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A Multicenter Evaluation of Blood Culture Practices, Contamination Rates, and the Distribution of Causative Bacteria.
Altindis, Mustafa; Koroglu, Mehmet; Demiray, Tayfur; Dal, Tuba; Ozdemir, Mehmet; Sengil, Ahmet Zeki; Atasoy, Ali Riza; Dogan, Metin; Cicek, Aysegul Copur; Ece, Gulfem; Kaya, Selcuk; Iraz, Meryem; Gultepe, Bilge Sumbul; Temiz, Hakan; Kandemir, Idris; Aksaray, Sebahat; Cetinkol, Yeliz; Sahin, Idris; Guducuoglu, Huseyin; Kilic, Abdullah; Kocoglu, Esra; Gulhan, Baris; Karabay, Oguz.
Afiliação
  • Altindis M; Department of Clinical Microbiology, Faculty of Medicine, Sakarya University, Sakarya, Turkey.
  • Koroglu M; Department of Clinical Microbiology, Faculty of Medicine, Sakarya University, Sakarya, Turkey.
  • Demiray T; Department of Clinical Microbiology, Training and Research Hospital, Sakarya University, Sakarya, Turkey.
  • Dal T; Department of Clinical Microbiology, School of Medicine, Yildirim Beyazit University, Ankara, Turkey.
  • Ozdemir M; Department of Clinical Microbiology, Meram Medical Faculty Hospital, Necmettin Erbakan University, Konya, Turkey.
  • Sengil AZ; Department of Medical Microbiology, Medical Faculty, Medipol University, Istanbul, Turkey.
  • Atasoy AR; Department of Clinical Microbiology, Faculty of Medicine, Sakarya University, Sakarya, Turkey.
  • Dogan M; Department of Clinical Microbiology, Meram Medical Faculty Hospital, Necmettin Erbakan University, Konya, Turkey.
  • Cicek AC; Department of Clinical Microbiology, School of Medicine, Recep Tayyip Erdogan University, Rize, Turkey.
  • Ece G; Department of Clinical Microbiology, School of Medicine, Izmir University, Izmir, Turkey.
  • Kaya S; Department of Clinical Microbiology, School of Medicine, Izmir Katip Celebi University, Izmir, Turkey.
  • Iraz M; Department of Clinical Microbiology, School of Medicine, Bezmi Alem University, Istanbul, Turkey.
  • Gultepe BS; Department of Clinical Microbiology, School of Medicine, Bezmi Alem University, Istanbul, Turkey.
  • Temiz H; Department of Clinical Microbiology, Diyarbakir Training and Research Hospital, Diyarbakir, Turkey.
  • Kandemir I; Department of Clinical Microbiology, School of Medicine, Dicle University, Diyarbakir, Turkey.
  • Aksaray S; Department of Clinical Microbiology, Haydarpasa Numune Hospital, Istanbul, Turkey.
  • Cetinkol Y; Department of Clinical Microbiology, School of Medicine, Ordu University, Ordu, Turkey.
  • Sahin I; Department of Clinical Microbiology, School of Medicine, Duzce University, Duzce, Turkey.
  • Guducuoglu H; Department of Clinical Microbiology, School of Medicine, Yuzuncuyil University, Van, Turkey.
  • Kilic A; Department of Clinical Microbiology, School of Medicine, Gulhane Military Medical School, Ankara, Turkey.
  • Kocoglu E; Department of Clinical Microbiology, School of Medicine, Abant Izzet Baysal University, Bolu, Turkey.
  • Gulhan B; Department of Clinical Microbiology, School of Medicine, Erzincan University, Erzincan, Turkey.
  • Karabay O; Department of Infection Diseases, School of Medicine, Sakarya University, Sakarya, Turkey.
Jundishapur J Microbiol ; 9(1): e29766, 2016 Jan.
Article em En | MEDLINE | ID: mdl-27099693
ABSTRACT

BACKGROUND:

The prognostic value of blood culture testing in the diagnosis of bacteremia is limited by contamination.

OBJECTIVES:

In this multicenter study, the aim was to evaluate the contamination rates of blood cultures as well as the parameters that affect the culture results. MATERIALS AND

METHODS:

Sample collection practices and culture data obtained from 16 university/research hospitals were retrospectively evaluated. A total of 214,340 blood samples from 43,254 patients admitted to the centers in 2013 were included in this study. The blood culture results were evaluated based on the three phases of laboratory testing the pre-analytic, the analytic, and the post-analytic phase.

RESULTS:

Blood samples were obtained from the patients through either the peripheral venous route (64%) or an intravascular catheter (36%). Povidone-iodine (60%) or alcohol (40%) was applied to disinfect the skin. Of the 16 centers, 62.5% have no dedicated phlebotomy team, 68.7% employed a blood culture system, 86.7% conducted additional studies with pediatric bottles, and 43.7% with anaerobic bottles. One center maintained a blood culture quality control study. The average growth rate in the bottles of blood cultures during the defined period (1259 - 26,400/year) was 32.3%. Of the growing microorganisms, 67% were causative agents, while 33% were contaminants. The contamination rates of the centers ranged from 1% to 17%. The average growth time for the causative bacteria was 21.4 hours, while it was 36.3 hours for the contaminant bacteria. The most commonly isolated pathogens were Escherichia coli (22.45%) and coagulase-negative staphylococci (CoNS) (20.11%). Further, the most frequently identified contaminant bacteria were CoNS (44.04%).

CONCLUSIONS:

The high contamination rates were remarkable in this study. We suggest that the hospitals' staff should be better trained in blood sample collection and processing. Sterile glove usage, alcohol usage for disinfection, the presence of a phlebotomy team, and quality control studies may all contribute to decreasing the contamination rates. Health policy makers should therefore provide the necessary financial support to obtain the required materials and equipment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article