1. A Randomized Comparison Study of Lyophilized Nile Tilapia Skin and Silver-Impregnated Sodium Carboxymethylcellulose for the Treatment of Superficial Partial-Thickness Burns.
- Author
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Júnior, Edmar Maciel Lima, Filho, Manoel Odorico de Moraes, Costa, Bruno Almeida, Fechine, Francisco Vagnaldo, Rocha, Marina Becker Sales, Vale, Mariana Lima, Diógenes, Ana Kely de Loyola, Uchôa, Alex Marques do Nascimento, Júnior, Francisco Raimundo Silva, Martins, Camila Barroso, Bandeira, Tereza de Jesus Pinheiro Gomes, Rodrigues, Felipe Augusto Rocha, Paier, Carlos Roberto Koscky, Moraes, Maria Elisabete Amaral de, Lima Júnior, Edmar Maciel, de Moraes Filho, Manoel Odorico, Silva Júnior, Francisco Raimundo, and de Moraes, Maria Elisabete Amaral
- Subjects
NILE tilapia ,CARBOXYMETHYLCELLULOSE ,DRUG efficacy ,SODIUM ,BIOLOGICAL dressings ,SKIN ,SURGICAL dressings ,PAIN ,PAIN tolerance ,TREATMENT for burns & scalds ,PILOT projects ,WOUND healing ,RESEARCH ,PAIN measurement ,ARTIFICIAL skin ,ANALGESICS ,BURNS & scalds ,RESEARCH methodology ,MEDICAL cooperation ,EVALUATION research ,COMPARATIVE studies ,RANDOMIZED controlled trials ,FISHES ,CELLULOSE ,SILVER ,LONGITUDINAL method - Abstract
Glycerolized Nile tilapia skin (NTS) showed promising results when used for burn treatment in phases II and III randomized controlled trials. This pilot study aims to evaluate the effectiveness of lyophilized NTS (LNTS) as a temporary skin substitute for superficial partial-thickness burns by comparing it with silver-impregnated sodium carboxymethylcellulose dressing. This was a randomized, prospective, open-label, and controlled pilot study conducted in Fortaleza, Brazil, from April 2019 to December 2019. The 24 participants had ≥18 and ≤70 years of age and superficial partial-thickness burns affecting up to 10% of TBSA. Primary outcomes were the number of dressings performed and pain intensity, assessed via the Visual Analogue Scale and the Electronic von Frey. Secondary outcomes were the level of pain-related anxiety, assessed via the Burns Specific Pain Anxiety Scale, and analgesic consumption. In the test group, the number of dressings and the patient-reported pain after dressing-related procedures were lower. Analgesic intake, pain-related anxiety, and both patient-reported and objectively measured pain before dressing-related procedures were similar for the treatment groups. No adverse effects were detected. LNTS shares the same characteristics of an "'ideal'" wound dressing demonstrated by glycerolized NTS in previous studies. Also, it demonstrated noninferiority for burn management when compared with silver-impregnated sodium carboxymethylcellulose dressing. The safety and efficacy of LNTS demonstrated in this pilot study may allow the development of larger phases II and III RCTs in a near future. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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