Dosage adjustment in medical patients with renal impairment at Groote Schuur Hospital.Failure to adjust dosing of renally excreted drugs in patients with renal impairment may lead to adverse effects, including nephrotoxicity neph·ro·tox·ic·i·ty
The quality or state of being toxic to kidney cells.
nephrotoxicity(ne·fr . The incidence of in-hospital acute kidney injury attributed to drug nephrotoxicity is estimated at 19%.1 Drug-induced nephrotoxicity and adverse effects can be reduced by adjusting the dosing of renally excreted drugs according to the patient's estimated glomerular filtration rate The Estimated Glomerular Filtration Rate (eGFR) is a calculated estimate of the actual glomerular filtration rate and is based on your serum creatinine concentration; the calculation uses a formula that also can include your age, gender, height, and weight; in some formulas, race may also (eGFR), but this is often neglected by prescribers. In renally impaired patients, 29-74% of drug prescriptions requiring dose adjustment are not appropriately adjusted. (2-7)
We conducted a retrospective cross-sectional study to determine the prevalence of incorrect dosing of renally eliminated drugs among general medical patients with renal impairment at Groote Schuur Hospital 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. (GSH GSH reduced glutathione.
reduced glutathione. ), Cape Town. We aimed to determine what proportion of drugs prescribed to patients with renal impairment (defined as an eGFR of [less than or equal to]50 ml per minute per 1.73 m2) in the general medical wards required dose adjustment; and to determine whether drug doses were appropriately adjusted in these patients, using Drug Prescribing in Renal Failure renal failure
Acute or chronic malfunction of the kidneys resulting from any of a number of causes, including infection, trauma, toxins, hemodynamic abnormalities, and autoimmune disease, and often resulting in systemic symptoms, especially edema, as our reference for dose adjustments. (8)
We reviewed folders of all patients admitted to the general medical wards of GSH between 1 January and 31 March 2008. The serum creatinine concentration, measured on the day of admission to the medical ward, was extracted. If this had not been measured at that time, the creatinine result with which the patient was referred to the medical ward from casualty or a referring hospital was used. eGFR was calculated using the abbreviated Modification of Diet in Renal Disease Renal disease
Mentioned in: Glycogen Storage Diseases
hypertension High blood pressure Cardiovascular disease An abnormal ↑ systemic arterial pressure, corresponding to a systolic BP of > 160 mm Hg study equation (MDRD MDRD Modification of Diet in Renal Disease
MDRD Mobilization, Deployment, Redeployment and Demobilization
MdRD Median Round Delay
MDRD Maximum Deflection Ratio Detector ): eGFR=186 x [(Scr/88.4).sup.-1.154] x [(age).sup.-0.203] x (0.742 if female) x (1.212 if African-American). (9-11) This formula requires age, sex, creatinine and ethnicity as inputs. As recommended by the South African Renal Society, the adjustment factor recommended for African-American patients was included in the equation for black patients, and omitted in those of other ethnicity. (11) We categorised patient ethnicity as black if the patient was recorded as Xhosa-speaking in the admission record. We included all patients with renal impairment, defined as an eGFR [less than or equal to]50 ml per minute per 1.73 [m.sup.2], who received treatment in the medical ward for at least 1 day after a serum creatinine test was performed. Drug details were extracted from prescription charts on the day that the clinical notes indicated that the renal function was reviewed. When no mention of the renal function was made in the clinical notes, we extracted prescribed drugs from prescription charts at least 1 day after the serum creatinine was measured. This step ensured that prescribers had had a 1-day period after renal function was assessed in which to adjust drug doses. We used Drug Prescribing in Renal Failure to identify drugs requiring dose adjustment, and to determine if the appropriate dose adjustment for the patient's eGFR had occurred. (8)
Data management and analysis
Data from the patient folders were entered into an AccessTM database. Statistical analyses were performed using Stata 10.0 (Stata Corporation, College Station, Texas College Station is a city in Brazos County, Texas, situated in Central Texas. It is located in the heart of the Brazos Valley. The city is located within the most populated region of Texas, near to three of the 10 largest cities in the United States - Houston, Dallas, and San , USA). Numerical variables were summarised using median and range or interquartile range (IQR IQR Interquartile Range (statistics)
IQR Internet Quick Reference
IQR Individual Qualification Record
IQR Internal Quality Review ). Associations between categorical variables were explored using the chi-square test of association.
Ethical approval was obtained from the Human Research Ethics Committee of the Faculty of Health Sciences, University of Cape Town
“UCT” redirects here. For other uses, see UCT (disambiguation). .
Between January and March 2008, 433 patients were admitted to the general medical wards. We located and assessed 317 folders, of which 303 had complete notes. The eGFR was >50 ml per min per 1.73 [m.sup.2] in 204 patients, and 2 patients with renal impairment were transferred from the ward to the intensive care unit within 24 hours of admission. Therefore, 97 patients fulfilled our inclusion criteria and were included in the final analysis: 32% (97/301) of medical admissions.
