TY - JOUR
T1 - Geographic Variations in Diagnosis and Treatment of Ankylosing Spondylitis in the United States
T2 - A Real-World Study
AU - Deodhar, Atul
AU - Kruzikas, Denise
AU - Zhou, Lili
AU - Biljan, Ana
AU - Saffore, Christopher D.
N1 - Funding Information:
Atul Deodhar has received consultancy fees from and participated in advisory boards for AbbVie, Amgen, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Eli Lilly, Glaxo Smith & Kline, Janssen, Novartis, Pfizer, UCB and received research grants from AbbVie, Eli Lilly, Glaxo Smith & Kline, Novartis, Pfizer, UCB. Denise Kruzikas, Ana Biljan, and Christopher Saffore are employees of AbbVie and own AbbVie stock. Lili Zhou was an employee of AbbVie at the time this study was conducted.
Funding Information:
This work was supported by AbbVie Inc. AbbVie sponsored the study, funded the Rapid Service Fee and Open Access charge, contributed to the design, participated in collection, analysis, and interpretation of data, and in writing, reviewing, approval of the final version and funded the Rapid Service Fee and Open Access Fee. No honoraria or payments were made for authorship.
Funding Information:
This work was supported by AbbVie Inc. AbbVie sponsored the study, funded the Rapid Service Fee and Open Access charge, contributed to the design, participated in collection, analysis, and interpretation of data, and in writing, reviewing, approval of the final version and funded the Rapid Service Fee and Open Access Fee. No honoraria or payments were made for authorship. Medical writing assistance was provided by Alan Saltzman, PhD, CMPP, of Fishawack Facilitate Ltd, part of Fishawack Health, Conshohocken, PA, and was funded by AbbVie Inc., North Chicago, IL. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. All authors contributed to the study conception and design, material preparation, data collection, and analysis. All authors were involved in the preparation and critical review of the manuscript and read and approved the final manuscript. Presented at the European League Against Rheumatism (EULAR) 2021 Virtual Congress, 2?5 June 2021 Poster POS0943. Atul Deodhar has received consultancy fees from and participated in advisory boards for AbbVie, Amgen, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Eli Lilly, Glaxo Smith & Kline, Janssen, Novartis, Pfizer, UCB and received research grants from AbbVie, Eli Lilly, Glaxo Smith & Kline, Novartis, Pfizer, UCB. Denise Kruzikas, Ana Biljan, and Christopher Saffore are employees of AbbVie and own AbbVie stock. Lili Zhou was an employee of AbbVie at the time this study was conducted. All database records were de-identified and compliant with US patient confidentiality requirements, including the Health Insurance Portability and Accountability Act of 1996. Because of this, institutional review board approval was not required. The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
Publisher Copyright:
© 2021, The Author(s).
PY - 2022/4
Y1 - 2022/4
N2 - Introduction: Diagnosis difficulties are common for ankylosing spondylitis (AS) patients, leading to inadequate and inconsistent treatment. We evaluated the national and geographic variability in disease diagnosis and treatment in the United States. Methods: This retrospective, cross-sectional analysis utilized the IBM® MarketScan® Administrative Claims Database from 2014 to 2019. AS patients ≥ 18 years of age with continuous medical and pharmacy enrollment during the calendar year and complete geographic information during the study period were included. Patient cohorts assessed were D1 (≥ 1 AS diagnoses within each calendar year of assessment between 2014 and 2019), D2 (≥ 2 non-rheumatologist AS diagnoses), and D3 (≥ 2 rheumatologist AS diagnoses). For D2 and D3, diagnoses were ≥ 6 months apart, but within 18 months. Annual AS diagnostic prevalence and treatment rates were determined from 2014 to 2019 nationally and per state in 2019. Treatments assessed were disease-modifying antirheumatic drugs (DMARDs), opioids, nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and methotrexate. Results: Nationally, AS diagnostic prevalence increased from 2014 to 2019, with 2019 rates of 9.6 (D1), 5.1 (D2), and 3.5 (D3) per 10,000 persons. Diagnostic prevalence varied between states, which was not explained by age, sex, racial distribution, or rheumatologists per capita. Nationally, a greater percentage of D3 patients vs. D1 and D2 patients received biologic/targeted synthetic DMARDs (bDMARD/tsDMARDs) and conventional synthetic DMARD. Opioid use ranged from 37 to 40% in 2019 and decreased from 2014 for all cohorts. Corticosteroid and methotrexate use decreased slightly, while NSAID and bDMARD/tsDMARD use generally increased from 2014 to 2019. Conclusions: AS diagnostic prevalence is increasing nationally, though it remains low among some states. bDMARD/tsDMARDs use was more common among patients treated by rheumatologists. Opioid and corticosteroid use is decreasing, though national rates remain high with significant state variability. Further education is needed, particularly in states with low prevalence and inadequate treatment, to improve diagnosis and treatment.
AB - Introduction: Diagnosis difficulties are common for ankylosing spondylitis (AS) patients, leading to inadequate and inconsistent treatment. We evaluated the national and geographic variability in disease diagnosis and treatment in the United States. Methods: This retrospective, cross-sectional analysis utilized the IBM® MarketScan® Administrative Claims Database from 2014 to 2019. AS patients ≥ 18 years of age with continuous medical and pharmacy enrollment during the calendar year and complete geographic information during the study period were included. Patient cohorts assessed were D1 (≥ 1 AS diagnoses within each calendar year of assessment between 2014 and 2019), D2 (≥ 2 non-rheumatologist AS diagnoses), and D3 (≥ 2 rheumatologist AS diagnoses). For D2 and D3, diagnoses were ≥ 6 months apart, but within 18 months. Annual AS diagnostic prevalence and treatment rates were determined from 2014 to 2019 nationally and per state in 2019. Treatments assessed were disease-modifying antirheumatic drugs (DMARDs), opioids, nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and methotrexate. Results: Nationally, AS diagnostic prevalence increased from 2014 to 2019, with 2019 rates of 9.6 (D1), 5.1 (D2), and 3.5 (D3) per 10,000 persons. Diagnostic prevalence varied between states, which was not explained by age, sex, racial distribution, or rheumatologists per capita. Nationally, a greater percentage of D3 patients vs. D1 and D2 patients received biologic/targeted synthetic DMARDs (bDMARD/tsDMARDs) and conventional synthetic DMARD. Opioid use ranged from 37 to 40% in 2019 and decreased from 2014 for all cohorts. Corticosteroid and methotrexate use decreased slightly, while NSAID and bDMARD/tsDMARD use generally increased from 2014 to 2019. Conclusions: AS diagnostic prevalence is increasing nationally, though it remains low among some states. bDMARD/tsDMARDs use was more common among patients treated by rheumatologists. Opioid and corticosteroid use is decreasing, though national rates remain high with significant state variability. Further education is needed, particularly in states with low prevalence and inadequate treatment, to improve diagnosis and treatment.
KW - Ankylosing spondylitis
KW - Biologic disease-modifying antirheumatic drugs
KW - Conventional synthetic disease-modifying antirheumatic drugs
KW - Diagnosis
KW - Epidemiology
KW - Opioids
KW - Real world
KW - States
KW - Targeted immunomodulator
KW - United States
UR - http://www.scopus.com/inward/record.url?scp=85121484230&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85121484230&partnerID=8YFLogxK
U2 - 10.1007/s40744-021-00406-9
DO - 10.1007/s40744-021-00406-9
M3 - Article
AN - SCOPUS:85121484230
SN - 2198-6576
VL - 9
SP - 447
EP - 463
JO - Rheumatology and Therapy
JF - Rheumatology and Therapy
IS - 2
ER -