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Excited Catatonia in Autism Spectrum Disorder

A Case Series

Bibliographic Data

ID15519989
AuthorsNora Burns (0000-0002-1709-1733, Ark Medical Center, corresponding author), Nora Kathleen Burns, Kathleen Grissett (Ark Medical Center), Marc Macaluso (Ark Medical Center), Mohsin Raza (0000-0002-2711-5663, Ark Medical Center), Barbara Gracious (0000-0003-1882-465X, Ark Medical Center)
Year2021
Volume12
Pages674335-674335
Publication date2021-05-11
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2021.674335
PMID34045985
OpenAlexW3158879457
LanguageEN
Citations received2
References cited19

Introduction: Autistic catatonia is an under-recognized debilitating syndrome with long-lasting negative effects for families, healthcare workers, and high-cost to the healthcare system. In this report, we describe two cases of excited catatonia in young men diagnosed with autism. Both endured a delay to diagnosis and difficulty to obtain appropriate treatment. Main concern: Each patient had a change in behavior from their baseline but with differences in severity and onset. The diagnosis in the first patient was made after only 3 months as the change was dramatic and sudden. Yet, despite a confirmed diagnosis, it was difficult to treat as the importance of M-ECT was not recognized by the clinicians. The second patient had been suffering for more than 5 years with a slow progression of worsening aggressive symptoms. The aggression was so uncontrollable that the patient required sedation, intubation and daily ECT. Both suffered from agitation, unprovoked aggression, urinary incontinence, stereotypic, and OCD behaviors and compulsive masturbation. Primary Diagnosis, intervention/outcomes: Both patients were diagnosed with autism, one high-functioning, attending high school and working a part-time job, the second low-functioning, nearly non-verbal, isolated to home and ABA school. The first patient's diagnosis of catatonia was only suspected after five psychiatric admissions and more than 20 medication trials. Lorazepam challenge was effective, he was treated with a short series of ECT but each time the treatments were tapered, the aggression returned. Ultimately, stabilized on weekly ECT. The second patient's behavior was escalating over a 5 month period, to the point, the aggression was uncontrollable. He presented to the ED under involuntary hold and the behavior could not be stabilized to the point that emergent ECT was initiated. Conclusion: Two cases of autistic catatonia diagnosed and treated within a year time span at a small community hospital indicates that this diagnosis is more common than previously recognized. We propose screening all patients with neurodevelopmental disorders with the Bush-Francis and Kanner scales to diagnose and treat them appropriately

Aggression · Anesthesia · Autism · Autism spectrum disorder · Catatonia · Intervention (counseling · Lorazepam · Psychiatry · Schizophrenia (object-oriented programming · Sedation · Urinary incontinence · Bipolar Disorder and Treatment · Electroconvulsive Therapy Studies · Medicine · Psychology · Treatment of Major Depression · Pediatrics

  • Case report

    Open Access•Nighat Jahan Nadeem, A A R Moawad et al.•Frontiers in Psychiatry•2024

  • Early-onset catatonia associated with SHANK3 mutations

    Open Access•Dirk Dhossche, Dirk M Dhossche et al.•Frontiers in Psychiatry•2023

Unique citing works2
Citations per year0,67
Citation span2023 - 2024 (2)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 2

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