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. 2019 Nov 12;19:306. doi: 10.1186/s12877-019-1327-4

Table 1.

Studies of subjects ≥65 years included in the meta-analysis

Author Year Drug & Dose Time (weeks) N Mean Age (years) Qualitya Scale Primary outcome Statistical benefit
Evans 1997 [14]b FLU 20 mg 8 62 82 Lowd HDRS-17 Response No
Fraguas 2009 [15]bc CIT 20-40 mg 8 37 74 Low HDRS-17 Response No
Hewett 2010 [16] BUP 105–300 mg 10 418 71 Lowd MADRS Change from baseline Inconsistente
Kasper 2005 [17]

ESC 10 mg

FLU 20 mg

8 517 75 Moderated MADRS Change from baseline No
Katona 2012 [18] DUL 60 mg 8 452 71 Highd HDRS-24 Change from baseline Yes
Raskin 2008 [19] b DUL 60 mg 8 311 73 Lowd HDRS-17

Response/

remission

Yes
Robinson 2014 [20]b DUL 60 mg 12 + 24 extension 370 73 Low-d HDRS-17 Maier subscale Change from baseline No
Roose 2004 [21] CIT 10–20 mg 8 174 80 Highd HDRS

Response/

remission

No
Schatzberg 2006 [22]b

FLU 40–60 mg

VEN 150–225 mg

8 300 71 Highd HDRS-21

Response/

remission

No

a Quality based on Cochrane risk of bias criteria; b Enrolled subjects with dementia/did not explicitly exclude dementia subjects; c Subjects had heart failure; d Trial had industry funding/industry employees as authors; e The pre-specified ANCOVA analysis was not statistically significant (p = 0.09). Post-hoc rank-based ANCOVA analysis was statistically significant (p = 0.03). Response was statistically significant (p = 0.01), but remission was not statistically significant (p = 0.17)

FLU Fluoxetine, CIT Citalopram, BUP Buspirone, ESC Escitalopram, DUL Duloxetine, VEN Venlafaxine, HDRS Hamilton Depression Rating Scale, MADRS Montgomery-Åsberg Depression Rating Scale