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A cohort study of therapeutic prescriptions after the end of phytotherapy drug reimbursement by French Social Security.

机译:法国社会保障局对植物疗法药物报销结束后的治疗处方进行了一项队列研究。

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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. Copyright ? 2012 John Wiley & Sons, Ltd.
机译:2006年3月,法国终止了用于治疗轻度焦虑症和失眠症的植物疗法药物的报销。这项研究的目的是调查停止植物疗法报销的短期影响。我们监测了在报销期结束前的12个月内至少接受过一次催眠和镇静植物疗法药物治疗的27?422患者的处方,并与他们取得了联系在接下来的12个月内至少与他们的开处方医生联系一次。在取消报销前的24个月内从满足相同纳入标准的患者中招募了对照队列,并对接下来的12个月内的处方进行监测。通过比较这些人群中的处方转换,可以估算出报销结束后的影响。在报销结束之前,有7684(28%)名被列为除草剂的患者具有相关的药品销售许可批准(DMAA)指征。催眠药和镇静药共同处方涉及40%的患者。在4646名仅接受处方药治疗的DMAA患者中,只有640例(14%)在报销结束后才改用催眠药或镇静剂,其中3266例(70%)停止了所有治疗,而740例(16%)采用了未报销的植物疗法处方。与对照组相比,需要报销的患者更有可能转用精神药物(OR?=?1.46)。在其有效性或严重程度较低的证据不足的情况下,结束对普通药物的报销其目标病理应附有处方药参与者的信息或建议。版权? 2012年John Wiley&Sons,Ltd.

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