全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Impact of Inappropriate Empiric Antimicrobial Therapy on Mortality of Septic Patients with Bacteremia: A Retrospective Study

DOI: 10.1155/2012/765205

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background. Inappropriate empiric antimicrobials could be a major cause of unfavorable mortality rates in co-morbid patients. This study aimed to assess the prevalence and impact of first-dose and 24-hour inappropriate antimicrobials on mortality rates of bacteremic septic patients. Methods. A retrospective cohort study was employed. Case record forms of patients diagnosed as sepsis, severe sepsis, or septic shock with positive hemoculture during 2009 were retrieved from the medical wards, Siriraj Hospital. Demographic data, antimicrobial use, types of bacteria isolated from blood and susceptibilities, patients’ comorbidities, 28-day and overall mortality rates were collected and analyzed. Results. There were 229 cases, mean age (SD) of 63.5 (17.2) years and mean (SD) APACHE II score of 24.7 (6.8). The prevalence of first-dose and 24-hour inappropriate antimicrobials was 29.7% and 25.3%, respectively. The 28-day and overall mortality rates between first-dose inappropriate and appropriate antimicrobial were 67.6% versus 60.2% ( ) and 75.0% versus 68.3% ( ), consequently. Patients with septic shock and inappropriate first-dose antimicrobials significantly had higher 28-day mortality rate (61.6% versus 41.9%; ). Conclusion. Higher mortality rates in bacteremic septic patients were substantially associated with inappropriate first-dose antimicrobials and 3-hour delayed antimicrobial administration after sepsis diagnosis. 1. Background Sepsis is one of the most serious conditions related to high mortality in approximately 0.1–5 per 100 cases admitted to the hospital, and it also accounts for 5–15 percent of cases with overall infections. In 2007, there were 201 (5.8%) cases diagnosed as sepsis from 3,451 patients admitted to the medical wards in the Siriraj Hospital, of which 38.8% developed septic shock. Inappropriate antimicrobial therapy administration during the first 24 hours was observed in 34.2%. The mortality rate of patients with sepsis and septic shock was as high as 34.3% and 52.6%, respectively [1]. Two important factors on antimicrobial therapy pertaining to adverse events and death in septic patients were the initiation of inappropriate antimicrobial therapy [2] and the delay of appropriate antimicrobial therapy [3]. Inappropriate empiric antimicrobial therapy was attributed to 46.5% of cases, with 35% overall mortality [3]. The elapsed time to appropriate antimicrobial therapy was crucial for the mortality in patients with severe sepsis and septic shock [4]. The Surviving Sepsis Campaign’s 2008 “International guidelines for the management of

References

[1]  N. Angkasekwinai, P. Rattanaumpawan, and V. Thamlikitkul, “Epidemiology of sepsis in Siriraj Hospital 2007,” Journal of the Medical Association of Thailand, vol. 92, supplement 2, pp. S68–S78, 2009.
[2]  A. Kumar, P. Ellis, Y. Arabi et al., “Initiation of inappropriate antimicrobial therapy results in a fivefold reduction of survival in human septic shock,” Chest, vol. 136, no. 5, pp. 1237–1248, 2009.
[3]  D. F. Gaieski, M. E. Mikkelsen, R. A. Band et al., “Impact of time to antibiotics on survival in patients with severe sepsis or septic shock in whom early goal-directed therapy was initiated in the emergency department,” Critical Care Medicine, vol. 38, no. 4, pp. 1045–1053, 2010.
[4]  A. Kumar, D. Roberts, K. E. Wood et al., “Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock,” Critical Care Medicine, vol. 34, no. 6, pp. 1589–1596, 2006.
[5]  R. P. Dellinger, M. M. Levy, J. M. Carlet et al., “Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2008,” Critical Care Medicine, vol. 36, no. 1, pp. 296–327, 2008.
[6]  R. C. Bone, R. A. Balk, F. B. Cerra et al., “Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine. 1992,” Chest, vol. 101, no. 6, pp. 1644–1655, 1992.
[7]  W. A. Knaus, E. A. Draper, D. P. Wagner, and J. E. Zimmerman, “APACHE II: a severity of disease classification system,” Critical Care Medicine, vol. 13, no. 10, pp. 818–829, 1985.
[8]  J. S. Garner, W. R. Jarvis, T. G. Emori, T. C. Horan, and J. M. Hughes, “CDC Defionitions for nosocomial infections, 1988,” American Journal of Infection Control, vol. 16, no. 3, pp. 128–140, 1988.
