2 y,   Gr1: [bar.X]=67.1 y,
  1994                    range=1-33 y           range=55-84 y
                        Gr2: [bar.X]=9.3 y,    Gr2: [bar.X]=60.9 y,
                          range=2-30 y           range=43-77 y
Johannsen et al, (36)   N/A                    Gr1: [bar.X]=59 y,
  1994                                           range=36-76 y
                                               Gr2: [bar.X]=62 y,
                                                 range=56-73 y
Palmgren et al, (37)    Gr1: [bar.X]=13.4 y,   Gr1: F: [bar.X]=61.1 y,
  1989                    range=1-45 y           range=29-76 y
                        Gr2: [bar.X]=15.5 y,     M: [bar.X]=66.0 y,
                          range=4-30             range=56-73 y
                                               Gr2: F: [bar.X]=57.5 y,
                                                 range=39-70 y
                                                 M: [bar.X]=68.0 y,
                                                 range=66-70
Walker et al, (38)      Gr1: [bar.X]=11 y,     Gr1: [bar.X]=60 y,
  1987                    range=1-40 y           range=23-74 y
                        Gr2: [bar.X]=6 y,      Gr2: [bar.X]=61.5 y,
                          range=                 range=35-73 y
                          0.25-38 y

Author/Year             Intervention

Goats et al, (34)       Gr1: 5-kHz pulse repetition
  1996                    rate, spot size of 0.125
                          [cm.sup.2] in contact with the
                          skin and 8.1 J/[cm.sup.2]
                          applied to each aspect
                          of the joint, Ga-Al-As
                          LLLT
Hall et al, (35)        Gr1: Go-Al-As LLLT in
  1994                    contact with the skin for
                          18 min, wavelength of
                          820 nm (cluster and
                          single), spot size of
                          0.1 [cm.sup.2]
                        Single-probe: pulsing
                          frequency of 5 kHz,
                          actual output of 40 mW,
                          irradiance of 400 mW/
                          [cm.sup.2], applied at the
                          radial, ulnar, and
                          ventral aspects of the
                          first to fifth MCP and PIP
                          joints of the most
                          affected hand,
                          90 s/joint (3.6 J/joint,
                          36 J/[cm.sup.2] for each joint)
                        Cluster probe: 31 diodes
                          (8x880 nm, 10x870
                          nm, 14x950 nm,
                          1x820 nm), total power
                          output of 60 mW,
                          applied over the dorsal
                          and ventral aspects of
                          the hand for 180 s
                          (minimal exposure=2.7
                          J/[cm.sup.2], maximal
                          exposure=4.5 J/[cm.sup.2])
Johannsen et al, (36)   Gr1: Go-Al-As LLLT,
  1994                    wavelength of 830 nm,
                          continuous LLLT beam,
                          spot size of 0.07 [cm.sup.2],
                          effect of 21 mW, 23.2 J
                          applied per treatment
                          with 2.9 J on 4 points
                          (2 anterolateral and 2
                          posterolateral) around
                          each of the 2 most
                          painful MCP joints on
                          the most affected hand
Palmgren et al, (37)    Gr1: LLLT, 820 nm,
  1989                    polarized, 15 mW,
                          narrow profile Go-Al-As
                          semiconductor LLLT
                          diode, continuous-wave;
                          diode area of 0.1256
                          [cm.sup.2], applied for 60 s
                          on each lateral side of
                          the second to fifth MCP
                          and PIP joints of the most
                          affected hand
Walker et al, (38)      Gr1: helium-neon LLLT,
  1987                    632.5 nm, 1 mW, 20
                          Hz, maximal output of
                          0.95 mW at the fiber
                          optic tip (spot size of 4
                          [mm.sup.2]), actual output of
                          0.4776 mW, pulsed,
                          applied bilaterally for
                          20 s on each site on the
                          skin overlying the radial,
                          median, and saphenous
                          nerves, also applied on
                          the skin overlying the
                          painful joints (4 min total
                          joint exposure for the
                          first 4 wk, 6 min for the
                          next 3 wk, and 8 min for
                          the last 3 wk)

                                                     Concurrent
Author/Year             Comparison Group             Therapy

Goats et al, (34)       Gr2: placebo (identical in   Patient's regular
  1996                    external appearance          medication
                          but having no output)
Hall et al, (35)        Gr2: placebo                 Patient's regular
  1994                                                 medication
Johannsen et al, (36)   Gr2: placebo                 Patient's regular
  1994                                                 medication
Palmgren et al, (37)    Gr2: placebo                 Patient's regular
  1989                                                 medication
Walker et al, (38)      Gr2: placebo                 N/A
  1987

                        Frequency        Follow-up    Quality
Author/Year             and Duration     Duration     (R, B, W)

Goats et al, (34)       2 times a week   3 and 6 mo   1, 2, 0
  1996                    for 4 wk
Hall et al, (35)        3 times a week   2 and 4 mo   1, 2, 1
  1994                    for 4 wk
Johannsen et al, (36)   3 times a week   None         2, 2, 1
  1994                    for 1 mo
Palmgren et al, (37)    3 times a week   None         1, 2, 1
  1989                    for 4 wk
Walker et al, (38)      3 times a week   None         1, 2, 1
  1987                    for 10 wk

(a) LLLT=low-level laser therapy, R=randomization: 2 points maximum
(Jadad scale (33)), B=blinding: 2 points maximum (Jadad scale (33)),
W=withdrawals: 1 point maximum (Jadad scale (33)), RCT=randomized
controlled trial, Gr=group, RA=rheumatoid arthritis,
MCP=metacarpophalangeal, PIP=proximal interphalangeal,
Ga-Al-As=gallium-aluminum-arsenide, N/A=not available, F=female,
M=male, ARA=American Rheumatism Association.

Appendix 3.

