TY - JOUR
T1 - Evidence for the benefits of nonantipsychotic pharmacological augmentation in the treatment of depression
AU - Chang, Chia Ming
AU - Sato, Soichiro
AU - Han, Changsu
N1 - Funding Information:
Conflict of interest Drs Chang and Sato have received honoraria from Korea Otsuka International Asia and Arab. Dr Han has received research grants from GlaxoSmithKline Korea, Eisai Korea, Korea Otsuka International Asia and Arab, Hanlim Pharmaceutical, Janssen Pharmaceuticals Korea, Eli Lilly and Co. Korea, Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea, Korean Research Foundation, and Otsuka Korea. Dr Han has also received honoraria from GlaxoSmithKline Korea, Lundbeck Korea, AstraZeneca Korea, Janssen Pharmaceuticals Korea, Eisai Korea, Abott Korea, Eli Lilly and Company Korea, Norvatis Korea and Otsuka Korea.
PY - 2013/5
Y1 - 2013/5
N2 - Failure to achieve an adequate response after initial antidepressant treatment in patients with depression is common and remains a clinical challenge. In recent years, some atypical antipsychotic agents have been approved by the US Food and Drug Administration for use in an augmentation strategy for major depressive disorder, and other agents are already in common use in clinical practice. We conducted a search of MEDLINE for relevant studies of augmentation strategies using randomized controlled trials and meta-analyses, and we summarize and discuss the various agents other than atypical antipsychotics. Lithium and thyroid hormone augmentation may improve the response of tricyclic antidepressants but not that of selective serotonin reuptake inhibitors. The efficacy of augmentation with modafinil, buspirone, methylphenidate, folic acid, pindolol and lamotrigine is limited or equivocal. Most of the studies have not focused on treatment-resistant depression (TRD). More trials are needed to help develop evidence-based options for augmentation in TRD.
AB - Failure to achieve an adequate response after initial antidepressant treatment in patients with depression is common and remains a clinical challenge. In recent years, some atypical antipsychotic agents have been approved by the US Food and Drug Administration for use in an augmentation strategy for major depressive disorder, and other agents are already in common use in clinical practice. We conducted a search of MEDLINE for relevant studies of augmentation strategies using randomized controlled trials and meta-analyses, and we summarize and discuss the various agents other than atypical antipsychotics. Lithium and thyroid hormone augmentation may improve the response of tricyclic antidepressants but not that of selective serotonin reuptake inhibitors. The efficacy of augmentation with modafinil, buspirone, methylphenidate, folic acid, pindolol and lamotrigine is limited or equivocal. Most of the studies have not focused on treatment-resistant depression (TRD). More trials are needed to help develop evidence-based options for augmentation in TRD.
UR - http://www.scopus.com/inward/record.url?scp=84886281128&partnerID=8YFLogxK
U2 - 10.1007/s40263-012-0030-1
DO - 10.1007/s40263-012-0030-1
M3 - Review article
C2 - 23712796
AN - SCOPUS:84886281128
SN - 1172-7047
VL - 27
SP - S21-S27
JO - CNS Drugs
JF - CNS Drugs
IS - SUPPL.1
ER -