Logo of jkmsThis ArticleThis JournalJKMS Journal of Korean Medical ScienceAboutFor Contributorse-Submission
J Korean Med Sci. 2010 Jul; 25(7): 992–998.
Published online 2010 Jun 18. doi:  10.3346/jkms.2010.25.7.992
PMCID: PMC2890898

Bloodstream Infections and Clinical Significance of Healthcare-associated Bacteremia: A Multicenter Surveillance Study in Korean Hospitals


Recent changes in healthcare systems have changed the epidemiologic paradigms in many infectious fields including bloodstream infection (BSI). We compared clinical characteristics of community-acquired (CA), hospital-acquired (HA), and healthcare-associated (HCA) BSI. We performed a prospective nationwide multicenter surveillance study from 9 university hospitals in Korea. Total 1,605 blood isolates were collected from 2006 to 2007, and 1,144 isolates were considered true pathogens. HA-BSI accounted for 48.8%, CA-BSI for 33.2%, and HCA-BSI for 18.0%. HA-BSI and HCA-BSI were more likely to have severe comorbidities. Escherichia coli was the most common isolate in CA-BSI (47.1%) and HCA-BSI (27.2%). In contrast, Staphylococcus aureus (15.2%), coagulase-negative Staphylococcus (15.1%) were the common isolates in HA-BSI. The rate of appropriate empiric antimicrobial therapy was the highest in CA-BSI (89.0%) followed by HCA-BSI (76.4%), and HA-BSI (75.0%). The 30-day mortality rate was the highest in HA-BSI (23.0%) followed by HCA-BSI (18.4%), and CA-BSI (10.2%). High Pitt score and inappropriate empirical antibiotic therapy were the independent risk factors for mortality by multivariate analysis. In conclusion, the present data suggest that clinical features, outcome, and microbiologic features of causative pathogens vary by origin of BSI. Especially, HCA-BSI shows unique clinical characteristics, which should be considered a distinct category for more appropriate antibiotic treatment.

Keywords: Bloodstream infection, Bacteremia, Community-acquired, Hospital-acquired, Healthcare-associated


Bloodstream infection (BSI) is potentially life-threatening condition with a case fatality rate of 30-40% (1). If BSI is clinically suspected, clinicians should choose antibiotics based on the type of infection, underlying disease, patient age, infecting pathogen, and site of acquisition of infection (2).

BSI can be classified as community-acquired (CA), hospitalacquired (HA), or healthcare-associated (HCA) depending on the site of acquiring infection and risk factors. Of 3 epidemiologic categories, HCA-BSI is a recently developed category that is traditionally classified as CA-BSI (3-5).

Clinically, the characteristics of HA-BSI can be separated from those of CA-BSI in many factors such as pathogen distribution, type of infection and their susceptibility patterns. Staphlylococcus and catheter-related infection were predominant in HA-BSI, while Escherichia coli and urinary tract infection were generally predominant in CA-BSI (6-8). With regard to HCA-BSI, previous studies showed that the clinical characteristics were not similar to those of CA-BSI (3, 5, 9). And the susceptibility patterns of HCA-BSI were similar to those of HA-BSI (5, 9). Generally, the concept of HCA-BSI has been accepted to be an independent epidemiologic category of BSI. However, so far the detailed data of clinical characteristics of HCA-BSI were not sufficient. Also, the independent risk factors for mortality of each BSI have not been compared yet.

In this study, we compared clinical characteristics of 3 BSI groups including HCA-BSI, instead of investigating one pathogen or one source. And we performed additional analysis to evaluate risk factors for mortality according to the epidemiologic type of infection.


