EFICACIA Y SEGURIDAD DE DOS FORMULACIONES DE ACIDO MICOFENOLICO EN NIÑOS CON TRASPLANTE RENAL





EFICACIA Y SEGURIDAD DE DOS FORMULACIONES DE ACIDO MICOFENOLICO EN NIÑOS CON TRASPLANTE RENAL

(especial para SIIC © Derechos reservados)
La conversión de micofenolato de mofetilo a mcofenolato sódico con capa entérica es eficaz y segura en niños con trasplante renal. Los síntomas gastrointestinales son menores con la formulación de capa entérica.
Autor:
Mara Medeiros
Columnista Experta de SIIC

Institución:
Hospital Infantil de México Federico Gómez


Artículos publicados por Mara Medeiros
Coautor
Mara Medeiros* 
Dra., Hospital Infantil de México Federico Gómez, México, México*
Aprobación
9 de Noviembre, 2010
Primera edición
17 de Noviembre, 2010
Segunda edición, ampliada y corregida
7 de Junio, 2021

Artículo completo

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Extensión:  +/-3.03 páginas impresas en papel A4
Exclusivo para suscriptores/assinantes

Clasificación en siicsalud
Artículos originales > Expertos de Iberoamérica >
página   www.siicsalud.com/des/expertocompleto.php/

Especialidades
Principal: Nefrología y Medio Interno, Trasplantes
Relacionadas: Farmacología, Inmunología, Medicina Farmacéutica, Pediatría



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Enviar correspondencia a:
Mara Medeiros, Laboratorio de Investigación en Nefrología y Metabolismo Mineral Hospital Infantil de México Federico Gómez, 06720, Dr. Marques 162 Col. Doctores, Mexico DF, México
Bibliografía del artículo
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Van Hest RM, Mathot RA, Vulto AG, Ijzermans JN, Van Gelder T. Within-patient variability of mycophenolic acid exposure: therapeutic drug monitoring from a clinical point of view. Ther Drug Monit 28:31-4, 2006.
Weber LT, Shipkova M, Armstrong VW, Wagner N, Schutz E, Mehls O et al. The pharmacokinetic-pharmacodynamic relationship for total and free mycophenolic Acid in pediatric renal transplant recipients: a report of the german study group on mycophenolate mofetil therapy. J Am Soc Nephrol 13:759-68, 2002.
Bremer S, Vethe NT, Rootwelt H, Bergan S. Expression of IMPDH1 is regulated in response to mycophenolate concentration. Int Immunopharmacol 9:173-80, 2009.
Sombogaard F, Peeters AM, Baan CC, Mathot RA, Quaedackers ME, Vulto AG et al. Inosine monophosphate dehydrogenase messenger RNA expression is correlated to clinical outcomes in mycophenolate mofetil-treated kidney transplant patients, whereas inosine monophosphate dehydrogenase activity is not. Ther Drug Monit 31:549-56, 2009.
Bolin P, Tanriover B, Zibari GB, Lynn ML, Pirsch JD, Chan L et al. Improvement in 3-month patient-reported gastrointestinal symptoms after conversion from mycophenolate mofetil to enteric-coated mycophenolate sodium in renal transplant patients. Transplantation 84:1443-51, 2007.
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Van Gelder T, Shaw LM. The rationale for and limitations of therapeutic drug monitoring for mycophenolate mofetil in transplantation. Transplantation 80:S244-53, 2005.
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United States Patent. Patent Number 6,306,900 B1. Enteric coated pharmaceutical compositions. Available from: www.google.com.mx/patents?id=DA8IAAAAEBAJ&printsec=claims&zoom#v=onepage&q=&f=false. Accesed January, 25, 2010.
Budde K, Knoll G, Curtis J, Chan L, Pohanka E, Gentil M et al. Long-term safety and efficacy after conversion of maintenance renal transplant recipients from mycophenolate mofetil (MMF) to enteric-coated mycophenolate sodium (EC-MPA, myfortic). Clin Nephrol 66:103-11, 2006.
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Heller T, Geide A, Bonitz U, Wegner U, Grone HJ, Armstrong VW et al. Effect of the antioxidant idebenone on adverse events under mycophenolate mofetil therapy in a rat model. Transplantation 85:739-47, 2008.
Kamar N, Rostaing L. Negative impact of one-year anemia on long-term patient and graft survival in kidney transplant patients receiving calcineurin inhibitors and mycophenolate mofetil. Transplantation 85:1120-4, 2008.
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