Summary
The goal of this observational study is to examine the factors associated with the transition from medical exposure to opioids with "signposts" of future opioid use disorder among adolescent surgical patients. The main question aims to identify factors (moderators, mediators, and covariates) associated with risk factors for opioid use disorder (ROUD) in the 12 months following major surgery with opioid exposure among adolescents aged 12-17. Participants will be asked to complete electronic surveys pre- and post-operatively and approve the collection of peri-operative data from the Electronic Medical Record to assess correlations.
Conditions
Opioid Use Disorder, Pain, Chronic
Recruitment Status
Not yet recruiting
Detailed Description
This project will collect data from a diverse sample of 10,000 dyads, including adolescent (aged 12-17 years, inclusive) patients undergoing major surgery with planned post-operative opioid analgesic use. and a parent (Total N=20,000) to identify ROUD that may occur within the 12 months after surgery. The resulting data repository will allow clinician scientists and physicians to develop research-informed pain management protocols for adolescent surgical patients to reduce the risk of OUD in this vulnerable population. Using a novel combination of data sources (electronic medical records (EMR), patient-reported outcomes, and parent-reported outcomes), this study investigates the twin problems of postoperative pain and ROUD in adolescent surgical patients. Using real-world evidence to evaluate longitudinal behaviors and outcomes. This project will provide insights into the associations between post-operative pain management and ROUD in adolescents. Findings could yield information about potential risks, which may inform future studies and ultimately lead to new screening tools to assess risk before opioid prescribing, updated protocols for managing pain intra-operatively and post-operatively in high-risk populations, updated patient and family education materials to reduce risks for those undergoing painful procedures, and revised recommendations for monitoring for patients being treated for pain. Furthermore, the project enables the establishment of an infrastructure among pediatric surgical centers that can be used for future projects to evaluate the best postoperative outcomes for youth. Aim 1: Machine learning models will be used to develop and validate screening algorithms to detect "early warning signs" or Risk factors for Opioid Use Disorder (ROUD). The features in these models will include the pre-, intra-, and post-operative EMR-derived data elements and the survey data. Models will fit against the primary outcome described above. Model evaluation will be done via cross-validation, where the models will be fit on a randomly selected training set of patients and evaluated on the remaining held-out subset of the patients to be used exclusively for testing the performance of the final models. Aim 2: Develop and validate a prediction model designed to predict a clinical trajectory of post-surgical opioid use and pain. The model will use clustering to identify typical patient trajectories of opioid use and will use similar prediction and validation techniques as in Aim 1.
Eligibility Criteria
Adolescent Inclusion Criteria
Be between the ages of 12 to 17 years old, inclusive, and scheduled to undergo a selected surgical procedure, including but not limited to general, orthopedic, thoracic, and spinal surgeries at a participating site within SPAIN.
Be willing and able to provide informed assent and have a parent/caregiver willing to provide informed consent.
Parent/Caregiver inclusion criteria
Be a parent or legal guardian of an eligible adolescent.
Be willing and able to provide written informed consent.
Adolescent Participant Exclusion Criteria
Adolescents meeting any of the following criteria will be excluded from study participation:
Adolescents who have been prescribed opioids in the past 2 years for pain due to a chronic medical condition, such as sickle cell disease, arthritis, or cancer.
Adolescents who do not have a caregiver who is willing to co-participate in the study.
Adolescents who cannot speak or read English at a 4th-grade level as determined by medical or research staff.
Adolescents that are currently in the custody of the Department of Youth Services, jail/prison, or other overnight facility as required by court of law or have pending legal action that could prevent participation in study activities.
Adolescents that are currently in the custody of the Department of Children and Families or living with a foster family.
Adolescents that are currently pregnant or parenting.
Adolescents that self or parent report ever having been diagnosed with opioid use disorder or prescribed buprenorphine, methadone, or naltrexone to treat opioid use disorder.
Parent/Caregivers Exclusion Criteria:
Parents/Caregivers meeting any of the following criteria will be excluded from study participation:
Parents/Caregivers that cannot speak or read English or Spanish at a 4th grade level as determined by medical or research staff.
Parents/Caregivers that are currently incarcerated.
Parents/Caregivers that are in physical or mental distress that precludes study participation as determined by clinical or study staff.
Gender
All
Min Age
12 Years
Max Age
17 Years
Download Date
April 10, 2024
Principal Investigator
Sharon Levy
Primary Contact Information
Melissa.Brogna@childrens.harvard.edu
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For more information on this trial, visit clinicaltrials.gov.
Contact
For more information and to contact the study team: