Efficacy and safety of extended-release dinalbuphine sebacate for postoperative analgesia: A systematic review and meta-analysis

被引:0
作者
Hsieh, Yu-Lien [1 ]
Wang, Chi-Fei [1 ]
Lin, Chung-Ren [1 ,2 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Anesthesiol, Tainan, Taiwan
[2] Natl Cheng Kung Univ Med Coll & Hosp, Dept Anesthesiol, 138 Sheng Li Rd, Tainan 704, Taiwan
关键词
Analgesia; Dinalbuphine sebacate; Postoperative pain; PATIENT-CONTROLLED ANALGESIA; INTRAMUSCULAR INJECTION; LAPAROSCOPIC CHOLECYSTECTOMY; PAIN MANAGEMENT; ADVERSE EVENTS; MORPHINE; NALBUPHINE; RATIO;
D O I
10.1097/FS9.0000000000000154
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundMultimodal analgesia, which combines multiple medications with different analgesic mechanisms, is recommended for optimizing postoperative pain control and minimizing opioid-related side effects. Dinalbuphine sebacate (DNS), a prodrug of nalbuphine, has a 7-day long-acting analgesic effect on moderate to severe postoperative pain. We conducted a systematic review and meta-analysis to analyze the efficacy and safety of DNS for postoperative pain management.Materials and MethodsWe systematically searched PubMed, EMBASE, and the Cochrane Central Register of Controlled Trials to identify randomized controlled trials of DNS for postoperative analgesia. We assessed the quality of all included studies using the risk-of-bias tool. The primary outcome was postoperative pain score, and the secondary outcomes included analgesic consumption, need for rescue analgesics, adverse events, and length of hospital stay. A meta-analysis was performed for the pooled data, and the level of evidence was rated using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) system.ResultsWe included five randomized controlled trials with 497 patients who underwent surgery. Compared with the control group, DNS significantly reduced the visual analog scale from postoperative 48 hours {mean difference (MD): -37.54 (95% confidence interval [CI]: -70.47, -4.62)} to 7 days [MD: -165.99 (95% CI: -231.44)] and decreased the requirement for rescue analgesics [relative risk: 0.89 (95% CI: 0.81, 0.97)]. No significant difference was observed in visual analog scale scores within postoperative 24 hours [MD: -10.13 (95% CI: -30.11, 9.85)] or in total analgesic consumption. Patients receiving DNS had a higher risk of dizziness and injection site reactions, without an increased occurrence of other adverse events.ConclusionsWith a low to moderate level of evidence, intramuscular DNS provides long-lasting analgesia from postoperative 48 hours to 7 days and may reduce the requirement for postoperative rescue analgesics. However, DNS does not offer additional pain relief within the first 24 hours postoperatively. Further high-quality studies are warranted.PROSPERO (International Prospective Register of Systematic Reviews) registry identifier: CRD42023494130.ConclusionsWith a low to moderate level of evidence, intramuscular DNS provides long-lasting analgesia from postoperative 48 hours to 7 days and may reduce the requirement for postoperative rescue analgesics. However, DNS does not offer additional pain relief within the first 24 hours postoperatively. Further high-quality studies are warranted.PROSPERO (International Prospective Register of Systematic Reviews) registry identifier: CRD42023494130.
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页码:53 / 59
页数:7
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