Anesthesiologic management of pregnant women with SARS-COV-2 infection undergoing cesarean delivery

A. Coviello, C. Posillipo, L. Golino, C. De Angelis, E. Gragnano, G. Saccone, M. Ianniello, G. Castellano, A. Marra, A. Maresca, M. Vargas, G. Servillo
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引用次数: 2

Abstract

Background: Pregnant women are usually more susceptible to infection due to typical physiological and mechanical changes, such as increased heart rate, stroke volume and pulmonary residual capacity. The aim of this study was to evaluate an innovative anesthesiologic opioid-free management protocol in symptomatic pregnant women, with COVID-19 and with oxygen therapy, undergoing cesarean delivery with spinal anesthesia. Methods: With the patient in the sitting position, spinal anesthesia was performed at the L1-L2 level. Vertebral level has been identified starting from the sacrum, we counted the laminae in the caudal-to-cephalad direction, which was then marked with a surgical pen. The technique was performed in asepsis, in the subarachnoid space after vision of clear Cephalo-Spinal Fluid (CSF) in the spinal needle 27 Gauge, without letting out the CSF, bupivacaine 0.5% 10 mg, dexmedetomidine 10 μg and dexamethasone 4 mg was injected. Results: During the study period, 40 pregnant women with one or more symptoms and supplemental oxygen (FiO2 35-40%) who underwent cesarean delivery were included in the study. All pregnant women had pain visual analog scale (VAS) <3, and no pregnant women required rescue dose. Adverse effects, such as nausea, vomiting, shivering, or pruritus were not recorded in any case. After a mean of 2.5 hours from the spinal anesthesia, all the included women had a complete motility of the lower limbs and were able to mobilize independently within 12 hours after delivery. Mean time to first latus was about 8 hours after delivery. Conclusions: Pregnant women in COVID-19 can safely receive intrathecal dexamethasone and dexmedetomidine during planned cesarean delivery. © 2021 The Author(s). Published by IMR Press.
SARS-COV-2感染孕妇剖宫产的麻醉处理
背景:孕妇由于心率、脑卒中量和肺残容量增加等生理和机械变化,更易感染。本研究的目的是评估一种创新的麻醉无阿片类药物管理方案,适用于有症状的COVID-19孕妇,在脊髓麻醉下剖宫产。方法:患者坐位,在L1-L2水平行脊髓麻醉。从骶骨开始确定椎体水平,我们计算了尾侧到头侧方向的椎板,然后用手术笔标记。在无菌条件下,于蛛网膜下腔内,用27号针观察清楚脑脊液后,不放空脑脊液,注射布比卡因0.5% 10 mg,右美托咪定10 μg,地塞米松4 mg。结果:在研究期间,40例有一种或多种症状并需补充氧气(FiO2 35-40%)的剖宫产孕妇被纳入研究。所有孕妇均有疼痛视觉模拟评分(VAS) <3,无孕妇需要抢救剂量。不良反应,如恶心,呕吐,颤抖,或瘙痒没有记录在任何情况下。脊髓麻醉平均2.5小时后,所有纳入的妇女在分娩后12小时内下肢活动完全,能够独立活动。分娩后平均8小时到达初产。结论:COVID-19孕妇在计划剖宫产期间可安全地接受地塞米松和右美托咪定鞘内注射。©2021作者。IMR出版社出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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