[9]  P. Y. Bochud, M. Bonten, O. Marchetti, and T. Calandra, “Antimicrobial therapy for patients with severe sepsis and septic shock: an evidence-based review,” Critical Care Medicine, vol. 32, no. 11, supplement, pp. S495–S512, 2004.
[10]  M. M. Levy, M. P. Fink, J. C. Marshall et al., “2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference,” Critical Care Medicine, vol. 31, no. 4, pp. 1250–1256, 2003.
[11]  A. Kumar, R. Zarychanski, B. Light et al., “Early combination antibiotic therapy yields improved survival compared with monotherapy in septic shock: a propensity-matched analysis,” Critical Care Medicine, vol. 38, no. 9, pp. 1773–1785, 2010.
[12]  “Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia,” American Journal of Respiratory and Critical Care Medicine, vol. 171, no. 4, pp. 388–416, 2005.
[13]  A. Kumar, C. Haery, B. Paladugu et al., “The duration of hypotension before the initiation of antibiotic treatment is a critical determinant of survival in a murine model of Escherichia coli septic shock: association with serum lactate and inflammatory cytokine levels,” Journal of Infectious Diseases, vol. 193, no. 2, pp. 251–258, 2006.
[14]  H. W. Boucher, G. H. Talbot, J. S. Bradley et al., “Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America,” Clinical Infectious Diseases, vol. 48, no. 1, pp. 1–12, 2009.
[15]  W. A. Knaus, X. Sun, P. O. Nystrom, and D. P. Wagner, “Evaluation of definitions for sepsis,” Chest, vol. 101, no. 6, pp. 1656–1662, 1992.
[16]  J. N. Krieger, D. L. Kaiser, and R. P. Wenzel, “Urinary tract etiology of bloodstream infections in hospitalized patients,” Journal of Infectious Diseases, vol. 148, no. 1, pp. 57–62, 1983.
[17]  L. Leibovici, M. Paul, O. Poznanski et al., “Monotherapy versus β-lactam-aminoglycoside combination treatment for gram-negative bacteremia: a prospective, observational study,” Antimicrobial Agents and Chemotherapy, vol. 41, no. 5, pp. 1127–1133, 1997.
[18]  E. H. Ibrahim, G. Sherman, S. Ward, V. J. Fraser, and M. H. Kollef, “The influence of inadequate antimicrobial treatment of bloodstream infections on patient outcomes in the ICU setting,” Chest, vol. 118, no. 1, pp. 146–155, 2000.
[19]  G. Behrendt, S. Schneider, H. R. Brodt, G. Just-Nübling, and P. M. Shah, “Influence of antimicrobial treatment on mortality in septicemia,” Journal of Chemotherapy, vol. 11, no. 3, pp. 179–186, 1999.
[20]  R. Zaragoza, A. Artero, J. J. Camarena, S. Sancho, R. González, and J. M. Nogueira, “The influence of inadequate empirical antimicrobial treatment on patients with bloodstream infections in an intensive care unit,” Clinical Microbiology and Infection, vol. 9, no. 5, pp. 412–418, 2003.
[21]  S. Blot, K. Vandewoude, D. de Bacquer, and F. Colardyn, “Nosocomial bacteremia caused by antibiotic-resistant gram-negative bacteria in critically ill patients: clinical outcome and length of hospitalization,” Clinical Infectious Diseases, vol. 34, no. 12, pp. 1600–1606, 2002.
[22]  M. Paul, V. Shani, E. Muchtar, G. Kariv, E. Robenshtok, and L. Leibovici, “Systematic review and meta-analysis of the efficacy of appropriate empiric antibiotic therapy for sepsis,” Antimicrobial Agents and Chemotherapy, vol. 54, no. 11, pp. 4851–4863, 2010.
[23]  T. P. Lodise, P. S. McKinnon, L. Swiderski, and M. J. Rybak, “Outcomes analysis of delayed antibiotic treatment for hospital-acquired Staphylococcus aureus bacteremia,” Clinical Infectious Diseases, vol. 36, no. 11, pp. 1418–1423, 2003.
[24]  A. F. Shorr, S. T. Micek, E. C. Welch, J. A. Doherty, R. M. Reichley, and M. H. Kollef, “Inappropriate antibiotic therapy in Gram-negative sepsis increases hospital length of stay,” Critical Care Medicine, vol. 39, no. 1, pp. 46–51, 2011.
