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. 2019 Mar 19;2019(3):CD003690. doi: 10.1002/14651858.CD003690.pub4
Study Reason for exclusion
Aizawa 1977 Methods: double‐blind RCT
 Participants: cerebrovascular disorders (including arteriosclerosis)
 Intervention: cyclandelate for 4 weeks
 Outcomes: data not currently available for those with 'emotionalism' at baseline
Allen 2018 Methods: not a RCT, i.e. non‐interventional, cross‐sectional, case control study
Participants: nursing home residents with documented diagnosis of pseudobulbar affect
Intervention: dextromethorphan/quinidine
Atarashi 1988 Methods: randomisation unclear
 Participants: stroke, including cerebral arteriosclerosis
 Intervention: no placebo comparison
Bassi 1984 Methods: non‐random, open‐label
 Participants: chronic cerebrovascular disorders
 Intervention: no placebo comparison
Chen 2010 Methods: not a RCT, i.e. case report and literature review
Intervention: quetiapine
Colamonico 2012 Methods: not a RCT, i.e. survey of to estimate the impact or burden of pseudobulbar affect
D'Amico 2017 Methods: non‐random, open‐label
Doody 2014 Participants: ineligible study population, i.e. participants were adults who had pseudobulbar affect after being diagnosed with dementia/Alzheimer's Disease
Formella 2017a Methods: non‐random, open‐label
Formella 2017b Methods: non‐random, open‐label
Kim 2017a Outcomes: data not currently available for those with 'emotionalism' at baseline pretreatment
Kim 2017b Methods: not a RCT, i.e. review of the most common poststroke mood and emotional disturbances
Lawson 1969 Methods: randomised
 Participants: hypertensive or ischaemic cerebral disease (number with stroke unclear)
 Intervention: method of randomisation makes placebo comparison ineffectual ‐ no appropriate washout period
Manzo 1998 Methods: not a RCT, i.e. qualitative study of pseudobulbar affect
Moller 2007 Methods: randomised
 Participants: patients with stroke and pathological crying
 Intervention: citalopram for 30 days
 Outcomes: emotionalism not investigated
Muller 1999 Methods: quasi‐randomised, 2 active treatments
 Participants: brain injury
 Intervention: no placebo comparison
Narushima 2002 Methods: double‐blind, randomised
 Participants: poststroke
 Intervention: prevention of depression
 Outcomes: emotionalism not investigated
Ohtomo 1985 Methods: double‐blind, randomised
 Participants: cerebrovascular disorders, including arteriosclerosis
 Intervention: tiapride for 5 weeks
 Outcomes: data not currently available for those with 'emotionalism' at baseline
Otomo 1984 Methods: double‐blind, randomised
 Participants: cerebrovascular disorders
 Outcomes: emotionalism not investigated
Rasmussen 2000 Methods: double‐blind, randomised
 Participants: poststroke without depression, emotionalism not assessed at baseline
Sauve 2017 Participants: ineligible study population, i.e. participants were adults who had pseudobulbar affect after being diagnosed with dementia/Alzheimer's Disease
Schiffer 1985 Methods: double‐blind, cross‐over
 Participants: ineligible study population, i.e. multiple sclerosis (not stroke)
Seliger 1992 Method: non‐random, open‐label
 Participants: patients with stroke or multiple sclerosis (not stroke) and emotional incontinence
Udaka 1984 Methods: non‐random, open‐label
 Participants: ineligible study population, i.e. diffuse cerebrovascular disease (not stroke)
Work 2011 Methods: not a RCT, i.e. a survey to estimate the overall prevalence of pseudobulbar affect and quantify the extent to which it is diagnosed and treated
Yang 2015 Methods: not a RCT, i.e. a literature review
Participants: adults with pseudobulbar affect
Intervention: dextromethorphan/quinidine

RCT: randomised controlled trial