烧伤创面感染的当前问题。

D Dodd, H R Stutman
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引用次数: 0

摘要

正如我们所强调的,高风险烧伤儿童烧伤创面感染的诊断可能是困难的,并且取决于高度的怀疑和一致的观察者对烧伤创面部位的日常临床评估。适当的预防措施包括在处理伤口部位时仔细洗手和使用手套,并预防性地使用局部抗菌剂,如SSD霜。伤口治疗应包括常规有力的手术治疗。应每周进行伤口监测培养,以确定定植的紧急情况,并在适当的情况下帮助选择经验性抗菌方案。对于病因不明或感染部位不明的重症患儿,强烈建议进行伤口活检,进行组织学检查和定量培养。如果,尽管采取了这些措施,脓毒症仍然发生,那么必须根据经验开始全身性抗生素治疗,作为外科手术的辅助治疗。在等待血液和伤口活检培养的明确结果时,了解在伤口上定植的微生物将有助于选择抗生素方案。如果没有这些信息,早期烧伤败血症治疗应侧重于革兰氏阳性菌,而后期的感染应引起医院病原体的怀疑,如铜绿假单胞菌、其他肠杆菌和白色念珠菌。初始方案可能包括萘西林加头孢他啶或氨基糖苷,根据前面提到的考虑进行厌氧覆盖。一旦确定了病原体,就必须对治疗方法进行相应的修改。两性霉素B和无环鸟苷的使用应根据烧伤部位的阳性培养以及全身传播的证据进行指导。现有的研究尚未明确经验性免疫疗法静脉注射丙种球蛋白在烧伤儿童中的作用。因此,虽然特异性免疫球蛋白(铜绿假单胞菌,金黄色葡萄球菌)的发展可能在将来证明是有用的,但目前不建议使用它。鉴于可能在烧伤创面上定植的生物的多样性,被动免疫可能在治疗感染方面比在预防感染方面更有用。从铜绿假单胞菌到肺炎克雷伯菌或阴沟杆菌的转换,在大多数情况下都不是特别有益的。同样,对免疫系统在烧伤败血症倾向中的作用的进一步了解可能会指导疫苗或免疫调节剂的开发,从而降低严重烧伤儿童和成人的感染风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current issues in burn wound infections.

As we have emphasized, the diagnosis of burn wound infections in the high-risk burned child can be difficult and depends on a very high degree of suspicion and daily clinical evaluation of the burn wound site by consistent observers. Appropriate precautions include meticulous hand-washing and the use of gloves when handling the wound site and prophylactic application of a topical antibacterial agent such as SSD cream. Wound therapy should include routine vigorous surgical débridement. Surveillance wound cultures should be done weekly to determine the emergency of colonization and aid in the selection of empiric antimicrobial regimens when these are appropriate. Wound biopsy for histological examination and quantitative culture is highly recommended in the severely ill child with an unclear etiology or site of infection. If, despite these measures, sepsis ensues, then systemic antibiotics must be started empirically as an adjuctive therapy to surgical débridement. Knowledge of the organisms colonizing a wound will prove useful in choosing an antibiotic regimen while awaiting definitive results of blood and wound biopsy cultures. Without this information, early burn sepsis therapy should focus on gram-positive organisms, while infection later in the course should raise suspicion of nosocomial pathogens such as P. aeruginosa, other enteric bacilli, and C. albicans. An initial regimen might include nafcillin plus ceftazidime or an aminoglycoside, with anaerobic coverage depending on considerations noted previously. Once the causative agent is identified, therapy must be modified accordingly. Amphotericin B and acyclovir use should be guided by positive cultures from the burn wound site along with systemic evidence of dissemination. Available studies do not yet make clear the role of empiric immunotherapy with intravenous gamma globulin in the burned child. Therefore, its use cannot be recommended at the present time, although the development of specific immunoglobulins (P. aeruginosa, S. aureus) may prove useful in the future. In view of the multiplicity of organisms that may colonize burn wounds, it is likely that passive immunization may be more useful in the treatment of infection than in its prevention. The switch from P. aeruginosa to, for example, Klebsiella pneumoniae or E. cloacae, is not apt to be particularly beneficial in most circumstances. Similarly, an increased understanding of the role of the immune system in the propensity to burn sepsis may guide the development of vaccines or immunomodulators that decrease the risk of infection in seriously burned children and adults.

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