Included Trials for Therapeutic Ultrasound (a)

Author/        Sample                                Symptom
Year           Size      Population Details          Duration

Konrad, (45)   RCT       Inclusion criteria:         Gr1: [bar.X]=4 y,
  1994           50        patients with RA (onset     SD=1.5 y
               Gr1: 25     of disease at least 1 y   Gr2: [bar.X]=5 y,
               Gr2: 25     earlier, functional         SD=1.75
                           class I or II, medium
                           activity of
                           RA-erythrocyte
                           sedimentation rate,
                           C-reactive protein)

Author/
Year           Age                   Intervention

Konrad, (45)   Gr1: [bar.X]=7.3 y,   Gr1: US applied in water
  1994           SD=9 y                to the dorsal and
               Gr2: [bar.X]=5.9 y,     palmar aspects of the
                 SD=8.75 y             hand, 0.5 W/[cm.sup.2],
                                       continuous with circular
                                       round head, 10 min on
                                       alternate days for 3 wk
                                       for a total of 10
                                       sessions

Author/                                 Concurrent   Frequency
Year           Comparison Group         Therapy      and Duration

Konrad, (45)   Gr2: placebo (inactive   N/A          10 sessions
  1994           US in water applied                   (3 wk)
                 to the palmar and
                 dorsal aspects of
                 the hand)

Author/        Follow-up   Quality
Year           Duration    (R, B, W)

Konrad, (45)   None        1, 1, 1
  1994

(a) R=randomization: 2 points maximum (Jadad scale (33)), B=blinding: 2
points maximum (Jadad scale (33)), W=withdrawals: 1 point maximum
(Jadad scale (33)), RCT=randomized controlled trial, Gr=group,
RA=rheumatoid arthritis, US=ultrasound.

Appendix 4.

Included Trials for Thermotherapy (a)

                        Sample
Author/Year             Size        Population Details

Bulstrode et al, (53)   RCT         Inclusion criteria: patients who
  1986                  Total: 24     had chronic RA (<1 y) and
                        Gr1 : 15      clinically obvious effusion of
                        Gr2: 9        one or both knee joints
Dellhag et al, (54)     RCT         Inclusion criteria: patients had
  1992                  Total: 52     to reside in the city of
                        Grl: 13       Gothenburg, be no older
                        Gr2: 11       than 70 y, and have
                        Gr3: 15       functional class I or II
                        Gr4: 13       chronic RA, have hand
                        F: 33         problems defined as a
                        M: 19         decrease in ROM or grip
                                      force

                        Symptom
Author/Year             Duration   Age                 Intervention

Bulstrode et al, (53)   N/A        N/A                 Gr1: ice packs
  1986
Dellhag et al, (54)     6-10 y     F: [bar.X]=51.8 y   Gr1: wax bath
  1992                             M: [bar.X]=56.3 y     and exercises
                                                       Gr2: exercises
                                                         only
                                                       Gr3: wax bath
                                                         only

                        Comparison        Concurrent
Author/Year             Group             Therapy

Bulstrode et al, (53)   Gr2: control      Supervised regimen
  1986                    (no ice           of static
                          packs)            quadriceps
                                            femoris muscle
                                            exercises 3 times
                                            daily
Dellhag et al, (54)     Gr4: control      None
  1992                    (unknown
                          intervention)

                        Frequency           Follow-up        Quality
Author/Year             and Duration        Duration         (R, B, W)

Bulstrode et al, (53)   Once a day for      End of           1, 0, 0
  1986                    10 min              intervention
                                              after 5 d
Dellhag et al, (54)     Five repetitions    End of           1, 0, 0
  1992                    for the             intervention
                          exercises           after
                          (each session       4 wk
                          was 20 min)
                        Wax bath: both
                          hands dipped
                          5 times into
                          wax, wrapped
                          in paper, and
                          fitted in quilt
                          mittens for 20
                          min
                        Intervention 3
                          times a week

(a) R=randomization: 2 points maximum (Jadad scale (33)), B=blinding: 2
points maximum (Jadad scale (33)), W=withdrawals: 1 point maximum
(Jadad scale (33)), RCT=randomized controlled trial, Gr=group,
RA=rheumatoid arthritis, N/A=not available, F=female, M=male, ROM=range
of motion. The data in this table have been previously published in a
table in another article (Brosseau L, Robinson V, Pellaud L, et al.
Efficacy of thermotherapy for rheumatoid arthritis: a meta-analysis.
Physical Therapy Reviews. 2002;7:5-15) and are used here with
permission of the publisher.

Appendix 5.

Included Trials for TENS (a)

                      Sample
Author/Year           Size      Population Details

Abelson et a1, (75)   RCT       Inclusion criteria: patients
  1983                34          with chronic RA
                      Gr1: 18     (according to ARA
                      Gr2: 16     criteria (4)) and chronic
                                  wrist involvement
Langley et al, (76)   RCT       Inclusion criteria: patients
  1984                22          with chronic RA
                      Gr1: 11     (according to ARA
                      Gr2: 11     criteria (4)), chronic hand
                                  involvement, and pain
                                  in one or both hands
Mannheimer            RCT       Inclusion criteria: patients
  et al, (77) 1978    38          with RA (including
                      Gr1: 19     spontaneous pain or
                      Gr2: 19     pain on loading from
                                  the wrist, the MCP
                                  joints, and the PIP
                                  joints)

                      Symptom
Author/Year           Duration               Age

Abelson et a1, (75)   Gr1: [bar.X]=12 y,     Gr1: [bar.X]=57 y,
  1983                  SD=8 y                 SD=8 y
                      Gr2: [bar.X]=13 y,     Gr2: [bar.X]=55 y,
                        SD=6.75 y              SD=7 y
Langley et al, (76)   Gr1: [bar.X]=11.3 y,   Gr1: [bar.X]=54.9 y,
  1984                  SD=7.5 y               SD=15.3 y
                      Gr2: [bar.X]=10.7 y,   Gr2: [bar.X]=53.4 y,
                        SD=10.7                SD=14.1 y
Mannheimer            Range: 1-44 y          Range: 20-69 y
  et al, (77) 1978

