Printer Friendly

Effect of adding intrathecal dexmedetomidine as an adjuvant to hyperbaric bupivacaine for elective cesarean section.


Subarachnoid block with 0.5% hyperbaric bupivacaine is the most commonly used anesthetic technique for lower segment cesarean section (LSCS). (1) Blockade to T4 dermatome is necessary to perform cesarean delivery without maternal discomfort. (2) This high level is commonly associated with hypotension and attendant decreased utero-placental perfusion. Reducing the volume of local anesthetic agent to avoid hypotension carries a risk of limited duration of action and hence lack of postoperative analgesia. (3) When only local anesthetic is used, postoperative opioid analgesic requirement is higher. (4)

[alpha]2 adrenergic receptor agonists due to their sedative, analgesic, perioperative sympatholytic and hemodynamic stabilizing properties may be useful as adjuvants to intrathecal local anesthetics. Intrathecal clonidine used in elective cesarean deliveries is shown to have anti-hyperalgesic and analgesic effects. (5) Dexmedetomidine, a highly selective [alpha]2 adrenergic receptor agonist is being safely used as an adjuvant for subarachnoid block in urological, orthopedic and lower abdominal surgical procedures. (6) But, its use with intrathecal local anesthetic agents for cesarean delivery has not been extensively studied. Hence, the present trial was conducted to study the efficacy of addition of dexmedetomidine to intrathecal hyperbaric bupivacaine for elective LSCS.


After institutional ethical committee approval, this prospective study was conducted in 60 parturients between ages of 18 to 35 years and a height of 150-170 cm with ASA physical status II undergoing elective LSCS under subarachnoid block in a tertiary care obstetric hospital attached to a medical college in south India.

Subjects with pre-existing medical and obstetric co morbidities, bleeding diatheses, local infection, raised intracranial pressure, known hypersensitivity to study drugs, patient refusal for spinal technique and emergency LSCS were excluded from the study.

Based on our pilot study, taking a difference in the duration of sensory and motor block of 30 min between the two groups as clinically significant, to have an 80% power in the present study with a simple stratified two sample t-based 95% confidence interval ([alpha] = 0.05), 26 parturients were to be recruited in each arm of the study. For adequate sampling size with dropout compensation, 60 subjects were recruited for the study and randomly divided into two groups with 30 parturients (n = 30) in each group by shuffled sealed envelope method to receive either 0.5% hyperbaric bupivacaine 9 mg (1.8 ml) with dexmedetomidine 5 [micro]g (0.2 ml) (Group D) or 0.5% hyperbaric bupivacaine 9 mg (1.8 ml) with 0.9% NaCl solution 0.2 ml (Group C).

Data were collected in pretested performa meeting the objectives of the study. Preoperative assessment was done for each patient and written informed consent was taken. All parturients were premedicated on the night before surgery with tablet ranitidine 150 mg, and kept nil per os after that. All patients were transported to OT in left lateral position where they were preloaded with Ringer's lactate 500 ml half an hour before anesthesia. All patients received preoperative aspiration prophylaxis with inj ranitidine 50 mg IV and inj metoclopramide 10 mg IV. Routine ASA monitoring was established.

The study drugs were prepared by the senior anesthesiologist who was not involved in further observations of the parturients. Under aseptic precautions, with patients in right lateral position, lumbar puncture (midline approach) was performed at the level of L3-L4 using 26 G Quincke spinal needles and study drug was injected by the principal investigator after confirmation of clear and free flow of cerebrospinal fluid. Sensory blockade was tested using pinprick method with a blunt 27G hypodermic needle every 15 sec till the onset of sensory blockade and thereafter at 2 min intervals till the maximum level of sensory blockade was achieved and subsequently at every 5 min during first 30 min, then at every 15 min up to 120 min, and thereafter at 30 min intervals until complete recovery. For the purpose of the present study, loss of pin prick sensation at T10 level was defined as the onset of sensory blockade. Time taken for maximum sensory blockade was defined as the time from the completion of the injection of the study drug to the maximum sensory blockade attained. Duration of sensory blockade was the time taken from the time of injection till the subject felt sensation at S1. Duration of pain relief was defined as the time from spinal injection to the first request for analgesics (VAS > 5). Inj diclofenac 75 mg IM was used as rescue analgesic with a maximum dose of 150 mg in 24 h.

