Okazaki Hirotake, Shirakabe Akihiro, Hata Noritake, Kobayashi Nobuaki, Matsushita Masato, Shibata Yusaku, Nishigoori Suguru, Uchiyama Saori, Kiuchi Kazutaka, Asai Kuniya, Shimizu Wataru
Division of Intensive Care Unit, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan.
Heart Vessels. 2018 Dec;33(12):1496-1504. doi: 10.1007/s00380-018-1204-7. Epub 2018 Jun 26.
Atherosclerotic diseases sometimes contribute to acute heart failure (AHF). The aim of the present study is to elucidate the prognostic impact of AHF with atherosclerosis. A total of 1226 AHF patients admitted to the intensive care unit were analyzed. AHF associated with atherosclerosis was defined by the etiology: atherosclerosis-AHF group (n = 708) (patients whose etiologies were ischemic heart disease or hypertensive heart disease) or AHF not associated with atherosclerosis (non-atherosclerosis-AHF) group (n = 518). Kaplan-Meier curves showed that the survival rate of the atherosclerosis-AHF group was significantly better than that of the non-atherosclerosis-AHF group within 730 days of follow-up. Regarding pre-hospital medications, atherosclerosis-AHF patients were more likely to be administered nitroglycerin (20.3 vs. 13.7%, p = 0.003), nicorandil (18.8 vs. 7.5%, p < 0.001), angiotensin-converting enzyme inhibitor (ACE-I) or angiotensin II receptor blocker (ARB) (46.5 vs. 38.6%, p = 0.006), β-blocker (33.2 vs. 26.6%, p = 0.014) and statin (30.1 vs. 22.4%, p = 0.003) because of a previous coronary event or atherosclerotic diseases. In sub-group analysis of medication including administered ≥ 3 drugs within 5 medications and ACE-I/ARB, atherosclerosis-AHF significantly decreased the rate of all-cause death within 180 days (hazard ratio (HR) 0.215, 95% CI 0.078-0.593 and HR 0.395, 95% CI 0.244-0.641, respectively) with a significant interaction (p value for interaction 0.022 and 0.005, respectively). Kaplan-Meier curves showed that the 180-days survival rate of the atherosclerosis-AHF group with ACE-I/ARB and ≥ 3 drugs were significantly better than other groups. The AHF patients associated with atherosclerosis lead to be a good long-term outcome. A relationship may exist between efficient treatment including ACE-Is before admission and a good outcome in mid-term.
动脉粥样硬化性疾病有时会导致急性心力衰竭(AHF)。本研究的目的是阐明合并动脉粥样硬化的AHF对预后的影响。对1226例入住重症监护病房的AHF患者进行了分析。根据病因将合并动脉粥样硬化的AHF定义为:动脉粥样硬化性AHF组(n = 708)(病因是缺血性心脏病或高血压性心脏病的患者)或不合并动脉粥样硬化的AHF组(非动脉粥样硬化性AHF组)(n = 518)。Kaplan-Meier曲线显示,在随访的730天内,动脉粥样硬化性AHF组的生存率显著高于非动脉粥样硬化性AHF组。关于院前用药,由于既往有冠状动脉事件或动脉粥样硬化性疾病,动脉粥样硬化性AHF患者更有可能使用硝酸甘油(20.3%对13.7%,p = 0.003)、尼可地尔(18.8%对7.5%,p < 0.001)、血管紧张素转换酶抑制剂(ACE-I)或血管紧张素II受体阻滞剂(ARB)(46.5%对38.6%,p = 0.006)、β受体阻滞剂(33.2%对26.6%,p = 0.014)和他汀类药物(30.1%对22.4%,p = 0.003)。在包括5种药物中使用≥3种药物以及ACE-I/ARB的用药亚组分析中,动脉粥样硬化性AHF显著降低了180天内的全因死亡率(风险比(HR)分别为0.215,95%置信区间0.078 - 0.593和HR 0.395,95%置信区间0.244 - 0.641),且存在显著交互作用(交互作用的p值分别为0.022和0.005)。Kaplan-Meier曲线显示,使用ACE-I/ARB且使用≥3种药物的动脉粥样硬化性AHF组的180天生存率显著高于其他组。合并动脉粥样硬化的AHF患者长期预后良好。入院前包括ACE-I在内的有效治疗与中期良好预后之间可能存在关联。