The analgesic efficacy of ultrasound guided transversus abdominis plane (TAP) block after laparascopic appendicectomy in children: a prospective randomised trial

Authors
Category Primary study
Registry of TrialsANZCTR
Year 2008
INTERVENTION: All patients will receive a standardised general anaesthetic. This will involve a rapid sequence induction with propofol (3 mg/kg) by an intravenous injection and suxamethonium (1.5‐2 mg/kg) by an intravenous injection and continued paralysis with atracurium (initially 0.5 mg/kg intravenous followed by 0.2 mg/kg intravenous at approximately 30 minute intervals). Anaesthesia will be further maintained with nitrous oxide 70 % in O2 and sevoflurane (titrated to effect). All patients will receive intravenous (IV) fentanyl (1 mcg/kg) at the commencement of surgery and ondansetron (200 mcg/kg) to a maximum of 4 mg IV towards the end of the procedure. Standard monitoring including electrocardiogram, non‐invasive arterial blood pressure, arterial oxygen saturation and end tidal carbon dioxide monitoring will be used throughout. The surgical technique will also be standardised. All patients will have laparoscopy port sites infiltrated by the surgeons as per routine practice with 0.5 ml/kg of 0.2% Ropivacaine (1 mg/kg total ropivacaine). Technique for Ultrasound guided TAP block. Laparascopic appendicectomy requires that the TAP block be placed bilaterally. A 38 mm linear array Ultrasound probe transducer (Sonosite Micromaxx (Registered) SonoSite, Inc. 21919 30th Drive SE Bothell, WA) is placed in either flank with the probe orientated on a line joining the umbilicus and the 3rd / 4th lumbar vertebrae. A needle is advanced under aseptic conditions from an injection point on the antero‐lateral abdominal wall, at about the level of the umbilicus, in the plane of the ultrasound. The needle is advanced until the tip lies between the transversus abdominus and the internal oblique muscles. A total of 1 ml/kg of 0.2% ropivacaine (2 mg/kg total ropivacaine) is drawn up. Half of this volume is injected on the left hand side and the other half on the Right hand side. A remaining 0.5 ml/kg or 0.2 % ropivacaine (1 mg/kg total ropivacaine) will be available to the surgeons for infiltration of port sites. Total dose of ropivacaine will be restricted to 3 mg / kg in according with published dose recommendations. CONDITION: Post‐operative pain after laparscopic appendicectomy PRIMARY OUTCOME: Primary outcome: Reduced PCA morphine consumption in the first 16 hours from the completion of anaesthesia. INCLUSION CRITERIA: Any consented patient aged 7‐16 years who is scheduled for laparoscopic appendicectomy. Post‐operatively each patient will be prescribed intravenous Patient Controlled analgesia with morphine as per the Sydney Children’s Hospital protocol and regular paracetamol 15 mg/kg Per Orum every 4 hours. The Sydney Children's Hospital protocol is to draw up 750 microg / kg of morphine into a 50 ml syringe and dilute to 50 ml with normal saline. The patient will be prescribed 1 ml intravenous boluses as required with a machine lockout period of 5 minutes. This will mean that each bolus of intravenous morphine will be 15 microg/kg. There must be no background infusion on the Patient controlled analgesia (PCA). No other analgesics are to be prescribed during the first 16 hours post‐operatively unless commenced by the Acute Pain Service. Patients must also be prescribed post‐operatively ondansetron 200 microg/kg intravenous (to a maximum of 4 mg) every 8 hours when necessary. SECONDARY OUTCOME: Increased time from the completion of anaesthesia to the first dose of PCA morphine Increased time to first supplemental analgesia from the completion of anaesthesia Reduced morphine PCA consumption from 8 hours after the completion of anaesthesia to 16 hours after the completion of anaesthesia Reduced Pain in the recovery ward measured by VAS at the time of recovery ward discharge Reduced Pain measured by Visual analogue scale at 10 to 12 hours after the completion of anaesthesia Reduced Pain measured by Visual analogue scale at 6 to 8 hours after the completion of anaesthesia Reduced PCA morphine consumption in the first 8 hours after the completion of anaesthesia Reduced Postoperative vomiting and nausea measured by number of antiemtic administrations in the first 16 hours following completion of anaesthesia Reduced sedation scores at the time of recovery ward discharge Reduced time to Hospital discharge
Epistemonikos ID: 1eefd520750e76a5782c73e08122c933230baaae
First added on: Aug 21, 2024