What predicts attrition in second step medication treatments for depression?: a STAR*D Report
- PMID: 18611293
- PMCID: PMC5885751
- DOI: 10.1017/S1461145708009073
What predicts attrition in second step medication treatments for depression?: a STAR*D Report
Abstract
Attrition rates are high during treatment for major depressive disorder (MDD), and patients who drop out are less likely to reach remission. This report evaluates the incidence, timing, and predictors of attrition during second-step medication treatment. Outpatients in the multisite Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study receiving a medication augmentation (n=563) or medication switch (n=723) for non-psychotic MDD after an unsatisfactory outcome with citalopram were evaluated to determine attrition rates and pretreatment sociodemographic or clinical predictors of attrition. Twenty percent of participants receiving a medication augmentation and 27% receiving a medication switch dropped out before 12 wk in the second treatment step. Remission rates were lower for dropouts [7% vs. 43% (medication augmentation); 12% vs. 31% (medication switch)]. For medication augmentation, Black and other non-Caucasian races, Hispanic ethnicity, younger age, family history of drug abuse, concurrent drug abuse, sociodemographic disadvantage, less symptom improvement with initial citalopram treatment, and greater symptom severity when beginning augmentation were associated with attrition. For medication switch, Black and other non-Caucasian races, younger age, more melancholic features, and lower exit doses but more severe side-effects with citalopram treatment were associated with attrition. Minority status, younger age, and greater difficulty with the first treatment step are risk factors for attrition in the second treatment step. Focus on patients with attrition risk factors for medication augmentation or switch strategies may enhance retention and improve outcomes.
Conflict of interest statement
Diane Warden, Ph.D., M.B.A. currently owns stock in Pfizer, Inc. has owned stock in Bristol–Myers Squibb Company within the last 5 years. A. John Rush, M.D. has received research support from the National Institute of Mental Health, the Robert Wood Johnson Foundation, and the Stanley Medical Research Institute; has been on the advisory boards and/or consultant for Advanced Neuromodulation Systems, Inc., AstraZeneca, Best Practice Project Management, Inc., Bristol–Myers Squibb Company, Cyberonics, Inc., Eli Lilly and Company, Gerson Lehman Group, GlaxoSmithKline, Jazz Pharmaceuticals, Magellan Health Services, Merck & Co., Inc., Neuronetics, Ono Pharmaceutical, Organon USA Inc., Pam Lab, Personality Disorder Research Corp., Pfizer Inc., The Urban Institute, and Wyeth–Ayerst Laboratories Inc.; has been on the speakers’ bureaux for Cyberonics, Inc., Forest Pharmaceuticals, Inc., and GlaxoSmithKline; has equity holdings (excluding mutual funds/blinded trusts) in Pfizer Inc.; and has royalty income affiliations with Guilford Publications and Healthcare Technology Systems, Inc. Stephen R. Wisniewski, Ph.D. has been a consultant for Cyberonics, Inc. (2005–2006), ImaRx Therapeutics, Inc. (2006), Bristol– Myers Squibb Company (2007), Organon (2007), and Case-Western University (2007). Ira M. Lesser, M.D. has received grant support from the National Institute of Mental Health and Aspect Medical Systems, and has served on the speakers’ bureau of Medical Education Speakers Network. Susan G. Kornstein, M.D. has received grant/research support from the Department of Health and Human Services, the National Institute of Mental Health, Pfizer, Inc., Bristol–Myers Squibb Company, Eli Lilly and Company, Forest Laboratories, Inc., GlaxoSmithKline, Inc., Mitsubishi-Tokyo, Merck, Inc., Biovail Laboratories, Inc., Wyeth, Inc., Berlex Laboratories, Novartis Pharmaceuticals, Inc., Sepracor, Inc., Boehringer-Ingelheim, Sanofi-Synthelabo, and AstraZeneca. She has served on advisory boards for and/or received honoraria from Pfizer, Inc., Wyeth, Inc., Eli Lilly and Company, Bristol–Myers Squibb Company, Warner-Chilcott, Inc., Biovail Laboratories, Berlex Laboratories, Forest Laboratories, Neurocrine, and Sepracor, Inc., and has received