An equity-based examination of access to follow-up care from psychiatric hospitalization before and after the introduction of Ontario's new physician billing structure for virtual care

  • Funded by Canadian Institutes of Health Research (CIHR)
  • Total publications:0 publications

Grant number: 475524

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Key facts

  • Disease

    COVID-19
  • start year

    2022
  • Known Financial Commitments (USD)

    $77,083.46
  • Funder

    Canadian Institutes of Health Research (CIHR)
  • Principal Investigator

    Hamovitch Emily K
  • Research Location

    Canada
  • Lead Research Institution

    Hospital for Sick Children (Toronto)
  • Research Priority Alignment

    N/A
  • Research Category

    Secondary impacts of disease, response & control measures

  • Research Subcategory

    Indirect health impacts

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Adolescent (13 years to 17 years)Children (1 year to 12 years)

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Mental health disorders are common among Canadian youth with high rates of hospital readmission. Timely follow-up care following psychiatric hospitalization improves outcomes but its uptake is poor and inequitable. While Health Quality Ontario issued a standard for adolescents with depression to receive follow-up care within 7 days of discharge, Ontario hospitals are not consistently following this standard. Virtual care may reduce barriers to follow-up care but may also increase inequities. During the COVID-19 pandemic, a new billing structure was implemented which formalized the use of virtual care. Whether this change in billing structure impacts access to follow-up care for children/adolescents is unknown. This study aims to determine patterns of virtual follow-up care access before and after the introduction of Ontario's billing change as well as characteristics (socioeconomic status, gender, location and immigrant status) of those receiving virtual follow-up care. The research will characterize hospital-level patterns regarding the provision of follow-up care and examine reasons for these differences from the perspective of healthcare personnel. A mixed methods approach will be used. For the quantitative portion, health administrative data at ICES will be analyzed to determine changes in rates of virtual follow-up care for children/adolescents before and after the new billing structure. These data will be used to determine characteristics of those receiving follow-up care and to identify hospital-level patterns. Qualitatively, interviews will be conducted with hospital physicians who refer to follow-up care and leaders from high and low performing hospitals. The study will provide evidence on how virtual care impacts the provision of follow-up care and whether it is delivered equitably. It will identify whether and why variations exist across hospitals regarding follow-up care for children/adolescents following psychiatric hospitalization.