| Abscess contents, aspirated fluid |
As much as possible in sterile disposable container. |
Disinfect skin with 70% alcohol before aspiration.
Use swab to collect only if volume is insufficient for aspiration. Aspirate material from under the margin of the lesion/abscess. Laboratory may provide 7H9 broth for transport of small volumes of aspirates. |
| Blood |
5ml of plain blood inoculated directly into Myco-F-Lytic vial.** On rare occasions, if blood culture vials are not available, blood and bone marrow may be submitted in Vacutainer tubes containing SPS, heparin or citrate. EDTA tubes are not acceptable |
Disinfect skin with 70% alcohol.
Disinfect cap of Myco-F-Lytic vial with alcohol.
Mix the contents immediately after collection. Mainly performed for immunocompromised patients, particularly those with AIDS. Please indicate such underlying condition on the form as prolonged culture incubation may be required. |
| Body fluids (pleural, pericardial, peritoneal, etc) |
As much as possible (minimum 10 - 15ml) in a sterile leak-proof, screw-capped, single-use container. |
Disinfect skin with 70% alcohol if collecting by needle and syringe. |
| Bone |
Bone in sterile disposable container with no fixative or preservative. |
Do not submit specimen in formalin. |
| Bone marrow |
Inoculate directly into Myco-F-Lytic vial.** If direct molecular testing is required, then at least 3 ml in a sterile, screw-capped disposable container. |
As for blood |
| Bronchoalveolar lavage or bronchial washing/brushing |
³ 5 ml in sterile disposable container |
Avoid contaminating bronchoscope with tap water as free-living saprophytic mycobacteria may produce false-positive results. |
| CSF |
³2 ml in sterile disposable container |
Disinfect skin before aspiration. Do not refrigerate or freeze. |
| Gastric lavage |
³5 - 10 ml in sterile disposable container. Collect in the morning soon after patient awakens in order to obtain sputum swallowed during sleep. |
Collect fasting early morning specimen on three consecutive days.
Use sterile saline.
Collect in container containing 60 mg of sodium carbonate per 30 ml of total fluid if delivery is expected to be delayed for > 4 hours.*** |
| Laryngeal swabs |
Unless the patient is suspected to have laryngeal TB, laryngeal swabs are not recommended for diagnosing pulmonary TB due to the following reasons:
1. Difficulty in proper collection and the procedure may pose a biosafety risk.
2. The amount of material collected on the swab is limited.
3. Risk of sharps injury from broken glass containers.
|
|
| Lymph node |
Node or portion of node in sterile disposable container with no fixative or preservative. Minute amounts may be submitted in a 1-2 ml of sterile saline. |
Collect aseptically. Select caseous portion if available. Do not freeze, immerse in formalin or other preservatives or wrap in gauze. |
| Skin lesion material |
Send biopsy specimen or aspirate in sterile disposable container with no fixative or preservative. |
For cutaneous ulcers, collect biopsy sample from periphery of lesion or aspirate material from under margin of lesion.
Swabs in transport medium (Amies or Stuarts) are acceptable only if biopsy sample or aspirate is not obtainable. If infection was acquired in Africa, Australia, Mexico, South America, Indonesia, New Guinea or Malaysia, state this on request form, because Mycobacterium ulcerans requires prolonged incubation for primary isolation. |
| Sputum |
5 - 10ml in sterile, wax-free disposable specimen container. |
Instruct patient to rinse mouth before sputum is collected. Collect an early-morning specimen from deep productive cough on at least three consecutive days - this provides the best yield. If this is not possible, separate collections of 3 consecutive samples in an 8 to 24 hour period is acceptable; one of which should be a first morning specimen.
Do not pool specimens (e.g. 24-hr pooled sputum); such samples and saliva are unacceptable.
Induced sputum can be collected from patients who cannot or find it difficult to expectorate.
