grant

Establishing and Implementing Pneumonia Diagnosis in ED Older Adults: A Mixed Methods Approach

Organization OHIO STATE UNIVERSITYLocation Columbus, UNITED STATESPosted 15 Sept 2022Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY202521+ years old65 and older65 or older65 years of age and older65 years of age or more65 years of age or older65+ years65+ years oldAccident and Emergency departmentAccuracy of DiagnosisAddressAdoptionAdultAdult HumanAdverse effectsAged 65 and OverAntibiotic AgentsAntibiotic DrugsAntibioticsBacteriaBacterial InfectionsBacterial PneumoniaBiological MarkersBlood SerumBlood leukocyteBlood monocyteCOVID-19 affectedCOVID-19 consequenceCOVID-19 effectCOVID-19 impactCOVID-19 impactedCXRCaringCessation of lifeClinicalCommunitiesDeathDefensinsDevelopmentDiagnosisDiagnosticDiagnostic testsDisablingED PhysicianED patientED visitER patientER physicianER visitEarly DiagnosisEmergency DepartmentEmergency Department PhysicianEmergency Department patientEmergency MedicineEmergency PhysicianEmergency Room patientEmergency care visitEmergency department visitEmergency hospital visitEmergency roomEmergency room physicianEmergency room visitEnsureEventFaceFemaleFutureGenesGeriatricsGoalsGuidelinesHealthHistoryHumanImageInfectionInnate Immune SystemInnate ImmunityInvestigationLength of StayLeukocytesLeukocytes Reticuloendothelial SystemLifeMapsMarrow leukocyteMarrow monocyteMeasuresMethodologyMethodsMiscellaneous AntibioticMissionModelingModern ManMorbidityMorbidity - disease rateNative ImmunityNatural ImmunityNon-Specific ImmunityNonspecific ImmunityNumber of Days in HospitalOutcomeParticipantPathway interactionsPatient CarePatient Care DeliveryPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPhysiciansPneumoniaProteinsQualifyingRecommendationRecording of previous eventsResearch PriorityRuralSepsisSerumSourceSubgroupSymptomsTestingTheoretical Domains frameworkThinkingThoracic RadiographyTimeUnited StatesValidationViralViral DiseasesViral PneumoniaVirusVirus DiseasesWhite Blood CellsWhite CellWidthWorkabove age 65accurate diagnosisadult youthadulthoodadverse consequenceadverse outcomeafter age 65age 65 and greaterage 65 and olderage 65 or olderageage of 65 years onwardaged 65 and greateraged 65+aged ≥65alpha-Defensinsanti-microbial peptidebacteria infectionbacteria pathogenbacteria pneumoniabacterial diseasebacterial pathogenbarriers to implementationbio-markersbiologic markerbiomarkercare for patientscare of patientscaring for patientschest X raychest Xraychest radiographyclinical careclinical diagnosticsclinical predictorsco-infectionco-morbidco-morbiditycoinfectioncomorbiditycomputer based predictionconcept mappingconcept mapscoronavirus disease 2019 consequencecoronavirus disease 2019 effectcoronavirus disease 2019 impactcoronavirus disease-19 impactdevelopmentaldiagnostic accuracydiagnostic approachdiagnostic criteriadiagnostic strategyearly detectionexperiencefacesfacialfuture implementationgeriatric medicinehistorieshospital dayshospital length of stayhospital stayhuman old age (65+)imagingimplementation barriersimplementation challengesimplementation scienceimplementation studyimplementation trialimprovedlung failurelung radiographymalemedical diagnosticmonocytemortalitynew diagnosticsnew markernext generation diagnosticsnovelnovel biomarkernovel diagnosticsnovel markerolder adultolder adulthoodover 65 yearspathogenpathogenic bacteriapathogenic viruspathwaypatient oriented outcomespredictive modelingpreventpreventingprospectivepulmonary failureradiographic chest imageradiographic lung imagethoracic radiogramthorax radiographythoughtstoolusabilityvalidation studiesvalidationsviral infectionviral pathogenvirus infectionvirus pathogenvirus-induced diseasewhite blood cellwhite blood corpuscleyoung adultyoung adult ageyoung adulthoodα-Defensins≥65 years
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Full Description

PROJECT SUMMARY/ABSTRACT
In the time it takes to read this application, 20 older adults (age≥65 years) will die of pneumonia in the

United States. Annually over 500,000 older adults received treatment in emergency departments (ED) for

pneumonia. Unfortunately, ED physicians cannot accurately diagnose pneumonia in older adults because of

atypical symptoms, chest x-ray inaccuracy, comorbidities, failure of pulmonary clinical prediction rules

established with younger adults, and poor accuracy of available biomarkers. Emergency physician’s inability to

diagnose pneumonia in older adults leads to delayed diagnosis, inadequate treatment, worsening infection,

longer lengths of stay (6.6 days vs. 5.4), and mortality.

Pneumonia can be caused by bacterial and viral pathogens alone or in combination. Bacterial

pneumonia alone causes the adverse outcomes and faces the diagnostic challenges just described. The

presence of viral pneumonia further complicates diagnosis. Bacterial and viral co-infection in all adults increase

odds of death by 2.1 with expected greater deleterious effects on older adults. Unfortunately, when viral

sources are detected our current diagnostic approach fails to reliably identify bacterial sources in the event of

co-infections. This can lead to inappropriate care and highlights the importance of ensuring fast, accurate

diagnosis of both bacterial and viral pneumonia.

Unfortunately, available tests (serum, imaging) and patient presentation (symptoms, exam, and history)

are unreliable for diagnosing pneumonia in older adult ED patients. Our previous results reveal that novel tests

may improve diagnostic accuracy of pneumonia (antimicrobial peptides [AMPs] and monocyte distribution

width [MDW]). AMPs are a part of the innate immune system and respond in minutes to bacteria and viruses.

Monocyte distribution width measures the distribution of size of leukocytes and increases in ED sepsis.

This project seeks to build on previous investigations to improve the diagnostic accuracy of pneumonia

in older adult ED patients with the long-term goal of improving clinical care and decreasing the morbidity and

mortality associated with pneumonia. Aim #1 examines the potential for novel tests (AMPs and MDW) to

diagnose pneumonia alone and in combination with patient presentation/symptoms and existing diagnostic

studies. This aim will consider pneumonia caused by bacterial pathogens, viral pathogens and the combination

separately to create and determine the accuracy of a diagnostic pathway. Aim #2 will employ group concept

mapping guided by the Theoretical Domains Framework to engage emergency physicians to identify facilitators

and barriers to implementation of a diagnostic pathway in emergency medicine to inform future studies. Aim #3

pilots the Aim #1 diagnostic pathway. If successful, this proposal will produce a diagnostic pathway for

pneumonia in older adult ED patients and provide the groundwork for a successful validation and

implementation study of this diagnostic pathway.

Grant Number: 3K76AG074941-04S1
NIH Institute/Center: NIH

Principal Investigator: Katherine Buck

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