剖腹产后凸畸形产妇的脊柱麻醉——来自印度一家三级护理中心的回顾性研究

IF 0.2 Q4 ANESTHESIOLOGY
Ranju Singh, Rashi Sardana, Pooja Singh
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引用次数: 0

摘要

引言:妊娠期后凸畸形是一种罕见但严重的疾病,通常需要剖腹产。在这些病例中既使用了全身麻醉,也使用了区域麻醉,但有关脊髓麻醉(SA)结果的数据有限。方法:我们进行了一项回顾性研究,以确定在印度一家三级护理医院接受剖腹产的后凸畸形患者。将接受SA的产妇与接受全身麻醉的产妇(GA组)在心肺参数、产妇结局和新生儿结局方面进行比较。结果:与SA组相比,GA组的心肺参数(包括肺功能测试、右心房压和心脏射血分数)明显较差。GA组的所有患者都需要机械通气,而SA组没有患者需要机械通气。SA组术中低血压更为常见。与SA组相比,GA组的新生儿结局更糟,1分钟和5分钟时的Apgar评分更低,入院人数更多。两组均未发生孕产妇或新生儿死亡。结论:SA可以成功地治疗计划为CD的后凸畸形产妇,并具有良好的孕产妇和新生儿结局。GA可用于伴有心肺并发症的严重后凸畸形产妇。SA治疗严重后凸畸形的安全性需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spinal anaesthesia in kyphoscoliotic parturients undergoing caesarean delivery – A retrospective study from a tertiary care centre in India
Introduction: Kyphoscoliosis with pregnancy is a rare but serious disorder which often requires caesarean delivery. Both general and regional anaesthesia have been used in these cases but data regarding outcomes with spinal anaesthesia (SA) are limited. Methods: We conducted a retrospective study to identify patients with kyphoscoliosis undergoing caesarean delivery at a tertiary care hospital in India. Those parturients who received SA were compared with those receiving general anaesthesia (GA group) with respect to cardiorespiratory parameters, maternal outcomes and neonatal outcomes. Results: The GA group had significantly worse cardiorespiratory parameters including pulmonary function tests, right atrial pressures and cardiac ejection fraction as compared to SA group. All the GA group patients required mechanical ventilation while no patients in the SA group needed mechanical ventilation. Intraoperative hypotension was more common in the SA group. Neonatal outcomes were worse in the GA group with lower Apgar scores at 1 and 5 min and more nursery admissions than the SA group. No maternal or neonatal deaths occurred in either group. Conclusion: Kyphoscoliotic parturients scheduled for CD can be successfully managed with SA with good maternal and neonatal outcomes. GA may be reserved for severe kyphoscoliotic parturients with cardiorespiratory complications. The safety of SA in severe kyphoscoliosis requires further studies.
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