Ms. A, an 87-year-old woman, was admitted to a geriatric psychiatry unit with a diagnosis of delirium due to a urinary tract infection. She had a history of major depression and was maintained with desipramine, 50 mg b.i.d., and sertraline, 100 mg/day. The urinary tract infection was treated with trimethoprim/sulfamethoxazole, 160/800 mg b.i.d., for 5 days. The delirium precipitated a major depressive episode, and Ms. A was referred for ECT. A computed tomography scan of her head revealed moderate cerebral atrophy and minor periventricular deep white matter disease but no focal lesions.
The first ECT treatment, delivered in the right unilateral configuration, lasted 75 seconds. Fifteen minutes after the procedure ended Ms. A had a generalized tonic-clonic seizure that was terminated with methohexital, 60 mg i.v. Once the seizure ended, she became more alert.
On the psychiatry unit Ms. A was obtunded and had slight clonic movements of the left side of her face. Lorazepam, 2 mg i.v., was administered and followed by loading with phenytoin, 1.4 mg i.v. An EEG revealed no normal background activity and almost continuous electrographic seizures over the right hemisphere of the brain. Ms. A was transferred to the intensive care unit, where repeat EEGs showed no signs of ictal activity. The neurology service felt that further ECT was not an option given the focality of her seizure. Ms. A was discharged to a nursing home, where she was eventually lost to follow-up.
We present this case as an unexpected event developing after a first ECT treatment. Further research into possible predictive factors for unexpected post-ECT seizures is needed.