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Manual of Commercial Methods in Clinical Microbiology


Manual of Commercial Methods in Clinical Microbiology


International Edition 2nd Edition

von: Allan L. Truant

167,99 €

Verlag: Wiley-Blackwell
Format: PDF
Veröffentl.: 28.03.2016
ISBN/EAN: 9781119021865
Sprache: englisch
Anzahl Seiten: 616

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Beschreibungen

<p><i>The Manual of Commercial Methods in Clinical Microbiology 2<sup>nd</sup> Edition, International Edition</i> reviews in detail the current state of the art in each of the disciplines of clinical microbiology, and reviews the sensitivities, specificities and predictive values, and subsequently the effectiveness, of commercially available methods – both manual and automated. This text allows the user to easily summarize the available methods in any particular field, or for a specific pathogen – for example, what to use for an Influenza test, a Legionella test, or what instrument to use for identification or for an antibiotic susceptibility test. </p> <p><i>The Manual of Commercial Methods in Clinical Microbiology, 2<sup>nd</sup> Edition, International Edition</i> presents a wealth of relevant information to clinical pathologists, directors and supervisors of clinical microbiology, infectious disease physicians, point-of-care laboratories, professionals using industrial applications of diagnostic microbiology and other healthcare providers. The content will allow professionals to analyze all commercially available methods to determine which works best in their particular laboratory, hospital, clinic, or setting. </p> Updated to appeal to an international audience, The Manual of <i>Commercial Methods in Clinical Microbiology</i>, <i>2<sup>nd</sup> Edition, International Edition</i> is an invaluable reference to those in the health science and medical fields.
<p>Important Notice, xiii<br />Preface to the Second Edition, xiv</p> <p>Foreword, xvi</p> <p>Acknowledgments, xvii</p> <p>Rising Sun Chair, xviii</p> <p>Contributors, xix</p> <p><b>1 Role of the US Food and Drug Administration in the Regulation of Clinical Microbiology Devices, 1</b><br /><i>Kathleen B. Whitaker, Sally A. Hojvat, and Estelle Russek-Cohen</i></p> <p>1.1 Historical overview of in vitro diagnostics, 1</p> <p>1.2 Current microbiology device review regulatory pathways: practical considerations, 2</p> <p>1.3 Assay performance characteristics: “Statistics 101” for diagnostic device developers, 7</p> <p>1.4 Common issues with new FDA submissions, 8</p> <p>References, 10</p> <p><b>2 Commercial Blood Culture Systems and Methods, 11</b><br /><i>Michael L. Wilson, Melvin P. Weinstein, and L. Barth Reller</i></p> <p>2.2 Automated blood culture systems, 12</p> <p>2.3 Molecular and other methods, 18</p> <p>2.4 Future directions, 19</p> <p>References, 19</p> <p><b>3 Rapid Devices and Instruments for the Identification of Aerobic Bacteria, 21</b><br /><i>Laura J. Chandler, P. Rocco LaSala, and Susan Whittier</i></p> <p>3.1 Introduction, 21</p> <p>3.2 Major methods currently available, 21</p> <p>3.3 Commercial systems for identification of Gram-positive organisms, 29</p> <p>3.4 Commercial systems for identification of Gram-negative organisms, 38</p> <p>3.5 Commercial methods for identification of microorganisms directly in blood culture bottles, 46</p> <p>3.6 Commercial molecular methods for identification