COMPARISON OF THE COMBINATION OF CAUDALLY ADMINISTERED BUPIVACAINE AND RECTALLY ADMINISTERED DICLOFENAC WITH CAUDALLY ADMINISTERED BUPIVACAINE ALONE FOR POSTOPERATIVE HERNIOTOMY PAIN MANAGEMENT IN CHILDREN

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COMPARISON OF THE COMBINATION OF CAUDALLY ADMINISTERED BUPIVACAINE AND RECTALLY ADMINISTERED DICLOFENAC WITH CAUDALLY ADMINISTERED BUPIVACAINE ALONE FOR POSTOPERATIVE HERNIOTOMY PAIN MANAGEMENT IN CHILDREN

ABSTRACT

The use of caudally administered bupivacaine is a standard practice of providing

perioperative analgesia for children undergoing infraumbilical procedures. However, the

duration of action of caudal bupivacaine is relatively short. Methods to prolong the duration of

action of bupivacaine include co-administration of caudal bupivacaine and preservative-free

drugs like opioids, ketamine and clonidine. But the side-effects of such mixtures make the use

of alternative methods imperative.

The use of rectal diclofenac as adjunct to caudal bupivacaine might provide superior quality

of postoperative analgesia compared to caudal bupivacaine alone, with relatively less side

effects. It was therefore hypothesised that the combination of caudally administered

bupivacaine and rectal diclofenac would provide a better quality of postoperative analgesia

than caudal bupivacaine alone. The aim of this study therefore, was to compare the quality of

postoperative analgesia achieved with the combination of caudally administered bupivacaine

and rectally administered diclofenac to caudally administered bupivacaine alone in children

undergoing herniotomy.

Following the institution’s Ethics Committee approval, 62 patients aged between 1 and

6 years scheduled for herniotomy were recruited and randomised to two groups (31 in each

group). Baseline haemodynamic parameters were recorded and anaesthesia was induced with

halothane in 100% oxygen using facemask. Plain bupivacaine 1ml/kg of 0.25% was caudally

administered in group I patients. Group II patients received a combination of caudal

bupivacaine 1ml/kg of 0.25% and rectal diclofenac 1mg/kg.

Anaesthesia was maintained with halothane 0.5 to 1.5% in 100% oxygen with patients

breathing spontaneously. Intraoperative haemodynamic parameters were monitored.

Postoperative pain was assessed for 24 hours using the Objective Pain Scale. The primary

outcome measure was the proportion of pain-free patients at pain assessment intervals. Data

were analysed using SPSS 11.0. Continuous data were compared using t-test while categorical

data were compared using Fisher’s exact test. P-values < 0.05 were considered significant.

There was no difference in the proportion of pain-free patients in both groups in the first 4

hours observation period. However, significant difference in the proportion of patients who

were pain-free was first observed at 6 hours postoperatively with eleven patients (35.48%) in

group I and 29 (93.5%) in group II having no pain (P <0.001). At 12 hours, 15 patients (48.38%)

were pain free in group I as against 25 (80.64%) in group II (P=0.02). No difference was

observed between both groups at 24 hours (P=0.24).

Time to first analgesic requirement was 6.83±2.67 hours in group I and 14.03 ± 2.51 hours

in group II with a marked significant difference (P <0.001). The mean paracetamol

consumption in 24 hours was significantly higher in group I (532.90±119.05mg) compared to

311.60 ±71.28mg in group II (P <0.001). The frequency of paracetamol administration was

more in group I (3.32 ±0.48) as against 2.06±0.25 in group II (P <0.001). However, changes in

the intraoperative haemodynamic parameters were comparable in both groups. The incidence

of complications were also similar in both groups (p=1.00).

This study showed that the use of the combination of caudally administered bupivacaine

and rectally administered diclofenac is superior to caudally administered bupivacaine alone for

postoperative analgesia in patients undergoing herniotomy

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