Colchicine to Reduce Atrial Fibrillation in the Postoperative Period of Myocardial Revascularization / Colchicina para Redução de Fibrilação Atrial em Pós-Operatório de Revascularização Miocárdica

Abstract Background: The high prevalence of atrial fibrillation (AF) in the postoperative period of myocardial revascularization surgery increases morbidity and mortality. Objective: To assess the efficacy of colchicine to prevent AF in the postoperative period of myocardial revascularization surgery, the impact of AF on hospital length of stay and death, and to identify its risk factors. Methods: Between May 2012 and November 2013, 140 patients submitted to myocardial revascularization surgery were randomized, 69 to the control group and 71 to the colchicine group. Colchicine was used at the dose of 1 mg orally, twice daily, preoperatively, and of 0.5 mg, twice daily, until hospital discharge. A single dose of 1 mg was administered to those admitted 12 hours or less before surgery. Results: The primary endpoint was AF rate in the postoperative period of myocardial revascularization surgery. Colchicine group patients showed no reduction in AF incidence as compared to control group patients (7.04% versus 13.04%, respectively; p = 0.271). There was no statistically significant difference between the groups regarding death from any cause rate (5.6% versus 10.1%; p = 0,363) and hospital length of stay (14.5 ± 11.5 versus 13.3 ± 9.4 days; p = 0.490). However, colchicine group patients had a higher infection rate (26.8% versus 8.7%; p = 0.007). Conclusion: The use of colchicine to prevent AF after myocardial revascularization surgery was not effective in the present study. Brazilian Registry of Clinical Trials number RBR-556dhr.

Resumo Fundamento: A alta prevalência de fibrilação atrial (FA) no pós-operatório de cirurgia de revascularização miocárdica ocasiona maior morbidade e mortalidade. Objetivos: Avaliar a eficácia da colchicina como profilaxia para FA no pós-operatório de cirurgia de revascularização miocárdica, o impacto da FA sobre o tempo de internação hospitalar e óbito e identificar fatores de risco para o seu aparecimento. Métodos: Entre maio de 2012 e novembro de 2013, 140 pacientes submetidos à cirurgia de revascularização miocárdica foram randomizados, 69 no grupo controle e 71 no grupo colchicina. A colchicina foi utilizada na dose de 1 mg via oral, duas vezes ao dia, no pré-operatório, e 0,5 mg, duas vezes ao dia, até a alta hospitalar. Dose única de 1 mg foi administrada aos internados 12 horas ou menos antes da cirurgia. Resultados: O desfecho primário foi a taxa de FA no pós-operatório de cirurgia de revascularização miocárdica. Os pacientes do grupo colchicina não apresentaram redução na incidência de FA em comparação aos do grupo controle (7,0% versus 13,0%, respectivamente; p = 0,271). Não houve diferença estatisticamente significativa entre os grupos em relação à taxa de óbito por qualquer causa (5,6% versus 10,1%; p = 0,363) e ao tempo de internação (14,5 ± 11,5 versus 13,3 ± 9,4 dias; p = 0,490). Porém, o grupo colchicina apresentou maior taxa de infecção (26,8% versus 8,7%; p = 0,007). Conclusões: O uso da colchicina para profilaxia da FA no pós-operatório de revascularização miocárdica não se mostrou eficaz neste estudo. Registro Brasileiro de Ensaios Clínicos número RBR-556dhr.

Colchicine to Reduce Atrial Fibrillation in the Postoperative Period of Myocardial Revascularization.

