A consensus conference to define the utility of advanced infectious disease diagnostics in solid organ transplant recipients
The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence‐based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was co...
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Published in | American journal of transplantation Vol. 22; no. 12; pp. 3150 - 3169 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Limited
01.12.2022
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Subjects | |
Online Access | Get full text |
ISSN | 1600-6135 1600-6143 1600-6143 |
DOI | 10.1111/ajt.17147 |
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Abstract | The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence‐based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was convened on December 7, 2021, to define the utility of novel infectious disease diagnostics in organ transplant recipients. The conference represented a collaborative effort by experts in transplant infectious diseases, diagnostic stewardship, and clinical microbiology from centers across North America to evaluate current uses, unmet needs, and future directions for assays in 5 categories including (1) multiplex molecular assays, (2) rapid antimicrobial resistance detection methods, (3) pathogen‐specific T‐cell reactivity assays, (4) next‐generation sequencing assays, and (5) mass spectrometry‐based assays. Participants reviewed and appraised available literature, determined assay advantages and limitations, developed best practice guidance largely based on expert opinion for clinical use, and identified areas of future investigation in the setting of transplantation. In addition, attendees emphasized the need for well‐designed studies to generate high‐quality evidence needed to guide care, identified regulatory and financial barriers, and discussed the role of regulatory agencies in facilitating research and implementation of these assays. Findings and consensus statements are presented.
This meeting report summarizes findings from an AST‐sponsored consensus conference to define best practice uses, unmet needs and future directions for advanced infectious diseases diagnostics in solid organ transplant recipients. |
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AbstractList | The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence-based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was convened on December 7, 2021, to define the utility of novel infectious disease diagnostics in organ transplant recipients. The conference represented a collaborative effort by experts in transplant infectious diseases, diagnostic stewardship, and clinical microbiology from centers across North America to evaluate current uses, unmet needs, and future directions for assays in 5 categories including (1) multiplex molecular assays, (2) rapid antimicrobial resistance detection methods, (3) pathogen-specific T-cell reactivity assays, (4) next-generation sequencing assays, and (5) mass spectrometry-based assays. Participants reviewed and appraised available literature, determined assay advantages and limitations, developed best practice guidance largely based on expert opinion for clinical use, and identified areas of future investigation in the setting of transplantation. In addition, attendees emphasized the need for well-designed studies to generate high-quality evidence needed to guide care, identified regulatory and financial barriers, and discussed the role of regulatory agencies in facilitating research and implementation of these assays. Findings and consensus statements are presented. The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence‐based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was convened on December 7, 2021, to define the utility of novel infectious disease diagnostics in organ transplant recipients. The conference represented a collaborative effort by experts in transplant infectious diseases, diagnostic stewardship, and clinical microbiology from centers across North America to evaluate current uses, unmet needs, and future directions for assays in 5 categories including (1) multiplex molecular assays, (2) rapid antimicrobial resistance detection methods, (3) pathogen‐specific T‐cell reactivity assays, (4) next‐generation sequencing assays, and (5) mass spectrometry‐based assays. Participants reviewed and appraised available literature, determined assay advantages and limitations, developed best practice guidance largely based on expert opinion for clinical use, and identified areas of future investigation in the setting of transplantation. In addition, attendees emphasized the need for well‐designed studies to generate high‐quality evidence needed to guide care, identified regulatory and financial barriers, and discussed the role of regulatory agencies in facilitating research and implementation of these assays. Findings and consensus statements are presented. This meeting report summarizes findings from an AST‐sponsored consensus conference to define best practice uses, unmet needs and future directions for advanced infectious diseases diagnostics in solid organ transplant recipients. The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence-based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was convened on December 7, 2021, to define the utility of novel infectious disease diagnostics in organ transplant recipients. The conference represented a collaborative effort by experts in transplant infectious diseases, diagnostic stewardship, and clinical microbiology from centers across North America to evaluate current uses, unmet needs, and future directions for assays in 5 categories including (1) multiplex molecular assays, (2) rapid antimicrobial resistance detection methods, (3) pathogen-specific T-cell reactivity assays, (4) next-generation sequencing assays, and (5) mass spectrometry-based assays. Participants reviewed and appraised available literature, determined assay advantages and limitations, developed best practice guidance largely based on expert opinion for clinical use, and identified areas of future investigation in the setting of transplantation. In addition, attendees emphasized the need for well-designed studies to generate high-quality evidence needed to guide care, identified regulatory and financial barriers, and discussed the role of regulatory agencies in facilitating research and implementation of these assays. Findings and consensus statements are presented.The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence-based recommendations to inform their optimal use in