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美国初次骨折患者后续骨折的发生率和成本。

Prevalence and Cost of Subsequent Fractures Among U.S. Patients with an Incident Fracture.

机构信息

1 Center for Observational and Real-World Evidence, Merck & Co., Kenilworth, New Jersey.

2 Center for Observational and Real-World Evidence, Merck & Co., Kenilworth, New Jersey (deceased).

出版信息

J Manag Care Spec Pharm. 2017 Apr;23(4):461-471. doi: 10.18553/jmcp.2017.23.4.461.

Abstract

BACKGROUND

The prevalence and cost of subsequent fractures among patients with an incident fracture are not well defined.

OBJECTIVE

To assess the prevalence of, and costs associated with, subsequent fractures in the year after an incident fracture.

METHODS

This was a retrospective claims database analysis using data from Humana Medicare Advantage claims (Medicare group) and Optum Insight Clinformatics Data Mart commercial claims (commercial group). Patients included in the study had a claim for a qualifying fracture occurring between January 2008 and December 2013 (index fracture), were continuously enrolled in the health plan for ≥ 1 year before and after the index fracture, and were aged ≥ 65 years in the Medicare group or ≥ 50 years in the commercial group at the time of the index fracture. Subsequent fractures were identified by ICD-9-CM codes and were defined as the second fracture occurring ≥ 3 to ≤ 12 months after the index fracture (≥ 6 to ≤ 12 months for fractures at the same site as the index fracture). Rates of subsequent fractures were calculated as the number of patients who had a subsequent fracture divided by the total sample size. After propensity matching of demographic and clinical variables, we determined the total medical and pharmacy costs accrued within 1 year of the index fracture by patients with and without a subsequent fracture. Health care costs were compared between patients with and without a subsequent fracture using McNemar's test.

RESULTS

A total of 45,603 patients were included in the Medicare group, and 54,145 patients were included in the commercial group. In the Medicare group, 7,604 (16.7%) patients experienced a subsequent fracture. The proportion of patients with a subsequent fracture was highest among patients with multiple index fractures (26.2%, n = 905), followed by those with hip (25.5%, n = 1,280) and vertebral (20.2%, n = 1,908) index fractures. In the commercial group, 6,256 (11.6%) patients experienced a subsequent fracture. The proportion of patients with a subsequent fracture paralleled those observed in the Medicare group: 24.5% (n = 808) in patients with multiple index fractures, 22.0% (n = 525) in those with hip fracture, and 14.5% (n = 841) in those with vertebral fracture. For vertebral, hip, and nonhip nonvertebral fractures, subsequent fractures were most frequently of the same type as the index fracture. The mean total health care cost (sum of medical and pharmacy costs) in the year following the incident fracture for the Medicare group was $27,844 and differed significantly between patients with and without a subsequent fracture ($34,897 vs. $20,790; P < 0.001). The mean total health care cost in the year following the incident fracture for the commercial group was $29,316 and also differed significantly between patients with and without a subsequent fracture ($39,501 vs. $19,131; P < 0.001).

CONCLUSIONS

Among patients with an incident fracture, those who experienced a subsequent fracture in the following year had significantly higher health care costs than those who did not. A subsequent fracture is most likely to be of the same type as the initial fracture.

DISCLOSURES

This study was funded by Merck & Co. Other than through the employer relationships disclosed here, Merck & Co did not have a role in the study design, data collection, interpretation of the data, in writing of the manuscript, or in the decision to submit the manuscript for publication. Weaver and Marvos are employees of Merck & Co. Sajjan was an employee of Merck & Co. and owned stock in the company at the time of the study. Lewiecki has received consulting and/or speaker honoraria from Merck, AbbVie, AgNovos Healthcare, Alexion Pharmaceuticals, Amgen, Eli Lilly and Company, Radius Health, Shire, and TheraNova. Lewiecki has received research grant support from Merck, Amgen, and Eli Lilly and Company and serves as a board member for the National Osteoporosis Foundation, the International Society for Clinical Densitometry, and the Osteoporosis Foundation of New Mexico. Harris has received consulting honoraria from Merck, Alexion Pharmaceuticals, Amgen, Eli Lilly and Company, Gilead Sciences, Primus Pharmaceuticals, and Radius Health. Study concept and design were contributed by Weave and Sajjan. Lewiecki collected the data, and data interpretation was performed by all the authors. The manuscript was written and revised by Weaver, Lewiecki, and Harris.