The median age of patients with renal impairment was 46 years; 52% were female; the median number of drugs prescribed per patient was 6 (range 1-15) and 55% (53/97) had [greater than or equal to]5 drugs prescribed. The median eGFR was 19 ml per min per 1.73m2 (IQR 9-33), with a median creatinine of 448 [micro]mol/l (IQR 314-950) (Table I).
There were 615 prescription entries for the 97 patients with renal impairment. In total, 110 different drugs were prescribed, and some prescribed on multiple occasions. Dose adjustment was required in 19% (117/615) of prescription entries. Of the 117 prescription entries, only 37 were correctly dose adjusted (32%).
Co-amoxiclavulanic acid was the most frequently prescribed drug that required dose adjustment, which was done in 21% (5/24) of cases; followed by atenolol atenolol /aten·o·lol/ (ah-ten´ah-lol) a cardioselective ß used in the treatment of hypertension and chronic angina pectoris and the prophylaxis and treatment of myocardial infarction and cardiac arrhythmias. and gliclazide, adjusted in 26% (5/19) of cases and 25% (2/8) of cases respectively. Of the most frequently prescribed drugs, ethambutol ethambutol /etham·bu·tol/ (e-tham´bu-tol) an antibacterial, specifically effective against Mycobacterium; used with one or more other antituberculous drugs in the treatment of pulmonary tuberculosis, administered as the was the only drug correctly dose adjusted in all cases (6/6). Ciprofloxacin ciprofloxacin /cip·ro·flox·a·cin/ (sip?ro-flok´sah-sin) a synthetic antibacterial effective against many gram-positive and gram-negative bacteria; used as the hydrochloride salt.
n. and digoxin digoxin: see digitalis. both required dose adjustment in 5 cases, and remained unadjusted in all cases.
Of the 97 patients, 71% (69/97) received ?1 drug that required dose adjustment (median 1; range 1-5). Only 12% (8/69) of patients had all of their drugs correctly adjusted; 29% (20/69) of patients had some drugs correctly adjusted; 59% (41/69) of patients had no drugs correctly adjusted.
On univariate analysis, we found no association between dose adjustment and sex, age, extent of renal impairment or the number of prescription items. Nine patients were documented to have received dialysis before or on the day when the prescription was reviewed for dose adjustment. No patients receiving dialysis had all of their prescription items correctly adjusted, and 89% (8/9) had one or more inappropriately dosed prescription entries.
Renal impairment occurred in 32% (97/301) of patients admitted for [less than or equal to]24 hours in the general medical wards at GSH. Dose adjustment was required in 19% of prescription entries in patients with renal impairment, and only 32% of those prescriptions were correctly dose adjusted. One or more drugs requiring dose adjustment were prescribed to 71% (69/97) of patients with renal impairment. In most patients prescribed drugs requiring dose adjustment (59%), none was correctly adjusted. Worryingly, 8/9 dialysed patients had at least one prescription item incorrectly dosed.
To our knowledge, this is the first study in general medical patients with renal impairment of the frequency of dose adjustment of renally excreted drugs in South Africa. Our findings are in keeping with international studies, which found inappropriate dose adjustment in 29-74% of patients with renal impairment. (2-7)
Failure to adjust drug doses has several possible explanations. Prescribers might not review renal function results before prescribing. Reference texts to guide adjustment in renal impairment might not be freely available in the hospital wards. Prescribers who do not routinely check whether dose adjustment is required in patients with renal impairment might selectively adjust drugs that are well-known to require dose adjustment, and be unaware of the need for dose adjustment of other drugs. Prescribers might have used different methods from ours to calculate and define renal impairment, such as only using serum creatinine as an indicator of renal impairment rather than calculating the eGFR. This omission might have resulted in significant renal impairment being missed in lighter patients. The hospital laboratory does not routinely calculate creatinine clearances when a creatinine test is requested, and clinicians would therefore have to calculate the clearance themselves before prescribing. When calculating eGFR, prescribers might have used the Cockroft-Gault formula (eGFR=[(140-age) x weight]/ Scr x 0.85 if female) rather than the MDRD formula. (10) The Cockroft-Gault formula is unlikely to have been used to calculate eGFR in many of the patients in our study, because weight is a variable required when using the Cockroft-Gault formula, and weight was only documented in 60% of patients with renal impairment. Lastly, a critically ill patient may experience rapid changes in renal function, making eGFR extremely difficult and unreliable. The limitations of currently available eGFR equations have been widely acknowledged in patients with acute renal impairment. (12,13) Prescribers might have opted not to dose adjust in patients with acute deterioration in renal function, with the expectation that renal function would improve and out of concern for under-dosing.
