Medical bacteriology : a practical approach /

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Bibliographic Details
Imprint:Oxford ; New York : IRL Press at Oxford University Press, 1989.
Description:xix, 321 p. : ill. ; 24 cm.
Language:English
Series:Practical approach series
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/1042561
Hidden Bibliographic Details
Other authors / contributors:Hawkey, P. M. (Peter M.)
Lewis, D. A. (Deirdre A.)
ISBN:0199630089 : $69.00 (U.S.)
0199630097 (pbk.) : $46.00 (U.S.)
Notes:Includes bibliographies and index.
Table of Contents:
  • Protocol List
  • Abbreviations
  • Contributors
  • 1. Bacteriology of urine
  • 1. Introduction
  • 2. Specimen collection and transport
  • 2.1. Collection
  • 2.2. Transport
  • 3. Microscopy and other rapid screening methods
  • 3.1. Reagent strips/dipsticks
  • 3.2. Microscopy
  • 3.3. Automated screening methods for urine
  • 4. Interpretation of findings on microscopy
  • 4.1. Leukocytes
  • 4.2. Red cells
  • 4.3. Epithelial cells
  • 4.4. Bacteria
  • 4.5. Casts and crystals
  • 5. Culture
  • 5.1. Choice of media
  • 5.2. Culture methods
  • 5.3. Localization of site of infection
  • 5.4. Culture of urine for Mycobacterium tuberculosis
  • 6. Interpretation of culture results
  • 6.1. The concept of significant bacteriuria
  • 6.2. Interpretation and reporting of specimens from patients with indwelling catheters and ileal conduits
  • 6.3. Interpretation and reporting of suprapubic aspirate and ureteric catheter specimens
  • 6.4. Asymptomatic bacteriuria of pregnancy
  • 7. Identification of bacteria
  • 7.1. Yeasts
  • 7.2. Identification of difficult or 'fastidious' organisms
  • 8. Sensitivity testing
  • 8.1. Choice of first-line and second-line agents for sensitivity testing
  • 8.2. Primary sensitivity testing
  • 8.3. Reporting of sensitivities
  • 9. Further tests
  • 9.1. Detection of antimicrobial substances in urine (51)
  • References
  • 2. Bacteriology of normally sterile body fluids
  • 1. Introduction
  • 2. Methods for the examination of blood
  • 2.1. Principles of blood culture
  • 2.2. Principles of blood culture methods
  • 2.3. Blood culture methods
  • 2.4. Blood culture diagnosis of catheter-related sepsis
  • 2.5. Alternative methods to broth cultures
  • 3. Methods for the examination of cerebrospinal fluid
  • 3.1. Introduction
  • 3.2. Bacteriological aspects of specimen collection
  • 3.3. Microscopy
  • 3.4. Culture
  • 3.5. Additional tests
  • 3.6. Interpretation of results
  • 3.7. Tuberculous meningitis (TBM)
  • 4. Methods for the examination of peritoneal dialysis effluents
  • 4.1. Definition of CAPD peritonitis
  • 4.2. Sampling PDE
  • 4.3. Interpretation of culture results
  • 4.4. Identification and sensitivity testing
  • 4.5. Culture negative peritonitis
  • 5. Methods for the examination of serous fluids
  • 5.1. Examination of non-purulent serous fluids
  • References
  • 3. Bacteriology of the respiratory tract
  • 1. Introduction
  • 2. Upper respiratory tract
  • 2.1. The nose
  • 2.2. The nasopharynx
  • 2.3. The throat
  • 2.4. The ear
  • 2.5. The maxillary sinuses
  • 3. Lower respiratory tract (LRT)
  • 3.1. Specimen collection
  • 3.2. Routine microscopy and culture
  • 3.3. Special microscopy and culture
  • 3.4. Non-cultural methods of diagnosis
  • References
  • 4. Bacteriology of the genital tract
  • 1. Introduction