of bacteria isolated in culture, 48</p> <p>3.7 Emerging technologies for the identification of organisms: mass spectrometry, 49</p> <p>References, 49</p> <p><b>4 Rapid Devices and Instruments for the Identification of Anaerobic Bacteria, 56</b><br /><i>Christopher L. Emery, Maria D. Appleman, Jean A. Siders, and Thomas E. Davis</i></p> <p>4.1 Introduction and clinical considerations, 56</p> <p>4.2 Steps in the diagnosis of anaerobic bacterial infections, 57</p> <p>4.3 Commercial kit requiring 24 h of anaerobic incubation, 64</p> <p>4.4 Commercial enzyme kits for identification after four hours of aerobic incubation, 64</p> <p>4.5 Identification by gene sequencing, 71</p> <p>4.6 Identification by chemical methods, 71</p> <p>4.7 Immunodiagnostic and molecular methods for diagnosis of Clostridium difficile infection, 74</p> <p>References, 82</p> <p><b>5 Rapid Antigen Devices and Instruments for the Detection and Identification of Viruses, 87</b><br /><i>Wallace H. Greene, Marilyn A. Menegus, and Allan L. Truant</i></p> <p>5.1 Influenza viruses, 88</p> <p>5.2 Respiratory syncytial virus, 91</p> <p>5.3 Immunofluorescence staining of respiratory viruses, 92</p> <p>5.4 Herpes simplex virus, varicella zoster virus, cytomegalovirus, 93</p> <p>5.5 Gastrointestinal viruses, 94</p> <p>References, 95</p> <p><b>6 Molecular Tests for the Identification of Viruses, 97</b><br /><i>Scott Duong and Christine C. Ginocchio</i></p> <p>6.1 Introduction, 97</p> <p>6.2 Respiratory viral infections, 97</p> <p>6.3 Enteric viruses, 105</p> <p>6.4 Enterovirus and parechovirus, 107</p> <p>6.5 Herpesviruses, 108</p> <p>6.6 Viral infections associated with transplantation, 109</p> <p>6.7 Implementation and additional considerations, 112</p> <p>References, 113</p> <p><b>7 Viral Hepatitis, 121</b><br /><i>Emily Jeanne Cartwright and Yun F. (Wayne) Wang</i></p> <p>7.1 Introduction/background, 121</p> <p>7.2 Clinical manifestations, epidemiology, and diagnostic considerations by virus, 121</p> <p>7.3 Commercial methods, 127</p> <p>7.4 Summary, 131</p> <p>References, 132</p> <p><b>8 Human Papillomaviruses, 135</b><br /><i>N. Esther Babady</i></p> <p>8.1 Background, 135</p> <p>8.2 Commercial assays, 136</p> <p>8.3 Current challenges and future directions, 143</p> <p>References, 144</p> <p><b>9 Human Immunodeficiency Virus, 149</b><br /><i>Richard L. Hodinka</i></p> <p>9.1 Introduction, 149</p> <p>9.2 Markers of HIV infection, 150</p> <p>9.3 HIV screening, 151</p> <p>9.4 Laboratory-based immunoassays, 152</p> <p>9.5 Rapid, less-sophisticated immunoassays, 154</p> <p>9.6 Specimen matrices for HIV screening, 157</p> <p>9.7 Confirmatory and supplemental tests, 157</p> <p>9.8 Serological testing of neonates, 159</p> <p>9.9 p24 Antigen detection, 160</p> <p>9.10 Qualitative molecular detection, 161</p> <p>9.11 Quantification of HIV RNA, 162</p> <p>9.12 Phenotypic and genotypic assays for drug resistance, 165</p> <p>References, 167</p> <p><b>10 Chlamydia, 175</b><br /><i>Claudiu I. Bandea, Robert C. Jerris, and Carolyn M. Black</i></p> <p>10.1 Introduction, 175</p> <p>10.2 Epidemiology, 176</p> <p>10.3 Biology, 177</p> <p>10.4 Natural history, 178</p> <p>10.5 Clinical symptoms and sequelae, 178</p> <p>10.6 Treatment, 179</p> <p>10.7 Laboratory testing for C. trachomatis, 179</p> <p>References, 183</p> <p><b>11 Rickettsiae and Tick-Borne Diseases, 184</b><br /><i>Natalie Williams-Bouyer, Donald H. Bouyer, and Michael