Reversible complete Heart block in a Pregnant Woman responding to Steroids: A rare Case Report

Manjappa Mahadevappa, Soumya Patil, Rishi Tripathi, Virupaksha Ajjammanavar, Prashanth Kulkarni
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Abstract

Complete heart block (CHB) is the total absence of conduction from atria to ventricles with an escape rhythm most commonly arising from the AVN or His bundle. CHB in pregnancy is very rare, and most reported cases are due to congenital variety, where the pre-existing CHB from birth is either detected incidentally or presented with symptoms during pregnancy. Pregnancy is associated with various physiological changes, such as a pro-inflammatory, hypercoagulable state with possible oedema of the heart's conduction system, which may rarely give rise to CHB. There are no clear guidelines to manage CHB complicating pregnancy. An asymptomatic 27-year-old lady with G2P1L1, 39 weeks of gestation with breech presentation, was referred for delivery given the low maternal heart rate of 40 bpm. Per abdominal examination revealed a term size uterus with active contractions and a fetal heart rate of 140bpm. An ECG revealed a CHB with an escape rate of 40 bpm. Other routine investigations were normal, with negative serological evaluation for hepatitis B, C, and HIV. ANA and Anti-Ro ⁄ SSA antibodies. She underwent an emergency LSCS under spinal anaesthesia with a backup temporary pacemaker (TPM). She received a short course of empirical steroid therapy for three days as there were no obvious secondary causes for CHB, which reverted to sinus rhythm after 48 hours. CHB complicating pregnancy with or without symptoms may require definitive therapy in the form of permanent pacemaker implantation. However, the insertion of a TPM for managing pregnancy is controversial as opinion in the literature is divided. There are no reports of CHB occurring in pregnancy without congenital or other known acquired causes. In the reported case, the CHB reverted to sinus rhythm with a short course of IV steroid therapy without any subsequent need for a PPM implantation. Congenital CHB remains the most common cause of rarely seen CHB complicating pregnancy. Through the conduction system oedema and inflammation, physiological changes in gestation may rarely cause CHB during pregnancy. In the absence of congenital CHB and other demonstrable acquired causes, a short course of steroid therapy may reverse the CHB avoiding PPM implantation as shown in the reported case.
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对类固醇有反应的孕妇可逆完全心脏传导阻滞:一例罕见病例报告
完全性心脏传导阻滞(CHB)是指心房到心室的传导完全阻断,并伴有逃逸节律,最常见的是由AVN或His束引起。妊娠期慢性乙型肝炎非常罕见,大多数报告的病例是由于先天性变异,从出生时就存在的慢性乙型肝炎要么是偶然发现的,要么是在妊娠期间出现症状的。妊娠与多种生理变化有关,如促炎、高凝状态,心脏传导系统可能出现水肿,这很少引起慢性乙型肝炎。没有明确的指导方针来管理CHB合并妊娠。一位27岁无症状的G2P1L1女性,妊娠39周,臀位出现,由于产妇心率低至每分钟40次,被推荐分娩。腹部检查显示足月大小的子宫,积极收缩,胎心率140bpm。心电图显示心律失常,心率为每分钟40次。其他常规检查正常,乙型、丙型肝炎和艾滋病毒血清学评估阴性。ANA和Anti-Ro / SSA抗体。她在脊髓麻醉下使用备用临时起搏器(TPM)接受了紧急LSCS。由于CHB无明显继发原因,患者接受了3天的短期类固醇治疗,48小时后恢复为窦性心律。慢性乙型肝炎合并妊娠伴有或无症状可能需要永久性起搏器植入的最终治疗形式。然而,插入TPM管理妊娠是有争议的,因为意见在文献中是分裂的。在没有先天性或其他已知获得性原因的情况下,没有妊娠期发生CHB的报道。在报告的病例中,CHB在短期静脉类固醇治疗后恢复为窦性心律,随后无需植入PPM。先天性慢性乙型肝炎仍然是罕见的慢性乙型肝炎并发妊娠的最常见原因。通过传导系统水肿和炎症,妊娠期生理变化很少引起妊娠期慢性乙型肝炎。在没有先天性CHB和其他明显的后天原因的情况下,短期类固醇治疗可以逆转CHB,避免PPM植入,正如报告的病例所示。
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