Al-Balushi Sara, Alam Mohammed Fasihul, Abid Abdul Rehman, Sharfi Amal
Department of Pharmacy, Heart Hospital, Hamad Medical Corporation, Doha, Qatar.
Department of Public Health, College of Health Sciences, Health Cluster, Qatar University, Doha, Qatar.
Heart Views. 2021 Jul-Sep;22(3):165-173. doi: 10.4103/HEARTVIEWS.HEARTVIEWS_23_20. Epub 2021 Oct 11.
Ivabradine is recommended in heart failure (HF) patients to reduce cardiovascular death and hospitalization due to worsening of HF symptoms.
To study the effect of Ivabradine in addition to guideline-directed medical therapy (GDMT) in a group of HF patients with HR more than 70 bpm, HF with reduced ejection fraction (HFrEF) left ventricular ejection fraction (LVEF ≤ 40%), and New York Heart Association class II-IV.
The study was conducted at Heart Hospital, Hamad Medical Corporation, Qatar. HF patients with age > 18 years, LVEF ≤40%, on GDMT, and HR of ≥70 bpm were included. The study population was divided into two groups: ivabradine group and non-ivabradine group. The primary outcomes were risk, number and length of hospitalizations due to worsening HF, and cardiovascular mortality. The secondary outcome was all-cause mortality. Baseline characteristics were collected at enrollment. Study outcomes were compared in the two groups by applying Chi-square and Fisher's exact tests. Logistic regression model was applied to assess both hospitalizations and cardiovascular mortality.
A total of 111 patients were studied, 37 (33.94%) ivabradine group and 74 (66.67%) non-ivabradine group. Risk of hospitalization was lower in Ivabradine group compared to non-Ivabradine group (odds ratio: 0.43, 95% confidence interval [CI]: 0.16-1.015, P = 0.094). Average length of hospitalization in ivabradine and non-ivabradine groups was 12.54 and 8.91 days, respectively (incidence rate ratio [IRR]: 1.63, 95% CI: 0.79-3.38, = 0.187). Compared to non-ivabradine, ivabradine patients had lower number of hospitalizations (IRR: 1.13, 95% CI: 0.61-2.11, = 0.694). Death rate in both ivabradine and non-ivabradine groups was 3.
Ivabradine along with GDMT reduces the risk of hospitalization due to worsening HF symptoms. Ivabradine had no significant effect on cardiovascular mortality and all-cause mortality. HFrEF non-Arabs patients have lower risk, number and length of hospitalization, and mortality compared to Arabs.
伊伐布雷定被推荐用于心力衰竭(HF)患者,以降低因HF症状恶化导致的心血管死亡和住院风险。
研究在一组心率超过70次/分钟、射血分数降低的心力衰竭(HFrEF)(左心室射血分数[LVEF]≤40%)且纽约心脏协会II-IV级的HF患者中,在指南指导的药物治疗(GDMT)基础上加用伊伐布雷定的效果。
该研究在卡塔尔哈马德医疗公司心脏医院进行。纳入年龄>18岁、LVEF≤40%、接受GDMT且心率≥70次/分钟的HF患者。研究人群分为两组:伊伐布雷定组和非伊伐布雷定组。主要结局是因HF恶化导致的住院风险、次数和时长,以及心血管死亡率。次要结局是全因死亡率。在入组时收集基线特征。通过卡方检验和费舍尔精确检验比较两组的研究结局。应用逻辑回归模型评估住院情况和心血管死亡率。
共研究了111例患者,伊伐布雷定组37例(33.94%),非伊伐布雷定组74例(66.67%)。与非伊伐布雷定组相比,伊伐布雷定组的住院风险更低(优势比:0.43,95%置信区间[CI]:0.16 - 1.015,P = 0.094)。伊伐布雷定组和非伊伐布雷定组的平均住院时长分别为12.54天和8.91天(发病率比[IRR]:1.63,95% CI:0.79 - 3.38,P = 0.187)。与非伊伐布雷定组相比,伊伐布雷定组患者的住院次数更少(IRR:1.13,95% CI:0.61 - 2.11,P = 0.694)。伊伐布雷定组和非伊伐布雷定组的死亡率均为3。
伊伐布雷定与GDMT联合使用可降低因HF症状恶化导致的住院风险。伊伐布雷定对心血管死亡率和全因死亡率无显著影响。与阿拉伯患者相比,非阿拉伯HFrEF患者的住院风险、次数和时长以及死亡率更低。