Long-Term Follow-Up Cares and Check Initiative: A Program to Advance Long-Term Follow-Up in Newborns Identified with a Disease through Newborn Screening

• Published in: International journal of neonatal screening 2024-04, Vol.10 (2), p.34
• Main Authors: Lietsch, Mei, Chan, Kee, Taylor, Jennifer, Lee, Bo Hoon, Ciafaloni, Emma, Kwon, Jennifer M, Waldrop, Megan A, Butterfield, Russell J, Rathore, Geetanjali, Veerapandiyan, Aravindhan, Kapil, Arya, Parsons, Julie A, Gibbons, Melissa, Brower, Amy
• Format: Article
• Language: English
• Subjects: Brief Report; Collaboration; Computational linguistics; Data collection; Data entry; Design; Diseases; Early intervention; Evidence-based medicine; Families & family life; Infants (Newborn); Laboratories; Language processing; Literature reviews; long-term follow-up (LTFU); Medical screening; Natural language interfaces; Newborn babies; newborn screening (NBS); Parents & parenting; Pediatrics; Pharmaceutical industry; Prenatal education; Project evaluation; Public health; spinal muscular atrophy (SMA); Stakeholders; Visualization (Computers)
• ISSN: 2409-515X; 2409-515X
• DOI: 10.3390/ijns10020034

In the United States and around the world, newborns are screened on a population basis for conditions benefiting from pre-symptomatic diagnosis and treatment. The number of screened conditions continues to expand as novel technologies for screening, diagnosing, treating, and managing disease are discovered. While screening all newborns facilitates early diagnosis and treatment, most screened conditions are treatable but not curable. Patients identified by newborn screening often require lifelong medical management and community support to achieve the best possible outcome. To advance the long-term follow-up of infants identified through newborn screening (NBS), the Long-Term Follow-up Cares and Check Initiative (LTFU-Cares and Check) designed, implemented, and evaluated a system of longitudinal data collection and annual reporting engaging parents, clinical providers, and state NBS programs. The LTFU-Cares and Check focused on newborns identified with spinal muscular atrophy (SMA) through NBS and the longitudinal health information prioritized by parents and families. Pediatric neurologists who care for newborns with SMA entered annual data, and data tracking and visualization tools were delivered to state NBS programs with a participating clinical center. In this publication, we report on the development, use of, and preliminary results from the LTFU-Cares and Check Initiative, which was designed as a comprehensive model of LTFU. We also propose next steps for achieving the goal of a national system of LTFU for individuals with identified conditions by meaningfully engaging public health agencies, clinicians, parents, families, and communities.