J. Loeffelholz</i></p> <p>11.1 Introduction, 184</p> <p>11.2 Overview of tick-borne diseases, 184</p> <p>11.3 Newly emerging tick-borne disease, 191</p> <p>References, 191</p> <p><b>12 Mycoplasma, 195</b><br /><i>Ken B. Waites and Cécile Bébéar</i></p> <p>12.1 Introduction and clinical considerations, 195</p> <p>12.2 Culture-based diagnosis, 197</p> <p>12.3 Serological diagnosis, 202</p> <p>12.4 Molecular detection systems, 206</p> <p>12.5 Antimicrobial susceptibility testing, 209</p> <p>12.6 Future directions, 210</p> <p>References, 211</p> <p><b>13 Commercial Methods for Identification and Susceptibility Testing of Fungi, 214</b><br /><i>Stephen A. Moser and Jason Wicker</i></p> <p>13.1 Direct examination and detection methods, 214</p> <p>13.2 Culture and detection, 220</p> <p>13.3 Identification systems, 224</p> <p>13.4 Molecular testing, 236</p> <p>13.5 Susceptibility testing, 248</p> <p>References, 261</p> <p><b>14 Mycobacteria, 273</b><br /><i>Xiang Yang Han</i></p> <p>14.1 Introduction, 273</p> <p>14.2 Specimen processing, 273</p> <p>14.3 Acid-fast staining reagents, 273</p> <p>14.4 Direct detection of mycobacteria from clinical specimens, 274</p> <p>14.5 Blood-culture recovery of mycobacteria, 275</p> <p>14.6 Mycobacteria-culturing methods and systems, 276</p> <p>14.7 Identification of mycobacteria, 278</p> <p>14.8 Susceptibility tests for mycobacteria, 280</p> <p>14.9 Immunodiagnosis of tuberculosis, 281</p> <p>14.10 Conclusion, 281</p> <p>References, 281</p> <p><b>15 Diagnostic Medical Parasitology, 284</b><br /><i>Lynne S. Garcia and Gary W. Procop</i></p> <p>15.1 Diagnostic parasitology testing, 284</p> <p>15.2 Solicitation of product information, 287</p> <p>15.3 Specimen collection systems, 287</p> <p>15.4 Fresh stool specimen collection, 287</p> <p>15.5 Preservation of stool specimens, 289</p> <p>15.6 Intestinal tract specimens (stool), 294</p> <p>15.7 Ova and parasite examination, 297</p> <p>15.8 Molecular methods, 297</p> <p>15.9 Other diagnostic methods, 303</p> <p>15.10 Collection of specimens from other body sites, 303</p> <p>15.11 Blood collection, 303</p> <p>15.12 Malaria rapid diagnostic tests, 305</p> <p>References, 307</p> <p><b>16 Molecular Microbiology, 309</b><br /><i>Raghava Potula and Yi-Wei Tang</i></p> <p>16.1 Introduction, 309</p> <p>16.2 Specimen processing and nucleic acid extraction platforms, 309</p> <p>16.3 Amplification methods and platforms, 310</p> <p>16.4 Amplicon detection and identification platforms, 313</p> <p>16.5 Future directions, 316</p> <p>16.6 Summary, 316</p> <p>References, 316</p> <p><b>17 Automated Immunoassay Analyzers, 319</b><br /><i>Richard L. Hodinka and Matthew J. Binnicker</i></p> <p>References, 333</p> <p><b>18 Molecular Typing Instruments and Methods, 336</b><br /><i>Ruth Ann Luna</i></p> <p>18.1 Introduction, 336</p> <p>18.2 Background, 336</p> <p>18.3 Current molecular typing methodologies, 337</p> <p>18.4 Comparison of typing techniques, 340</p> <p>18.5 Summary, 343</p> <p>References, 343</p> <p><b>19 Commercial Methods in Clinical Veterinary Microbiology, 346</b><br /><i>Thomas J. Inzana, Xiang-Jin Meng, Tanja Opriessnig, and Lora Ballweber</i></p> <p>19.1 Collection and transportation of clinical samples, 347</p> <p>19.2 Selection of diagnostic laboratories and tests, 348</p> <p>19.3 Pathology and histopathology, 349</p> <p>19.4 Quality control of veterinary diagnostic assays: sensitivity and specitivity, 