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舒巴坦治疗涉及多重耐药醋酸钙不动杆菌-鲍曼不动杆菌复合体的肺炎。

Sulbactam treatment for pneumonia involving multidrug-resistant Acinetobacter calcoaceticus-Acinetobacter baumannii complex.

机构信息

From the Division of Infectious Diseases, Department of Internal Medicine, Chang Gung Memorial Hospital at Chia-Yi , Chia-Yi, Taiwan , ROC.

出版信息

Infect Dis (Lond). 2015 Jun;47(6):370-8. doi: 10.3109/00365548.2014.995129. Epub 2015 Mar 6.

Abstract

BACKGROUND

Multidrug-resistant (MDR) Acinetobacter calcoaceticus-Acinetobacter baumannii (Acb) complex has become an important cause of nosocomial pneumonia. Sulbactam is a β-lactamase inhibitor with antimicrobial activity against MDR Acb complex.

METHODS

To investigate outcomes of pneumonia involving MDR Acb complex treated with sulbactam or ampicillin/sulbactam for at least 7 days, we conducted a retrospective study of 173 adult patients over a 34 month period.

RESULTS

Of 173 patients, 138 (79.8%) received combination therapy, mainly with carbapenems (119/138, 86.2%). The clinical response rate was 67.6% and the 30 day mortality rate was 31.2%. The independent predictors of clinical failure were malignancy, bilateral pneumonia and shorter duration of treatment. In patients with sulbactam-susceptible strains, there was no difference in clinical and microbiological outcome between combination therapy and monotherapy. Compared to the sulbactam-susceptible group, the sulbactam-resistant group had a lower rate of airway eradication, a longer duration of treatment and a higher rate of combination therapy with predominantly carbapenems (p < 0.05). There was no significant difference between the two groups in clinical resolution and 30 day mortality rates.

CONCLUSIONS

Sulbactam could be a treatment option for pneumonia involving MDR Acb complex, and combination therapy with carbapenems could be considered for sulbactam-resistant cases.

摘要

背景

耐多药(MDR)醋酸钙不动杆菌-鲍曼不动杆菌(Acb)复合群已成为医院获得性肺炎的重要病因。舒巴坦是一种β-内酰胺酶抑制剂,对 MDR Acb 复合群具有抗菌活性。

方法

为了研究至少使用舒巴坦或氨苄西林/舒巴坦治疗 7 天以上的 MDR Acb 复合群肺炎的结局,我们对 34 个月期间的 173 例成年患者进行了回顾性研究。

结果

173 例患者中,138 例(79.8%)接受了联合治疗,主要与碳青霉烯类药物联合治疗(119/138,86.2%)。临床缓解率为 67.6%,30 天死亡率为 31.2%。临床治疗失败的独立预测因素为恶性肿瘤、双侧肺炎和治疗时间较短。对于舒巴坦敏感株的患者,联合治疗与单药治疗在临床和微生物学结局方面没有差异。与舒巴坦敏感组相比,舒巴坦耐药组的气道清除率较低,治疗时间较长,且主要采用碳青霉烯类药物联合治疗的比例较高(p<0.05)。两组患者在临床缓解率和 30 天死亡率方面无显著差异。

结论

舒巴坦可能是治疗 MDR Acb 复合群肺炎的一种治疗选择,对于舒巴坦耐药株,可以考虑联合使用碳青霉烯类药物。

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