Predictors of mortality for methicillin-resistant Staphylococcus aureus health-care-associated pneumonia -: Specific evaluation of vancomycin pharmacokinetic indices

被引:179
作者
Jeffres, Meghan N.
Isakow, Warren
Doherty, Joshua A.
McKinnon, Peggy S.
Ritchie, David J.
Micek, Scott T.
Kollef, Marin H.
机构
[1] Washington Univ, Sch Med, Dept Pulm & Crit Care Med, St Louis, MO 63110 USA
[2] BJC Healthcare, Med Informat, St Louis, MO USA
[3] Barnes Jewish Hosp, Dept Pharm, St Louis, MO 63110 USA
关键词
antibiotics; methicillin resistance; pneumonia; Staphylococcus aureus;
D O I
10.1378/chest.130.4.947
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The goal of this investigation was to determine whether vancomycin pharmacokinetie indexes (eg, serum trough concentrations or area under the concentration curve [AUC] values) were associated with mortality for patients with health-care-associated pneumonia (HCAP) attributed to methicillin-resistant Staphylococcus aureus (MRSA). Design: A retrospective, single-center, observational cohort study. Setting: Barnes-Jewish Hospital, a 1,200-bed urban teaching facility. Patients: Adult patients requiring hospitalization who were identified as having HCAP attributed to MRSA by BAL semi-quantitative cultures. Interventions: Retrospective data collection from automated hospital, microbiology, and pharmacy databases. Measurements and main results: One hundred two patients with MRSA HCA-P were identified over a 6.5-year period. Thirty-two patients (31.4%) died during their hospitalization. The mean (+/- SD) vancomycin trough concentrations (13.6 +/- 5.9 vs 13.9 +/- 6.7 mu g/mL, respectively; p = 0.866) and AUC values (351 +/- 143 vs 354 +/- 109 mu g/h/mL, respectively; p = 0.941) did not differ between survivors and nonsurvivors. The stratification of the vancomycin trough concentrations and AUC values yielded no relationship with hospital mortality. Conclusions: We found no evidence that greater vancomycin trough concentrations or AUC values correlated with hospital outcome. Based on these results, aggressive dosing strategies for vancomycin (eg, trough concentrations of > 15 mu g/mL) may not offer any advantage over traditional dose targets (range, 5 to 15 mu g/mL).
引用
收藏
页码:947 / 955
页数:9
相关论文
共 43 条
[11]   Treatment of gram-positive nosocomial pneumonia - Prospective randomized comparison of quinupristin/dalfopristin versus vancomycin [J].
Fagon, JY ;
Patrick, H ;
Haas, DW ;
Torres, A ;
Gibert, C ;
Cheadle, WG ;
Falcone, RE ;
Anholm, JD ;
Paganin, F ;
Fabian, TC ;
Lilienthal, F .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (03) :753-762
[12]   Severe community-onset pneumonia in healthy adults caused by methicillin-resistant Staphylococcus aureus carrying the Panton-Valentine leukocidin genes [J].
Francis, JS ;
Doherty, MC ;
Lopatin, U ;
Johnston, CP ;
Sinha, G ;
Ross, T ;
Cai, M ;
Hansel, NN ;
Perl, T ;
Ticehurst, JR ;
Carroll, K ;
Thomas, DL ;
Nuermberger, E ;
Bartlett, JG .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (01) :100-107
[13]   Epidemiological and microbiological characterization of infections caused by Staphylococcus aureus with reduced susceptibility to vancomycin, United States, 1997-2001 [J].
Fridkin, SK ;
Hageman, J ;
McDougal, LK ;
Mohammed, J ;
Jarvis, WR ;
Perl, TM ;
Tenover, FC .
CLINICAL INFECTIOUS DISEASES, 2003, 36 (04) :429-439
[14]   Health care-associated bloodstream infections in adults: A reason to change the accepted definition of community-acquired infections [J].
Friedman, ND ;
Kaye, KS ;
Stout, JE ;
McGarry, SA ;
Trivette, SL ;
Briggs, JP ;
Lamm, W ;
Clark, C ;
MacFarquhar, J ;
Walton, AL ;
Reller, LB ;
Sexton, DJ .
ANNALS OF INTERNAL MEDICINE, 2002, 137 (10) :791-797
[15]   Association between Staphylococcus aureus strains carrying gene for Panton-Valentine leukocidin and highly lethal necrotising pneumonia in young immunocompetent patients [J].
Gillet, Y ;
Issartel, B ;
Vanhems, P ;
Fournet, JC ;
Lina, G ;
Bes, M ;
Vandenesch, F ;
Piémont, Y ;
Brousse, N ;
Floret, D ;
Etienne, J .
LANCET, 2002, 359 (9308) :753-759
[16]   Pulmonary manifestations in children with invasive community-acquired Staphylococcus aureus infection [J].
Gonzalez, BE ;
Hulten, KG ;
Dishop, MK ;
Lamberth, LB ;
Hammerman, WA ;
Mason, EO ;
Kaplan, SL .
CLINICAL INFECTIOUS DISEASES, 2005, 41 (05) :583-590
[17]   Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility [J].
Hiramatsu, K ;
Hanaki, H ;
Ino, T ;
Yabuta, K ;
Oguri, T ;
Tenover, FC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (01) :135-136
[18]   Treatment outcomes for serious infections caused by methicillin-resistant Staphylococcus aureus with reduced vancomycin susceptibility [J].
Howden, BP ;
Ward, PB ;
Charles, PGP ;
Korman, TM ;
Fuller, A ;
du Cros, P ;
Grabsch, EA ;
Roberts, SA ;
Robson, J ;
Read, K ;
Bak, N ;
Hurley, J ;
Johnson, PDR ;
Morris, AJ ;
Mayall, BC ;
Grayson, ML .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (04) :521-528
[20]   In vitro evaluation of BAL9141, a novel parenteral cephalosporin active against oxacillin-resistant staphylococci [J].
Jones, RN ;
Deshpande, LM ;
Mutnick, AH ;
Biedenbach, DJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (06) :915-932