BACKGROUND: The high prevalence of atrial fibrillation (AF) in the postoperative period of myocardial revascularization surgery increases morbidity and mortality. OBJECTIVE: To assess the efficacy of colchicine to prevent AF in the postoperative period of myocardial revascularization surgery, the impact of AF on hospital length of stay and death, and to identify its risk factors. METHODS: Between May 2012 and November 2013, 140 patients submitted to myocardial revascularization surgery were randomized, 69 to the control group and 71 to the colchicine group. Colchicine was used at the dose of 1 mg orally, twice daily, preoperatively, and of 0.5 mg, twice daily, until hospital discharge. A single dose of 1 mg was administered to those admitted 12 hours or less before surgery. RESULTS: The primary endpoint was AF rate in the postoperative period of myocardial revascularization surgery. Colchicine group patients showed no reduction in AF incidence as compared to control group patients (7.04% versus 13.04%, respectively; p = 0.271). There was no statistically significant difference between the groups regarding death from any cause rate (5.6% versus 10.1%; p = 0,363) and hospital length of stay (14.5 ± 11.5 versus 13.3 ± 9.4 days; p = 0.490). However, colchicine group patients had a higher infection rate (26.8% versus 8.7%; p = 0.007). CONCLUSION: The use of colchicine to prevent AF after myocardial revascularization surgery was not effective in the present study. Brazilian Registry of Clinical Trials number RBR-556dhr.

Evaluation of topical metronidazole in the healing wounds process: an experimental study.

OBJECTIVE: To assess the efficacy of a topical 4% metronidazole solution in wound healing by secondary intention in rats. METHODS: We made circular wounds two inches in diameter at the back of rats and studied healing at 3, 7, 14 and 21 days. The wound contraction and epithelialization were assessed by peripheral digital planimetry and myofibroblasts by immunohistochemistry with a-SMA. RESULTS: There was no difference between groups regarding wound contraction. In wounds treated with metronidazole peripheral epithelialization was evident early on day 3 (p <0.001) and there were no differences in other periods. In the control group, the number of myofibroblasts was higher on day 7 (p = 0.003) and day 14 (p = 0.001) and in the experimental group it was suggestively higher on day 3 (p = 0.06). CONCLUSION: Metronidazole 4% solution at a dose of 50 mg/kg applied topically to wounds healing by secondary intention facilitates early peripheral epithelialization, does not interfere with wound contraction and delays the appearance of myofibroblasts.

Avaliação do uso tópico do metronidazol no processo de cicatrização de feridas: um estudo experimental / Evaluation of topical metronidazole in the healing wounds process: an experimental study

OBJETIVO: Avaliar a ação do metronidazol em solução a 4 por cento, tópico, em feridas com cicatrização por segunda intenção em ratos. MÉTODOS: Fez-se feridas circulares com dois centímetros de diâmetro no dorso de ratos e estudou-se a cicatrização em 3, 7, 14 e 21 dias. A contração da ferida e a epitelização periférica foram avaliadas por planimetria digital e os miofibroblastos pela imunoistoquímica com a-SMA. RESULTADOS: Não houve diferença entre os grupos em relação à contração ferida. Nas feridas tratadas com metronidazol a epitelização periférica precoce foi evidente no 3°dia (p<0,001) e não houve diferenças nos demais períodos. No grupo controle, o número de miofibroblastos foi maior no 7° dia (p=0,003) e no 14° dia (p=0,001), e no grupo experimento, foi sugestivamente maior no 3° dia (p=0,06). CONCLUSÃO: O metronidazol, solução a 4 por cento, na dose de 50mg/kg/dia, aplicado de forma tópica nas feridas com cicatrização por segunda intenção, facilita a epitelização periférica precoce, não interfere na contração da ferida e atrasa o aparecimento dos miofibroblastos.

OBJECTIVE: To assess the efficacy of topical a 4 percent metronidazole solution in wounds healing by secondary intention in rats. METHODS: We made circular wounds two inches in diameter at the back of rats and studied healing at 3, 7, 14 and 21 days. The wound contraction and epithelialization were assessed by peripheral digital planimetry and myofibroblasts by immunohistochemistry with a-SMA. RESULTS: There was no difference between groups regarding wound contraction. In wounds treated with metronidazole peripheral epithelialization was evident early on day 3 (p <0.001) and there were no differences in other periods. In the control group, the number of myofibroblasts was higher on day 7 (p = 0.003) and day 14 (p = 0.001) and in the experimental group it was suggestively higher on day 3 (p = 0.06). CONCLUSION: Metronidazole 4 percent solution at a dose of 50 mg/kg applied topically to wounds healing by secondary intention facilitates early peripheral epithelialization, does not interfere with wound contraction and delays the appearance of myofibroblasts.