Institute of Applied Health Research, University of Birmingham, Birmingham.
Public Health England, London.
Br J Gen Pract. 2021 Feb 25;71(704):e219-e225. doi: 10.3399/bjgp20X714065. Print 2021.
Initiation of statins for the primary prevention of cardiovascular disease (CVD) should be based on CVD risk estimates, but their use is suboptimal.
To investigate the factors influencing statin prescribing when clinicians code and do not code estimated CVD risk (QRISK2).
A historical cohort of patients who had lipid tests in a database (IQVIA Medical Research Data) of UK primary care records.
The cohort comprised 686 560 entries (lipid test results) between 2012 and 2016 from 383 416 statin-naive patients without previous CVD. Coded QRISK2 scores were extracted, with variables used in calculating QRISK2 and factors that might influence statin prescribing. If a QRISK2 score was not coded, it was calculated post hoc. The outcome was initiation of a statin within 60 days of the lipid test result.
Of the entries, 146 693 (21.4%) had a coded QRISK2 score. Statins were initiated in 6.6% (95% confidence interval [CI] = 6.4% to 6.7%) of those with coded and 4.1% (95% CI = 4.0% to 4.1%) of uncoded QRISK2 (<0.001). Statin initiations were consistent with National Institute for Health and Care Excellence guideline recommendations in 85.0% (95% CI = 84.2% to 85.8%) of coded and 44.2% (95% CI = 43.5% to 44.9%) of uncoded QRISK2 groups (<0.001). When coded, QRISK2 score was the main predictor of statin initiation, but total cholesterol was the main predictor when a QRISK2 score was not coded.
When a QRISK2 score is coded, prescribing is more consistent with guidelines. With no QRISK2 score, prescribing is mainly based on total cholesterol. Using QRISK2 is associated with statin prescribing that is more likely to benefit patients. Promoting the routine CVD risk estimation is essential to optimise decision making.
启动他汀类药物用于心血管疾病(CVD)的一级预防应基于 CVD 风险估计,但他汀类药物的使用并不理想。
调查临床医生编码和不编码估计 CVD 风险(QRISK2)时影响他汀类药物处方的因素。
这是一个在英国初级保健记录 IQVIA 医疗研究数据数据库中进行的患者血脂检测的历史队列。
该队列包括 2012 年至 2016 年期间 383416 例无他汀类药物治疗史且无既往 CVD 的他汀类药物初治患者的 686560 个血脂检测结果。提取了编码 QRISK2 评分,使用了 QRISK2 计算中使用的变量和可能影响他汀类药物处方的因素。如果未编码 QRISK2 评分,则在事后进行计算。结果是在血脂检测结果后 60 天内开始使用他汀类药物。
在这些检测结果中,有 146693 例(21.4%)具有编码 QRISK2 评分。编码 QRISK2 评分的患者中,他汀类药物的使用率为 6.6%(95%置信区间[CI]为 6.4%至 6.7%),未编码 QRISK2 评分的患者中,他汀类药物的使用率为 4.1%(95% CI 为 4.0%至 4.1%)(<0.001)。编码 QRISK2 评分的患者中,85.0%(95% CI 为 84.2%至 85.8%)符合国家卫生与保健卓越研究所指南建议,未编码 QRISK2 评分的患者中,44.2%(95% CI 为 43.5%至 44.9%)符合国家卫生与保健卓越研究所指南建议(<0.001)。当 QRISK2 评分被编码时,评分是他汀类药物起始治疗的主要预测因素,但当 QRISK2 评分未被编码时,总胆固醇是主要预测因素。
当 QRISK2 评分被编码时,处方与指南更一致。当没有 QRISK2 评分时,处方主要基于总胆固醇。使用 QRISK2 与更有可能使患者受益的他汀类药物处方相关。推广常规 CVD 风险评估对于优化决策至关重要。