Canadian Network for Mood and Anxiety Treatments (CANMAT) Clinical guidelines for the management of major depressive disorder in adults. Ill. Pharmacotherapy

被引:325
作者
Lam, Raymond W. [1 ]
Kennedy, Sidney H. [2 ]
Grigoriadis, Sophie [2 ]
McIntyre, Roger S. [2 ]
Milev, Roumen [3 ]
Ramasubbu, Rajamannar [4 ]
Parikh, Sagar V. [2 ]
Patten, Scott B. [4 ]
Ravindran, Arun V. [2 ]
机构
[1] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[2] Univ Toronto, Toronto, ON M5S 1A1, Canada
[3] Queens Univ, Kingston, ON K7L 3N6, Canada
[4] Univ Calgary, Calgary, AB T2N 1N4, Canada
基金
加拿大健康研究院;
关键词
Depressive disorders; MDD; Antidepressant; Pharmacotherapy; Canadian; Guidelines; Systematic review; Treatment; Adverse effects; Treatment-resistant depression; SEROTONIN-REUPTAKE INHIBITORS; STAR-ASTERISK-D; RANDOMIZED CONTROLLED-TRIALS; PERSISTENT PULMONARY-HYPERTENSION; COGNITIVE-BEHAVIORAL THERAPY; SSRI-RESISTANT DEPRESSION; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; ANTIDEPRESSANT MEDICATION; POSTPARTUM DEPRESSION;
D O I
10.1016/j.jad.2009.06.041
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: In 2001, the Canadian Psychiatric Association and the Canadian Network for Mood and Anxiety Treatments (CANMAT) partnered to produce evidence-based clinical guidelines for the treatment of depressive disorders. A revision of these guidelines was undertaken by CANMAT in 2008-2009 to reflect advances in the field. Methods: The CANMAT guidelines are based on a question-answer format to enhance accessibility to clinicians. An evidence-based format was used with updated systematic reviews of the literature and recommendations were graded according to Level of Evidence using pre-defined criteria. Lines of Treatment were identified based on criteria that included Levels of Evidence and expert clinical support. This section on "Pharmacotherapy" is one of 5 guideline articles. Results: Despite emerging data on efficacy and tolerability differences amongst newer antidepressants, variability in patient response precludes identification of specific first choice medications for all patients. All second-generation antidepressants have Level 1 evidence to support efficacy and tolerability and most are considered first-line treatments for MDD. First-generation tricyclic and monoamine oxidase inhibitor antidepressants are not the focus of these guidelines but generally are considered second- or third-line treatments. For inadequate or incomplete response, there is Level 1 evidence for switching strategies and for add- on strategies including lithium and atypical antipsychotics. Limitations: Most of the evidence is based on trials for registration and may not reflect real-world effectiveness. Conclusions: Second-generation antidepressants are safe, effective and well tolerated treatments for MDD in adults. Evidence-based switching and add-on strategies can be used to optimize response in MDD that is inadequately responsive to monotherapy. (C) 2009 Published by Elsevier B.V.
引用
收藏
页码:S26 / S43
页数:18
相关论文
共 147 条
[1]   Safety of fluoxetine during the first trimester of pregnancy: a meta-analytical review of epidemiological studies [J].
Addis, A ;
Koren, G .
PSYCHOLOGICAL MEDICINE, 2000, 30 (01) :89-94
[2]   Placebo-controlled study of relapse prevention with risperidone augmentation in older patients with resistant depression [J].
Alexopoulos, George S. ;
Canuso, Carla M. ;
Gharabawi, Georges M. ;
Bossie, Cynthia A. ;
Greenspan, Andrew ;
Turkoz, Ibrahim ;
Reynolds, Charles .
AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2008, 16 (01) :21-30
[3]   Evidence-based guidelines for treating depressive disorders with antidepressants: A revision of the 2000 British Association for Psychopharmacology guidelines [J].
Anderson, I. M. ;
Ferrier, I. N. ;
Baldwin, R. C. ;
Cowen, P. J. ;
Howard, L. ;
Lewis, G. ;
Matthews, K. ;
McAllister-Williams, R. H. ;
Peveler, R. C. ;
Scott, J. ;
Tylee, A. .
JOURNAL OF PSYCHOPHARMACOLOGY, 2008, 22 (04) :343-396
[4]   Meta-analytical studies on new antidepressants [J].
Anderson, IM .
BRITISH MEDICAL BULLETIN, 2001, 57 :161-178
[5]   Antidepressant medication use and risk of persistent pulmonary hypertension of the newborn [J].
Andrade, Susan E. ;
McPhillips, Heather ;
Loren, David ;
Raebel, Marsha A. ;
Lane, Kimberly ;
Livingston, James ;
Boudreau, Denise M. ;
Smith, David H. ;
Davis, Robert L. ;
Willy, Mary E. ;
Platt, Richard .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2009, 18 (03) :246-252
[6]  
[Anonymous], 2008, COCHRANE DATABASE SY
[7]   Patients with severe depression may benefit from buspirone augmentation of selective serotonin reuptake inhibitors:: Results from a placebo-controlled, randomized, double-blind, placebo wash-in study [J].
Appelberg, BG ;
Syvälahti, EK ;
Koskinen, TE ;
Mehtonen, OP ;
Muhonen, TT ;
Naukkarinen, HH .
JOURNAL OF CLINICAL PSYCHIATRY, 2001, 62 (06) :448-452
[8]   Antidepressant medications and other treatments of depressive disorders:: a CINP Task Force report based on a review of evidence [J].
Baghai, Thomas C. ;
Baldwin, David S. ;
Barrett, Barbara ;
Baumann, Pierre ;
Ghalib, Kareem ;
Goodwin, Guy ;
Grunze, Heinz ;
Knapp, Martin ;
Leonard, Brian E. ;
Markowitz, John C. ;
Padberg, Frank ;
Pinder, Roger ;
Sartorius, Norman ;
Brand, Ursula ;
Fink, Max ;
Furukawa, Toshiaki A. ;
Fountoulakis, Konstantinos N. ;
Jensen, Peter ;
Kanba, Shigenobu ;
Riecher-Roessler, Anita .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 :S1-S121
[9]   Discontinuation symptoms in depression and anxiety disorders [J].
Baldwin, David S. ;
Montgomery, Stuart A. ;
Nil, Rico ;
Lader, Malcolm .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 (01) :73-84
[10]   Paroxetine and congenital malformations:: Meta-analysis and consideration of potential confounding factors [J].
Bar-Oz, Benjamin ;
Einarson, Thomas ;
Einarson, Adrienne ;
Boskovic, Radinka ;
O'Brien, Lisa ;
Malm, Heli ;
Berard, Anick ;
Koren, Gideon .
CLINICAL THERAPEUTICS, 2007, 29 (05) :918-926