French National Health Insurance (Caisse Nationale de l'Assurance Maladie/Cnam), 50 avenue du Pr. André Lemierre, 75 986, Paris Cedex 20, France.
Pharmacologie Médicale, Faculté de Médecine, Université de Toulouse UPS, Inserm CERPOP, CHU, Toulouse, France.
Drug Saf. 2021 Dec;44(12):1323-1339. doi: 10.1007/s40264-021-01117-4. Epub 2021 Oct 6.
Nationwide prevalence of potentially harmful drug prescribing during pregnancy is unknown in France, and several risk classification systems (RCS) exist to guide prescribers.
The aim of this study was to estimate the nationwide prevalence of potentially harmful drug prescribing during pregnancy in France and to describe maternal characteristics associated with this prescription.
This drug utilisation study, conducted on the French health databases (67 million beneficiaries), included all pregnancies beginning in 2016-2017, regardless of pregnancy outcome. Potentially harmful drug prescribing was defined as at least one reimbursement during pregnancy of Swedish RCS category D drugs, Australian RCS category D/X drugs, or contraindicated drugs in France for drugs not listed in these two RCSs. Maternal characteristics associated with potentially harmful drug prescribing were described using a univariate logistic regression analysis.
Among the 1,844,447 pregnant women identified, the prevalence of potentially harmful drug prescribing was higher according to the Australian RCS (3.9%) than according to the Swedish RCS (2.2%), with good agreement between the two RCSs (Kappa = 0.81 [0.74-0.87]). This prevalence increased to 9.2% and 6.9%, respectively, when considering contraindications in France. Prescribing of teratogenic drugs, including retinoids and valproate, was highest during the first trimester, whereas prescribing of foetotoxic drugs decreased after the first trimester but remained high for nonsteroidal anti-inflammatory drugs (N = 10,021). In women with no chronic diseases, polymedication (five or more drugs) was the strongest maternal characteristic associated with potentially harmful drug prescribing in both RCSs.
Potentially harmful drug prescribing during pregnancy is not uncommon in France. This study supports the comparative analysis of RCS to assess potentially harmful drug prescribing in claims databases.
法国全国范围内孕妇潜在有害药物处方的流行情况尚不清楚,并且存在几种风险分类系统(RCS)来指导处方开具者。
本研究旨在估计法国全国范围内孕妇潜在有害药物处方的流行情况,并描述与该处方相关的产妇特征。
这项药物利用研究在法国健康数据库(6700 万受益人群)中进行,包括所有在 2016-2017 年开始的妊娠,无论妊娠结局如何。潜在有害药物处方的定义是在怀孕期间至少有一次报销瑞典 RCS 类别 D 药物、澳大利亚 RCS 类别 D/X 药物或法国禁用药物的情况,而这些 RCS 中未列出的药物除外。使用单变量逻辑回归分析描述与潜在有害药物处方相关的产妇特征。
在确定的 1844447 名孕妇中,根据澳大利亚 RCS(3.9%),而非瑞典 RCS(2.2%),潜在有害药物处方的流行率更高,两种 RCS 之间具有良好的一致性(Kappa=0.81 [0.74-0.87])。当考虑法国的禁忌症时,这一流行率分别上升至 9.2%和 6.9%。致畸药物(包括视黄醇和丙戊酸)的处方率在妊娠早期最高,而妊娠后期胎儿毒性药物的处方率下降,但非甾体抗炎药(N=10021)的处方率仍较高。在没有慢性疾病的女性中,多药治疗(五种或更多药物)是两种 RCS 中与潜在有害药物处方最相关的产妇特征。
法国孕妇潜在有害药物处方并不罕见。本研究支持使用 RCS 进行比较分析,以评估索赔数据库中潜在有害药物的处方情况。