Telavancin versus Vancomycin for HospitalAcquired Pneumonia due to Gram-positive Pathogens

被引:206
作者
Rubinstein, Ethan [1 ]
Lalani, Tahaniyat [2 ,3 ]
Corey, G. Ralph [2 ,3 ]
Kanafani, Zeina A. [11 ]
Nannini, Esteban C. [12 ]
Rocha, Marcelo G. [16 ]
Rahav, Galia [17 ]
Niederman, Michael S. [4 ,5 ]
Kollef, Marin H. [6 ]
Shorr, Andrew F. [7 ]
Lee, Patrick C. [8 ]
Lentnek, Arnold L. [9 ]
Luna, Carlos M. [13 ]
Fagon, Jean-Yves [18 ]
Torres, Antoni [19 ]
Kitt, Michael M.
Genter, Fredric C. [10 ]
Barriere, Steven L. [10 ]
Friedland, H. David
Stryjewski, Martin E. [2 ,14 ,15 ]
机构
[1] Univ Manitoba, Fac Med, Infect Dis Sect, Dept Internal Med & Med Microbiol, Winnipeg, MB R3E 0W3, Canada
[2] Duke Univ, Med Ctr, Dept Med, Duke Clin Res Inst, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Med, Div Infect Dis, Durham, NC 27710 USA
[4] Winthrop Univ Hosp, Mineola, NY 11501 USA
[5] SUNY Stony Brook, Stony Brook, NY 11794 USA
[6] Washington Univ, Sch Med, Pulm & Crit Care Div, St Louis, MO USA
[7] Washington Hosp Ctr, Washington, DC 20010 USA
[8] Baystate Med Ctr, Springfield, MA USA
[9] Wellstar Infect Dis, Marietta, GA USA
[10] Theravance Inc, San Francisco, CA USA
[11] Amer Univ Beirut, Med Ctr, Beirut, Lebanon
[12] Univ Nacl Rosario, Sch Med, Dept Infect Dis, RA-2000 Rosario, Santa Fe, Argentina
[13] Univ Buenos Aires, Hosp Clin, Div Pulm Dis, Dept Internal Med, Buenos Aires, DF, Argentina
[14] Clin Norberto Quirno, Ctr Educ Med & Invest, Dept Med, Buenos Aires, DF, Argentina
[15] Clin Norberto Quirno, Ctr Educ Med & Invest, Div Infect Dis, Buenos Aires, DF, Argentina
[16] Intens Care Unit, Porto Alegre, RS, Brazil
[17] Sheba Med Ctr, Div Infect Dis, Dept Med, Tel Hashomer, Israel
[18] Univ Paris 05, Assistance Publ Hop Paris, Paris, France
[19] Univ Barcelona, Hosp Clin Barcelona, Div Pulm Med, Clin Inst Thorax,Inst Invest Biomed August Pi & S, Barcelona, Spain
关键词
INTENSIVE-CARE UNITS; IN-VITRO ACTIVITY; NOSOCOMIAL PNEUMONIA; DOUBLE-BLIND; LIPOGLYCOPEPTIDE; EPIDEMIOLOGY; INFECTIONS; INTEGRITY; MEMBRANE; DISRUPTS;
D O I
10.1093/cid/ciq031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Telavancin is a lipoglycopeptide bactericidal against gram-positive pathogens. Methods. Two methodologically identical, double-blind studies (0015 and 0019) were conducted involving patients with hospital-acquired pneumonia (HAP) due to gram-positive pathogens, particularly methicillin-resistant Staphylococcus aureus (MRSA). Patients were randomized 1:1 to telavancin (10 mg/kg every 24 h) or vancomycin (1 g every 12 h) for 7-21 days. The primary end point was clinical response at follow-up/test-of-cure visit. Results. A total of 1503 patients were randomized and received study medication (the all-treated population). In the pooled all-treated population, cure rates with telavancin versus vancomycin were 58.9% versus 59.5% (95% confidence interval [CI] for the difference, -5.6% to 4.3%). In the pooled clinically evaluable population (n = 654), cure rates were 82.4% with telavancin and 80.7% with vancomycin (95% CI for the difference, -4.3% to 7.7%). Treatment with telavancin achieved higher cure rates in patients with monomicrobial S. aureus infection and comparable cure rates in patients with MRSA infection; in patients with mixed gram-positive/gram-negative infections, cure rates were higher in the vancomycin group. Incidence and types of adverse events were comparable between the treatment groups. Mortality rates for telavancin-treated versus vancomycin-treated patients were 21.5% versus 16.6% (95% CI for the difference, -0.7% to 10.6%) for study 0015 and 18.5% versus 20.6% (95% CI for the difference, -7.8% to 3.5%) for study 0019. Increases in serum creatinine level were more common in the telavancin group (16% vs 10%). Conclusions. The primary end point of the studies was met, indicating that telavancin is noninferior to vancomycin on the basis of clinical response in the treatment of HAP due to gram-positive pathogens.
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页码:31 / 40
页数:10
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