MYASTHENIA GRAVIS IN PREGNANCY: ACHIEVING OPTIMAL OUTCOMES THROUGH PRECISION CARE – A CASE SERIES FROM SOUTH INDIA & REVIEW OF LITERATURE

Dhanya R Shenoy, N. Navakumar, Vidyalekshmy R, Brinda Sabu, Roshini Ambat, Sajitlh Mohan, Lumiya Malik, Suresh Chandran
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Abstract

Introduction: Myasthenia Gravis (MG) is an autoimmune neuromuscular disorder affecting skeletal muscles, particularly in women of reproductive age. Though uncommon with a prevalence of only 0.3 to 2.8 per 100,000, the incidence peaks during 2nd and 3rd decades of life, and can have signicant impact in pregnancy. The course of the disease in pregnancy is not entirely understood. Methodology: A retrospective case series analysis of 4 cases were carried out for a period of 5 years from 2018 in a tertiary care centre in South India to identify and describe the disease course in pregnancy and effect of disease in the pregnant women and their fetuses. From this study, we aimed to describe the disease course of MG in pregnancy and formulate an optimal management plan, learning from our experience. Results: All patients included in the study were in a state of remission prior to conception. With vigilant monitoring and collaborative multidisciplinary approach, two patients successfully carried their pregnancies to term without encountering any complications, maintaining a stable course throughout the antenatal, intrapartum, and postpartum periods. However, one patient experienced an acute exacerbation upon contracting COVID-19 category C. Subsequently, her pregnancy was complicated by late-onset fetal growth restriction, preterm premature rupture of membranes (PPROM), preterm birth and postpartum exacerbation. Despite these challenges, both maternal and fetal outcomes were favorable, attributed to meticulous surveillance and critical care interventions. Another patient experienced an exacerbation at 10 weeks of gestation but otherwise had an uneventful pregnancy, labour, and postpartum recovery. Conclusion: One third of Myasthenia gravis patients can have exacerbations in pregnancy with a small but signicant subset experiencing potentially life threatening Myasthenic crisis. All necessary precautions should be pro-actively taken to prevent factors that could trigger a myasthenic crisis, including cautious drug selection during anaesthesia and the avoidance of medications that may exacerbate MG during acute infections. Caesarean section should be for obstetric indications only. Managing myasthenia gravis in pregnancy is quite challenging and requires multidisciplinary input with close monitoring and follow up.
妊娠期肌无力:通过精准护理实现最佳疗效--来自南印度的系列病例及文献综述
简介重症肌无力(MG)是一种影响骨骼肌的自身免疫性神经肌肉疾病,尤其多发于育龄妇女。虽然这种疾病并不常见,发病率仅为每十万人中 0.3 至 2.8 例,但其发病率在生命的第二和第三个十年达到高峰,并可能对妊娠产生重大影响。该病在妊娠期的发病过程尚不完全清楚。研究方法:自2018年起,我们在印度南部的一家三级医疗中心对4个病例进行了为期5年的回顾性病例系列分析,以确定和描述妊娠期的疾病过程以及疾病对孕妇及其胎儿的影响。通过这项研究,我们旨在描述妊娠期 MG 的病程,并借鉴我们的经验,制定最佳管理方案。研究结果所有参与研究的患者在受孕前均处于缓解状态。在严密的监测和多学科协作下,两名患者成功怀上了宝宝,没有出现任何并发症,在整个产前、产中和产后期间都保持了稳定的病程。然而,其中一名患者在感染 COVID-19 C 类疾病后病情急性加重。随后,她的妊娠因晚期胎儿生长受限、早产胎膜早破(PPROM)、早产和产后病情加重而变得复杂。尽管遇到了这些挑战,但产妇和胎儿的预后都很好,这要归功于精心的监护和重症监护干预。另一名患者在妊娠 10 周时病情加重,但在妊娠、分娩和产后恢复过程中一切顺利。结论三分之一的重症肌无力患者会在妊娠期病情加重,其中一小部分患者可能会出现危及生命的肌无力危象。应积极采取一切必要的预防措施,防止可能引发肌无力危象的因素,包括在麻醉期间谨慎选择药物,避免使用可能在急性感染期间加重 MG 的药物。剖腹产只能用于产科适应症。治疗妊娠期肌无力是一项相当具有挑战性的工作,需要多学科参与,并进行密切监测和随访。
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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