Objectives | Endpoint | Data Source |
---|---|---|
Primary | ||
To compare the odds of post-extraction opioid prescriptions to AYA under the intervention condition relative to the control condition | Study condition comparison of the patient-level odds of post-extraction opioid prescription | EHR |
Secondary | ||
To compare provider-perceived intervention appropriateness and feasibility before and after intervention implementation | Differential pre- to post-intervention change by provider in the rating of intervention feasibility and appropriateness | Provider survey before and after transition period |
To compare provider-perceived appropriateness and feasibility of decreasing opioid prescribing to AYA before and after intervention implementation | Differential pre- to post-intervention change by provider in the rating of opioid prescribing reduction feasibility and appropriateness | Provider survey before and after transition period |
To compare AYA self-reported pain level within 10 days after tooth extraction based on self-reported opioid use. | Comparison of worst, least, and average pain over the 10 days after extraction based on self-reported opioid use | Patient survey within 6–10 days after tooth extraction |
To compare AYA self-reported pain interference within 10 days after tooth extraction based on self-reported opioid use. | Comparison of average pain interference T-score (NIH PROMIS Pediatric Short Form v1.0 – Pain Interference 8a, or NIH PROMIS Adult Short Form v1.0 – Pain Interference 6b) based on self-reported opioid use. | Patient survey within 6–10 days after tooth extraction |
To compare AYA self-reported satisfaction with pain management within 10 days after tooth extraction based on self-reported opioid use | Comparison of average overall pain satisfaction based on self-reported opioid use. | Patient survey within 6–10 days after tooth extraction |