Literature DB >> 28333757

The Septic Shock 3.0 Definition and Trials: A Vasopressin and Septic Shock Trial Experience.

James A Russell1, Terry Lee, Joel Singer, John H Boyd, Keith R Walley.   

Abstract

OBJECTIVES: The Septic Shock 3.0 definition could alter treatment comparisons in randomized controlled trials in septic shock. Our first hypothesis was that the vasopressin versus norepinephrine comparison and 28-day mortality of patients with Septic Shock 3.0 definition (lactate > 2 mmol/L) differ from vasopressin versus norepinephrine and mortality in Vasopressin and Septic Shock Trial. Our second hypothesis was that there are differences in plasma cytokine levels in Vasopressin and Septic Shock Trial for lactate less than or equal to 2 versus greater than 2 mmol/L.
DESIGN: Retrospective analysis of randomized controlled trial.
SETTING: Multicenter ICUs.
METHODS: We compared vasopressin-to-norepinephrine group 28- and 90-day mortality in Vasopressin and Septic Shock Trial in lactate subgroups. We measured 39 cytokines to compare patients with lactate less than or equal to 2 versus greater than 2 mmol/L. PATIENTS: Patients with septic shock with lactate greater than 2 mmol/L or less than or equal to 2 mmol/L, randomized to vasopressin or norepinephrine.
INTERVENTIONS: Concealed vasopressin (0.03 U/min.) or norepinephrine infusions.
MEASUREMENTS AND MAIN RESULTS: The Septic Shock 3.0 definition would have decreased sample size by about half. The 28- and 90-day mortality rates were 10-12 % higher than the original Vasopressin and Septic Shock Trial mortality. There was a significantly (p = 0.028) lower mortality with vasopressin versus norepinephrine in lactate less than or equal to 2 mmol/L but no difference between treatment groups in lactate greater than 2 mmol/L. Nearly all cytokine levels were significantly higher in patients with lactate greater than 2 versus less than or equal to 2 mmol/L.
CONCLUSIONS: The Septic Shock 3.0 definition decreased sample size by half and increased 28-day mortality rates by about 10%. Vasopressin lowered mortality versus norepinephrine if lactate was less than or equal to 2 mmol/L. Patients had higher plasma cytokines in lactate greater than 2 versus less than or equal to 2 mmol/L, a brisker cytokine response to infection. The Septic Shock 3.0 definition and our findings have important implications for trial design in septic shock.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28333757     DOI: 10.1097/CCM.0000000000002323

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  17 in total

Review 1.  The intensive care medicine research agenda on septic shock.

Authors:  Anders Perner; Anthony C Gordon; Derek C Angus; Francois Lamontagne; Flavia Machado; James A Russell; Jean-Francois Timsit; John C Marshall; John Myburgh; Manu Shankar-Hari; Mervyn Singer
Journal:  Intensive Care Med       Date:  2017-05-12       Impact factor: 17.440

2.  Implementation of the Sepsis-3 definition in German university intensive care units : A survey.

Authors:  U Keppler; T Schmoch; B H Siegler; M A Weigand; F Uhle
Journal:  Anaesthesist       Date:  2018-06-26       Impact factor: 1.041

Review 3.  Vasopressor therapy in critically ill patients with shock.

Authors:  James A Russell
Journal:  Intensive Care Med       Date:  2019-10-23       Impact factor: 17.440

Review 4.  Update of Sepsis in the Intensive Care Unit.

Authors:  Kelly Roveran Genga; James A Russell
Journal:  J Innate Immun       Date:  2017-07-12       Impact factor: 7.349

5.  Vasopressin in septic shock: an individual patient data meta-analysis of randomised controlled trials.

Authors:  Myura Nagendran; James A Russell; Keith R Walley; Stephen J Brett; Gavin D Perkins; Ludhmila Hajjar; Alexina J Mason; Deborah Ashby; Anthony C Gordon
Journal:  Intensive Care Med       Date:  2019-05-06       Impact factor: 17.440

6.  Rapidly Improving ARDS in Therapeutic Randomized Controlled Trials.

Authors:  Edward J Schenck; Clara Oromendia; Lisa K Torres; David A Berlin; Augustine M K Choi; Ilias I Siempos
Journal:  Chest       Date:  2018-10-22       Impact factor: 9.410

7.  Identification of Acute Kidney Injury Subphenotypes with Differing Molecular Signatures and Responses to Vasopressin Therapy.

Authors:  Pavan K Bhatraju; Leila R Zelnick; Jerald Herting; Ronit Katz; Carmen Mikacenic; Susanna Kosamo; Eric D Morrell; Cassianne Robinson-Cohen; Carolyn S Calfee; Jason D Christie; Kathleen D Liu; Michael A Matthay; William O Hahn; Victoria Dmyterko; Natalie S J Slivinski; Jim A Russell; Keith R Walley; David C Christiani; W Conrad Liles; Jonathan Himmelfarb; Mark M Wurfel
Journal:  Am J Respir Crit Care Med       Date:  2019-04-01       Impact factor: 21.405

8.  Predictors of response to fixed-dose vasopressin in adult patients with septic shock.

Authors:  Gretchen L Sacha; Simon W Lam; Abhijit Duggal; Heather Torbic; Stephanie N Bass; Sarah C Welch; Robert S Butler; Seth R Bauer
Journal:  Ann Intensive Care       Date:  2018-03-06       Impact factor: 6.925

9.  Hyperoxia toxicity in septic shock patients according to the Sepsis-3 criteria: a post hoc analysis of the HYPER2S trial.

Authors:  Julien Demiselle; Martin Wepler; Clair Hartmann; Peter Radermacher; Frédérique Schortgen; Ferhat Meziani; Mervyn Singer; Valérie Seegers; Pierre Asfar
Journal:  Ann Intensive Care       Date:  2018-09-17       Impact factor: 6.925

Review 10.  Hemodynamic support in the early phase of septic shock: a review of challenges and unanswered questions.

Authors:  Olivier Lesur; Eugénie Delile; Pierre Asfar; Peter Radermacher
Journal:  Ann Intensive Care       Date:  2018-10-29       Impact factor: 6.925

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.