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2013-2014 年法国数据库分析:在绝经后骨质疏松症限定适应证下依降钙素治疗的患者特征和使用模式。

Profile of Women Initiated on Denosumab and Pattern of Use in a Restricted Postmenopausal Osteoporosis Indication: A French Database Analysis Over the Period 2013-2014.

机构信息

Cemka, Bourg-la-Reine, France.

UMS 011, Institut National de la Santé et Recherche Médicale, Villejuif, France.

出版信息

Adv Ther. 2019 Apr;36(4):969-975. doi: 10.1007/s12325-019-00919-4. Epub 2019 Mar 5.

Abstract

INTRODUCTION

French authorities have approved the reimbursement of denosumab as a second-line therapy after bisphosphonates (BPs) in women presenting with postmenopausal osteoporosis (PMO) at high risk of fracture. By using a nationally representative claims database, we analyzed the pattern of denosumab use. The objectives of this study were to describe the profile of women initiated with denosumab over the 14-month period after launch and to check as far back as possible for the appropriateness of its use regarding the restrictions brought by French health authorities.

METHODS

A retrospective study using a national representative claims database, i.e., the "Echantillon Généraliste des Bénéficiaires" (EGB), was performed. The population was composed of women aged ≥ 40 years old who had an initiation of a PMO treatment in 2013 or 2014. The denosumab women's profiles were compared with those of women that started any other PMO treatment (except denosumab) over the same period.

RESULTS

In 2013 and 2014, we identified 256 women who initiated denosumab. Denosumab was primarily prescribed by specialists (75%) compared with the other PMO treatments (37.6%). Patients on denosumab were significantly older, 73.2 versus 69.1 years old, and they more frequently had a history of fractures (20.7% versus 17.4%, NS) and chronic uptake of high-dose steroids (25% versus 22.8%, NS). Of the women initiated with denosumab, 93.8% had undergone a previous PMO treatment (during the 2005-2014 period). In 92.9% of cases, it was a BP alone or in association.

CONCLUSION

This study suggests satisfactory compliance of prescribers concerning the restriction of the reimbursed indication of denosumab in second line after bisphosphonates with 6.2% possible inappropriate prescriptions.

FUNDING

Amgen.

摘要

简介

法国当局已批准地舒单抗作为绝经后骨质疏松症(PMO)高危骨折女性在使用双膦酸盐(BP)后的二线治疗药物进行报销。通过使用全国代表性的索赔数据库,我们分析了地舒单抗的使用模式。本研究的目的是描述在推出后 14 个月内开始使用地舒单抗的女性的概况,并尽可能追溯其使用的合理性,以符合法国卫生当局的限制。

方法

使用全国代表性的索赔数据库,即“Echantillon Généraliste des Bénéficiaires”(EGB)进行回顾性研究。该人群由 2013 年或 2014 年开始 PMO 治疗的年龄≥40 岁的女性组成。将地舒单抗女性的特征与同期开始任何其他 PMO 治疗(除地舒单抗外)的女性特征进行比较。

结果

2013 年和 2014 年,我们确定了 256 名开始使用地舒单抗的女性。与其他 PMO 治疗(37.6%)相比,地舒单抗主要由专科医生开具(75%)。使用地舒单抗的患者年龄明显较大,为 73.2 岁,而 69.1 岁,且骨折史(20.7%对 17.4%,无统计学意义)和慢性高剂量类固醇摄入(25%对 22.8%,无统计学意义)更为常见。在开始使用地舒单抗的女性中,93.8%的人曾接受过 PMO 治疗(2005-2014 年期间)。在 92.9%的情况下,是单独使用 BP 或联合使用。

结论

这项研究表明,在双膦酸盐后作为二线治疗药物使用地舒单抗的报销适应证限制方面,处方医生的遵从性令人满意,可能存在 6.2%的不适当处方。

资金来源

安进。

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