  • 1.1. Normal vaginal flora
  • 1.2. Changes in normal vaginal flora
  • 1.3. Pathogens associated with specific clinical conditions
  • 2. Collection and transport of specimens
  • 3. Assessment of specimens in the laboratory
  • 3.1. Microscopy
  • 3.2. Detection of antigen in specimens by enzyme immunoassay
  • 4. Culture
  • 4.1. Selective medium for the isolation of N. gonorrhoeae
  • 4.2. Blood agar and blood agar with neomycin
  • 4.3. MacConkey's agar
  • 4.4. Chlamydia transport medium
  • 5. Serological methods
  • 5.1. Serological diagnosis of syphilis
  • 5.2. Serological diagnosis of chlamydial infections
  • 6. Molecular methods
  • 6.1. Chlamydial trachomatis
  • 6.2. Neisseria gonorrhoeae
  • 6.3. Treponema pallidum
  • 7. Antibiotic susceptibility testing
  • 7.1. Antibiotic susceptibility testing of N. gonorrhoeae
  • 7.2. Antibiotic sensitivity testing of other pathogens
  • References
  • 5. Bacteriology of superficial and deep tissue infection
  • 1. Introduction
  • 1.1. Taking good samples
  • 1.2. Transport
  • 2. General methods
  • 2.1. Pus
  • 2.2. Swabs
  • 2.3. Fluids
  • 2.4. Tissue
  • 3. Anaerobic methods
  • 3.1. Gas-liquid chromatography (GLC)
  • 3.2. Culture of anaerobes
  • 3.3. Identification of anaerobes
  • 3.4. Anaerobic sensitivity testing
  • 4. Skin and soft tissue infections
  • 4.1. Pyoderma and cellulitis
  • 4.2. Wound infections
  • 4.3. Gangrene, myositis, and fasciitis
  • 4.4. Burns, varicose ulcers, ischaemic ulcers, pressure sores
  • 4.5. Sinuses
  • 4.6. Fistulae
  • 4.7. Vesicles and bullae
  • 4.8. Suppurative lymphadenitis
  • 4.9. Chronic ulcers
  • 5. Infection associated with the gastrointestinal tract
  • 5.1. Intra-abdominal abscess
  • 5.2. Peritonitis
  • 5.3. Wound infections
  • 5.4. Biliary infections
  • 5.5. Liver abscesses
  • 5.6. Abscesses
  • 6. Gynaecological and post-partum infections
  • 6.1. Post-operative infections
  • 6.2. Tubo-ovarian sepsis
  • 6.3. Infection associated with intrauterine contraceptive devices (IUCDs)
  • 6.4. Post-partum infections
  • 7. Infections of the skeletal system
  • 7.1. Acute osteomyelitis
  • 7.2. Chronic osteomyelitis
  • 8. Joint infections
  • 8.1. Prosthetic joint infections
  • 9. CNS infections
  • 9.1. Cerebral abscess
  • 10. Eye infections
  • 10.1. Acute conjunctivitis
  • 10.2. Endophthalmitis
  • 10.3. Periocular infections
  • References
  • 6. Bacteriology of intestinal disease
  • 1. Introduction
  • 2. Bacterial enteric pathogens
  • 3. Culture media
  • 3.1. Media for the isolation of salmonellae and shigellae
  • 3.2. Screening identification media for salmonellae and shigellae
  • 3.3. Media for the isolation of Escherichia coli 0157, Yersinia enterocolitica, and other commonly encountered gastrointestinal pathogens
  • 4. Routine specimen processing
  • 4.1. Specimen collection
  • 4.2. Microscopy
  • 4.3. Culture
  • 4.4. Reading the plates
  • 4.5. Serotyping of salmonellae and shigellae
  • 4.6. Biochemical identification
  • 4.7. Sensitivity testing of salmonellae and shigellae
  • 4.8. Reporting to the clinician
  • 5. Specimen processing for organisms other than salmonellae, shigellae, and campylobacters
  • 5.1. Escherichia coli
  • 5.2. Yersinia enterocolitica
  • 5.3. Vibrio cholerae and V. parahaemolyticus
  • 5.4. Clostridium difficile
  • 5.5. 'Food poisoning' due to Clostridium perfringens, Staphylococcus aureus, and Bacillus cereus
