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Predictability of Nonremitting Depression After First 2 Weeks of Antidepressant Treatment: A VAST-D Trial Report.
Hicks, Paul B; Sevilimedu, Varadan; Johnson, Gary R; Tal, Ilanit; Chen, Peijun; Davis, Lori L; Vertrees, Julia E; Mohamed, Somaia; Zisook, Sidney.
Afiliación
  • Hicks PB; Department of Psychiatry Baylor Scott & White Health.
  • Sevilimedu V; Texas A&M College of Medicine Temple Texas.
  • Johnson GR; Yale University School of Public Health New Haven Connecticut.
  • Tal I; Cooperative Studies Program Coordinating Center Veterans Affairs (VA) Connecticut Healthcare System West Haven.
  • Chen P; Cooperative Studies Program Coordinating Center Veterans Affairs (VA) Connecticut Healthcare System West Haven.
  • Davis LL; VA San Diego Healthcare System San Diego.
  • Vertrees JE; Louis Stokes Cleveland VA Medical Center Clevelend.
  • Mohamed S; Tuscaloosa VA Medical Center Tuscaloosa Alabama.
  • Zisook S; University of Alabama School of Medicine Birmingham.
Psychiatr Res Clin Pract ; 1(2): 58-67, 2019 Oct.
Article en En | MEDLINE | ID: mdl-36101874
Objective: In this secondary analysis of data from the Veterans Affairs Augmentation and Switching Treatments for Improving Depression Outcomes (VAST-D) study, the authors sought to determine the effectiveness of early improvement (or lack thereof) for predicting remission from depression with antidepressant therapy. Methods: This study used data from the VAST-D study, a multisite, randomized, single-blind trial with parallel assignment to one of three medication interventions for 1,522 veterans whose major depressive disorder was unresponsive to at least one course of antidepressant treatment meeting minimal standards for dosage and duration. The authors calculated the positive predictive value (PPV) and negative predictive value (NPV) of early improvement on remission, response, or greater than minimal improvement from depression for various degrees of improvement (10%-50%) on the Quick Inventory of Depressive Symptomatology-Clinician Rated (QIDS-C) at 1, 2, 4, and 6 weeks. Results: The end of week 2 of treatment was identified as the best time to evaluate early improvement. The presence of a ≥20% drop from the baseline QIDS-C score by the end of week 2 resulted in a PPV for remission of 38% and an NPV of 93% by week 12. Extending the observational window to week 6 minimally improved NPV (97%). This association did not differ across treatment groups. Conclusions: A lack of early improvement at the end of week 2 of antidepressant therapy can be used to inform clinical decisions on the likelihood of nonremission of depression during the subsequent 10 weeks, even when dosage optimization is incomplete.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Psychiatr Res Clin Pract Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Psychiatr Res Clin Pract Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos