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The real world experience of pediatric primary hyperoxaluria patients in the PEDSnet clinical research network.

Authors :
Ching, Christina B.
Dickinson, Kimberley
Karafilidis, John
Marchesani, Nicole
Mucha, Lisa
Antunes, Nuno
Razzaghi, Hanieh
Utidjian, Levon
Yonekawa, Karyn
Coplen, Douglas E.
Muneeruddin, Samina
DeFoor, William
Rove, Kyle O.
Forrest, Christopher B.
Tasian, Gregory E.
Source :
European Journal of Pediatrics. Sep2023, Vol. 182 Issue 9, p4027-4036. 10p. 4 Charts.
Publication Year :
2023

Abstract

The rarity of primary hyperoxaluria (PH) challenges our understanding of the disease. The purpose of our study was to describe the course of clinical care in a United States cohort of PH pediatric patients, highlighting health service utilization. We performed a retrospective cohort study of PH patients < 18 years old in the PEDSnet clinical research network from 2009 to 2021. Outcomes queried included diagnostic imaging and testing related to known organ involvement of PH, surgical and medical interventions specific to PH-related renal disease, and select PH-related hospital service utilization. Outcomes were evaluated relative to cohort entrance date (CED), defined as date of first PH-related diagnostic code. Thirty-three patients were identified: 23 with PH type 1; 4 with PH type 2; 6 with PH type 3. Median age at CED was 5.0 years (IQR 1.4, 9.3 years) with the majority being non-Hispanic white (73%) males (70%). Median follow-up between CED and most recent encounter was 5.1 years (IQR 1.2, 6.8). Nephrology and Urology were the most common specialties involved in care, with low utilization of other sub-specialties (12%-36%). Most patients (82%) had diagnostic imaging used to evaluate kidney stones; 11 (33%) had studies of extra-renal involvement. Stone surgery was performed in 15 (46%) patients. Four patients (12%) required dialysis, begun in all prior to CED; four patients required renal or renal/liver transplant. Conclusion: In this large cohort of U.S. PH children, patients required heavy health care utilization with room for improvement in involving multi-disciplinary specialists. What is Known: • Primary hyperoxaluria (PH) is rare with significant implications on patient health. Typical involvement includes the kidneys; however, extra-renal manifestations occur. • Most large population studies describe clinical manifestations and involve registries. What is New: • We report the clinical journey, particularly related to diagnostic studies, interventions, multispecialty involvement, and hospital utilization, of a large cohort of PH pediatric patients in the PEDSnet clinical research network. • There are missed opportunities, particularly in that of specialty care, that could help in the diagnosis, treatment, and even prevention of known clinical manifestations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03406199
Volume :
182
Issue :
9
Database :
Academic Search Index
Journal :
European Journal of Pediatrics
Publication Type :
Academic Journal
Accession number :
172951543
Full Text :
https://doi.org/10.1007/s00431-023-05077-y