Study design and data collection

This study was a prospective nationwide surveillance of BSI in 9 university hospitals in various regions of Korea from October 2006 to September 2007. The participating institutions included Kyunghee East-West Neo Medical Center (800-bed, Seoul), Samsung Medical Center (1,270-bed, Seoul), Kangbuk Samung Hospital (620-bed, Seoul), Konkuk University Hospital (820-bed, Seoul), Kyungpook National University Hospital (850-bed, Daegu), Keimyung University Dongsan Medical Center (910-bed, Daegu), Chungnam National University Hospital (980-bed, Daejeon), Chonnam National University Hospital (850-bed, Gwangju), and Jeju National University Hospital (300-bed, Jeju). The following data were collected from all cases of BSI; demographic information, underlying disease, comorbid conditions, microbiological data, sources of infection, and other important clinical parameters at the time of infection. The main clinical outcome was measured by the 30-day mortality rate.

Study population

All blood isolates during the study period from the participating hospitals were reviewed for clinical significance. Cases that showed clinical features of Systemic Inflammatory Response Syndrome (SIRS) were included in this study. SIRS was defined by the presence of at least two of the following signs and symptoms: tachycardia (pulse rate >90 beats/min); tachypnea (respiratory rate >20/min); fever (body temperature >38℃) or hypothermia (body temperature <36℃); leukocytosis (white blood cell count >12,000 cells/µL) or leukopenia (white blood cell count <4,000 cells/µL) (10). The site of infection causing BSI was estimated by infectious disease specialist at participating institutions. All underlying diseases and comorbid conditions for each patient were included in the analysis. And only the first bacteremic episode for each patient was included.


BSI cases were classified as CA, HA, or HCA depending on the site of acquiring infection and risk factors. HA-BSI was defined if blood culture was positive >48 hr from admission or who had been discharged from an acute care hospital within the past 10 days. HCA-BSI was defined if patients had a history of hospitalization for 2 or more days in the previous 90 days; receipt of intravenous (IV) medication or home wound care in the previous 30 days; receipt of hemodialysis; or residence in a nursing home or long-term care facility (3, 5, 9). CA-BSI was defined if patients had the first positive blood culture <48 hr after admission and who did not have any risk factors for HCA-BSI. Neutropenia was defined as an absolute neutrophil count below 500/µL. Corticosteroid use was noted only if the patient had recently received the equivalent of 30 mg of prednisone daily for at least seven days, or 20 mg each day for 14 days. Receipt of immunosuppressant was defined as use of any immunosuppressive drug (e.g., cyclosporine, antineoplastic chemotherapy) in the previous 30 days. Prior antibiotic use was defined as use of antimicrobial agent for >3 days in the previous 30 days. High alcohol uptake was noted if the patient had ingested >100 g of alcohol every day. Severe sepsis was defined as sepsis associated with the presence of at least one or more following signs of organ dysfunction; metabolic acidosis, acute alteration in mental status, oliguria, and/or adult respiratory distress syndrome (11). The Pitt score was calculated within 2 days prior to or on the day of first positive blood culture on the basis of 5 parameters (fever, hypotension, mechanical ventilation, cardiac arrest, and mental status) (12). The initial empirical antibiotic therapy was considered 'appropriate' if the initial antibiotics, which were administered within 24 hr after acquisition of blood culture samples, included at least one antibiotic that was active in vitro and when the dosage and route of administration confirmed with current medical standards. Otherwise, initial antibiotic therapy was considered 'inappropriate' (13). The 'improvement' of treatment outcome was defined as partial resolution of presenting signs and test results (e.g., fever, elevated leukocyte) of the infection (14).

Microbiological tests

All isolates identified from each hospital were transported to the central laboratory of the Asian-Pacific Research Foundation for Infectious Diseases (ARFID), Seoul, Republic of Korea. Antibiotic susceptibility testing was performed in this laboratory using the modified broth microdilution method. Minimum inhibitory concentration (MIC) breakpoints and quality control protocols were used according to the standards established by the Clinical and Laboratory Standards Institute (CLSI) (15).

