Successful bilateral electroconvulsive therapy for catatonia presenting with novel climbing behavior in an adolescent with CACNA1A pathogenic variant and autism spectrum disorder: a case report - Scorecard - MDSpire
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Successful bilateral electroconvulsive therapy for catatonia presenting with novel climbing behavior in an adolescent with CACNA1A pathogenic variant and autism spectrum disorder: a case report
Clinical Scorecard: Effective Bilateral Electroconvulsive Therapy for Catatonia with Unusual Climbing Behavior in a Teenager with a CACNA1A Pathogenic Variant and Autism Spectrum Disorder: A Case Study
At a Glance
Category
Detail
Condition
Catatonia in adolescent with CACNA1A pathogenic variant and autism spectrum disorder
Key Mechanisms
CACNA1A variant associated with deficits in neuronal communication and neurotransmitter release, contributing to neurodevelopmental disorders and catatonia
Target Population
Adolescents with neurodevelopmental disorders including ASD and CACNA1A pathogenic variants presenting with catatonia
Care Setting
Specialized inpatient child psychiatry unit and outpatient ECT consultation
Key Highlights
Bilateral electroconvulsive therapy (ECT) was safely and effectively used to treat catatonia in a teenager with a CACNA1A pathogenic variant and ASD.
Unique catatonic symptom included novel climbing behavior conceptualized as perseverative stereotypy related to catatonia.
Monitoring treatment response utilized clinician-rated Busch-Francis Catatonia Rating Scale, parent-reported Catatonia Impact Scale, and behavioral observations, all showing significant improvement.
Guideline-Based Recommendations
Diagnosis
Consider catatonia diagnosis in neurodevelopmental disorders with new or worsening symptoms such as negativism, withdrawal, stereotypies, and regression including incontinence.
Use validated rating scales such as Busch-Francis Catatonia Rating Scale and Catatonia Impact Scale for assessment.
Management
First-line pharmacological treatment includes benzodiazepines (e.g., clonazepam).
In cases refractory to pharmacotherapy, consider bilateral electroconvulsive therapy (ECT) with clinical consensus.
Exercise caution with ECT in patients with CACNA1A variants due to potential risk of neurological complications, but bilateral ECT can be well tolerated and effective.
Monitoring & Follow-up
Use multi-source monitoring including clinician ratings, parent reports, and behavioral observations to assess treatment response.
Track symptom severity with scales such as BFCRS and CIS throughout treatment.
Risks
Potential for prolonged neurological deficits and MRI changes post-ECT in patients with CACNA1A variants; monitor closely.
Safety concerns related to novel behaviors (e.g., climbing) require close supervision.
Patient & Prescribing Data
Adolescent male with ASD, intellectual disability, ADHD, and CACNA1A pathogenic variant presenting with catatonia.
Initial benzodiazepine (clonazepam) and valproic acid showed limited improvement; bilateral ECT led to significant symptom reduction and was well tolerated.
Clinical Best Practices
Obtain thorough baseline assessment including neuropsychiatric history and use of validated catatonia rating scales.
Consider genetic factors such as CACNA1A variants when evaluating neurodevelopmental patients with catatonia.
Use a multidisciplinary approach including psychiatry, neurology, behavior analysis, and family input for diagnosis and monitoring.
Initiate benzodiazepines as first-line treatment and escalate to bilateral ECT if inadequate response.
Monitor for and contextualize unusual behaviors (e.g., climbing) as possible catatonic symptoms.
Ensure close safety monitoring during treatment due to risk of impulsivity and novel perseverative behaviors.
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