A meta-analysis on the effectiveness of postoperative analgesia with intrathecal nalbuphine versus intrathecal fentanyl as neuraxial adjuvants in cesarean section.
Aileen P Balatbat | Joy Ann R Lim
Discipline: medicine by specialism
Abstract:
Background: Inadequately treated postoperative pain can contribute significantly to morbidity in
women undergoing cesarean section. Recent studies showed that nalbuphine and fentanyl has promising
result as neuraxial adjuvants in terms of postoperative analgesia and with lower incidents of adverse
effect when use in cesarean section.
Objective: To compare postoperative analgesia with intrathecal nalbuphine versus intrathecal fentanyl
as neuraxial adjuvants in cesarean section.
Methods: A meta-analysis following the PRISMA guidelines was performed. Articles were searched
through the Cochrane Library, PubMed.Gov and Pubmed Central, Google Scholar, HERDIN, WPRIM
and ProQuest Guideline Central using different search strategies such as keywords and MeSH term.
Cochrane version 2 risk-of-bias tool for randomized trials (RoB 2) was used to assess for quality.
Quantitative data were pooled and analyzed using Review Manager 5.4.
Results: A total of four trials, involving 425 full term pregnant women were compared. The pooled mean
difference showed significantly longer duration of postoperative analgesia (MD=21.12 minutes,
95%CI=11.13,31.11, I2=73%), pooled risk ratio showed lesser risk for pruritus (RR=0.09,
95%CI=0.02,0.50, I2 = 0%) and postoperative nausea and vomiting (RR=0.38, 95%CI= 0.19,0.78, I2 =
11%) who received intrathecal nalbuphine compared to intrathecal fentanyl.
Conclusions: The results of this meta-analysis demonstrates that the use of intrathecal nalbuphine
appears to have longer duration of postoperative analgesia and lesser incidence of PONV and pruritus
than fentanyl. However, due to the presence of heterogeneity it warrants that the results should be treated
with caution especially with the possibility of publication bias.
Recommendations: Better literature search through inclusion of high-quality studies from relevant
databases and strict adherence on the uniformity of the dosage and methods used are very crucial to
achieve the target clinical outcomes and minimize the publication bias.
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