Sicras Mainar A, Fernández de Bobadilla J, Rejas Gutiérrez J, García Vargas M
Servicios Asistenciales, Badalona.
An Med Interna. 2006 Aug;23(8):361-8. doi: 10.4321/s0212-71992006000800003.
Lack of compliance is a major factor responsible for the differences between clinical trial results and real effectiveness in daily medical practice, contributing to an insufficient control of the cardiovascular risk factors (CVRF). Knowledge of the factors contributing to lack of compliance is limited, and in Spain data are scarce. The objectives of this study are: a) to indirectly determine the level of compliance among patients with hypertension and/or dyslipidemia; and b) to determine factors associated with compliance.
9,001 hypertensive and/or dyslipidemic patients from four primary care centres in Catalonia were enrolled in Disease Management programmes during the previous four years. Compliance was estimated by the relationship between the amount of dispensed and prescribed pills: a) the levels of compliance of dyslipidemic patients without hypertension (DL-non HT), hypertensive patients with dyslipidemia (HT+DL) and hypertensives without dyslipidemia (HT-non DL) were compared; and b) an stepwise, multivariate, descriptive; multiple regression model was designed in order to explain compliance.
依从性不佳是导致临床试验结果与日常医疗实践中实际疗效存在差异的主要因素,这使得心血管危险因素(CVRF)的控制不足。导致依从性不佳的因素相关知识有限,且在西班牙此类数据稀缺。本研究的目的是:a)间接确定高血压和/或血脂异常患者的依从性水平;b)确定与依从性相关的因素。
来自加泰罗尼亚四个初级保健中心的9001例高血压和/或血脂异常患者在过去四年中参加了疾病管理项目。通过配药数量与处方数量的关系来估计依从性:a)比较无高血压的血脂异常患者(DL-非HT)、伴有血脂异常的高血压患者(HT+DL)和无血脂异常的高血压患者(HT-非DL)的依从性水平;b)设计一个逐步的、多变量的、描述性的多元回归模型以解释依从性。