Blood cultures are collected whenever there is reason to suspect bacteremia or septicemia. Although mild transitory bacteremia is a frequent finding in many infections, a persistent, continuous, or recurrent bacteremia indicates a more serious condition that may require immediate treatment. The expeditious detection and identification of pathogens (bacteria, fungi, viruses, and parasites) in the blood may aid in making a clinical and etiologic diagnosis.
Bacteremia
Septicemia
Shock
Unexplained postoperative shock
Postoperative shock after genitourinary tract manipulation or surgery
Unexplained fever with a duration of several days
Chills and fever in patients with:
Infected burns
Urinary tract infection (UTI)
Rapidly progressing tissue infection
Postoperative wound sepsis
Indwelling venous or arterial catheter
Debilitated patients receiving:
Antibiotic drugs
Corticosteroids
Immunosuppressives
Antimetabolites
Parenteral hyperalimentation
Following body piercing (nose, tongue, nipples, penis, umbilicus) with signs of infection and bacteremia
During an acute febrile illness, immediately draw two separate blood samples from separate sites. Obtain cultures prior to starting antimicrobial therapy, when possible, because antimicrobial therapy may interfere with bacterial growth.
For fever of unknown origin, two blood cultures can be initially drawn 510 minutes apart. If necessary, two more sets of samples can be drawn 2448 hours later.
In cases of acute endocarditis, draw blood cultures 60 minutes apart. If results are negative at 24 hours, two more sets of samples may be obtained.
Parasites in the blood (Plasmodium, Trypanosoma, and Babesia) are usually detected by direct microscopic observation.
For infants and small children, only 15 mL of blood can safely be drawn for culture. Quantities less than 1 mL may be insufficient to detect bacterial organisms. In adults, cultures should optimally be 2030 mL of blood.
Procedure for Blood Culture
During venipuncture, because of the high potential for infecting the patient, aseptic technique must be used. Key points are listed as follows:
Observe standard precautions. Perform hand hygiene and don gloves.
Scrub the proposed puncture site with an antiseptic agent such as chlorhexidine. Allow to dry for 12 minutes.
Cleanse the rubber stoppers of culture bottles with chlorhexidine and allow to air-dry.
Perform venipuncture with a sterile syringe and needle; avoid contamination of the cleansed puncture site.
Withdraw about 1030 mL of blood into a 20-mL syringe or directly into the culture tubes. Because of the danger of accidental needle sticks, the practice of changing needles to transfer the specimen into blood culture bottles has been replaced by direct injection with the original phlebotomy needle.
If two culture bottles are to be inoculated (one anaerobic and one aerobic), first inoculate the aerobic bottle with the optimal, manufacturer-recommended volume and then inoculate the anaerobic bottle with the remaining, being careful not to overinoculate. Be certain to inoculate each bottle with the optimum blood volume.
Mix both bottles gently.
Remove and discard gloves. Perform hand hygiene.
Label specimens with the patients name, date, and tests ordered and immediately transfer them to the laboratory.
Procedural Alert
Handle all blood specimens according to standard precautions.
After disinfection, do not palpate the venipuncture site unless sterile gloves are worn. Palpation is the greatest potential cause of blood culture contamination.
Specimens can be drawn from two or three different sites to exclude a skin-contaminating organism.
Collection of more than three blood cultures in a 24-hour period does not improve the detection of bacteria.
It is recommended to draw blood below an intravenous line (if possible) to prevent dilution of the sample.
Negative cultures: If all cultures, subcultures (if performed), and Gram-stained smears are negative, the blood culture may be reported as no growth after 57 days of incubation.
Positive cultures: Pathogens most commonly found in blood cultures include:
Bacteroides spp.
Brucella spp.
Enterobacteriaceae
Pseudomonas aeruginosa
Haemophilus influenzae
Listeria monocytogenes
Streptococcus pneumoniae
Enterococcus spp.
Staphylococcus aureus, Staphylococcus epidermidis
Streptococcus spp. including beta-hemolytic streptococci
Candida albicans
Clostridium perfringens
Pretest Patient Care
Explain purpose of and procedure for culture. Obtain and document pertinent history of signs and symptoms of infection.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Review test results; report and record findings. Modify the nursing care plan as needed. Monitor for bacteremia, septicemia, and other febrile illness. Counsel the patient appropriately about treatment (triple antibiotic therapy).
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
Clinical Alert
The healthcare provider should be notified immediately about positive culture results so that treatment and isolation precautions are appropriate.
Blood cultures are subject to contamination, especially by skin bacteria. These skin organisms should be identified if possible.