Vancomycin, Daptomycin, Antistaphylococcal β-Lactam, and Trimethoprim-Sulfamethoxazole Monotherapy and Combination Therapy in the Management of Methicillin-Resistant Staphylococcus aureus: A Network Meta-Analysis

被引:4
作者
Xu, Xiaonan [1 ]
Lu, Ni [2 ]
Song, Pan [3 ]
Zhou, Mingzhen [2 ]
Li, Yuanxiao [1 ]
Wang, Zirui [2 ]
Gao, Xin [2 ]
机构
[1] Lanzhou Univ, Dept Pediat, Hosp 2, Lanzhou, Peoples R China
[2] Lanzhou Univ, Clin Med Coll, Lanzhou, Peoples R China
[3] Sichuan Univ, Inst Urol, Dept Urol, West China Hosp, Chengdu, Peoples R China
关键词
vancomycin; daptomycin; beta-lactams; network meta-analysis; MRSA; MRSA BACTEREMIA; CEFTAROLINE; INFECTIONS; TRIMETHOPRIM/SULFAMETHOXAZOLE; SUSCEPTIBILITY; GLYCOPEPTIDE;
D O I
10.3389/fphar.2022.805966
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The aim was to evaluate the efficacy and safety of vancomycin or daptomycin (VAN/DAP), antistaphylococcal beta-lactam (ASBL), trimethoprim-sulfamethoxazole (TMP-SMX), and combination therapy of VAN/DAP + ASBL in the management of methicillin-resistant Staphylococcus aureus (MRSA). Methods: Databases including PubMed, Cochrane Library, Embase database, and google scholar were searched on 1 September 2021. The randomized control trials (RCTs) and comparable clinical studies of VAN/DAP, VAN/DAP + ASBL, ASBL, and TMP-SMX in the management of MRSA were identified. A network meta-analysis was conducted with STATA 14.0. Results: Seven RCTs and two matched cohorts with 1,048 patients were included in the analysis. The pooled results showed that VAN/DAP + ASBL had a significantly lower rate of persistent bacteremia > 3 days than VAN/DAP alone [OR:0.46, 95%CI (0.26, 0.81), p < 0.001]. No obvious differences were observed in the outcomes of all-cause mortality, relapsed bacteremia, microbiological treatment failure, embolic or metastatic infection, and total adverse events. However, the ranking results showed that VAN/DAP + ASBL had slightly better efficacy (all-cause mortality, persistent bacteremia > 3 days, duration of bacteremia, microbiological treatment failure, and relapsed bacteremia) but slightly higher adverse events than VAN/DAP alone. No obvious differences in the comparisons of VAN/DAP vs. ASBL, and VAN/DAP vs TMP-SMX in the analyzed outcomes. The ranking results revealed that ASBL and TMP-SMX did not have better efficacy or lower adverse events compared with the treatment of VAN/DAP. Conclusion: The efficacy of VAN/DAP + ASBL was slightly but not significantly better than VAN/DAP alone in the management of MRSA.
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页数:9
相关论文
共 37 条
[1]   Monotherapy with Vancomycin or Daptomycin versus Combination Therapy with β-Lactams in the Treatment of Methicillin-Resistant Staphylococcus Aureus Bloodstream Infections: A Retrospective Cohort Analysis [J].
Alosaimy, Sara ;
Sabagha, Noor L. ;
Lagnf, Abdalhamid M. ;
Zasowski, Evan J. ;
Morrisette, Taylor ;
Jorgensen, Sarah C. J. ;
Trinh, Trang D. ;
Mynatt, Ryan P. ;
Rybak, Michael J. .
INFECTIOUS DISEASES AND THERAPY, 2020, 9 (02) :325-339
[2]   Ceftaroline fosamil monotherapy for methicillin-resistant Staphylococcus aureus bacteremia: a comparative clinical outcomes study [J].
Arshad, Samia ;
Huang, Vanthida ;
Hartman, Pamela ;
Perri, Mary B. ;
Moreno, Daniela ;
Zervos, Marcus J. .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2017, 57 :27-31
[3]   In MRSA bacteremia, adding a β-lactam to usual care did not improve a composite outcome at 90 days [J].
Atalla, Eleftheria ;
Mylonakis, Eleftherios .
ANNALS OF INTERNAL MEDICINE, 2020, 172 (12) :JC67-JC67
[4]   What Is Driving the Epidemiology of Methicillin-Resistant Staphylococcus aureus Infections in Europe? [J].
Borg, Michael A. ;
Camilleri, Liberato .
MICROBIAL DRUG RESISTANCE, 2021, 27 (07) :889-894
[5]   Treatment of Methicillin-Resistant Staphylococcus aureus Infections with a Minimal Inhibitory Concentration of 2 μg/mL to Vancomycin: Old (Trimethoprim/Sulfamethoxazole) versus New (Daptomycin or Linezolid) Agents [J].
Campbell, Michelle L. ;
Marchaim, Dror ;
Pogue, Jason M. ;
Sunkara, Bharath ;
Bheemreddy, Suchitha ;
Bathina, Pradeep ;
Pulluru, Harish ;
Chugh, Neelu ;
Wilson, Melanie N. ;
Moshos, Judy ;
Ku, Kimberley ;
Hayakawa, Kayoko ;
Martin, Emily T. ;
Lephart, Paul R. ;
Rybak, Michael J. ;
Kaye, Keith S. .
ANNALS OF PHARMACOTHERAPY, 2012, 46 (12) :1587-1597
[6]   Conceptual and Technical Challenges in Network Meta-analysis [J].
Cipriani, Andrea ;
Higgins, Julian P. T. ;
Geddes, John R. ;
Salanti, Georgia .
ANNALS OF INTERNAL MEDICINE, 2013, 159 (02) :130-W54
[7]   Combination of Vancomycin and β-Lactam Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia: A Pilot Multicenter Randomized Controlled Trial [J].
Davis, Joshua S. ;
Sud, Archana ;
O'Sullivan, Matthew V. N. ;
Robinson, James O. ;
Ferguson, Patricia E. ;
Foo, Hong ;
van Hal, Sebastiaan J. ;
Ralph, Anna P. ;
Howden, Benjamin P. ;
Binks, Paula M. ;
Kirby, Adrienne ;
Tong, Steven Y. C. .
CLINICAL INFECTIOUS DISEASES, 2016, 62 (02) :173-180
[8]   β-Lactams Enhance Vancomycin Activity against Methicillin-Resistant Staphylococcus aureus Bacteremia Compared to Vancomycin Alone [J].
Dilworth, Thomas J. ;
Ibrahim, Omar ;
Hall, Pamela ;
Sliwinski, Jora ;
Walraven, Carla ;
Mercier, Renee-Claude .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (01) :102-109
[9]   Experimental study on the efficacy of combinations of glycopeptides and β-lactams against Staphylococcus aureus with reduced susceptibility to glycopeptides [J].
Domenech, A ;
Ribes, S ;
Cabellos, C ;
Taberner, F ;
Tubau, F ;
Domínguez, MA ;
Montero, A ;
Liñares, J ;
Ariza, J ;
Gudiol, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (04) :709-716
[10]  
Eliakim-Raz N, 2017, J ANTIMICROB CHEMOTH, V72, P882, DOI [10.1093/jac/dkw510, 10.1093/jac/dkx213]