TY - JOUR
T1 - Continuous neuromuscular blockade following successful resuscitation from cardiac arrest
T2 - A randomized trial
AU - Moskowitz, Ari
AU - Andersen, Lars W.
AU - Rittenberger, Jon C.
AU - Swor, Robert
AU - Seethala, Raghu R.
AU - Kurz, Michael C.
AU - Berg, Katherine M.
AU - Chase, Maureen
AU - Cocchi, Michael N.
AU - Grossestreuer, Anne V.
AU - Liu, Xiaowen
AU - Holmberg, Mathias J.
AU - Callaway, Clifton W.
AU - Donnino, Michael W.
N1 - Funding Information:
The primary study was funded by a Grant-in-Aid from the American Heart Association (14GRNT2001002), and additional biomarker substudies were supported by the National Institutes of Health (NIH) (K24HL127101). Dr Moskowitz and Dr Berg are supported by grants from the NIH (K23GM128005 and K23 HL128814, respectively). Dr Grossestreuer receives support from Harvard Catalyst|The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, NIH Award UL 1TR002541) and financial contributions from Harvard University and its affiliated academic healthcare centers.
Publisher Copyright:
© 2020 The Authors.
PY - 2020
Y1 - 2020
N2 - BACKGROUND: Neuromuscular blockade (NMB) agents are often administered to control shivering during targeted temperature management following cardiac arrest. In this study, we hypothesized that early, continuous NMB would result in a greater reduction in serum lactate levels among comatose patients after cardiac arrest. METHODS AND RESULTS: Randomized trial of continuous NMB for 24 hours versus usual care following cardiac arrest conducted at 5 urban centers in the United States. Adult patients who achieved return of spontaneous circulation, remained unresponsive, and underwent targeted temperature management after cardiac arrest were included. The primary outcome was change in lactate over 24 hours. A total of 83 patients were randomized, and 80 were analyzed (37 and 43 in the NMB and usual care arms, respectively). There was no significant interaction between time and treatment group with respect to change in lactate over 24 hours (median lactate change from 4.2 to 2.0 mmol/L [−2.2 mmol/L] in the NMB arm versus 4.0 to 1.7 mmol/L [−2.3 mmol/L] in the usual care arm; geometric mean difference, 1.3 [95% CI, 1.0–1.8]; P=0.07 for the interaction term). There was no difference in hospital survival (38% [NMB] versus 33% [usual care]; P=0.63) or survival with good functional outcome (30% [NMB] versus 21% [usual care]; P=0.35). There were no adverse events in either arm attributed to study interventions. CONCLUSIONS: Continuous NMB compared with usual care did not reduce lactate over the first 24 hours after enrollment compared with usual care. There was no difference in overall hospital survival, hospital survival with good neurologic outcome, or adverse events. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02260258.
AB - BACKGROUND: Neuromuscular blockade (NMB) agents are often administered to control shivering during targeted temperature management following cardiac arrest. In this study, we hypothesized that early, continuous NMB would result in a greater reduction in serum lactate levels among comatose patients after cardiac arrest. METHODS AND RESULTS: Randomized trial of continuous NMB for 24 hours versus usual care following cardiac arrest conducted at 5 urban centers in the United States. Adult patients who achieved return of spontaneous circulation, remained unresponsive, and underwent targeted temperature management after cardiac arrest were included. The primary outcome was change in lactate over 24 hours. A total of 83 patients were randomized, and 80 were analyzed (37 and 43 in the NMB and usual care arms, respectively). There was no significant interaction between time and treatment group with respect to change in lactate over 24 hours (median lactate change from 4.2 to 2.0 mmol/L [−2.2 mmol/L] in the NMB arm versus 4.0 to 1.7 mmol/L [−2.3 mmol/L] in the usual care arm; geometric mean difference, 1.3 [95% CI, 1.0–1.8]; P=0.07 for the interaction term). There was no difference in hospital survival (38% [NMB] versus 33% [usual care]; P=0.63) or survival with good functional outcome (30% [NMB] versus 21% [usual care]; P=0.35). There were no adverse events in either arm attributed to study interventions. CONCLUSIONS: Continuous NMB compared with usual care did not reduce lactate over the first 24 hours after enrollment compared with usual care. There was no difference in overall hospital survival, hospital survival with good neurologic outcome, or adverse events. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02260258.
KW - Biomarkers
KW - Cardiopulmonary resuscitation
KW - Clinical trial
KW - Heart arrest
KW - Hypothermia
KW - Neuromuscular blockade
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U2 - 10.1161/JAHA.120.017171
DO - 10.1161/JAHA.120.017171
M3 - Article
C2 - 32851921
AN - SCOPUS:85090178603
SN - 2047-9980
VL - 9
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
IS - 17
M1 - e017171
ER -