糖尿病足发作:糖尿病患者严重脓毒症的处理。

Kisshan Raj Balakrishnan, Dharshanan Raj Selva Raj, Sabyasachi Ghosh, Gregory Aj Robertson
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引用次数: 0

摘要

糖尿病足发作(DFA)是糖尿病足病最严重的表现,患者通常表现为严重的败血症,可危及肢体或生命。DFA可分为两大类:典型和非典型。典型的DFA继发于足部严重感染,通常由皮肤完整性的轻微破坏引起,使病原体进入并增殖。由于神经病变、微血管疾病和高血糖等潜在的糖尿病病理生理,这种形式往往进展迅速,从而促进感染扩散和组织坏死。这种形式的DFA可以表现为许多严重的感染病理之一,包括化脓性炎、坏死性筋膜炎和肌坏死,所有这些都可以导致全身性败血症和多器官衰竭。然而,非典型DFA主要不是由感染引起的。它可继发于缺血或沙氏关节病。典型DFA的治疗包括及时诊断、积极控制感染和多学科联合治疗。治疗可以根据当前国际糖尿病足工作组/美国传染病学会糖尿病足感染指南,以及英国骨科足和踝关节学会血管学会联合指南进行指导。本文强调了早期识别、综合管理策略的重要性,以及进一步研究建立标准化方案和改善DFA患者临床结果的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diabetic foot attack: Managing severe sepsis in the diabetic patient.

Diabetic foot attack (DFA) is the most severe presentation of diabetic foot disease, with the patient commonly displaying severe sepsis, which can be limb or life threatening. DFA can be classified into two main categories: Typical and atypical. A typical DFA is secondary to a severe infection in the foot, often initiated by minor breaches in skin integrity that allow pathogens to enter and proliferate. This form often progresses rapidly due to the underlying diabetic pathophysiology of neuropathy, microvascular disease, and hyperglycemia, which facilitate infection spread and tissue necrosis. This form of DFA can present as one of a number of severe infective pathologies including pyomyositis, necrotizing fasciitis, and myonecrosis, all of which can lead to systemic sepsis and multi-organ failure. An atypical DFA, however, is not primarily infection-driven. It can occur secondary to either ischemia or Charcot arthropathy. Management of the typical DFA involves prompt diagnosis, aggressive infection control, and a multidisciplinary approach. Treatment can be guided by the current International Working Group on the Diabetic Foot/Infectious Diseases Society of America guidelines on diabetic foot infections, and the combined British Orthopaedic Foot and Ankle Society-Vascular Society guidelines. This article highlights the importance of early recognition, comprehensive management strategies, and the need for further research to establish standardized protocols and improve clinical outcomes for patients with DFA.

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