Table 1:
Summary of Considerations for Determining Eligibility and Suitability for Neurosurgical Intervention for Patients With OCD
| Entity | Eligibility guidance | Additional considerations |
|---|---|---|
| Committee for Neurosurgery for Psychiatric Disorders, part of the World Society for Stereotactic and Functional Neurosurgery (WSSFN) and the European Society for Stereotactic and Functional Neurosurgery (ESSFN)a Consensus Guidelines24 |
|
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| Indian Psychiatric Society,31 Indian Society for Stereotactic and Functional Neurosurgery, and The Neuromodulation Society Consensus Criteria 201929 |
|
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| Royal College of Psychiatrists Position Statement 2017 (UK)28 |
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Abbreviations: GAF, Global Assessment of Functioning; OCD, obsessive–compulsive disorder; Y-BOCS, Yale-Brown Obsessive–Compulsive Scale.
Partnering with the working group “Deep Brain Stimulation in Psychiatry: Guidance for Responsible Research and Application”, the Psychiatric Neurosurgery Committee of the American Society for Stereotactic and Functional Neurosurgery (ASSFN), the Latin American Society for Stereotactic and Functional Neurosurgery (SLANFE), the Asian-Australasian Society for Stereotactic and Functional Neurosurgery (AASSFN), and the World Psychiatric Association (WPA).
Lack of efficacy or disabling side effects.
For example, pharmacotherapy and behavioural therapy. As outlined by Visser-Vanderwalle et al30: “insufficient response to, at minimum: 2 selective serotonin reuptake inhibitors (SSRIs) at the maximum tolerated dose for at least 12 weeks; clomipramine at a maximum tolerated dosage for at least 12 weeks; 1 augmentation trial with an antipsychotic for at least 8 weeks, in combination with one of the aforementioned drugs; and a complete trial of exposure-based cognitive behavioural therapy (CBT) confirmed by a psychotherapist.”
Includes systematic treatment trials not discontinued prematurely due to mild side effects as follows: at least 3 months of ≥2 SSRIs and clomipramine, plus augmentation with at least 1 antipsychotic for at least 8 weeks and adequate trial of exposure and response prevention (ERP) CBT (≥20 sessions) or inability to tolerate the anxiety caused by therapy.29