The effect of adding dexmedetomidine or dexamethasone to bupivacaine-fentanyl mixture in spinal anesthesia for cesarean section.

IF 1.5 Q3 PHARMACOLOGY & PHARMACY Journal of Anaesthesiology, Clinical Pharmacology Pub Date : 2024-01-01 Epub Date: 2024-03-14 DOI:10.4103/joacp.joacp_396_22
Sameh Abdelkhalik Ahmed, Hashem Adel Lotfy, Tarek Abdel Hay Mostafa
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Abstract

Background and aims: Many strategies are available to prevent spinal-induced hypotension in cesarean section, especially the use of a low dose of spinal anesthesia combined with adjuvants. This study investigated the effect of adding either dexmedetomidine or dexamethasone to the intrathecal bupivacaine-fentanyl mixture on the postoperative analgesia duration, after elective cesarean section.

Material and methods: This prospective, randomized, double-blind study was conducted on 90 full-term parturients undergoing elective cesarean section, who were randomly distributed into three groups. They all received spinal anesthesia with the bupivacaine-fentanyl mixture (2.5 ml), in addition to 0.5 ml normal saline (control group), 5 μg dexmedetomidine dissolved in 0.5 ml normal saline (dexmedetomidine group), or 2 mg dexamethasone (dexamethasone group). The time to the first request of morphine rescue analgesia was recorded, in addition to the total dose of morphine consumed in the first 24 h after surgery, the postoperative numerical rating score (NRS), and maternal and fetal outcomes.

Results: As compared to the control group and the dexamethasone group, the use of dexmedetomidine as an additive to the bupivacaine-fentanyl mixture significantly prolonged the time to the first request of rescue analgesia, decreased postoperative morphine consumption, and decreased the pain score 4 and 6 h after surgery. There was an insignificant difference between the control and dexamethasone groups.

Conclusion: The use of dexmedetomidine as an additive to bupivacaine-fentanyl mixture in spinal anesthesia for cesarean section prolonged the postoperative analgesia and decreased the postoperative opioid consumption in comparison to the addition of dexamethasone or normal saline.

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在剖腹产脊髓麻醉中加入右美托咪定或地塞米松的效果。
背景和目的:目前有许多策略可用于预防剖宫产术中脊髓诱发的低血压,尤其是使用低剂量脊髓麻醉联合辅助剂。本研究探讨了在选择性剖宫产术后,在鞘内布比卡因-芬太尼混合物中加入右美托咪定或地塞米松对术后镇痛持续时间的影响:这项前瞻性、随机、双盲研究的对象是90名接受择期剖宫产手术的足月产妇,她们被随机分为三组。他们都接受了布比卡因-芬太尼混合物(2.5 毫升)的脊髓麻醉,此外还接受了 0.5 毫升生理盐水(对照组)、5 微克右美托咪定溶于 0.5 毫升生理盐水(右美托咪定组)或 2 毫克地塞米松(地塞米松组)的麻醉。除了术后 24 小时内消耗的吗啡总剂量、术后数字评分(NRS)以及母体和胎儿结局外,还记录了首次要求使用吗啡镇痛的时间:与对照组和地塞米松组相比,使用右美托咪定作为布比卡因-芬太尼混合物的添加剂能显著延长首次要求镇痛的时间,减少术后吗啡用量,并降低术后4小时和6小时的疼痛评分。对照组和地塞米松组之间的差异不明显:结论:与添加地塞米松或生理盐水相比,在剖宫产脊髓麻醉中使用右美托咪定作为布比卡因-芬太尼混合物的添加剂可延长术后镇痛时间并减少术后阿片类药物的用量。
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来源期刊
CiteScore
1.90
自引率
6.70%
发文量
129
期刊介绍: The JOACP publishes original peer-reviewed research and clinical work in all branches of anaesthesiology, pain, critical care and perioperative medicine including the application to basic sciences. In addition, the journal publishes review articles, special articles, brief communications/reports, case reports, and reports of new equipment, letters to editor, book reviews and obituaries. It is international in scope and comprehensive in coverage.
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