Expert consensus on evidence-based recommendations for the diagnosis, treatment, and follow-up of X-linked hypophosphatemic rickets (XLH)

Introduction: X-linked hypophosphatemic rickets is a hereditary condition causing disruptions in bone mineral homeostasis. The morbidity associated with this condition has exhibited variability in previous decades, possibly stemming from variations in case definitions and diagnostic confirmation pro...

Full description

Autores:
Cárdenas-Aguilera, Juan Guillermo
Medina-Orjuela, Adriana
Meza-Martínez, Adriana Isabel
Prieto, Juan Carlos
Zarante-Bahamón, Ana María
Cáceres-Mosquera, Jimena Adriana
Mejía-Gaviria, Natalia
Serrano-Gayubo, Ana Katherina
Baquero-Rodríguez, Richard
Chacón-Acevedo, Kelly
Guerrero-Tinoco, Gustavo Adolfo
Uribe-Ríos, Alejandro
García-Rueda, María Fernanda
Abad-Londoño, Verónica
Nossa-Almanza, Sergio Alejandro
Aroca-Martínez, Gustavo
Román-González, Alejandro
Endo-Cáceres, Jorge Alberto
Llano-Linares, Juan Pablo
Florenzano, Pablo
Díaz-Curiel, Manuel
Vaisbich, María Helena
Zanchetta, María Belén
Guerra-Hernández, Norma Elizabeth
Enrique Stefano, Eduardo
Brunetto, Oscar
Tipo de recurso:
Fecha de publicación:
2024
Institución:
Universidad Simón Bolívar
Repositorio:
Repositorio Digital USB
Idioma:
eng
OAI Identifier:
oai:bonga.unisimon.edu.co:20.500.12442/14256
Acceso en línea:
https://hdl.handle.net/20.500.12442/14256
https://doi.org/10.22265/acnef.11.1
https://revistanefrologia.org/index.php/rcn/issue/view/40
Palabra clave:
Rickets
Hypophosphatemic
Fibroblast Growth Factor-23
Diagnosis
Therapeutics
Consensus
Raquitismo
Hipofosfatemia
Factor de crecimiento de fibroblastos-23
Diagnóstico
Rapéutica
Consenso
Rights
openAccess
License
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Description
Summary:Introduction: X-linked hypophosphatemic rickets is a hereditary condition causing disruptions in bone mineral homeostasis. The morbidity associated with this condition has exhibited variability in previous decades, possibly stemming from variations in case definitions and diagnostic confirmation procedures. Objective: Our aim was to generate evidence-informed recommendations for the diagnosis, treatment, and follow-up of patients with suspected or diagnosed XLH. Methodology: Integration of a literature review with a modified Delphi method, guided by expert consensus. Results: Following the screening and selection of 1041 documents, 41 were chosen to address the queries posed by the developer group. Experts, consulted through a modified Delphi consensus, endorsed 97 recommendations on the diagnosis, treatment, and follow-up of patients with suspected or diagnosed XLH. Notably, the quality of the evidence was deemed to be low. Conclusions: The recommendations proposed here will allow early and timely diagnosis of Xlinked hypophosphatemic rickets, while optimizing resources for its treatment and follow-up. In addition, it will help clarify the burden of the disease and improve health outcomes for this population.