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Diabetic patients frequently develop wounds, which can be colonized by bacteria, mainly Staphylococcus aureus and Pseudomonas aeruginosa, with the ability to form biofilms. This study aimed to evaluate the colonization and biofilm formation of Staphylococcus aureus and Pseudomonas aeruginosa in chronic wounds of diabetic patients treated with a bioactive dressing (EGF-CMC), which consisted of a 2% carboxymethylcellulose (CMC) hydrogel loaded with epidermal growth factor (EGF). This randomized clinical trial was conducted with 25 participants: 14 treated with EGF-CMC hydrogel and 11 treated with CMC hydrogel for 12 weeks. Participants with type 2 diabetes mellitus were selected. All had diabetic foot ulcers or chronic venous ulcers. Swab collections were performed on weeks 1, 6, and 12. The laboratory analyses included the identification of strains, microbial quantification, virulence gene investigation, and the evaluation of biofilm formation. In total, 13 S. aureus strains and 15 P. aeruginosa strains were isolated. There were no statistically significant differences regarding bacterial loads and virulence genes. However, EGF-CMC-hydrogel-treated wounds were colonized by strains with lower biofilm formation abilities. The probability of isolating biofilm-producing strains from CMC-hydrogel-treated wounds was 83% greater than the probability of isolating biofilm-producing strains from EGF-CMC-treated wounds.
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The Brazilian Practice Guidelines for Stroke Rehabilitation - Part II, developed by the Scientific Department of Neurological Rehabilitation of the Brazilian Academy of Neurology (Academia Brasileira de Neurologia, in Portuguese), focuses on specific rehabilitation techniques to aid recovery from impairment and disability after stroke. As in Part I, Part II is also based on recently available evidence from randomized controlled trials, systematic reviews, meta-analyses, and other guidelines. Part II covers disorders of communication, dysphagia, postural control and balance, ataxias, spasticity, upper limb rehabilitation, gait, cognition, unilateral spatial neglect, sensory impairments, home rehabilitation, medication adherence, palliative care, cerebrovascular events related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, the future of stroke rehabilitation, and stroke websites to support patients and caregivers. Our goal is to provide health professionals with more recent knowledge and recommendations for better rehabilitation care after stroke.
As Diretrizes Brasileiras de Reabilitação do Acidente Vascular Cerebral (AVC) - Parte II, desenvolvida pelo Departamento Científico de Reabilitação Neurológica da Academia Brasileira de Neurologia é voltada para intervenções específicas de técnicas de reabilitação de déficits neurológicos e incapacidades. Seguindo o mesmo modelo da Parte I, a Parte II também se baseia em estudos randomizados, revisões sistemáticas, metanálises e outras diretrizes sobre o mesmo tema. A segunda parte aborda os distúrbios da comunicação, disfagia, controle postural e equilíbrio, ataxias, espasticidade, reabilitação do membro superior, marcha, cognição, negligência espacial unilateral, déficits sensoriais, reabilitação domiciliar, aderência ao uso de medicamentos, cuidados paliativos, o futuro da reabilitação no AVC, e websites de orientação sobre AVC para pacientes e cuidadores. Nosso objetivo é fornecer aos profissionais envolvidos na reabilitação conhecimento atualizado e recomendações para um melhor cuidado no pós-AVC.
