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口服β-内酰胺类药物与氟喹诺酮类药物和复方磺胺甲噁唑用于大肠杆菌、奇异变形杆菌和肺炎克雷伯菌菌血症的降阶梯治疗。

Oral β-lactams vs fluoroquinolones and trimethoprim/sulfamethoxazole for step-down therapy for Escherichia coli, Proteus mirabilis, and Klebsiella pneumoniae bacteremia.

机构信息

Department of Pharmacy, Dr. P. Phillips Hospital/Orlando Health, Orlando, FL, USA.

Department of Pharmacy, Dell Seton Medical Center at the University of Texas, Austin, TX, USA.

出版信息

Am J Health Syst Pharm. 2023 Feb 21;80(Suppl 1):S33-S41. doi: 10.1093/ajhp/zxac202.

DOI:10.1093/ajhp/zxac202
PMID:35868628
Abstract

PURPOSE

To compare rates of treatment failure for patients with bloodstream infections (BSIs) due to Escherichia coli, Klebsiella pneumoniae, or Proteus mirabilis who received oral step-down antibiotic therapy with either a fluoroquinolone (FQ) or trimethoprim/sulfamethoxazole (SXT) to rates for those who received an oral β-lactam (BL).

METHODS

This retrospective, multicenter, cohort study included 397 unique adult hospitalized patients with a BSI due to E. coli, K. pneumoniae, or P. mirabilis at 6 hospitals in central Texas between July 11, 2016, and July 11, 2018. The primary outcome was a composite of treatment failure comprising 30-day readmission due to recurrence, 30-day all-cause mortality, and change in oral antibiotic. Secondary outcomes included 90-day development of Clostridioides difficile infection, 90-day colonization with a multidrug-resistant organism, 90-day all-cause readmission, hospital length of stay, and the individual components of the primary outcome.

RESULTS

Of the 397 patients included, 200 received oral step-down therapy with a BL while 197 received an FQ or SXT. Most patients had an infection due to E. coli (82.8%) and a urinary source of infection (85%). Median total duration of therapy was 14 days in both groups. No difference in treatment failure was identified between the groups treated with a BL and FQ/SXT (7% vs 5.8%, P = 0.561). Median hospital length of stay was the only secondary endpoint in which there was an observed difference (6 vs 5 days, P = 0.04).

CONCLUSION

We observed no difference in treatment failure rates for patients receiving an oral BL compared to an oral FQ or SXT for step-down therapy of BSIs due to E. coli, K. pneumoniae, and P. mirabilis.

摘要

目的

比较大肠杆菌、肺炎克雷伯菌或奇异变形杆菌引起血流感染(BSI)的患者接受氟喹诺酮(FQ)或复方磺胺甲噁唑(SXT)降阶梯口服抗生素治疗与接受口服β-内酰胺(BL)治疗的治疗失败率。

方法

这是一项回顾性、多中心队列研究,纳入了 2016 年 7 月 11 日至 2018 年 7 月 11 日德克萨斯州中部 6 家医院的 397 例因大肠杆菌、肺炎克雷伯菌或奇异变形杆菌引起 BSI 的成年住院患者。主要结局是由 30 天内因复发而再次入院、30 天内全因死亡率和口服抗生素变化组成的复合治疗失败。次要结局包括 90 天内艰难梭菌感染、90 天内多药耐药菌定植、90 天内全因再入院、住院时间和主要结局的各个组成部分。

结果

在纳入的 397 例患者中,200 例接受 BL 降阶梯治疗,197 例接受 FQ 或 SXT 治疗。大多数患者的感染源为大肠杆菌(82.8%)和尿路感染(85%)。两组的总治疗时间中位数均为 14 天。BL 组和 FQ/SXT 组治疗失败率无差异(7%比 5.8%,P=0.561)。观察到住院时间是唯一存在差异的次要终点(6 天比 5 天,P=0.04)。

结论

我们观察到,对于大肠杆菌、肺炎克雷伯菌和奇异变形杆菌引起的 BSI 接受 BL 降阶梯治疗的患者与接受 FQ 或 SXT 治疗的患者相比,治疗失败率无差异。

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