Antibiotic Treatment Strategies for Community-Acquired Pneumonia in Adults

被引:256
作者
Postma, Douwe F. [1 ,2 ,3 ,5 ]
van Werkhoven, Cornelis H. [1 ]
van Elden, Leontine J. R. [6 ]
Thijsen, Steven F. T. [7 ]
Hoepelman, Andy I. M. [2 ,3 ]
Kluytmans, Jan A. J. W. [8 ]
Boersma, Wim G. [9 ]
Compaijen, Clara J. [10 ]
van der Wall, Eva [11 ]
Prins, Jan M. [12 ]
Oosterheert, Jan J. [2 ,3 ]
Bonten, Marc J. M. [1 ,4 ]
机构
[1] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, NL-3508 GA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Internal Med, NL-3508 GA Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Infect Dis, NL-3508 GA Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Dept Med Microbiol, NL-3508 GA Utrecht, Netherlands
[5] Diakonessenhuis Utrecht, Dept Internal Med, Utrecht, Netherlands
[6] Diakonessenhuis Utrecht, Dept Pulmonol, Utrecht, Netherlands
[7] Diakonessenhuis Utrecht, Dept Med Microbiol, Utrecht, Netherlands
[8] Amphia Ziekenhuis Breda, Dept Med Microbiol, Breda, Netherlands
[9] Med Ctr Alkmaar, Dept Pulmonol, Alkmaar, Netherlands
[10] Kennemer Gasthuis Haarlem, Dept Internal Med, Haarlem, Netherlands
[11] Spaarne Ziekenhuis, Dept Pulmonol, Hoofddorp, Netherlands
[12] Acad Med Ctr Amsterdam, Dept Internal Med, Amsterdam, Netherlands
关键词
BETA-LACTAM MONOTHERAPY; ATYPICAL PATHOGENS; ECONOMIC BURDEN; CLINICAL-TRIALS; THERAPY; DESIGN; GUIDELINES; NONINFERIORITY; AZITHROMYCIN; MANAGEMENT;
D O I
10.1056/NEJMoa1406330
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The choice of empirical antibiotic treatment for patients with clinically suspected community-acquired pneumonia (CAP) who are admitted to non-intensive care unit (ICU) hospital wards is complicated by the limited availability of evidence. We compared strategies of empirical treatment (allowing deviations for medical reasons) with beta-lactam monotherapy, beta-lactam-macrolide combination therapy, or fluoroquinolone monotherapy. METHODS In a cluster-randomized, crossover trial with strategies rotated in 4-month periods, we tested the noninferiority of the beta-lactam strategy to the beta-lactam-macrolide and fluoroquinolone strategies with respect to 90-day mortality, in an intention-to-treat analysis, using a noninferiority margin of 3 percentage points and a two-sided 90% confidence interval. RESULTS A total of 656 patients were included during the beta-lactam strategy periods, 739 during the beta-lactam-macrolide strategy periods, and 888 during the fluoroquinolone strategy periods, with rates of adherence to the strategy of 93.0%, 88.0%, and 92.7%, respectively. The median age of the patients was 70 years. The crude 90-day mortality was 9.0% (59 patients), 11.1% (82 patients), and 8.8% (78 patients), respectively, during these strategy periods. In the intention-to-treat analysis, the risk of death was higher by 1.9 percentage points (90% confidence interval [CI], -0.6 to 4.4) with the beta-lactam-macrolide strategy than with the beta-lactam strategy and lower by 0.6 percentage points (90% CI, -2.8 to 1.9) with the fluoroquinolone strategy than with the beta-lactam strategy. These results indicated noninferiority of the beta-lactam strategy. The median length of hospital stay was 6 days for all strategies, and the median time to starting oral treatment was 3 days (interquartile range, 0 to 4) with the fluoroquinolone strategy and 4 days (interquartile range, 3 to 5) with the other strategies. CONCLUSIONS Among patients with clinically suspected CAP admitted to non-ICU wards, a strategy of preferred empirical treatment with beta-lactam monotherapy was noninferior to strategies with a beta-lactam-macrolide combination or fluoroquinolone monotherapy with regard to 90-day mortality.
引用
收藏
页码:1312 / 1323
页数:12
相关论文
共 40 条
  • [1] [Anonymous], 2012, ANTIMICROBIAL RESIST
  • [2] Cause-specific long-term mortality rates in patients recovered from community-acquired pneumonia as compared with the general Dutch population
    Bruns, A. H. W.
    Oosterheert, J. J.
    Cucciolillo, M. C.
    El Moussaoui, R.
    Groenwold, R. H. H.
    Prins, J. M.
    Hoepelman, A. I. M.
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2011, 17 (05) : 763 - 768
  • [3] Consort 2010 statement: extension to cluster randomised trials
    Campbell, Marion K.
    Piaggio, Gilda
    Elbourne, Diana R.
    Altman, Douglas G.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2012, 345
  • [4] Dutch National Institute for Public Health and the Environment, 2014, VIR WEEKST
  • [5] Empiric antibiotic coverage of atypical pathogens for community-acquired pneumonia in hospitalized adults
    Eliakim-Raz, Noa
    Robenshtok, Eyal
    Shefet, Daphna
    Gafter-Gvili, Anat
    Vidal, Liat
    Paul, Mical
    Leibovici, Leonard
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2012, (09):
  • [6] Moxifloxacin monotherapy versus β-lactam mono- or combination therapy in hospitalized patients with community-acquired pneumonia
    Ewig, S.
    Hecker, H.
    Suttorp, N.
    Marre, R.
    Welte, T.
    [J]. JOURNAL OF INFECTION, 2011, 62 (03) : 218 - 225
  • [7] Does Empiric Therapy for Atypical Pathogens Improve Outcomes for Patients with CAP?
    File, Thomas M., Jr.
    Marrie, Thomas J.
    [J]. INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2013, 27 (01) : 99 - +
  • [8] A review of Streptococcus pneumoniae infection treatment failures associated with fluoroquinolone resistance
    Fuller, JD
    Low, DE
    [J]. CLINICAL INFECTIOUS DISEASES, 2005, 41 (01) : 118 - 121
  • [9] β-Lactam Monotherapy vs β-Lactam-Macrolide Combination Treatment in Moderately Severe Community-Acquired Pneumonia A Randomized Noninferiority Trial
    Garin, Nicolas
    Genne, Daniel
    Carballo, Sebastian
    Chuard, Christian
    Eich, Gerhardt
    Hugli, Olivier
    Lamy, Olivier
    Nendaz, Mathieu
    Petignat, Pierre-Auguste
    Perneger, Thomas
    Rutschmann, Olivier
    Seravalli, Laurent
    Harbarth, Stephan
    Perrier, Arnaud
    [J]. JAMA INTERNAL MEDICINE, 2014, 174 (12) : 1894 - 1901
  • [10] Grobbee DE, 1997, BRIT MED J, V315, P1151