Quality of motor blockade was assessed by modified Bromage scale. (7) Time for two segments sensory regression time, total duration of sensory and motor blockade and total duration of analgesia were noted. Hemodynamic parameters like heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial blood pressure (MAP), respiratory parameters like respiratory rate (RR) and Sp[O.sup.2], sedation score using Ramsay sedation score (RSS) were recorded every 2 min up to 10 min, every 5 min till 40 min, then every 10 min till the end of surgery. Any reduction of SBP more than 20% below baseline or fall in SBP less than 90 mmHg was considered as hypotension 3 mg IV increments if necessary. Neonatal APGAR scores were assessed by attending pediatrician at 1st and 5th min. Postoperative pain was assessed at 30 min, hourly for the next 6 h, and 2 hourly till 24 h using visual analogue scale (0-10) and time to rescue analgesic request were recorded. Subjects were also monitored for occurrence of adverse events after spinal injection like nausea, vomiting, desaturation, hypotension, bradycardia (requiring inj atropine), excessive sedation and others, if any.

Statistical analysis:

All the data were entered in Microsoft Excel and analysed using Statistical Package for Social Science (SPSS) version 22.0. Descriptive statistical methods were used to summarize the data. Student's t-test and Chi square test were used for continuous and categorical variables respectively. p < 0.05 was considered significant.


The parturients in both groups were comparable with respect to demographic characteristics. All the parturients completed the study (Table 1).

Sensory and motor blockade characteristics are shown in Table 2.

The mean time of onset of analgesia to T10 level was significantly faster in Group D compared to Group C (p < 0.001). The maximum sensory levels obtained in two groups were comparable and sufficient for the surgery (T3-T8). Peak sensory level was achieved earlier in Group D compared to Group C (p = 0.023). The mean time for two segment sensory regression was significantly prolonged in Group D compared to Group C (p < 0.001). The time taken for sensory regression of the blockade to S1 level was more in Group D compared to Group C (p < 0.001). Duration of analgesia was prolonged in Group D compared to Group C.

24 hours postoperative VAS scores were consistently low in Group D compared to Group C (Figure 1).

The time of onset of Bromage Grade I and IV motor block was rapid in Group D compared to Group C (p < 0.001). The duration of motor block was less in Group D than Group C (p < 0.001).

The RSS measured at various intervals in both groups were almost similar and all parturients had RSS [less than or equal to] 2. Neonatal APGAR scores at 1 and 5 min were comparable between Group D and Group C.

There were no significant alterations in the hemodynamic parameters (HR, SBP DBP and MAP) between the two groups. Variations in HR and MAP are shown in Figures 2 and 3

There was no significant difference between Group D and C with respect to respiratory rate, oxygen saturation (Sp[O.sub.2]) and the incidence of bradycardia and hypotension. The mean consumption of mephentermine and atropine for treatment of hypotension and bradycardia were similar and the differences were statistically not significant.

Both the groups were observed for occurrence of possible adverse effects like nausea, vomiting, pruritus, shivering and respiratory depression. Incidence of these adverse effects were low and not significant. (Table 3)


Neuraxial block for LSCS has become increasingly popular, as data indicating decreased maternal morbidity with regional anesthesia have accumulated. (8,9) In this era of advanced obstetric care, spinal anesthesia for LSCS continues to be the technique favoured by most anesthesiologists due to its ease and reliability, rapid onset of analgesia, motor blockade and muscle relaxation and also for having a definitive end point. (10) Although various local anesthetics can be used for spinal blockade, hyperbaric bupivacaine 10 to 15 mg is frequently used to achieve an adequate (T4) block level. In our institution, considering the patients' demographic profile and as proposed by Danelli G et al (11), 9 mg 0.5% hyperbaric bupivacaine is the dose of spinal local anesthetic used in parturients of height 150-170 cm.

