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在低产超广谱β-内酰胺酶(ESBL)人群中,头孢呋辛与哌拉西林/他唑巴坦作为菌血症经验性治疗药物的比较。

Cefuroxime compared to piperacillin/tazobactam as empirical treatment of bacteremia in a low Extended-spectrum beta-lactamase (ESBL) prevalence cohort.

作者信息

Thønnings Sara, Jansåker Filip, Gradel Kim Oren, Styrishave Bjarne, Knudsen Jenny Dahl

机构信息

Department of Clinical Microbiology, Copenhagen University Hospital, Hvidovre, Denmark.

Toxicology Laboratory, Analytical BioSciences, Department of Pharmacy, University of Copenhagen, Copenhagen, Denmark.

出版信息

Infect Drug Resist. 2019 May 13;12:1257-1264. doi: 10.2147/IDR.S197735. eCollection 2019.

Abstract

On January 18, 2010, a part of the capital region of Denmark shifted the empirical treatment of febrile conditions from cefuroxime to piperacillin/tazobactam. We compare empirical treatment with piperacillin/tazobactam versus cefuroxime for bacteremia with regard to 14 days mortality, in a low prevalence cohort of Extended-spectrum beta-lactamase-producing . From January 18, 2010 to December 31, 2012, we conducted a retrospective cohort study including patients with bacteremia from six university hospitals in Copenhagen, Denmark. Clinical and laboratory information was obtained from a bacteremia research database, including information on comorbidity, and we used Cox proportional hazard analysis to asses all-cause 14 days mortality. A total of 568 patients receiving either cefuroxime (n=377) or piperacillin/tazobactam (n=191) as empirical therapy were included. In the Cox proportional hazard model, cefuroxime treatment was significantly associated with death (mortality rate ratio 3.95, CI 1.12-13.90). Other variables associated with death were health care related infection (MRR 3.20, CI 1.67-6.15), hospital-acquired infection (MRR 2,17, CI 1.02-4.62), admission at intensive care unit (MRR 20.45, 5.31-78.82), and combination therapy with ciprofloxacin (MRR 2.14, CI 0.98-4.68). Empiric cefuroxime treatment of bacteremia was significantly associated with higher 14 days mortality in comparison with piperacillin/tazobactam.

摘要

2010年1月18日,丹麦首都地区的部分地区将发热病症的经验性治疗药物从头孢呋辛改为哌拉西林/他唑巴坦。我们在产超广谱β-内酰胺酶的低患病率队列中,比较哌拉西林/他唑巴坦与头孢呋辛用于菌血症经验性治疗的14天死亡率。2010年1月18日至2012年12月31日,我们进行了一项回顾性队列研究,纳入了丹麦哥本哈根六家大学医院的菌血症患者。临床和实验室信息从菌血症研究数据库中获取,包括合并症信息,我们使用Cox比例风险分析来评估全因14天死亡率。共有568例接受头孢呋辛(n = 377)或哌拉西林/他唑巴坦(n = 191)作为经验性治疗的患者被纳入研究。在Cox比例风险模型中,头孢呋辛治疗与死亡显著相关(死亡率比3.95,CI 1.12 - 13.90)。与死亡相关的其他变量包括医疗保健相关感染(MRR 3.20,CI 1.67 - 6.15)、医院获得性感染(MRR 2.17,CI 1.02 - 4.62)、入住重症监护病房(MRR 20.45,5.31 - 78.82)以及与环丙沙星联合治疗(MRR 2.14,CI 0.98 - 4.68)。与哌拉西林/他唑巴坦相比,菌血症的经验性头孢呋辛治疗与14天更高的死亡率显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49fa/6526191/899121ab7d0b/IDR-12-1257-g0001.jpg

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