开放性和闭合性骨折后的深度感染。

Michael Polmear,Jennifer E Hagen,Gregory M Schrank,Marilyn Heng,Francesc A Marcano-Fernández,Kyle J Jeray,Mark J Gage,Gerard P Slobogean,Sheila Sprague,Terrie Vasilopoulos,
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Significance was set at p < 0.05.\r\n\r\nRESULTS\r\nAmong the 2 primary studies, a total of 484 cases (defined as an anatomic fracture area; some patients had multiple fractures, which were each defined as a case if they developed an infection) had culture samples taken from deep or organ tissue. The culture positivity rate was 96.7% (95% CI, 94.7% to 98.0% [468 of 484 cases]). There were no significant differences (p = 0.507) in culture positivity between open fractures (97.2% [95% CI, 94.5% to 98.6%]; 273 of 281 cases) and closed fractures (96.1% [95% CI, 92.4% to 98.0%]; 195 of 203 cases). There was information on microbial species in 84.4% (395) of 468 cases. For patients with positive cultures, 43.3% (171 of 395 cases) were polymicrobial infections. Open fractures (47.8% [111 of 232 cases]), compared with closed fractures (36.8% [60 of 163 cases]), were more likely to be polymicrobial (p = 0.029). Staphylococcus aureus microbes (methicillin-sensitive S. aureus, methicillin-resistant S. aureus, and coagulase-negative S. aureus) accounted for 43.3% (462 of 1,066) of all positive cultures. The median time to infection was 58.5 days (95% CI, 49.0 to 67.0 days). The median time to infection was not significantly different in cases of open fractures (61.0 days [95% CI, 51.0 to 71.0 days]) compared with closed fractures (54.0 days [95% CI, 43.0 to 67.0 days]) (hazard ratio [HR], 0.92 [95% CI, 0.72 to 1.12]). SSIs associated with gram-negative bacteria had a shorter median time to infection at 46.0 days (95% CI, 36.0 to 58.0 days) compared with SSIs not associated with gram-negative bacteria at 70.0 days (95% CI, 56.0 to 88.0 days) (HR, 1.79 [95% CI, 1.55 to 2.03]). 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引用次数: 0

