27 Influence of routine cardiac rhythm assessment in the long-term management of channelopathy patients

HM Sulaiman, R. Hackett, M. Hogg, E. Banks, A. Muir
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Abstract

27 Table 1Rhythm disturbances identified in follow up of channelopathy patients Diagnosis Gene testing result Monitoring method Symptoms Rhythm disturbance Alteration to treatment 1 OOHCA Query LQTS Gene negative ICD yes syncope NCT/inappropriate shock BBlocker changed to verapamil 2 OOHCA Query BrS Gene negative ICD none NCT Medication change 3 LQTS KCNQ1 ILR yes palpitations & pre-syncope AF anticoagulation 4 Screening LQTS No gene testing ILR yes palpitations, pre-syncope & syncope SVT EPS/ablation 5 LQTS KCNQ1 Holter none 22% VEs, 7 beats NSVT ICD offered 6 LQTS KCNQ1 Holter yes palpitations PAT BBlocker commenced 7 BrS SCN5a VUS Holter yes palpitations Atrial PACs, NCT, conduction disease, NSVT ICD offered and declined *OOHCA: Out of hospital cardiac arrest, LQTS= LQT syndrome, BrS: Brugada syndrome, BBlocker: beta-blocker, NCT: narrow complex tachycardia, AF: atrial fibrillation, SVT: supraventricular tachycardia, NSVT: non-sustained ventricular tachycardia, PAT: paroxysmal atrial tachycardia, PACs: paroxysmal atrial complex, VE: ventricular ectopic, ILR: implantable loop recorder, ICD: Implantable cardiac defibrillator, EPS: EP study.ConclusionIn our selected channelopathy patients, we demonstrated that the yield of routine monitoring arrangement is low at 10% despite 50% of patients reporting concerning cardiac symptoms. A large proportion of our cohort continue to await rhythm assessment due to delays in scheduling from the Covid-19 pandemic but 93% have had no change in management to date. As of March 2021 mortality was only 1% with just a single patient dying of a suspected dysrhythmia. There is a lack of international guideline on timing of follow up investigation in routine management of channelopathies, but our cohort suggests that routine Holter monitoring in asymptomatic LQTS and BrS does not significantly alter sudden cardiac de th (SCD) risk management. We educate our ICC channelopathy patients’ to report their symptoms to facilitate prompt rhythm assessment, and given pressures on current health systems, perhaps focusing on these symptomatic patients would be an appropriate use of resources.
常规心律评估对通道病变患者长期治疗的影响
27表1通道病变患者随访中发现的节律障碍诊断基因检测结果监测方法症状节律障碍治疗改变1 OOHCA查询LQTS基因阴性ICD是晕厥NCT/不合适的休克阻滞剂改为维拉帕米2 OOHCA查询BrS基因阴性ICD无NCT药物改变3 LQTS KCNQ1 ILR是心悸和晕厥前房颤抗凝4筛选LQTS无基因检测ILR是心悸,先期晕厥和晕厥SVT EPS/消融5 LQTS KCNQ1 Holter无22% VEs, 7次非SVT ICD提供6 LQTS KCNQ1 Holter yes心悸PAT阻滞剂开始使用7 BrS SCN5a VUS Holter yes心悸心房PACs, NCT,传导疾病,NSVT ICD提供和拒绝*OOHCA:院外心脏骤停,LQTS= LQT综合征,BrS: Brugada综合征,阻滞剂:β -阻滞剂,NCT:狭窄复杂心动过速,AF:房颤,SVT:室上性心动过速,NSVT:非持续性室性心动过速,PAT:阵发性房性心动过速,PACs:阵发性房性复合体,VE:室性异位,ILR:植入式环路记录仪,ICD:植入式心脏除颤器,EPS: EP研究。结论:在我们选择的通道病变患者中,我们证明常规监测安排的成功率低至10%,尽管50%的患者报告有心脏症状。由于Covid-19大流行导致日程安排延迟,我们的大部分队列继续等待节律评估,但迄今为止,93%的患者在管理方面没有变化。截至2021年3月,死亡率仅为1%,只有一名患者死于疑似心律失常。对于通道病变常规治疗的随访调查时间,目前缺乏国际指南,但我们的队列研究表明,无症状LQTS和BrS的常规动态心电图监测并没有显著改变心脏猝死(SCD)风险管理。我们教育ICC通道病患者报告他们的症状,以促进及时的心律评估,鉴于当前卫生系统的压力,也许关注这些有症状的患者将是资源的适当利用。
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