害怕生物丢失(FOMO):糖尿病足和骨髓炎管理机会

Morgan Morelli, Andrea Son, Yanis Bitar, Michelle Hecker
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引用次数: 0

摘要

背景:糖尿病足感染和下肢骨髓炎住院是常见的。使用经验性抗生素治疗耐甲氧西林金黄色葡萄球菌(MRSA)和铜绿假单胞菌也很常见。指南根据疾病的严重程度、MRSA和铜绿假单胞菌的危险因素以及当地流行情况推荐抗生素治疗。我们评估了经验性抗生素治疗与培养结果和最终抗生素治疗之间的一致性,重点是MRSA和铜绿假单胞菌。我们还评估了MRSA和假单胞菌风险因素对这些微生物培养结果的预测程度。方法:我们对2021年所有诊断为糖尿病足感染或下肢骨髓炎的住院患者进行了一项队列研究。如果患者患有国际疾病分类第十版(ICD-10)诊断代码为M86、E10.621、E11.621或E08.621,则纳入患者。如果抗生素用于其他适应症或年龄为18岁,则排除患者。在多次住院的患者中,仅包括第一次住院。经验性抗生素治疗包括由入院小组开始使用的抗生素。最终抗生素治疗包括在入院时完成或出院时规定的最终抗生素疗程。MRSA危险因素包括过去一年内MRSA阳性培养,90天内静脉注射抗生素住院,静脉注射药物或血液透析。假单胞菌的危险因素包括过去一年内铜绿假单胞菌培养阳性或90天内静脉注射抗生素住院。结果:2021年,260例疑似糖尿病足感染或下肢骨髓炎的独特患者入院。68例患者住院1次。分别对224例(86%)和214例(82%)患者进行经验性抗mrsa和抗假单胞菌治疗。分别对76例(30%)和51例(20%)患者进行了明确的抗mrsa和抗假单胞菌治疗。在195例进行伤口培养的患者中,分别有29例(15%)和18例(9%)的MRSA和P. aeruginosa培养呈阳性(图)。MRSA危险因素预测MRSA阴性培养的阴性预测值为91%。假单胞菌危险因素预测铜绿假单胞菌阴性培养的阴性预测值为95%。结论:我们的数据表明,糖尿病足感染和下肢骨髓炎的经验性抗mrsa和抗假单胞菌治疗有机会大幅减少。耐甲氧西林金黄色葡萄球菌和假单胞菌危险因素的缺失在预测这些微生物的阳性培养缺失方面是相当好的。披露:没有
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Fear of missing organisms (FOMO): Diabetic foot and osteomyelitis management opportunities
Background: Hospitalizations for diabetic foot infections and lower-extremity osteomyelitis are common. Use of empiric antibiotic therapy for methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa is also common. Guidelines recommend antibiotic therapy based on severity of illness, risk factors for MRSA and P. aeruginosa , and local prevalence. We evaluated the concordance between empiric antibiotic therapy and both culture results and definitive antibiotic therapy with a focus on MRSA and P. aeruginosa . We also evaluated how well MRSA and pseudomonal risk factors were predictive of culture results with these organisms. Methods: We conducted a cohort study of all patients admitted to our hospital system in 2021 with a diagnosis of a diabetic foot infection or lower-extremity osteomyelitis. Patients were included if they had an International Classification of Disease, Tenth Revision (ICD-10) diagnosis code of M86, E10.621, E11.621, or E08.621. Patients were excluded if antibiotics were for another indication or if they were aged <18 years. In patients with multiple hospitalizations only the first hospitalization was included. Empiric antibiotic therapy included antibiotics started by the admitting team. Definitive antibiotic therapy included the final antibiotic course either completed during admission or prescribed at the time of discharge. MRSA risk factors included prior positive culture with MRSA within the last year, hospitalization with IV antibiotics within 90 days, intravenous drug use, or hemodialysis. Pseudomonal risk factors included prior positive culture with P. aeruginosa within the last year or hospitalization with IV antibiotics within 90 days. Results: In 2021, 260 unique patients were admitted with suspected diabetic foot infections or lower-extremity osteomyelitis. 68 patients had >1 admission. Empiric anti-MRSA and antipseudomonal therapy was administered to 224 (86%) and 214 (82%) patients, respectively. Definitive anti-MRSA and antipseudomonal therapy was administered to 76 (30%) and 51 (20%) patients, respectively. Of the 195 patients who had wound cultures, 29 (15%) and 18 (9%) had positive cultures for MRSA and P. aeruginosa respectively (Fig.). The negative predictive value of MRSA risk factors for predicting a negative culture with MRSA was 91%. The negative predictive value of pseudomonal risk factors for predicting a negative culture with P. aeruginosa was 95%. Conclusions: Our data suggest an opportunity for substantial reductions in empiric anti-MRSA and antipseudomonal therapy for diabetic foot infection and lower-extremity osteomyelitis. The absence of MRSA and pseudomonal risk factors was reasonably good at predicting the absence of a positive culture with these organisms. Disclosure: None
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