Asunto(s)
Rehabilitación de Accidente Cerebrovascular , Accidente Cerebrovascular , Humanos , Brasil , COVID-19 , Accidente Cerebrovascular/complicaciones , Accidente Cerebrovascular/tratamiento farmacológico , Rehabilitación de Accidente Cerebrovascular/métodos , Ensayos Clínicos Controlados Aleatorios como Asunto , Metaanálisis como Asunto , Revisiones Sistemáticas como AsuntoRESUMEN
Objetivo: Analisar as produções científicas sobre a efetividade do Fator de crescimento epitelial recombinante humano na cicatrização de feridas diabéticas. Métodos: Trata-se de uma revisão sistemática da literatura, a busca foi realizada nas bases de dados: Pubmed; Scopus e Lilacs. Resultados: Foram selecionados 21 artigos, sendo a maioria estudos experimentais (48%). A cicatrização completa de lesões tratadas com Fator de crescimento epitelial recombinante humano foi relatada por 17 artigos (81%). O aumento do tecido de granulação foi relatado em nove publicações (43%). Da mesma maneira, a diminuição da área da lesão foi descrita em dois artigos incluídos (10%). Duas publicações descrevem a diminuição do número de amputações e do estresse oxidativo e 62% dos artigos abordaram eventos adversos associados ao uso do produto (13/21), dos quais foram prioritários a ocorrência de tremores, dor local, calafrios, náuseas, infecção superficial, sensação de queimação e hematomas, considerados eventos adversos leves. Apenas um estudo apresentou a ocorrência de dor no peito como evento adverso grave. Conclusão: O fator de crescimento epitelial recombinante humano é indicado para uso tópico no tratamento de feridas diabéticas, evidenciando boa eficácia, porém mais estudos clínicos devem ser desenvolvidos. (AU)
Objective: To analyse the scientific studies of Human recombinant epithelial growth factor for the healing of diabetic wounds. Methods: A thorough review of the literature was performed in the following databases: PubMed, Scopus and LILACS. Results: 21 articles were selected, most studies were experimental (48%). Complete healing of Human recombinant epithelial growth factor-treated lesions has been reported by 17 articles (81%). Increased granulation tissue has been reported in nine publications (43%). Similarly, the reduction of the lesion area was described in two included articles (10%). Two publication describes the decrease in the number of amputations and oxidative stress and 62% of the articles addressed adverse events associated with the use of the product (13/21), of which the occurrence of tremors, local pain, chills, nausea, superficial infection, burning sensation and bruising were considered priority, considered adverse events light. Only one study showed chest pain as a serious adverse event. Conclusion: Although Human recombinant epithelial growth factor is indicated for topical use in the treatment of diabetic wounds and demonstrates good efficacy, more clinical studies should be developed. (AU)
Objetivo: Analizar la producción científica sobre la efectividad de Factor de crecimiento epitelial humano recombinante en la curación de heridas diabéticas. Métodos: Esta es una revisión sistemática de la literatura, la búsqueda se realizó en las bases de datos: Pubmed; Scopus y lilas. Resultados: Se seleccionaron 21 artículos. La mayoría de los estudios fueron experimentales (48%). 17 artículos informaron sobre la curación completa de lesiones tratadas con factor de crecimiento epitelial humano recombinante (81%). El aumento en el tejido de granulación se informó en nueve publicaciones (43%). Asimismo, se utilizó una reducción en el área de la lesión en dos artículos incluidos (10%). Dos publicaciones describen una disminución en el número de amputaciones y estrés oxidativo y el 62% de los artículos abordaron eventos adversos asociados con el uso del producto (13/21), que son las prioridades prioritarias en la aparición de temblores, dolor local, escalofríos, náuseas, infección superficial, sensación de ardor y hematomas, reflejos de eventos adversos leves. Solo un estudio muestra la aparición de dolor torácico como un evento adverso grave. Conclusión: Factor de crecimiento epitelial humano recombinante está indicado para uso tópico en el tratamiento de heridas diabéticas, mostrando buena eficacia, pero se deben desarrollar más estudios clínicos. (AU)
Asunto(s)
Pie Diabético , Cicatrización de Heridas , Enfermería , Factor de Crecimiento EpidérmicoRESUMEN
The aim of the study was to evaluate the healing process of chronic wounds treated with carboxymethylcellulose loaded with recombinant human epidermal growth factor in patients with diabetes. The case series consisted of 10 patients treated at the university hospital for 12 weeks. Data were analyzed using SPSS version 22.0. according to the intention to treat the principle, without the loss or exclusion of the participants. The sample consisted of 70% (7/10) males with a mean age of 61.9 years (±9.4); all (100%) had diabetes mellitus and 70% (7/10) had systolic hypertension associated with diabetes mellitus. Sixty percent (6/10) presented lesions of diabetic etiology and 40% (4/10) presented lesions of venous etiology; 70% (7/10) had had lesions for less than 5 years. The mean glycated hemoglobin was 7.8% (±2.7%), while the mean ankle-arm index (AAI) was 0.94 (±0.21). The mean initial area of all wounds was 13.4 cm², and the mean final area was 7.8 cm2, with a reduction rate of 28.9% over the 12 weeks of treatment. The reduction rate of diabetic ulcers was higher (33.4%) than that of venous ulcers (22.1%). Regarding the type of tissue, there was an increase in granulation and epithelialization, and a decrease in slough and the amount of exudate that were statistically significant (p = 0.021). No participant had severe or local adverse events during the study period. Epidermal growth factor was effective in the treatment of chronic wounds, especially diabetic ulcers, resulting in the reduction of the wound area and the improvement of tissue and exudate quality.