The cesarean sections done under spinal anesthesia are often associated with visceral pain, nausea, and vomiting. (2) Studies have reported that in cesarean sections, spinal anesthesia, using only local anesthetic (without any additive) has a short duration of effect, and is insufficient for preventing the above side effects especially during uterine manipulation and peritoneum closure, and that it leads to postoperative analgesic requirement at an earlier stage. (12) Though a long acting local anesthetic with high-potency and differential sensorial-motor blockade, bupivacaine doesn't obliterate visceral pain and does not have advantage of prolonged postoperative analgesia. (13) Lipophilic opioids like fentanyl are commonly used adjuvants to overcome these shortcomings, but there are some concerns about disadvantages of opioids use in this setting. The use of non-selective [alpha]2-agonists like clonidine as intravenous adjuvants has shown to be without the side effects of opioids e.g. respiratory depression and pruritus, while providing improved perioperative analgesia and beneficial sedation. Clonidine has also been used intrathecally as an adjuvant with bupivacaine up to a dose of 1 [micro]g/kg in various surgeries and in parturients undergoing LSCS, without significant maternal and neonatal side-effects. (14,15) But, the usual dose of clonidine (15-150[micro]g) may be sometimes associated with bradycardia, hypotension and sedation. (4)

Dexmedetomidine is a highly selective [alpha]2-agonist with a selectivity ratio for the [alpha]2 receptor to [alpha]1 receptor of 1600:1, as compared with a ratio of 220:1 for clonidine. (16) It acts pre-junctional to reduce neurotransmitter release and post-junctional to cause hyperpolarization and reduction of impulse transmission. Intrathecal [alpha]2 receptor agonism in the dorsal horn of the spinal cord can produce anti nociceptive action for both somatic and visceral pain. (17) Highly selective [alpha]2 agonism of dexmedetomidine produces better hemodynamic stability and preserves baroreceptor reflex and heart rate response to pressors. (18)

Intravenous dexmedetomidine has been reported to produce favorable maternal and fetal outcome in labor analgesia and cesarean delivery. (19) No adverse effects were reported with the use of IV dexmedetomidine in a pregnant patient undergoing neurosurgery. (20) In a pregnant patient with Klippel-Feil syndrome with difficult airway, IV dexmedetomidine was successfully used to facilitate fiberoptic intubation before administration of general anesthesia without any untoward maternal and neonatal adverse effects. (21)

Ala-Kokko TI et al. working with clonidine and dexmedetomidine on isolated perfused human placenta observed that the highly lipophilic dexmedetomidine disappeared from maternal circulation earlier than clonidine but appeared in fetal circulation later than clonidine suggesting higher placental retention. (22) This may be advantageous in labor analgesia and anesthesia for cesarean delivery. As such, dexmedetomidine, by virtue of its increased [alpha]2 selectivity, limited effects on uteroplacental blood flow, and minimal placental transfer is advantageous over clonidine.

Intrathecal dexmedetomidine is an off label use. Fyneface-Ogan S. et al. using low dose bupivacaine and dexmedetomidine for single-shot intrathecal labor analgesia, observed that the combination produced prolonged analgesia without significant motor block. They reported no adverse neonatal effects. (23)

In various studies where intrathecal dexmedetomidine (dose ranging from 3 to 15 [micro]g) was used for orthopedic, endo-urological, lower abdominal and perianal surgeries no neurological symptoms or signs have been reported on short term follow up. (8,24,25)

The concerns about demyelination caused by high doses of epidurally administered dexmedetomidine in rabbits reported by Konakci S et al. in the year 200826 have been addressed well by Zhang H et al. in 2013. (27) They studied the molecular mechanisms underlying the analgesic property of intrathecal dexmedetomidine and evaluated its neurotoxicity in vivo and in vitro experimental study on mice. They observed that in addition to prolongation of analgesia, dexmedetomidine by itself may be neuroprotective and has a potential protective property on local anesthetic-induced neurotoxicity.

The optimal dose of intrathecal dexmedetomidine has not been established. Based on the effects on [alpha]2 receptors and the characteristics of neuraxial block when these two drugs are added as adjuvants, 3 [micro]g of dexmedetomidine is claimed to be equipotent to 30 [micro]g of clonidine intrathecally. (28) An optimal intrathecal dexmedetomidine dose necessary for sensory and motor blockade appears to be in between 2.5 [micro]g and 10 [micro]g, 5 [micro]g of dexmedetomidine being the optimum. (29,30) Hence for the present study we selected 5 [micro]g dexmedetomidine as adjuvant.

Our findings of rapid onset and delayed offset of sensory block with prolonged duration of analgesia are consistent with earlier studies. We also observed rapid onset of motor block. As most authors have defined onset of motor block as time taken to reach modified Bromage grade III block we could not compare our results with earlier studies. The mechanism of such faster onset is not well understood, but may be due to direct action of [alpha]-2 agonists on [micro]-motor neurons in ventral horn of spinal cord and facilitation of local anesthetic action. (31) We also found significant prolongation in duration of motor block which has been reported by most authors except Li Z et al.,32 who found no significant prolongation of motor block. The hemodynamic stability and minimal sedation with dexmedetomidine in the present study correlates with similar findings by other investigators. (30,32,33)

Neonatal assessment using APGAR scores at 1 and 5 min in both the groups in the present study were normal. Other researchers also found no significant effect of dexmedetomidine on APGAR scores and umbilical blood gas analysis. (23,30,32,33) No neurobehavioral scoring and umbilical artery blood gas analysis were conducted in this study as they are not routinely done in our institution.


To conclude, the results of the present study indicate that 5 [micro]g dexmedetomidine as an intrathecal adjuvant to 9 mg 0.5% hyperbaric bupivacaine for cesarean section is useful as it hastens the onset of sensory and motor block and prolongs postoperative analgesia and motor blockade, without producing significant hemodynamic changes, sedation and neonatal adverse effects.

Conflict of interest: None declared by the authors

Authors' contribution:

SMR: Conduction of the study work, data collection, preparation of manuscript

DG: Concept, review of articles, manuscript editing


(1.) Traynor AJ, Aragon M, Ghosh D, Choi RS, Dingmann C, Vu Tran Z, et al. Obstetric anesthesia workforce survey: A 30-year update. Anesth Analg. 2016;122(6):1939-46. doi: 10.1213/ANE.0000000000001204 [Free full text] [PubMed]

(2.) Braveman FR, Scavone BM, Blessing ME, Wong CA. Obstetrical anesthesia. Chapter 40 In Barash P, Cullen BF, Stoelting RK, Cahalan M, Stock MC, & Ortega R. Clinical Anesthesia. 7th ed. Lippincott Williams and Wilkins; 2013;1144-1177.

(3.) Agarwal A, Kishore K. Complications and controversies of regional anesthesia: A review. Indian J Anaesth 2009;53:543-53. [PubMed] [Free full text]

(4.) Elia N, Culebras X, Mazza C, Schiffer E, Tramer MR. Clonidine as an adjuvant to intathecal local anesthetics for surgery: Systematic review of randomized trials. Reg Anesth Pain Med 2008;33(2):159-67. DOI: 10.1016/j.rapm.2007.10.008 [PubMed]

(5.) Lavand'homme PM, Roelants F, Waterloos H, Collet V, De Kock MF. An evaluation of the postoperative antihyperalgesic and analgesic effects of intrathecal clonidine administered during elective cesarean delivery. Anesth Analg. 2008;107(3):948-55. DOI: 10.1213/ ane.0b013e31817f1595 [PubMed] [Free full text]

(6.) Wu H-H, Wang H-T, Jin J-J, Cui G-B, Zhou K-C. Does dexmedetomidine as a neuraxial adjuvant facilitate better anesthesia and analgesia? a systematic review and meta-analysis. PLoS One. 2014;9(3):e93114. DOI: 10.1371/journal.pone.00931 14 [PubMed] [Free full text]

(7.) Al-Ghanem SM, Massad IM, AlMustafa MM, Al-Zaben KR, Qudaisat IY Qatawneh AM, et al. Effect of adding dexmedetomidine versus fentanyl to intrathecal bupivacaine on spinal block characteristics in gynecological procedure. Amer Jour of Appl Scien 2009;6(5):882-7. DOI : 10.3844/ajassp.2009.882.887

(8.) Hawkins JL, Chang J, Palmer SK, et al. Anesthesia-related maternal mortality in the United States: 1979-2002. Obstetric Gynecol. 2011;117:69-74. DOI: 10.1097/ AOG.0b013e31820093a9 [PubMed] [Free full text]

