Fang Shawn Foo MBChB, FRACP , Mildred Lee BTech, MSc , Wil Harrison MBChB, FRACP , Geoffrey C. Clare MBChB, FRACP , Martin K. Stiles MBChB, PhD, FRACP , Andrew Gavin MBChB, FRACP , Matthew Webber MBChB, FRACP , Andrew Martin MBChB, FRACP , Rod Jackson MBChB, PhD, FNZCPH, FRSNZ , Andrew J. Kerr MBChB, MD, FRACP
{"title":"Long-Term Clinical Outcomes and Predictors of Mortality in Implantable Cardioverter-Defibrillator Recipients in New Zealand (ANZACS-QI 83)","authors":"Fang Shawn Foo MBChB, FRACP , Mildred Lee BTech, MSc , Wil Harrison MBChB, FRACP , Geoffrey C. Clare MBChB, FRACP , Martin K. Stiles MBChB, PhD, FRACP , Andrew Gavin MBChB, FRACP , Matthew Webber MBChB, FRACP , Andrew Martin MBChB, FRACP , Rod Jackson MBChB, PhD, FNZCPH, FRSNZ , Andrew J. Kerr MBChB, MD, FRACP","doi":"10.1016/j.hlc.2025.03.015","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>The long-term clinical outcomes of implantable cardioverter-defibrillator (ICD) recipients across New Zealand are unknown. This study aims to compare the all-cause mortality of primary and secondary prevention ICD recipients in New Zealand and identify predictors of mortality.</div></div><div><h3>Method</h3><div>Patients who received a primary or secondary prevention ICD in New Zealand between 2016 and 2020 were identified using the Aotearoa NZ All Cardiology Services Quality Improvement Cardiac Implanted Device Registry [ANZACS-QI DEVICE], a national registry for cardiac implantable electronic devices. Patients with infiltrative cardiomyopathies, congenital heart disease, and channelopathies were excluded. The primary outcome was all-cause mortality. Secondary outcomes were cardiovascular (CVD) mortality, non-CVD mortality, heart failure hospitalisation, and ventricular arrhythmia hospitalisation. Log-rank tests on Kaplan–Meier curves and 4-year Kaplan–Meier event rates were reported. Cox regression multivariate analysis was performed to identify predictors of all-cause mortality.</div></div><div><h3>Results</h3><div>There were 1,990 patients, including 1,067 (53.6%) primary prevention and 923 (46.4%) secondary prevention ICD recipients, with a mean follow-up of 4.0±1.5 years. The median age was 62 years, 29.6% were Māori or Pacific Islanders.</div><div>At 4 years, the all-cause mortality was higher in the primary prevention group than in the secondary prevention group (17.1% vs 11.8%; p=0.002). This was due to a higher rate of CVD mortality (11.9% vs 7.3%; p=0.008), with no significant difference in non-CVD mortality (5.9% vs 4.8%; p=0.093). Compared with the secondary prevention group, the primary prevention group had more heart failure hospitalisations (30.2% vs 17.9%; p<0.001) but fewer ventricular arrhythmia hospitalisations (14.8% vs 29.0%; p<0.001).</div><div>Significant predictors of mortality in multivariate regression analyses were Māori or Pacific Islander ethnicity (primary prevention hazard ratio [HR] 2.12; p<0.001; secondary prevention HR 1.71; p=0.018); older age (per 10-year increase in age: primary prevention HR 1.33; p=0.003; secondary prevention HR 1.72; p<0.001), and poorer renal function (per 10 mL/min/1.73m<sup>2</sup> decrease: primary prevention HR 1.21; p<0.001; secondary prevention HR 1.25; p<0.001). Previous myocardial infarction was not a significant predictor of mortality in either cohort.</div></div><div><h3>Conclusions</h3><div>In New Zealand ICD recipients, long-term all-cause mortality and CVD mortality rates were higher in primary prevention than secondary prevention ICD implants. Non-CVD mortality was low and similar in both cohorts, consistent with appropriate patient selection. The higher mortality observed for Māori and Pacific Islander patients require further investigation.</div></div>","PeriodicalId":13000,"journal":{"name":"Heart, Lung and Circulation","volume":"34 9","pages":"Pages 891-899"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heart, Lung and Circulation","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1443950625002112","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Background
The long-term clinical outcomes of implantable cardioverter-defibrillator (ICD) recipients across New Zealand are unknown. This study aims to compare the all-cause mortality of primary and secondary prevention ICD recipients in New Zealand and identify predictors of mortality.