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The Guidelines for Stroke Rehabilitation are the result of a joint effort by the Scientific Department of Neurological Rehabilitation of the Brazilian Academy of Neurology aiming to guide professionals involved in the rehabilitation process to reduce functional disability and increase individual autonomy. Members of the group participated in web discussion forums with predefined themes, followed by videoconference meetings in which issues were discussed, leading to a consensus. These guidelines, divided into two parts, focus on the implications of recent clinical trials, systematic reviews, and meta-analyses in stroke rehabilitation literature. The main objective was to guide physicians, physiotherapists, speech therapists, occupational therapists, nurses, nutritionists, and other professionals involved in post-stroke care. Recommendations and levels of evidence were adapted according to the currently available literature. Part I discusses topics on rehabilitation in the acute phase, as well as prevention and management of frequent conditions and comorbidities after stroke.
Asunto(s)
Neurología , Médicos , Rehabilitación de Accidente Cerebrovascular , Accidente Cerebrovascular , Brasil , HumanosRESUMEN
Abstract The Brazilian Practice Guidelines for Stroke Rehabilitation - Part II, developed by the Scientific Department of Neurological Rehabilitation of the Brazilian Academy of Neurology (Academia Brasileira de Neurologia, in Portuguese), focuses on specific rehabilitation techniques to aid recovery from impairment and disability after stroke. As in Part I, Part II is also based on recently available evidence from randomized controlled trials, systematic reviews, meta-analyses, and other guidelines. Part II covers disorders of communication, dysphagia, postural control and balance, ataxias, spasticity, upper limb rehabilitation, gait, cognition, unilateral spatial neglect, sensory impairments, home rehabilitation, medication adherence, palliative care, cerebrovascular events related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, the future of stroke rehabilitation, and stroke websites to support patients and caregivers. Our goal is to provide health professionals with more recent knowledge and recommendations for better rehabilitation care after stroke.
Resumo As Diretrizes Brasileiras de Reabilitação do Acidente Vascular Cerebral (AVC) - Parte II, desenvolvida pelo Departamento Científico de Reabilitação Neurológica da Academia Brasileira de Neurologia é voltada para intervenções específicas de técnicas de reabilitação de déficits neurológicos e incapacidades. Seguindo o mesmo modelo da Parte I, a Parte II também se baseia em estudos randomizados, revisões sistemáticas, metanálises e outras diretrizes sobre o mesmo tema. A segunda parte aborda os distúrbios da comunicação, disfagia, controle postural e equilíbrio, ataxias, espasticidade, reabilitação do membro superior, marcha, cognição, negligência espacial unilateral, déficits sensoriais, reabilitação domiciliar, aderênciaao usode medicamentos, cuidados paliativos,ofuturodareabilitação no AVC, e websites de orientação sobre AVC para pacientes e cuidadores. Nosso objetivo é fornecer aos profissionais envolvidos na reabilitação conhecimento atualizado e recomendações para um melhor cuidado no pós-AVC.
RESUMEN
ABSTRACT The Guidelines for Stroke Rehabilitation are the result of a joint effort by the Scientific Department of Neurological Rehabilitation of the Brazilian Academy of Neurology aiming to guide professionals involved in the rehabilitation process to reduce functional disability and increase individual autonomy. Members of the group participated in web discussion forums with predefined themes, followed by videoconference meetings in which issues were discussed, leading to a consensus. These guidelines, divided into two parts, focus on the implications of recent clinical trials, systematic reviews, and meta-analyses in stroke rehabilitation literature. The main objective was to guide physicians, physiotherapists, speech therapists, occupational therapists, nurses, nutritionists, and other professionals involved in post-stroke care. Recommendations and levels of evidence were adapted according to the currently available literature. Part I discusses topics on rehabilitation in the acute phase, as well as prevention and management of frequent conditions and comorbidities after stroke.