  • 5.6. Helicobacter pylori
  • References
  • 7. Antimicrobial susceptibility testing
  • 1. Introduction
  • 2. Disc diffusion methods for antimicrobial susceptibility testing
  • 2.1. Factors affecting diffusion tests
  • 2.2. Methods of disc diffusion susceptibility testing
  • 2.3. Selection of agents for routine testing
  • 2.4. Specific problems in testing
  • 2.5. Quality assurance
  • 2.6. Primary susceptibility tests
  • 3. Methods for determining minimum inhibitory concentrations
  • 3.1. Agar dilution
  • 3.2. Broth dilution methods
  • 3.3. Etest
  • 4. Breakpoint methods
  • 5. Serum bactericidal tests and determination of minimum bactericidal concentrations
  • 6. Automated methods
  • 7. Expert systems
  • 8. Clinical relevance and epidemiological outputs
  • References
  • 8. Antimicrobial assays
  • 1. Introduction
  • 2. Clinical application of antimicrobial assays
  • 2.1. General considerations
  • 2.2. Indications for monitoring
  • 3. Taking specimens for assays
  • 4. Methods of assay
  • 4.1. Characteristics of assay methods: microbiological vs. non-microbiological
  • 5. Microbiological assays
  • 6. Immunoassays
  • 6.1. General principles
  • 6.2. Reagent constitution and storage
  • 6.3. Calibration
  • 6.4. Internal control
  • 6.5. Fluorescence polarization immunoassay (FPIA)
  • 7. High performance liquid chromatography (HPLC)
  • 7.1. General principles and terms
  • 7.2. Characteristics
  • 7.3. Principles of separation--reverse phase
  • 7.4. Equipment
  • 7.5. Sample preparation
  • 7.6. Calibration
  • 7.7. Methods for individual antimicrobials
  • 8. Quality assurance
  • 8.1. Internal controls
  • 8.2. External quality assessment (EQA)
  • 9. Clinical interpretation
  • References
  • 9. Laboratory computing in medical microbiology
  • 1. Introduction
  • 2. Laboratory computers in microbiology
  • 2.1. Stand-alone systems (Laboratory Information Management Systems--LIMS)
  • 2.2. Systems integrated with other hospital systems (Hospital Information Systems--HIS)
  • 2.3. Feeder systems to electronic patient records (Integrated Laboratory Information Management Systems--ILIMS)
  • 3. Core elements of a microbiology computer system
  • 3.1. Requesting
  • 3.2. Result entry
  • 3.3. Validation, system actions, and authorization
  • 3.4. Returning results to requesters
  • 4. Secondary functions
  • 4.1. Access, security, and audit
  • 4.2. Laboratory management functions
  • 4.3. Data extraction
  • 5. System maintenance and development
  • 6. Procurement of a new system
  • References
  • 10. Quality control and quality assurance
  • 1. Introduction
  • 2. Personnel
  • 2.1. Recruitment policies and staffing structures
  • 2.2. Training and organization
  • 2.3. Standard operating procedures
  • 2.4. Logistics and organization
  • 2.5. Specimen collection and transport
  • 2.6. Specimen handling and report validation
  • 3. Culture media quality issues
  • 3.1. Storage conditions
  • 3.2. Preparation of culture media
  • 3.3. User problems
  • 4. Maintenance and storage of control organisms
  • 4.1. Long-term storage
  • 4.2. Short-term storage for ready access
  • 5. Equipment monitoring
  • 5.1. Temperature control
  • 5.2. Control of anaerobic cabinets
  • 5.3. pH meter electrodes
  • 5.4. Autoclaves and preparators
  • 5.5. Pipettes
  • 6. Quality control of laboratory tests and reagents