                                                              Concur-
                                               Comparison     rent
Author/Year           Intervention             Group          Therapy

Abelson et a1, (75)   Gr1: one TENS            Gr2: placebo   N/A
  1983                  session a week for
                        3 wk
Langley et al, (76)   Gr1: 20 min of high-     Gr2: 20 min    N/A
  1984                  frequency TENS           of placebo
                        (continuous square       TENS
                        wave pulses of
                        0.2 ms at 100
                        Hz), monophasic
                        pulses via 2
                        surface electrodes.
                        Electrodes were
                        wet pad type with
                        surface area of
                        9.08 [cm.sup.2].
                        Electrodes were
                        placed
                        immediately
                        proximal to the
                        patient's wrist,
                        with one electrode
                        on the volar
                        surface and the
                        other electrode on
                        the palmar surface.
Mannheimer            Conventional HF/LF       Placebo        N/A
  et al, (77) 1978      TENS, 5 min a            controlled
                        day for 15 d, wrist
                        (dorsal and volar)
                        and back (either
                        side of the spinal
                        process),
                        0-120 V, 0.2 ms,
                        45-170 Hz,
                        electrodes had
                        area of 9 [cm.sup.2]

                      Frequency
                      and            Follow-up   Quality
Author/Year           Duration       Duration    (R, B, W)

Abelson et a1, (75)   1 session a    None        1, 1, 0
  1983                  week for
                        3 wk, 15
                        min per
                        session
Langley et al, (76)   1 session      None        1, 2, 1
  1984
Mannheimer            15 sessions    None        1, 0, 0
  et al, (77) 1978      (one daily
                        5-min
                        session)

(a) TENS=transcutaneous electrical nerve stimulation, R=randomization:
2 points maximum (Jadad scale (33)), B=blinding: 2 points maximum
(Jadad scale (33)), W=withdrawals: 1 point maximum (Jadad scale (33)),
RCT=randomired controlled trial, RA=rheumatoid arthritis, Gr=group,
N/A=not available, MCP=metacarpophalangeal, PIP=proximal
interphalangeal, HF=high frequency, LF=low frequency. The data in this
table have been previously published in a table in another article
(Brosseau L., Yonge K, Marchand S, et al. Efficacy of transcutaneous
electrical nerve stimulation (TENS) for rheumatoid arthritis: a
systematic review. Physical Therapy Reviews. 2003;7:199-208) and are
used here with permission of the publisher.


Appendix 6.

Clinical Practice Guidelines

Low-level Loser Therapy (LLLT)

LLLT applied to the foot, knee, or hand versus a placebo, level I (RCT): grade A for pain at 3 months (clinically important benefit); grade C for function, tender joints, muscle force, and ROM at 3 and 6 months (no benefit). Patients with chronic RA.

Therapeutic Ultrasound

Therapeutic ultrasound performed on the hand in water versus a placebo, level I (RCT): grade A for tender joints at 10 weeks (clinically important benefit); grade C for swollen joints and morning stiffness at 10 weeks (no benefit). Patients with RA involving the hand (functional class I or II, chronic stage).

Thermotherapy

Cryotherapy applied to the knee joint versus a control, level I (RCT): grade C for thermographic index (measurement [in degrees Celsius] obtained using infrared thermography of the joint) at 5 days (na benefit). Patients with chronic RA, and with obvious effusion of joints.

Wax applied to the hand and wrist versus a control, level I (RCT): grade C for pain, ROM, muscle force, and function at 1 month (na benefit). Patients with functional class I or II with hands affected.

Wax applied to the hand or wrist and hand exercises versus a control, level I (RCT): grade A for ROM at 1 month (clinically important benefit), grade C+ for pain and stiffness at 1 month (clinical benefit), grade C for muscle force and function at 1 month (no benefit). Patients with functional class I or II with hands affected.

Transcutaneous Electrical Nerve Stimulation (TENS)

Low-frequency TENS applied to the hand and wrist versus no stimulation, level I (RCT): grade A for pain at 3 weeks (clinically important benefit), grade C+ for power at 3 weeks (clinical benefit), grade C for work at 3 weeks (no benefit). Patients with chronic RA.

High-frequency TENS applied to the hand and wrist versus placebo, level I (RCT): grade C for pain and joint tenderness, same day (no benefit). Patients with chronic RA.

High- versus low-frequency TENS applied to the hand and wrist, level I (RCT): grade C+ for global patient [(patient's assessment of overall disease activity or improvement).sup.33] at 2 weeks (clinical benefit). Patients with chronic RA.
Table 1.

Included Studies for Low-Level Laser Therapy (a)

                       Study
Study                  Design   Population        Outcomes

Goats et al (34)       RCT      RA affecting 2    Pain, function, knee
                                  or more           ROM, ankle ROM,
                                  tibiofemoral,     morning stiffness,
                                  talocrural,       rheumatoid factor
                                  subtalar, or      positive,
                                  MCP joints;       suprapatellor
                                  mean age:         swelling, and
                                  Gr1=57 y,         walking speed
                                  Gr2=74 y
Hall et al (35)        RCT      RA class II or    Pain, tender joints,
                                  III; active       function, MCP and
                                  synovitis of      PIP joint ROM,
                                  some or all       grip force, MCP
                                  of the MCP        and PIP joint
                                  and PIP           swelling, and
                                  joints; mean      morning stiffness
                                  age: Gr1=67.1     duration
                                  y, Gr2=60.9 y
Johannsen et al (36)   RCT      RA class I or     Pain, flexibility
                                  II; mean age:     (fingertip-to-palm
                                  Gr1=59 y,         distance), morning
                                  Gr2=62 y          stiffness not
                                                    improved, and grip
                                                    force
Palmgren et al (37)    RCT      RA class I or     Flexibility
                                  II; mean age:     (fingertip-to-palm
                                  Gr1 males=66      distance), morning
                                  y, Gr1            stiffness, grip
                                  females=61.1      force, PIP joint
                                  y, Gr2            swelling, and
                                  males=68 y,       morning stiffness
                                  Gr2               duration
                                  females=57.5
                                  y
Walker et al (38)      RCT      RA; mean age:     Pain
                                  Gr1=61.5 y,
                                  Gr2=60 7

(a) RCT=randomized controlled trial, RA=rheumatoid arthritis,
MCP=metacarpophalangeal, PIP=proximal interphalangeal, ROM=range
of motion, Gr1=group 1, Gr2=group 2.

