Using Quality Improvement to Expand and Align State Public Health Long-Term Follow-up Data Collection Across Newborn Screening Conditions.


Journal

Journal of public health management and practice : JPHMP
ISSN: 1550-5022
Titre abrégé: J Public Health Manag Pract
Pays: United States
ID NLM: 9505213

Informations de publication

Date de publication:
06 Sep 2024
Historique:
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: aheadofprint

Résumé

Despite the undeniable success of newborn screening (NBS), numerous barriers exist regarding long-term follow-up (LTFU) of children with conditions included in NBS. Furthermore, there is a focus on condition-specific follow-up with no national guidelines for standard quality measures collected by state public health LTFU programs. Minnesota Department of Health (MDH) Longitudinal Follow-up for NBS. A state public health LTFU for NBS quality improvement (QI) project was carried out with collaboration between MDH project team members and a QI Steering Team who provided clinical, public health, education, caregiver, and community perspectives and expertise to MDH. Relevant measures were selected from existing data elements, and additional measures were developed based on exchange between MDH project team and the QI Steering Team. Potential data sources were explored and prioritized. Processes for querying existing data sources such as death records were refined, new sources such as electronic health records and paper/PDF health records were established, and data collection was piloted. The Minnesota Electronic Disease Surveillance System was modified, and an electronic data form was created to promote consistent data abstraction from sources. Throughout the project, progress was evaluated and shared. At project conclusion, MDH project team and the QI Steering Team reviewed project outcomes and approaches to evolve the project into ongoing surveillance. Five common public health LTFU measures were determined. Overall, 77% of attempted measures were successfully collected. Primary and secondary data sources were adopted. In addition, collected data resulted in 7% of cases that were closed to further public health LTFU, often related to a move out of state. This project established the feasibility of state public health LTFU surveillance of outcomes and health care use by collecting a common data set applicable across NBS conditions.

Identifiants

pubmed: 39250312
doi: 10.1097/PHH.0000000000002056
pii: 00124784-990000000-00343
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors have indicated no potential conflicts of interest to disclose.

Références

Sontag MK, Yusuf C, Grosse SD, et al. Infants with congenital disorders identified through newborn screening—United States, 2015-2017. MMWR Morb Mortal Wkly Rep. 2020;69(36):1265-1268. doi:10.15585/mmwr.mm6936a6.
doi: 10.15585/mmwr.mm6936a6
Wang Y, Caggana M, Sango-Jordan M, Sun M, Druschel CM. Long-term follow-up of children with confirmed newborn screening disorders using record linkage. Genet Med. 2011;13(10):881-886. doi:10.1097/GIM.0b013e31821e485b.
doi: 10.1097/GIM.0b013e31821e485b
Darby E, Thompson J, Johnson C, Singh S, Ojodu J. Establishing a national community of practice for newborn screening follow-up. Int J Neonatal Screen. 2021;7(3):49. doi:10.3390/ijns7030049.
doi: 10.3390/ijns7030049
Health Resources & Services Administration. The role of quality measures to promote long-term follow-up of children identified by newborn screening programs. https://www.hrsa.gov/sites/default/files/hrsa/advisory-committees/heritable-disorders/reports-recommendations/role-quality-measures-nbs-sept2018-508c.pdf. Presented by the Follow-up and Treatment Workgroup to the Advisory Committee on Heritable Disorders in Newborns and Children on February 8, 2018. Accessed February 23, 2024.
Health Resources & Services Administration. Recommended Uniform Screening Panel. https://www.hrsa.gov/advisory-committees/heritable-disorders/rusp. As of January 2023. Accessed June 26, 2024.
Minnesota Department of Health. Newborn Screening Panel and Timeline Minnesota’s Newborn Screening Panel. https://www.health.state.mn.us/people/newbornscreening/program/newbornscreeningpanel.html. Last updated February 26, 2024. Accessed June 26, 2024.
Association of Public Health Laboratories. Newborn Screening Systems Quality Improvement Projects. https://www.aphl.org/rfp/Pages/NBS-Systems-Quality-Improvement-Projects.aspx Published June 3, 2019. Accessed February 23, 2024.
Ogrinc G, Davies L, Goodman D, Batalden P, Davidoff F, Stevens D. SQUIRE 2.0 (Standards for Quality Improvement Reporting Excellence): revised publication guidelines from a detailed consensus process. BMJ Qual Saf. 2016;25(12):986-992. doi:10.1136/bmjqs-2015-004411.
doi: 10.1136/bmjqs-2015-004411
Institute for Healthcare Improvement. How to Improve: model for improvement. https://www.ihi.org/resources/how-to-improve. Accessed February 23, 2024.
Hinton CF, Mai CT, Nabukera SK, et al. Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings. Genet Med. 2014;16(6):484-490. doi:10.1038/gim.2013.177.
doi: 10.1038/gim.2013.177
Brower A, Chan K, Hartnett M, Taylor J. The longitudinal pediatric data resource: facilitating longitudinal collection of health information to inform clinical care and guide newborn screening efforts. Int J Neonatal Screen. 2021;7(3):37. doi:10.3390/ijns7030037.
doi: 10.3390/ijns7030037
Bailey DB Jr. Early intervention and newborn screening: parallel roads or divergent highways? Infants & Young Children. 2021;34(1):3-16. doi:10.1097/IYC.0000000000000181.
doi: 10.1097/IYC.0000000000000181
Kemper AR, Boyle CA, Aceves J, et al. Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services’ Advisory Committee on heritable disorders and genetic diseases in newborns and children. Genet Med. 2008;10(4):259-261. doi:10.1097/GIM.0b013e31816b64f9.
doi: 10.1097/GIM.0b013e31816b64f9
Centers for Disease Control and Prevention. End of the federal COVID-19 Public Health Emergency (PHE) declaration. https://www.cdc.gov/coronavirus/2019-ncov/your-health/end-of-phe.html. Updated September 12, 2023. Accessed February 23, 2024.
Lebrun-Harris LA, Sappenfield OR, Warren MD. Missed and delayed preventive health care visits among US children due to the COVID-19 pandemic. 433021. 2022;137(2):336-343. doi:10.1177/00333549211061322.
doi: 10.1177/00333549211061322
Council of State and Territorial Epidemiologists. Conditions available in RCKMS as of October 2023. Reportable Conditions Knowledge Management System (RCKMS). https://www.rckms.org/wp-content/uploads/2023/10/Conditions-available-in-RCKMS-October-2023.pdf. Updated October 2023. Accessed February 21, 2024.

Auteurs

Kristi Bentler (K)

Author Affiliations: Children and Youth with Special Health Needs, Minnesota Department of Health, St Paul, Minnesota (Mss Bentler, Barber, and Lintelmann, Dr Dierking, and Ms Hauser); Pediatric Otolaryngology, Children's Minnesota, Minneapolis, Minnesota (Dr Meyer); Department of Otolaryngology-Head & Neck Surgery, University of Minnesota, Minneapolis, Minnesota (Dr Meyer); and Newborn Screening and Genetics, Association of Public Health Laboratories Bethesda, Maryland (Ms Comer).

Classifications MeSH