Pharmacological augmentation strategies for treatment-resistant obsessive-compulsive disorder

被引:20
作者
Walsh, KH [1 ]
McDougle, CJ [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Psychiat, James Whitcomb Riley Hosp Children, Indianapolis, IN 46202 USA
关键词
neuroleptics; obsessive-compulsive disorder; pharmacological augmentation; serotonin re-uptake inhibitors; treatment resistance;
D O I
10.1517/14656566.5.10.2059
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
First-line treatment for obsessive-compulsive disorder (OCD) has been well-established for over a decade, although newer medications, such as citalopram and venlafaxine, have emerged to take a place among the older more established serotonin re-uptake inhibitors (SRIs). Unfortunately, as many as 50% of all patients with OCD will have symptoms refractory to a single medication treatment trial, and a smaller percentage will remain refractory after two or more trials. The optimal dosage and duration for first-line trials have been established. Many strategies exist for patients who do not respond to first-or second-line medication trials, including behavioural therapy, switching to newer Sills, and augmentation with additional medications. This review will focus on medication strategies for augmenting SRI treatment response in OCD treatment, including neuroleptic and serotonergic agents. Future investigations should include more controlled studies and investigate medications that are less likely to trigger extrapyramidal symptoms, diabetes mellitus and weight gain.
引用
收藏
页码:2059 / 2067
页数:9
相关论文
共 100 条
[51]   Behavioral versus pharmacological treatments of obsessive compulsive disorder: a meta-analysis [J].
Kobak, KA ;
Greist, JH ;
Jefferson, JW ;
Katzelnick, DJ ;
Henk, HJ .
PSYCHOPHARMACOLOGY, 1998, 136 (03) :205-216
[52]   Olanzapine augmentation for treatment-resistant obsessive-compulsive disorder [J].
Koran, LM ;
Ringold, AL ;
Elliott, MA .
JOURNAL OF CLINICAL PSYCHIATRY, 2000, 61 (07) :514-517
[53]   Will pindolol augment the response to a serotonin reuptake inhibitor in obsessive-compulsive disorder? [J].
Koran, LM ;
Mueller, K ;
Maloney, A .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1996, 16 (03) :253-254
[54]   Lamotrigine augmentation of serotonin re-uptake inhibitors in obsessive-compulsive disorder [J].
Kumar, TCR ;
Khanna, S .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2000, 34 (03) :527-528
[55]  
LEONARD HL, 1992, AM J PSYCHIAT, V149, P1244
[56]   CLONAZEPAM AS AN AUGMENTING AGENT IN THE TREATMENT OF CHILDHOOD-ONSET OBSESSIVE-COMPULSIVE DISORDER [J].
LEONARD, HL ;
TOPOL, D ;
BUKSTEIN, O ;
HINDMARSH, D ;
ALLEN, AJ ;
SWEDO, SE .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 1994, 33 (06) :792-794
[57]   Obsessive-compulsive symptoms induced by atypical antipsychotics. A review of the reported cases [J].
Lykouras, L ;
Alevizos, B ;
Michalopoulou, P ;
Rabavilas, A .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2003, 27 (03) :333-346
[58]  
Marazziti D, 1999, AM J PSYCHIAT, V156, P1834
[59]   Citalopram in refractory obsessive-compulsive disorder: an open study [J].
Marazziti, D ;
Dell'Osso, L ;
Gemignani, A ;
Ciapparelli, A ;
Presta, S ;
Di Nasso, E ;
Pfanner, C ;
Cassano, GB .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2001, 16 (04) :215-219
[60]   A PILOT-STUDY OF COMBINED TRAZODONE AND TRYPTOPHAN IN OBSESSIVE-COMPULSIVE DISORDER [J].
MATTES, JA .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1986, 1 (02) :170-173