For induced sputum, use sterile hypertonic saline. Avoid sputum contamination with nebuliser reservoir water. Indicate induced sputum on request form as these watery specimens resemble saliva. |
| Stool |
³1g in sterile, disposable wax-free container |
Collect specimen directly into container or transfer from bedpan. Recommended only for detection of Mycobacterium avium complex (MAC) involvement in the gastrointestinal tracts of patients with AIDS. Refrigerate if delay in transportation is expected, but do not freeze. |
| Tissue biopsy sample |
1g of tissue, if possible, in sterile disposable container with no fixative or preservative. Minute amounts may be submitted in a 1-2 ml of sterile saline. |
Collect aseptically. Select caseous portion if available. Do not freeze, immerse in formalin or other preservatives or wrap in gauze |
| Transtracheal aspirate |
As much as possible in a sterile, leak-proof disposable container |
|
| Urine |
Clean the urethral area with distilled or cooled boiled water (tap water may contain saprophytic bacteria).
Mid-stream urine is not advised. Collect at least 40ml in a sterile, leak-proof disposable container.
Collect as much as possible of suprapubic urine in sterile disposable container. |
Collect first morning specimen on three consecutive days. The first morning void provides the best yield. Specimens collected at other times are diluted and not optimal. An early morning midstream urine is acceptable only if a whole early morning urine sample is not available.
24-hour pooled specimens or urine from catheter bag are unacceptable.
Specimens of < 40ml are unacceptable unless a larger volume is not obtainable.
A small fraction of patients undergoing BCG immunotherapy for bladder cancer may have local or even disseminated disease from BCG. For 95% of such patients, serious side effects do not occur and BCG isolation from urine does not have clinical significance. Routine urine culture for mycobacteria in this setting are not recommended. |
| Wound material |
See biopsy or aspirate |
Due to limited material collected, swabs are acceptable only if biopsy or aspirate is not obtainable; negative results may not be reliable. If used, send the swab in transport medium (Amies or Stuarts). Negative results are not reliable. |
| Specimens for nucleic acid amplification (ProbeTec DTB) |
All specimens as for culture. Turbid and grossly bloody specimens may contain inhibitors or give rise to false-positives due to high background.
If critical, blood/bone marrow specimens should be sent in plain tubes. Specimens sent in heparin-containing containers; blood in Myco-F-Lytic or on slides are not suitable. |
To avoid false positives from cross contamination, specimens should not be pre-processed in other labs. If delay in delivery is expected, store at 4ºC. |
| Blood for Quantiferon testing |
Quantiferon Gold-in-tubes are available from the SGH SOC Lab at Blk 3 or CTBL.
Collect whole blood (1ml per tube, accepted range = 0.8-1.2 ml) in the Quantiferon-Gold tubes in correct order: Nil (Grey cap with a white ring), TB-Ag (Red cap with a white ring) then Mitogen (Purple cap with a white ring).
The black mark on the side of the tubes indicates the 1 ml fill volume, and the prevacuumed tubes have been validated by the manufacturer for volumes ranging from 0.8 to 1.2 ml.
|
Use a butterfly needle or vacutainer system - using hypodermic syringes increases the risk of sharps injury. Purge the contents of the butterfly tubing with a plain tube first.
Labelling -
1. Label all 3 tubes with the patient’s particulars, taking care to avoid obscuring the area where the blood filling and the black volume marks can be observed.
2. Indicate on the tubes or request form the date and time of specimen collection. For CPOE orders, print the barcodes just prior to the collection.
To avoid overfilling -
1. Before specimen collection, allow the tubes to equilibrate to room temperature (17-25ºC).
2. Do not choose a limb that has an intravenous drip attached or force blood into the tubes with a syringe.
3. Remove the tourniquet once blood enters the first tube. Note that the tubes draw blood relatively slowly; keep the tube on the needle for 2-3 seconds once the tube appears to have completed filling.
4. If the level of blood in any tube is not close to or exceeds the indicator line, another blood sample should be obtained.
Mixing
Post collection, mix the blood with the tube contents by shaking tubes 10 times, to ensure that the entire inner surface of the tubes are coated with blood. Foaming may be expected and this will not affect the result. The shaking should not be so hard as to disrupt the gel at the base of the tubes as this may cause aberrant results.
Transportation
Transport the tubes at room temperature (22 +/- 5ºC). It is not necessary for them to be transported upright. Transport to SOC Lab Level 1 before 4pm on the same day or hand-deliver directly to CTBL.
Timing
Specimens must be received at CTBL within 16 hours of sample collection on Mon-Fri between 8.30 am - 6.30 pm. They will not be accepted on Saturday, Sunday and on the eve of public holidays.
|