Recovery and subsequent recurrence in patients with recurrent major depressive disorder

التفاصيل البيبلوغرافية
العنوان: Recovery and subsequent recurrence in patients with recurrent major depressive disorder
المؤلفون: Peter Holland, Martin B. Keller, Boadie W. Dunlop, Philip T. Ninan, Weihang Bao
المصدر: Journal of Psychiatric Research. 46:708-715
بيانات النشر: Elsevier BV, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Venlafaxine Hydrochloride, Poison control, Venlafaxine, Kaplan-Meier Estimate, Placebo, Article, law.invention, Drug Delivery Systems, Double-Blind Method, Randomized controlled trial, Risk Factors, law, Internal medicine, Secondary Prevention, medicine, Humans, Psychiatry, Biological Psychiatry, Depression (differential diagnoses), Psychiatric Status Rating Scales, Depressive Disorder, Major, business.industry, Hazard ratio, Recovery of Function, Cyclohexanols, medicine.disease, Psychiatry and Mental health, Treatment Outcome, Antidepressive Agents, Second-Generation, Major depressive disorder, Female, business, Follow-Up Studies, medicine.drug
الوصف: In contrast to "remission" from an episode of major depressive disorder (MDD), for which there is general agreement in the literature, the optimal definition of "recovery" from MDD is uncertain. Previous definitions of recovery have used inconsistent thresholds for symptom severity and duration of wellness. To address the effects of duration and degree of recovery from an episode of MDD on recurrence risk, and the impact of maintenance antidepressant treatment on recurrence, we analyzed 258 patients from a randomized, double-blind study of outpatients with recurrent MDD. All patients had responded to 8½ months of venlafaxine extended release and were subsequently randomized to receive venlafaxine ER or placebo during 2 consecutive 12-month maintenance phases. Four definitions of recovery were used to evaluate recovery rates and time to recurrence: (1) 17-item Hamilton Depression Rating Scale (HAM-D(17)) total score ≤3 with duration ≥120 days; (2) HAM-D(17) ≤3 with duration ≥56 days; (3) HAM-D(17) ≤7 with duration ≥120 days; and (4) HAM-D(17) ≤7 with duration ≥56 days. Recovery definitions using lower symptom severity and longer duration thresholds produced lower rates of recurrence. Patients on placebo were more likely to have a recurrence than patients on venlafaxine ER, with hazard ratio (HR) ranging from 2.5 among patients who recovered by the most relaxed criteria (definition 4), to 5.3 among patients who recovered by the most stringent criteria (definition 1). We conclude that protection against recurrence derives from the degree and duration of recovery, particularly for patients maintained on antidepressant medication.
تدمد: 0022-3956
DOI: 10.1016/j.jpsychires.2012.03.002
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0ae38c51f5962c4eaabfe2f7797b91
https://doi.org/10.1016/j.jpsychires.2012.03.002
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....cd0ae38c51f5962c4eaabfe2f7797b91
قاعدة البيانات: OpenAIRE
الوصف
تدمد:00223956
DOI:10.1016/j.jpsychires.2012.03.002