349</p> <p>19.5 Veterinary virology, 350</p> <p>19.6 Veterinary bacteriology, 359</p> <p>19.7 Veterinary mycology, 365</p> <p>19.8 Veterinary parasitology, 366</p> <p>Acknowledgements, 371</p> <p>References, 371</p> <p><b>20 Microbiology Laboratory Information Systems, 377</b><br /><i>Raymond D. Aller and Vincent Salazar</i></p> <p>20.1 In general, microbiology laboratory information systems fit one of three categories, 377</p> <p>20.2 What are the key features of software to support management of microbiology?, 378</p> <p>20.3 Microbiology information systems have evolved over several decades, 380</p> <p>20.4 Criteria for comparison of current systems, 382</p> <p>20.5 Specialized software, 382</p> <p>20.6 Selecting an information system for your laboratory, 383</p> <p>20.7 Cases, 383</p> <p>20.8 Management of the laboratory information system, 384</p> <p>20.9 Personnel management, 384</p> <p>References, 385</p> <p><b>21 Emerging Infectious Diseases, 386</b><br /><i>Brett Laurence, Julie Collins, Carolyn Fernandes, Rafik Samuel, and Byungse Suh</i></p> <p>21.1 Introduction, 386</p> <p>21.2 Plasmodium knowlesi, 386</p> <p>21.3 Clostridium difficile, 389</p> <p>21.4 Pandemic H1N1 influenza, 391</p> <p>21.5 Escherichia coli O104:H4, 393</p> <p>21.6 Cryptococcus gattii, 394</p> <p>21.7 Borrelia miyamotoi, 396</p> <p>21.8 Rickettsia parkeri, 397</p> <p>21.9 Mycobacterium lepromatosis, 398</p> <p>21.10 Bocavirus, 400</p> <p>21.11 Human metapneumovirus, 400</p> <p>21.12 Severe fever with thrombocytopenia syndrome virus, 402</p> <p>21.13 Zika virus, 403</p> <p>References, 404</p> <p><b>22 Automated and Manual Systems for Antimicrobial Susceptibility Testing of Bacteria, 414</b><br /><i>Alan T. Evangelista and James A. Karlowsky</i></p> <p>22.1 Introduction, 414</p> <p>22.2 Evaluation of commercial AST performance, 415</p> <p>22.3 Automated broth microdilution AST systems, 415</p> <p>22.4 Semiautomated and manual broth microdilution AST systems, 422</p> <p>22.5 Manual and semiautomated agar antimicrobial gradient diffusion and disk diffusion susceptibility tests, 423</p> <p>22.6 Phenotypic detection of antimicrobial resistance using chromogenic media, 425</p> <p>22.7 Genotypic detection of antimicrobial resistance determinants in positive blood cultures, 427</p> <p>22.8 Next generation methods for antimicrobial susceptibility testing, 428</p> <p>References, 430</p> <p><b>23 Bioterrorism, 433</b><br /><i>James W. Snyder and Michael A. Pentella</i></p> <p>23.1 Introduction, 433</p> <p>23.2 History of bioterrorism, 433</p> <p>23.3 Bioterrorism in the future, 434</p> <p>23.4 Laboratory Response Network, 435</p> <p>23.5 Rapid methods, 436</p> <p>23.6 Conclusion, 436</p> <p>References, 436</p> <p><b>24 Clinical Microbiology: Looking Ahead, 438</b><br /><i>Natalie N. Whitfield, Raquel M. Martinez, and Donna M. Wolk</i></p> <p>24.1 Introduction, 438</p> <p>24.2 Connectivity between extraction and amplification platforms, 439</p> <p>24.3 Polymerase chain reaction and RT-PCR: detection and characterization, 441</p> <p>24.4 Other amplification methods, 447</p> <p>24.5 Probe technology, 448</p> <p>24.6 Mass spectrometry, 449</p> <p>24.7 DNA sequencing, 451</p> <p>24.8 Emerging technology, 452</p> <p>24.9 Other strategies and concepts that will impact clinical microbiology, 459</p> <p>24.10 Some new responsibilities for the coming years, 460</p> <p>24.11 Summary, 462</p> <p>References, 463</p> <p>International