急性冠脉综合征患者住院和30个月死亡率参数的回顾性评价

B. Alan, L. Kayikçioğlu, Irmak SAYIN ALAN
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引用次数: 0

摘要

目的:本研究的目的是回顾性评估在医学院附属医院诊断为急性冠脉综合征(ACS)并住院治疗的患者的临床资料和治疗策略,以研究这些资料对心血管事件发生和30个月死亡率的影响。方法:回顾性筛选2007年6月至2008年12月在医学院附属医院心内科门诊诊断为ACS的患者,采用患者档案资料和电子数据记录系统信息,并通过电话对患者进行评估。住院死亡和长期随访死亡是研究的终点。采用SPSS (Version 15.0)进行统计学分析。结果:985例确诊为ACS、住院并在医院治疗的患者纳入研究。根据诊断将901例患者分类为:UAP 339例(38%),NSTEMI 206例(23%),STEMI 356例(39%)。男性占78.4%,女性占21.6%。发现高血压、高脂血症、肥胖危险因素、有心血管病史的病例属于NSTEMI和UAP组,所占比例较大。其中,UAP诊断病例最多,STEMI诊断病例住院前使用受体阻滞剂、钙管阻滞剂、ACE抑制剂、ARB、利尿剂、他汀类药物、贝特、硝酸盐等药物组比例最小。住院死亡率经常出现,STEMI病例为7.6%,NSTEMI病例为2.4%,UAP病例为0.6%。所有诊断组随访30个月进行长期死亡率评估。随访期间观察到70例(7.8%)死亡。根据诊断组,UAP死亡22例(6.5%),NSTEMI死亡22例(10.7%),STEMI死亡26例(7.3%)。长期生存(30个月)与住院和出院时他汀类药物使用无显著相关性(p值分别为0.1和0.16)。大约30个月的生存率与住院时ACE抑制剂/ARB抑制剂的使用以及出院时ACE抑制剂/ARB抑制剂的使用之间存在显著相关性(p = 0.007和p = 0.004)。同一时期的生存率与院内β受体阻滞剂的使用有显著的相关性(p = 0.01)。出院时-受体阻滞剂的使用与长期生存无显著相关性(p = 0.779)。结论:纳入901例ACS诊断患者的单中心回顾性扫描研究的结果与GRACE和欧洲心脏调查前瞻性研究的结果相似,这些研究是在多中心环境中进行的,在人数较少的患者中进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrospective Evaluation of In-Hospital and Thirty-Month Mortality Parameters in Cases of Acute Coronary Syndrome
Objectives: The aim of this study is to retrospectively assess, from the hospital records of patients, the clinical data of patients and the treatment strategies practiced on patients who were diagnosed as Acute Coronary Syndrome (ACS) and hospitalized and treated in the Hospital of Faculty of Medicine to research the effect of these data on occurrence of cardiovascular events and 30 months mortality. Methods: It is a retrospective screening study in which patients hospitalized with the diagnosis of ACS between June 2007 and December 2008 in the Hospital of Faculty of Medicine Cardiology Clinic are evaluated by using patient file information and electronic data recording system information, and by calling patients. In-hospital and long-term follow-up deaths were the endpoints of the study. Statistical analysis was performed using SPSS (Version 15.0). Results: 985 patients were included in the study who were diagnosed as ACS, hospitalized and treated in the hospital. The categorization of the patients subjected to the analysis (n:901) according to their diagnosis is as follows: 339 (38%) cases diagnosed as UAP, 206 (23%) cases diagnosed as NSTEMI, and 356 (39%) cases diagnosed as STEMI. 78,4 % of cases were male while 21,6 % were female. It was found that cases with hypertension, hyperlipidemia, obesity risk factor, and with a history of cardiovascular disease fall into the NSTEMI and UAP groups with a larger proportion. Among the groups, the UAP diagnosed cases have the largest and the STEMI diagnosed cases have the smallest ratio of using medicine groups such as beta blocker, calcium-canal blocker, ACE inhibitor, ARB, diuretic, statin, fibrate and nitrate before being hospitalized. In-hospital mortality was frequently encountered with a percentage of 7.6 % in STEMI cases, 2.4 % in NSTEMI cases, and 0.6 % in UAP cases. 30-months of follow-up data were obtained in all diagnosis groups for long-term mortality assessment. 70 (7.8 %) deaths were observed within the follow-up. According to diagnosis groups, death was observed in 22 (6.5 %) of UAP cases, 22 (10.7 %) of NSTEMI cases, and 26 (7.3 %) of STEMI cases. Correlation between long-term survival (30 months) and in-hospital statin usage and statin usage in discharge was not significant (p value respectively 0.1 and 0.16). Correlation between an approximate 30-months-survival and in-hospital ACE inhibitor/ARB inhibitor usage and ACE inhibitor/ARB inhibitor usage during discharge was significant (p = 0.007 and p = 0.004). It is also found that there was a significant correlation between survival in the same period of time and in-hospital beta blocker usage (p = 0.01). There was not a significant correlation between beta blocker usage during discharge and long-term survival (p = 0.779). Conclusion: Results of the unicentral retrospective scanning study which involves 901 ACS diagnosed patients prove to be similar to the ones obtained from GRACE and Euro Heart Survey prospective studies which were carried out in multi-central environment and among outnumbered patients.
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