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协作性初级保健中心血管风险降低(CCARP)研究。

The Collaborative Cardiovascular Risk Reduction in Primary Care (CCARP) study.

机构信息

College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

出版信息

Pharmacotherapy. 2010 Aug;30(8):766-75. doi: 10.1592/phco.30.8.766.

Abstract

STUDY OBJECTIVE

To evaluate whether a simple pharmacist protocol, consisting of patient screening and cardiovascular risk stratification, identification and reminders about uncontrolled risk factors, and drug adherence support, can significantly reduce cardiovascular risk.

DESIGN

Prospective, randomized, controlled pilot study.

SETTING

Large primary care medical clinic in Saskatoon, Saskatchewan, Canada.

PATIENTS

One hundred seventy-six adult patients (mean age 60 yrs) who exhibited a 10-year Framingham risk score of 15% or greater, or a coronary artery disease risk equivalent (coronary artery disease, peripheral artery disease, cerebrovascular disease, or diabetes mellitus).

INTERVENTION

Eligible patients initially met with the pharmacist to receive general counselling about cardiovascular disease and were then randomly assigned to receive ongoing follow-up by the pharmacist (follow-up group [88 patients]) or to return to usual care (single-contact group [88 patients]) for a minimum of 6 months.

MEASUREMENTS AND MAIN RESULTS

The primary end point was mean reduction in the 10-year Framingham risk score. Secondary end points included individual modifiable risk factors (systolic and diastolic blood pressures; total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol [HDL], and triglyceride levels; total cholesterol:HDL ratio; and hemoglobin A(1c) value), as well as statin utilization, initiation, and adherence rates. Baseline characteristics were similar across both groups. Neither the mean reduction in 10-year risk (-2.68 for the follow-up group and -1.25 for the single-contact group, one-tailed p=0.098) nor individual risk factors were significantly different between groups. The proportion of patients exhibiting statin adherence of 80% or greater did not significantly differ between groups at study end (73.1% [57/78] and 80.0% [52/65], respectively, p=0.333). However, 85.2% (75/88) in the follow-up group continued with statin therapy at the end of the study compared with 67.0% (59/88) in the single-contact group (p=0.005). Statin initiations were more frequent in the follow-up group than in the single-contact group (75.0% [30/40) vs 48.9% [22/45], p=0.013).

CONCLUSION

This simple cardiovascular care protocol for nonspecialist pharmacists did not result in a clear improvement to cardiovascular risk reduction success among patients in a primary care medical clinic. The intervention did, however, appear to improve statin utilization.

摘要

研究目的

评估由药剂师实施的一项简单方案是否能显著降低心血管风险,该方案包括患者筛选和心血管风险分层、识别和提醒未得到控制的危险因素、以及药物依从性支持。

设计

前瞻性、随机、对照试验研究。

地点

加拿大萨斯喀彻温省萨斯卡通市的一个大型初级保健医疗诊所。

患者

176 名成年患者(平均年龄 60 岁),其Framingham 10 年风险评分大于等于 15%,或存在冠状动脉疾病风险等同物(冠心病、外周动脉疾病、脑血管疾病或糖尿病)。

干预措施

符合条件的患者最初与药剂师会面,接受有关心血管疾病的一般咨询,然后被随机分配到由药剂师进行的持续随访组(88 名患者)或仅接受单次接触的常规护理组(88 名患者),至少随访 6 个月。

测量和主要结果

主要终点是Framingham 10 年风险评分的平均降低幅度。次要终点包括单个可改变的危险因素(收缩压和舒张压;总胆固醇、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇[HDL]和甘油三酯水平;总胆固醇:HDL 比值;以及血红蛋白 A1c 值),以及他汀类药物的使用率、起始率和依从率。两组的基线特征相似。两组患者Framingham 10 年风险的平均降低幅度(随访组为-2.68,单次接触组为-1.25,单侧 p=0.098)或个体危险因素均无显著差异。研究结束时,两组患者他汀类药物依从性达到 80%或以上的比例无显著差异(分别为 73.1%[57/78]和 80.0%[52/65],p=0.333)。然而,随访组 85.2%(88 名中的 75 名)的患者在研究结束时继续使用他汀类药物治疗,而单次接触组的比例为 67.0%(88 名中的 59 名)(p=0.005)。与单次接触组相比,随访组的他汀类药物起始率更高(75.0%[30/40] vs 48.9%[22/45],p=0.013)。

结论

在初级保健医疗诊所中,这种针对非专家药剂师的简单心血管护理方案并未显著改善患者的心血管风险降低效果。然而,该干预措施似乎确实提高了他汀类药物的使用率。

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