Revista Brasileira de Ortopedia (Aug 2007)
O efeito do laser de baixa energia no crescimento bacteriano "in vitro" Low level laser effect in "in vitro" bacterial growth
Abstract
OBJETIVO: Avaliar, por meio de estudo bacteriológico in vitro, o efeito de dois tipos de laser de baixa energia (LBE) sobre diferentes populações bacterianas habitualmente presentes em feridas pós-traumáticas. MÉTODOS: Foram colhidos swabs diretamente do sítio de infecção de pacientes internados com osteomielite pós-traumática crônica. As bactérias isoladas foram Acinetobacter baumanii complex, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonela sp, Serratia sp e Staphylococcus aureus. O material coletado foi semeado em meio ágar-sangue, através de alça estéril, utilizando-se 30 placas de Petri para cada germe. Foram utilizados dois aparelhos de LBE: Ibramed Laser Pulse #01189, com 15W/904nm por 200 segundos, e Phisiolux dual Bioset #9909001, com 20W/904nm por 230 segundos. Nos grupos I (n = 10) e II (n = 10), as bactérias sofreram irradiação pelo laser. O grupo III (n = 10) serviu de controle, não sendo irradiado. As bactérias dos grupos I e II foram irradiadas em câmara de fluxo laminar, previamente esterilizada por raio ultravioleta. O laser foi administrado de forma direta, central e perpendicularmente à superfície de cultivo das bactérias, com distância-padrão de 1cm, através de orifício confeccionado na tampa das placas. O crescimento bacteriano foi analisado após 12 e 24 horas da irradiação. Os resultados foram processados estatisticamente, utilizando-se o teste não-paramétrico de Kruskall-Wallis, com nível de significância p OBJECTIVE: To perform an in vitro bacteriologic study to evaluate the effect of two types of low level laser (LLL) on different bacterial populations usually present in post-traumatic wounds. METHODS: Swabs were prepared directly at the infection site of patients hospitalized with chronic post-traumatic osteomyelitis. Isolated bacteria were Acinetobacter baumanii complex, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonela sp, Serratia sp, and Staphylococcus aureus. The material collected was seeded in agar-blood medium with a sterile loop, using 30 Petri dishes for each germ. Two LLL devices were used: Ibramed Laser Pulse #01189, with 15W/904nm for 200 seconds, and Phisiolux dual Bioset #9909001, with 20W/904nm for 230 seconds. In groups I (n = 10) and II (n = 10), bacteria were irradiated with laser. Group III (n = 10) was the control group and was not irradiated. Bacteria in groups I and II were submitted to radiation in a laminar flow chamber that was previously sterilized with UV rays, and the laser was directly, centrally, and perpendicularly applied to the bacteria cultivation surface, from a standard distance of one centimeter, through an orifice made in the lid of the dishes. Bacterial growth was analyzed 12 and 24 hours after the irradiation. Results were statistically processed using the non-parametric test of Kruskall-Wallis, with a significance level p < 5%. RESULTS: A similar behavior was seen in the bacterial population of the three groups studied after 12 and 24 hours of irradiation with the two types of LLL, and there was no statistically significant difference in the bacterial growth between groups I and II and between these two groups and group III (control). CONCLUSION: In the conditions of this study, the effect of LLL showed to be innocuous for the increase in the number of units forming bacterial colonies, in the doses used in this study, as an adjuvant for the wound healing process, even under contamination by the bacteria being evaluated.
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