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CO2-Lasertonsillotomy Under Local Anesthesia in Adults
Published on: November 6, 2019
Ropivacaine Versus Bupivacaine in Pediatric Tonsillectomy: A Systematic Review and Meta-Analysis
Ebraheem Albazee1,2, Khaled Alenezi3, Abdulwahab Alkandari3
1Otorhinolaryngology-Head and Neck Surgery Kuwait Institute for Medical Specializations (KIMS) Kuwait City Kuwait.
Insights
Ropivacaine and bupivacaine provide similar pain relief after tonsillectomy in children. Ropivacaine showed a slight advantage in reducing pain at 24 hours post-surgery, with comparable safety profiles.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Pharmacology
Background:
- Tonsillectomy is a common pediatric surgical procedure.
- Postoperative pain management is crucial for recovery.
- Local anesthetic infiltration in the tonsillar fossa is a potential strategy for pain control.
Purpose of the Study:
- To compare the analgesic efficacy and safety of ropivacaine versus bupivacaine for local anesthetic infiltration in the tonsillar fossa during pediatric tonsillectomy.
- To evaluate postoperative pain scores, time to first analgesic requirement, and complication rates.
Main Methods:
- A systematic review and meta-analysis of eligible randomized controlled trials (RCTs) was conducted.
- Data sources included CENTRAL, PubMed, Web of Science, Scopus, and Google Scholar.
- Risk of bias was assessed using Cochrane's Risk of Bias Tool (RoB-2).
- Standardized mean difference (SMD) and risk ratio (RR) with 95% confidence intervals (CI) were used for data synthesis.
Main Results:
- Seven RCTs involving 375 pediatric patients were analyzed.
- No significant differences in pain scores were observed between ropivacaine and bupivacaine at 1, 2, 4, 6-8, and 12 hours post-tonsillectomy.
- Ropivacaine demonstrated a statistically significant superior analgesic effect at 24 hours post-surgery (SMD = -0.23, 95% CI [-0.43, -0.03]).
- Time to first analgesic requirement and complication rates were comparable between the two agents.
Conclusions:
- Ropivacaine and bupivacaine exhibit comparable clinical analgesic efficacy and safety profiles for local anesthetic infiltration in pediatric tonsillectomy.
- Ropivacaine may offer a slight advantage in pain reduction at 24 hours postoperatively.
Objective:
To evaluate the analgesic efficacy and safety of local anesthetic infiltration in the tonsillar fossa using ropivacaine compared to bupivacaine in pediatric patients undergoing tonsillectomy.
Data Sources:
CENTRAL, PubMed, Web of Science, Scopus, and Google Scholar.
Review Methods:
Eligible randomized controlled trials (RCTs) were evaluated for risk of bias using Cochrane's Risk of Bias Tool (RoB-2). The primary outcome was postoperative pain within the first 24 hours following tonsillectomy. Secondary outcomes included the time to first analgesic requirement and complication rates (ie, bleeding, airway obstruction, local anesthetic toxicity, and nausea). Data were synthesized using the standardized mean difference (SMD) for continuous outcomes and risk ratio (RR) for dichotomous outcomes, both reported with 95% confidence intervals (CI).
Results:
Seven RCTs with a total of 375 patients were analyzed. Regarding posttonsillectomy pain scores, there was no significant difference between ropivacaine and bupivacaine at 1 hour (SMD = -0.01, 95% confidence interval [CI] [-0.36, 0.34]), 2 hours (SMD = 0.03, 95% CI [-0.45, 0.51]), 4 hours (SMD = -0.17, 95% CI [-0.39, 0.06]), 6-8 hours (SMD = 0.04, 95% CI [-0.38, 0.46]), and 12 hours (SMD = -0.23, 95% CI [-0.62, 0.15]). However, at 24 hours, ropivacaine demonstrated a superior effect compared to bupivacaine (SMD = -0.23, 95% CI [-0.43, -0.03]). There was no significant difference between ropivacaine and bupivacaine in terms of time to first analgesia and complication rates (P > .05).
Conclusion:
This meta-analysis demonstrated that ropivacaine and bupivacaine offer comparable clinical analgesic efficacy and safety profiles in pediatric patients undergoing tonsillectomy.
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