严重Takotsubo型心肌病的不祥三联征。

Journal of Medical Cases Pub Date : 2022-07-01 Epub Date: 2022-07-20 DOI:10.14740/jmc3946
Abdalaziz Awadelkarim, Ahmed S Yassin, Mohammed Ali, John Dayco, Eltaib Saad, Isra Idris, Rashid Alhusain, Joseph Sebastian, Luis Afonso
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摘要

26-52%的Takotsubo型心肌病(TCM)患者QT间期延长。它被认为是由心脏复极储备减少引起的,反映了中医观察到的短暂性心肌损伤。心动过缓引起的QT间期延长可因中药的出现而被放大,这两种药物的结合可能会导致点扭转(TdP)的显著风险。我们提出一个独特的情况下,80岁的女性与中医相关的心脏骤停。患者患有长QT综合征,中医心肌损伤导致三度房室传导阻滞和随后的心动过缓引起的TdP。由于缺乏强有力的文献,在中医背景下,对于三度房室传导阻滞的处理尚无明确的指导方针。在我们的病例中,由于复发性室性心动过速(VT)和心室颤动(VF)骤停,我们选择在高心室率下进行临时起搏,然后使用双心室植入式心律转复除颤器(BiV/ICD)。随访3个月后发现左室功能障碍改善,QT间期延长缓解。然而,注意到的房室传导缺陷仍然存在。在现有的文献中,我们确定了五个报告的病例,与我们的病人的表现相似。所确定的病例为无明显心脏病史的中老年女性,她们表现出与高级别房室传导阻滞、获得性长QT综合征和心动过缓性TdP快速进展相关的相似中医三联征,导致在入院前24 - 48小时内几乎心脏骤停。监测纠正QT (QTc),纠正电解质异常,并尽量减少延长QT的药物对中医患者至关重要。识别中医患者的房室传导缺陷是至关重要的,特别是当它与QT间期明显延长相关时。这种情况未得到充分认识,可能是致命的,需要密切监测和及时干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Ominous Triad of Severe Takotsubo Cardiomyopathy.

QT prolongation is present in 26-52% of cases of Takotsubo cardiomyopathy (TCM). It has been postulated to result from reduced cardiac repolarization reserve and reflects the transient myocardial insult observed in TCM. Bradycardia-induced QT interval prolongation is amplified by the occurrence of TCM, a combination that potentially carries a significant risk for torsade de pointes (TdP). We present a unique case of an 80-year-old female with TCM-related cardiac arrest. The patient had acquired long QT syndrome in which TCM myocardial insult led to the precipitation of a third-degree atrioventricular (AV) block and subsequent bradycardia-induced TdP. Due to the lack of robust literature, there is no clear guideline in the management of third-degree AV block in the setting of TCM. In our case, because of recurrent ventricular tachycardia (VT) and ventricular fibrillation (VF) arrest, we opted for temporary pacing at a high ventricular rate, followed by a biventricular implantable cardioverter-defibrillator (BiV/ICD). Follow-up 3 months later revealed improvement of left ventricular (LV) dysfunction and resolution of QT prolongation. However, the noticed AV conduction defects persisted. In the available literature, we identified five reported cases that bear similarity with our patient's presentation. The identified cases were middle-aged to elderly females with no significant cardiac history, who exhibited a similar triad of TCM associated with high-grade AV block, acquired long QT syndrome, and a rapid progression of bradycardia-induced TdP, resulting in a near cardiac arrest within the first 24 - 48 h of admission. It is crucial to monitor corrected QT (QTc), correct electrolyte abnormalities, and minimize QT-prolonging medications in patients with TCM. The recognition of AV conduction defects in patients with TCM is critical, especially if it is associated with significant QT prolongation. Such situations are underrecognized, and are potentially fatal, necessitating close monitoring and timely intervention.

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