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Efficacy of intralesional recombinant human epidermal growth factor in diabetic foot ulcers in Mexican patients: A randomized double‐blinded controlled trial
Authors:Ramiro Gomez‐Villa MD  Francisco Aguilar‐Rebolledo MD  PhD  Adriana Lozano‐Platonoff MD  Juan Miguel Teran‐Soto MD  Maria Rosy Fabian‐Victoriano ETN  Nicole Stephanie Kresch‐Tronik MD  Ximena Garrido‐Espíndola ETN  Adriana Garcia‐Solis MD  Augusto Bondani‐Guasti MD  PhD  Guillermo Bierzwinsky‐Sneider MD  José Contreras‐Ruiz MD
Affiliation:1. Interdisciplinary Wound and Ostomy Care Center, Division of Dermatology, Dr. Manuel Gea Gonzalez General Hospital, , Mexico City, Mexico;2. Center for Advanced Medicine (CIMA, A.C.), , Xalapa, Veracruz;3. Division of Internal Medicine, Dr. Manuel Gea Gonzalez General Hospital, , Mexico City, Mexico;4. Mexican Association of Pharmacology (AMEFAR), , Mexico City, Mexico
Abstract:
The healing process in diabetic foot ulcer (DFU) is hindered by factors such as chronic inflammation, defects in fibroblast function, poor angiogenesis, and lack of cell migration. Recombinant human epidermal growth factor (rhEGF) has been shown to enhance extracellular matrix formation, cellular proliferation, and angiogenesis. Therefore, intralesional application of rhEGF in DFU could accelerate wound healing. Our objective was to determine the efficacy and safety of rhEGF in patients with DFU. A randomized, double‐blinded, placebo‐controlled study was conducted comparing a thrice‐per‐week intralesional application of rhEGF (75 μg) or placebo in patients with DFU for 8 weeks. The number of completely healed ulcers, size, and wound bed characteristics were evaluated to determine the efficacy of rhEGF. Adverse events were recorded and analyzed to establish its safety. A total of 34 patients were recruited for the study. After three dropouts, we were able to follow and analyze 16 patients in the placebo group and 15 patients in the rhEGF study to the end of the trial. Baseline testing showed that both groups were similar. Compared to the placebo group, more ulcers achieved complete healing in the rhEGF group (rhEGF, n = 4; placebo, n = 0; p = 0.033); ulcers in the rhEGF group decreased in area size (12.5 cm2 [rhEGF] vs. 5.2 cm2 [placebo]; p = 0.049); and more epithelial islands in the wound bed were present (28% vs. 3%; p = 0.025). Mild transitory dizziness was the only side effect that was more frequently noted in the rhEGF group. Our results showed that in patients with DFU who received standard care, intralesional rhEGF application resulted in complete healing in more patients, promoted the epithelialization of the wound bed, and significantly reduced the area of the DFU treated. Therefore, rhEGF resulted in better outcomes for patients suffering from DFU.
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