Deep brain stimulation of the nucleus accumbens for severe self-injurious behaviour in children: long-term outcomes from a first-in-human pilot trial.

Mol PsychiatryJun 22, 2026 (epub)
Clinical ResearchNeurosurgeryPediatricsPsychiatryOpen access

Karim Mithani, Sara Breitbart, Thiemo Dinger et al.

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In 30 seconds

This prospective, single-centre, first-in-human clinical trial assessed bilateral nucleus accumbens deep brain stimulation in six children and adolescents aged 7–14 years with profound autism and treatment-refractory self-injurious behaviour. Participants were followed for at least 24 months (mean 32.5 months; range 25.8–56.0). The study reports sustained reductions in the frequency and severity of self-injury, repetitive and obsessive-compulsive behaviours, alongside clinically meaningful quality-of-life improvements. One device-related infection required hardware removal; self-injury returned to baseline and improved rapidly after re-implantation in that participant.

Key findings

  • All six participants had sustained reductions in self-injury frequency and severity during follow-up of at least 24 months.
  • The cohort also showed reductions in repetitive and obsessive-compulsive behaviours and clinically meaningful quality-of-life improvements.
  • One serious adverse event was a device-related infection requiring explantation; self-injury relapsed to baseline and improved rapidly after re-implantation.

Why it matters

Severe self-injury in children with profound autism can cause permanent injury, and the abstract describes limited effective treatment options. These long-term observations suggest that targeting reward and behavioural regulation circuitry may be associated with durable improvement in self-injury and related outcomes. The small, uncontrolled pilot provides an early signal rather than definitive evidence of efficacy or safety.

What to keep in mind

The trial was a single-centre pilot involving only six participants, with no comparator group described in the abstract.

Source

Published in Mol Psychiatry. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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