grant

Sickle Cell Improvement: ENhancing Care in the Emergency Department (SCIENCE)

Organization NEMOURS CHILDREN'S HOSPITAL, DELAWARELocation WILMINGTON, UNITED STATESPosted 1 Sept 2021Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY20250-11 years oldAbnormal HemoglobinsAccident and Emergency departmentAccountingAcuteAcute PainAcutely painfulAdherenceAdoptionAffectAmerican Society of HematologyApplied ResearchApplied ScienceBlackBlack raceBlood DiseasesBlood erythrocyteCaringCategoriesChildChild CareChild YouthChildren (0-21)ChronicClinicalClinical TreatmentCollaborationsDataDiscipline of NursingDiseaseDisorderDissemination and ImplementationDoseED careED visitER careER visitEducationEducational aspectsEffectivenessEmergency CareEmergency DepartmentEmergency Department careEmergency MedicineEmergency Room careEmergency care visitEmergency department visitEmergency health careEmergency hospital visitEmergency medical careEmergency roomEmergency room visitEngineeringErythrocytesErythrocyticEvidence based practice guidelinesFamilyFeedbackFoundationsFundingGoalsGrantGuideline AdherenceGuidelinesHb SS diseaseHbSS diseaseHealthHematologic DiseasesHematological DiseaseHematological DisorderHemoglobin S DiseaseHemoglobin sickle cell diseaseHemoglobin sickle cell disorderHereditaryHospital AdmissionHospitalizationInheritedInstitutionInterventionInterviewJournalsMagazineMarrow erythrocyteMedicineModificationNHLBINational Academy of SciencesNational Heart, Lung, and Blood InstituteNew EnglandNortheastern United StatesNursingNursing FieldNursing ProfessionOpiatesOpioidOutcomePainPain ControlPain TherapyPain managementPainfulPathway interactionsPatientsPersonsProtocolProtocols documentationPuericultureQOCQOLQOL improvementQuality of CareQuality of lifeRE-AIMRandomizedReach, Effectiveness, Adoption, Implementation, and MaintenanceRecurrenceRecurrentRed Blood CellsRed CellRegistriesReportingResearch MethodologyResearch MethodsSickle CellSickle Cell AnemiaSiteStressStructureTestingTheoretical Domains frameworkTimeUnited StatesUnited States National Academy of SciencesUniversitiesVisitVulnerable PopulationsWashingtonWorkanalytical methodblood corpusclesblood disorderclinical interventionclinical therapydata toolsdesigndesigningeffectiveness and implementation trialeffectiveness/implementation hybrid trialeffectiveness/implementation trialevidence baseevidence based guidelinesevidence based recommendationsgroup interventionhospitalization ratesimplementation facilitationimplementation outcomesimplementation researchimplementation scienceimplementation strategyimprovedimprovements in QOLimprovements in quality of lifekidsmultidisciplinarypain interventionpain scorepain treatmentpathwaypediatric emergencyquality of life improvementrandomisationrandomizationrandomly assignedreach, efficacy, adoption, implementation, and maintenanceresearch and methodssickle RBCsickle cell diseasesickle cell disordersickle diseasesickle erythrocytesickle red blood cellsicklemiasicklingstrategies for implementationtreatment adherencetreatment compliancetreatment guidelinestrial regimentrial treatmentvaso-occlusive crisisvaso-occlusive painvasoocclusive crisisvasoocclusive painvulnerable groupvulnerable individualvulnerable peopleyoungster
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Full Description

Sickle cell disease (SCD) is an inherited blood disorder affecting approximately 36,000 children in the United States, approximately 90% of whom are Black. The disease is characterized by recurrent, severe pain crises which result in high rates of emergency department visits and hospitalizations, and decreased quality of life. The National Heart, Lung and Blood Institute, as well as the American Society of Hematology, have endorsed pain management guidelines regarding the timeliness of care for children presenting with these acute pain crises. These evidence-based guidelines are infrequently followed, resulting in increased pain and hospitalizations. A lack of systematic care has been proposed as a significant contributor to lack of guideline adherence and the New England Journal of Medicine recently called for the institution of SCD- specific pain management protocols to reduce time to opioid administration.
Our long-term goal is to improve the care and health outcomes of children with acute painful vaso-occlusive crisis treated in the emergency department. Our overall aim is to test a care pathway using multifaceted implementation strategies to increase guideline adherent care for children in the emergency department with acute painful vaso-occlusive crisis. Our primary aims are: 1) To compare the primary implementation outcomes of Reach, Adoption, and Implementation for the care pathway for treatment of children with acute painful vaso- occlusive crisis in the emergency department, between control and intervention groups and 2) To compare the primary clinical outcomes of guideline adherent care for opioid dose timing, hospitalization rates, and pain scores for the care pathway for the treatment of children with acute painful vaso-occlusive crises in the emergency department between control and intervention groups. We will test these aims using a randomized, multicenter stepped wedge design to conduct a type III hybrid effectiveness-implementation trial of the care pathway. Our proposal will institute the care pathway across seven emergency departments with the goal of improving guideline adherent care for children with SCD presenting with an acute pain crisis, thereby improving

pain, decreasing hospitalizations and improving quality of life for this vulnerable population.

Grant Number: 5U01HL159850-05
NIH Institute/Center: NIH

Principal Investigator: David Brousseau

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