战场上适宜的外用抗菌药物预防大鼠烧伤创面脓毒症的比较。

David S Kauvar, Eric Acheson, Joanna Reeder, Kristin Roll, David G Baer
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引用次数: 18

摘要

局部抗菌素治疗有可能限制受污染战场伤害的死亡率和发病率。许多可用的特工都不适合在战场上使用;然而,醋酸马菲尼德溶液(MAS)作为烧伤敷料的辅助治疗已经被证实有效,并且先前的研究表明马菲尼德作为一种直接的化疗药物是有希望的。71只雄性Sprague-Dawley大鼠接受20% TBSA全层烫伤。伤口接种含有每毫升铜绿假单胞菌1244 (ATCC 27317) 1 × 10菌落形成单位的溶液。采用10%醋酸马夫尼特乳膏(MAC)、5% MAS、5%盐酸马夫尼特溶液(MHS)和4%葡萄糖酸氯己定溶液(CHG)进行处理。每日直接涂抹于创面,连用10天。对动物进行了21天的监测,如果它们因败血症而表现出垂死状态,就对它们实施安乐死。阴性对照组(未治疗)至研究完成的生存率为25%(3/12)。阳性对照组(MAC)生存率为100%。与未治疗的对照组相比,没有一个试验组表现出显著的生存率;MAS为5/12(42%)生存率(P = 0.67), CHG为4/12(33%)生存率(P = 1.0), MHS为2/12(17%)生存率(P = 1.0)。第1天各组体重无显著差异。到第6天,与MAC组相比,所有试验剂组的体重都明显偏轻。这种趋势随着体重过轻的动物死亡而消失。当我们使用这些药物时,我们没有证明这些药物对伤口败血症的显著预防作用。这些技术不应取代现有的烧伤护理。水性直接外用抗菌剂比面霜和敷料在战场上使用具有后勤优势,并且应该继续寻找在受伤点或附近使用的战场便利剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of battlefield-expedient topical antimicrobial agents for the prevention of burn wound sepsis in a rat model.

Topical antimicrobial therapy has the potential to limit the mortality and morbidity of contaminated battlefield injuries. Many agents available are ill-suited for use on the battlefield; however, mafenide acetate solution (MAS) has known efficacy as a burn dressing adjunct, and previous work with mafenide as a direct chemotherapeutic has shown promise. A total of 71 male Sprague-Dawley rats underwent a 20% TBSA full-thickness scald. Wounds were inoculated with a solution containing 1 x 10 colony-forming units per milliliter of Pseudomonas aeruginosa 1244 (ATCC 27317). Treatments with 10% mafenide acetate cream (MAC), 5% MAS, 5% mafenide hydrochloride solution (MHS), and 4% chlorhexidine gluconate solution (CHG) were established. Agents were applied directly to the wound daily for 10 days. Animals were monitored for 21 days and euthanized if they manifested a moribund state as a result of sepsis. Survival to study completion in the negative control group (no treatment) was 25% (3/12). Survival in the positive control group (MAC) was 100%. None of the test agent groups demonstrated significant survival over the untreated controls; MAS resulted in 5/12 (42%) survival (P = .67), CHG in 4/12 (33%) survival (P = 1.0), and MHS resulted in 2/12 (17%) survival (P = 1.0). There were no significant differences in group weights on day 1. By day 6, all test agent groups were significantly underweight compared with the MAC group. This trend resolved as underweight animals died. We did not demonstrate significant prevention of wound sepsis with these agents as we used them. These techniques should not be substituted for established burn care. Aqueous direct topical antimicrobial agents have logistical advantages over creams and dressing soaks for field use, and the search for a battlefield-expedient agent for use at or near the point of wounding should continue.

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