Congenital Hypothyroidism Long-Term Follow-up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Project

dc.contributor.authorWintergerst, Kupper
dc.contributor.authorGembel, Gina
dc.contributor.authorKreipe, Tracey
dc.contributor.authorZeller, Patrick
dc.contributor.authorEugster, Erica
dc.contributor.authorYoung, Bill
dc.contributor.authorAndruszewski, Karen
dc.contributor.authorKleyn, Mary
dc.contributor.authorCunningham, Troi
dc.contributor.authorFawbush, Sandy
dc.contributor.authorVanderburg, Nancy
dc.contributor.authorSockalosky, Joe
dc.contributor.authorMenon, Ram
dc.contributor.authorLinard, Sharon
dc.contributor.authorHoffman, Gary
dc.contributor.authorGorman, Lisa
dc.contributor.departmentDepartment of Pediatrics, IU School of Medicineen_US
dc.date.accessioned2016-03-04T22:17:00Z
dc.date.available2016-03-04T22:17:00Z
dc.date.issued2015-06
dc.description.abstractThe Region 4 Midwest Genetics Collaborative, made up of seven regional states (Illinois, Indiana, Kentucky, Michigan, Minnesota, Ohio, and Wisconsin), brought together pediatric endocrinologists, state laboratory experts, public health follow-up specialists, and parents of children with congenital hypothyroidism (CH) to identify the three-year follow-up management and education patterns of primary care clinicians and pediatric endocrinologists in the care of children diagnosed with CH by state newborn screening (NBS) programs. Among a number of challenges, each state had different NBS methods, data systems, public health laws, and institutional review board (IRB) requirements. Furthermore, the diagnosis of CH was complicated by the timing of the NBS sample, the gestational age, weight, and co-morbidities at delivery. There were 409 children with CH identified through NBS in 2007 in the seven state region. The clinician of record and the parents of these children were invited to participate in a voluntary survey. Approximately 64 % of clinician surveys were collected with responses to questions relating to treatment, monitoring practices, educational resources, genetic counseling, and services provided to children with confirmed CH and their families. Nearly one-quarter (24 %) of parents surveyed responded to questions relating to treatment, education, genetic counseling, resources, and services they received or would like to receive. De-identified data from six of the seven states were compiled for analysis, with one state being unable to obtain IRB approval within the study timeline. The data from this collaborative effort will improve state follow-up programs and aid in developing three-year follow-up guidelines for children diagnosed with CH. To aid in the facilitation of similar public health studies, this manuscript highlights the challenges faced, and focuses on the pathway to a successful multi-state public health endeavor.en_US
dc.identifier.citationWintergerst, K., Gembel, G., Kreipe, T., Zeller, P., Eugster, E., Young, B., … Gorman, L. (2015). Congenital Hypothyroidism Long-Term Follow-up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Project. Journal of Genetic Counseling, 24(3), 464–472. http://doi.org/10.1007/s10897-014-9790-8en_US
dc.identifier.urihttps://hdl.handle.net/1805/8723
dc.language.isoen_USen_US
dc.publisherSpringer International Publishingen_US
dc.relation.isversionof10.1007/s10897-014-9790-8en_US
dc.relation.journalJournal of Genetic Counselingen_US
dc.rightsAttribution 3.0 United States
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/
dc.sourcePMCen_US
dc.subjectCongenital hypothyroidismen_US
dc.subjectPublic healthen_US
dc.subjectLong-term follow-upen_US
dc.titleCongenital Hypothyroidism Long-Term Follow-up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Projecten_US
dc.typeArticleen_US
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