继发于永久性起搏器导联的严重三尖瓣狭窄。

Journal of Medical Cases Pub Date : 2022-08-01 Epub Date: 2022-08-19 DOI:10.14740/jmc3900
Asif Khan, Ahmad Mustafa, Joanne Ling, James Lafferty
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引用次数: 1

摘要

三尖瓣狭窄(TS)是一种罕见的瓣膜异常,通常与风湿性心脏病的二尖瓣狭窄有关。TS现在经常被描述为永久性起搏器导联,无论是否存在感染性心内膜炎。我们描述了一个案例的女性与TS继发永久性心脏起搏器导联在没有感染性心内膜炎被管理在孕前期。她最初为中重度TS做了球囊瓣膜成形术,随后怀孕和分娩无并发症。然而,在她第二次怀孕前进行评估时,再次发现她患有严重的TS。我们假设永久性起搏器导联的存在导致了第一次手术后早期再狭窄的发展。重复球囊瓣膜成形术不成功,最终她成功地进行了三尖瓣置换术,几年后没有超声心动图或再狭窄的临床迹象。继发于永久性起搏器导联的TS的治疗方法包括医学治疗、球囊瓣膜成形术(有或没有去除起搏器导联)或三尖瓣置换术。总的来说,缺乏任何一种选择的长期结果的数据,这使得管理具有挑战性。
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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Severe Tricuspid Stenosis Secondary to Permanent Pacemaker Lead.

Tricuspid stenosis (TS) is a rare valvular abnormality and generally associated with mitral stenosis in cases of rheumatic heart disease. TS is now frequently being described in the setting of permanent pacemaker leads, either with or without the presence of infective endocarditis. We describe a case of a female with TS secondary to permanent pacemaker leads in the absence of infective endocarditis being managed during the pre-conception period. She initially had a balloon valvuloplasty done for moderate to severe TS and subsequently conceived and delivered without complications. However, upon being evaluated before her second pregnancy, she was again found to have severe TS. We hypothesize that the presence of permanent pacemaker lead contributed to the development of early restenosis after the first procedure. A repeat balloon valvuloplasty was unsuccessful and she ultimately underwent successful tricuspid valve replacement with no echocardiographic or clinical signs of restenosis years later. The options for management of TS secondary to permanent pacemaker lead include medical management, balloon valvuloplasty (with or without removal of pacemaker lead), or tricuspid valve replacement. Overall, there is a scarcity of data on long-term outcomes of either option making the management challenging.

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