Durability of clinical benefit with transcranial magnetic stimulation (TMS) in the treatment of pharmacoresistant major depression: assessment of relapse during a 6-month, multisite, open-label study

التفاصيل البيبلوغرافية
العنوان: Durability of clinical benefit with transcranial magnetic stimulation (TMS) in the treatment of pharmacoresistant major depression: assessment of relapse during a 6-month, multisite, open-label study
المؤلفون: Peter B. Rosenquist, John P. O'Reardon, Sheila M. Dowd, Philip G. Janicak, H. Brent Solvason, Sarah H. Lisanby, Shirlene Sampson, Mark A. Demitrack, William S. Gilmer, Colleen Loo, Alan F. Schatzberg, William M. McDonald, Andrew D. Krystal, Ziad Nahas, James Kimball, W. Vaughn McCall, Lauren B. Marangell, Mustafa H. Husain
المصدر: Brain Stimulation, Vol 3, Iss 4, Pp 187-199 (2010)
بيانات النشر: Elsevier, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Adult, medicine.medical_specialty, genetic structures, medicine.medical_treatment, Biophysics, Kaplan-Meier Estimate, law.invention, lcsh:RC321-571, treatment resistance, Randomized controlled trial, Double-Blind Method, law, Recurrence, Internal medicine, Hamd, medicine, Humans, Prospective Studies, Psychiatry, Prospective cohort study, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, Depressive Disorder, Major, antidepressant, General Neuroscience, Therapeutic effect, clinical trial, Middle Aged, medicine.disease, Transcranial Magnetic Stimulation, Antidepressive Agents, Transcranial magnetic stimulation, Clinical trial, Treatment Outcome, Tolerability, TMS, Major depressive disorder, Female, Neurology (clinical), Psychology, major depression, maintenance of effect, Follow-Up Studies
الوصف: Background Although transcranial magnetic stimulation (TMS) can be an effective acute antidepressant treatment, few studies systematically examine persistence of benefit. Objective We assessed the durability of antidepressant effect after acute response to TMS in patients with major depressive disorder (MDD) using protocol-specified maintenance antidepressant monotherapy. Methods Three hundred one patients were randomly assigned to active or sham TMS in a 6-week, controlled trial. Nonresponders could enroll in a second, 6-week, open-label study. Patients who met criteria for partial response (i.e., >25% decrease from the baseline HAMD 17) during either the sham-controlled or open-label study (n = 142) were tapered off TMS over 3 weeks, while simultaneously starting maintenance antidepressant monotherapy. Patients were then followed for 24 weeks in a naturalistic follow-up study examining the long-term durability of TMS. During this durability study, TMS was readministered if patients met prespecified criteria for symptom worsening (i.e., a change of at least one point on the CGI-S scale for 2 consecutive weeks). Relapse was the primary outcome measure. Results Ten of 99 (10%; Kaplan-Meier survival estimate=12.9%) patients relapsed . Thirty-eight (38.4%) patients met criteria for symptom worsening and 32/38 (84.2%) reachieved symptomatic benefit with adjunctive TMS. Safety and tolerability were similar to acute TMS monotherapy. Conclusions These initial data suggest that the therapeutic effects of TMS are durable and that TMS may be successfully used as an intermittent rescue strategy to preclude impending relapse.
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d71ae389331d48fb9d1837a9c248b6
http://www.sciencedirect.com/science/article/pii/S1935861X10001105
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....e7d71ae389331d48fb9d1837a9c248b6
قاعدة البيانات: OpenAIRE