Table 2.

Excluded Studies for Low-Level Laser Therapy (LLLT)

Study                  Reason for Exclusion

Asada et al (39)       No control group
Bliddal et al (40)     Subjects served as their own control--LLLT
                         potential systemic effect
Goldman et al (41)     Subjects served as their own control--LLLT
                         potential systemic effect
Heussler et al (42)    Subjects served as their own control--LLLT
                         potential systemic effect
Oyamada et al (43)     The abstract did not provide enough
                         statistical data to be analyzed
Walker et al (44)      Duplicate of Walker et al (38)

Table 3.

Included Studies for Therapeutic Ultrasound (a)

              Study
Study         Design   Population            Outcomes

Konrad (45)   RCT      Classical or          Change in the following:
                         definite RA of        ROM, grip force, number
                         both hands; pain,     of painful
                         swelling, and         articulations, number of
                         limitation of         swollen articulations,
                         movement              circumference of the PIP
                                               joints, and duration of
                                               morning stiffness

(a) RCT=randomized controlled trial, RA=rheumatoid arthritis,
PIP=proximal interphalangeal, ROM=range of motion.

Table 4.

Excluded Studies for Therapeutic Ultrasound

Study                         Reason for Exclusion

Berliner and Piegsa (46)      Subjects without known pathology or
                                impairments
Bromley et al (47)            Subjects without known pathology or
                                impairments
El-Hadidi and El-Garf (48)    Measures effect of medication
Hawkes et al (49)             Head-to-head study
Herrera-Lasso et al (50)      No patients with rheumatoid arthritis
Kitchen and                   Literature review
  Partridges (51)
Nykanen (52)                  No patients with rheumatoid arthritis

Table 5.

Included Studies for Thermotherapy (a)

                       Study
Study                  Design   Population        Outcomes

Bulstrode et al (53)   RCT      Classical or      Swelling/
                                  definite RA;      inflammation and
                                  effusion of 1     joint circumference
                                  or both knee
                                  joints
Dellhag et al (54)     RCT      RA class I and    Flexion and extension
                                  II and hand       of the dominant
                                  problems          hand (ROM), grip
                                  (decreased        force, pain
                                  ROM or grip       (nonresisted motion
                                  force); age:      with both hands),
                                  no older than     and stiffness (both
                                  70 y              hands)

(a) RCT=randomized controlled trial, RA=rheumatoid arthritis, ROM-range
of motion.

Table 6.

Excluded Studies for Thermotherapy

Study                           Reason for Exclusion

Abramson et al (55)             No clinical outcome
Amundson (56)                   Not a clinical trial
Bromley et al (47)              Subjects without known pathology or
                                  impairments
Curkovic et al (57)             No sufficient statistical data
Devereaux et al (58)            No control group
DonTigny and Sheldon (59)       No subjects with rheumatoid arthritis
Feibel and Fast (60)            Not a clinical trial
Haines (61)                     No subjects with rheumatoid arthritis;
                                  survey to estimate the number of
                                  hospitals that find it worthwhile to
                                  use cold therapy
Halliday et al (62)             No control group
Harris and Millard (63)         No description of the statistical
                                  procedure used, no P values, and no
                                  standard deviations available
Hawkes et al (62)               Head-to-head study
Hoyrup and Kjorvel (64)         Subjects with traumas
Ivey et al (65)                 Head-to-head study
Kirk and Kersley (66)           Head-to-head study
Mainardi et al (67)             No control group; subjects served as
                                  their own controls
Oosterveld et al (68)           Subjects without known pathology or
                                  impairments
Oosterveld and Rasker (69)      Mixed population, with rheumatoid
                                  arthritis in minority
Oosterveld and Rasker (70)      Literature review
Rembe (71)                      Patients postsurgery
Weinberger et al (72)           No clinical outcome
Whipple-Ellsworth et al (73)    Subjects without known pathology or
                                  impairments
Williams et al (74)             Head-to-head study

Table 7.

Included Studies for Transcutaneous Electrical Nerve Stimulation (a)

                        Study
Study                   Design   Population        Outcomes

Abelson et al (75)      RCT      Chronic RA and    Pain and muscle
                                   chronic wrist     force
                                   involvement;
                                   mean age:
                                   Gr1: 57 y,
                                   Gr2: 55 y
Langley et al (76)      RCT      Chronic RA with   Pain, joint
                                   hand              tenderness score,
                                   involvement       and number of
                                   and pain in 1     tender joints
                                   or both
                                   hands; mean
                                   age: Gr1=54.9
                                   y, Gr2=53.4 y
Mannheimer et al (77)   RCT      RA with           Patient global
                                   spontaneous       (patient's
                                   pain or pain      assessment of
                                   on resistance     overall disease
                                   from the          activity or
                                   wrist, MCP,       improvement (33)):
                                   and PIP           number of patients
                                   joints; age:      improved
                                   20-69 y

(a) RCT=randomized controlled trial, RA-rheumatoid arthritis,
MCP=metacarpophalangeal, PIP=proximal interphalangeal, Gr1=group 1,
Gr2=group 2.

Table 8.

Excluded Studies for Transcutaneous Electrical Nerve Stimulation

Study                      Reason for Exclusion

Angulo and Colwell (78)    Majority of subjects had osteoarthritis
Bruce et al (79)           Only 2 subjects per group
Herrera-Lasso et al (50)   No subjects with rheumatoid arthritis
Kumar and Redford (80)     Subjects served as their own control
Levy et al (81)            Not rheumatoid arthritis
                             population--rabbit joints
Moystad et al (82)         Data could not be used

Table 9.

Low-Level Laser Therapy (LLLT) Versus Placebo: Pain at 10 Weeks

                        Intervention                        No. of
Study                   Group           Outcome             Subjects

Goats et al (34)        LLLT            Pain 10-cm VAS      25
                        Placebo         Pain 10-cm VAS      10
Hall et al (35)         LLLT            Pain on activity    20
                                          10-cm VAS
                        Placebo         Pain on activity    20
                                          10-cm VAS
Walker et al (38)       LLLT            Pain 10-cm VAS      34
                        Placebo         Pain 10-cm VAS      38
Johannsen et al (36)    LLLT            Pain: 0-12 scale    10
                        Placebo         Pain: 0-12 scale    12

                                                    End-of-
                        Intervention    Baseline    Study      Absolute
Study                   Group           Mean        Mean       Benefit

Goats et al (34)        LLLT            5.52        5.16       -1.47
                        Placebo         4.83        5.94
Hall et al (35)         LLLT            5.20        4.00       -1.20
                        Placebo         4.30        4.30
Walker et al (38)       LLLT            4.58        3.67       -0.91
                        Placebo         5.21        5.21
Johannsen et al (36)    LLLT            7.00        4.50       -1.50
                        Placebo         6.50        5.50

                                        Relative
                                        Difference
                                        in Change
                        Intervention    From
Study                   Group           Baseline

Goats et al (34)        LLLT            -28%
                        Placebo
Hall et al (35)         LLLT            -25%
                        Placebo
Walker et al (38)       LLLT            -19%
                        Placebo
Johannsen et al (36)    LLLT            -22%
                        Placebo

(a) VAS=visual analog scale.

Table 10.

Low-Level Laser Therapy (LLLT) Versus Placebo: Fingertip-to-Palm
Distance

                      Intervention                            No. of
Study                   Group          Outcome               Subjects

Johannsen et al (36)    LLLT           Fingertip-to-palm     10
                                         distance (cm)
                        Placebo        Fingertip-to-palm     12
                                         distance (cm)
Palmgren et al (37)     LLLT           Finger pulp-to-palm   19
                                         distance (mm)
                        Placebo        Finger pulp-to-palm   16
                                         distance (mm)

                        Intervention   Baseline     End-of-Study
Study                   Group          Mean         Mean

Johannsen et al (36)    LLLT           0.25         0
                        Placebo        1            1.25
Palmgren et al (37)     LLLT           7            0
                        Placebo        5            6

                                                    Relative
                                                    Difference
                                                    in Change
                        Intervention   Absolute     from
Study                   Group          Benefit      Baseline

Johannsen et al (36)    LLLT           -0.5          -76%
                        Placebo
Palmgren et al (37)     LLLT           -8.0         -142%
                        Placebo

Table 11.

Low-Level Laser Therapy (LLLT) Versus Placebo: Grip Force

                       Intervention                         No. of
Study                  Group          Outcome               Subjects

Palmgren et al (37)    LLLT           Grip force (kPa) at   19
                                        10 wk
                       Placebo        Grip force (kPa) at   16
                                        10 wk
Hall et al (35)        LLLT           Grip force (mm Hg)    20
                                        at 10 wk
                       Placebo        Grip force (mm Hg)    20
                                        at 10 wk
Johannsen et al (36)   LLLT           Grip force (kg) at    10
                                        10 wk
                       Placebo        Grip force (kgl at    12
                                        10 wk

                       Intervention   Baseline       End-of-Study
Study                  Group          Mean           Mean

Palmgren et al (37)    LLLT            2.5             3.3
                       Placebo         2.1             1.8
Hall et al (35)        LLLT           80              86
                       Placebo        95             105
Johannsen et al (36)   LLLT           6.2              7
                       Placebo        5.3              6.5

                                                     Relative
                                                     Difference
                                                     in Change
                       Intervention   Absolute       From
Study                  Group          Benefit        Baseline

Palmgren et al (37)    LLLT            1.1           47%
                       Placebo
Hall et al (35)        LLLT           -4.0           -7% (favors
                                                       placebo)
                       Placebo

Johannsen et al (36)   LLLT           -0.4           -7% (favors
                                                       placebo)
                       Placebo

Table 12.

Ultrasound Versus Placebo: Grip Force, Range of Motion (ROM],
Swollen Joints, Tender Joints, and Morning Stiffness at 10 Weeks

               Intervention                             No. of
Study          Group          Outcome                   Subjects

Konrad (45)    Ultrasound     Painful articulations     25
                                (tender joints)
               Placebo        Painful articulations     25
                                (tender joints)
Konrad (45)    Ultrasound     Swollen articulations     25
                                (swollen joints)
               Placebo        Swollen articulations     25
                                (swollen joints)
Konrad (45)    Ultrasound     Morning stiffness         25
                                (min)
               Placebo        Morning stiffness         25
                                (min)
Konrad (45)    Ultrasound     Dorsal flexion of wrist   25
                                (ROM in degrees)
               Placebo        Dorsal flexion of wrist   25
                                (ROM in degrees)
Konrad (45)    Ultrasound     Grip force                25
               Placebo        Grip force                25

               Intervention   Baseline        End-of-Study
Study          Group          Mean            Mean

Konrad (45)    Ultrasound      6.2             4.8

               Placebo         6.2             6.0

Konrad (45)    Ultrasound      6.12            4.84

               Placebo         6.12            5.86

Konrad (45)    Ultrasound     69.6            31.4

               Placebo        69.6            59.94

Konrad (45)    Ultrasound     Not available   Not available

               Placebo        Not available   Not available

Konrad (45)    Ultrasound     Not available   Not available
               Placebo        Not available   Not available

                                              Relative
                                              Difference
                                              in Change
               Intervention   Absolute        From
Study          Group          Benefit         Baseline

Konrad (45)    Ultrasound     -1.20           -9%
               Placebo
Konrad (45)    Ultrasound     -1.02           -3%
               Placebo
Konrad (45)    Ultrasound     28.54           -41
               Placebo
Konrad (45)    Ultrasound      1.90
               Placebo
Konrad (45)    Ultrasound     28.07
               Placebo

Table 13.

