Micaela Ebert MD, Ines Masmoudi MD, Mandy Flechsig MD, Julia Mayer MD, Stefan Ulbrich MD, Leonhard Schleußner MD, Thomas Gaspar MD, Angela Zedda MD, Axel Linke MD, Sergio Richter MD
{"title":"不同类型室性心动过速伴低钾血症的处理和结局","authors":"Micaela Ebert MD, Ines Masmoudi MD, Mandy Flechsig MD, Julia Mayer MD, Stefan Ulbrich MD, Leonhard Schleußner MD, Thomas Gaspar MD, Angela Zedda MD, Axel Linke MD, Sergio Richter MD","doi":"10.1016/j.hroo.2025.05.030","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Hypokalemia is a potentially reversible cause of ventricular tachyarrhythmias (VTAs) such as polymorphic ventricular tachycardia/ventricular fibrillation (PMVT/VF) and sustained monomorphic ventricular tachycardia (SMVT). Despite its established role in arrhythmogenesis, the clinical implications of hypokalemia in patients with distinct VTA subtypes remain poorly understood.</div></div><div><h3>Objective</h3><div>The aims of this study were to study the clinical characteristics, management, and outcome of patients with hypokalemia-associated VTAs and to investigate the prognosis of distinct VTA subtypes after correction of hypokalemia with or without additional VT–targeted therapies (VTTTs), such as catheter ablation or antiarrhythmic drugs.</div></div><div><h3>Methods</h3><div>Consecutive patients admitted with hypokalemia-associated VTAs were analyzed after hypokalemia correction. Patients were categorized by VTA subtype and followed for VT recurrence, 24-month VT-free survival, and all-cause mortality. Those with other reversible causes of VTAs were excluded.</div></div><div><h3>Results</h3><div>Sixty-five patients (mean age 69 ± 12 years; 20% (n = 13) women; mean left ventricular ejection fraction 32% ± 13%; 54% (n = 35) with New York Heart Association class III/IV; 8% (n = 5) with a left ventricular assist device) were studied; 68% (n = 44) presented with SMVT. Patients with SMVT were younger (65 ± 11 years vs 77 ± 10 years; <em>P</em> < .001) and had more advanced left ventricular dilation (left ventricular end-diastolic diameter 64 ± 12 mm vs 57 ± 12 mm; <em>P</em> = .03). Over a median follow-up of 18 months, 24-month VT-free survival was 28%. Patients with SMVT had higher VT recurrence (50% vs 10%; <em>P</em> = .002) and lower 24-month VT-free survival (16% vs 52%; <em>P</em> = .005) than did those with PMVT/VF. Among patients with SMVT, those receiving VTTTs (36%, (n = 16/44)) showed improved 24-month VT-free survival compared with hypokalemia correction alone (31% vs 7%; <em>P</em> = .02).</div></div><div><h3>Conclusion</h3><div>Hypokalemia-associated VTAs are associated with advanced heart failure and linked to poor outcomes, especially in patients with SMVT. Although potassium correction may be sufficient for patients with hypokalemia-associated PMVT/VF, those with SMVT require additional VTTTs to improve outcomes.</div></div>","PeriodicalId":29772,"journal":{"name":"Heart Rhythm O2","volume":"6 9","pages":"Pages 1391-1400"},"PeriodicalIF":2.9000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Management and outcome of different types of ventricular tachycardia associated with hypokalemia\",\"authors\":\"Micaela Ebert MD, Ines Masmoudi MD, Mandy Flechsig MD, Julia Mayer MD, Stefan Ulbrich MD, Leonhard Schleußner MD, Thomas Gaspar MD, Angela Zedda MD, Axel Linke MD, Sergio Richter MD\",\"doi\":\"10.1016/j.hroo.2025.05.030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Hypokalemia is a potentially reversible cause of ventricular tachyarrhythmias (VTAs) such as polymorphic ventricular tachycardia/ventricular fibrillation (PMVT/VF) and sustained monomorphic ventricular tachycardia (SMVT). Despite its established role in arrhythmogenesis, the clinical implications of hypokalemia in patients with distinct VTA subtypes remain poorly understood.</div></div><div><h3>Objective</h3><div>The aims of this study were to study the clinical characteristics, management, and outcome of patients with hypokalemia-associated VTAs and to investigate the prognosis of distinct VTA subtypes after correction of hypokalemia with or without additional VT–targeted therapies (VTTTs), such as catheter ablation or antiarrhythmic drugs.</div></div><div><h3>Methods</h3><div>Consecutive patients admitted with hypokalemia-associated VTAs were analyzed after hypokalemia correction. Patients were categorized by VTA subtype and followed for VT recurrence, 24-month VT-free survival, and all-cause mortality. Those with other reversible causes of VTAs were excluded.