[25]  S. Reisfeld, M. Paul, B. S. Gottesman, P. Shitrit, L. Leibovici, and M. Chowers, “The effect of empiric antibiotic therapy on mortality in debilitated patients with dementia,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 30, no. 6, pp. 813–818, 2011.
[26]  J. A. Cortés, D. C. Garzón, J. A. Navarrete, and K. M. Contreras, “Impact of inappropriate antimicrobial therapy on patients with bacteremia in intensive care units and resistance patterns in Latin America,” Revista Argentina de Microbiologia, vol. 42, no. 3, pp. 230–234, 2010.
[27]  C. Permpikul, S. Tongyoo, R. Ratanarat, W. Wilachone, and A. Poompichet, “Impact of septic shock hemodynamic resuscitation guidelines on rapid early volume replacement and reduced mortality,” Journal of the Medical Association of Thailand, vol. 93, supplement 1, pp. S102–109, 2010.
[28]  C. I. Kang, S. H. Kim, W. B. Park et al., “Bloodstream infections caused by antibiotic-resistant gram-negative bacilli: risk factors for mortality and impact of inappropriate initial antimicrobial therapy on outcome,” Antimicrobial Agents and Chemotherapy, vol. 49, no. 2, pp. 760–766, 2005.
[29]  O. Zarkotou, S. Pournaras, P. Tselioti et al., “Predictors of mortality in patients with bloodstream infections caused by KPC-producing Klebsiella pneumoniae and impact of appropriate antimicrobial treatment,” Clinical Microbiology and Infection, vol. 17, no. 12, pp. 1798–1803, 2011.
[30]  M. T. Johnson, R. Reichley, J. Hoppe-Bauer, W. M. Dunne, S. Micek, and M. Kollef, “Impact of previous antibiotic therapy on outcome of Gram-negative severe sepsis,” Critical Care Medicine, vol. 39, no. 8, pp. 1859–1865, 2011.
[31]  K. P. Abhilash, B. Veeraraghavan, and O. C. Abraham, “Epidemiology and outcome of bacteremia caused by extended spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella spp. in a tertiary care teaching hospital in south India,” The Journal of the Association of Physicians of India, vol. 58, supplement, pp. 13–17, 2010.
[32]  A. Apisarnthanarak, W. Buppunharun, S. Tiengrim, P. Sawanpanyalert, and N. Aswapokee, “An overview of antimicrobial susceptibility patterns for gram-negative bacteria from the National Antimicrobial Resistance Surveillance Thailand (NARST) program from 2000 to 2005,” Journal of the Medical Association of Thailand, vol. 92, pp. S91–S94, 2009.
[33]  P. Kiratisin, A. Apisarnthanarak, C. Laesripa, and P. Saifon, “Molecular characterization and epidemiology of extended-spectrum-β-lactamase-producing Escherichia coli and Klebsiella pneumoniae isolates causing health care-associated infection in Thailand, where the CTX-M family is endemic,” Antimicrobial Agents and Chemotherapy, vol. 52, no. 8, pp. 2818–2824, 2008.
[34]  J. C. Lucet, S. Chevret, D. Deeré et al., “Outbreak of multiply resistant enterobacteriaceae in an intensive care unit: epidemiology and risk factors for acquisition,” Clinical Infectious Diseases, vol. 22, no. 3, pp. 430–436, 1996.
[35]  C. Pe?a, M. Pujol, C. Ardanuy et al., “Epidemiology and successful control of a large outbreak due to Klebsiella pneumoniae producing extended spectrum β-lactamases,” Antimicrobial Agents and Chemotherapy, vol. 42, no. 1, pp. 53–58, 1998.
[36]  D. L. Paterson, W. C. Ko, A. Von Gottberg et al., “International prospective study of Klebsiella pneumoniae Bacteremia: implications of extended-spectrum β-Lactamase production in Nosocomial infections,” Annals of Internal Medicine, vol. 140, no. 1, pp. 26–32, 2004.
[37]  J. Rodríguez-Ba?o, E. Picón, P. Gijón et al., “Community-onset bacteremia due to extended-spectrum β-lactamase- producing Escherichia coli: risk factors and prognosis,” Clinical Infectious Diseases, vol. 50, no. 1, pp. 40–48, 2010.
[38]  D. L. Paterson, W. C. Ko, A. Von Gottberg et al., “Antibiotic therapy for Klebsiella pneumoniae bacteremia: implications of production of extended-spectrum β-lactamases,” Clinical Infectious Diseases, vol. 39, no. 1, pp. 31–37, 2004.
