TY - JOUR
T1 - Antimicrobial de-escalation in critically ill patients
T2 - a position statement from a task force of the European Society of Intensive Care Medicine (ESICM) and European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Critically Ill Patients Study Group (ESGCIP)
AU - Tabah, Alexis
AU - Bassetti, Matteo
AU - Kollef, Marin H.
AU - Zahar, Jean Ralph
AU - Paiva, José Artur
AU - Timsit, Jean Francois
AU - Roberts, Jason A.
AU - Schouten, Jeroen
AU - Giamarellou, Helen
AU - Rello, Jordi
AU - De Waele, Jan
AU - Shorr, Andrew F.
AU - Leone, Marc
AU - Poulakou, Garyphallia
AU - Depuydt, Pieter
AU - Garnacho-Montero, Jose
N1 - Funding Information:
Dr. Tabah has nothing to disclose. Dr. Bassetti reports grants and personal fees from PFIZER, grants and personal fees from MSD, grants and personal fees from MENARINI, grants and personal fees from ANGELINI, personal fees from ASTELLAS, personal fees from NABRIVA, grants and personal fees from PARATEK, personal fees from GILEAD, personal fees from BASILEA, personal fees from CIDARA, personal fees from MOLTENI, outside the submitted work. Dr. Kollef’s efforts are supported by the Barnes-Jewish Hospital Foundation. Dr. Zahar reports personal fees from MSD, personal fees from Correvio, personal fees from Pfizer, outside the submitted work. Dr. Paiva has nothing to disclose. Dr. Timsit reports grants and personal fees from Pfizer, grants and personal fees from Merck, personal fees from Astellas, grants and personal fees from Biomerieux, personal fees from 3 M, during the conduct of the study; personal fees from Nabriva, personal fees from Bayer pharma, outside the submitted work. Dr. Roberts reports personal fees and non-financial support from Biomerieux, grants and personal fees from MSD, personal fees from Astellas, personal fees from Infectopharm, grants from The Medicines Company, outside the submitted work. Dr. Schouten has nothing to disclose. Dr. Giamarellou has received research grants from Pfizer, MSD, Angelini. Dr. Rello reports personal fees from Navriba, grants from BAYER, personal fees from Pfizer, personal fees from Anchoagen, outside the submitted work. Dr. De Waele reports grants from Research Foundation Flanders, during the conduct of the study; other from Bayer, other from Pfizer, other from MSD, other from Grifols, other from Accelerate, outside the submitted work. Dr Shorr has served as a speaker for, received research support from, or been a consultant to: Astellas, Merck, Nabriva, Paratek, Shinogi, and Tetraphase. Dr. Leone reports personal fees from MSD, personal fees from Pfizer, during the conduct of the study; grants, personal fees and non-financial support from AMOMED, personal fees from AGUETTANT, personal fees from ASPEN, personal fees from OCTAPHARMA, personal fees from ORION, outside the submitted work. Dr. Poulakou reports personal fees from Angelini, personal fees from MSD, grants and personal fees from Pfizer, grants from Roche, outside the submitted work. Dr. Depuydt has nothing to disclose. Dr. Garnacho-Montero has nothing to disclose.
Publisher Copyright:
© 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Background: Antimicrobial de-escalation (ADE) is a strategy of antimicrobial stewardship, aiming at preventing the emergence of antimicrobial resistance (AMR) by decreasing the exposure to broad-spectrum antimicrobials. There is no high-quality research on ADE and its effects on AMR. Its definition varies and there is little evidence-based guidance for clinicians to use ADE in the intensive care unit (ICU). Methods: A task force of 16 international experts was formed in November 2016 to provide with guidelines for clinical practice to develop questions targeted at defining ADE, its effects on the ICU population and to provide clinical guidance. Groups of 2 experts were assigned 1–2 questions each within their field of expertise to provide draft statements and rationale. A Delphi method, with 3 rounds and an agreement threshold of 70% was required to reach consensus. Results: We present a comprehensive document with 13 statements, reviewing the evidence on the definition of ADE, its effects in the ICU population and providing guidance for clinicians in subsets of clinical scenarios where ADE may be considered. Conclusion: ADE remains a topic of controversy due to the complexity of clinical scenarios where it may be applied and the absence of evidence to the effects it may have on antimicrobial resistance.
AB - Background: Antimicrobial de-escalation (ADE) is a strategy of antimicrobial stewardship, aiming at preventing the emergence of antimicrobial resistance (AMR) by decreasing the exposure to broad-spectrum antimicrobials. There is no high-quality research on ADE and its effects on AMR. Its definition varies and there is little evidence-based guidance for clinicians to use ADE in the intensive care unit (ICU). Methods: A task force of 16 international experts was formed in November 2016 to provide with guidelines for clinical practice to develop questions targeted at defining ADE, its effects on the ICU population and to provide clinical guidance. Groups of 2 experts were assigned 1–2 questions each within their field of expertise to provide draft statements and rationale. A Delphi method, with 3 rounds and an agreement threshold of 70% was required to reach consensus. Results: We present a comprehensive document with 13 statements, reviewing the evidence on the definition of ADE, its effects in the ICU population and providing guidance for clinicians in subsets of clinical scenarios where ADE may be considered. Conclusion: ADE remains a topic of controversy due to the complexity of clinical scenarios where it may be applied and the absence of evidence to the effects it may have on antimicrobial resistance.
KW - Antimicrobial de-escalation
KW - Antimicrobial resistance
KW - De-escalation
KW - Stewardship
UR - http://www.scopus.com/inward/record.url?scp=85075663010&partnerID=8YFLogxK
U2 - 10.1007/s00134-019-05866-w
DO - 10.1007/s00134-019-05866-w
M3 - Article
C2 - 31781835
AN - SCOPUS:85075663010
SN - 0342-4642
VL - 46
SP - 245
EP - 265
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 2
ER -