Phisquare Institute-Fondation Transplantation, Paris, France.
Pharmacoepidemiol Drug Saf. 2013 Jul;22(7):760-8. doi: 10.1002/pds.3382. Epub 2012 Dec 4.
The reimbursement of phytotherapy drugs for the treatment of mild anxiety and insomnia ended in March 2006 in France. The aim of this study is to investigate the short-term impact of stopping phytotherapy reimbursement.
We monitored the prescriptions of 27,422 patients who received hypnotic and sedative phytotherapy drug treatment at least once in the 12 months preceding the end of reimbursement and made contact with their prescribing physician at least once in the following 12 months. A control cohort was recruited from patients fulfilling the same inclusion criteria in the 24 months before de-reimbursement and their prescriptions in the following 12 months were monitored. The impact of the end of reimbursement is estimated comparing prescription switches in these cohorts.
Before the end of reimbursement, 7684 (28%) patients being prescribed delisted phytotherapy drugs had the relevant drug marketing authorization approval (DMAA) indications. Co-prescriptions of hypnotic and sedative drugs concerned 40% of patients. Of the 4646 DMAA patients exclusively prescribed phytotherapy, 640 (14%) switched to hypnotic or sedative drugs only after the end of reimbursement, 3266 (70%) stopped all treatments and 740 (16%) carried on with a non-reimbursed phytotherapy prescription. When compared to the control cohort, patients exposed to de-reimbursement were more likely to switch to psychotropic drugs (OR = 1.46).
Ending the reimbursement of common drugs on the basis of insufficient evidence regarding their effectiveness or the low level of severity of their target pathologies should be accompanied by information or advice to prescribing health care actors.
法国于 2006 年 3 月停止报销草药治疗轻度焦虑和失眠的费用。本研究旨在调查停止报销草药治疗费用的短期影响。
我们监测了至少在报销结束前 12 个月内接受过催眠和镇静草药治疗的 27422 名患者的处方,并在随后的 12 个月内至少与他们的开处方医生联系一次。从符合报销前 24 个月相同纳入标准的患者中招募了一个对照组,并监测他们在接下来的 12 个月内的处方。通过比较这两个队列的处方转换来评估报销结束的影响。
在报销结束前,7684 名(28%)开列被取消报销资格的草药的患者有相关药物上市许可批准(DMAA)适应证。40%的患者同时开催眠和镇静药物。在仅开列 DMAA 的 4646 名患者中,640 名(14%)在报销结束后仅转而使用催眠或镇静药物,3266 名(70%)停止所有治疗,740 名(16%)继续使用未报销的草药处方。与对照组相比,暴露于取消报销的患者更有可能转而使用精神药物(OR=1.46)。
在缺乏关于其有效性或目标病理严重程度低的证据的情况下,基于常见药物的报销应伴有信息或建议给开处方的医疗保健行为者。