Ice Packs Versus Control at 5 Days

                       Intervention                          No. of
Study                  Group           Outcome               Subjects

Bulstrode et al (53)   Ice packs       Thermographic index   15
                       Control         Thermographic index    9

                                                            Relative
                                                            Difference
                                                            in Change
                       Baseline   End-of-Study   Absolute   From
Study                  Mean       Mean           Benefit    Baseline

Bulstrode et al (53)   5.0        4.6            -0.3       -6%
                       5.3        5.2

Table 14.

Wax Only Versus Control at 1 Month: Range of Motion (ROM), Grip,
Pain, Stiffness (a)

                     Intervention                              No. of
Study                Group          Outcome                    Subjects

Dellhag et al (54)   E: Wax only    ROM: flexion in dominant   15
                                      hand (in millimeters)
                     C: Untreated   ROM: flexion in dominant   13
                                      hand (in millimeters)
Dellhag et al (54)   E: Wax only    Grip function test:        15
                                      0-80 points
                     C: Untreated   Grip function test:        13
                                      0-80 points
Dellhag et al (54)   E: Wax only    Pinch function test:       15
                                      0-32 points
                     C: Untreated   Pinch function test:       13
                                      0-32 points
Dellhag et al (54)   E: Wax only    Grip force (in newtons)    15
                                      (average of dominant
                                      hand)
                     C: Untreated   Grip force (in newtons]    13
                                      (average of dominant
                                      hand)
Dellhag et al (54)   E: Wax only    Pain on nonresisted        15
                                      motion: both hands,
                                      0-100-mm VAS
                     C: Untreated   Pain on nonresisted        13
                                      motion: both hands,
                                      0-100-mm VAS
Dellhag et al (54)   E: Wax only    Stiffness: both hands,     15
                                      0-100-mm VAS
                     C: Untreated   Stiffness: both hands,     13
                                      0-100-mm VAS

                     Intervention    Baseline      End-of-Study
Study                Group           Mean          Mean

Dellhag et al (54)   E: Wax only     43.0          42.9
                     C: Untreated    59.4          62.0
Dellhag et al (54)   E: Wax only     75.5          75.0
                     C: Untreated    75.2          75.0
Dellhag et al (54)   E: Wax only     29.3          28.3
                     C: Untreated    29.5          29.2
Dellhag et al (54)   E: Wax only     72.9          75.9
                     C: Untreated    82.6          85.4
Dellhag et al (54)   E: Wax only     20.3          25.9
                     C: Untreated    27.7          33.1
Dellhag et al (54)   E: Wax only     23.7          27.0
                     C: Untreated    36.0          30.2

                                                  Relative Difference
                     Intervention    Absolute     in Change From
Study                Group           Benefit      Baseline

Dellhag et al (54)   E: Wax only     -2.7         -5%
                     C: Untreated
Dellhag et al (54)   E: Wax only     -0.3         -1%
                     C: Untreated
Dellhag et al (54)   E: Wax only     -0.7         -2%
                     C: Untreated
Dellhag et al (54)   E: Wax only      0.2          0%
                     C: Untreated
Dellhag et al (54)   E: Wax only      0.2          1%
                     C: Untreated
Dellhag et al (54)   E: Wax only      9.1         31% (favors control)
                     C: Untreated

(a) E=experimental group, C=control group, VAS-visual analog scale.

Table 15.

Wax and Exercise Versus Control at 1 Month: Range of Motion (ROM),
Grip, Pain, Stiffness (a)

                     Intervention                             No. of
Study                Group                 Outcome            Subjects

Dellhag et al (54)   E: Wax and exercise   ROM: flexion       13
                                             in dominant
                                             hand (in
                                             millimeters)
                     C: Untreated          ROM: flexion       13
                                             in dominant
                                             hand (in
                                             millimeters)
Dellhag et al (54)   E: Wax and exercise   Grip function      13
                                             test: 0-80
                                             points
                     C: Untreated          Grip function      13
                                             test: 0-80
                                             points
Dellhag et al (54)   E: Wax and exercise   Pinch function     13
                                             test: 0-32
                                             points
                     C: Untreated          Pinch function     13
                                             test: 0-32
                                             points
Dellhag et al (54)   E: Wax and exercise   Grip force         13
                                             (in newtons)
                                             (average of
                                             dominant hand)
                     C: Untreated          Grip force         13
                                             (in newtons)
                                             (average of
                                             dominant hand)
Dellhag et al (54)   E: Wax and exercise   Pain on            13
                                             nonresisted
                                             motion: both
                                             hands,
                                             0-100-mm VAS
                     C: Untreated          Pain on            13
                                             nonresisted
                                             motion: both
                                             hands,
                                             0-100-mm VAS
Dellhag et al (54)   E: Wax and exercise   Pain on            13
                                             nonresisted
                                             motion: both
                                             hands,
                                             0-100-mm VAS
                     C: Untreated          Pain on            13
                                             nonresisted
                                             motion: both
                                             hands,
                                             0-100-mm VAS

