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quality metric regarding blood cultures is the contamination rate. There has been a long-standing recommendation that blood culture contamination rates be kept at or below 3%

for hospitalized patients. This figure is not derived from anything more than the belief that it generally is not possible to maintain rates below 1% and that rates above 5% result in a confounding of the clinician’s ability to distinguish between contaminants and pathogens. Because blood cul-ture contaminants result in increased health care costs, contamination rates above 5% also are associated with in-creased costs. Whether the 3% figure is realistic for outpa-tient settings, particularly in emergency departments, is another unanswered question. For patient safety, quality, and costs, it makes sense to target the lowest possible con-tamination rates, but targeting specific rates should be done with the understanding that different contamination rates occur in different settings.

Another common assessment of quality is the number of blood cultures drawn per septic episode. As noted previously, interpretation of blood culture results depends heavily upon drawing both an adequate volume of blood and more than one culture. Determining the clinical importance of isolates recovered from single blood cultures can be impossible de-pending on the type of isolate recovered. At the same time, collecting more blood cultures than is necessary is wasteful, contributes to phlebotomy-caused anemia, and results only in recovery of more contaminants. For both reasons, labora-tories should monitor the number of blood cultures collected per septic episode.

A third important measurement is the adequacy of fill of blood culture bottles. Weighing filled bottles and comparing weights against those of a known standard most readily achieve this goal. Bottles filled with inadequate volumes of blood diminish yield and should be reported to the provider, with a recommendation to recollect the blood culture. Ade-quacy of filling should be monitored through time and by site so that any patterns of underfilling (or overfilling) can be identified and the appropriate corrective action taken.

SUMMARY

Detection of bacteremia and fungemia remains one of the most important roles of clinical microbiology laboratories.

Despite the development and introduction of a number of novel technologies, the blood culture using liquid-based media still remains the only practicable approach for routine patient care. Molecular detection methods show promise, but the available methods do not have the sensitivityof blood cultures (except for a select few pathogens), provide only limited information regarding antimicrobial suscepti-bility testing, if used alone would not allow for retention of isolates for epidemiologic investigations, at this time are not effectivefor detecting polymicrobial isolates, and are more expensive to use on a routine basis. Other methods such as MALDI-TOF (MS) also can achieve similar results for rapid identification of microorganisms isolated on solid media but currently are not cleared by the FDA for identifi-cation of pathogens directly from blood cultures. Experience has shown that novel technologies rarely replace older tech-nologies but rather serve as adjunctmethods to enhance older technologies. Because the isolation of pathogens from blood serves multiple clinical roles—prognosis, guiding ther-apy, monitoring response to therther-apy, and epidemiology—

any approach to the laboratory detection of bacteremia and fungemia mustbe able tofulfill each of these roles. It is unlikely that any new technology will replace blood cultures entirely in the foreseeable future. What already is happening is that newer technologies are being integrated with blood cultures into an algorithmic approach that takes advantage of the benefits of each method.

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