Infection Control and Hospital Epidemiology Publication Info
For individual subscriptions, please contact the The University of Chicago Press
University of Chicago Press Customer Service:
1.877.705.1878 (toll-free, U.S. & Canada)
1.773.753.3347 (international)
subscriptions@press.uchicago.edu
For information about institutional access to this title, please visit the Institutional Subscriptions page.
Risk Factors for and Clinical Outcomes of Bloodstream Infections Caused by Extended‐Spectrum Beta‐Lactamase–Producing Klebsiella pneumoniae
Formats Available in JSTOR: PDF
Abstract(back to top)
OBJECTIVE. To evaluate risk factors and treatment outcomes of bloodstream infections caused by extended‐spectrum beta‐lactamase–producing Klebsiella pneumoniae (ESBL‐KP).
DESIGN. Retrospective case–control study. Stored blood isolates of K. pneumoniae were tested for ESBL production by NCCLS guidelines, double‐disk synergy test, or both.
SETTING. A 1,500‐bed, tertiary‐care university hospital and referral center.
PATIENTS. Sixty case‐patients with bacteremia due to ESBL‐KP were compared with 60 matched control‐patients with non–ESBL‐KP.
RESULTS. There were no significant differences in age, gender, APACHE II score, or underlying diseases between the groups. Independent risk factors for infections caused by ESBL‐KP were urinary catheterization, invasive procedure within the previous 72 hours, and an increasing number of antibiotics administered within the previous 30 days. Complete response rate, evaluated 72 hours after initial antimicrobial therapy, was higher among control‐patients (13.3% vs 36.7%; P = .003). Treatment failure rate was higher among case‐patients (35.0% vs 15%; P = .011). Overall 30‐day mortality rate was 30% for case‐patients and 28.3% for control‐patients (P = .841). Case‐patients who received imipenem or ciprofloxacin as a definitive antibiotic had 10.5% mortality. The mortality rate for initially ineffective therapy was no higher than that for initially effective therapy (9.1% vs 11.1%; P = 1.000), but statistical power was low for evaluating mortality in the absence of septic shock.
CONCLUSION. For K. pneumoniae bacteremia, patients with ESBL‐KP had a higher initial treatment failure rate but did not have higher mortality if antimicrobial therapy was appropriately adjusted in this study with limited statistical power.
Bibliographic Information(back to top)
- Risk Factors for and Clinical Outcomes of Bloodstream Infections Caused by Extended‐Spectrum Beta‐Lactamase–Producing Klebsiella pneumoniae
- Cheol‐In Kang , MD, Sung‐Han Kim , MD, Dong Min Kim , MD, Wan Beom Park , MD, Ki‐Deok Lee , MD, Hong‐Bin Kim , MD, Myoung‐don Oh , MD, Eui‐Chong Kim , MD and Kang‐Won Choe , MD
- Infection Control and Hospital Epidemiology
- Vol. 25, No. 10 (October 2004) (pp. 860-867)
Notes and References(back to top)
This item contains 1 note(s).
Notes
Drs. Kang, S‐H. Kim, D. M. Kim, Park, Lee, H‐B. Kim, Oh, and Choe are from the Department of Internal Medicine and Dr. E‐C. Kim is from the Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, South Korea. Drs. Oh, E‐C. Kim, and Choe are also from the Clinical Research Institute, Seoul National University Hospital, Seoul, South Korea.Address reprint requests to Myoung‐don Oh, MD, Department of Internal Medicine, Seoul National University College of Medicine, 28 Yongon‐dong Chongno‐gu, Seoul 110‐744, Republic of Korea.Presented in part at the 13th European Congress of Clinical Microbiology and Infectious Diseases; May 10‐13, 2003; Glasgow, United Kingdom.
Items Citing this Item (back to top)
8 item(s) in JSTOR cite this item
- Debby Ben‐David , MD; Yasmin Maor , MD; Nathan Keller , MD; Gili Regev‐Yochay , MD; Ilana Tal , MS; Dalit Shachar , RN; Amir Zlotkin , PhD; Gill Smollan , MD; Galia Rahav , MDVol. 31, No. 6 (June 2010) pp. 620-626Stable URL: http://www.jstor.org/stable/10.1086/652528
- Elizabeth Cerceo , MD; Ebbing Lautenbach , MD, MPH, MSCE; Darren R. Linkin , MD, MSCE; Warren B. Bilker , PhD; Ingi Lee , MD, MSCEVol. 30, No. 5 (May 2009) pp. 479-483Stable URL: http://www.jstor.org/stable/10.1086/597061
- Anucha Apisarnthanarak , MD; Pattarachai Kiratisin , MD, PhD; Linda M. Mundy , MDVol. 29, No. 11 (November 2008) pp. 1026-1034Stable URL: http://www.jstor.org/stable/10.1086/591864
- C. Laurent MDMDRNRNMD, PhDMScMD, PhDMD, PhD; H. Rodriguez-Villalobos MDMDRNRNMD, PhDMScMD, PhDMD, PhD; F. Rost MDMDRNRNMD, PhDMScMD, PhDMD, PhD; H. Strale MDMDRNRNMD, PhDMScMD, PhDMD, PhD; J.-L. Vincent MDMDRNRNMD, PhDMScMD, PhDMD, PhD; A. Deplano MDMDRNRNMD, PhDMScMD, PhDMD, PhD; M. J. Struelens MDMDRNRNMD, PhDMScMD, PhDMD, PhD; B. Byl MDMDRNRNMD, PhDMScMD, PhDMD, PhDVol. 29, No. 6 (June 2008) pp. 517-524Stable URL: http://www.jstor.org/stable/10.1086/588004
- Anucha Apisarnthanarak , MD; Pattarachai Kiratisin , MD, PhD; Payawan Saifon , BSc; Rungrueng Kitphati , MD; Surang Dejsirilert , MSc; Linda M. Mundy , MDVol. 28, No. 7 (July 2007) pp. 873-876Stable URL: http://www.jstor.org/stable/10.1086/518725
- Emily P. Hyle , MD; Warren B. Bilker , PhD; Leanne B. Gasink , MD, MSCE; Ebbing Lautenbach , MD, MPH, MSCEVol. 28, No. 6 (June 2007) pp. 647-654Stable URL: http://www.jstor.org/stable/10.1086/516798
- Anucha Apisarnthanarak , MD; Linda M. Mundy , MDVol. 27, No. 3 (March 2006) p. 325Stable URL: http://www.jstor.org/stable/10.1086/503018
- Cheol‐In Kang , MD; Sung‐Han Kim , MD; Wan Beom Park , MD; Ki‐Deok Lee , MD; Hong‐Bin Kim , MD; Eui‐Chong Kim , MD; Myoung‐don Oh , MD; Kang‐Won Choe , MDVol. 26, No. 1 (January 2005) pp. 88-92Stable URL: http://www.jstor.org/stable/10.1086/502492