Key result
Prospective screening for depressive symptoms up to three months after intracerebral hemorrhage detected symptoms in 22.4% of patients compared to only 3.8% identified via diagnostic codes in standard care (OR 7.20).
Why the study?
It was not well described how often depressive symptoms are ascertained and treated in large unselected cohorts of ICH patients, or if they represent a target to improve outcomes.
Does prospective screening improve the detection of depressive symptoms in patients with intracerebral hemorrhage compared to standard clinical care?
Observational (n=3,538)
Yes
Does prospective screening improve the detection of depressive symptoms in patients with intracerebral hemorrhage compared to standard clinical care?
Depressive symptoms are common after intracerebral hemorrhage but are significantly under-diagnosed and under-treated in routine clinical practice compared to active screening.
Prospective screening detects more post-ICH depressive symptoms than routine care; hypothesis-generating for implementation trials before practice change.
INTRODUCTION: Depressive symptoms in patients with intracerebral hemorrhage (ICH) are common and are associated with worse outcomes. It is not well described how often depressive symptoms are ascertained and treated in large unselected cohorts of patients, and whether depressive symptoms would be a potential target for improving outcomes. METHODS: Data were electronically retrieved from a multi-center EHR repository in Chicago, IL, from 2006 to 2012 ("multicenter cohort"). In the multicenter cohort, we retrieved diagnostic codes and medication data from four university health systems across Chicago. In the single center cohort, we prospectively screened for depressive symptoms (NIH Patient Reported Outcomes Measurement Information System, PROMIS, T Score ≥ 60), at one, three and twelve months after ICH onset. It should be noted that not all depressive symptoms are optimally characterized through diagnostic codes. RESULTS: Diagnostic codes for depressive symptoms up to three months after ICH onset were recorded in 132 of 3422 (3.8%) of the multicenter cohort; fewer than 10% of patients received a typical medication to treat depressive symptoms, and < 2% one month later. In the single-center cohort, PROMIS assessments were indicative of depressive symptoms in 26 of 116 (22.4%), and depressive symptoms were more likely to be found with screening (OR 7.20, 95% CI 4.5-11.5, P < 0.0001). Results were similar up to 12 months after ICH. CONCLUSIONS: Depressive symptoms in patients with ICH are more common than medication treatment or a coded diagnosis in a multi-center cohort, and are a potential opportunity for additional treatment to improve outcomes. There are currently no AHA/ASA treatment guidelines for depression screening of patients with ICH.
No takes yet. Share an insight, caveat, or question.
Francis et al. (2018) conducted an observational in Intracerebral hemorrhage (n=3,538). Prospective screening for depressive symptoms vs. Standard care (diagnostic codes) was evaluated on Detection of depressive symptoms up to three months after ICH onset (OR 7.20, 95% CI 4.5-11.5, p=<0.0001). Prospective screening for depressive symptoms up to three months after intracerebral hemorrhage detected symptoms in 22.4% of patients compared to only 3.8% identified via diagnostic codes in standard care (OR 7.20).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: