1 Center for Observational and Real-World Evidence, Merck & Co., Kenilworth, New Jersey.
2 New Mexico Clinical Research & Osteoporosis Center, Albuquerque, New Mexico.
J Manag Care Spec Pharm. 2017 Jul;23(7):735-744. doi: 10.18553/jmcp.2017.23.7.735.
Although treatment for osteoporosis is recommended by U.S. clinical guidelines, a lack of diagnosis and treatment is common among patients with osteoporotic fractures.
To determine the rates of osteoporosis diagnosis and treatment before and after various types of fractures.
This was a retrospective claims analysis using data from the 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 (the 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. Fragility fractures and osteoporosis diagnoses were identified from ICD-9-CM codes. Treatment for osteoporosis included oral and injectable therapies identified by National Drug Code numbers and Healthcare Common Procedure Coding System codes. Diagnosis and treatment rates were assessed during the 1-year periods before and after the index fracture. All analyses were conducted by fracture type (vertebral, hip, nonhip/nonvertebral [NHNV], and multiple), with stratification by age and sex. No comparisons were made between the Medicare and Commercial groups; rather, McNemar tests were used to compare prefracture versus postfracture diagnosis and treatment rates within each group.
For inclusion in the Medicare group, 45,603 patients were identified, and 54,145 patients were identified for the Commercial group. In the prefracture period, the osteoporosis diagnosis rates ranged from 12.0% (NHNV) to 21.5% (vertebral) in the Medicare group and from 5.3% (NHNV) to 12.1% (vertebral) in the Commercial group. In the postfracture period, diagnosis rates significantly increased (P < 0.001)-and nearly doubled-for all fracture types but did not exceed 42.1% (vertebral) in the Medicare group and 27.7% (vertebral) in the Commercial group. Pre-index treatment rates were similarly low, ranging from 9.4% (hip) to 16.6% (vertebral) among Medicare patients, and 7.5% (NHNV) to 14.4% (vertebral) in Commercial patients. Osteoporosis treatment rates improved significantly in the postfracture year, ranging from 12.5% (NHNV) to 26.5% (vertebral) among Medicare patients, and 8.3% (NHNV) to 21.4% (vertebral) in Commercial patients. Larger increases in diagnosis rates and smaller increases in treatment rates were observed in stratified analyses of men and women and of different age groups, with women and older patients having higher overall rates of diagnosis and treatment before and after fracture.
In men and women, osteoporosis diagnosis rates were low before the index fracture and improved substantially after the fracture, yet still remained low overall (under 50%). Osteoporosis treatment rates among patients experiencing a fracture were low before the index fracture and improved only minimally afterwards.
This study was funded by Merck & Co. Other than through the employer relationship 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 is an employee 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 & Co., AbbVie, AgNovos Healthcare, Alexion Pharmaceuticals, Amgen, Eli Lilly and Company, Radius Health, Shire, and TheraNova, along with research grant support from Merck & Co., 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 & Co., Alexion Pharmaceuticals, Amgen, Eli Lilly and Company, Gilead Sciences, Primus Pharmaceuticals, and Radius Health. Study concept and design were contributed by Weaver and Sajjan. Sajjan collected the data, and data interpretation was performed by all the authors. The manuscript was written and revised by Weaver, Lewiecki, and Harris.
尽管美国临床指南推荐骨质疏松症的治疗,但患有骨质疏松性骨折的患者常存在诊断和治疗不足的情况。
确定各种类型骨折前后骨质疏松症的诊断和治疗率。
这是一项回顾性索赔分析,使用 Humana Medicare Advantage 索赔(医疗保险组)和 Optum Insight Clinformatics Data Mart 商业索赔(商业组)的数据。研究纳入的患者在 2008 年 1 月至 2013 年 12 月期间发生符合条件的骨折(索引骨折),在索引骨折前后至少连续 1 年参加健康计划,并且在医疗保险组中年龄≥65 岁或在商业组中年龄≥50 岁。使用国际疾病分类第 9 版临床修正编码(ICD-9-CM)代码识别脆性骨折和骨质疏松症诊断。使用国家药品代码编号和医疗保健通用程序编码系统代码识别骨质疏松症的治疗方法。在索引骨折前后的 1 年期间评估诊断和治疗率。所有分析均按骨折类型(椎体、髋部、非髋/非椎体[NHNV]和多处)进行,并按年龄和性别进行分层。医疗保险组和商业组之间未进行比较;而是在每个组内使用 McNemar 检验比较骨折前与骨折后的诊断和治疗率。
纳入医疗保险组的患者有 45603 例,纳入商业组的患者有 54145 例。在骨折前时期,医疗保险组中 NHNV 的骨质疏松症诊断率为 12.0%(NHNV)至 21.5%(椎体),商业组中 NHNV 的骨质疏松症诊断率为 5.3%(NHNV)至 12.1%(椎体)。在骨折后时期,诊断率显著增加(P<0.001)-所有骨折类型的诊断率几乎翻了一番-但在医疗保险组中未超过 42.1%(椎体),在商业组中未超过 27.7%(椎体)。骨折前的治疗率也同样较低,医疗保险组中从髋部的 9.4%(髋部)到椎体的 16.6%(椎体),商业组中从 NHNV 的 7.5%(NHNV)到椎体的 14.4%(椎体)。在骨折后的年份中,骨质疏松症治疗率显著提高,从医疗保险组中 NHNV 的 12.5%(NHNV)到椎体的 26.5%(椎体),商业组中 NHNV 的 8.3%(NHNV)到椎体的 21.4%(椎体)。在男女和不同年龄组的分层分析中观察到诊断率的较大增加和治疗率的较小增加,女性和老年患者在骨折前后的诊断和治疗总体率较高。
在男性和女性中,骨折前的骨质疏松症诊断率较低,骨折后显著提高,但总体仍较低(低于 50%)。骨折前骨质疏松症治疗率较低,骨折后仅略有改善。
这项研究由默克公司资助。除了此处披露的雇主关系外,默克公司在研究设计、数据收集、数据解释、手稿撰写或决定提交手稿供发表方面没有任何作用。Weaver 是默克公司的员工。Sajjan 是默克公司的员工,在研究期间拥有该公司的股票。Lewiecki 曾收到过默克公司、AbbVie、AgNovos Healthcare、Alexion Pharmaceuticals、Amgen、Eli Lilly and Company、Radius Health、Shire 和 TheraNova 的咨询和/或演讲酬金,以及默克公司、Amgen 和 Eli Lilly and Company 的研究资助,并担任国家骨质疏松基金会、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 曾收到过 Merck & Co.、Alexion Pharmaceuticals、Amgen、Eli Lilly and Company、Gilead Sciences、Primus Pharmaceuticals 和 Radius Health 的咨询酬金。研究概念和设计由 Weaver 和 Sajjan 贡献。Sajjan 收集了数据,所有作者进行了数据解释。手稿由 Weaver、Lewiecki 和 Harris 撰写和修订。