Abstract
AUTOMATIC REFERRALS WITHIN A CYSTIC FIBROSIS MULTIDISCIPLINARY CLINIC IMPROVE PATIENT EVALUATION AND MANAGEMENT. BackgroundCystic fibrosis (CF) affects multiple systems beyond the pulmonary system, including the gastrointestinal and endocrine systems. Many CF clinics focus on pulmonary effects, initiating referrals to other specialties only when a condition has been identified by the primary pulmonary team. Unfortunately, many extrapulmonary manifestations of cystic fibrosis may be overlooked. Thus, implementing a multidisciplinary clinic with automatic referrals to designated subspecialists may improve patient care. MethodsThis retrospective review of medical records examined the effects of integrating a pediatric endocrinologist into the University of Massachusetts Memorial Medical Center Pediatric CF Clinic in March 2017. In this new CF/Endocrinology clinic, all patients scheduled to see a pulmonologist were automatically referred to pediatric endocrinology. We compared rates of referrals to pediatric endocrinology, oral glucose tolerance tests (OGTTs), and bone density (DEXA) scans before (2013–2016) and after (2017–2020) implementation of this clinic. We also recorded endocrine disorders being evaluated and/or treated after implementation. ResultsThe rate of referral to pediatric endocrinology increased from before (4%) to after (82%) (p < 0.0001) implementation of the CF/Endocrinology Clinic. OGTT and DEXA scan screening rates also increased from 7% to 65% (p < 0.0001) and from 6% to 63% (p = 0.0011), respectively. Before implementation, patients were evaluated by endocrinology primarily for CF-related diabetes. After implementation, the diversity of endocrine conditions under evaluation and/or management increased substantially; the most common were vitamin D insufficiency/deficiency (37.2% of clinic patients), glycemic dysregulation (36.8%), and poor weight gain/failure to thrive (17.5%). ConclusionImplementing a multidisciplinary CF clinic with automatic referrals to pediatric endocrinology improves patient care by promoting early detection and management of endocrine concerns that may have been overlooked and by increasing OGTT and DEXA screening rates.
Highlights
Cystic fibrosis (CF) is the most lethal autosomal recessive disorder in Caucasians, with a worldwide prevalence of 1/2500 live births
The percentage of CF pediatric patients in our clinic referred to pe diatric endocrinology increased from 4% prior to integration of a pedi atric endocrinologist in the clinic to 82% after integration (p < 0.0001)
oral glucose tolerance tests (OGTTs) and DEXA scan screening rates increased from 7% to 65% (p < 0.0001) and from 6% to 63% (p = 0.0011), respectively (Table 1)
Summary
Cystic fibrosis (CF) is the most lethal autosomal recessive disorder in Caucasians, with a worldwide prevalence of 1/2500 live births. It caused by a mutation of the cystic fibrosis transmembrane conductance regu lator (CFTR) gene. Many CF clinics focus predominantly on reducing pulmonary effects of this disease, initiating referrals to endocrinologists and gastroenter ologists only when a corresponding condition has been identified. When following this approach, many subtle non-pulmonary concerns may be overlooked, potentially impacting overall care in a negative manner
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Clinical & Translational Endocrinology
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.