Key result
Electroconvulsive therapy in a patient with atherosclerotic disease was associated with delirium, multi-infarct state, and cognitive deficits, suggesting potential for permanent ischaemic impairment.
Why the study?
Is ECT safe in patients with cerebrovascular disease?
Case Report (n=1)
Is ECT safe in patients with cerebrovascular disease?
ECT in patients with underlying atherosclerotic or cerebrovascular disease may precipitate permanent cognitive impairment due to cerebral ischemia.
May warrant caution with ECT and antidepressants in elderly vascular patients; leaves open questions on safe relapse management.
A 70‐year‐old man with a history of peripheral vascular disease was treated initially with antidepressants, then bilateral electroconvulsive therapy (ECT) for a depressive illness. Apart from an episode of delirium following ECT he recovered fully. Four years later he relapsed. Low‐dose antidepressants caused disorientation and oversedation, as did ECT. Shortly afterwards he developed a multi‐infarct state with Parkinsonian symptoms, transient schaemic attacks (TIAs) and cerebrovascular attacks (CVAs). His cognitive deficits implicated pathology in the frontal and subcortical areas of the brain. Postmortem examination confirmed widespread atherosclerotic disease, also cerebrovascular disease. The haemodynamic and cerebral effects of ECT are condidered in the context of vascular disease. It is postulated that ECT given to such patients might cause permanent impairment of cognitive function through ischaemia of an already compromised cerebral circulation. Suggestions are outlined regarding a policy for a more comprehensive assessment of patients with atherosclerotic disease. Deficiencies of ECT procedures are highlighted.
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Blackburn et al. (1994) conducted a case report in Depressive illness and cerebrovascular disease (n=1). Electroconvulsive therapy (ECT) was evaluated. Electroconvulsive therapy in a patient with atherosclerotic disease was associated with delirium, multi-infarct state, and cognitive deficits, suggesting potential for permanent ischaemic impairment.
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