National Reference Centre for Inherited Arrhythmia of Lyon (CERA), Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, 69500 Bron, France; Electrophysiology Unit, Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, 69500 Bron, France; Université Claude-Bernard Lyon-1, MeLiS, CNRS UMR 5284, INSERM U1314, Institut NeuroMyoGène, 69008 Lyon, France; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-Heart).
Electrophysiology Unit, Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, 69500 Bron, France; Paediatric and Congenital Heart Disease Medico-Surgical Unit, Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, 69500 Bron, France; Université Claude-Bernard Lyon-1, LabTau, Inserm, 69003 Lyon, France.
Arch Cardiovasc Dis. 2024 May;117(5):313-320. doi: 10.1016/j.acvd.2024.02.010. Epub 2024 Apr 24.
In patients with congenital long QT syndrome (LQTS), the risk of ventricular arrhythmia is correlated with the duration of the corrected QT interval and the changes in the ST-T wave pattern on the 12-lead surface electrocardiogram (12L-ECG). Remote monitoring of these variables could be useful.
To evaluate the abilities of two wearable electrocardiogram devices (Apple Watch and KardiaMobile 6L) to provide reliable electrocardiograms in terms of corrected QT interval and ST-T wave patterns in patients with LQTS.
In a prospective multicentre study (ClinicalTrials.gov identifier: NCT04728100), a 12L-ECG, a 6-lead KardiaMobile 6L electrocardiogram and two single-lead Apple Watch electrocardiograms were recorded in patients with LQTS. The corrected QT interval and ST-T wave patterns were evaluated manually.
Overall, 98 patients with LQTS were included; 12.2% were children and 92.8% had a pathogenic variant in an LQTS gene. The main genotypes were LQTS type 1 (40.8%), LQTS type 2 (36.7%) and LQTS type 3 (7.1%); rarer genotypes were also represented. When comparing the ST-T wave patterns obtained with the 12L-ECG, the level of agreement was moderate with the Apple Watch (k=0.593) and substantial with the KardiaMobile 6L (k=0.651). Regarding the corrected QT interval, the correlation with 12L-ECG was strong for the Apple Watch (r=0.703 in lead II) and moderate for the KardiaMobile 6L (r=0.593). There was a slight overestimation of corrected QT interval with the Apple Watch and a subtle underestimation with the KardiaMobile 6L.
In patients with LQTS, the corrected QT interval and ST-T wave patterns obtained with the Apple Watch and the KardiaMobile 6L correlated with the 12L-ECG. Although wearable electrocardiogram devices cannot replace the 12L-ECG for the follow-up of these patients, they could be interesting additional monitoring tools.
在患有先天性长 QT 综合征(LQTS)的患者中,室性心律失常的风险与校正 QT 间期的持续时间以及 12 导联体表心电图(12L-ECG)上 ST-T 波形态的变化相关。对这些变量进行远程监测可能会有所帮助。
评估两款可穿戴心电图设备(Apple Watch 和 KardiaMobile 6L)在提供 LQTS 患者校正 QT 间期和 ST-T 波形态可靠心电图方面的能力。
在一项前瞻性多中心研究(ClinicalTrials.gov 标识符:NCT04728100)中,记录了 LQTS 患者的 12L-ECG、6 导联 KardiaMobile 6L 心电图和两个单导联 Apple Watch 心电图。手动评估校正 QT 间期和 ST-T 波形态。
总体而言,共有 98 例 LQTS 患者纳入研究;其中 12.2%为儿童,92.8%存在 LQTS 基因致病性变异。主要基因型为 LQTS 1 型(40.8%)、LQTS 2 型(36.7%)和 LQTS 3 型(7.1%);也存在较罕见的基因型。在比较 12L-ECG 获得的 ST-T 波形态时,Apple Watch 的一致性为中度(k=0.593),KardiaMobile 6L 的一致性为高度(k=0.651)。关于校正 QT 间期,Apple Watch 与 12L-ECG 的相关性较强(导联 II 中 r=0.703),KardiaMobile 6L 的相关性为中度(r=0.593)。Apple Watch 会略微高估校正 QT 间期,而 KardiaMobile 6L 则会轻微低估校正 QT 间期。
在 LQTS 患者中,Apple Watch 和 KardiaMobile 6L 获得的校正 QT 间期和 ST-T 波形态与 12L-ECG 相关。虽然可穿戴心电图设备不能替代 12L-ECG 用于这些患者的随访,但它们可能是有趣的额外监测工具。