De-Implementing Opioid Use and Implementing Optimal Pain Management Following Dental Extractions
De-Implementing Opioid Use and Implementing Optimal Pain Management Following Dental Extractions
批准号:
9438338
负责人:
Shannon Gwin Mitchell
金额:
$78.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2021-08-31
关键词:
Absence of pain sensationAcetaminophenAcuteAdverse effectsAnalgesicsAppointmentAutomobile DrivingCenters for Disease Control and Prevention (U.S.)ClinicalCluster randomized trialConsumptionDataDecision MakingDentalDentistsDoseDrug MonitoringDrug PrescriptionsEducationElectronic Health RecordElementsEpidemicEvidence based practiceGoalsIncidenceLanguageMedication ManagementMethodsMorphineNon-Steroidal Anti-Inflammatory AgentsOperative Surgical ProceduresOpioidOpioid AnalgesicsOverdosePainPain managementPatient-Focused OutcomesPatientsPharmaceutical PreparationsPostoperative PainPostoperative PeriodProviderPublic HealthRandomizedRecommendationRecording of previous eventsReportingRiskSafetySymptomsTechniquesTestingTimeUnited StatesVisitarmchronic painclinical decision-makingcomparative efficacydisorder preventionelectronic dataevidence baseinnovationnovelopioid useprescription opioidprogramsshared decision makingsupport toolssystematic reviewthird molar extractiontooltrial design
中文摘要
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英文摘要
Project Summary
The primary objective of this project is to de-implement the use of opioid analgesics for the management of
postoperative pain following dental extractions and to implement effective alternative pain management. We
propose a cluster-randomized trial design in which dental practitioners will be randomly assigned to 1 of 3
conditions involving different implementation strategies. The first condition, Standard Practice, will serve as a
control condition. The second condition will implement a clinical decision support (CDS) tool that will extract
patient history and interface with the state prescription drug monitoring program to provide personalized
recommendations for analgesic prescribing and offer language for discussing optimal, evidence-based non-
opioid pain management with dental extraction patients. The third condition will involve an enhanced version of
the CDS (CDS-E) that will also include information regarding optimal, evidence-based, non-opioid pain
management delivered directly to the patient both before and following the dental extraction visit. We will
examine opioid and non-opioid prescribing data from the electronic health record across study arms as well as
other provider- and patient-focused outcomes using mixed methods.
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