(9.) Sia AT, Fun WL, Tan TU. The ongoing challenges of regional and general anaesthesia in obstetrics: Best Pract Res Clin Obstet Gynaecol. 2010;24(3):303-12. DOI: 10.1016/j. bpobgyn.2009.12.001 [PubMed]

(10.) Chestnut DH, Wong CA, Tsen LC, Kee WDN, Beilin Y Mhyre JM, et al. Anesthesia for cesarean delivery. Chapter 26. In: (Eds). Chestnut's Obstetric Anesthesia: Principles and Practice, Philadelphia: Elsevier Saunders. 2014;545-603.

(11.) Danelli G, Zangrillo A, Nucera D, Giorgi E, Fanelli G, Senatore R, et al. The minimum effective dose of 0.5% hyperbaric spinal bupivacaine for cesarean section. Minerva Anesthesiol. 2001;67:573-7. [PubMed]

(12.) Roofthooft E, Van de Velde M. Lowdose spinal anaesthesia for caesarean section to prevent spinal-induced hypotension. Curr Opin Anaesthesiol. 2008;21(3):259-62. DOI: 10.1097/ ACO.0b013e3282ff5e41 [PubMed]

(13.) Berde CB, & Strichartz GR. Local Anesthetics, Chapter 36. In: Miller RD, Cohen NH, Eriksson LI, Fleisher LA, Weiner-Kronish JP &Young WL. (Eds). Miller's Anesthesia. Philadelphia: Elsevier Saunders; 2015;8(1):120534.

(14.) van Tuijl I, van Klei WA, van der Werff DB, Kalkman CJ. The effect of addition of intrathecal clonidine to hyperbaric bupivacaine on postoperative pain and morphine requirements after caesarean section: a randomized controlled trial. Br J Anaesth 2006;97(3):365-70. DOI: 10.1093/ bja/ael182 [PubMed] [Free full text]

(15.) Kothari N, Bogra J, Chaudhary AK. Evaluation of analgesic effects of intrathecal clonidine along with bupivacaine in cesarean section. Saudi J Anaesth 2011 Jan-Mar; 5(1):31-5. DOI: 10.4103/1658-354X. 76499 [PubMed] [Free full text]

(16.) Vuyk J, Sitsen E,& Reekers M.(2015) Intravenous Anesthetics, Chapter 36. In: Miller RD, Cohen NH, Eriksson LI, Fleisher LA, Weiner-Kronish JP &Young WL. (Eds). Miller's Anesthesia. Philadelphia: Elsevier Saunders. 2015;8(1): 957-1008.

(17.) Liu YL, Zhou LJ, Hu NW, Xu JT, Wu CY Zhang T, et al. Tumor necrosis factor alpha induces long-term potentiation of C-fiber evoked field potentials in spinal dorsal horn in rats with nerve injury: the role of NF-kappa B, JNK and p38 MAPK. Neuropharmacology. 2007;52:708-15. DOI: 10.1016/j. neuropharm.2006.09.011 [PubMed]

(18.) Bajwa SJ, Kulshrestha A. Dexmedetomidine: An adjuvant making large inroads into clinical practice. Ann Med Health Sci Res. 2013;3(4):47583. DOI: 10.4103/2141-9248.122044 [PubMed]

(19.) Palanisamy A, Klickovich RJ, Ramsay M, Ouyang DW, Tsen LC. Intravenous dexmedetomidine as an adjunct for labor analgesia and cesarean delivery anesthesia in a parturient with a tethered spinal cord. Int Journ Obstet Anesth. 2009;18(3):258-61. DOI: 10.1016/j.ijoa.2008.10.002 [PubMed]

(20.) Souza KM, Anzoategui LC, Pedroso WCJ, Gemperli WA. Dexmedetomidine in general anesthesia for surgical treatment of cerebral aneurysm in pregnant patient with specific hypertensive disease of pregnancy case report. Rev Bras Anestesiol. 2005;55(2):212-6. [PubMed]

