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Lowering Expectations: Glucocorticoid Tapering Among Veterans With Rheumatoid Arthritis Achieving Low Disease Activity on Stable Biologic Therapy.
Wallace, Beth I; England, Bryant R; Baker, Joshua F; Rojas, Jorge; Sauer, Brian C; Roul, Punyasha; Kunkel, Gary A; Braaten, Tawnie J; Petro, Alison; Mikuls, Ted R; Cannon, Grant W.
Afiliación
  • Wallace BI; Center for Clinical Management Research, VA Ann Arbor Healthcare System and University of Michigan, Ann Arbor.
  • England BR; University of Nebraska Medical Center and Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha.
  • Baker JF; Hospital of the University of Pennsylvania and Philadelphia VA Medical Center, Philadelphia.
  • Rojas J; VA Salt Lake City Healthcare System, Salt Lake City, Utah, and VA Puget Sound Healthcare System, Seattle, Washington.
  • Sauer BC; VA Salt Lake City Healthcare System, Salt Lake City, Utah.
  • Roul P; University of Nebraska Medical Center, Omaha.
  • Kunkel GA; VA Salt Lake City Healthcare System and University of Utah, Salt Lake City.
  • Braaten TJ; VA Salt Lake City Healthcare System and University of Utah, Salt Lake City.
  • Petro A; University of Nebraska Medical Center, Omaha.
  • Mikuls TR; University of Nebraska Medical Center and Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha.
  • Cannon GW; VA Salt Lake City Healthcare System, Salt Lake City, Utah, and VA Puget Sound Healthcare System, Seattle, Washington.
ACR Open Rheumatol ; 5(9): 437-442, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37491906
ABSTRACT

OBJECTIVE:

In the Steroid EliMination In Rheumatoid Arthritis (SEMIRA) trial, 65% of patients with rheumatoid arthritis (RA) in low disease activity (LDA) on stable biologic therapy successfully tapered glucocorticoids. We aimed to evaluate real-world rates of glucocorticoid tapering among similar patients in the Veterans Affairs Rheumatoid Arthritis registry.

METHODS:

Within a multicenter, prospective RA cohort, we used registry data and linked pharmacy claims from 2003 to 2021 to identify chronic prednisone users achieving LDA after initiating a new biologic or targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD). We defined the index date as first LDA occurring 60 to 180 days after b/tsDMARD initiation. The primary outcome of successful tapering, assessed at day 180 after LDA, required a 30-day averaged prednisone dose both less than or equal to 5mg/day and at least 50% lower than at the index date. The secondary outcome was discontinuation, defined as a prednisone dose of 0 mg/day at days 180 through 210. We used univariate statistics to compare patient characteristics by fulfillment of the primary outcome.

RESULTS:

We evaluated 100 b/tsDMARD courses among 95 patients. Fifty-four courses resulted in successful tapering; 33 resulted in discontinuation. Positive rheumatoid factor, higher erythrocyte sedimentation rate, more background DMARDs, shorter time from b/tsDMARD initiation to LDA, and higher glucocorticoid dose 30 days before LDA were associated with greater likelihood of successful tapering.

CONCLUSION:

In a real-world RA cohort of chronic glucocorticoid users in LDA, half successfully tapered and a third discontinued prednisone within 6 months of initiating a new b/tsDMARD. Claims-based algorithms of glucocorticoid tapering and discontinuation may be useful to evaluate predictors of tapering in administrative data sets.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: ACR Open Rheumatol Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: ACR Open Rheumatol Año: 2023 Tipo del documento: Article
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