Why the study?
Do symptoms of depression and anxiety predict participation in a randomized study for prevention of post-ACS depression in patients with acute coronary syndrome?
Do symptoms of depression and anxiety predict participation in a randomized study for prevention of post-ACS depression in patients with acute coronary syndrome?
Symptoms of depression and anxiety are highly prevalent in post-ACS patients but do not predict their willingness to participate in depression prevention trials.
Answers are grounded in this paper and cite their sources.
Depression and anxiety symptoms do not bias post-ACS trial participation; leaves open whether older age affects enrollment.
BACKGROUND: The prevalence of depression and anxiety in patients after acute coronary syndrome (ACS) is higher than in the general population. In a study on prevention of post-ACS depression, more than half of eligible patients declined participation. AIMS: The aim of this study was to evaluate whether symptoms of depression and anxiety in participants and non-participants predicted participation in the study. METHODS: This substudy was conducted between May 2005 and April 2007. Patients with ACS, eligible for the study (n=302) were asked four questions on depression and anxiety from the Primary Care Evaluation of Mental Disorders (PRIME-MD) screening questionnaire. RESULTS: The PRIME-MD screening data were available on 232 patients (76.8% of eligible patients). Thirty-eight (35.5%) of 107 participants and 30 (24.0%) of 125 non-participants had a positive screening for depression (NS), and 47 (43.9%) participants and 55 (44%) non-participants were screened positive for anxiety (NS). Non-participants were older (P=0.002), while no significant differences in gender or cardiac diagnosis were found. CONCLUSIONS: Symptoms of depression and anxiety were highly prevalent in patients after ACS but did not predict participation in the study of prevention of depression.
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Hansen et al. (2010) studied this question.
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