Statistical analysis

Student's t-test was used to compare continuous variables (age and PITT score), and chi-square or Fisher's exact test was used to compare categorical variables (underlying diseases, comorbid conditions, microorganism distributions, sources of infection, and treatment outcome). For pairwise comparisons, 3×2 table (3 epidemiologic type of BSI) was broken down into three 2×2 tables (CA vs. HCA, HA vs. HCA, CA vs. HA). To determine the independent risk factors for mortality, a multiple logistic regression analysis was used. P values <0.05 were considered statistically significant. The SPSS for Windows software package (version 11.5) was used for this analysis.


This study was performed with an exemption of the deliberation permitted by the Institutional Review Board at East-West Neo Medical Center (2009-075). All data collected from this study were kept confidential.


Patient characteristics

A total of 1,605 blood isolates were obtained from 9 hospitals between October 2006 and September 2007. Of these 1,605 isolates, 461 isolates (28.7%) were not considered true pathogens because there were no compatible clinical features of SIRS. Among 1,144 isolates included in the study, HA-BSI accounted for 48.8% (558/1,144), CA-BSI for 33.2% (380/1,144), and HCA-BSI for 18.0% (206/1,144).

The mean age was the highest in patients with CA-BSI (57.0±20.7), followed by HCA-BSI (53.7±20.7), and HA-BSI (47.3±23.7) (Table 1). With regard to underlying diseases, solid tumor and hematologic malignancy was the most common disease in HCA-BSI group (54.9%) and HA-BSI group (24.6%), respectively. Compared with other groups, patients with CA-BSI were significantly less likely to have solid tumor (24.2%, 32.4%, 54.9% in CA-BSI, HA-BSA, and HCA-BSI, P<0.005, respectively) and hematologic malignancy (3.4%, 24.6%, 16.0% in CA-BSI, HA-BSA, and HCA-BSI, P<0.005, respectively).

Table 1
Patient characteristics of bloodstream infection by epidemiologic type of infection

Patients with HA-BSI or HCA-BSI were more likely to have severe comorbidities (neutropenia, receipt of steroids, receipt of immunosuppressant, or prior antibiotic use) compared with CA-BSI group (for neutropenia, 8.9%, 28.3%, 25.2% in CA-BSI, HA-BSI, and HCA-BSI, P<0.005; for receipt of steroid, 4.7%, 28.1%, 24.3%, P<0.005; for receipt of immunosuppressant, 9.2%, 33.2%, 31.6%, P<0.005; for prior antibiotic use, 7.1%, 54.7%, 14.6%, respectively, P<0.005).

Pathogen distribution

Of all BSI isolates, 59.2% were Gram-negative aerobes, and 38.9% were Gram-positive aerobes. As a total, E. coli (27.8%) was the most common isolate followed by Klebsiella pneumoniae (13.6%), S. aureus (12.4%), coagulase-negative Staphylococcus (9%), Enterococcus species (7.1%) (Table 2). The prevalence of E. coli was the highest in CA-BSI group, and the incidence of E. coli varied by type of BSI (47.1%, 14.9%, 27.2% in CA-BSI, HA-BSA, and HCA-BSI, respectively, P<0.005). Of CA-BSI isolates, the incidence of Gram-negative aerobes (70.5%) was more than two times higher than that of Gram-positive aerobes (28.2%). E. coli (47.1%) and K. pneumoniae (12.6%) represent more than half of the isolates in CA-BSI followed by S. aureus (7.4%), Streptococcus viridans group (5.0%). Of HA-BSI isolates, 49.1% were Gram-negative aerobes, and 48.0% were Gram-positive aerobes. The most common isolate of HA-BSI was S. aureus (15.2%) followed by coagulase-negative Staphylococcus (15.1%), and E. coli (14.9%). The pattern of isolates in HCA-BSI was more similar to that in CA-BSI than that in HA-BSI. Of HCA-BSI isolates, Gram-negative aerobes (65.5%) were more common than Gram-positive aerobes (34.0%) like CA-BSI. However, isolate distributions of CA-BSI and HCA-BSI group were not identical. While E. coli (47.1% vs. 27.2% in CA-BSI vs. HCA-BSI, P<0.001) and Streptococcus pneumoniae (3.9% vs. 1.0% in CA-BSI vs. HCA-BSI, P=0.04) were recovered more frequently in CA-BSI, S. aureus (7.4% vs. 14.1% in CA-BSI vs. HCA-BSI, P=0.009) and P. aeruginosa (2.9% vs. 7.8% in CA-BSI vs. HCA-BSI, P=0.007) were more prevalent in HCA-BSI.