[39]  A. Endimiani, F. Luzzaro, M. Perilli et al., “Bacteremia due to Klebsiella pneumoniae isolates producing the TEM-52 extended-spectrum β-Lactamase: treatment outcome of patients receiving imipenem or ciprofloxacin,” Clinical Infectious Diseases, vol. 38, no. 2, pp. 243–251, 2004.
[40]  J. Oteo, M. Pérez-Vázquez, and J. Campos, “Extended-spectrum β-lactamase producing Escherichia coli: changing epidemiology and clinical impact,” Current Opinion in Infectious Diseases, vol. 23, no. 4, pp. 320–326, 2010.
[41]  P. Kansakar, D. Dorji, P. Chongtrakool, S. Mingmongkolchai, B. Mokmake, and P. Dubbs, “Local dissemination of multidrug-resistant Acinetobacter baumannii clones in a Thai Hospital,” Microbial Drug Resistance, vol. 17, no. 1, pp. 109–119, 2011.
[42]  K. Lolans, T. W. Rice, L. S. Munoz-Price, and J. P. Quinn, “Multicity outbreak of carbapenem-resistant Acinetobacter baumannii isolates producing the carbapenemase OXA-40,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 9, pp. 2941–2945, 2006.
[43]  S. Anunnatsiri and P. Tonsawan, “Risk factors and clinical outcomes of multidrug-resistant Acinetobacter baumannii bacteremia at a university hospital in Thailand,” Southeast Asian Journal of Tropical Medicine and Public Health, vol. 42, no. 3, pp. 693–703, 2011.
[44]  M. Dizbay, O. G. Tunccan, B. E. Sezer, and K. Hizel, “Nosocomial imipenem-resistant Acinetobacter baumannii infections: epidemiology and risk factors,” Scandinavian Journal of Infectious Diseases, vol. 42, no. 10, pp. 741–746, 2010.
[45]  E. Tacconelli, M. A. Cataldo, G. de Pascale et al., “Prediction models to identify hospitalized patients at risk of being colonized or infected with multidrug-resistant Acinetobacter baumannii calcoaceticus complex,” Journal of Antimicrobial Chemotherapy, vol. 62, no. 5, pp. 1130–1137, 2008.
[46]  J. Y. Jung, M. S. Park, S. E. Kim et al., “Risk factors for multi-drug resistant Acinetobacter baumannii bacteremia in patients with colonization in the intensive care unit,” BMC Infectious Diseases, vol. 10, article 228, 2010.
[47]  A. S. Levin, A. A. Barone, J. Pen?o et al., “Intravenous colistin as therapy for nosocomial infections caused by multidrug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii,” Clinical Infectious Diseases, vol. 28, no. 5, pp. 1008–1011, 1999.
[48]  J. Garnacho-Montero, C. Ortiz-Leyba, F. J. Jiménez-Jiménez et al., “Treatment of multidrug-resistant Acinetobacter baumannii ventilator-associated pneumonia (VAP) with intravenous colistin: a comparison with imipenem-susceptible VAP,” Clinical Infectious Diseases, vol. 36, no. 9, pp. 1111–1118, 2003.
[49]  P. Koomanachai, S. Tiengrim, P. Kiratisin, and V. Thamlikitkul, “Efficacy and safety of colistin (colistimethate sodium) for therapy of infections caused by multidrug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii in Siriraj Hospital, Bangkok, Thailand,” International Journal of Infectious Diseases, vol. 11, no. 5, pp. 402–406, 2007.
[50]  D. Curcio, F. Fernandez, J. Vergara, W. Vazquez, and C. M. Luna, “Late onset ventilator-associated pneumonia due to multidrug-resistant Acinetobacter spp.: experience with tigecycline,” Journal of Chemotherapy, vol. 21, no. 1, pp. 58–62, 2009.
[51]  G. Metan, E. Alp, O. Yildiz, D. Percin, B. Aygen, and B. Sumerkan, “Clinical experience with tigecycline in the treatment of carbapenem-resistant Acinetobacter infections,” Journal of Chemotherapy, vol. 22, no. 2, pp. 110–114, 2010.
[52]  M. Paul, G. Kariv, E. Goldberg et al., “Importance of appropriate empirical antibiotic therapy for methicillin-resistant Staphylococcus aureus bacteraemia,” Journal of Antimicrobial Chemotherapy, vol. 65, no. 12, Article ID dkq373, pp. 2658–2665, 2010.