  • 6.1. Chemicals and dyes
  • 6.2. Staining techniques
  • 6.3. Kits and identification systems
  • 6.4. United Kingdom National External Quality Assessment Scheme (UKNEQAS)
  • 6.5. Internal quality control
  • 7. Near patient testing
  • 8. Audit and error logging
  • 9. Conclusions
  • References
  • 11. Laboratory investigation of health care-associated infection
  • 1. Introduction
  • 1.1. Administration
  • 2. Sample collection
  • 2.1. Surveillance
  • 2.2. Sampling protocols
  • 3. Specimen processing
  • 3.1. Criteria for organism identification
  • 3.2. Use of selective and differential media
  • 4. Bacterial typing systems
  • 4.1. Principles and use of bacterial typing systems
  • 4.2. Biotyping
  • 4.3. Antibiogram and resistogram typing
  • 4.4. Serotyping
  • 4.5. Bacteriophage typing
  • 4.6. Bacteriocin typing
  • 4.7. Molecular typing methods
  • References
  • 12. Epidemiological methods in the investigation of acute bacterial infections
  • 1. Introduction
  • 2. Basic concepts in infectious disease epidemiology
  • 2.1. Reservoir of infection
  • 2.2. Source of infection
  • 2.3. Mode of transmission
  • 2.4. Occurrence
  • 2.5. Incubation period
  • 2.6. Host response
  • 2.7. Analysis and presentation of data
  • 2.8. Communicability
  • 3. Epidemiological methods
  • 3.1. Descriptive methods
  • 4. Analytical methods
  • 4.1. Case-control studies
  • 4.2. Cohort studies
  • 4.3. Statistical analysis of case-control and cohort studies
  • 5. A practical approach to the investigation of an acute incident
  • 5.1. Identification and confirmation of the problem
  • References
  • I. Staining procedures
  • 1. Gram's stain (Preston and Morrell's modification)
  • 1.1. Solutions required
  • 1.2. Staining procedure
  • 2. Giemsa stain
  • 2.1. Solutions required
  • 2.2. Staining procedure
  • 3. Stains for acid-fast bacilli
  • 3.1. Auramine phenol
  • 3.2. Ziehl-Neelsen
  • 3.3. Kinyoun's acid-fast stain
  • 4. Stains for metachromatic (volutin) granules
  • 4.1. Loeffler's methylene blue
  • 4.2. Albert's stain, modified
  • 4.3. Neisser's stain
  • 5. Spore stain (Schaeffer and Fulton's method)
  • 5.1. Staining procedure
  • II. Bacteriological media not usually commercially available
  • 1. Transport media
  • 1.1. Chlamydia transport medium
  • 2. Selective/differential media
  • 2.1. Deoxycholate citrate, crystal violet, cefazolin, rhamnose agar (DCCR)
  • 2.2. Deoxyribonuclease, toluidine blue, cefalothin agar (DTBCA)
  • 2.3. Leeds Acinetobacter medium (LAM)
  • 2.4. MacConkey, inositol, carbenicillin agar (MICA)
  • 2.5. Nalidixic acid, cetrimide agar
  • 2.6. Phenanthroline, C-3911 agar
  • 2.7. Proteeae identification medium
  • 2.8. Salt, phenolphthalein, methicillin agar (SPMA)
  • 2.9. Toluidine blue deoxynucleic acid agar (TDA)
  • 2.10. Vancomycin imipenem agar (VIA)
  • References
  • III. Principles of biochemical tests for the identification of bacteria
  • 1. Introduction
  • 1.1. Catalase test
  • 1.2. Citrate test
  • 1.3. Decarboxylase and dehydrolase tests
  • 1.4. Hippurate hydrolysis test
  • 1.5. Hydrogen sulfide test
  • 1.6. Indole test
  • 1.7. Methyl red and Voges-Proskauer test
  • 1.8. Nitrate reduction test
  • 1.9. ONPG (o-nitrophenyl-[beta]-D-galactopyranoside) test
  • 1.10. Oxidase test
  • 1.11. Phenylalanine deaminase test
  • 1.12. Urease test
  • References
  • IV. Epidemiological questionnaire
  • Index