Table 2
Microorganism distribution of bloodstream infection by epidemiologic type of infection

With regard to resistant pathogens, extended spectrum beta-lactamase (ESBL)-producing E. coli was most frequently recovered in patients with HA-BSI (31.3%), followed by HCA-BSI (14.2%) and CA-BSI (3.3%) (HA-BSI vs. CA-BSI, P<0.001; HA-BSI vs. HCA-BSI, P=0.021; HCA-BSI vs. CA-BSI, P=0.002). ESBL-producing K. pneumoniae was common in patients with HA-BSI (18.9%), followed by HCA-BSI (14.7%) and CA-BSI (4.1%). Although, it did not show the statistical difference for the prevalence of ESBL-producing K. pneumoniae (HA-BSI vs HCA-BSI, P=0.593; HCA-BSI vs. CA-BSI, P=0.092) except between HA-BSI and CA-BSI (P=0.018). Methicillin-resistant Staphylococcus aureus (MRSA) was higher in HA-BSI (69.4%), compared with HCA-BSI (31.0%, P<0.001) and CA-BSI group (17.8%, P<0.001).

Primary infection

The primary infections causing BSI significantly varied by type of BSI. The most common primary infection of CA-BSI were urinary tract infection (UTI) (31.3%) and intra-abdominal infection (30.5%) (Table 3). In contrast, primary bacteremia (53.2%) was the most common in HA-BSI group followed by intra-abdominal infection (17.6%), and pneumonia (14.2%). The most common primary infection of HCA-BSI was primary bacteremia (39.8%) like HA-BSI, and followed by intra-abdominal infection (27.2%) and UTI (14.2%).

Table 3
Primary sources of bloodstream infection by epidemiologic type of infection

Clinical outcomes

Severity index on admission measured by Pitt bacteremia score in patients with HCA-BSI (2.2±3.0) was significantly higher than that in CA-BSI group (1.5±2.6) (P=0.012) (Table 4). And, the incidence of severe sepsis in HCA-BSI group (36.9%) was also higher than that in CA-BSI (23.4%, P=0.001).

Table 4
Clinical outcome of bloodstream infection by epidemiologic type of infection

The rate of appropriate empirical antibiotic therapy was the highest in CA-BSI group (89.0%), followed by HCA-BSI (76.4%), and HA-BSI group (75.0%). Initial clinical improvement rate was more frequently observed in CA-BSI group (85.7%) than in HCA-BSI (68.64%, P<0.001) and HA-BSI group (68.5%, P<0.001).

The overall 30-day mortality rate in all patients with BSI was 18% (193/1,144). Mortality rate was significantly lower in CA-BSI group (10.2%) than in HCA-BSI (18.4%, P=0.007), and HA-BSI group (23.0%, P<0.001). Although, no significant difference was seen in mortality rate between HA-BSI and HCA-BSI group (P=0.188).

Risk factors for mortality

By univariate analysis, high Pitt score (>4), severe sepsis, inappropriate empirical antibiotic therapy were the common risk factors for all patients with BSI (Table 5). For demographics and comorbidities, old age (≥65 yr), underlying solid tumor, stroke, high alcohol uptake, neutropenia were the significant risk factors for mortality in CA-BSI group. In HA-BSI group, old age (≥65 yr), underlying congestive heart failure, receipt of immunosuppressant, prior antibiotic use, history of transplantation were the significant risk factors. In HCA-BSI group, underlying congestive heart failure was the significant risk factor. For infecting pathogens, E. coli was the negative predictive factor for 30-day mortality in CA-BSI group. Fungal infection was the significant risk factor for mortality in HA-BSI group. For primary infection, pneumonia was the significant risk factor for all patients with BSI.

