Sheerin Ian, Hamilton Greg, Humphrey Alistair, Scragg Alf
Department of Public Health and General Practice, Christchurch School of Medicine and Health Sciences, University of Otago, Christchurch.
N Z Med J. 2007 Sep 7;120(1261):U2714.
The aim was to audit patient records at selected general practices in Canterbury, New Zealand to assess the potential: (a) to improve identification and management of people with risk factors for cardiovascular disease (CVD); and (b) to develop a geographically distinct community database of CVD risk factor prevalence that could be used to plan public health programmes to improve cardiovascular health.
Patient records were audited in three general practices in a Canterbury rural town and information on cardiovascular risk factors recommended for the screening and management of CVD by the New Zealand Guidelines Group was extracted and entered into an electronic database. The data was analysed to assess the extent of recording of information on recommended risk factors.
Most patient records contained information on smoking, blood pressure and lipid profiles. Low levels of information recording were found for physical activity, body mass index (BMI), and family history. There were statistically significant differences between general practices in the type and coverage of information recorded, even for patients with diagnosed cardiovascular disease. Because of deficiencies in information, it was not possible to calculate CVD risk using the guidelines for 43% of patients. Some practices remain reliant on paper records which make it extremely difficult to undertake a systematic programme of screening and management of CVD risk factors.
Before it is practical to undertake a systematic screening programme for CVD risk factors in primary care, it is necessary to reduce reliance on paper records and to fully implement computerised patient management systems that allow for information storage and retrieval. In addition, it is essential to improve the systematic collection of key information in primary care that is used to assess risk of CVD.
旨在对新西兰坎特伯雷地区部分普通诊所的患者记录进行审查,以评估其潜在作用:(a) 改善对心血管疾病(CVD)风险因素人群的识别和管理;(b) 建立一个具有地域特色的CVD风险因素患病率社区数据库,用于规划改善心血管健康的公共卫生项目。
对坎特伯雷一个乡村小镇的三家普通诊所的患者记录进行审查,提取新西兰指南小组推荐的用于CVD筛查和管理的心血管风险因素信息,并录入电子数据库。对数据进行分析,以评估推荐风险因素信息的记录程度。
大多数患者记录包含吸烟、血压和血脂谱信息。发现身体活动、体重指数(BMI)和家族史的信息记录水平较低。即使对于已诊断患有心血管疾病的患者,不同普通诊所在记录信息的类型和覆盖范围上也存在统计学显著差异。由于信息不足,43%的患者无法按照指南计算CVD风险。一些诊所仍依赖纸质记录,这使得开展CVD风险因素的系统筛查和管理计划极为困难。
在初级保健中实际开展CVD风险因素的系统筛查计划之前,有必要减少对纸质记录的依赖,并全面实施允许信息存储和检索的计算机化患者管理系统。此外,必须改善初级保健中用于评估CVD风险的关键信息的系统收集。