RESUMO As Diretrizes Brasileiras para Reabilitação do AVC são fruto de um esforço conjunto do Departamento Científico de Reabilitação Neurológica da Academia Brasileira de Neurologia com o objetivo de orientar os profissionais envolvidos no processo de reabilitação para a redução da incapacidade funcional e aumento da autonomia dos indivíduos. Membros do grupo acima participaram de fóruns de discussão na web com pré-temas, seguidos de reuniões por videoconferência em que as controvérsias foram discutidas, levando a um consenso. Essas diretrizes, divididas em duas partes, focam as implicações de recentes ensaios clínicos, revisões sistemáticas e metanálises sobre reabilitação do AVC. O objetivo principal é servir de orientação a médicos, fisioterapeutas, fonoaudiólogos, terapeutas ocupacionais, enfermeiros, nutricionistas e demais profissionais envolvidos no cuidado pós-AVC. As recomendações e níveis de evidência foram adaptados de acordo com a literatura disponível atualmente. Aqui é apresentada a Parte I sobre tópicos de reabilitação na fase aguda, prevenção e tratamento de doenças e comorbidades frequentes após o AVC.
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ABSTRACT Objective: to validate the Portuguese version of the Leg Ulcer Measurement Tool regarding construct and reliability. Method: this is a methodological research study. Data collection was conducted between January and July 2019. A total of 105 participants were included for construct validation and internal consistency and, of these, 50 were selected for intra-observer stability. For the analysis of construct validity, factor analysis was performed; for internal consistency, Cronbach's alpha coefficient was calculated, and for stability, the intraclass correlation coefficient. Results: A total of 12items were confirmed for the Brazilian reality, meeting all the theoretical requirements of the factor analysis model. As for the internal consistency (reliability) analysis, the Cronbach's alpha coefficient values (α=0.711) showed that the set of items that make up the scale measures the same characteristics and presents internal consistency. In the global stability analysis (ICC=0.823), the Leg Ulcer Measurement Tool test and retest scores presented good agreement, showing that the adapted scale is stable. Conclusion: the Leg Ulcer Measurement Tool scale adapted to the Portuguese language contains 12 items, with scores varying from 0 to 4 and, thus, produces a score from 0 to 48 points. It presents construct validity analyzed by means of factor analysis and reliability in terms of internal consistency and stability.
RESUMEN Objetivo: validar el constructo y la confiabilidad de la versión en portugués de la escala Leg Ulcer Measurement Tool. Método: investigación metodológica. La recolección de datos tuvo lugar entre enero y julio de 2019. Se incluyó a 105 participantes para la validación del constructo y la consistencia interna y, de ellos, 50 para la estabilidad intraobservador. Para el análisis de validez de constructo, se realizó un análisis factorial; para la consistencia interna, se calculó el coeficiente alfa de Cronbach y, para la estabilidad, el coeficiente de correlación intraclase. Resultados: se confirmaron 12 ítems para la realidad brasileña, cumpliendo con todos los requisitos teóricos del modelo de análisis factorial. En relación con el análisis de la consistencia interna (confiabilidad), los valores del coeficiente alfa de Cronbach (α=0,711) demostraron que el conjunto de ítems que componen la escala mide las mismas características y presenta consistencia interna. En el análisis de la estabilidad global (ICC=0,823), las puntuaciones test-retest de la escala Leg Ulcer Measurement Tool presentaron buena concordancia, demostrando así que la escalaadaptada es estable. Conclusión: la escala Leg Ulcer Measurement Tool adaptada para el idioma portuguéscontiene 12 ítems, con valores de 0 a 4 y, por lo tanto, genera una puntuación que varía entre 0 y 48 puntos. Presenta validez de constructo, la cual se analizó por medio del análisis factorial y confiabilidad en términos de consistencia interna y estabilidad.
RESUMO Objetivo: validar o construto e a confiabilidade da versão em português da escala Leg Ulcer Measurement Tool. Método: trata-se de uma pesquisa metodológica. A coleta de dados foi realizada entre janeiro e julho de 2019. Foram incluídos 105 participantes para a validação de construto e consistência interna e, desses, 50 participantes para a estabilidade intraobservador. Para a análise de validade de construto, foi realizada a análise fatorial; para a consistência interna, foi calculado o coeficiente alfa de Cronbach e para a estabilidade, o coeficiente de correlação intraclasse. Resultados: foram confirmados 12 itens para a realidade brasileira, cumprindo todas as exigências teóricas do modelo da análise fatorial. Quanto à análise da consistência interna (confiabilidade), os valores do coeficiente de alfa de Cronbach (α=0,711) demonstraram que o conjunto de itens que compõem a escala mede as mesmas características e apresenta consistência interna. Na análise da estabilidade global (ICC=0,823), os escores da Leg Ulcer Measurement Tool no teste e reteste apresentaram boa concordância, demonstrando que a escalaadaptada é estável. Conclusão: A escala Leg Ulcer Measurement Tool adaptada para a língua portuguesa contém 12 itens, com pontuação de 0 a 4, e produz, assim, um escore que varia de 0 a 48 pontos. Apresenta validade de construto analisada pela análise fatorial e confiabilidade em termos de consistência interna e estabilidade.