Table 5
Risk factors associated with 30 day mortality in bloodstream infection by epidemiologic type of infection

By multivariate analysis, high Pitt score (CA-BSI, OR 28.3, P<0.001; HA-BSI, OR 2.2, P=0.003; HCA-BSI, OR 7.8, P=0.001) and ineffective empirical antibiotic therapy (CA-BSI, OR 5.1, P=0.01; HA-BSI, OR 2.2, P=0.003; HCA-BSI, OR 6.0, P=0.001) were the common independent risk factors in all patients with BSI (Table 6). Severe sepsis (OR 5.5, 95% CI 3.2-9.5, P<0.001), pneumonia (OR 3.0, 95% CI 1.6-5.6, P<0.001), and prior antibiotic use (OR 1.7, 95% CI 1.0-2.9, P=0.03) were the independent risk factors in patients with HA-BSI.

Table 6
Independent risk factors for mortality in bloodstream infection by epidemiologic type of infection


This study was a nationwide surveillance of BSI in Korean hospitals. In this study, we compared clinical and microbiological characteristics of 3 types of BSI.

With regard to prevalent pathogens by the epidemiologic type, Gram-negative bacilli (especially E. coli and K. pneumoniae) in CA-BSI were due to higher incidence of UTI and intra-abdominal infection, while Gram-positive cocci (especially staphylococci) in HA-BSI were due to primary bacteremia which were frequently associated with cather-related infection. In HCA-BSI, Gram-negative bacilli were also the prevalent pathogen like CA-BSI, because the incidences of UTI and intra-abdominal infection were higher than that of primary bacteremia. However, the proportion of Gram-negative bacilli in HCA-BSI was differed from that in CA-BSI.

Cheong et al. (16) previously reported that the prevalence of ESBL-producing E.coli in HCA-BSI (6.7%) was higher than that in CA-BSI (3.2%), although it did not show the statistical difference between 2 groups. In addition, Kang et al. (17) reported that more than half (63.2%) of community-onset BSIs caused by ESBL-producing E. coli were HCA-BSI. Our study also showed the similar result that the prevalence of ESBL-producing E. coli in HCA-BSI and HA-BSI group was higher than that in CA-BSI. With regard to S. aureus bacteremia, previous reports showed that the prevalence of MRSA was the highest in in HA-BSI (33.8-61%) followed by HCA-BSI (29.4-52%) and CA-BSI (11-21.2%) (3, 10, 18). And, our study also showed the similar result.

In general, early and appropriate antibiotic therapy significantly affects the overall mortality in BSI (19, 20). Previous studies reported that 10-40% of BSI cases received inappropriate empirical therapy, which was more frequent in cases of HA-BSI and HCA-BSI (9, 21, 22). Our data was also consistent with this finding that initial antibiotic therapy was more frequently inappropriate in HA-BSI and HCA-BSI cases than in CA-BSI. Given the different pathogens and antimicrobial resistance in HCA-BSI compared with CA-BSI, empirical antibiotic choice should be different in HCA-BSI from those in CA-BSI cases.

Previously, high severity index on admission and inappropriate empirical antibiotic therapy were known as significant risk factors in BSI (16, 19, 23). Pazos et al. (23) reported that septic shock, and inappropriate antibiotic therapy were found to be risk factors for mortality in overall BSI. And, Cheong et al. (16) also reported that high Charlson's index, high Pitt score, and acute renal failure were found to be risk factors for mortality in E. coli bacteremia. In our study, high Pitt score and inappropriate empirical antibiotic therapy were shown to be the common independent risk factors in every BSI group including HCA-BSI on multivariate analysis.

