Corresponding Bundle Element:
Blood cultures obtained prior to antibiotic administration.
Related Measures
Timing of Blood Cultures
Background:
The incidence of sepsis and bacteremia in critically ill patients has been increasing in the past two decades. [8,9] Thirty percent to 50 percent of patients presenting with a clinical syndrome of severe sepsis or shock have positive blood cultures. Therefore, blood should be obtained for culture in any critically ill septic patient.
Collecting blood cultures prior to antibiotic administration offers the best hope of identifying the organism that caused severe sepsis in an individual patient. Failure to check blood cultures prior to antibiotic infusion will perhaps affect the growth of any blood borne bacteria and prevent a culture from becoming positive later.
Collection Strategy:
Two or more blood cultures are recommended. [1] In patients with suspected catheter-related infection, a pair of blood cultures obtained through the catheter hub and a peripheral site should be obtained simultaneously. If the same organism is recovered from both cultures, the likelihood that the organism is causing the severe sepsis is enhanced. In addition, if the culture drawn through the vascular access device is positive much earlier than the peripheral blood culture (i.e., > 2 hours earlier), it may offer support that the vascular access device is the source of the infection. [2] Volume of blood may also be important. [3]
Indications:
Fever, chills, hypothermia, leukocytosis, left shift of neutrophils, neutropenia, and the development of otherwise unexplained organ dysfunction, e.g., renal failure or signs of hemodynamic compromise, are specific indications for obtaining blood for culture. Blood cultures should be taken as soon as possible after the onset of fever or chills.
While it remains difficult to predict bacteremia in patients with sepsis [4], a number of clinical and laboratory parameters are independently correlated with the presence of bacteria in the blood of patients when infection is suspected. These include chills, hypoalbuminemia, the development of renal failure, and a diagnosis of urinary tract infection [4,5]; other criteria are new fever, hypothermia, leukocytosis and left shift of neutrophils, neutropenia, and signs of hemodynamic compromise. [6] Peaking fever appears to be more sensitive than leukocytosis to predict bacteremia [7]; however, fever and low-grade bacteremia can be continuous, such as in endocarditis.
References:
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Smith-Elekes S, Weinstein MP.
Blood cultures. Infectious Disease Clinics of North America. 1993;7:221–234.
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- Crowe M, Ispahani P, Humphreys H, et al. Bacteraemia in the adult intensive care unit of a teaching hospital in Nottingham, UK, 1985–1996. European Journal of Clinical Microbiology and Infectious Diseases. 1998;17:377–384.
- Martin GS, Mannino DM, Eaton S, et al. The epidemiology of sepsis in the United States from 1979 through 2000. New England Journal of Medicine. 2003;348:1546–1554.
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