Presentation on theme: "Chapter 26 Specimen Collection and Processing for Microbiology"— Presentation transcript:
1Chapter 26 Specimen Collection and Processing for Microbiology Wang Hui
2General specimen collection and processing issue First part of this chapter
3Specimen CollectionSuccessful laboratory diagnosis of a microbial infection depends on many factors beginning with a well-collected sample.Proper specimen selection, collection, and transport are all essential to ensure that a specimen is representative of the disease process and minimally contaminated with microorganisms present in adjacent tissues.
4Site and TimingCollect the sample from the correct anatomic site . eg. a superficial sample of a lesion is not useful in identifying the cause of a deep wound infection.The timing of sample collection is also important. eg, when submitting a specimen for bacterial culture, samples should be collected before the administration of antibiotics
5Collection Techniques Sterile technique and equipment.Sufficient volumeAfter collection, the specimen must be placed in an appropriately labeled leak-proof container.
6Requisition slipEach specimen must be accompanied by a requisition slip to evaluate the specimen appropriately and relay the test results back to health care provider without delay.The requisition slip should contain these information :patient name, age, gender, identification number, location, name of health- care provider, time and date of collection, specimen type, diagnosis, and test(s) requested.
7Transport of Specimens Rapid, optimally in less than 2 hours.For delays in transport, most specimens should be refrigerated.Exceptions: blood, cerebrospinal fluid (CSF), and specimens to be examined for anaerobes, fastidious organisms such as Neisseria gonorrboeae and Bordetella pertussis, and Trichomonas vaginalis, all of which should be maintained at room temperature.
8Specimen rejection criteria(1) Improper transport temperatureImproper transport container or mediumProlonged transport timeUnlabeled or mislabeled specimenBroken or cracked containerLeaking specimen
9Specimen rejection criteria(2) Dried-out specimenInappropriate specimen for test requestedInadequate volumeSpecimen in fixative (for culture)Duplicate sample in 24-hr period (for urine, sputum, feces culture)
10Specimen rejection criteria(3) When specimens are rejected, the health care provider is notified so that another specimen may be properly submitted.If information on the requisition is incomplete, laboratory personnel should ask a responsible person to provide the information before processing the specimen further.If a specimen is mislabeled, the sample should be recollected. Relabeling of a specimen is acceptable only for difficult to collect specimens, such as tissue obtained during a surgical procedure or CSF.
11Specimen not routinely accepted for anaerobic culture(1) Throat, nasopharyngeal, or gingival swabsSputaBronchial wash, lavage, or brush (except when collected with a protected double lumen catheter)Gastric and bowel contents
12Specimen not routinely accepted for anaerobic culture(2) Ileostomy and colostomy effluentVoided or catheterized urineFemale genital tract specimens collected through the vaginaSurface swabs of ulcers, wound, and abscesses
13Standard PrecautionsAll specimens should be presumed to contain transmissible agents and therefore should be collected and handled using standard precautions.Use of gloves, gown, mask, and protective eyewear when there is a risk of coming in contact with the specimenIn most clinical laboratories, a special area is designed for processing clinical samples for culture.
14Clinical Diagnosis by Microbiology Laboratory method(1) Direct ExaminationGram stain (general)acid-fast bacilli (AFB) (mycobacteria )KOH and/or calcofluor white preparation (fungi )wet mount (parasites), etc.Other techniques for directly examining specimens :direct fluorescent antibody stains (DFA),enzyme immunoassays (EIAs),DNA hybridization or amplification assays, etc.
15Clinical Diagnosis by Microbiology Laboratory method(2) Isolate, Culture and IdentificationA combination of media types is used to isolate bacteria and fungi (include enriched, nonselective, selective, or differential media);Viruses can only be cultured within mammalian cells, three main categories: primary, low-passage finite and continuous cell linesCulture of parasites is generally not performed.
16Clinical Dignosis by Microbiology Laboratory method(3) Lengths of culture timeMost routine bacterial cultures are incubated for 2 to 3 days.Mycobacterial and fungal cultures are in-cubated for as long as 6 weeks.Viral cell cultures are incubated for varying lengths of time depending on the specimen source and the growth rate of the viruses that are typically recovered from that site
17Clinical Dignosis by Microbiology Laboratory method(4) The condition of incubation35℃ for bacteria and viruses30℃ for fungiVarious atmospheric conditions may be utilized including ambient, CO2 enriched, microaerophilic and anaerobic.
18Specific recommendations for each specimen type The second part of this chapter
19Blood - specimen collection(1) In general, blood for culture should not be obtained using an intravascular device.When performing a venipuncture, the skin must be adequately disinfected to minimize contamination with normal skin flora.Blood should be collected and incubated into the blood culture bottles using the same needle.
