Medical bacteriology : a practical approach /
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Imprint: | Oxford ; New York : IRL Press at Oxford University Press, 1989. |
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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 |
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