Evolution of renal function in patients with diabetic foot ulcer treated with Heberprot-P®

Authors

Keywords:

diabetic foot, diabetic kidney disease, Heberprot-P®.

Abstract

Introduction: Diabetic foot ulcer represents a complication of diabetes mellitus. Heberprot-P® is a medicine for its treatment, whose active substance is a human growth factor that could be associated with the onset of kidney disease.

Objective: To describe the evolution of renal function after treatment with Heberprot-P® in patients with diabetic foot ulcer.

Methods: Prospective descriptive study in 90 patients diagnosed with diabetic foot ulcer treated with Heberprot-P®. The variables analyzed were: microalbuminuria, creatinine, uric acid and glomerular filtration, at baseline, 6 months and post-treatment year. Relative frequencies of qualitative variables were determined, and mean and standard deviation of quantitative variables. Friedman test for two independent samples, U Mann Whitney and Chi square independence test were performed.

Results: The quantitative variables of renal function did not vary significantly. At baseline, the glomerular filtrate was 67.1 ml/min; and at both 6 months and a year, 67.2 ml/min. The mean creatinine at 6 months was 86.2 μmol/L; and after a year, 86.1 μmol/L. Uric acid increased its value from 331.7 mmol/L to 345.6 mmol/L at 6 months; and at 340 mmol/L after a year. Urinary albumin excretion improved significantly during the study.

Conclusions: Patients with diabetic foot ulcer treated with Heberprot-P® showed no impairment of renal function during the first year of treatment. Urinary albumin excretion improved and the rest of the variables remained stable.

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Published

2022-10-31

How to Cite

1.
Yanes Quesada M, Cruz Hernández J, Choque López F, Conesa González AI, Peña Gener R, Ortiz Peña Y, et al. Evolution of renal function in patients with diabetic foot ulcer treated with Heberprot-P®. RCACV [Internet]. 2022 Oct. 31 [cited 2024 Nov. 27];23(3). Available from: https://revangiologia.sld.cu/index.php/ang/article/view/386

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