grant

The Pediatric Advanced Cancer Experience (PACE): Measuring Quality of End-of-Life Care for Children with Cancer

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 1 Apr 2021Deadline 28 Feb 2027
NIHUS FederalResearch GrantFY20250-11 years old21+ years oldAI basedAcademyAddressAdultAdult HumanAdvanced CancerAdvanced Malignant NeoplasmAdvisory CommitteesAwardBereavementCancersCare GiversCaregiversCaringCessation of lifeChildChild CareChild YouthChildhoodChildhood CancersChildren (0-21)ClinicalCognitiveCohort StudiesConcurrent StudiesDataData CollectionData SourcesDeathDevelopment PlansElectronic Health RecordEquityEvaluationFaceFamilyFoundationsGoalsHealth CareHealth Care UtilizationHospicesHospital AdmissionHospitalizationIntubationInvestigationInvestigatorsKnowledgeLeadershipLength of StayLibrariesLifeMalignant Childhood NeoplasmMalignant Childhood TumorMalignant NeoplasmsMalignant Pediatric NeoplasmMalignant Pediatric TumorMalignant TumorMalignant childhood cancerManualsMeasurementMeasuresMedicineMentorshipMethodsMinorityNatural Language ProcessingNon-accidentalNonaccidentalNumber of Days in HospitalOutcomePainPainfulPalliative CarePalliative TherapyPalliative TreatmentParentsPatient Outcomes AssessmentsPatient Reported MeasuresPatient Reported OutcomesPatientsProceduresProcessProcess MeasurePropertyProviderPsychometricsPuericultureQOCQuality of CareQuestionnaire DesignsQuestionnairesReportingResearchResearch PersonnelResearch TechnicsResearch TechniquesResearchersSamplingScienceStructureSurvey InstrumentSurveysSymptomsTask ForcesTestingTrainingTraining ActivityValidationWorkadulthoodadvisory teamartificial intelligence basedcancer carecancer in a childcancer in childrencare deliverycare resource usecare resource utilizationcare resourcescareercareer developmentchild with cancerchildhood malignancyclinician communicationcohortcomfort carecommunicate to clinicianscommunicate to providerscommunicate with clinicianscommunicate with doctorscommunicate with providersdesigndesigningdoctor communicationelectronic health care recordelectronic health medical recordelectronic health plan recordelectronic health registryelectronic medical health recordend of lifeend of life careend-of-lifeevidence baseexperienceexperimentexperimental researchexperimental studyexperimentsfacesfacialgoal concordant caregoal concordant managementgoal concordant treatmenthealth assessmenthealth care resource usehealth care resource utilizationhealth care resourceshealth care service usehealth care service utilizationhospice enrollmenthospice environmenthospice usehospice utilizationhospital dayshospital length of stayhospital stayimprovedkidsmalignancymulti-modalitymultimodalitynatural language understandingneoplasm/cancernovelpalliative interventionparentpatient centeredpatient orientedpediatricpediatric cancerpediatric malignancypreferenceprogramsprospectiveprovider communicationskillstooltraining moduletrendvalidationsyoungster
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Full Description

PROJECT SUMMARY
Although cure rates for childhood cancer have increased over several decades, cancer remains the leading

cause of non-accidental death in children. Yet, there are no existing quality measures to define optimal end-of-

life care (EOLC) for children with cancer. A lack of standards for EOLC contributes to high healthcare utilization

for children with advanced, incurable cancer, as well as widely variable palliative care provision. For adults with

cancer, high quality EOLC is defined at least in part by measures to reduce use of intensive healthcare

resources, such as avoidance of hospital stays in the last weeks of life and prompt referral to hospice. In

contrast, attributes of high quality EOLC for children with cancer have not been previously elucidated. To

address this gap in knowledge, the overall objectives of this proposal are to prioritize family-centered quality

measures for EOLC and to pioneer complementary approaches to assess care quality for children with

advanced cancer. Specific aims are to: (1) establish a priority list of EOLC quality measures, from the

perspective of parents of children with cancer; (2) characterize EOLC process measures for children who died

of cancer, using natural language processing in electronic health records; and (3) develop and pilot the

“Pediatric Advanced Cancer Experience” (PACE) questionnaire to prospectively appraise care quality for

children with advanced cancer. Completion of these aims will lay the foundation for the first multi-center, multi-

modal evaluation of end-of-life care quality in children with cancer. The long term goal of Dr. Ananth’s research

program is to build a platform for systematically measuring, reporting, and incentivizing high quality EOLC in

children with cancer, facilitating goal-concordant care delivery. Through the proposed research, Dr. Ananth

seeks to advance the science of measuring EOLC quality in childhood cancer. Dr. Ananth is supported by an

outstanding mentorship team and scientific advisory committee, with substantial expertise spanning patient-

reported outcomes, artificial intelligence-based techniques for research, and pediatric palliative care

investigation. Dr. Ananth will pursue formal training in patient-centered quality measurement, natural language

processing, and questionnaire design and validation, concurrently building skills in leadership of a multi-center

consortium. Collectively, the research in this proposal and career development plan will amply prepare her for

an independent career focused on enhancing quality of care for children with advanced, incurable cancer.

Grant Number: 5K08CA259222-05
NIH Institute/Center: NIH

Principal Investigator: Prasanna Ananth

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