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To investigate whether the addition of human recombinant epidermal growth factor (h-EGF) to 2% carboxymethyl cellulose gel is more effective in diabetic wound healing than standard treatment, a pilot, double-blind, randomized and controlled clinical trial with therapeutic intervention was performed at a university hospital. The sample consisted of 25 patients (14 in the intervention group that used rh-EGF and 11 in the control group that used 2% carboxymethyl cellulose gel). Data were tabulated in SPSS and analysed by intention to treat, without loss or exclusion of participants. Twenty-five subjects participated with a mean age of 60.6 years, a predominance of males in both groups and 100% prevalence of type-2 diabetes. Within 12 weeks, complete wound healing occurred in three ulcers in the intervention group versus one ulcer in the control group. The percent reduction in the wound area was significantly higher in the intervention group than in the control group (p = 0.049). Concerning the types of tissue, an increase in granulation and epithelial tissue and a reduction in exudate levels were observed in both groups. Decreased slough occurred only in the intervention group. No participant experienced serious or local adverse events during the study period. This study shows that h-EGF is effective, with a statistically significant reduction in wound area, improvement of tissue quality, and safe treatment of chronic wounds. In addition, this study demonstrated that blinding of participants during research using h-EGF is feasible.
Asunto(s)
Diabetes Mellitus Tipo 2 , Método Doble Ciego , Factor de Crecimiento Epidérmico , Humanos , Úlcera de la Pierna/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Cicatrización de HeridasRESUMEN
Este estudo teve como objetivo analisar a efetividade clínica do gel contendo fator de crescimento epidérmico recombinante humano (rhEGF) no processo de reparo tecidual de feridas crônicas, comparado com o Gel de Carboximetilcelulose a 2%. Material e Método: Trata-se de um ensaio clínico randomizado, controlado e cego com intervenção terapêutica realizado em um hospital universitário. O período de coleta foi de novembro de 2016 a janeiro de 2018. A amostra foi constituída de 19 pacientes. A randomização foi realizada por meio do software Excel 2010, alocando os participantes de forma aleatória em grupo intervenção (EGF) e controle (Gel de Carboximetilcelulose a 2%). Este estudo foi aprovado pelo Comitê de Ética em Pesquisa da Faculdade de Medicina, sob o protocolo nº 1602.173 de 16 de junho de 2016. Os dados foram analisados no Excel 2010, BioSat 5.0 e SPSS 20.0. Os participantes foram na sua maioria do sexo masculino (74%) com idade média de 62,8 anos. Em relação às doenças de base, associadas a maior parte dos participantes (47%) apresentavam Hipertensão Arterial Sistólica (HAS) e Insuficiência Venosa Crônica (IVC) associada a Diabetes Mellitus. Em relação às características clínicas das feridas, o grupo Intervenção (EGF) apresentou redução da área da ferida estatisticamente significativa (p=0.019) ao longo das 12 semanas de tratamento. Já o grupo Controle apresentou redução da área da ferida, mas não estatisticamente significativa (p=0,216). Ao comparar ambos os tratamentos na consulta 1, 6 e 12, observou-se que não houve diferença estatisticamente significativa na redução da área da lesão (p=o.751). Quanto ao tipo de tecido o grupo Intervenção apresentou aumento dos tecidos de granulação e de epitelização e redução do esfacelo e do exsudato, não sendo estatisticamente significativo. No grupo Controle (Gel de Carboximetilcelulose a 2%) observou-se aumento do tecido de granulação e epitelização e diminuição dos tecidos desvitalizados e do exsudato (p=0.048). Em relação aos aspectos clínicos do exsudato presente no leito da lesão, nas 12 semanas de tratamento ambos os grupos foram estatisticamente significativos. Quanto aos eventos adversos, nenhum dos participantes apresentou eventos adversos graves ou locais como dor de forte intensidade, eczema e prurido, durante o período de seguimento do estudo. Ambos os tratamentos se mostraram seguros e eficazes no tratamento de feridas crônicas, não houve perdas e exclusões de participantes após a randomização
