共 18 条
Endocarditis Caused by Highly Penicillin-Resistant Viridans Group Streptococci: Still Room for Vancomycin-Based Regimens
被引:14
|作者:
Pericas, Juan M.
[1
,2
,7
]
Nathavitharana, Ruvandhi
[3
]
Garcia-de-la-Maria, Cristina
[1
,7
,8
]
Falces, Caries
[1
,7
]
Ambrosioni, Juan
[1
,7
]
Almela, Manel
[1
,7
,9
]
Garcia-Gonzalez, Javier
[1
,7
,8
]
Quintana, Eduard
[1
,7
,10
]
Marco, Francesc
[6
,9
]
Moreno, Asuncion
[1
,7
]
Bayer, Arnold S.
[4
,5
]
Miro, Jose M.
[1
,7
]
Karchmer, Adolf W.
[3
]
Tellez, Adrian
[7
]
Hernandez-Meneses, Marta
[7
]
Casals, Climent
Vila, Jordi
[9
]
Sandoval, Elena
[10
]
Pare, Juan C.
[10
]
Falces, Carlos
[10
]
Pereda, Daniel
[10
]
Cartana, Ramon
[10
]
Ninot, Salvador
[10
]
Azqueta, Manel
[10
]
Sitges, Marta
[10
]
Vidal, Barbara
[10
]
Pomar, Jose L.
[10
]
Castella, Manuel
[10
]
Tolosana, Jose M.
[10
]
Ortiz, Jose
[10
]
Fita, Guillermina
[11
]
Rovira, Irene
[11
]
Fuster, David
[12
]
Ramirez, Jose
[13
]
Brunet, Merce
[14
]
Soy, Dolors
[15
]
Castro, Pedro
[16
]
Llopis, Jaume
[17
]
Garcia-Pares, Delia
[7
]
机构:
[1] Univ Barcelona, Inst Invest Biomed Pi & Sunyar IDIBAPS, Hosp Clin Barcelona, Barcelona, Spain
[2] Hosp Arnau Vilanova, IRB Lleida, Clin Direct Infect Dis & Clin Microbiol, Lleida, Spain
[3] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Internal Med, Div Infect Dis, Boston, MA 02115 USA
[4] LA Biomed Res Inst, Torrance, CA USA
[5] UCLA, Geffen Sch Med, Los Angeles, CA USA
[6] Univ Barcelona, ISGIobal, Hosp Clin Barcelona, Barcelona, Spain
[7] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Infect Dis Serv, Barcelona, Spain
[8] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Expt Endocarditis Lab, Barcelona, Spain
[9] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Microbiol Serv, Barcelona, Spain
[10] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Cardiovasc Inst, Barcelona, Spain
[11] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Anesthesiol Dept, Barcelona, Spain
[12] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Nucl Med Serv, Barcelona, Spain
[13] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Pathol Dept, Barcelona, Spain
[14] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Toxicol Serv, Barcelona, Spain
[15] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Pharm Serv, Barcelona, Spain
[16] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Intens Care Unit, Barcelona, Spain
[17] Univ Barcelona, Sch Med, Hosp Clin IDIBAPS, Dept Stat,Fac Biol, Barcelona, Spain
基金:
美国国家卫生研究院;
关键词:
animal models;
combination therapy;
high-level penicillin resistance;
in vitro;
infective endocarditis;
viridans group streptococci;
IN-VITRO ACTIVITY;
STAPHYLOCOCCUS-AUREUS;
INFECTIVE ENDOCARDITIS;
DAPTOMYCIN;
THERAPY;
SUSCEPTIBILITY;
COMBINATION;
AMPICILLIN;
ANTIBIOTICS;
DALBAVANCIN;
D O I:
10.1128/AAC.00516-19
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Optimal treatment options remain unknown for infective endocarditis (IE) caused by penicillin-resistant (PEN-R) viridans group streptococcal (VGS) strains. The aims of this study were to report two cases of highly PEN-R VGS IE, perform a literature review, and evaluate various antibiotic combinations in vitro and in vivo. The following combinations were tested by time-kill studies and in the rabbit experimental endocarditis (EE) model: PEN-gentamicin, ceftriaxone-gentamicin, vancomycin-gentamicin, daptomycin-gentamicin, and daptomycin-ampicillin. Case 1 was caused by Streptococcus parasanguinis (PEN MIC, 4 mu g/ml) and was treated with vancomycin plus cardiac surgery. Case 2 was caused by Streptococcus mitis (PEN MIC, 8 mu g/ml) and was treated with 4 weeks of vancomycin plus gentamicin, followed by 2 weeks of vancomycin alone. Both patients were alive and relapse-free after >= 6 months follow-up. For the in vitro studies, except for daptomycin-ampicillin, all combinations demonstrated both synergy and bactericidal activity against the S. parasanguinis isolate. Only PEN-gentamicin, daptomycin-gentamicin, and daptomycin-ampicillin demonstrated both synergy and bactericidal activity against the S. minis strain. Both strains developed high-level daptomycin resistance (HLDR) during daptomycin in vitro passage. In the EE studies, PEN alone failed to clear S. minis from vegetations, while ceftriaxone and vancomycin were significantly more effective (P < 0.001). The combination of gentamicin with PEN or vancomycin increased bacterial eradication compared to that with the respective monotherapies. In summary, two patients with highly PEN-R VGS IE were cured using vancomycin-based therapy. In vivo, regimens of gentamicin plus either beta-lactams or vancomycin were more active than their respective monotherapies. Further clinical studies are needed to confirm the role of vancomycin-based regimens for highly PEN-R VGS IE. The emergence of HLDR among these strains warrants caution in the use of daptomycin therapy for VGS IE.
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