Method
Patients who received a primary or secondary prevention ICD in New Zealand between 2016 and 2020 were identified using the Aotearoa NZ All Cardiology Services Quality Improvement Cardiac Implanted Device Registry [ANZACS-QI DEVICE], a national registry for cardiac implantable electronic devices. Patients with infiltrative cardiomyopathies, congenital heart disease, and channelopathies were excluded. The primary outcome was all-cause mortality. Secondary outcomes were cardiovascular (CVD) mortality, non-CVD mortality, heart failure hospitalisation, and ventricular arrhythmia hospitalisation. Log-rank tests on Kaplan–Meier curves and 4-year Kaplan–Meier event rates were reported. Cox regression multivariate analysis was performed to identify predictors of all-cause mortality.
Results
There were 1,990 patients, including 1,067 (53.6%) primary prevention and 923 (46.4%) secondary prevention ICD recipients, with a mean follow-up of 4.0±1.5 years. The median age was 62 years, 29.6% were Māori or Pacific Islanders.
At 4 years, the all-cause mortality was higher in the primary prevention group than in the secondary prevention group (17.1% vs 11.8%; p=0.002). This was due to a higher rate of CVD mortality (11.9% vs 7.3%; p=0.008), with no significant difference in non-CVD mortality (5.9% vs 4.8%; p=0.093). Compared with the secondary prevention group, the primary prevention group had more heart failure hospitalisations (30.2% vs 17.9%; p<0.001) but fewer ventricular arrhythmia hospitalisations (14.8% vs 29.0%; p<0.001).
Significant predictors of mortality in multivariate regression analyses were Māori or Pacific Islander ethnicity (primary prevention hazard ratio [HR] 2.12; p<0.001; secondary prevention HR 1.71; p=0.018); older age (per 10-year increase in age: primary prevention HR 1.33; p=0.003; secondary prevention HR 1.72; p<0.001), and poorer renal function (per 10 mL/min/1.73m2 decrease: primary prevention HR 1.21; p<0.001; secondary prevention HR 1.25; p<0.001). Previous myocardial infarction was not a significant predictor of mortality in either cohort.
Conclusions
In New Zealand ICD recipients, long-term all-cause mortality and CVD mortality rates were higher in primary prevention than secondary prevention ICD implants. Non-CVD mortality was low and similar in both cohorts, consistent with appropriate patient selection. The higher mortality observed for Māori and Pacific Islander patients require further investigation.
背景:新西兰植入式心脏转复除颤器(ICD)受者的长期临床结果尚不清楚。本研究旨在比较新西兰一级和二级预防ICD受者的全因死亡率,并确定死亡率的预测因素。方法:2016年至2020年期间在新西兰接受一级或二级预防ICD的患者使用Aotearoa新西兰所有心脏病学服务质量改进心脏植入设备登记处[ANZACS-QI Device]进行识别,该登记处是心脏植入电子设备的国家登记处。排除有浸润性心肌病、先天性心脏病和血管病变的患者。主要结局为全因死亡率。次要结局是心血管(CVD)死亡率、非CVD死亡率、心力衰竭住院和室性心律失常住院。报告Kaplan-Meier曲线的Log-rank检验和4年Kaplan-Meier事件发生率。采用Cox回归多因素分析确定全因死亡率的预测因素。结果:1990例患者,其中一级预防1067例(53.6%),二级预防923例(46.4%),平均随访4.0±1.5年。年龄中位数为62岁,29.6%为Māori或太平洋岛民。4年时,一级预防组的全因死亡率高于二级预防组(17.1% vs 11.8%;p = 0.002)。这是由于心血管疾病死亡率较高(11.9% vs 7.3%;p=0.008),非心血管疾病死亡率无显著差异(5.9% vs 4.8%;p = 0.093)。与二级预防组相比,一级预防组有更多的心力衰竭住院(30.2% vs 17.9%;p2降低:一级预防HR 1.21;结论:在新西兰ICD受术者中,一级预防的长期全因死亡率和心血管疾病死亡率高于二级预防ICD植入者。两组患者的非心血管疾病死亡率都很低且相似,这与适当的患者选择一致。Māori和太平洋岛民患者观察到的较高死亡率需要进一步调查。
期刊介绍:
Heart, Lung and Circulation publishes articles integrating clinical and research activities in the fields of basic cardiovascular science, clinical cardiology and cardiac surgery, with a focus on emerging issues in cardiovascular disease. The journal promotes multidisciplinary dialogue between cardiologists, cardiothoracic surgeons, cardio-pulmonary physicians and cardiovascular scientists.