摘要

本研究的目的是描述来自PREP-IT调查员的prep和水- prep研究中手术部位感染(SSI)患者的培养和物种形成结果。方法收集疑似SSI患者的深层或器官组织样本进行培养。培养阳性率以百分数和精确的二项95%置信区间(CI)估计。微生物种类以百分比报告。采用比例z检验对开放骨折和闭合骨折进行比较。p < 0.05为显著性。结果在2项初步研究中,共有484例(定义为解剖性骨折区;一些患者有多处骨折,如果他们发生了感染,每一个都被定义为一个病例),培养样本取自深部或器官组织。培养阳性率为96.7% (95% CI, 94.7% ~ 98.0%[484例中468例])。开放性骨折患者的培养阳性差异无统计学意义(p = 0.507) (97.2% [95% CI, 94.5% ~ 98.6%];281例中273例)和闭合性骨折(96.1% [95% CI, 92.4% ~ 98.0%];203例中的195例)。468例患者中有395例(84.4%)有微生物种类信息。在395例培养阳性患者中,43.3%(171例)为多微生物感染。开放性骨折(47.8%[232例中的111例])比闭合性骨折(36.8%[163例中的60例])更容易出现多微生物(p = 0.029)。金黄色葡萄球菌微生物(甲氧西林敏感金黄色葡萄球菌、耐甲氧西林金黄色葡萄球菌和凝固酶阴性金黄色葡萄球菌)占所有阳性培养物的43.3%(1066例中有462例)。感染的中位时间为58.5天(95% CI, 49.0 ~ 67.0天)。开放性骨折的中位感染时间(61.0天[95% CI, 51.0 ~ 71.0天])与闭合性骨折(54.0天[95% CI, 43.0 ~ 67.0天])相比无显著差异(风险比[HR], 0.92 [95% CI, 0.72 ~ 1.12])。与革兰氏阴性菌相关的ssi相比,与革兰氏阴性菌相关的ssi感染的中位时间较短,为46.0天(95% CI, 36.0至58.0天),而与革兰氏阴性菌无关的ssi感染的中位时间为70.0天(95% CI, 56.0至88.0天)(HR, 1.79 [95% CI, 1.55至2.03])。与单微生物感染患者(78.6天[95% CI, 57.2至86.8天])相比,多微生物感染患者的中位感染时间(47.0天[95% CI, 38.8至52.1天])也更短(HR, 1.26 [95% CI, 1.03至1.49])。结论SSI患者组织标本微生物培养率高。开放性骨折中革兰氏阴性菌比例较高。革兰氏阴性感染也与早期感染有关。临床医生应该毫不犹豫地为疑似SSI的患者采集深层组织培养样本,并应做好应对多种微生物感染的准备。证据等级:诊断性三级。有关证据水平的完整描述,请参见作者说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Infections After Open and Closed Fractures.
BACKGROUND The purpose of this study was to describe the culture and speciation results of patients with surgical site infection (SSI) from the PREPARE and Aqueous-PREP studies from the PREP-IT Investigators. METHODS Patients with suspected SSI underwent collection of deep or organ tissue samples for culture. The culture positivity rate was estimated as a percentage along with the exact binomial 95% confidence interval (CI). Microbial species were reported as percentages. Comparisons between open and closed fractures were conducted with the Z-test for proportions. Significance was set at p < 0.05. RESULTS Among the 2 primary studies, a total of 484 cases (defined as an anatomic fracture area; some patients had multiple fractures, which were each defined as a case if they developed an infection) had culture samples taken from deep or organ tissue. The culture positivity rate was 96.7% (95% CI, 94.7% to 98.0% [468 of 484 cases]). There were no significant differences (p = 0.507) in culture positivity between open fractures (97.2% [95% CI, 94.5% to 98.6%]; 273 of 281 cases) and closed fractures (96.1% [95% CI, 92.4% to 98.0%]; 195 of 203 cases). There was information on microbial species in 84.4% (395) of 468 cases. For patients with positive cultures, 43.3% (171 of 395 cases) were polymicrobial infections. Open fractures (47.8% [111 of 232 cases]), compared with closed fractures (36.8% [60 of 163 cases]), were more likely to be polymicrobial (p = 0.029). Staphylococcus aureus microbes (methicillin-sensitive S. aureus, methicillin-resistant S. aureus, and coagulase-negative S. aureus) accounted for 43.3% (462 of 1,066) of all positive cultures. The median time to infection was 58.5 days (95% CI, 49.0 to 67.0 days). The median time to infection was not significantly different in cases of open fractures (61.0 days [95% CI, 51.0 to 71.0 days]) compared with closed fractures (54.0 days [95% CI, 43.0 to 67.0 days]) (hazard ratio [HR], 0.92 [95% CI, 0.72 to 1.12]). SSIs associated with gram-negative bacteria had a shorter median time to infection at 46.0 days (95% CI, 36.0 to 58.0 days) compared with SSIs not associated with gram-negative bacteria at 70.0 days (95% CI, 56.0 to 88.0 days) (HR, 1.79 [95% CI, 1.55 to 2.03]). There was also a shorter median time to infection for patients with polymicrobial infections (47.0 days [95% CI, 38.8 to 52.1 days]) compared with patients with monomicrobial infections (78.6 days [95% CI, 57.2 to 86.8 days]) (HR, 1.26 [95% CI, 1.03 to 1.49]). CONCLUSIONS In patients with SSI, tissue samples yielded high rates of microbial culture results. There was a higher proportion of gram-negative organisms in open fractures. Gram-negative infections were also associated with earlier time to infection. Clinicians should not hesitate to take deep-tissue culture samples in patients with suspected SSI and should be prepared to encounter polymicrobial infections. LEVEL OF EVIDENCE Diagnostic Level III. See Instructions for Authors for a complete description of levels of evidence.
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