Improving End-of-Life Care for Hospitalized Patients with Lewy Body Disorders
Project Number1K23AG086669-01
Contact PI/Project LeaderAAMODT, WHITLEY
Awardee OrganizationUNIVERSITY OF PENNSYLVANIA
Description
Abstract Text
PROJECT SUMMARY
Lewy body disorders, a subset of Alzheimer’s disease and related disorders (ADRDs), are the second most
common neurodegenerative disorders worldwide and the 14th leading cause of death in the United States.
Lewy body ADRDs are progressive, incurable, and mortality rates are rising, making end-of-life (EoL) care a
significant public health concern. The majority of persons with Lewy body ADRDs are hospitalized in their last
6 months of life with high rates of intensive care unit admission, in-hospital death, and low rates of discharge to
hospice care. Because these markers of poor care quality are often incongruent with patient care preferences,
urgent interventions are needed to improve EoL care quality in acute care hospitals. Despite this critical need,
there are two fundamental knowledge gaps in developing inpatient EoL interventions for persons with Lewy
body ADRDs: 1) lack of a prognostic model to determine risk of 6-month mortality and 2) lack of a validated
tool to measure EoL care quality. This proposal requests support for a mentored career development award for
Dr. Whitley Aamodt, a movement disorders specialist, neurodegenerative neurologist, and clinical researcher
at the University of Pennsylvania. The overarching goal of this project is to improve prognostication and EoL
care quality for hospitalized persons with Lewy body ADRDs by identifying patients at the greatest risk of death
and ensuring that hospital-based care is appropriate and aligned with care preferences. In Aim 1, Dr. Aamodt
will use comprehensive Medicare data to develop a risk-prediction model for 6-month all-cause mortality in a
nationally representative sample of hospitalized patients with Lewy body ADRDs using advanced predictive
modeling. This model will be externally validated in a second cohort of Medicare beneficiaries from the post-
pandemic period. In Aim 2, Dr. Aamodt will create, test, and externally validate a patient-centered EoL care
quality instrument based on data gathered from diverse Lewy body ADRD patients, care partners, and
practitioners using qualitative research methods and factor analysis. In executing these aims, Dr. Aamodt will
obtain additional training in neuroepidemiology, biostatistics, and qualitative research under the guidance of
mentors and advisors in epidemiologic research methods (John Farrar, MD, PhD), neurodegenerative disease
epidemiology and health services research (Allison Willis, MD, MS), predictive modeling (Warren Bilker, PhD),
qualitative research methods (Katharine Rendle, PhD, MPH), and palliative care research (Scott Halpern, MD,
PhD). The results of this project will provide fundamental knowledge about hospitalized patients with Lewy
body ADRDs nearing EoL and will guide the development of future interventions to improve EoL care quality.
This work aligns with the strategic goal of the National Institute on Aging to address EoL care needs in ADRDs.
Through the research training and mentorship gained during this career development award, Dr. Aamodt will
establish herself as an independent investigator in the field of applied epidemiology, outcomes research, and
palliative and EoL care for aging Americans with neurodegenerative diseases.
Public Health Relevance Statement
PROJECT NARRATIVE
Lewy body disorders, a subset of Alzheimer’s disease and related disorders (ADRDs), are progressive,
incurable, and the 14th leading cause of death in the United States. Because most persons with Lewy body
ADRDs are hospitalized in their last 6 months of life with high rates of intensive, inappropriate care, hospital-
based interventions are needed to improve end-of-life care quality for this growing population. The goal of this
project is to improve prognostication and end-of-life care quality measurement in Lewy body ADRDs, which will
be used to inform future interventions that promote improved care quality, more thoughtful resource allocation,
and reduced Medicare spending at end-of-life.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAdmission activityAgeAgingAlzheimer's DiseaseAlzheimer's disease related dementiaAmericanApplied SkillsAttitudeBiometryBradykinesiaCalibrationCaringCause of DeathCessation of lifeClinicalDataDeath RateDementiaDevelopmentDimensionsDiscriminationDiseaseDisease ProgressionDoctor of PhilosophyEnsureEpidemiologyEuroQOLFactor AnalysisFoundationsFundingFutureGoalsGrantHallucinationsHealthHealth Services ResearchHealth systemHospice CareHospitalizationHospitalsInpatientsIntensive Care UnitsInterventionK-Series Research Career ProgramsKnowledgeLearningLewy BodiesLewy Body DementiaLewy Body DiseaseLifeLogistic RegressionsMalignant NeoplasmsMeasurementMeasuresMedicareMentorsMentorshipModelingMovement DisordersMultiple System AtrophyNational Institute on AgingNerve DegenerationNeurodegenerative DisordersNeuroepidemiologyNeurologistOnline SystemsOutcomeOutcomes ResearchOutpatientsPalliative CareParkinson DiseasePatient CarePatientsPennsylvaniaPersonsPopulationPopulations at RiskPositioning AttributePsychosesPublic HealthQualitative ResearchQuality IndicatorQuality of CareQuality of lifeReportingRequest for ProposalsResearchResearch MethodologyResearch PersonnelResearch TrainingResource AllocationReview LiteratureRiskSamplingSpecialistSurveysSymptomsTarget PopulationsTechniquesTestingTimeTrainingTreatment EfficacyUnited StatesUniversitiesWorkacute carebeneficiarycare preferencecareercohortcomorbiditycomorbidity Indexdesignend of lifeend of life careepidemiology studyfallsfrailtyhealth beliefhigh riskhospice environmenthospital careimprovedindexinginstrumentmalemortalitymortality riskmotor symptomnon-motor symptompalliativepatient orientedpilot testpost-pandemicpredictive modelingprognostic modelprognosticationrisk prediction modelsexskillssuccesssupportive environmenttool
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