TY - JOUR
T1 - Very early administration of progesterone for acute traumatic brain injury
AU - Wright, David W.
AU - Yeatts, Sharon D.
AU - Silbergleit, Robert
AU - Palesch, Yuko Y.
AU - Hertzberg, Vicki S.
AU - Frankel, Michael
AU - Goldstein, Felicia C.
AU - Caveney, Angela F.
AU - Howlett-Smith, Harriet
AU - Bengelink, Erin M.
AU - Manley, Geoffrey T.
AU - Merck, Lisa H.
AU - Janis, L. Scott
AU - Barsan, William G.
AU - Frankel, Michael
AU - Merck, Lisa H.
AU - Espinoza, Tamara R.
AU - Salomone, Jeffrey P.
AU - Dhall, Sanjay S.
AU - Hudgins, Patricia A.
AU - Allen, Jason W.
AU - Goldstein, Felicia
AU - Hertzberg, Vicki
AU - Rogers, Susan D.
AU - Marie Calcaterra, Anna
AU - Howlett-Smith, Harriet
AU - Lane, Bethany
AU - Lunney, Michael P.
AU - Renee Cook, N.
AU - Hall, Alex
AU - Hall, Andy
AU - McDougal, Andrea
AU - Subramanian, Anuradha
AU - Pradilla, Gustavo
AU - Stein, Donald G.
AU - Silbergleit, Robert
AU - Barsan, William G.
AU - Pancioli, Arthur
AU - Lowenstein, Daniel
AU - Meurer, William J.
AU - Morgenstern, Lewis B.
AU - Stevenson, Valerie
AU - Bengelink, Erin
AU - Harney, Deneil
AU - De Yampert, Andrace
AU - Mawocha, Samkeliso
AU - Pinkerton, Joy
AU - Caveney, Angela
AU - Yeatts, Sharon
AU - Creed Pettigrew, L.
N1 - Publisher Copyright:
Copyright © 2014 Massachusetts Medical Society. All rights reserved.
PY - 2014/12/25
Y1 - 2014/12/25
N2 - BACKGROUND Traumatic brain injury (TBI) is a major cause of death and disability worldwide. Progesterone has been shown to improve neurologic outcome in multiple experimental models and two early-phase trials involving patients with TBI. METHODS We conducted a double-blind, multicenter clinical trial in which patients with severe, moderate-to-severe, or moderate acute TBI (Glasgow Coma Scale score of 4 to 12, on a scale from 3 to 15, with lower scores indicating a lower level of consciousness) were randomly assigned to intravenous progesterone or placebo, with the study treatment initiated within 4 hours after injury and administered for a total of 96 hours. Efficacy was defined as an increase of 10 percentage points in the proportion of patients with a favorable outcome, as determined with the use of the stratified dichotomy of the Extended Glasgow Outcome Scale score at 6 months after injury. Secondary outcomes included mortality and the Disability Rating Scale score. RESULTS A total of 882 of the planned sample of 1140 patients underwent randomization before the trial was stopped for futility with respect to the primary outcome. The study groups were similar with regard to baseline characteristics; the median age of the patients was 35 years, 73.7% were men, 15.2% were black, and the mean Injury Severity Score was 24.4 (on a scale from 0 to 75, with higher scores indicating greater severity). The most frequent mechanism of injury was a motor vehicle accident. There was no significant difference between the progesterone group and the placebo group in the proportion of patients with a favorable outcome (relative benefit of progesterone, 0.95; 95% confidence interval [CI], 0.85 to 1.06; P = 0.35). Phlebitis or thrombophlebitis was more frequent in the progesterone group than in the placebo group (relative risk, 3.03; CI, 1.96 to 4.66). There were no significant differences in the other prespecified safety outcomes. CONCLUSIONS This clinical trial did not show a benefit of progesterone over placebo in the improvement of outcomes in patients with acute TBI.
AB - BACKGROUND Traumatic brain injury (TBI) is a major cause of death and disability worldwide. Progesterone has been shown to improve neurologic outcome in multiple experimental models and two early-phase trials involving patients with TBI. METHODS We conducted a double-blind, multicenter clinical trial in which patients with severe, moderate-to-severe, or moderate acute TBI (Glasgow Coma Scale score of 4 to 12, on a scale from 3 to 15, with lower scores indicating a lower level of consciousness) were randomly assigned to intravenous progesterone or placebo, with the study treatment initiated within 4 hours after injury and administered for a total of 96 hours. Efficacy was defined as an increase of 10 percentage points in the proportion of patients with a favorable outcome, as determined with the use of the stratified dichotomy of the Extended Glasgow Outcome Scale score at 6 months after injury. Secondary outcomes included mortality and the Disability Rating Scale score. RESULTS A total of 882 of the planned sample of 1140 patients underwent randomization before the trial was stopped for futility with respect to the primary outcome. The study groups were similar with regard to baseline characteristics; the median age of the patients was 35 years, 73.7% were men, 15.2% were black, and the mean Injury Severity Score was 24.4 (on a scale from 0 to 75, with higher scores indicating greater severity). The most frequent mechanism of injury was a motor vehicle accident. There was no significant difference between the progesterone group and the placebo group in the proportion of patients with a favorable outcome (relative benefit of progesterone, 0.95; 95% confidence interval [CI], 0.85 to 1.06; P = 0.35). Phlebitis or thrombophlebitis was more frequent in the progesterone group than in the placebo group (relative risk, 3.03; CI, 1.96 to 4.66). There were no significant differences in the other prespecified safety outcomes. CONCLUSIONS This clinical trial did not show a benefit of progesterone over placebo in the improvement of outcomes in patients with acute TBI.
UR - http://www.scopus.com/inward/record.url?scp=84920059259&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84920059259&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa1404304
DO - 10.1056/NEJMoa1404304
M3 - Article
C2 - 25493974
AN - SCOPUS:84920059259
SN - 0028-4793
VL - 371
SP - 2457
EP - 2466
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 26
ER -