[53]  V. Schneider-Lindner, J. A. Delaney, S. Dial, A. Dascal, and S. Suissa, “Antimicrobial drugs and community-acquired methicillin-resistant Staphylococcus aureus, United Kingdom,” Emerging Infectious Diseases, vol. 13, no. 7, pp. 994–1000, 2007.
[54]  S. J. Spindel, L. J. Strausbaugh, and C. Jacobson, “Infections caused by Staphylococcus aureus in a Veterans' Affairs nursing home care unit: a 5-year experience,” Infection Control and Hospital Epidemiology, vol. 16, no. 4, pp. 217–223, 1995.
[55]  J. D. Szumowski, K. M. Wener, H. S. Gold et al., “Methicillin-resistant Staphylococcus aureus colonization, behavioral risk factors, and skin and soft-tissue infection at an ambulatory clinic serving a large population of hiv-infected men who,” Clinical Infectious Diseases, vol. 49, no. 1, pp. 118–121, 2009.
[56]  S. H. Kim, K. H. Kim, H. B. Kim et al., “Outcome of vancomycin treatment in patients with methicillin-susceptible Staphylococcus aureus bacteremia,” Antimicrobial Agents and Chemotherapy, vol. 52, no. 1, pp. 192–197, 2008.
[57]  A. Kumar, N. Safdar, S. Kethireddy, and D. Chateau, “A survival benefit of combination antibiotic therapy for serious infections associated with sepsis and septic shock is contingent only on the risk of death: a meta-analytic/meta-regression study,” Critical Care Medicine, vol. 38, no. 8, pp. 1651–1664, 2010.
[58]  J. A. Russell, “Management of sepsis,” The New England Journal of Medicine, vol. 355, no. 16, pp. 1699–1713, 2006.
[59]  D. Vogelaers, D. de Bels, F. Forêt et al., “Patterns of antimicrobial therapy in severe nosocomial infections: empiric choices, proportion of appropriate therapy, and adaptation rates—a multicentre, observational survey in critically ill patients,” International Journal of Antimicrobial Agents, vol. 35, no. 4, pp. 375–381, 2010.
[60]  A. Y. Peleg and D. C. Hooper, “Hospital-acquired infections due to gram-negative bacteria,” The New England Journal of Medicine, vol. 362, no. 19, pp. 1804–1813, 2010.
[61]  S. Deuster, I. Roten, and S. Muehlebach, “Implementation of treatment guidelines to support judicious use of antibiotic therapy,” Journal of Clinical Pharmacy and Therapeutics, vol. 35, no. 1, pp. 71–78, 2010.
[62]  E. van Gastel, M. Costers, W. E. Peetermans, and M. J. Struelens, “Nationwide implementation of antibiotic management teams in Belgian hospitals: a self-reporting survey,” Journal of Antimicrobial Chemotherapy, vol. 65, no. 3, Article ID dkp470, pp. 576–580, 2010.
[63]  E. Raineri, A. Pan, P. Mondello, A. Acquarolo, A. Candiani, and L. Crema, “Role of the infectious diseases specialist consultant on the appropriateness of antimicrobial therapy prescription in an intensive care unit,” American Journal of Infection Control, vol. 36, no. 4, pp. 283–290, 2008.
[64]  P. Lesprit, L. Merabet, J. Fernandez, P. Legrand, and C. Brun-Buisson, “Improving antibiotic use in the hospital: focusing on positive blood cultures is an effective option,” Presse Medicale, vol. 40, no. 6, pp. e297–e303, 2011.
[65]  S. Diamantis, C. Rioux, C. Bonnal et al., “Evaluation of initial antibiotic therapy for bacteremia and role of an antibiotic management team for antibiotic stewardship,” Medecine et Maladies Infectieuses, vol. 40, no. 11, pp. 637–643, 2010.
[66]  A. Corona, G. Bertolini, J. Lipman, A. P. Wilson, and M. Singer, “Antibiotic use and impact on outcome from bacteraemic critical illness: the BActeraemia Study in Intensive Care (BASIC),” Journal of Antimicrobial Chemotherapy, vol. 65, no. 6, pp. 1276–1285, 2010.
[67]  S. Harbarth, V. Nobre, and D. Pittet, “Does antibiotic selection impact patient outcome?” Clinical Infectious Diseases, vol. 44, no. 1, pp. 87–93, 2007.
[68]  C. Pe?a, C. Gudiol, L. Calatayud et al., “Infections due to Escherichia coli producing extended-spectrum β-lactamase among hospitalised patients: factors influencing mortality,” Journal of Hospital Infection, vol. 68, no. 2, pp. 116–122, 2008.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413