                                                           End-of-
                     Intervention           Baseline       Study
Study                Group                  Mean           Mean

Dellhag et al (54)   E: Wax and exercise    62.3           52.1
                     C: Untreated           59.4           62.0
Dellhag et al (54)   E: Wax and exercise    72.3           74.8
                     C: Untreated           75.2           75.0
Dellhag et al (54)   E: Wax and exercise    27.4           29.3
                     C: Untreated           29.5           29.2
Dellhag et al (54)   E: Wax and exercise    72.4           79.2
                     C: Untreated           82.6           85.4
Dellhag et al (54)   E: Wax and exercise    29.3           22.1
                     C: Untreated           27.7           33.1
Dellhag et al (54)   E: Wax and exercise    39.3           24.9
                     C: Untreated           36             30.2

                                                           Relative
                                                           Diffe-
                                                           rence in
                                                           Change
                     Intervention           Absolute       From
Study                Group                  Benefit        Baseline

Dellhag et al (54)   E: Wax and exercise    -12.8          -21%
                     C: Untreated
Dellhag et al (54)   E: Wax and exercise      2.7            5%
                     C: Untreated
Dellhag et al (54)   E: Wax and exercise      2.2            8%
                     C: Untreated
Dellhag et al (54)   E: Wax and exercise      4              5%
                     C: Untreated
Dellhag et al (54)   E: Wax and exercise    -12.6          -44%
                     C: Untreated
Dellhag et al (54)   E: Wax and exercise     -8.6          -23%
                     C: Untreated

(a) E=experimental group, C=control group, VAS-visual analog scale.

Table 16.

Transcutaneous Electrical Nerve Stimulation (TENS) Versus
Control (No TENS): Pain at 3 Weeks (a)

                     Intervention                      No. of
Study                Group          Outcome            Subjects

Abelson et al (75)   TENS           Pain VAS 100 mm    18
                     Placebo        Pain VAS 100 mm    16

                     Intervention   Baseline           End-of-Study
Study                Group          Mean               Mean

Abelson et al (75)   TENS           60.5               18.5
                     Placebo        75.0               78.0

                                                       Relative
                                                       Difference
                                                       in Change
                     Intervention   Absolute           From
Study                Group          Benefit            Baseline

Abelson et al (75)   TENS           -45                -67%
                     Placebo

(a) VAS=visual analog scale.

Table 17.

Transcutaneous Electrical Nerve Stimulation (TENS) Versus
Control (No TENS): Power and Work Scores

                     Intervention                        No. of
Study                Group          Outcome              Subjects

Abelson et al (75)   TENS           Power (in watts)     18
                                      for hand muscles
                                      (not precise)
                                      at 3 wk
                     Placebo        Power (in watts)     16
                                      for hand muscles
                                      (not precise)
                                      at 3 wk
Abelson et a1 (75)   TENS           Work score           18
                                      (in joules) for
                                      hand muscles
                                      (not precise)
                                      at 3 wk
                     Placebo        Work score           16
                                      (in joules) for
                                      hand muscles
                                      (not precise)
                                      at 3 wk

                     Intervention     Baseline        End-of-Study
Study                Group            Mean            Mean

Abelson et al (75)   TENS             1.64            2.38
                     Placebo          1.91            1.67
Abelson et al (75)   TENS             0.82            0.96
                     Placebo          0.69            0.67

                                                      Relative
                                                      Difference
                                                      in Change
                     Intervention     Absolute        From
Study                Group            Benefit         Baseline

Abelson et al (75)   TENS             0.98            55
                     Placebo
Abelson et al (75)   TENS             0.16             5%
                     Placebo

Table 18.

High-Frequency Transcutaneous Electrical Nerve Stimulation (TENS)
Versus Placebo (No TENS): Joint Tenderness

                     Intervention                              No. of
Study                Group                 Outcome             Subjects

Langley et al (76)   High-frequency TENS   Joint tenderness    11
                                             scale
                                             (0-22) (a)
                     Placebo               Joint tenderness    11
                                           scale (0-22) (a)

                     Intervention          Baseline     End-of-Study
Study                Group                 Mean         Mean

Langley et al (76)   High-frequency TENS   28           15
                     Placebo               48           35

                                                        Relative
                                                        Difference
                                                        in Change
                     Intervention          Absolute     From
Study                Group                 Benefit      Baseline

Langley et al (76)   High-frequency TENS   0            0%
                     Placebo

(a) The scale from 0 to 22 is not consistent with baseline
and final scores >22.

Table 19.

High-Frequency Versus Low-Frequency Transcutaneous Electrical Nerve
Stimulation (TENS): Patient Global (Patient's Assessment of Overall
Disease Activity or Improvement (33) at 2 Weeks

                                                              No. of
                                                              Subjects
Author                  Group (a)                Outcome      Improved

Mannheimer et al (77)   E: High-frequency TENS   Patient      18
                                                 global;
                                                 number of
                                                 subjects
                                                 improved
                        C: Low frequency TENS    Patient      14
                                                 global;
                                                 number of
                                                 subjects
                                                 improved

                                                  Total   Risk
Author                  Group (a)                 N       Occurrence

Mannheimer et al (77)   E: High-frequency  TENS   19      95
                        C: Low frequency TENS     19      74%

                                                  Risk
Author                  Group (a)                 Difference

Mannheimer et al (77)   E: High-frequency  TENS   21%
                        C: Low frequency TENS

(a) E=experimental group, C = control group.


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To make random in arrangement, especially in order to control the variables in an experiment.
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Fictional characters
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LSW Light Support Weapon
LSW Least Significant Word
LSW Last Seen Wearing
LSW Long Suffering Wife
LSW Laboratory Safety Workshop
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Transdermal.
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A type of disease involving inflammation of muscles, joints, and other tissues.

