Changes in cotherapies after initiation of disease‐modifying antirheumatic drug therapy in patients with rheumatoid arthritis
Objective We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the use of corticosteroids, nonsteroidal antiinflammatory drugs (NSAIDs), and narcotics. Methods Using administrative databases, we assembled 4 re...
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Published in | Arthritis care & research (2010) Vol. 63; no. 10; pp. 1415 - 1424 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.10.2011
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Subjects | |
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Abstract | Objective
We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the use of corticosteroids, nonsteroidal antiinflammatory drugs (NSAIDs), and narcotics.
Methods
Using administrative databases, we assembled 4 retrospective cohorts of RA patients (1998–2005) and identified 5 groups initiating DMARD regimens: methotrexate (MTX) with (new MTX) or without (first MTX) use of other nonbiologic DMARDs in the previous year; new hydroxychloroquine (HCQ) and/or sulfasalazine (SSZ; new HCQ/SSZ) and new leflunomide (new LEF), both with previous use of MTX; and new tumor necrosis factor α (TNFα) antagonists (new anti‐TNF). We compared within‐person differences in any use of cotherapies (≥1 prescription) between the 6 months before and the 6–12 months after DMARD initiation.
Results
Among 32,476 DMARD initiators, the prevalence of corticosteroid, NSAID, and narcotic use increased by 15%, 5%, and 6%, respectively, in the 6 months before initiation compared to the previous 6 months, suggesting worsening of the disease. In the 6–12 months after initiation for most initiator groups, more patients stopped using corticosteroids and NSAIDs than started, with overall decreases of 8.9% (95% confidence interval [95% CI] 8.4–9.4%) for corticosteroids and 12.9% (95% CI 12.3–13.4%) for NSAIDs. The proportion of narcotic users changed little (overall decrease of 2.5%; 95% CI 1.9–3.0%).
Conclusion
Use of all 3 cotherapies increased in the 6 months before initiation of new DMARD regimens for RA. Use of corticosteroids and NSAIDs decreased modestly 6–12 months after initiation, but there was only a very small decrease in narcotic use. These differential changes require further study. |
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AbstractList | Abstract
Objective
We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the use of corticosteroids, nonsteroidal antiinflammatory drugs (NSAIDs), and narcotics.
Methods
Using administrative databases, we assembled 4 retrospective cohorts of RA patients (1998–2005) and identified 5 groups initiating DMARD regimens: methotrexate (MTX) with (new MTX) or without (first MTX) use of other nonbiologic DMARDs in the previous year; new hydroxychloroquine (HCQ) and/or sulfasalazine (SSZ; new HCQ/SSZ) and new leflunomide (new LEF), both with previous use of MTX; and new tumor necrosis factor α (TNFα) antagonists (new anti‐TNF). We compared within‐person differences in any use of cotherapies (≥1 prescription) between the 6 months before and the 6–12 months after DMARD initiation.
Results
Among 32,476 DMARD initiators, the prevalence of corticosteroid, NSAID, and narcotic use increased by 15%, 5%, and 6%, respectively, in the 6 months before initiation compared to the previous 6 months, suggesting worsening of the disease. In the 6–12 months after initiation for most initiator groups, more patients stopped using corticosteroids and NSAIDs than started, with overall decreases of 8.9% (95% confidence interval [95% CI] 8.4–9.4%) for corticosteroids and 12.9% (95% CI 12.3–13.4%) for NSAIDs. The proportion of narcotic users changed little (overall decrease of 2.5%; 95% CI 1.9–3.0%).
Conclusion
Use of all 3 cotherapies increased in the 6 months before initiation of new DMARD regimens for RA. Use of corticosteroids and NSAIDs decreased modestly 6–12 months after initiation, but there was only a very small decrease in narcotic use. These differential changes require further study. Objective. We hypothesized that initiation of a new disease-modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the use of corticosteroids, nonsteroidal antiinflammatory drugs (NSAIDs), and narcotics.Methods. Using administrative databases, we assembled 4 retrospective cohorts of RA patients (1998-2005) and identified 5 groups initiating DMARD regimens: methotrexate (MTX) with (new MTX) or without (first MTX) use of other nonbiologic DMARDs in the previous year; new hydroxychloroquine (HCQ) and/or sulfasalazine (SSZ; new HCQ/SSZ)and new leflunomide (new LEF), both with previous use of MTX; and new tumor necrosis factor α (TNFα) antagonists(new anti-TNF). We compared within-person differences in any use of cotherapies (≥ prescription) between the 6 months before and the 6-12 months after DMARD initiation.Results. Among 32,476 DMARD initiators, the prevalence of corticosteroid, NSAID, and narcotic use increased by 15%, 5%,and 6%, respectively, in the 6 months before initiation compared to the previous 6 months, suggesting worsening of the disease. In the 6-12 months after initiation for most initiator groups, more patients stopped using corticosteroids and NSAIDs than started, with overall decreases of 8.9% (95% confidence interval [95% CI] 8.4-9.4%) for corticosteroids and 12.9% (95%CI 12.3-13.4%) for NSAIDs. The