(21.) Shah T, Badve M, Olajide K, Skorupan H, Waters J, Vallejo M. Dexmedetomidine for an awake fiber-optic intubation of a parturient with Klippel-Feil syndrome, Type I Arnold Chiari malformation and status post released tethered spinal cord presenting for repeat cesarean section. Clin and Practi. 2011;1(3):116-8. DOI: 10.4081/cp.2011.e57 [PubMed]

(22.) Ala-Kokko TI, Pienimaki P Lampela E, Hollmen AI, Pelkonen O, Vahakangas K. Transfer of clonidine and dexmedetomidine across the isolated perfused human placenta. Acta Anaesth Scand. 1997;41 (2):313-9. [PubMed]

(23.) Ogan SF, Job OG, Enyindah CE. Comparative Effects of Single Shot Intrathecal Bupivacaine with Dexmedetomidine and Bupivacaine with Fentanyl on Labor Outcome. ISRN Anesthesiology. 2012;816984:1-6. [Free full text]

(24.) Nayagam HA, Singh NR, Singh HS. A prospective randomised double blind study of intrathecal fentanyl and dexmedetomidine added to low dose bupivacaine for spinal anesthesia for lower abdominal surgeries. Indian J Anaesth. 2014; 58(4):430-5. DOI: 10.4103/0019-5049.138979 [PubMed] [Free full text]

(25.) Nethra SS, Sathesha M, Dixit A, Dongare PA, Harsoor SS, Devikarani D. Intrathecal dexmedetomidine as adjuvant for spinal anaesthesia for perianal ambulatory surgeries: A randomised double-blind controlled study. Indian J Anaesth. 2015;59(3):177-81. DOI: 1 0.41 03/001 9-5049.153040 [PubMed] [Free full text]

(26.) Konakci S, Adanir T, Yilmaz G, Rezanko T. The efficacy and neurotoxicity of dexmedetomidine administered via the epidural route. Eur J Anaesthesiol. 2008; 25(5):403-9. DOI: 10.1017/ S0265021507003079 [PubMed]

(27.) Zhang H, Zhou F, Li C, Kong M, Liu H, Zhang P et al. Molecular mechanisms underlying the analgesic property of intrathecal dexmedetomidine and its neurotoxicity evaluation: an in vivo and in vitro experimental study. PLoS One. 2013; 8(2):e55556(1-8). DOI: 10.1371/journal. pone.0055556 [PubMed] [Free full text]

(28.) Kanazi GE, Aouad MT, Jabbour-Khoury SI, Al Jazzar MD, Alameddine MM, Al-Yaman R, et al. Effect of low dose dexmedetomidine or clonidine on the characteristic of bupivacaine spinal block. Acta Anaesth Scand. 2006;50(2):222-7. DOI: 10.1111/j.1399-6576.2006.00919.x [PubMed]

(29.) Sullivan AF, Kalso EA, McQuay HJ, Dickenson AH. The antinociceptive actions of dexmedetomidine on dorsal horn neuronal responses in the anaesthetized rat. Eur J Pharmacol. 1992;215(1):127-33. [PubMed]

(30.) Mahdy WR, Abdullah SI. Effect of adding dexmedetomidine versus fentanyl to intrathecal bupivacaine on spinal block characteristics and neonatal outcome in uncomplicated cesarean delivery: a randomized double blind placebo controlled study. Meno Med Journ. 2011;24(1):221 32.

(31.) Yoshitomi T, Kohjitani A, Maeda S, Higuchi H, Shimada M, Miyawaki T. Dexmedetomidine enhances the local anesthetic action of lidocaine via an alpha-2A adrenoceptor. Anesth Analg. 2008;107(1):96-101. DOI: 10.1213/ ane.0b013e318176be73 [PubMed] [Free full text]

(32.) Li Z, Tian M, Zhang CY Li AZ, Huang AJ, Shi CX, et al. A randomised controlled trial to evaluate the effectiveness of intrathecal bupivacaine combined with different adjuvants (fentanyl, clonidine and dexmedetomidine) in caesarean section. Drug Res. 2015;65(11):5816. DOI: 10.1055/s-0034-1395614 [PubMed]