20Blood - specimen collection(2) Blood specimens should be collected before administering antimicrobial agents.Optimally, the specimen should be collected just before a fever spike; however, prac-tically, the specimen should be collected immediately after the spike.For adults, 20 to 30mL of blood should be collected per venipuncture. Less blood is required for children .
21Blood - specimen collection(3) For adult patient, two sets of cultures should be collected per febrile episode to help distinguish probable pathogens from pos-sible contaminantsNo more than four sets should be submitted in a 24-hour period.Inoculated blood culture vials should be held at room temperature until they reach the laboratory.
22Blood culture(1)Cultures for rapidly growing bacteria and yeast are usually incubated for 5 to 7 days.Cultures for mycobacteria and slowly grow-ing fungi are held for as long as 42 days.Many types of blood culture systems are a-vailable, including both manual and auto-mated. Each system utilizes a noninvasive method (i.e., colorimetric, fluorescent, or manometric methods for detecting CO2 or other gases) to monitor growth.
23Blood culture(2)As soon as growth is detected from the blood specimen, a stain is performed (Gram, acid-fast, or Giemsa stain) to determine the type of microorganism present.Positive stain results are considered a critical value and called directly to the patient’s health care provider .Then the specimen should be subcultured to solid media.
24Culture of catheter tips Performed to determine the source of a bacteremia.Semiquantitative catheter tip culture method :The segment is rolled across a blood agar plate four timesCultures yielding organisms present in more than 15 CFU are considered to be significant, potentially indicating a catheter-related in-fection.
25Cerebrospinal fluid (CSF)(1) Cerebrospinal fluid (CSF) is submitted for microbiological analysis when meningitis or encephalitis is suspected.For meningitis, the likely infection agent differs depending on the duration of symp-toms. The most likely bacterial agent of acute meningitis will also vary with the age of the individual and whether the disease is comunity or nosocomially acquired.
26Cerebrospinal fluid (CSF)(2) Most infectious cases of encephalitis are a result of viral infection, both arthropod and nonarthropod borne.Parasitic infections of the central nervous system also occur, with varying clinical presentations.
27Probable infectious cause of meningitis Duration of symptoms Probable Pathogen< 24 hr Pyogenic bacteria1-7 days Enteroviruses , Pyogenic bacteria≥4 wk Mycobacterium tuberculosisTreponema pallidumBrucella spp , Candida sppLeptospira interrogansBorrelia burgdorferiCryptococcus neoformamCoccidioides immitisHistoplasma capsulatum
28CSF - specimen collection Obtained by lumbar spinal punctureGenerally at least 0.5mL of CSF (smear, culture, antigen tests )For mycobacterial culture, at least 3mL (greater volumes increase recovery)
29CSF – transportationTransported to the laboratory promptly and processed as soon as possible.If a delay in processing is unavoidable, the specimen should be held at room temperature.If greater than 1.0mL of CSF is received for a given test the fluid is centrifuged to allow the test to be performed on the concentrate sediment
30CSF-laboratory diagnosis Gram stainantigen testsIndia ink test (Cryptococcus neoformans )dark-field microscopy of a concentrated specimen (Leptospires)acid-fast bacilli (AFB) (mycobacteria )bacterial cultureyeast and fungi cultureviral culture
31Gastrointestinal Tract(1) Feces, and in some cases rectal swabs, are submitted to the laboratory primarily to determine the etiologic agent infections diarrhea or food poisoning.Feces should be collected in a clean container with a tight lid and should not be contaminated with urine, barium, or toilet paper. Optimally be examined within 2 hours of collection.
32Gastrointestinal Tract(2) Rectal swabs should be placed in a tube transport system containing modified Stuart-’s medium.Unpreserved stool specimens should be maintained at refrigerator temperature dur-ing storage and transport.
33Gastrointestinal Tract(3) It is becoming standard practice to reject stool specimens for bacterial culture and parasite examination from patients who have been hospitalized longer than 3 days . For such patients, examination for the toxins produced by Clostridium difficile is recom-mended.
34Gastrointestinal Tract -laboratory diagnosis Bacterial cultureselective and differential medium (Mac Conkey agar, Hektoen enteric or xylose-lysine-desoxycholate agar,etc)Fungal culture of stool is not recommended.Viral cultureTo detect parasites, stool is examined microscopically for the presence of protozoa, helminth eggs, and larvae.
35Genital Tract(1)Genital tract specimens are sent to the laboratory for determining the cause of vari-ous clinical syndromes, including vulvova-ginitis, bacterial vaginosis, etc.Many specimens will be contaminated with the normal microbiota of the genital tract or skin; therefore, the microbiologist must differentiate the normal flora from potential pathogens.
