Hsieh T, Samson L M, Jabbour M, Osmond M H
Faculty of Medicine, Queen's University, Kingston, Ont.
CMAJ. 2000 Aug 22;163(4):393-6.
Early recognition and treatment are important factors that can help improve survival following necrotizing fasciitis. However, early recognition is complicated by the difficulty in distinguishing the infection from other, less serious soft-tissue infections such as cellulitis. We reviewed the charts of children presenting with necrotizing fasciitis at a tertiary care pediatric hospital in Ontario to document potential increases in the frequency of cases and to identify clinical and laboratory features that could help distinguish between necrotizing fasciitis and cellulitis.
Necrotizing fasciitis was defined as a soft-tissue infection characterized by necrosis of subcutaneous tissue and confirmed at surgery or on pathological examination. A retrospective chart review was conducted to identify cases of necrotizing fasciitis that occurred between June 1, 1983, and May 31, 1999. The characteristics of the identified cases, their clinical manifestations and the laboratory features at presentation were compared with those of matched controls admitted to the hospital with cellulitis.
In total, 8 cases of necrotizing fasciitis were identified during the study period. There were no cases from 1983 to 1987, 1 from 1988 to 1991, 1 from 1992 to 1995, and 6 cases from 1996 to 1999. Compared with the children who had cellulitis, those who had necrotizing fasciitis were more likely to present with a generalized erythematous rash (odds ratio [OR] 11.0; 95% confidence interval [CI] 1.5-81.6) and a toxic appearance (OR 23.0; 95% CI 2.0-262.5). They were also more likely than the children with cellulitis to have a history of fever (8/8 v. 10/24, p = 0.004), a higher temperature (mean 38.7 degrees C v. 37.8 degrees C, p = 0.006), a higher respiratory rate (mean 31.5 v. 25.4 breaths/min, p = 0.02) and a lower platelet count on presentation (mean 194.0 v. 299.3 x 10(9)/L, p = 0.03).
On presentation, factors that may help distinguish necrotizing fasciitis from cellulitis include a generalized erythematous rash, toxic appearance, fever and low platelet count.
早期识别和治疗是有助于改善坏死性筋膜炎患者生存率的重要因素。然而,由于难以将该感染与其他不太严重的软组织感染(如蜂窝织炎)区分开来,早期识别变得复杂。我们回顾了安大略省一家三级护理儿科医院中患有坏死性筋膜炎的儿童病历,以记录病例频率的潜在增加情况,并确定有助于区分坏死性筋膜炎和蜂窝织炎的临床和实验室特征。
坏死性筋膜炎被定义为一种以皮下组织坏死为特征的软组织感染,并经手术或病理检查确诊。进行了一项回顾性病历审查,以确定1983年6月1日至1999年5月31日期间发生的坏死性筋膜炎病例。将确诊病例的特征、临床表现和就诊时的实验室特征与因蜂窝织炎入院的匹配对照组进行比较。
在研究期间共确定了8例坏死性筋膜炎病例。1983年至1987年无病例,1988年至1991年有1例,1992年至1995年有1例,1996年至1999年有6例。与患有蜂窝织炎的儿童相比,患有坏死性筋膜炎的儿童更有可能出现全身性红斑疹(优势比[OR]11.0;95%置信区间[CI]1.5 - 81.6)和中毒面容(OR 23.0;95%CI 2.0 - 262.5)。他们也比患有蜂窝织炎的儿童更有可能有发热史(8/8对10/24,p = 0.004)、更高的体温(平均38.7摄氏度对37.8摄氏度,p = 0.006)、更高的呼吸频率(平均31.5对25.4次/分钟,p = 0.02)以及就诊时更低的血小板计数(平均194.0对299.3×10⁹/L,p = 0.03)。
就诊时,可能有助于区分坏死性筋膜炎和蜂窝织炎的因素包括全身性红斑疹、中毒面容、发热和低血小板计数。