Wearable cardioverter-defibritlator as a bridge to cardiac transplantation: A national database analysis

被引:35
作者
Opreanu, Madalina [1 ]
Wan, Chingping [2 ]
Singh, Vini [1 ]
Salehi, Negar [1 ]
Ahmad, Jaffri [1 ]
Szymkiewicz, Steven J. [2 ]
Thakur, Ranjan K. [1 ]
机构
[1] Michigan State Univ, Sparrow Thorac & Cardiovasc Inst, Lansing, MI USA
[2] Zoll Med Corp, Pittsburgh, PA USA
关键词
heart failure; heart transplantation; wearable carclioverter-defibrillator; sudden cardiac death; cardiac arrest; implantable cardioverter defibrillator; ATRIAL-FIBRILLATION; HEART-FAILURE; DEFIBRILLATOR IMPLANTATION; INTERNATIONAL SOCIETY; LUNG TRANSPLANTATION; EXPERIENCE; CANDIDATES;
D O I
10.1016/j.healun.2015.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Life-threatening ventricular arrhythmias (VAs) and sudden cardiac death (SCD) are common in patients awaiting heart transplantation (HT), and the implantable cardioverter-defibrillator (ICD) is often used for primary prevention in this setting. Use of ICDs in these patients is not without risks and is sometimes contraindicated. The wearable cardioverter-defibrillator (WCD) may be a reasonable alternative to bridge the period of risk leading up to HT. METHODS: We obtained a convenience sample of patients prescribed an WCD as a bridge therapy to HT. The available data consisted of demographics, cardiac transplantation status, associated comorbidities, device use, device-stored electrocardiogram (ECG) and reason for discontinuing the WCD. Statistical analyses were performed using SPSS version 17 and Graph Pad PRISM 5. RESULTS: The registry included 121 patients consisting of 83 (69%) men and 38 (31%) women. The mean age was 44 +/- 18 years. Mean ejection fraction was 25 +/- 15%. Non-ischemic cardiomyopathy (CMP) was the underlying diagnosis in 67 (55%) patients, whereas 21(17%) patients had ischemic CMP and 33 (27%) had a mixed or uncharacterized CMP. New York Heart Association Class III heart failure was present in 32% and 34% were in Class IV. Eighty-eight patients (73%) were being evaluated for HT or were on an HT waiting list, and 33 patients (27%) had had a prior HT, experienced rejection, and were awaiting re-transplantation. The patients wore the WCD for an average of 127 392 days (median 39 days) with average daily use of 17 +/- 7 hours (median 20 hours). Seven patients (6%) received appropriate WCD shocks. Fifty-one patients (42%) ended use after ICD implantation and 13 patients (11%) after HT. There were 11 deaths (9%). CONCLUSIONS: A significant proportion of patients on the HT waiting list will have VA. WCD use in our study showed high compliance and efficacy and a low complication rate, suggesting that the WCD is a reasonable bridge therapy for preventing SCD in patients awaiting HT. (C) 2015 International Society for Heart and Lung Transplantation. All rights reserved.
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收藏
页码:1305 / 1309
页数:5
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