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Anaesthesiologic protocol for kidney transplantation in two patients with Fabry Disease: a case series

Fabry's Disease is a rare genetic syndrome, with a classic X-linked alpha -galactosidase A deficiency phenotype, responsible for glico-sphyngolypids metabolism impairment with clinical effects in several organs and functions. We describe the anaesthesiologic implications of two patients with Fa...

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Detalles Bibliográficos
Autores principales: Sorbello, Massimiliano, Veroux, Massimiliano, Cutuli, Melania, Morello, Gianluigi, Paratore, Annalaura, Sidoti, Mirko Tindaro, Maugeri, Jessica Giuseppina, Gagliano, Massimiliano, Giuffrida, Giuseppe, Corona, Daniela, Veroux, Pierfrancesco
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596113/
https://www.ncbi.nlm.nih.gov/pubmed/19014714
http://dx.doi.org/10.1186/1757-1626-1-321
Descripción
Sumario:Fabry's Disease is a rare genetic syndrome, with a classic X-linked alpha -galactosidase A deficiency phenotype, responsible for glico-sphyngolypids metabolism impairment with clinical effects in several organs and functions. We describe the anaesthesiologic implications of two patients with Fabry disease who underwent a kidney transplantation from a deceased donor. We recommend careful preoperative evaluation, including cardiac sonography study and spirometry for Fabry disease patients, and according to our experience, we recommend advanced haemodynamic monitoring during surgery. Careful airway examination should be further performed, with particular attention to patient ventilability prediction and available alternative strategies for airway management in case of difficulties. A nephroprotective strategy and a particular care to the associated end-stage organ disease may significantly improve the long-term outcome of patients with Fabry Disease.