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1.
Medicine (Baltimore) ; 94(48): e2196, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26632907

RESUMEN

Transition from child to adult-oriented care is widely regarded a challenging period for young people with kidney transplants and is associated with a high risk of graft failure. We analyzed the existing transition structures in Germany and Austria using a questionnaire and retrospective data of 119 patients transferred in 2011 to 2012. Most centers (73%) confirmed agreements on the transition procedure. Patients' age at transfer was subject to regulation in 73% (18 years). Median age at transition was 18.3 years (16.5-36.7). Median serum creatinine increased from 123 to 132 µmol/L over the 12 month observation period before transfer (P = 0.002). A total of 25/119 patients showed increased creatinine ≥ 20% just before transfer. Biopsy proven rejection was found in 10/119 patients. Three patients lost their graft due to chronic graft nephropathy.Mean coefficient of variation (CoV%) of immunosuppression levels was 0.20 ± 0.1. Increased creatinine levels ≥ 20% just before transfer were less frequently seen in patients with CoV < 0.20 (P = 0.007). The majority of pediatric nephrology centers have internal agreements on transitional care. More than half of the patients had CoV of immunosuppression trough levels consistent with good adherence. Although, 20% of the patients showed increase in serum creatinine close to transfer.


Asunto(s)
Trasplante de Riñón/estadística & datos numéricos , Transición a la Atención de Adultos/organización & administración , Transición a la Atención de Adultos/estadística & datos numéricos , Adolescente , Adulto , Austria , Femenino , Alemania , Rechazo de Injerto/epidemiología , Humanos , Inmunosupresores/uso terapéutico , Masculino , Cumplimiento de la Medicación/estadística & datos numéricos , Estudios Retrospectivos , Adulto Joven
2.
Neuropediatrics ; 46(1): 49-51, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25305753

RESUMEN

BACKGROUND: Idiopathic intracranial hypertension is a clinical condition with elevated intracranial pressure of uncertain etiology. Although various underlying causes are suspected and familial occurrence has also been reported, however, it still remains an unexplained phenomenon. CASE REPORT: We report the case of dizygotic siblings with a known CYP24A1 mutation resulting in chronic hypercalcemia and impairment of kidney function. At the same point in time both of them developed intracranial hypertension resistant to conservative therapy necessitating therefore ventriculoperitoneal shunt implantation. In both children magnetic resonance imaging showed slightly hypoplastic sinus transversus as the potential underlying cause. CONCLUSION: The simultaneous clinical presentation could be due to a genetic factor or might be a component of the underlying disease or the consequence of its treatment. Further cases and clinical experience are needed to clarify this issue.


Asunto(s)
Hipercalcemia/complicaciones , Hipercalcemia/genética , Hipertensión Intracraneal/complicaciones , Acetazolamida/uso terapéutico , Anticonvulsivantes/uso terapéutico , Encéfalo/patología , Femenino , Fructosa/análogos & derivados , Fructosa/uso terapéutico , Humanos , Lactante , Hipertensión Intracraneal/diagnóstico , Hipertensión Intracraneal/genética , Imagen por Resonancia Magnética , Hermanos , Topiramato , Gemelos Dicigóticos
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