Section, 473</p> <p>Introduction, 473<br /><i>Allan L. Truant, Yi-Wei Tang, Ken B. Waites, Cécile Bébéar, and Robert Rennie</i></p> <p><b>25 Clinical Microbiology In Vitro Diagnostic Medical Devices in Argentina: Regulatory Requirements And Product Information, 475</b><br /><i>Marcela Echavarria and Mariela Aranda</i></p> <p>25.1 History, 475</p> <p>25.2 Regulation of clinical microbiology in vitro diagnostic medical devices in Argentina, 477</p> <p>References, 481</p> <p><b>26 Clinical Microbiology In Vitro Diagnostics in Australia: Regulatory Requirements and Product Information, 483</b><br /><i>Carola Venturini, Vitali Sintchenko, and Jonathan R. Iredell</i></p> <p>26.1 The Therapeutic Goods Administration, 483</p> <p>26.2 National Pathology Accreditation Advisory Council, 486</p> <p>26.3 National Association of Testing Authorities, 486</p> <p>26.4 RCPA quality assurance programs, 487</p> <p>26.5 Manufacturers and suppliers of IVDs, 487</p> <p>References, 489</p> <p><b>27 Clinical Microbiology In Vitro Diagnostic Devices in Canada: Regulatory Requirements and Product Information, 491</b><br /><i>James A. Karlowsky</i></p> <p>References, 493</p> <p><b>28 Clinical Microbiology In Vitro Diagnostics in China: Regulatory Requirements and Product Information, 494</b><br /><i>Shangwei Wu, Weiwei Zhao, Hongbo Li, and Dongfeng Tan</i></p> <p>28.1 The regulatory requirements for clinical microbiology in vitro diagnostics products in China, 494</p> <p>28.2 IVD product review: devices and instruments, 495</p> <p>References, 506</p> <p><b>29 Clinical Microbiology In Vitro Diagnostic Medical Devices in France: Regulatory Requirements and Product Information, 507</b><br /><i>Frederique Gouriet</i></p> <p>29.1 Regulatory requirements, 507</p> <p>29.2 European Directive 98/79/EC, 507</p> <p>29.3 Directive 98/79/EC in France, 514</p> <p>29.4 The implications of the regulatory level authorities, 514</p> <p>29.5 Assessment procedures, 514</p> <p>Reference, 514</p> <p><b>30 Clinical Microbiology In Vitro Diagnostic Medical Devices in India: Regulatory Requirements and Product Information, 515</b><br /><i>Abhijit Chaudhury</i></p> <p>References, 519</p> <p>Websites for reference, 519</p> <p><b>31 Clinical Microbiology In Vitro Diagnostics in Italy: Regulatory Requirements and Product Information, 520</b><br /><i>Simone Ambretti, Mariapaola Landini, Davide Gibellini, and Tiziana Lazzarotto</i></p> <p>31.1 Introduction, 520</p> <p>31.2 National classification of medical devices, 520</p> <p>31.3 Assessment procedures for IVD medical devices, 521</p> <p>31.4 Registration for manufacturers of IVD medical devices, 524</p> <p>Bibliography, 524</p> <p><b>32 Clinical Microbiology In Vitro Diagnostics in Japan: Regulatory Requirements and Product Information, 525</b><br /><i>Koji Kawakami and Yukie Yamauchi</i></p> <p>32.1 The regulatory structure of pharmaceuticals and clinical trials in Japan, 525</p> <p>32.2 The regulatory structure of in vitro diagnostic testing in Japan, 525</p> <p>32.3 Marketing of IVD reagents in Japan, 526</p> <p>32.4 Clinical efficiency study/correlation study, 527</p> <p>32.5 Marketing approval, 530</p> <p>32.6 National Health Insurance coverage of IVD reagents, 530</p> <p>Bibliography, 530</p> <p><b>33 Clinical Microbiology In Vitro Diagnostic Medical Devices in the Republic of Korea: Regulatory Requirements and Product Information, 531</b><br /><i>Jeong Hwan