Posttraumatic Stress Disorder, Depression, Anxiety, and Persistence of Methotrexate and TNF Inhibitors in Patients with Rheumatoid Arthritis.
Journal
ACR open rheumatology
ISSN: 2578-5745
Titre abrégé: ACR Open Rheumatol
Pays: United States
ID NLM: 101740025
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
09
07
2020
accepted:
26
07
2020
pubmed:
14
9
2020
medline:
14
9
2020
entrez:
13
9
2020
Statut:
ppublish
Résumé
To examine the relationship of posttraumatic stress disorder (PTSD) with earlier treatment discontinuation and medication adherence in US veterans with rheumatoid arthritis (RA). Veterans Affairs (VA) administrative data (2005-2014) were used to define unique dispensing episodes of methotrexate (MTX) and tumor necrosis factor inhibitors (TNFi) for veterans with RA. Diagnosis codes were used to categorize patients into mutually exclusive groups: PTSD (with/without depression/anxiety), depression/anxiety without PTSD, and neither psychiatric diagnosis. Multivariable Cox proportional hazards models were used to evaluate associations between psychiatric diagnoses and time to disease-modifying antirheumatic drug discontinuation (lapse in refill >90 days). Multivariable logistic regression was used to examine associations of diagnoses with medication nonadherence (proportion of days covered <0.8). There were 15 081 dispensing episodes of MTX and 8412 dispensing episodes of TNFi. PTSD was independently associated with a greater likelihood of earlier discontinuation of both MTX (hazard ratio [HR] 1.15 [1.10-1.21]) and TNFi (HR 1.20 [1.13-1.28]). Depression/anxiety had a comparable risk of discontinuation for both MTX (HR 1.14 [1.10-1.19]) and TNFi (HR 1.16 [1.10-1.22]). Depression/anxiety, but not PTSD, was associated with higher odds of MTX (odds ratio [OR] 1.12 [1.03-1.22]) and TNFi (OR 1.14 [1.02-1.27]) nonadherence. Veterans with RA and comorbid PTSD, depression, or anxiety had poor persistence of MTX and TNFi therapies. These results suggest that earlier discontinuation and low adherence to therapy among patients with RA with these psychiatric comorbidities may contribute to worse disease outcomes. Mechanisms by which these comorbidities contribute to lower adherence deserve further investigation and may lead to targeted interventions to improve disease outcomes.
Identifiants
pubmed: 32921004
doi: 10.1002/acr2.11175
pmc: PMC7571399
doi:
Types de publication
Journal Article
Langues
eng
Pagination
555-564Subventions
Organisme : NIH HHS
ID : K23-AR-064372
Pays : United States
Organisme : NIH HHS
ID : P50AR060772
Pays : United States
Organisme : Rheumatology Research Foundation
Organisme : NIH HHS
ID : R25AA020818
Pays : United States
Organisme : CSRD VA
ID : I01 CX001703
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR064372
Pays : United States
Organisme : Veterans Affairs Clinical Science Research & Development Merit Award
ID : I01 CX00170
Organisme : NIH HHS
ID : U54GM115458
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM115458
Pays : United States
Organisme : Veterans Affairs Merit Award
ID : BX0046000
Informations de copyright
© 2020 The Authors. ACR Open Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.
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