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Treatment and care to combat disease or alleviate pain or injury. Its tools include drugs, surgery, radiation therapy, mechanical devices, diet, and psychiatry.
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Of, relating to, or characteristic of psoriasis.
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In an artificial environment outside a living organism.
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Of, near, or situated in the part of the back and sides between the lowest ribs and the pelvis.
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Lightning.



[Middle English levene, levin; see leuk- in Indo-European roots.]
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CWY Clearway (aviation) 
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Ottawa Panel Members:

Ottawa Methods Group:

Lucie Brosseau, PhD, Physiotherapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa, Ottawa, Ontario, Canada

George A Wells, PhD, Department of Epidemiology and Community Medicine, University of Ottawa

Peter Tugwell, MD, MSc, Centre for Global Health, Institute of Population Health, Ottawa, Ontario, Canada

Mary Egan, PhD, Occupational Therapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa

Claire-Jehanne Dubouloz, PhD, Occupational Therapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa

Lynn Casimiro, MA, Physiotherapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa

Vivian A Robinson, MSc, Centre for Global Health, Institute of Population Health

Lucie Pelland, PhD, Physiotherapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa

Jessie McGowan, MLIS MLIS Master of Library and Information Science
MLIS Multilingual Information Society
MLIS Molecular Laser Isotope Separation
MLIS Masters of Library and Information Studies
MLIS Medical/Legal Information Services
, Director, Medical Library Centre for Global Health, Institute of Population Health

External Experts:

Mary Bell

For other people named Mary Bell, see Mary Bell (disambiguation).


Mary Flora Bell (born on May 26 1957 in Newcastle upon Tyne, England) was convicted in December 1968 of the murders of two boys, Martin Brown (four years old) and Brian Howe
, MD (Rheumatologist rheumatologist /rheu·ma·tol·o·gist/ (roo?mah-tol´ah-jist) a specialist in rheumatology.

rheu·ma·tol·o·gist
n.
A specialist in the diagnosis and treatment of rheumatic disorders.
), Sunnybrook and Women's College Health Sciences Centre, Toronto, Ontario, Canada

Hillel M Finestone, MD (Physiatrist), Sisters of Charity of Ottawa Health Service, Ottawa, Ontario, Canada

France Legare, MD (Evidence-Based Practice in Family Medicine), University of Laval, Quebec Laval (pronounced ) is a city and a region in southwestern Quebec, Canada in the Greater Montreal Area. It is located on Île Jésus, across the Rivière des Prairies from Montreal.  City, Quebec, Canada

Catherine Caron, MD (Family Physician), Sisters of Charity of Ottawa Health Service

Sydney Lineker, PT, MSc, The Arthritis Society, Ontario Division, Research Co-ordinator, Toronto, Ontario, Canada

Angela Haines-Wangda, PT, MSc, Ottawa Hospital, General Campus, Ottawa, Ontario, Canada

Marion Russell-Doreleyers, PT who practices acupuncture acupuncture (ăk`ypŭng'chər), technique of traditional Chinese medicine, in which a number of very fine metal needles are inserted into the skin at specially designated points. , MSC, Canadian Physiotherapy Association and Ottawa Arthritis Rehabilitation and Education Program, Ottawa, Ontario, Canada

Martha Hall, OT, MPA MPA

medroxyprogesterone acetate.
, Canadian Association of Occupational Therapists and Ottawa Arthritis Rehabilitation and Education Program

Paddy Cedar cedar, common name for a number of trees, mostly coniferous evergreens. The true cedars belong to the small genus Cedrus of the family Pinaceae (pine family). , patient with rheumatoid arthritis (named with her written permission)

Assistant Manuscript Writer:

Marnie Lamb, MA, School of Rehabilitation Sciences, Faculty of Health Sciences, University of Ottawa

APTA APTA American Physical Therapy Association.  is a sponsor of the Decade, an international, multidisciplinary mul·ti·dis·ci·pli·nar·y  
adj.
Of, relating to, or making use of several disciplines at once: a multidisciplinary approach to teaching. 
 initiative to improve health-related quality of life for people with musculoskeletal disorders.

Address all correspondence and requests for reprints to: Lucie Brosseau, PhD, Physiotherapy Program, School of Rehabilitation Sciences, Faculty of Health Sciences, 451 Smyth Rd, University of Ottawa, Ottawa, Ontario, Canada K1H 8MS(lbrossea@uottawama).

This study was financially supported by The Arthritis Society (Canada); the Ontario Ministry of Health and Long-Term Care long-term care (LTC),
n the provision of medical, social, and personal care services on a recurring or continuing basis to persons with chronic physical or mental disorders.
 (Canada); the Career Scientist Salary Support Program, University of Ottawa for Dr Brosseau; the University Research Chair Program for Dr Brosseau; and the Ministry of Human Resources The fancy word for "people." The human resources department within an organization, years ago known as the "personnel department," manages the administrative aspects of the employees. , Summer Students Program (Canada).

Acknowledgments: The Ottawa Panel is indebted in·debt·ed  
adj.
Morally, socially, or legally obligated to another; beholden.



[Middle English endetted, from Old French endette, past participle of endetter, to oblige
 to Ms Catherine Lamothe, Ms Shannon Rees, Mr Shaun Cleaver, Ms Lucie Lavigne, Mr Guillaume Leonard, Ms Marie-Andree Ouimet, Mr Martin Campbell, Ms Isabelle Blais Isabelle Blais is a Canadian actress. Born in 1975 in Trois-Rivières, Quebec, she is a graduate of the Montreal Conservatory of Dramatic Arts. She quickly charmed critics by her stage interpretation of Juliette in Romeo and Juliette, and in 2001, won their attention for her role in , Ms Simon Barsoum, Ms Judith Robitaille, and Ms Karin Phillips for their technical support and help in data extraction Data extraction is the act or process of retrieving (binary) data out of (usually unstructured or badly structured) data sources for further data processing or data storage (data migration). .
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