Our study has limitations. It was conducted retrospectively so as not to influence prescribing habits. Retrospective data collection may be hampered by missing and incomplete data, and we could not locate folders in 30% of medical admissions, which decreased our sample size. However, the patients with missing folders are unlikely to have differed in any systematic way from patients whose folders were located. It is therefore unlikely that inability to locate their folders introduced bias. As the study was retrospective, we could not determine what method, if any, prescribers used to identify renal impairment and assess the severity of renal impairment in patients in our study. We used the internationally recommended MDRD formula, which includes an adjustment factor in the equation for African-Americans to estimate GFR GFR - Grim File Reaper . (10) The South African Renal Society recommends use of this adjustment factor in black African patients, and omission of the adjustment factor in patients of all other ethnic backgrounds. (11) As this was a retrospective chart review, we could not acquire self-defined ethnicity data, or data on ethnic ancestry, from patients. We therefore identified black African patients as those who were recorded as Xhosa-speaking on their admission records, which might have resulted in misclassification of some patients. To our knowledge, there are no data on performance of the MDRD formula in a southern African population, and there may be differences between our population and the population in which the formula was originally developed and validated. Dose adjustment in rapidly changing renal function is controversial, and some of the failure to dose adjust might have been due to prescribers electing not to adjust dosing during acute renal impairment. Our study design did not allow us to differentiate between acute and chronic renal impairment. Lastly, prescribers might have used a different reference source from that which we used.
Studies have suggested methods to improve adherence to dose adjustment recommendations in renal impairment. Computer-guided drug dosing for inpatients with renal impairment has been shown to result in an increase in correct dosing of renally eliminated drugs. (20) Automated eGFR reporting in renal function reports are already standard practice in many South African private laboratories and may alert the prescribing clinician to the presence of significant renal impairment.
We found that clinicians frequently neglected to adjust doses in renally impaired patients. Renal impairment is common in medical inpatients, and it is therefore important to increase awareness of the importance of dose adjustment and improve adherence to dose adjustment recommendations. Increasing availability of reference texts in medical wards, providing clinicians with an eGFR with all creatinine results, and electronic aids to identify drugs requiring dose adjustment, should be considered.
We thank Professor Charles Swanepoel for his input.
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(8.) Aronoff GR, Bennett WM, Berns JS, et al. Drug Prescribing in Renal Failure: Dosing Guidelines for Adults and Children. 5th ed. Philadelphia: American College of Physicians, 2007.
(9.) Levey AS, Coresh J, Greene T, et al. Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate glomerular filtration rate
n. Abbr. GFR
The volume of water filtered out of the plasma through glomerular capillary walls into Bowman's capsules per unit of time. . Ann Intern Med 2006; 145(4): 247-254.
(10.) National Kidney Foundation. KDOQI KDOQI Kidney Disease Outcomes Quality Initiative (National Kidney Foundation) 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. for Chronic Kidney Disease Chronic kidney disease (CKD), also know as chronic renal disease, is a progressive loss of renal function over a period of months or years through five stages. Each stage is a progression through an abnormally low and progressively worse glomerular filtration rate, which is : Evaluation, Classification, and Stratification. 2002. http://www.kidney.org/PROFESSIONALS/ kdoqi/guidelines_ckd/p5_lab_g4.htm (accessed 30 June 2008).
(11.) South African Renal Society. Guidelines for the Optimal Care of Patients on Chronic Dialysis in South Africa. 2006. www.kznhealth.gov.za/medicine/sars.pdf (accessed 30 June 2009).
(12.) DeBellis RJ, Smith BS, Cawley PA, Burniske GM. Drug dosing in critically ill patients with renal failure: a pharmacokinetic approach. J Intensive Care Med 2000; 15(6): 273-313.
(13.) Lameire N, Hoste E. Reflections on the definition, classification, and diagnostic evaluation of acute renal failure. Curr Opin Crit Care 2004; 10(6): 468-475.
(14.) Chertow GM, Lee J, Kuperman GJ, et al. Guided medication dosing for inpatients with renal insufficiency. JAMA 2001; 286(22): 2839-2844.
Accepted 14 January 2010.
Division of Clinical Pharmacology, Department of Internal Medicine, University of Cape Town and Groote Schuur Hospital, Cape Town
Eric Decloedt, MB ChB, BSc Pharmacol (Hons)
Rory Leisegang, MB ChB, BSc Eng (Hons)
Marc Blockman, MB ChB, MMed (Clin Pharmacol), BPharm, Dip Int Res Ethics
Karen Cohen cohen
(Hebrew: “priest”) Jewish priest descended from Zadok (a descendant of Aaron), priest at the First Temple of Jerusalem. The biblical priesthood was hereditary and male. , MB ChB, FCFP FCFP Fibre Channel Functional Profile
FCFP Fueled Clad Fabrication Process
FCFP Fellow of College of Family Physicians of Canada (SA), MSc (Epid), Dip HIV HIV (Human Immunodeficiency Virus), either of two closely related retroviruses that invade T-helper lymphocytes and are responsible for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is responsible for the vast majority of AIDS in the United States. Man, Dip Obst
Corresponding author: E Decloedt (firstname.lastname@example.org)
Table I. Patient characteristics (N=97) Sex 50 (52%) female Ethnicity 33 (34%) black Median age (IQR) 46 (23-79) years Median weight (IQR) 64 (54-73) kg * Median creatinine (IQR) 448 (314-950) [micro]mol/l Median GFR (IQR) 19.2 (8.9-33.1) ml/min/1.73 [m.sup.2] Median drugs 6 (1-15) prescribed (range) [greater than or equal to] 5 drugs per script 53/97 (55%) * Weight available for only 58/97 (60%) patients.