首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Stroke monitoring on a national level: PERFECT Stroke, a comprehensive, registry-linkage stroke database in Finland.
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Stroke monitoring on a national level: PERFECT Stroke, a comprehensive, registry-linkage stroke database in Finland.

机译:在国家一级进行卒中监测:PERFECT Stroke,芬兰的一个完整的注册表链接卒中数据库。

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BACKGROUND AND PURPOSE: Stroke databases are established to systematically evaluate both the treatment and outcome of stroke patients and the structure and processes of stroke services. Comprehensive data collection on this common disease is resource-intensive, and national stroke databases often include only patients from selected hospitals. Here we describe an alternative national stroke database. METHODS: We established a nationwide stroke database with multiple administrative registry linkages at the individual-patient level. Information on comorbidities; treatments before, during, and after stroke; living status; recurrences; case fatality; and costs were collected for each hospital-treated stroke patient. RESULTS: The current database includes 94 316 patients with incident stroke between January 1999 and December 2007, with follow-up until December 2008. Annually, 10 500 new patients are being added. One-year recurrence was 13% and case fatality was 27% during the study period. In 2007, 86% of patients survived 1 month and 77% were living at home at 3 months, but the proportion treated in stroke centers (62%) or with nationally recommended secondary preventive medication after ischemic stroke (49%) was still suboptimal. CONCLUSIONS: In comparison with other national stroke databases, our method enables higher coverage and more thorough follow-up of patients. Information on long-term recurrences, case fatality, or costs is not often included in national stroke databases. Our database has low maintenance costs, but it lacks detailed data on in-hospital processes. Use of national administrative data, where such linkage is possible, saves resources, achieves high rates of long-term follow-up, and allows for comprehensive monitoring of the burden of the disease.
机译:背景与目的:建立卒中数据库以系统地评估卒中患者的治疗和结果以及卒中服务的结构和过程。关于这种常见疾病的全面数据收集需要大量资源,国家卒中数据库通常仅包括来自选定医院的患者。在这里,我们描述了另一种国家卒中数据库。方法:我们建立了一个全国性的卒中数据库,在个体患者一级具有多个行政登记处联系。有关合并症的信息;中风之前,之中和之后的治疗;生活状况;复发;病死率并为每位住院治疗的中风患者收取费用。结果:当前的数据库包括1999年1月至2007年12月之间的94 316名中风事件患者,并随访至2008年12月。每年,新增加10 500名患者。在研究期间,一年复发率为13%,病死率为27%。 2007年,有86%的患者生存了1个月,有77%的患者在3个月时在家中生活,但是在卒中中心(62%)或全国推荐的缺血性卒中后二级预防药物(49%)的治疗比例仍然不理想。结论:与其他国家卒中数据库相比,我们的方法可实现更高的覆盖率和更彻底的患者随访。国家中风数据库通常不包含有关长期复发,病死率或费用的信息。我们的数据库维护成本低,但缺乏医院内流程的详细数据。在可能的情况下使用国家行政数据,可以节省资源,实现长期的高随访率,并可以全面监测疾病的负担。

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