There is a limitation in this study. Our data were obtained from a few university hospitals that might lead to the bias of pathogen distribution, antimicrobial resistance or primary infection.

In conclusion, the present data suggest that clinical features, clinical outcome, and microbiologic features of causative pathogens vary by epidemiologic type of BSI. Especially, HCA-BSI shows a distinct entity of BSI with its unique epidemiology, microbiology, and treatment outcomes, which shares more similarity with HA-BSI. The only independent risk factors for mortality associated with HCA-BSI could not be found. However, considering the inappropriate empirical antibiotic therapy as a major independent risk factor for mortality, clinicians should be aware of this category for more appropriate antibiotics based on possible resistant pathogens.


This study was supported by a grant of the Korea Centers for Disease Control and Prevention (Serial number: 2007-E-00129-00, 2007-E00037-00).


1. Leibovici L, Samra Z, Konigsberger H, Drucker M, Ashkenazi S, Pitlik SD. Long-term survival following bacteremia or fungemia. JAMA. 1995;274:807–812. [PubMed]
2. Pedersen G, Schønheyder HC, Sørensen HT. Source of infection and other factors associated with case fatality in community-acquired bacteremia-a Danish population-based cohort study from 1992 to 1997. Clin Microbiol Infect. 2003;9:793–802. [PubMed]
3. Friedman ND, Kaye KS, Stout JE, Stout JE, McGarry SA, Trivette SL, Briggs JP, Lamm W, Clark C, MacFarquhar J, Walton AL, Reller LB, Sexton DJ. Healthcare-associated bloodstream infections in adults: a reason to change the accepted definition of community-acquired infections. Ann Intern Med. 2002;137:791–797. [PubMed]
4. Siegman-Igra Y, Fourer B, Orni-Wasserlauf R, Golan Y, Noy A, Schwartz D, Giladi M. Reappraisal of community-acquired bacteremia: a proposal of a new classification for the spectrum of acquisition of bacteremia. Clin Infect Dis. 2002;34:1431–1439. [PubMed]
5. Shorr AF, Tabak YP, Killian AD, Gupta V, Liu LZ, Kollef MH. Healthcare-associated bloodstream infection: a distinct entity? Insights from a large U.S. database. Crit Care Med. 2006;34:2588–2595. [PubMed]
6. Weinstein MP, Towns ML, Quartey SM, Mirrett S, Reimer LG, Parmigiani G, Reller LB. The clinical significance of positive blood cultures in the 1990s: a prospective comprehensive evaluation of the microbiology, epidemiology, and outcome of bacteremia and fungemia in adults. Clin Infect Dis. 1997;24:584–602. [PubMed]
7. Lark RL, Chenoweth C, Saint S, Zemencuk JK, Lipsky BA, Plorde JJ. Four year prospective evaluation of nosocomial bacteremia: epidemiology, microbiology, and patient outcome. Diagn Microbiol Infect Dis. 2000;38:131–140. [PubMed]
8. Lark RL, Saint S, Chenoweth C, Zemencuk JK, Lipsky BA, Plorde JJ. Four-year prospective evaluation of community-acquired bacteremia: epidemiology, microbiology, and patient outcome. Diagn Microbiol Infect Dis. 2001;41:15–22. [PubMed]
9. McDonald JR, Friedman ND, Stout JE, Sexton DJ, Kaye KS. Risk factors for ineffective therapy in patients with bloodstream infection. Arch Intern Med. 2005;165:308–313. [PubMed]
10. Rangel-Frausto MS, Pittet D, Costigan M, Hwang T, Davis CS, Wenzel RP. The natural history of the systemic inflammatory response syndrome (SIRS): a prospective study. JAMA. 1995;273:117–123. [PubMed]
11. American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. Crit Care Med. 1992;20:864–874. [PubMed]
12. Chow JW, Yu VL. Combination antibiotic versus monotherapy for gram-negative bacteremia: a commentary. Int J Antimicrob Agents. 1999;11:7–12. [PubMed]