the care of transplant recipients are lacking. A consensus conference sponsored by the American Society of Transplantation (AST) was convened on December 7, 2021, to define the utility of novel infectious disease diagnostics in organ transplant recipients. The conference represented a collaborative effort by experts in transplant infectious diseases, diagnostic stewardship, and clinical microbiology from centers across North America to evaluate current uses, unmet needs, and future directions for assays in 5 categories including (1) multiplex molecular assays, (2) rapid antimicrobial resistance detection methods, (3) pathogen-specific T-cell reactivity assays, (4) next-generation sequencing assays, and (5) mass spectrometry-based assays. Participants reviewed and appraised available literature, determined assay advantages and limitations, developed best practice guidance largely based on expert opinion for clinical use, and identified areas of future investigation in the setting of transplantation. In addition, attendees emphasized the need for well-designed studies to generate high-quality evidence needed to guide care, identified regulatory and financial barriers, and discussed the role of regulatory agencies in facilitating research and implementation of these assays. Findings and consensus statements are presented. |
Author | Razonable, Raymund Letourneau, Alyssa R. Miller, Steve Turbett, Sarah Kumar, Deepali Schwartz, Ilan Azar, Marwan M. Maron, Gabriela Bard, Jennifer Dien Gaston, David Koo, Sophia Simner, Patricia Danziger‐Isakov, Lara Prinzi, Andrea Gitman, Melissa Odom John, Audrey R. Hanisch, Benjamin Bhaskaran, Archana Basu, Sankha S. Silveira, Fernanda Banach, David B. Luong, Me‐Linh John, Teny M. Hanson, Kimberly Kotton, Camille Gandhi, Ronak |
Author_xml | – sequence: 1 givenname: Marwan M. orcidid: 0000-0001-5498-5042 surname: Azar fullname: Azar, Marwan M. email: marwan.azar@yale.edu organization: Yale University School of Medicine – sequence: 2 givenname: Sarah surname: Turbett fullname: Turbett, Sarah organization: Harvard Medical School – sequence: 3 givenname: David orcidid: 0000-0002-7320-5635 surname: Gaston fullname: Gaston, David organization: John's Hopkins University School of Medicine – sequence: 4 givenname: Melissa orcidid: 0000-0002-6960-0763 surname: Gitman fullname: Gitman, Melissa organization: Icahn School of Medicine at Mount Sinai – sequence: 5 givenname: Raymund orcidid: 0000-0001-5248-0227 surname: Razonable fullname: Razonable, Raymund organization: Mayo Clinic – sequence: 6 givenname: Sophia orcidid: 0000-0002-4973-7439 surname: Koo fullname: Koo, Sophia organization: Harvard Medical School – sequence: 7 givenname: Kimberly surname: Hanson fullname: Hanson, Kimberly organization: University of Utah School of Medicine – sequence: 8 givenname: Camille surname: Kotton fullname: Kotton, Camille organization: Harvard Medical School – sequence: 9 givenname: Fernanda surname: Silveira fullname: Silveira, Fernanda organization: University of Pittsburgh School of Medicine – sequence: 10 givenname: David B. surname: Banach fullname: Banach, David B. organization: University of Connecticut School of Medicine – sequence: 11 givenname: Sankha S. orcidid: 0000-0002-4931-7805 surname: Basu fullname: Basu, Sankha S. organization: Harvard Medical School – sequence: 12 givenname: Archana surname: Bhaskaran fullname: Bhaskaran, Archana organization: University of Minnesota Medical School – sequence: 13 givenname: Lara orcidid: 0000-0002-5691-5221 surname: Danziger‐Isakov fullname: Danziger‐Isakov, Lara organization: Cincinnati Children's Hospital Medical Center and University of Cincinnati – sequence: 14 givenname: Jennifer Dien surname: Bard fullname: Bard, Jennifer Dien organization: University of Southern California – sequence: 15 givenname: Ronak orcidid: 0000-0001-9442-0396 surname: Gandhi fullname: Gandhi, Ronak organization: Harvard Medical School – sequence: 16 givenname: Benjamin orcidid: 0000-0003-3387-9093 surname: Hanisch fullname: Hanisch, Benjamin organization: Children's National Hospital – sequence: 17 givenname: Teny M. surname: John fullname: John, Teny M. organization: The University of Texas MD Anderson Cancer Center – sequence: 18 givenname: Audrey R. orcidid: 0000-0001-8395-8537 surname: Odom John fullname: Odom John, Audrey R. organization: Children's Hospital of Pennsylvania – sequence: 19 givenname: Alyssa R. surname: Letourneau fullname: Letourneau, Alyssa R. organization: Harvard Medical School – sequence: 20 givenname: Me‐Linh orcidid: 0000-0003-3756-892X surname: Luong fullname: Luong, Me‐Linh organization: Centre de Recherche du Centre Hospitalier de l'Université de Montréal – sequence: 21 givenname: Gabriela orcidid: 0000-0001-5247-5399 surname: Maron fullname: Maron, Gabriela organization: St. Jude Children's Research Hospital – sequence: 22 givenname: Steve orcidid: 0000-0002-9188-3392 surname: Miller fullname: Miller, Steve organization: University of California San Francisco School of Medicine – sequence: 23 givenname: Andrea orcidid: 0000-0003-2949-5484 surname: Prinzi fullname: Prinzi, Andrea organization: Infectious Disease Medical Science Liaison – sequence: 24 givenname: Ilan orcidid: 0000-0002-7522-0281 surname: Schwartz fullname: Schwartz, Ilan organization: University of Alberta – sequence: 25 givenname: Patricia surname: Simner fullname: Simner, Patricia organization: John's Hopkins University School of Medicine – sequence: 26 givenname: Deepali orcidid: 0000-0003-1961-0477 surname: Kumar fullname: Kumar, Deepali organization: University of Toronto |
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Snippet | The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence‐based recommendations to inform their optimal... The last decade has seen an explosion of advanced assays for the diagnosis of infectious diseases, yet evidence-based recommendations to inform their optimal... |
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StartPage | 3150 |
SubjectTerms | Antimicrobial resistance Clinical microbiology clinical research/practice Consensus diagnostic techniques and imaging Humans infection and infectious agents infectious disease Infectious diseases Mass spectroscopy Medical diagnosis North America Organ Transplantation - adverse effects organ transplantation in general translational research/science Transplant Recipients Transplantation Transplants Transplants & implants |
Title | A consensus conference to define the utility of advanced infectious disease diagnostics in solid organ transplant recipients |
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