</div></div><div><h3>Results</h3><div>Sixty-five patients (mean age 69 ± 12 years; 20% (n = 13) women; mean left ventricular ejection fraction 32% ± 13%; 54% (n = 35) with New York Heart Association class III/IV; 8% (n = 5) with a left ventricular assist device) were studied; 68% (n = 44) presented with SMVT. Patients with SMVT were younger (65 ± 11 years vs 77 ± 10 years; <em>P</em> < .001) and had more advanced left ventricular dilation (left ventricular end-diastolic diameter 64 ± 12 mm vs 57 ± 12 mm; <em>P</em> = .03). Over a median follow-up of 18 months, 24-month VT-free survival was 28%. Patients with SMVT had higher VT recurrence (50% vs 10%; <em>P</em> = .002) and lower 24-month VT-free survival (16% vs 52%; <em>P</em> = .005) than did those with PMVT/VF. Among patients with SMVT, those receiving VTTTs (36%, (n = 16/44)) showed improved 24-month VT-free survival compared with hypokalemia correction alone (31% vs 7%; <em>P</em> = .02).</div></div><div><h3>Conclusion</h3><div>Hypokalemia-associated VTAs are associated with advanced heart failure and linked to poor outcomes, especially in patients with SMVT. Although potassium correction may be sufficient for patients with hypokalemia-associated PMVT/VF, those with SMVT require additional VTTTs to improve outcomes.</div></div>\",\"PeriodicalId\":29772,\"journal\":{\"name\":\"Heart Rhythm O2\",\"volume\":\"6 9\",\"pages\":\"Pages 1391-1400\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Heart Rhythm O2\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666501825001928\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heart Rhythm O2","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666501825001928","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
背景:低钾血症是室性心动过速(VTAs)的潜在可逆原因,如多形性室性心动过速/室颤(PMVT/VF)和持续性单形性室性心动过速(SMVT)。尽管低钾血症在心律失常发生中起着确定的作用,但低钾血症在不同VTA亚型患者中的临床意义仍然知之甚少。目的:研究低钾相关性VTA患者的临床特征、治疗和预后,并探讨不同VTA亚型患者在接受或不接受额外的vtt靶向治疗(vtts)(如导管消融或抗心律失常药物)纠正低钾血症后的预后。方法对连续入院的低钾血症相关VTAs患者进行低钾血症纠正后的分析。患者按室性心动过速亚型分类,随访室性心动过速复发、无室性心动过速24个月生存率和全因死亡率。排除有其他可逆原因的VTAs。结果65例患者(平均年龄69±12岁),女性占20% (n = 13);平均左室射血分数32%±13%;54% (n = 35)为纽约心脏协会III/IV级;8% (n = 5)使用左心室辅助装置;68% (n = 44)表现为SMVT。SMVT患者更年轻(65±11岁vs 77±10岁;P < .001),左室扩张更严重(左室舒张末期直径64±12 mm vs 57±12 mm; P = .03)。在18个月的中位随访中,24个月无vt生存率为28%。与PMVT/VF患者相比,SMVT患者有更高的VT复发率(50% vs 10%, P = 0.002)和更低的24个月无VT生存率(16% vs 52%, P = 0.005)。在SMVT患者中,接受vtts的患者(36%,(n = 16/44))与单纯低钾血症矫正相比,24个月无vtts生存率提高(31% vs 7%; P = 0.02)。结论低钾相关性VTAs与晚期心力衰竭相关,并与不良预后相关,尤其是在SMVT患者中。虽然钾矫正对低钾血症相关PMVT/VF患者可能足够,但SMVT患者需要额外的vttt来改善预后。
Management and outcome of different types of ventricular tachycardia associated with hypokalemia
Background
Hypokalemia is a potentially reversible cause of ventricular tachyarrhythmias (VTAs) such as polymorphic ventricular tachycardia/ventricular fibrillation (PMVT/VF) and sustained monomorphic ventricular tachycardia (SMVT). Despite its established role in arrhythmogenesis, the clinical implications of hypokalemia in patients with distinct VTA subtypes remain poorly understood.
Objective
The aims of this study were to study the clinical characteristics, management, and outcome of patients with hypokalemia-associated VTAs and to investigate the prognosis of distinct VTA subtypes after correction of hypokalemia with or without additional VT–targeted therapies (VTTTs), such as catheter ablation or antiarrhythmic drugs.
Methods
Consecutive patients admitted with hypokalemia-associated VTAs were analyzed after hypokalemia correction. Patients were categorized by VTA subtype and followed for VT recurrence, 24-month VT-free survival, and all-cause mortality. Those with other reversible causes of VTAs were excluded.
Results
Sixty-five patients (mean age 69 ± 12 years; 20% (n = 13) women; mean left ventricular ejection fraction 32% ± 13%; 54% (n = 35) with New York Heart Association class III/IV; 8% (n = 5) with a left ventricular assist device) were studied; 68% (n = 44) presented with SMVT. Patients with SMVT were younger (65 ± 11 years vs 77 ± 10 years; P < .001) and had more advanced left ventricular dilation (left ventricular end-diastolic diameter 64 ± 12 mm vs 57 ± 12 mm; P = .03). Over a median follow-up of 18 months, 24-month VT-free survival was 28%. Patients with SMVT had higher VT recurrence (50% vs 10%; P = .002) and lower 24-month VT-free survival (16% vs 52%; P = .005) than did those with PMVT/VF. Among patients with SMVT, those receiving VTTTs (36%, (n = 16/44)) showed improved 24-month VT-free survival compared with hypokalemia correction alone (31% vs 7%; P = .02).
Conclusion
Hypokalemia-associated VTAs are associated with advanced heart failure and linked to poor outcomes, especially in patients with SMVT. Although potassium correction may be sufficient for patients with hypokalemia-associated PMVT/VF, those with SMVT require additional VTTTs to improve outcomes.