Background: Mental health concerns in children with disabilities are common and have a significant and negative impact. Clinicians have reported high demand for this population to receive early, targeted, and family-centred mental health interventions.

Objective: We sought to map out and describe existing pediatric mental health services/resources for children with disabilities and their families across clinical sites and local and online communities.

Methods: Using a mixed-method triangulation study design, we outreached to clinical managers at the participating clinical sites and conducted a rapid online search of local in-person, telehealth, and web-based information. The nature, access method, admission criteria, target, focus, and other pertinent information were recorded and analyzed using descriptive statistics and a narrative synthesis approach.

Results: Eighty-one ( = 81) services/resources (in-person,  = 48; telehealth,  = 10; web-based information,  = 33) were identified. Few ( = 6, 13%) in-person services had a method of care access through an online booking portal. Nearly half of in-person resources ( = 23, 47%) had admission criteria specific for children with disabilities (e.g., diagnosis, age limit), and many ( = 32, 67%) required a formal referral. A small number of in-person and telehealth services targeted the mental health concerns of the entire family ( = 23, 47%;  = 2, 20%). Very few ( = 13, 16%) services incorporated follow-up support. Important gaps emerged for certain populations (e.g., children with cerebral palsy). Practitioners' inadequate training when intervening with co-existing mental health demands of children with disabilities was noted by clinical managers.

Conclusion: Findings could be used to create a user-friendly database to easily identify suitable services and to advocate for services/resources that are lacking.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267822PMC
http://dx.doi.org/10.3389/fresc.2023.1118769DOI Listing

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