地塞米松单用与经皮穴位电刺激或托咪司琼联合预防妇科腹腔镜手术患者术后恶心呕吐的比较

X. Y. Yang, J. Xiao, Y. H. Chen, Z. Wang, H. Wang, D. He, J. Zhang
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引用次数: 0

摘要

其中恶心和呕吐是次要终点,引发了对治疗力度不足和异质性增加的批评。目前的研究旨在通过评估术前加巴喷丁的综合效果来解决这些局限性,这些研究旨在探讨PONV作为主要终点。该方法表明术前加巴喷丁可减少术后恶心、呕吐和抢救止吐需求。对引用PONV终点(主要或次要)的所有纳入试验的进一步分析也得出结论,即术前加巴喷丁与PONV发生率、恶心、呕吐和救急止吐需求降低相关。这些发现,作为迄今为止最大队列试验汇总数据的结果,提示术前加巴喷丁在预防PONV中的作用。加巴喷丁减弱PONV的机制尚存争议。一些研究已经假设了脑后区域钙信号的减少,以及速激肽神经传递的减少。也有人建议减少术后炎症,从而减轻肠梗阻和随后的PONV。尽管如此,其他人指出减少围手术期阿片类药物需求与加巴喷丁相关的手术机制。人们可能会猜测,这些机制的某种组合可能是负责任的。尽管如此,加巴喷丁对中枢神经系统的影响必须得到承认。尽管目前的研究没有确定加巴喷丁与头晕/头晕、头痛和服药口之间的关联,但已有报道称术后可能出现过度镇静和头晕。然而,目前的调查确实发现了术后过度镇静和嗜睡的显著发生率。另一个悬而未决的问题是术前加巴喷丁是否对出院后PONV有影响。当然,当前的荟萃分析应该刺激许多相关领域的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dexamethasone Alone Versus in Combination With Transcutaneous Electrical Acupoint Stimulation or Tropisetron for Prevention of Postoperative Nausea and Vomiting in Gynaecological Patients Undergoing Laparoscopic Surgery
wherein nausea and vomiting were the secondary end points, triggering criticism about insufficient power and increased heterogeneity. The current study was tailored to address these limitations by assessing the pooled effects of preoperative gabapentin among studies designed to explore PONV as a primary end point. This approach showed that preoperative gabapentin reduced postoperative nausea, vomiting, and rescue antiemetic requirements. Additional analysis of all included trials that cited PONV end points (primary or secondary) also resulted in the conclusion that preoperative gabapentin was associated with a reduced incidence of PONV, nausea, vomiting, and rescue antiemetic requirement. These findings, as a result of pooled data from the largest cohort of trials to date, suggest a role for preoperative gabapentin in the prevention of PONV. The mechanism by which gabapentin attenuates PONV is debatable. Some studies have postulated a reduction in calcium signaling in the area postrema, as well as reduced tachykinin neurotransmission. Others have suggested a decrease in postoperative inflammation, thereby mitigating ileus and subsequent PONV. Still, others point to the reduction in perioperative opioid requirements associated with gabapentin as the operative mechanism. One might conjecture that some combination of these mechanisms may be responsible. Nonetheless, the central nervous system effects of gabapentin must be acknowledged. Potential excessive sedation and dizziness in the postoperative period have been reported, although the current study did not identify an association between gabapentin and dizziness/lightheadedness, headache, and drug mouth. The current investigation, however, did detect notable incidences of excessive postoperative sedation and somnolence. Another unanswered question is whether preoperative gabapentin has any effect on postdischarge PONV. Certainly, the current meta-analysis should stimulate further research in many germane areas.
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