The efficacy and safety of granisetron with ondansetron for the prevention of post-operative nausea and vomiting in patients undergoing cesarean section under spinal anesthesia

Supriya Singh, Sanni Deyol Gautam, Narendra Singh Bafila, Rajesh Kumar
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Abstract

Background: Spinal anesthesia often causes more post-operative nausea and vomiting (PONV). Cesarean-section patients have a significantly more PONV rate. Therefore, evidence-based knowledge about PONV prevention and care for high-risk individuals is urgently needed to reduce the consequences. Aims and Objectives: The aim of the study was to compare the efficacy and safety of granisetron with that of ondansetron in the prevention of PONV in patients undergoing cesarean section under spinal anesthesia. Materials and Methods: A total of 86 pregnant women with American Society of Anesthesiologists grade I–II scheduled for cesarean delivery under spinal anesthesia were enrolled. Patients were divided into two equal groups (n=43): Ten minutes before spinal anesthesia, patients in group B (granisetron) received 2 mg granisetron intravenously diluted to 10 mL with normal saline, whereas patients in group A (ondansetron) received 4 mg ondansetron. Results: There was no significant difference between Groups A and B in terms of the number of vomiting episodes between 0 and 6 h. Group A had significantly more episodes of nausea after 2 h than Group B after 0–2 h. After 2–6 h, however, the nausea was similar in all groups. Of the patients in Group A, 4 (9.3%) required antiemetic medication, in Group B, it was 2 (4.7%). In Group A, 8 patients (18.6%) and 6 patients (14%) complained of headache and dizziness, respectively; in Group B, 3 patients (7.0%) and (0%), respectively. Dizziness was significantly more pronounced in Group A than in Group B. Conclusion: The results of the study show that granisetron (2 mg) was more effective than ondansetron (4 mg) in minimizing PONV episodes in women undergoing spinal anesthesia for cesarean section. There were no significant side effects and both drugs were comparatively safe.
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格拉司琼与昂丹司琼用于预防脊髓麻醉下剖宫产术患者术后恶心和呕吐的有效性和安全性
背景:脊髓麻醉通常会引起更多的术后恶心和呕吐(PONV)。剖腹产患者的 PONV 发生率明显更高。因此,迫切需要以证据为基础的 PONV 预防知识和对高危人群的护理,以减少后果:该研究旨在比较格拉司琼和昂丹司琼对脊柱麻醉下剖宫产患者预防 PONV 的有效性和安全性:共招募了86名美国麻醉医师协会I-II级孕妇,计划在脊柱麻醉下进行剖宫产。患者被平均分为两组(43 人):在脊髓麻醉前十分钟,B组(格拉司琼)患者静脉注射用生理盐水稀释至10毫升的2毫克格拉司琼,而A组(昂丹司琼)患者则注射4毫克昂丹司琼:结果:A 组和 B 组在 0 至 6 小时内的呕吐次数没有明显差异,但 A 组在 2 小时后的恶心次数明显多于 B 组。在 A 组患者中,有 4 人(9.3%)需要服用止吐药,B 组为 2 人(4.7%)。在 A 组中,分别有 8 名患者(18.6%)和 6 名患者(14%)抱怨头痛和头晕;在 B 组中,分别有 3 名患者(7.0%)和 0 名患者(0%)抱怨头痛和头晕。A 组头晕症状明显比 B 组明显:研究结果表明,格拉司琼(2 毫克)比昂丹司琼(4 毫克)更能有效减少剖宫产椎管麻醉妇女的 PONV 发作。两种药物都没有明显的副作用,相对安全。
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