摘要

背景

患有骨折事件的患者随后骨折的患病率和成本尚不清楚。

目的

评估骨折事件后一年内随后骨折的患病率和相关成本。

方法

这是一项回顾性的理赔数据库分析,使用了 Humana Medicare Advantage 理赔(医疗保险组)和 Optum Insight Clinformatics Data Mart 商业理赔(商业组)的数据。研究纳入的患者在 2008 年 1 月至 2013 年 12 月期间发生了符合条件的骨折(索引骨折),在索引骨折之前和之后至少连续 1 年在健康计划中参保,在医疗保险组中年龄≥65 岁,或在商业组中年龄≥50 岁。随后骨折通过 ICD-9-CM 代码确定,并定义为索引骨折后 3 至 12 个月(对于与索引骨折相同部位的骨折,定义为 6 至 12 个月)发生的第二次骨折。随后骨折的发生率计算为发生随后骨折的患者人数除以总样本量。在对人口统计学和临床变量进行倾向匹配后,我们确定了索引骨折后 1 年内患者的总医疗和药房费用。使用 McNemar 检验比较有无随后骨折的患者之间的医疗保健费用。

结果

医疗保险组共纳入 45603 例患者,商业组共纳入 54145 例患者。在医疗保险组中,7604 例(16.7%)患者发生了随后骨折。在有多个索引骨折的患者中(26.2%,n=905),有随后骨折的患者比例最高,其次是髋部(25.5%,n=1280)和椎体(20.2%,n=1908)索引骨折。在商业组中,6256 例(11.6%)患者发生了随后骨折。有随后骨折的患者比例与医疗保险组观察到的比例相似:多发性索引骨折患者中 24.5%(n=808),髋部骨折患者中 22.0%(n=525),椎体骨折患者中 14.5%(n=841)。对于椎体、髋部和非髋非椎体骨折,随后骨折最常与索引骨折类型相同。医疗保险组中,在骨折事件后一年的总医疗保健费用(医疗和药房费用之和)为 27844 美元,且在有无随后骨折的患者之间差异显著(34897 美元与 20790 美元;P<0.001)。商业组中,在骨折事件后一年的总医疗保健费用为 29316 美元,且在有无随后骨折的患者之间也差异显著(39501 美元与 19131 美元;P<0.001)。

结论

在患有骨折事件的患者中,在接下来的一年中经历随后骨折的患者的医疗保健费用明显高于未经历随后骨折的患者。随后骨折最有可能与初始骨折类型相同。

披露

这项研究由默克公司资助。除了这里披露的雇主关系外,默克公司在研究设计、数据收集、数据解释、撰写手稿或决定提交手稿供发表方面没有任何作用。Weaver 和 Marvos 是默克公司的员工。Sajjan 曾是默克公司的员工,在研究期间拥有该公司的股票。Lewiecki 曾从默克、AbbVie、AgNovos Healthcare、Alexion Pharmaceuticals、Amgen、Eli Lilly and Company、Radius Health、Shire 和 TheraNova 获得咨询和/或演讲酬金。Lewiecki 从默克、Amgen 和 Eli Lilly and Company 获得研究资助,并担任国家骨质疏松症基金会、国际临床密度测定学会和新墨西哥州骨质疏松症基金会的董事会成员。Harris 曾从 Merck、Alexion Pharmaceuticals、Amgen、Eli Lilly and Company、Gilead Sciences、Primus Pharmaceuticals 和 Radius Health 获得咨询酬金。研究概念和设计由 Weaver 和 Sajjan 贡献。Lewiecki 收集数据,所有作者对数据进行解释。Weaver、Lewiecki 和 Harris 撰写和修订了手稿。

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