Department of Surgery, University of Cincinnati, Cincinnati, OH 45267-0558, USA.
United States Air Force School of Aerospace Medicine, En Route Care Training Department, University of Cincinnati, Cincinnati, OH 45267-0558, USA.
Mil Med. 2023 Nov 8;188(Suppl 6):295-303. doi: 10.1093/milmed/usad113.
Negative pressure wound therapy (NPWT) is utilized early after soft tissue injury to promote tissue granulation and wound contraction. Early post-injury transfers via aeromedical evacuation (AE) to definitive care centers may actually induce wound bacterial proliferation. However, the effectiveness of NPWT or instillation NPWT in limiting bacterial proliferation during post-injury AE has not been studied. We hypothesized that instillation NPWT during simulated AE would decrease bacterial colonization within simple and complex soft tissue wounds.
The porcine models were anesthetized before any experiments. For the simple tissue wound model, two 4-cm dorsal wounds were created in 34.9 ± 0.6 kg pigs and were inoculated with Acinetobacter baumannii (AB) or Staphylococcus aureus 24 hours before a 4-hour simulated AE or ground control. During AE, animals were randomized to one of the five groups: wet-to-dry (WTD) dressing, NPWT, instillation NPWT with normal saline (NS-NPWT), instillation NPWT with Normosol-R® (NM-NPWT), and RX-4-NPWT with the RX-4 system. For the complex musculoskeletal wound, hind-limb wounds in the skin, subcutaneous tissue, peroneus tertius muscle, and tibia were created and inoculated with AB 24 hours before simulated AE with WTD or RX-4-NPWT dressings. Blood samples were collected at baseline, pre-flight, and 72 hours post-flight for inflammatory cytokines interleukin (IL)-1β, IL-6, IL-8 and tumor necrosis factor alpha. Wound biopsies were obtained at 24 hours and 72 hours post-flight, and the bacteria were quantified. Vital signs were measured continuously during simulated AE and at each wound reassessment.
No significant differences in hemodynamics or serum cytokines were noted between ground or simulated flight groups or over time in either wound model. Simulated AE alone did not affect bacterial proliferation compared to ground controls. The simple tissue wound arm demonstrated a significant decrease in Staphylococcus aureus and AB colony-forming units at 72 hours after simulated AE using RX-4-NPWT. NS-NPWT during AE more effectively prevented bacterial proliferation than the WTD dressing. There was no difference in colony-forming units among the various treatment groups at the ground level.
The hypoxic, hypobaric environment of AE did not independently affect the bacterial growth after simple tissue wound or complex musculoskeletal wound. RX-4-NPWT provided the most effective bacterial reduction following simulated AE, followed by NS-NPWT. Future research will be necessary to determine ideal instillation fluids, negative pressure settings, and dressing change frequency before and during AE.
负压伤口治疗(NPWT)在软组织损伤后早期使用,以促进组织肉芽形成和伤口收缩。通过航空医疗后送(AE)在受伤后早期转移到确定性治疗中心实际上可能会导致伤口细菌增殖。然而,NPWT 或灌洗 NPWT 在限制受伤后 AE 期间细菌增殖方面的有效性尚未得到研究。我们假设,在模拟 AE 期间进行灌洗 NPWT 会减少简单和复杂软组织伤口内的细菌定植。
在进行任何实验之前,对猪模型进行麻醉。对于简单组织伤口模型,在 34.9±0.6kg 猪中创建了两个 4cm 的背部伤口,并在 4 小时模拟 AE 或地面对照前 24 小时接种鲍曼不动杆菌(AB)或金黄色葡萄球菌。在 AE 期间,动物随机分为五组之一:湿对干(WTD)敷料、NPWT、用生理盐水(NS-NPWT)灌洗 NPWT、用 Normosol-R®(NM-NPWT)灌洗 NPWT 和用 RX-4-NPWT 进行 RX-4 系统。对于复杂的肌肉骨骼伤口,在皮肤、皮下组织、腓骨第三肌和胫骨上创建后腿伤口,并在模拟 AE 前 24 小时用 WTD 或 RX-4-NPWT 敷料接种 AB。在飞行前和飞行后 72 小时采集血液样本,用于炎症细胞因子白细胞介素(IL)-1β、IL-6、IL-8 和肿瘤坏死因子 alpha。在飞行后 24 小时和 72 小时获取伤口活检,并定量细菌。在模拟 AE 期间和每次伤口重新评估时连续测量生命体征。
在地面或模拟飞行组之间或在两种伤口模型中均未观察到血流动力学或血清细胞因子的显著差异。与地面对照组相比,单纯 AE 本身并不影响细菌增殖。与地面水平相比,在使用 RX-4-NPWT 的模拟 AE 后 72 小时,简单组织伤口的金黄色葡萄球菌和 AB 菌落形成单位显著减少。AE 期间使用 NS-NPWT 比 WTD 敷料更有效地防止细菌增殖。在 AE 期间,不同治疗组之间的菌落形成单位没有差异。
AE 的低氧、低气压环境不会独立影响简单组织伤口或复杂肌肉骨骼伤口后的细菌生长。在模拟 AE 后,RX-4-NPWT 提供了最有效的细菌减少,其次是 NS-NPWT。在 AE 之前和期间,需要进一步研究确定理想的灌洗液、负压设置和敷料更换频率。