Ganapathi Sanjay, Jeemon Panniyammakal, Krishnasankar Rajasekharan, Kochumoni Rajamoni, Vineeth Purushothaman, Mohanan Nair Krishna Kumar, Valaparambil Ajit Kumar, Harikrishnan Sivadasanpillai
Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, 695011, Kerala, India.
ESC Heart Fail. 2020 Apr;7(2):467-473. doi: 10.1002/ehf2.12600. Epub 2020 Feb 3.
Long-term outcome data of acute decompensated heart failure (HF) are scarce from India. The aim of the study was to collect in-hospital and long-term outcome data of HF patients admitted during 2001-2010 in a tertiary-care centre in South India.
Consecutive patients admitted with first episode of decompensated HF were part of the registry. Data regarding diagnosis, risk factors, treatment, early (in-hospital), and late (5 and 10year) mortality outcomes were captured. During this period, 1502 patients were admitted with first episode of decompensated HF [37.7% of women, mean age of 51.1 (SD = 14.3) years]. Common causes were ischaemic heart disease (36.2%), rheumatic heart disease (34.3%), and cardiomyopathies (9.9%). HF with reduced ejection fraction (HFrEF) was present in 26.9% of patients, and 33.8% had atrial arrhythmias. Diabetes, hypertension, and renal dysfunction were prevalent in 27.4%, 28.6%, and 37.4%, respectively. Median duration of hospitalization was 6 days (interquartile range: 3-10), and 247 patients (16.4%) died during index admission. The total time at risk was 6248 person years, and 1051 patients died during the study period with a median survival time of 3.7 years. Overall mortality rate was 16.8 per 100 person years (95% CI: 15.8-17.9 per 100 person years). Older age [hazard ratio (HR) = 1.08, 95% CI: 1.02-1.14, P = 0.007], anaemia (HR = 1.34, 95% CI: 1.08-1.65, P = 0.007), renal dysfunction (HR = 1.38, 95% CI: 1.20-1.59, P < 0.001), HFpEF (HR = 0.61, 95% CI: 0.52-0.73, P < 0.001 against HFrEF), and the use of guideline-directed therapies (GDT; beta blockers: HR = 0.57, 95% CI: 0.49-0.66, P < 0.0001; and angiotensin converting enzyme inhibitor/angiotensin receptor blocker: HR = 0.59, 95% CI: 0.51-0.69, P < 0.001) were important predictors of mortality. Patients with HF and mid-range EF also benefited from GDT.
In our cohort, ischaemic and rheumatic heart diseases were the leading contributors for HF. Anaemia, renal dysfunction, poor ejection fraction, and suboptimal prescriptions of GDT were the main predictors of long-term mortality. Both patients with HFrEF and mid-range EF benefited from GDT.
印度急性失代偿性心力衰竭(HF)的长期预后数据匮乏。本研究的目的是收集2001年至2010年期间在印度南部一家三级医疗中心住院的HF患者的院内及长期预后数据。
首次因失代偿性HF入院的连续患者纳入登记研究。记录有关诊断、危险因素、治疗、早期(院内)和晚期(5年及10年)死亡率结局的数据。在此期间,1502例患者因首次失代偿性HF入院[女性占37.7%,平均年龄51.1(标准差=14.3)岁]。常见病因包括缺血性心脏病(36.2%)、风湿性心脏病(34.3%)和心肌病(9.9%)。26.9%的患者存在射血分数降低的HF(HFrEF),33.8%的患者有心房心律失常。糖尿病、高血压和肾功能不全的患病率分别为27.4%、28.6%和37.4%。住院中位时长为6天(四分位间距:3 - 10天),247例患者(16.4%)在本次住院期间死亡。总风险时间为6248人年,1051例患者在研究期间死亡,中位生存时间为3.7年。总体死亡率为每100人年16.8例(95%置信区间:每100人年15.8 - 17.9例)。年龄较大[风险比(HR)=1.08,95%置信区间:1.02 - 1.14,P = 0.007]、贫血(HR = 1.34,95%置信区间:1.08 - 1.65,P = 0.007)、肾功能不全(HR = 1.38,95%置信区间:1.20 - 1.59,P < 0.001)、射血分数保留的HF(HFpEF,与HFrEF相比,HR = 0.61,95%置信区间:0.52 - 0.73,P < 0.001)以及使用指南指导的治疗(GDT;β受体阻滞剂:HR = 0.57,95%置信区间:0.49 - 0.66,P < 0.0001;血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂:HR = 0.59,95%置信区间:0.51 - 0.69,P < 0.001)是死亡率的重要预测因素。HF且射血分数处于中等范围的患者也从GDT中获益。
在我们的队列中,缺血性和风湿性心脏病是HF的主要病因。贫血、肾功能不全、射血分数差以及GDT处方不达标是长期死亡率的主要预测因素。HFrEF和射血分数处于中等范围的患者均从GDT中获益。