Deep Wound Culture
Test Code
CXDWD
Description
Deep wound culture is used to determine infectious agents in normally sterile sites such as organs, deep abscesses and visceral/soft tissue below the dermis. This test is similar to Tissue Culture (CXTIS).
- This test includes Gram stain and culture.
- Specimens sent under anaerobic condition will be cultured for both aerobic and anaerobic pathogens. Specimens not sent under anaerobic conditions will only be examined for aerobic pathogens.
- Common sterile sources include: Lymph node, brain, heart, liver, spleen, vitreous fluid, kidney, pancreas, ovary, vascular tissue, abscesses, deep tissue.
- Organisms seen in the Gram stain or recovered in culture from a sterile source are considered a critical result. Critical results are called to the ordering physician in accordance with the NJH critical policy.
Collect
All specimen types should be collected in a sterile container, sterile syringe, or sterile swab (swabs are not recommended due to low specimen volume). Anaerobic culture will be added to the aerobic culture if any of the specimens below are collected anaerobically. This can be done by collecting the sample into a syringe with the air expelled, or collecting into anaerobic transport media.
Tissues, biopsies, and bone: Can be collected from any deep subcutaneous site. Specimen should be taken from within and adjacent to the area of infection. A few drops of sterile nonbacteriostatic saline can be added to prevent the specimen from drying out.
Preferred volume: 6 cm3
Minimum Volume: 1 cm3
Deep wounds: Debride wound, then thoroughly rinse with sterile saline. Only take specimen from viable tissue of wounds that appear to be infected or do not appear to be healing over a long period of time.
Fine needle aspirates & drainage from non-sterile sources (i.e. abscesses): Disinfect skin with 2% chlorhexidine or 70% alcohol followed by iodine solution. Remove iodine with 70% alcohol before collection. Aspirate with a needle and syringe. If the first attempt fails to produce pus, inject sterile saline subcutaneously, then repeat the aspiration. Expel the excess air, remove the needle, and cap the syringe before sending to the laboratory.
Preferred volume: 3 mL
Minimum Volume: 1 mL
Swabs: should be collected from a deep tissue site (non-cutaneous), and collection should be avoided if a tissue/biopsy or aspiration of the infected area can be performed because swabs typically have insufficient volume. Place the swab in an appropriate transport system and send to the laboratory.
Patient Prep
Avoid antibiotic administration prior to sample collection.
Unacceptable Conditions
- Specimens received outside of temperature storage requirements (DO NOT refrigerate)
- Specimens received outside of stability time frame
- Specimens received in formalin
- Specimens that do not meet the minimum volume requirement
- Specimens in non-sterile containers
- Specimens in expired transport media
- Specimens from a source not acceptable for this testing
- Specimens that are excessively leaking
- Mislabeled or unlabeled specimen (exception with attestation for specimens from irretrievable source, i.e tissue or bone)
- Anaerobic portion of testing will not be performed if the samples was not submitted under anaerobic conditions
Stability
- For optimal recovery of potential pathogens, specimens should arrive as soon as possible at room temperature (20-25°C)
- If transportation is delayed, specimens may be stored at room temperature (20-25°C) for 24 hours
Notes
Specimens from irretrievable sources will be processed with a disclaimer if specimen was received in sub optimal conditions.
Performed
7 days a week from 8am to 6pm
Methodology
Aerobic and anaerobic (if appropriately collected) bacterial culture
Turnaround Time
4 days
Department
Microbiology Lab
Study Offerings
CAP/CLIA
Related Tests
CXTIS, CXSWD
Reference Interval
- No growth for sterile sources
- Normal commensal flora may be observed some cases (e.g. GI flora or skin flora) due to non-sterile collection or non-sterile sources being submitted.
Interpretation
The table below describes reportable organisms and if antimicrobial susceptibility testing (AST) is routinely included. If susceptibilities are needed for an organism that AST is not routinely performed, please submit the request through EPIC using the OP Add-On/Comm Message type addressed to NJH LAB ADD-ON POOL.
Threshold for Reporting |
Organism |
Testing performed |
Any |
Aeromonas hydrophila |
ID and AST‡ |
Aracanobacterium haemolyticum |
ID and AST‡ |
|
Bacillus anthracis |
ID |
|
Bartonella spp. |
ID |
|
Burkholderia mallei |
ID |
|
Burkholderia pseudomallei |
ID |
|
Capnocytophaga spp. |
ID |
|
Clostridium novyi |
ID |
|
Clostridium prefringens |
ID |
|
Clostridium septicum |
ID |
|
Clostridium sordellii |
ID |
|
Corynebacterium diptheriae |
ID and AST‡ |
|
Corynebacterium kroppenstedtii |
ID and AST‡ |
|
Corynebacterium minutissimum |
ID and AST‡ |
|
Corynebacterium pseudotuberculosis |
ID and AST‡ |
|
Corynebacterium ulcerans |
ID and AST‡ |
|
Francisella tularensis |
ID |
|
Haemophilus ducreyi |
ID |
|
Neisseria gonorrhoeae |
ID |
|
Nocardia spp. |
ID and AST |
|
Pasteurella spp. |
ID; β-lactamase |
|
Pseudomonas aeruginosa |
ID and AST |
|
Staphylococcus aureus |
ID and AST |
|
Streptococcus pneumoniae |
ID and AST |
|
Streptococcus pyogenes (group A) |
ID |
|
Vibrio vulnificus |
ID and AST‡ |
|
Yersinia pestis |
ID |
|
Pure or Predominant |
Acinetobacter baumanni complex |
ID and AST |
Actinomyces spp. |
ID and AST‡ |
|
Bacteroides fragilis group |
ID and AST‡ |
|
Candida spp. |
ID |
|
Eikenella spp. |
ID and AST |
|
Enterobacterales (not listed separately) |
ID and AST |
|
Enterococcus spp. |
ID and AST |
|
Fusobacterium spp. |
ID and AST‡ |
|
Non-glucose fermenting GNR |
ID and AST |
|
Staphylococcus intermedius group |
ID and AST |
|
Staphylococcus lugdunensis |
ID and AST |
|
Staphylococcus schleiferi |
ID and AST |
|
Stenotrophomonas maltophilia |
ID and AST |
|
Streptococcus agalactiae (group B) |
ID |
|
Streptococcus anginosus |
ID and AST |
|
Pure |
Bacillus spp. (not anthracis) |
ID |
Coagulase-negative staphylococci (not listed individually) |
ID and AST |
|
Other anaerobes |
ID and AST‡ |
|
Viridans group Streptococcus |
ID and AST |
‡AST is not performed in house; isolate will be sent to reference lab for susceptibility testing
CPT Code
87205, 87070
New York Approved
Standard
FDA
Standard Method