36Genital Tract(2)Organisms such as N. gonorrhoeae, C. trachomatis, and Haemophilus ducreyi are always pathogenic, whereas organisms such as the Enterobacteriaceae, S. aureus, and group B streptococci are pathogenic only in some clinical situations.
37Genital Tract -laboratory diagnosis(1) direct Gram stain (only a few situations )eg., gram-negative diplococci within poly-morphonuclear leukocyteswet mount preparation of vaginal secretionsclue cells :epithelial cells covered with small coccobacillary bacteriavaginal pH normal≤4.5whiff test positive :generation of a pungent, fishy odor on addition of 10% KOH to the specimen
38Genital Tract -laboratory diagnosis(2) bacterial culture: depend on the source and the organisms likely to cause disease at that siteTissue and aspirates should be plated to media capable of recovering fastidious organisms.Specimens from the cervix, vagina, and urethra should at a minimum be evaluated for N. gonorrhoeae and C. trachomatis by culture or a direct detection method.
39Genital Tract -laboratory diagnosis(3) Fungal culture of female genital tract specimens is not productive.Viral culture remains the gold standard for detection of HSV.
40Lower Respiratory Tract primarily to determine the etiologic agent of pneumoniaSpecimen types:sputum (expectorated or induced), tracheal aspirates, transtracheal aspirates, bronchial washes, bronchial brushings, and bronchoalveolar lavage fluids.delivered promptly to the laboratory. if delays are unavoidable , refrigerated .
41Lower Respiratory Tract -laboratory diagnosis(1) Gram-stained smearlow-power magnification to determine the number of squamous epithelial cells and/or neutrophils presentoil immersion to determine the relative amounts of organisms presentIntracellular organisms should be specifical-ly noted.culture ,selective and nonselective media, In addition, a medium capable of recovering fastidious organisms
42Lower Respiratory Tract -laboratory diagnosis(2) bronchial brush specimens (0.01 to 0.001mL)a smear for Gram staining is prepared by cytocentrifugation, and 0.01mL of the speci-men is plated to appropriate media using a pipette or calibrated loop.bronchoalveolar lavage (10 to 100mL )a smear is prepared by cytocentrifugation and Gram stained (presence or absence of intracellular organisms), a mL aliquot of the specimen is inoculated onto agar media
43Upper Respiratory Tract Nasopharyngeal aspirates, washings, and swab specimens are primarily used for the diagnosis of viral respiratory infections but may also be submitted to diagnose pertussis, diphtheria, chlamydia infections, and candidiasis, as well as identify carriers of N. meningitidis or S. aureus.Throat swab specimens are generally collected to diagnose group A streptococcal pharyngitis or to detect shedding of viruses such as enteroviruses, HSV, or CMV.
44Tissuesprocured at great expense and considerable risk to the patient; therefore, for optimal evaluation enough material should be collected to allow both histopathologic and microbiologic examination.After collection, tissues should be placed in a sterile container and transported rapidly to the laboratory to prevent drying.
45Tissues -laboratory diagnosis homogenized by mincing with a sterile scalpel, grinding with a mortar and pestle or tissue grinderGram stain or other stainsexamined for presence of microorganisms, leukocytes, and squamous epithelial cellsroutine culture, liquid medium and enriched agar mediumbone marrow aspirates, in collection tubes for the lysis centrifugation blood culture system or in a sterile container
46UrineAcceptable methods of urine collection in-clude midstream clean catch, catheterization, and suprapubic aspiration. Foley catheter tips should not be accepted for culture.promptly to the laboratory and processed within 2 hours of collection . If delays are unavoidable, refrigerated.
47Urine -laboratory diagnosis Screening urine specimensGram staindipstick tests that combine nitrate reductase and leukocyte esteraseQuantitative bacterial culture0.001-mLplastic or wire calibrated loopblood and Mac-Conkey agars
48Skin and Subcutaneous Lesions(1) Ideally, the infected material is aspirated with a needle and syringe. For transport, the material is expelled into sterile container that is tightly capped and promptly delivered to the laboratory.If an aspirate cannot be obtained, swab specimens of exudate collected from the deep portion of the lesion are acceptable.For bacterial and fungal cultures, swabs may be placed in tube transport system contain-ing modified Stuart’s medium.
49Skin and Subcutaneous Lesions(2) To recover anaerobes, an additional swab specimen must be collected and placed in an anaerobic transport system.For viral culture, the specimen (aspirate or swab) should be placed in viral transport medium and kept on ice.If a delay in processing is unavoidable, specimens may be stored in the refrigerator, except those for recovery of anaerobes (room temperature )
50Skin and Subcutaneous Lesions -laboratory diagnosis Gram-stainappropriate media for cultureIf detection of mycobacteria is requested, specimens should be decontaminated and concentrated. The sediment is used to prepare a smear for staining for AFB and to inoculate mycobacterial media.