(33.) Sun Y, Xu Y, Wang GN. Comparative evaluation of intrathecal bupivacaine alone, bupivacaine-fentanyl, and bupivacaine dexmedetomidine in caesarean section. Drug Res. 2015;65(9):468-72. DOI: 10.1055/s0034-1387740 [PubMed]

Sushruth MR [1], Dinesh Govinda Rao [2]

[1] Senior Resident, Department of Anesthesiology, JSS Medical College, Mysore, Karnataka (India)

[2] Associate Professor, Department of Anesthesiology, Mysore Medical College, Mysore, Karnataka (India)

Correspondence: Dr Dinesh Govinda Rao, Associate Professor, Department of Anaesthesia, MMCRI, Mysore, Karnataka 570005 (India); Phone: 9845582006; E-mail:

Received: 07 May 2018

Reviewed: 19 May, 27 May, 30 May, 2 Jun 2018

Corrected: 19 Jun 2018

Revised: 23 Jun 2018

Accepted: 14 Aug 2018

Caption: Figure 1: Mean VAS scores for 24 hours in two groups

Caption: Figure 2: Comparative mean heart rates in two groups

Caption: Figure 3: Comparative mean arterial pressures in two groups
Table 1: Demographic characteristics

Variable                       Group D              Group C

Mean Age (y)              24.6 [+ or -] 2.9    25.2 [+ or -] 3.8
Mean Weight (kg)          59.7 [+ or -] 6.3    59.8 [+ or -] 5.6
Mean Height (cm)          155.9 [+ or -] 4.4   156.3 [+ or -] 4.5
Mean BMI (kg/[m.sup.2])    24.6 [+ or -] 2     24.4 [+ or -] 2.9

Variable                  p-value

Mean Age (y)               0.45
Mean Weight (kg)           0.95
Mean Height (cm)           0.73
Mean BMI (kg/[m.sup.2])    0.82

Table 2: Comparative block characteristics in two groups

Block Characteristics         Group D                Group C

Time for onset of         45 [+ or -] 11.3       68 [+ or -] 11.3
analgesia (sec)

Maximum sensory          T 5.6 [+ or -] 1.2     T5.7 [+ or -] 1.4

Time to peak sensory     3.98 [+ or -] 1.8      4.98 [+ or -] 1.6
level (min)

Time for two segment     140 [+ or -] 12.3      44.15 [+ or -] 6.5
sensory regression

Time taken for           364 [+ or -] 48.2      126.3 [+ or -]12.4
sensory regression
to S1 (min)

Duration of             420.3 [+ or -] 74.6     68.9 [+ or -] 11.1
analgesia (min)

Time for onset of        42.8 [+ or -] 15.6      67 [+ or -] 15.8
motor block (sec)

Time for maximum          3.8 [+ or -] 0.8       7.7 [+ or -] 2.8
motor block (min)

Duration of motor        341 [+ or -] 39.9     113.2 [+ or -] 11.6
block (min)

Block Characteristics   p-value

Time for onset of       < 0.001
analgesia (sec)

Maximum sensory          0.77

Time to peak sensory     0.023
level (min)

Time for two segment    < 0.001
sensory regression

Time taken for          < 0.001
sensory regression
to S1 (min)

Duration of             < 0.001
analgesia (min)

Time for onset of       < 0.001
motor block (sec)

Time for maximum        < 0.001
motor block (min)

Duration of motor       < 0.001
block (min)

Table 3: Comparative frequency of adverse effects in the

Adverse effects    Group D     Group C    p-value
                    n (%)       n (%)

Hypotension       8 (26.7)    8 (26.7)       1
Shivering             0        1 (3.3)      .32
Bradycardia        6 (20)      6 (20)        1
Pain                  0        3 (10)      0.07
Total             14 (46.7)   17 (56.7)    0.17
COPYRIGHT 2018 Anaesthesia, Pain and Intensive Care
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Sushruth, M.R.; Rao, Dinesh Govinda
Publication:Anaesthesia, Pain & Intensive Care
Article Type:Report
Date:Jul 1, 2018
Previous Article:Paraphenylenediamine poisoning: clinical features, complications and outcome in a tertiary care institute.
Next Article:Effects of ultrasound-guided intraarticular botox vs. corticosteroids for shoulder osteoarthritis.

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters