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Published in: Intensive Care Medicine 11/2018

01-11-2018 | Editorial

Do trials that report a neutral or negative treatment effect improve the care of critically ill patients? No

Authors: Jean-Louis Vincent, John J. Marini, Antonio Pesenti

Published in: Intensive Care Medicine | Issue 11/2018

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Excerpt

Randomized controlled trials (RCTs) with appropriate question selection, careful subject enrollment, adequate powering and assiduous execution of a well-designed protocol can provide convincing data that improve the strength of the evidence base guiding practice. However, many RCTs conducted in intensive care medicine have resulted in no significant differences in primary outcomes between the tested groups. This is particularly true for trials targeting mortality. Because patients in RCTs in critical care medicine—and patients in intensive care units (ICUs)—have wide variability in their risk of death, these patients will also have wide variability in the absolute benefit that they can derive from a given therapy. If the adverse effects of the therapy are not perfectly aligned with the treatment benefits, this will result in heterogeneity of the treatment effect, wherein different patients experience quite different and often unexpected results from therapy. As a consequence, in a negative RCT, there are patients who experience benefit and others who experience harm, all merged into the global result. Therefore, the results do not provide a definitive answer to the study question or enable reliable guidance or recommendations to be developed. Indeed, these negative clinical trials seldom convey useful information beyond that stemming from an examination of their subgroups, their possibly inopportune assumptions and their deficiencies of design. …
Literature
1.
go back to reference Goligher EC, Kavanagh BP, Rubenfeld GD, Adhikari NK, Pinto R, Fan E, Brochard LJ, Granton JT, Mercat A et al (2014) Oxygenation response to positive end-expiratory pressure predicts mortality in acute respiratory distress syndrome. A secondary analysis of the LOVS and ExPress trials. Am J Respir Crit Care Med 190:70–76CrossRef Goligher EC, Kavanagh BP, Rubenfeld GD, Adhikari NK, Pinto R, Fan E, Brochard LJ, Granton JT, Mercat A et al (2014) Oxygenation response to positive end-expiratory pressure predicts mortality in acute respiratory distress syndrome. A secondary analysis of the LOVS and ExPress trials. Am J Respir Crit Care Med 190:70–76CrossRef
2.
go back to reference Iwashyna TJ, Burke JF, Sussman JB, Prescott HC, Hayward RA, Angus DC (2015) Implications of heterogeneity of treatment effect for reporting and analysis of randomized trials in critical care. Am J Respir Crit Care Med 192:1045–1051CrossRef Iwashyna TJ, Burke JF, Sussman JB, Prescott HC, Hayward RA, Angus DC (2015) Implications of heterogeneity of treatment effect for reporting and analysis of randomized trials in critical care. Am J Respir Crit Care Med 192:1045–1051CrossRef
3.
go back to reference Venkatesh B, Finfer S, Cohen J, Rajbhandari D, Arabi Y, Bellomo R, Billot L, Correa M, Glass P et al (2018) Adjunctive glucocorticoid therapy in patients with septic shock. N Engl J Med 378:797–808CrossRef Venkatesh B, Finfer S, Cohen J, Rajbhandari D, Arabi Y, Bellomo R, Billot L, Correa M, Glass P et al (2018) Adjunctive glucocorticoid therapy in patients with septic shock. N Engl J Med 378:797–808CrossRef
4.
go back to reference Annane D, Renault A, Brun-Buisson C, Megarbane B, Quenot JP, Siami S, Cariou A, Forceville X, Schwebel C et al (2018) Hydrocortisone plus fludrocortisone for adults with septic shock. N Engl J Med 378:809–818CrossRef Annane D, Renault A, Brun-Buisson C, Megarbane B, Quenot JP, Siami S, Cariou A, Forceville X, Schwebel C et al (2018) Hydrocortisone plus fludrocortisone for adults with septic shock. N Engl J Med 378:809–818CrossRef
5.
go back to reference Asfar P, Meziani F, Hamel JF, Grelon F, Megarbane B, Anguel N, Mira JP, Dequin PF, Gergaud S et al (2014) High versus low blood-pressure target in patients with septic shock. N Engl J Med 370:1583–1593CrossRef Asfar P, Meziani F, Hamel JF, Grelon F, Megarbane B, Anguel N, Mira JP, Dequin PF, Gergaud S et al (2014) High versus low blood-pressure target in patients with septic shock. N Engl J Med 370:1583–1593CrossRef
6.
go back to reference Vincent JL (2012) Indications for blood transfusions: too complex to base on a single number? Ann Intern Med 157:71–72CrossRef Vincent JL (2012) Indications for blood transfusions: too complex to base on a single number? Ann Intern Med 157:71–72CrossRef
7.
go back to reference De Backer D, Vincent JL (2016) Early goal-directed therapy: do we have a definitive answer? Intensive Care Med 42:1048–1050CrossRef De Backer D, Vincent JL (2016) Early goal-directed therapy: do we have a definitive answer? Intensive Care Med 42:1048–1050CrossRef
8.
go back to reference Vincent JL, Brochard LJ (2017) Do we need randomized clinical trials in extracorporeal respiratory support? We are not sure. Intensive Care Med 43:1869–1871CrossRef Vincent JL, Brochard LJ (2017) Do we need randomized clinical trials in extracorporeal respiratory support? We are not sure. Intensive Care Med 43:1869–1871CrossRef
9.
go back to reference Gattinoni L, Marini JJ, Quintel M (2018) Time to rethink the approach to treating acute respiratory distress syndrome. JAMA 319:664–666CrossRef Gattinoni L, Marini JJ, Quintel M (2018) Time to rethink the approach to treating acute respiratory distress syndrome. JAMA 319:664–666CrossRef
Metadata
Title
Do trials that report a neutral or negative treatment effect improve the care of critically ill patients? No
Authors
Jean-Louis Vincent
John J. Marini
Antonio Pesenti
Publication date
01-11-2018
Publisher
Springer Berlin Heidelberg
Published in
Intensive Care Medicine / Issue 11/2018
Print ISSN: 0342-4642
Electronic ISSN: 1432-1238
DOI
https://doi.org/10.1007/s00134-018-5220-y

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