book royalties from Guilford Press. Michael E. Thase, M.D. has served in an advisory or consulting capacity to, or received speaker’s honoraria from, AstraZeneca, Bristol–Myers Squibb, Cephalon, Cyberonics, Inc., Eli Lilly and Company, GlaxoSmithKline, Janssen Pharmaceutica, MedAvante, Inc., Neuronetics, Inc., Novartis, Organon, Inc., Sanofi-Aventis, Sepracor, Inc., Shire US, Inc., and Wyeth Pharmaceuticals; has equity holdings in MedAvante, Inc.; and has received royalty/patent or other income from American Psychiatric Publishing, Inc., Guilford Publications, and Herald House. Sheldon H. Preskorn, M.D. has served or is serving in one or more of the following capacities: as a principal investigator, on the speakers’ bureau, and/or as a consultant for the following companies: Abbott Laboratories, AstraZeneca, Aventis, Biovail, Boehringer-Ingleheim, Bristol–Myers Squibb, E. Merck, Eisai, Eli Lilly, GlaxoSmithKline, Hoffman LaRoche, Janssen, Johnson & Johnson, Lundbeck, Merck, Neurosearch, Novartis, Organon, Otusak, Pfizer, Inc., Solvay, Somerset, Sumitomo, Wyeth, and Yamanouchi. Andrew A. Nierenberg, M.D. has received research support from Bristol–Myers Squibb, Cederroth, Cyberonics, Forest Pharmaceuticals, Eli Lilly & Co, GlaxoSmithKline, Janssen Pharmaceutica, Lichtwer Pharma, NARSAD, NIMH, Pfizer Pharmaceuticals, Stanley Foundation, and Wyeth–Ayerst. He has served on speakers’ bureaux with Bristol–Myers Squibb, Cyberonics, Forest Pharmaceuticals, Eli Lilly & Co., GlaxoSmithKline, and Wyeth–Ayerst and has provided advisory/consulting services to Abbott Laboratories, Brain Cells Inc., Bristol–Myers Squibb, Cederroth, Eli Lilly & Co, GlaxoSmithKline, Genaissance, Innapharma, Janssen Pharmaceutica, Novartis Pharmaceuticals, Pfizer Pharmaceuticals, Sepracor, Shire, and Somerset. Madhukar H. Trivedi, M.D. has been a consultant for Abbott Laboratories, Inc.; Akzo (Organon Pharmaceuticals Inc.); AstraZeneca; Bayer; Bristol–Myers Squibb Company; Cephalon, Inc.; Cyberonics, Inc.; Eli Lilly & Company; Fabre-Kramer Pharmaceuticals, Inc.; Forest Pharmaceuticals; Glaxo-SmithKline; Janssen Pharmaceutica Products, LP; Johnson & Johnson PRD; Eli Lilly & Company; Meade Johnson; Neuronetics; Parke-Davis Pharmaceuticals, Inc.; Pfizer, Inc.; Pharmacia & Upjohn; Sepracor; Solvay Pharmaceuticals, Inc.; VantagePoint; and Wyeth–Ayerst Laboratories. He has served on speakers’ bureaux for Abdi Brahim; Akzo (Organon Pharmaceuticals Inc.); Bristol–Myers Squibb Company; Cephalon, Inc.; Cyberonics, Inc.; Forest Pharmaceuticals; GlaxoSmithKline; Janssen Pharmaceutica Products, LP; Eli Lilly & Company; Pharmacia & Upjohn; Solvay Pharmaceuticals, Inc.; and Wyeth–Ayerst Laboratories. He has also received grant support from Bristol–Myers Squibb Company; Cephalon, Inc.; Corcept Therapeutics, Inc.; Cyberonics, Inc.; Eli Lilly & Company; Forest Pharmaceuticals; GlaxoSmithKline; Janssen Pharmaceutica; Merck; National Institute of Mental Health; National Alliance for Research in Schizophrenia and Depression; Novartis; Pfizer Inc.; Pharmacia & Upjohn; Predix Pharmaceuticals; Solvay Pharmaceuticals, Inc.; and Wyeth–Ayerst Laboratories.
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References
-
- Arnow BA, Blasey C, Manber R, Constantino MJ, Markowitz JC, Klein DN, Thase ME, Kocsis JH, Rush AJ. Dropouts versus completers among chronically depressed outpatients. Journal of Affective Disorders. 2007;97:197–202. - PubMed
-
- Cooper LA, Gonzales JJ, Gallo JJ, Rost KM, Meredith LS, Rubenstein LV, Wang NY, Ford DE. The acceptability of treatment for depression among African-American, Hispanic, and white primary care patients. Medical Care. 2003;41:479–489. - PubMed
-
- Demyttenaere K, Enzlin P, Dewe W, Boulanger B, De Bie J, De Troyer W, Mesters P. Compliance with antidepressants in a primary care setting, 1: Beyond lack of efficacy and adverse events. Journal of Clinical Psychiatry. 2001;62(Suppl 22):30–33. - PubMed
-
- Demyttenaere K, Van Ganse E, Gregoire J, Gaens E, Mesters P. Compliance in depressed patients treated with fluoxetine or amitriptyline. Belgian Compliance Study Group. International Clinical Psychopharmacology. 1998;13:11–17. - PubMed
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