The effectiveness of RSV immunoprophylaxis on the short- and long- term respiratory morbidity in children with Down syndrome
The effectiveness of RSV immunoprophylaxis on the short- and long- term respiratory morbidity in children with Down syndrome
批准号:
10398259
负责人:
PINGSHENG WU
金额:
$45.25万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
未结题
起止时间:
2019-02-12 至 2025-01-31
关键词:
6 year oldAcademyAdaptive Immune SystemAdherenceAdverse eventAmericanAnatomyAsthmaBirthChildChildhoodChromosome 21Chronic lung diseaseClinicalCohort StudiesCongenital chromosomal diseaseCost-Benefit AnalysisDataDepartment of DefenseDiseaseDown SyndromeEffectivenessEligibility DeterminationEnrollmentGuidelinesHealthHealth Care VisitHealthcare SystemsHospitalizationHumanImmune systemInfantInfectionKnowledgeLeadLifeLower Respiratory Tract InfectionLungMedicaidMilitary PersonnelMorbidity - disease rateObservational StudyOutcomePatientsPediatricsPharmacologyPhysiologicalPoliciesPolicy MakerPopulationPremature BirthPrevalencePreventive therapyQualifyingRandomized Clinical TrialsResearchResearch DesignRespiratory DiseaseRespiratory Syncytial Virus InfectionsRespiratory syncytial virusRiskRisk FactorsSafetySocioeconomic FactorsTennesseeTestingVariantViralVulnerable PopulationsWheezingclinical carecohortcongenital heart disordercostcost effectivenessdemographicshemodynamicshigh risk populationimmunoprophylaxisimprovedinfancymortalitypopulation basedpost-marketpreventprogramsrespiratoryrespiratory morbidityresponse
中文摘要
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英文摘要
PROJECT SUMMARY
Significance and Background: Children with Down syndrome (DS), irrespective of having other risk factors,
are at increased risk for respiratory syncytial virus (RSV) infection. Worldwide RSV is the most common cause
of lower respiratory tract infections (LRTI) in infants and young children. Early life RSV LRTI further adversely
influences the developing lung and immune system, and sets up children with DS for an increased risk of other
long term respiratory diseases. Children with DS may therefore potentially benefit from RSV
immunoprophylaxis, the only currently available pharmacological strategy to prevent RSV LRTI. However,
insufficient data limit routine use of RSV immunoprophylaxis in children with DS to the same qualifying
conditions as children without DS (premature birth < 29 weeks, chronic lung disease, or hemodynamically
significant congenital heart disease) per American Academy of Pediatrics guideline.
Objectives, Hypothesis and Specific Aims: Our overarching hypotheses are: 1) In children with DS RSV
LRTI early in life increases the risk of respiratory morbidity through age 6 years, 2) Administration of RSV
immunoprophylaxis reduces RSV LRTI morbidity and later respiratory morbidity caused by RSV LRTI early in
life, and 3) Administration of RSV immunoprophylaxis offsets the costs of both RSV LRTI related
hospitalization during the first 2 years of life and respiratory morbidity through age 6 years. To test the
hypotheses, we will: 1) Determine and quantify the prevalence of severe RSV LRTI in the first 2 years of life
and the association of RSV LRTI with respiratory morbidity through age 6 years; 2) Characterize the receipt of,
safety of, and adherence to RSV immunoprophylaxis; 3) Determine the short-term effectiveness of RSV
immunoprophylaxis on reducing RSV LRTI healthcare visits and the long-term effectiveness on childhood
respiratory outcomes, 4) Determine the cost-effectiveness of RSV immunoprophylaxis administration in
reducing RSV LRTI and later respiratory morbidity in children with DS.
Research Design: We will conduct a large population-based birth cohort study of 4,063 children with DS born
1996-2018 and enrolled in the Tennessee Medicaid Program or the Department of Defense military healthcare
system, the largest cohort ever conducted in this population.
Impact: The knowledge gaps about the burden of RSV infection and the effectiveness of RSV
immunoprophylaxis in children with DS leave policy makers, clinicians and patients unable to make informed
clinical decisions. The proposed research, the largest study ever conducted, is in direct response to the
American Academy of Pediatrics call for adequately powered studies to answer the question and inform policy
on effectiveness of RSV immunoprophylaxis in this high risk population. Results from this study will provide
information in informing clinical care and policy, and more importantly may improve human health in children
with DS with a readily available and safe therapy.
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