4.4 Article

Primary care management of major depression in patients aged ≥55 years: outcome of a randomised clinical trial

Journal

BRITISH JOURNAL OF GENERAL PRACTICE
Volume 58, Issue 555, Pages 680-686

Publisher

ROYAL COLL GENERAL PRACTITIONERS
DOI: 10.3399/bjgp08X342165

Keywords

disease management programme; general practice; major depression; older adults; screening; usual care

Funding

  1. Netherlands Organisation for Health Research and Development (ZonMw) [2200/0019]

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Background Late-life depression is associated with chronic illness, disability, and a poor prognosis. Primary care management may be in need of improvement. Aim To compare the effects of an intervention programme that aims to improve the identification, diagnosis, and treatment of depression in patients aged >= 55 years with the effects of usual care. Design of study Cluster randomised controlled trial. Setting General practices in the Netherlands. Method Trained GPs performed the intervention and their practice assistants conducted the screenings. Patients were screened with the 15-item Geriatric Depression Scale (GDS-15) and given a consultation with the GP who diagnosed depression with the mood module of the Primary Care Evaluation of Mental Disorders (PRIME-MD). Antidepressant treatment was proposed. Primary outcomes were measured with the Montgomery Asberg Depression Rating Scale (MADRS). Trained independent research assistants performed independent evaluations in both arms. Results Eighteen practices (23 GPs) were allocated to the intervention and 16 practices (20 GPs) to usual care. From June 2000 to September 2002, 3937 patients were screened; 579 patients had a positive score on the GDS-15, 178 had major depression, of whom 145 participated in the trial. MADRS scores for the intervention group dropped from 21.66 at baseline to 9.23 at 6 months, and the usual care group from 20.94 at baseline to 11.45 at 6 months. MADRS scores decreased during the year in both arms. For the intervention group, these scores increased between 6 and 12 months. Conclusion The programme resulted in lower MADRS scores in the intervention group than in the usual care group, but only at the end of the intervention, at 6 months after baseline.

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