This study aimed at the clinical effectiveness of the gel containing a human recombinant epidermal factor (rhEGF) in the tissue repair process in chronic wounds compared to Gel 2% carboxymethylcellulose. Material and Method: This is a randomized, controlled, controlled clinical trial conducted at a university hospital. The collection period was from November 2016 to January 2018. The date was 19 patients. Randomization was performed using Excel 2010 software, allocating participants randomly into intervention group (EGF) and control (Carboxymethyl Cellulose Gel 2%). This study was orthopedic in the date of 1602.173 of June 16, 2016. Data were published in Excel 2010, BioSat 5.0 and SPSS 20.0. The participants were mostly male (74%) with a mean of 62.8 years. In relation to the underlying diseases, they were associated with Chronic Venous Insufficiency (CVI) associated with Diabetes Mellitus (47%). Regarding clinical units of wounds, the Intervention Group (EGF) decreased in the area of health statistically significant (p = 0.019) over the 12 weeks of treatment. The control group, however, presented a reduction of the wound area, but not statistically significant (p = 0.216). To compare also the treatment at consultation 1, 6 and 12, clarify the ability to reduce the area of the lesion (p = 0,751). Regarding the type of tissue of the series Intervention group, granulation and epithelialization tissues and reduction of the sphincter and the exercise, not being statistically significant. In the control group (Gels Carboxymethylcellulose 2%) was observed increase of granulation tissue and epithelialization and reduction of devitalized tissue and exudate (p = 0.048). Regarding the clinical issues of the present study, there have been 12 weeks of treatment in statistically significant groups. Adverse events, to which adverse events graves or places such as the intensity of time, eczema and itching were submitted during the follow-up period of the study. Both treatments appear to be safe and do not proceed fiercely when there is no loss and exclusion of participants after randomization
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Pie Diabético , Factor de Crecimiento Epidérmico , Úlcera de la Pierna , Cicatrización de HeridasRESUMEN
Objetiva-se descrever o processo de cicatrização de pacientes com úlceras diabéticas tratadas com fator de crescimento epidérmico recombinante humano (rhEGF), e a colonização por Staphylococcus aureus e Pseudomonas aeruginosa. Estudo de casos de pacientes com úlceras diabéticas tratadas com rhEGF acompanhados ambulatorialmente em um hospital universitário. A coleta de dados ocorreu entre abril e agosto de 2017, com a obtenção de características clínicas, incluindo mensuração das áreas e registros fotográficos das lesões, bem como, coleta de material biológico por swab. A análise de dados foi feita por estatística descritiva. O cálculo da taxa apontou 100% de cicatrização no paciente 1 e 30% no paciente 2. Em relação ao tecido presente no leito da ferida, nota-se um aumento do tecido de granulação e epitelização e uma diminuição do tecido de esfacelo. Quanto ao exsudato, houve uma redução na quantidade presente na ferida ao fim do estudo. Não foram observados sinais clínicos de infecção nas feridas, os resultados das análises microbiológicas indicaram que a colonização microbiana por S. aureus e P. aeruginosa manteve-se no paciente 1 e foi minimizada no paciente 2. Concluise que a aplicação do rhEGF foi favorável na cicatrização de úlceras diabéticas e no controle microbiológico
The aim is to describe the healing process of patients with diabetic ulcers treated with recombinant human epidermal growth factor (rhEGF), and colonization by Staphylococcus aureus and Pseudomonas aeruginosa. Case study of patients with diabetic ulcers treated with rhEGF with outpatients in a university hospital. Data collection took place between April and August 2017, obtaining clinical characteristics, including measurement of areas and photographic records of the lesions, as well as collection of biological material by swab. The data analysis was done by descriptive statistics. The calculation of the rate indicated 100% healing in patient 1 and 30% in patient 2. In relation to the tissue present in the wound bed, there is an increase of granulation tissue and epithelization and a decrease of the shedding tissue. As for the exudate, there was reduction in the amount present in the wound at the end of the study. No clinical signs of infection were observed in the wounds. The results of the microbiological analyzes indicated that microbial colonization by S. aureus and P. aeruginosa was maintained in patient 1 and was minimized in patient 2. It concluded that the application of rhEGF was favorable in cicatrization of diabetic ulcers and in microbiological control