13. Kang CI, Kim SH, Park WB, Lee KD, Kim HB, Kim EC, Oh MD, Choe KW. Bloodstream infections caused by antibiotic-resistant gram-negative bacilli: risk factors for mortality and impact of inappropriate initial antimicrobial therapy on outcome. Antimicrob Agents Chemother. 2005;49:760–766. [PMC free article] [PubMed]
14. Kasiakou SK, Michalopoulos A, Soteriades ES, Samonis G, Sermaides GJ, Falagas ME. Combination therapy with intravenous colistin for management of infections due to multidrug-resistant Gram-negative bacteria in patients without cystic fibrosis. Antimicrob Agents Chemother. 2005;49:3136–3146. [PMC free article] [PubMed]
15. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing: Fifteenth Informational Supplement. Wayne, PA: CLSI; 2005. Document No. M100-S15.
16. Cheong HS, Kang CI, Kwon KT, Heo ST, Wi YM, Kim ES, Lee JS, Ko KS, Chung DR, Lee NY, Song JH, Peck KR. Clinical significance of healthcare-associated infections in community-onset Escherichia coli bacteraemia. J Antimicrob Chemother. 2007;60:1355–1360. [PubMed]
17. Kang CI, Cheong HS, Chung DR, Peck KR, Song JH, Oh MD, Choe KW. Clinical features and outcome of community-onset bloodstream infections caused by extended-spectrum beta-lactamase-producing Escherichia coli. Eur J Clin Microbiol Infect Dis. 2008;27:85–88. [PubMed]
18. Lesens O, Hansmann Y, Brannigan E, Hopkins S, Meyer P, O'Connel B, Prévost G, Bergin C, Christmann D. Healthcare-associated Staphylococcus aureus bacteremia and the risk for methicillin resistance: is the Center for Disease Control and Prevention definition for community acquired bacteremia still appropriate? Infect Control Hosp Epidemiol. 2005;26:204–209. [PubMed]
19. Ramphal R. Importance of adequate initial antimicrobial therapy. Chemotherapy. 2005;51:171–176. [PubMed]
20. Du B, Long Y, Liu H, Chen D, Liu D, Xu Y, Xie X. Extended spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae bloodstream infection: risk factors and clinical outcome. Intensive Care Med. 2002;28:1718–1723. [PubMed]
21. Elhanan G, Sarhat M, Raz R. Empiric antibiotic treatment and the misuse of culture results and antibiotic sensitivities in patients with community-acquired bacteraemia due to urinary tract infection. J Infect. 1997;35:283–288. [PubMed]
22. Byl B, Clevenbergh P, Jacobs F, Jacobs F, Struelens MJ, Zech F, Kentos A, Thys JP. Impact of infectious diseases specialists and microbiological data on the appropriateness of antimicrobial therapy for bacteremia. Clin Infect Dis. 1999;29:60–66. [PubMed]
23. Pazos Añón R, Fernández Rodríguez R, Paz Vidal I, Tinajas A, Cantón I, Abel V, González R, Martínez R, Gayoso P, Fernández Alvarez O. Prognostic factors of bacteremia: prospective study. An Med Interna. 2001;18:415–420. [PubMed]

Articles from Journal of Korean Medical Science are provided here courtesy of Korean Academy of Medical Sciences
PubReader format: click here to try


Save items

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


  • Compound
    PubChem chemical compound records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records. Multiple substance records may contribute to the PubChem compound record.
  • MedGen
    Related information in MedGen
  • PubMed
    PubMed citations for these articles
  • Substance
    PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.
  • Taxonomy
    Taxonomy records associated with the current articles through taxonomic information on related molecular database records (Nucleotide, Protein, Gene, SNP, Structure).
  • Taxonomy Tree
    Taxonomy Tree

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...