QT interval prolongation in Takotsubo syndrome: a frightening feature with no major prognostic impact.

IF 1.1 Q4 RESPIRATORY SYSTEM
Monaldi Archives for Chest Disease Pub Date : 2024-12-31 Epub Date: 2023-12-06 DOI:10.4081/monaldi.2023.2834
Ana Isabel Pinho, Cátia Oliveira, Luís Daniel Santos, Catarina Marques, André Cabrita, Paula Dias, Gonçalo Pestana, Carla Sousa, Rui André Rodrigues
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Abstract

Despite the frequent and often severe repolarization abnormalities seen in Takotsubo syndrome (TTS), the underlying mechanism of life-threatening arrhythmias is incompletely understood, and the risk remains uncertain. TTS is considered a potential cause of acquired long QT syndrome; however, there is no robust evidence that QT prolongation has a major prognostic impact on these patients' outcomes. Our aim was to assess the prevalence and clinical implications of acquired long QT during TTS events and compare in-hospital and long-term outcomes between patients with and without corrected QT interval (QTc) prolongation. This is a retrospective cohort study that included 113 patients admitted to our tertiary care hospital with a diagnosis of TTS. The cohort was divided into two groups: a long QTc group (QTc≥460 milliseconds in any electrocardiogram at admission or during hospitalization) and a normal QTc group. Baseline characteristics, occurrences during hospitalization, and outcome data were obtained from the revision of medical registries and hospital visits. Of the 113 patients, 107 (94.7%) were female. The mean age was 67.6±11.7 years. QTc prolongation was found in 38%. Demographic characteristics, relevant chronic medication, prevalence of cardiovascular risk factors, and other comorbidities were similar between the groups, except for a history of atrial fibrillation, which was more common in the long QTc group. Syncope was more prevalent in the long QTc group. In-hospital complications were not statistically different between patients with long and normal QTc (48.8% vs. 44.2%, p=0.637), including ventricular arrhythmias and complete atrioventricular block (both 4.7% vs. 1.4%, p=0.556). In-hospital mortality was 0.9%, corresponding to one patient in the long QTc group. The mean follow-up time was 4.8±3.8 years. 5-year all-cause mortality and the occurrence of the composite endpoint of major adverse cardiac and cerebrovascular events did not differ between the groups (p=0.511 and p=0.538, respectively). Our study found no association between prolonged QTc interval during TTS events and adverse prognosis since in-hospital and long-term outcomes were similar between the groups. Our findings suggest that, although QT prolongation is usually a frightening feature on ECG, this repolarization abnormality during the acute phase has no major prognostic implications in the TTS population.

Takotsubo综合征的QT间期延长:一个没有重大预后影响的可怕特征。
尽管Takotsubo综合征(TTS)经常出现严重的复极异常,但危及生命的心律失常的潜在机制尚不完全清楚,其风险仍不确定。TTS被认为是获得性长QT综合征的潜在原因;然而,没有强有力的证据表明QT间期延长对这些患者的预后有重大影响。我们的目的是评估TTS事件中获得性长QT的患病率和临床意义,并比较有和没有纠正QT间期(QTc)延长的患者的住院和长期结果。这是一项回顾性队列研究,纳入了113名诊断为TTS的三级医院患者。该队列分为两组:长QTc组(入院时或住院期间任何心电图QTc≥460毫秒)和正常QTc组。基线特征、住院期间的发生率和结果数据来自修订的医疗登记和医院就诊。113例患者中,女性107例(94.7%)。平均年龄67.6±11.7岁。38%的患者QTc延长。人口统计学特征、相关慢性药物治疗、心血管危险因素患病率和其他合并症在两组之间相似,但房颤史在长QTc组中更为常见。长QTc组晕厥更为普遍。长QTc患者和正常QTc患者的院内并发症无统计学差异(48.8%比44.2%,p=0.637),包括室性心律失常和完全性房室传导阻滞(均为4.7%比1.4%,p=0.556)。住院死亡率为0.9%,与长QTc组的1例患者相对应。平均随访时间4.8±3.8年。5年全因死亡率和主要心脑血管不良事件复合终点的发生率在两组间无差异(p=0.511和p=0.538)。我们的研究发现,TTS事件期间QTc间隔延长与不良预后之间没有关联,因为两组之间的住院和长期结局相似。我们的研究结果表明,尽管QT间期延长通常是心电图上的一个可怕特征,但急性期的复极异常对TTS人群的预后没有重大影响。
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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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
1
审稿时长
12 weeks
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