TY - JOUR
T1 - Time to antimicrobial therapy in septic shock patients treated with an early goal-directed resuscitation protocol
T2 - A post-hoc analysis of the ARISE trial
AU - ARISE Investigators
AU - The ARISE Working Committee
AU - The ARISE Management and Steering Committee
AU - The ARISE site investigators
AU - Bulle, Esther B.
AU - Peake, Sandra L.
AU - Finnis, Mark
AU - Bellomo, Rinaldo
AU - Delaney, Anthony
AU - Peake, C.
AU - Cameron, P. A.
AU - Higgins, A. M.
AU - Holdgate, A.
AU - Howe, B. D.
AU - Webb, S. A.R.
AU - Williams, P.
AU - Cooper, D. J.
AU - Cross, A.
AU - Gomersall, C.
AU - Graham, C.
AU - Holdgate, A.
AU - Howe, B. D.
AU - Jacobs, I.
AU - Johanson, S.
AU - Jones, P.
AU - Kruger, P.
AU - McArthur, C.
AU - Myburgh, J.
AU - Nichol, A.
AU - Pettilä, V.
AU - Rajbhandari, D.
AU - Williams, A.
AU - Williams, J.
AU - Williams, P.
AU - Bennett, V.
AU - Board, J.
AU - McCracken, P.
AU - McGloughlin, S.
AU - Nanjayya, V.
AU - Teo, A.
AU - Hill, E.
AU - Jones, P.
AU - O'Brien, E.
AU - Sawtell, F.
AU - Schimanski, K.
AU - Wilson, D.
AU - Bolch, S.
AU - Eastwood, G.
AU - Kerr, F.
AU - Peak, L.
AU - Young, H.
AU - Edington, J.
AU - Fletcher, J.
AU - Smith, J.
N1 - Publisher Copyright:
© 2020 Australasian College for Emergency Medicine
PY - 2020/10/9
Y1 - 2020/10/9
N2 - Objective: Intravenous antimicrobial therapy within 1 h of the diagnosis of septic shock is recommended in international sepsis guidelines. We aimed to evaluate the association between antimicrobial timing and mortality in patients presenting to the ED with septic shock. Methods: Post-hoc analysis of 1587 adult participants enrolled in the Australasian Resuscitation in Sepsis Evaluation (ARISE) multicentre trial of early goal-directed therapy for whom the time of initial antimicrobial therapy was recorded. We compared participants who had initiation of antimicrobials within the first hour (early) or later (delayed) of ED presentation. A propensity score model using inverse probability of treatment weighting was constructed to account for confounding baseline covariates. The primary outcome was 90-day mortality. Results: The median (interquartile range) time to initiating antimicrobials was 69 (39–112) min with 712 (44.9%) participants receiving the first dose within the first hour of ED presentation. Compared with delayed therapy, early administration was associated with increased baseline illness severity score and greater intensity of resuscitation pre-randomisation (fluid volumes, vasopressors, invasive ventilation). All-cause 90-day mortality was also higher; 22.6% versus 15.5%; unadjusted odds ratio (OR) 1.58 (95% confidence interval [CI] 1.16–2.15), P = 0.004. After inverse probability of treatment weighting, the mortality difference was non-significant; OR 1.30 (95% CI 0.95–1.76), P = 0.1. Live discharge rates from ICU (OR 0.81, 95% CI 0.72–0.91; P = 0.80) and hospital (OR 0.93, 95% CI 0.82–1.06; P = 0.29) were also not different between groups. Conclusion: In this post-hoc analysis of the ARISE trial, early antimicrobial therapy was associated with increased illness severity, but 90-day adjusted mortality was not reduced.
AB - Objective: Intravenous antimicrobial therapy within 1 h of the diagnosis of septic shock is recommended in international sepsis guidelines. We aimed to evaluate the association between antimicrobial timing and mortality in patients presenting to the ED with septic shock. Methods: Post-hoc analysis of 1587 adult participants enrolled in the Australasian Resuscitation in Sepsis Evaluation (ARISE) multicentre trial of early goal-directed therapy for whom the time of initial antimicrobial therapy was recorded. We compared participants who had initiation of antimicrobials within the first hour (early) or later (delayed) of ED presentation. A propensity score model using inverse probability of treatment weighting was constructed to account for confounding baseline covariates. The primary outcome was 90-day mortality. Results: The median (interquartile range) time to initiating antimicrobials was 69 (39–112) min with 712 (44.9%) participants receiving the first dose within the first hour of ED presentation. Compared with delayed therapy, early administration was associated with increased baseline illness severity score and greater intensity of resuscitation pre-randomisation (fluid volumes, vasopressors, invasive ventilation). All-cause 90-day mortality was also higher; 22.6% versus 15.5%; unadjusted odds ratio (OR) 1.58 (95% confidence interval [CI] 1.16–2.15), P = 0.004. After inverse probability of treatment weighting, the mortality difference was non-significant; OR 1.30 (95% CI 0.95–1.76), P = 0.1. Live discharge rates from ICU (OR 0.81, 95% CI 0.72–0.91; P = 0.80) and hospital (OR 0.93, 95% CI 0.82–1.06; P = 0.29) were also not different between groups. Conclusion: In this post-hoc analysis of the ARISE trial, early antimicrobial therapy was associated with increased illness severity, but 90-day adjusted mortality was not reduced.
KW - mortality
KW - septic shock
KW - timing anti-microbial agent
UR - http://www.scopus.com/inward/record.url?scp=85092373004&partnerID=8YFLogxK
U2 - 10.1111/1742-6723.13634
DO - 10.1111/1742-6723.13634
M3 - Article
C2 - 38019012
AN - SCOPUS:85092373004
SN - 1742-6731
VL - 33
SP - 409
EP - 417
JO - EMA - Emergency Medicine Australasia
JF - EMA - Emergency Medicine Australasia
IS - 3
ER -