Fosfomycin as salvage therapy for persistent methicillin-resistant Staphylococcus aureus bacteremia: A case series and review of the literature

被引:3
作者
Omori, Keitaro [1 ,2 ,3 ,8 ]
Kitagawa, Hiroki [1 ,3 ,4 ]
Takada, Masahiro [5 ,6 ]
Maeda, Ryuto [5 ,6 ]
Nomura, Toshihito [1 ,3 ]
Kubo, Yuko [3 ]
Shigemoto, Norifumi [1 ,3 ,4 ,7 ]
Ohge, Hiroki [1 ,3 ]
机构
[1] Hiroshima Univ Hosp, Dept Infect Dis, Hiroshima, Japan
[2] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Mol & Internal Med, Hiroshima, Japan
[3] Hiroshima Univ Hosp, Div Infect Control, Hiroshima, Japan
[4] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Surg, Hiroshima, Japan
[5] Natl Hosp Org Kure Med Ctr, Div Pharm, Hiroshima, Japan
[6] Chugoku Canc Ctr, Hiroshima, Japan
[7] Hiroshima Univ, Translat Res Ctr, Hiroshima, Japan
[8] 1-2-3 Kasumi,Minami Ku, Hiroshima 7348551, Japan
关键词
MRSA; Refractory bacteremia; Fosfomycin; Salvage therapy; Synergy; DAPTOMYCIN PLUS FOSFOMYCIN; IN-VITRO ACTIVITY; COMBINATION; VANCOMYCIN; OSTEOMYELITIS;
D O I
10.1016/j.jiac.2023.10.024
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Methicillin-resistant Staphylococcus aureus (MRSA) bacteremia can be persistent and refractory; however, the optimal approach for its treatment has not been determined. Although fosfomycin (FOM) has been shown to have synergistic effects with anti-MRSA agents in vitro, clinical experience with FOM combination therapy is limited. Thus, we present cases of persistent MRSA bacteremia that improved with the addition of FOM. In case 1, a 48year-old man with prosthetic vascular graft infection developed persistent MRSA bacteremia despite vancomycin (VCM) and daptomycin (DAP) administration. On day 46, after the first positive blood culture, we added FOM to DAP. The blood culture became negative on day 53. In case 2, an 85-year-old woman presented with pacemakerrelated MRSA bacteremia. She was treated with VCM, followed by DAP and DAP plus rifampicin. However, the bacteremia persisted for 32 days because of difficulties in immediate pacemaker removal. After adding FOM to DAP, the blood culture became negative on day 38. In case 3, a 57-year-old woman developed persistent MRSA bacteremia due to pulmonary valve endocarditis and pulmonary artery thrombosis after total esophagectomy for esophageal cancer. The bacteremia continued for 50 days despite treatment with DAP, followed by VCM, VCM plus minocycline, DAP plus linezolid (LZD), and VCM plus LZD. She was managed conservatively because of surgical complications. After adding FOM to VCM on day 51, the blood culture became negative on day 58. FOM combination therapy may be effective in eliminating bacteria and can serve as salvage therapy for refractory MRSA bacteremia.
引用
收藏
页码:352 / 356
页数:5
相关论文
共 28 条
  • [1] Fosfomycin as Partner Drug for Systemic Infection Management. A Systematic Review of Its Synergistic Properties from In Vitro and In Vivo Studies
    Antonello, Roberta Maria
    Principe, Luigi
    Maraolo, Alberto Enrico
    Viaggi, Valentina
    Pol, Riccardo
    Fabbiani, Massimiliano
    Montagnani, Francesca
    Lovecchio, Antonio
    Luzzati, Roberto
    Di Bella, Stefano
    [J]. ANTIBIOTICS-BASEL, 2020, 9 (08): : 1 - 74
  • [2] Efficacy of Linezolid and Fosfomycin in Catheter-Related Biofilm Infection Caused by Methicillin-Resistant Staphylococcus aureus
    Chai, Dong
    Liu, Xu
    Wang, Rui
    Bai, Yan
    Cai, Yun
    [J]. BIOMED RESEARCH INTERNATIONAL, 2016, 2016
  • [3] High-dose daptomycin and fosfomycin treatment of a patient with endocarditis caused by daptomycin-nonsusceptible Staphylococcus aureus: Case report
    Chen, Liang-Yu
    Huang, Cheng-Hsiung
    Kuo, Shu-Chen
    Hsiao, Chen-Yuan
    Lin, Mei-Lin
    Wang, Fu-Der
    Fung, Chang-Phone
    [J]. BMC INFECTIOUS DISEASES, 2011, 11
  • [4] Combination of Vancomycin and β-Lactam Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia: A Pilot Multicenter Randomized Controlled Trial
    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.
    [J]. CLINICAL INFECTIOUS DISEASES, 2016, 62 (02) : 173 - 180
  • [5] INVITRO ACTIVITY OF LY146032 ALONE AND IN COMBINATION WITH OTHER ANTIBIOTICS AGAINST GRAM-POSITIVE BACTERIA
    DEBBIA, E
    PESCE, A
    SCHITO, GC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (02) : 279 - 281
  • [6] Use of Antistaphylococcal β-Lactams to Increase Daptomycin Activity in Eradicating Persistent Bacteremia Due to Methicillin-Resistant Staphylococcus aureus: Role of Enhanced Daptomycin Binding
    Dhand, Abhay
    Bayer, Arnold S.
    Pogliano, Joseph
    Yang, Soo-Jin
    Bolaris, Michael
    Nizet, Victor
    Wang, Guiquing
    Sakoulas, George
    [J]. CLINICAL INFECTIOUS DISEASES, 2011, 53 (02) : 158 - 163
  • [7] Fosfomycin
    Falagas, Matthew E.
    Vouloumanou, Evridiki K.
    Samonis, George
    Vardakas, Konstantinos Z.
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2016, 29 (02) : 321 - 347
  • [8] García-de-la-Mària C, 2018, ANTIMICROB AGENTS CH, V62, DOI [10.1128/AAC.02633-17, 10.1128/aac.02633-17]
  • [9] Emergence of resistance to daptomycin in a cohort of patients with methicillin-resistant Staphylococcus aureus persistent bacteraemia treated with daptomycin
    Gasch, O.
    Camoez, M.
    Dominguez, M. A.
    Padilla, B.
    Pintado, V.
    Almirante, B.
    Martin, C.
    Lopez-Medrano, F.
    Ruiz de Gopegui, E.
    Blanco, J. R.
    Garcia-Pardo, G.
    Calbo, E.
    Montero, M.
    Granados, A.
    Jover, A.
    Duenas, C.
    Pujol, M.
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (02) : 568 - 571
  • [10] Diagnosis and treatment of bacteremia and endocarditis due to Staphylococcus aureus. A clinical guideline from the Spanish Society of Clinical Microbiology and Infectious Diseases (SEIMC)
    Gudiol, Francesc
    Maria Aguado, Jose
    Almirante, Benito
    Bouza, Emilio
    Cercenado, Emilia
    Angeles Dominguez, M.
    Gasch, Oriol
    Lora-Tamayo, Jaime
    Miro, Jose M.
    Palomar, Mercedes
    Pascual, Alvaro
    Pericas, Juan M.
    Pujol, Miguel
    Rodriguez-Bano, Jesus
    Shaw, Evelyn
    Soriano, Alex
    Valles, Jordi
    [J]. ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2015, 33 (09): : 625 - 625