Regional Pharmacovigilance Centre of Limoges, Department of Pharmacology-Toxicology and Pharmacovigilance, CHU Limoges, Limoges, France.
UR 24134 (VieSanté- Vieillissement, Fragilité, Prévention, e-Santé), IFR OMEGA HEALTH, Université de Limoges, Limoges, France.
Br J Clin Pharmacol. 2023 Jan;89(1):390-400. doi: 10.1111/bcp.15510. Epub 2022 Sep 7.
In the last French study in 2007, the incidence of hospital admissions (HAs) related to adverse drug reactions (ADRs) was 3.6%. The objective was to assess the current ADR-HA incidence in France and to describe both its characteristics and preventability.
A prospective multicentre study was conducted among randomly selected French public hospital medical wards (April-July 2018). Patients admitted during a week period were included. ADR-HA cases were collected by the French Regional Pharmacovigilance Centres network. An independent committee validated potential cases and ADR preventability.
ADR-HA incidence was 8.5% (95% confidence interval [CI]: 7.6-9.4%), increasing with age (3.3% [95%CI: 1.8-5.5%] ≤16 y vs. 10.6% [95%CI: 9.3-12.0%] ≥65 y). The most common ADRs were haemorrhagic events (8.8%), haematological disorders (6.5%), acute renal failure (6.3%), fluid and electrolyte disorders (6.0%), and falls (5.2%). New drugs were involved: targeted therapies (22.8% of antineoplastics), direct oral anticoagulants (29.6% of antithrombotics) and incretin-based drugs (20.0% of antidiabetics). ADRs were preventable in 16.1% of cases because the drugs involved had not been used in accordance with monographies, package leaflets or other therapeutic guidelines. The main situations of noncompliance addressed either dose or duration of use (27.9%), warning (23.2%), use precaution (18.6%) and inappropriate self-medication or misuse by patients (11.6%).
In France, ADR-HA incidence dramatically increased over the last decade. A significant proportion was related to new pharmacological classes and considered as preventable. These findings should lead to in-depth thought on preventive actions on at-risk drug classes.
在 2007 年的最后一项法国研究中,与药物不良反应(ADR)相关的住院(HA)发生率为 3.6%。本研究旨在评估法国当前的 ADR-HA 发生率,并描述其特征和可预防程度。
这是一项在法国公立医疗机构中进行的前瞻性多中心研究(2018 年 4 月至 7 月)。选择一周内住院的患者进行研究。通过法国地区药物警戒中心网络收集 ADR-HA 病例。一个独立委员会验证潜在病例和 ADR 可预防程度。
ADR-HA 的发生率为 8.5%(95%置信区间[CI]:7.6-9.4%),随年龄增加而升高(3.3%[95%CI:1.8-5.5%]≤16 岁 vs. 10.6%[95%CI:9.3-12.0%]≥65 岁)。最常见的 ADR 是出血事件(8.8%)、血液系统疾病(6.5%)、急性肾功能衰竭(6.3%)、体液和电解质紊乱(6.0%)和跌倒(5.2%)。新的药物涉及靶向治疗(22.8%的抗肿瘤药物)、直接口服抗凝剂(29.6%的抗血栓药物)和基于肠促胰岛素的药物(20.0%的抗糖尿病药物)。16.1%的 ADR 可预防,因为所涉及的药物未按照专论、药品说明书或其他治疗指南使用。不遵守的主要情况是剂量或使用时间(27.9%)、警告(23.2%)、使用注意事项(18.6%)和患者自行用药或用药不当(11.6%)。
在法国,ADR-HA 的发生率在过去十年中急剧增加。相当一部分与新的药物类别有关,且被认为是可预防的。这些发现应促使深入思考针对高危药物类别的预防措施。