proportion of narcotic users changed little (overall decrease of 2.5%; 95% CI 1.9-3.0%).Conclusion. Use of all 3 cotherapies increased in the 6 months before initiation of new DMARD regimens for RA. Use of corticosteroids and NSAIDs decreased modestly 6-12 months after initiation, but there was only a very small decrease in narcotic use. These differential changes require further study. Objective We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the use of corticosteroids, nonsteroidal antiinflammatory drugs (NSAIDs), and narcotics. Methods Using administrative databases, we assembled 4 retrospective cohorts of RA patients (1998–2005) and identified 5 groups initiating DMARD regimens: methotrexate (MTX) with (new MTX) or without (first MTX) use of other nonbiologic DMARDs in the previous year; new hydroxychloroquine (HCQ) and/or sulfasalazine (SSZ; new HCQ/SSZ) and new leflunomide (new LEF), both with previous use of MTX; and new tumor necrosis factor α (TNFα) antagonists (new anti‐TNF). We compared within‐person differences in any use of cotherapies (≥1 prescription) between the 6 months before and the 6–12 months after DMARD initiation. Results Among 32,476 DMARD initiators, the prevalence of corticosteroid, NSAID, and narcotic use increased by 15%, 5%, and 6%, respectively, in the 6 months before initiation compared to the previous 6 months, suggesting worsening of the disease. In the 6–12 months after initiation for most initiator groups, more patients stopped using corticosteroids and NSAIDs than started, with overall decreases of 8.9% (95% confidence interval [95% CI] 8.4–9.4%) for corticosteroids and 12.9% (95% CI 12.3–13.4%) for NSAIDs. The proportion of narcotic users changed little (overall decrease of 2.5%; 95% CI 1.9–3.0%). Conclusion Use of all 3 cotherapies increased in the 6 months before initiation of new DMARD regimens for RA. Use of corticosteroids and NSAIDs decreased modestly 6–12 months after initiation, but there was only a very small decrease in narcotic use. These differential changes require further study. |
Author | Curtis, Jeffrey R. Herrinton, Lisa Ouellet‐Hellstrom, Rita Liu, Liyan Solomon, Daniel H. Mitchel, Edward F. Stein, C. Michael Kawai, Vivian K. Chen, Lang Grijalva, Carlos G. Arbogast, Patrick G. Delzell, Elizabeth Griffin, Marie R. |
Author_xml | – sequence: 1 givenname: Vivian K. surname: Kawai fullname: Kawai, Vivian K. – sequence: 2 givenname: Carlos G. surname: Grijalva fullname: Grijalva, Carlos G. – sequence: 3 givenname: Patrick G. surname: Arbogast fullname: Arbogast, Patrick G. – sequence: 4 givenname: Jeffrey R. surname: Curtis fullname: Curtis, Jeffrey R. – sequence: 5 givenname: Daniel H. surname: Solomon fullname: Solomon, Daniel H. – sequence: 6 givenname: Elizabeth surname: Delzell fullname: Delzell, Elizabeth – sequence: 7 givenname: Lang surname: Chen fullname: Chen, Lang – sequence: 8 givenname: Rita surname: Ouellet‐Hellstrom fullname: Ouellet‐Hellstrom, Rita – sequence: 9 givenname: Lisa surname: Herrinton fullname: Herrinton, Lisa – sequence: 10 givenname: Liyan surname: Liu fullname: Liu, Liyan – sequence: 11 givenname: Edward F. surname: Mitchel fullname: Mitchel, Edward F. – sequence: 12 givenname: C. Michael surname: Stein fullname: Stein, C. Michael – sequence: 13 givenname: Marie R. surname: Griffin fullname: Griffin, Marie R. email: marie.griffin@vanderbilt.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22121511$$D View this record in MEDLINE/PubMed |
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Notes | Dr. Herrinton has received research support from Centocor, Genentech, and Procter & Gamble. Dr. Curtis has received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from Abbott, Centocor, Pfizer, and BMS, and (more than $10,000 each) from Amgen, Consortium of Rheumatology Researchers of North America, Roche/Genentech, and UCB. Dr. Griffin has received consultant fees, speaking fees and/or honoraria (less than $10,000 each) from Rocky Mountain Poison and Drug Center funded by McNeil. Dr. Solomon has received research support from Abbott and Amgen. Dr. Delzell has received research support from Amgen. |
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We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the... Objective. We hypothesized that initiation of a new disease-modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would decrease the... Abstract Objective We hypothesized that initiation of a new disease‐modifying antirheumatic drug (DMARD) for treatment of rheumatoid arthritis (RA) would... |
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SubjectTerms | Adrenal Cortex Hormones - administration & dosage Adult Aged Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Antirheumatic Agents - administration & dosage Arthritis, Rheumatoid - drug therapy Cohort Studies Drug Administration Schedule Drug Therapy, Combination Female Humans Hydroxychloroquine - administration & dosage Isoxazoles - administration & dosage Male Methotrexate - administration & dosage Middle Aged Narcotics - administration & dosage Retrospective Studies Sulfasalazine - administration & dosage Time Factors Treatment Outcome Tumor Necrosis Factor-alpha - antagonists & inhibitors |
Title | Changes in cotherapies after initiation of disease‐modifying antirheumatic drug therapy in patients with rheumatoid arthritis |
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