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Use of Rapamycin in Pediatric Patients with Autosomal Domina | 21666

Allgemeinmedizin: Open Access

ISSN - 2327-5146

Abstrakt

Use of Rapamycin in Pediatric Patients with Autosomal Dominant Polycystic Kidney Disease

Liern JM, Codianni P, Mora F, Blumenthal L and Vallejo G

Background: Autosomal dominant polycystic disease (ADPKD) is characterized by the development of renal cysts. Objectives: 1) To assess the kidney and cyst volume growth in patients treated with Rapamycin compared to patients who receive standard ADPKD treatment. 2) Evaluate the occurrence of adverse effects related to the use of Rapamycin. 3) To assess the changes in blood pressure, proteinuria and estimated Glomerular Filtration rate (eGFR). Materials and Methods: During 24 months were randomized 12 patients with ADPKD in a Rapamycin group (6 patients, received rapamycin 2-3 mg/m2/day, max. 5mg/día) and a Control group (standard treatment). Results: Of the 12 patients, 6 entered the Rapamycin group and had a total renal volume and cystic volume increase at study completion of 13% and 32% respectively. In the Control group (6 patients) the increases were 11% and 23% respectively. The eGFR was normal for both groups. The proteinuria for rapamycin group and control group was initially 7.3 mg/m²/hour and 6 mg/m2/hour respectively, at the end was normal for both groups. 3 patients had arterial hypertension, but at the 24th month, were normal. The adverse effects were: Anemia, diarrhea and oral sores. Conclusions: Rapamycin not decrease the kidney volume and cystic. There was no significant increase in proteinuria or eGFR decrease. Mean blood pressure remained normal.

Haftungsausschluss: Dieser Abstract wurde mit Hilfe von Künstlicher Intelligenz übersetzt und wurde noch nicht überprüft oder verifiziert