Shin</i></p> <p>Bibliography, 534</p> <p><b>34 Clinical Microbiology In Vitro Diagnostic Medical Devices in South Africa: Regulatory Requirements and Product Information, 535</b><br /><i>Abdool Kader Peer</i></p> <p>34.1 Regulatory requirements, 535</p> <p>34.2 Product information, 536</p> <p>Reference, 536</p> <p><b>35 Clinical Microbiology In Vitro Diagnostic Medical Devices in the UK: Regulatory Requirements and Product Information, 537</b><br /><i>Timothy D. McHugh, Jim F. Huggett, and Simon Rattenbury</i></p> <p>35.1 Background, 537</p> <p>35.2 Definitions, 537</p> <p>35.3 Conformity assessment, 545</p> <p>35.4 Other considerations, 545</p> <p>Bibliography, 545</p> <p>Appendix: Manufacturers, Distributors and Vendors, 546<br /><i>Raquel DeLeon-Gonsalves and Allan L. Truant</i></p> <p>Index, 581</p>
<p>"The second edition of the Manual of Commercial Methods in Clinical Microbiology: International Edition is intended to be a current reference of commercially available tests, devices, and instruments used in clinical microbiology. The first edition contained 18 chapters that focused on US regulatory issues, rapid detection systems for bacteria and viruses, blood culture systems, diagnostic parasitology, automated serology, susceptibility testing, molecular methods, laboratory information systems, and specific pathogens such as HIV, Chlamydia, Mycoplasma, Mycobacterium, and emerging organisms. The second edition has been greatly updated and expanded to 35 chapters including new chapters on virology, viral hepatitis, automated molecular typing systems, specific pathogens such as human papillomavirus and rickettsiae, tickborne diseases, and bioterrorism. Additionally, there are 11 new chapters containing a synopsis of international clinical microbiology products and the regulatory requirements of selected countries including several in Europe and Asia, as well as Canada, Australia, South Africa, and Argentina.</p> <p>The content of this book focuses primarily on human clinical microbiology; however, both the first and second editions include a chapter on Commercial Methods in Clinical Veterinary Microbiology coauthored by microbiologists from 3 colleges of veterinary medicine. That chapter is an informed summary that reveals issues associated with the use of human diagnostic systems in veterinary microbiology and includes references that document the accuracy of such systems when used to analyze samples of various animal origins....</p> <p>Although the majority of the book focuses on available tests for human pathogens, a reasonable amount of the reference information will be useful for veterinary diagnostic microbiologists. The inclusion of the chapter on veterinary clinical veterinary microbiology integrates the reference material in an informative manner. It is a comprehensive reference of available commercial diagnostic systems for laboratory managers seeking tools for enhancing efficiency and accuracy." (<b>Journal of the American Veterinary Medical Association, 15th Dec 2017<b>)</p>
<p><strong>The Editor-in-Chief, Allan L. Truant</strong> is a Professor of Pathology and Laboratory Medicine, Microbiology and Immunology, and Internal Medicine at the Lewis Katz School of Medicine at Temple University, and Director of Clinical Microbiology, Immunology and Virology Laboratories at the Temple University Hospital in Philadelphia, PA.

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