Abstract
BackgroundDepression is a common complication of traumatic brain injury (TBI). New evidence suggests that antidepressant medication may be no more effective than placebo in this population.Main bodySelective serotonin reuptake inhibitors are recommended as first-line treatment for depression in contemporary expert consensus clinical practice guidelines for management of TBI. This recommendation is based on multiple prior meta-analyses of clinical trials in depression after TBI as well as depression in the general population. The evidence is mixed. A recent clinical trial and new meta-analysis including that trial found no benefit of antidepressants for depression following TBI. We argue that this finding should not change practice, i.e., patients who present with depression after TBI should still be considered for antidepressant treatment, because they may (1) benefit from robust placebo effects, (2) benefit from an alternative or adjunctive medication if the agent prescribed first does not achieve a depression remission, and (3) make improvements that are not captured well by traditional depression outcome measures, which are confounded by TBI sequelae. Patients with mild TBI are especially appropriate for antidepressant therapy because they, on average, more closely resemble patients with no known TBI history enrolled in typical primary Major Depressive Disorder clinical trials than patients enrolled in TBI trials in placebo-controlled trials published to date.ConclusionTBI, and especially mild TBI, is not a contraindication for antidepressant therapy. Health providers should routinely screen and initiate treatment for depression after TBI.
Highlights
Prior meta-analyses have concluded that antidepressant medications are effective for depression in a variety of Silverberg and Panenka BMC Psychiatry (2019) 19:100II error), we argue here that proactive treatment should be considered, especially in mild traumatic brain injury (TBI), for the following reasons.First, when non-randomized and open-label studies were included in the Kreitzer et al [9] study as well as prior meta-analyses on the same topic [6, 10], the treatment effect was significant
Depression is common after traumatic brain injury (TBI), with at least 1 in 5 patients meeting criteria for a Major Depressive Episode within the first six months [1,2,3]
II error), we argue here that proactive treatment should be considered, especially in mild TBI, for the following reasons
Summary
Depression is common after traumatic brain injury (TBI), with at least 1 in 5 patients meeting criteria for a Major Depressive Episode within the first six months [1,2,3]. This rate is similar across the spectrum of TBI severity. Depression may magnify the burden of physical and cognitive symptoms as well as functional disability after TBI [2, 4], making it an important treatment target
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