From the, Department of Clinical Epidemiology, Leibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.
Department of Biometry and Data Management, Leibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.
J Intern Med. 2020 Feb;287(2):171-179. doi: 10.1111/joim.12990. Epub 2019 Nov 11.
To compare diclofenac use before and after implementation of European risk minimization measures in 2013, focusing on diclofenac initiators and prevalence of congestive heart failure (NYHA class II-IV), ischaemic heart disease, peripheral arterial disease and cerebrovascular disease (new contraindications) in these patients in Germany.
We included adults with health insurance coverage on 1 January 2011 (cohort 2011) or 1 January 2014 (cohort 2014) and during a 1-year pre-observation period. We defined diclofenac initiators as persons filling a prescription of systemic diclofenac in 2011 (cohort 2011) or 2014 (cohort 2014) and without such a prescription during the respective pre-observation period.
Each cohort comprised >10 million persons. Between 2011 and 2014, the age-standardized proportion of persons initiating diclofenac decreased by 29% (from 8.2% to 5.8%) amongst female patients and by 26% (from 8.5% to 6.3%) amongst male patients; in the subgroup of persons with new contraindications, this proportion decreased by 33% (from 9.8% to 6.6%) amongst female patients and by 31% (from 10.0% to 6.7%) amongst male patients. Amongst diclofenac initiators, the proportion of those with new contraindications did not change between 2011 (12.0%) and 2014 (11.8%).
The overall decline of about 30% in diclofenac initiation between 2011 and 2014 was largely independent of the presence or absence of new contraindications. The proportion of diclofenac initiators with a new contraindication remained at a high level (more than one in ten patients), demonstrating the need for research at the prescriber level (e.g. interventional studies) and further measures to improve patient safety.
比较 2013 年实施欧洲风险最小化措施前后双氯芬酸的使用情况,重点关注这些患者中新出现的充血性心力衰竭(NYHA II-IV 级)、缺血性心脏病、外周动脉疾病和脑血管疾病(新的禁忌症)的双氯芬酸起始者和流行率。
我们纳入了 2011 年 1 月 1 日(队列 2011 年)或 2014 年 1 月 1 日(队列 2014 年)有健康保险的成年人,并在 1 年的预观察期内。我们将双氯芬酸起始者定义为 2011 年(队列 2011 年)或 2014 年(队列 2014 年)开具全身用双氯芬酸处方且在各自预观察期内无此类处方的患者。
每个队列都包含超过 1000 万人。2011 年至 2014 年间,女性患者中开始使用双氯芬酸的人数比例从 8.2%降至 5.8%,标准化年龄后降幅为 29%;男性患者中这一比例从 8.5%降至 6.3%,标准化年龄后降幅为 26%;在具有新禁忌症的亚组中,女性患者中这一比例从 9.8%降至 6.6%,降幅为 33%;男性患者中这一比例从 10.0%降至 6.7%,降幅为 31%。在双氯芬酸起始者中,2011 年(12.0%)和 2014 年(11.8%)之间新禁忌症患者的比例没有变化。
2011 年至 2014 年间,双氯芬酸的使用量总体下降约 30%,这在很大程度上与新禁忌症的存在与否无关。具有新禁忌症的双氯芬酸起始者的比例仍处于较高水平(超过每 10 名患者中就有 1 名),这表明需要在处方医生层面(例如干预性研究)进行研究,并采取进一步措施提高患者安全性。