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来自商业保险人群的新诊断类风湿关节炎患者的治疗模式

Treatment Patterns of Newly Diagnosed Rheumatoid Arthritis Patients from a Commercially Insured Population.

作者信息

Kern David M, Chang Lawrence, Sonawane Kalyani, Larmore Cynthia J, Boytsov Natalie N, Quimbo Ralph A, Singer Joseph, Hinton John T, Wu Sze-Jung, Araujo Andre B

机构信息

HealthCore, Inc, Wilmington, DE, USA.

Eli Lilly and Company, Indianapolis, IN, USA.

出版信息

Rheumatol Ther. 2018 Dec;5(2):355-369. doi: 10.1007/s40744-018-0114-6. Epub 2018 May 30.

Abstract

INTRODUCTION

To describe treatment patterns in newly diagnosed rheumatoid arthritis (RA) patients in a large, nationally representative managed-care database.

METHODS

Newly diagnosed RA patients were identified from 07/01/2006-08/31/2014. Patients had ≥ 1 RA diagnosis by a rheumatologist, or ≥ 2 non-rheumatologist RA diagnoses ≥ 30 days apart, or RA diagnosis followed by a disease-modifying antirheumatic drug (DMARD) prescription fill within 1 year. Patients were ≥ 18 years old at index (earliest date fulfilling diagnostic criteria) and had ≥ 6 and 12 months of pre- and post-index health plan enrollment, respectively. Patterns of DMARD treatment, including conventional synthetic DMARDs (csDMARD), tumor necrosis factor inhibitors (TNFi), non-TNFi, and Janus kinase inhibitors (JAKi), were captured during follow-up.

RESULTS

Of the 63,101 RA patients identified, 73% were female; mean age was 57 years. During an average of 3.5 ± 2.1 years of follow-up, 45% of patients never received a DMARD, 52% received a csDMARD (94 ± 298 mean ± SD days from index), 16% a TNFi (315 ± 448 days), 4% a non-TNFi (757 ± 660 days), and < 1% a JAKi. Among DMARD recipients, the most common treatment patterns were: receiving csDMARDs only (68%), adding a TNFi as second-line therapy after initiation of a csDMARD (12%), and receiving only a TNFi (6%) during follow-up. Among those not on DMARDs, the all-cause usage of an opioid was 56% and 19% had chronic opioid use (≥ 180 days supplied).

CONCLUSIONS

Despite American College of Rheumatology recommendations for DMARD treatment of RA, nearly half of newly diagnosed RA patients received no DMARD therapy during follow-up. These data identify a treatment gap in RA management.

FUNDING

Eli Lilly & Company.

摘要

引言

在一个具有全国代表性的大型管理式医疗数据库中描述新诊断类风湿性关节炎(RA)患者的治疗模式。

方法

从2006年7月1日至2014年8月31日确定新诊断的RA患者。患者经风湿病学家诊断为≥1次RA,或经非风湿病学家诊断≥2次且间隔≥30天,或在RA诊断后1年内开具改善病情抗风湿药(DMARD)处方。患者在索引日期(满足诊断标准的最早日期)时≥18岁,且分别有≥6个月和12个月的索引前和索引后健康计划登记。在随访期间记录DMARD治疗模式,包括传统合成DMARD(csDMARD)、肿瘤坏死因子抑制剂(TNFi)、非TNFi和Janus激酶抑制剂(JAKi)。

结果

在确定的63101例RA患者中,73%为女性;平均年龄为57岁。在平均3.5±2.1年的随访期间,45%的患者从未接受过DMARD治疗,52%接受过csDMARD治疗(自索引日期起平均94±298天),16%接受过TNFi治疗(315±448天),4%接受过非TNFi治疗(757±660天),<1%接受过JAKi治疗。在接受DMARD治疗的患者中,最常见的治疗模式为:仅接受csDMARD治疗(68%),在开始csDMARD治疗后作为二线治疗加用TNFi(12%),以及在随访期间仅接受TNFi治疗(6%)。在未接受DMARD治疗的患者中,阿片类药物的全因使用率为56%,19%长期使用阿片类药物(供应≥180天)。

结论

尽管美国风湿病学会对RA的DMARD治疗有相关建议,但近一半新诊断的RA患者在随访期间未接受DMARD治疗。这些数据揭示了RA管理中的治疗差距。

资助

礼来公司。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36ce/6251837/2a7df9a74c9a/40744_2018_114_Fig1_HTML.jpg

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