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Transversus Abdominis Plane Versus Caudal Block for Pediatrics

Phase 1
Completed
Conditions
Lower Abdominal Surgery
Interventions
Other: Caudal block
Other: Transversus abdominis plane block
Registration Number
NCT02398123
Lead Sponsor
Mansoura University
Brief Summary

The transversus abdominis plane (TAP) block is a relatively simple technique that provides myocutaneous anesthesia that, as part of a multimodal analgesic treatment, may be useful in the prevention and treatment of parietal postoperative pain.

Initial experience with ultrasound TAP block demonstrated efficacy of the echo guided technique in different surgical procedures such as cesarean section, appendicectomy, laparoscopic cholecystectomy, infra umbilical surgery in adult and pediatric patients. Recently published clinical trials suggest that TAP block may represents an effective alternative to epidural anesthesia but further studies in larger population are necessary.

Transversus-abdominis plane (TAP) block was found to increase analgesic consumption low thoracic-epidural analgesia (TEA) in ischemic heart disease patients after abdominal laparotomy (2). Others found comparable results between continuous transversus abdominis plane technique and epidural analgesia in regard to pain, analgesic use and satisfaction after abdominal surgery(3). The TAP block affords effective analgesia with opioid sparing effects, technical simplicity, and long duration of action. Some disadvantages include the need for bilateral block for midline incisions and absence of effectiveness for visceral pain (4). TAP block has been associated with good pain relief and decreased intraoperative and postoperative opioids requirements after laparoscopic surgery (5). The analgesic efficacy of the TAP block has been demonstrated in prospective randomized trials compared with placebo, in different surgical procedures such as abdominal surgery, hysterectomy, retro pubic prostatectomy, Caesarean section, laparoscopic cholecystectomy, and appendicectomy (6, 7, 8, 9, 5 and 10 respectively). All these studies have reported superiority of the TAP block in terms of reduction in visual analogue scale scores and morphine consumption. In this study the investigators try to compare Transversus Abdominis Plane (TAP) blocks versus caudal block for postoperative pain control after lower abdominal surgeries in pediatrics.

Detailed Description

Children aged 1-7 years undergoing lower abdominal surgeries would be recruited in this randomized study.

Children would be monitored by electrocardiogram, pulse oximeter and non-invasive blood pressure.

After preoxygenation for three minutes, anesthesia would be induced with 8% sevoflurane inhalation in 33% oxygen and 66% nitrous oxide; 1ug/kg fentanyl is administered intravenously. Then laryngeal mask is inserted when conditions are satisfactory (jaw relaxed, lash reflex disappeared, no coughing, gagging, swallowing).

Anesthesia would be maintained with 2% sevoflurane and nitrous oxide.

An increase in blood pressure or heart rate by more than 15% from preoperative value was defined as insufficient analgesia and was treated with fentanyl 0.5 µ/kg. Saline dextrose5% (1:1) solution was infused in a dose of 12 ml/ kg /h.

Children were transferred from PACU to day-surgery unit (DSU) if they achieved Modified Aldrete Score of ten.

Patients received rectal paracetamol 15 mg/ kg every 6 hours. Tramadol 1mg/kg is rescue analgesic.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
28
Inclusion Criteria
  • Children
  • Lower abdominal surgery
Exclusion Criteria
  • Allergy to study medications
  • Contraindications to caudal block
  • Contraindications to transversus abdominis block

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Caudal blockCaudal blockCaudal block
Transversus abdominis plane blockTransversus abdominis plane blockTransversus Abdominis Plane block
Transversus abdominis plane blockBupivacaineTransversus Abdominis Plane block
Caudal blockBupivacaineCaudal block
Primary Outcome Measures
NameTimeMethod
Time for first analgesic request24 hours after surgery

By investigators until hospital discharge, then through telephone interview with parents after that

Secondary Outcome Measures
NameTimeMethod
Parent satisfaction scores24 hours after surgery

By investigators until hospital discharge, then through telephone interview with parents after that

Total opioid consumption24 hours after surgery

By investigators until hospital discharge, then through telephone interview with parents after that

Sedation level12 hours after surgery

Sedation level would be evaluated using a four-point sedation scale, 0=eyes open spontaneously, 1=eyes open to speech, 2=eyes open when shaken, 3=un arousable.

Modified Children's Hospital of Eastern Ontario Pain Scale (CHEOPS),2 h, 4 h, 6 h, 8 h, 10 h, 12 h, 18 h, 24 h after surgery

By investigators until hospital discharge, then through telephone interview with parents after that

Trial Locations

Locations (1)

Mansoura University

🇪🇬

Mansoura, DK, Egypt

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