Early short course of neuromuscular blocking agents in patients with COVID-19 ARDS: a propensity score analysis

被引:8
|
作者
Li Bassi, Gianluigi [1 ,2 ,3 ,4 ,5 ,6 ]
Gibbons, Kristen [7 ]
Suen, Jacky Y. [1 ,2 ]
Dalton, Heidi J. [8 ]
White, Nicole [4 ]
Corley, Amanda [1 ,2 ]
Shrapnel, Sally [2 ,9 ]
Hinton, Samuel [2 ]
Forsyth, Simon [2 ]
Laffey, John G. [10 ,11 ]
Fan, Eddy [12 ]
Fanning, Jonathon P. [1 ,2 ,5 ,6 ]
Panigada, Mauro [13 ]
Bartlett, Robert [14 ]
Brodie, Daniel [15 ,16 ]
Burrell, Aidan [17 ]
Chiumello, Davide [18 ,19 ]
Elhazmi, Alyaa [20 ]
Esperatti, Mariano [21 ]
Grasselli, Giacomo [19 ]
Hodgson, Carol [17 ]
Ichiba, Shingo [22 ]
Luna, Carlos [23 ]
Marwali, Eva [24 ]
Merson, Laura [25 ]
Murthy, Srinivas [26 ,27 ]
Nichol, Alistair [17 ,28 ,29 ]
Ogino, Mark [30 ]
Pelosi, Paolo [31 ,32 ]
Torres, Antoni [3 ,33 ]
Ng, Pauline Yeung [34 ]
Fraser, John F. [1 ,3 ,4 ,5 ,6 ]
机构
[1] Prince Charles Hosp, Crit Care Res Grp, 627 Rode Rd, Brisbane, Qld 4032, Australia
[2] Univ Queensland, Brisbane, Qld, Australia
[3] Inst Invest Biomed August Pi i Sunyer, Barcelona, Spain
[4] Queensland Univ Technol, Brisbane, Qld, Australia
[5] UnitingCare Hosp, Brisbane, Qld, Australia
[6] Wesley Med Res, Brisbane, Qld, Australia
[7] Univ Queensland, Child Hlth Res Ctr, Brisbane, Qld, Australia
[8] Heart & Vasc Inst, INOVA Fairfax Med Ctr, Falls Church, VA USA
[9] Australian Res Council, Ctr Excellence Engn Quantum Syst EQUS CE170100009, Brisbane, Qld, Australia
[10] Natl Univ Ireland, Sch Med, Anaesthesia & Intens Care Med, Galway, Ireland
[11] Galway Univ Hosp, Galway, Ireland
[12] Univ Toronto, Interdept Div Crit Care Med, Toronto, ON, Canada
[13] Policlin Milano, Fdn IRCCS Ca Granda Osped Maggiore, Milan, Italy
[14] Univ Michigan, Med Ctr, Ann Arbor, MI USA
[15] New York Presbyterian Hosp, Columbia Coll Phys & Surg, Dept Med, New York, NY USA
[16] New York Presbyterian Hosp, Ctr Acute Resp Failure, New York, NY USA
[17] Monash Univ, Sch Publ Hlth, Australian & New Zealand Intens Care Res Ctr, Melbourne, Vic, Australia
[18] Osped San Paolo, Milan, Italy
[19] Univ Milan, Milan, Italy
[20] King Faisal Specialist Hosp & Res Ctr, Riyadh, Saudi Arabia
[21] Univ Nacl Mar Del Plata, Escuela Med, Hosp Privado Comunidad, Mar Del Plata, Argentina
[22] Nippon Med Coll Hosp, Tokyo, Japan
[23] UBA, Hosp Clin, Neumonol, Buenos Aires, DF, Argentina
[24] Natl Cardiovasc Ctr Harapan Kita, Jakarta, Indonesia
[25] Univ Oxford, Ctr Trop Med & Global Hlth, ISARIC, Oxford, England
[26] Univ British Columbia, Dept Pediat, Fac Med, Vancouver, BC, Canada
[27] BC Childrens Hosp Res Inst, Vancouver, BC, Canada
[28] St Vincents Univ Hosp, Clin Res Ctr, Univ Coll Dublin, Dublin, Ireland
[29] Alfred Hosp, Dept Intens Care, Melbourne, Vic, Australia
[30] Nemours Alfred I duPont Hosp Children, Wilmington, DE USA
[31] Univ Genoa, Dept Surg Sci & Integrated Diagnost, Genoa, Italy
[32] San Martino Policlin Hosp, Anesthesia & Crit Care, IRCCS Oncol & Neurosci, Genoa, Italy
[33] Hosp Clin Barcelona, Barcelona, Spain
[34] Univ Hong Kong, Dept Med, Pok Fu Lam, Hong Kong, Peoples R China
基金
比尔及梅琳达.盖茨基金会; 英国医学研究理事会; 欧盟地平线“2020”;
关键词
NEW-YORK-CITY; EPIDEMIOLOGY; COHORT; GUIDELINES; BLOCKERS; OUTCOMES; CARE;
D O I
10.1186/s13054-022-03983-5
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: The role of neuromuscular blocking agents (NMBAs) in coronavirus disease 2019 (COVID-19) acute respiratory distress syndrome (ARDS) is not fully elucidated. Therefore, we aimed to investigate in COVID-19 patients with moderate-to-severe ARDS the impact of early use of NMBAs on 90-day mortality, through propensity score (PS) matching analysis. Methods: We analyzed a convenience sample of patients with COVID-19 and moderate-to-severe ARDS, admitted to 244 intensive care units within the COVID-19 Critical Care Consortium, from February 1, 2020, through October 31, 2021. Patients undergoing at least 2 days and up to 3 consecutive days of NMBAs (NMBA treatment), within 48 h from commencement of IMV were compared with subjects who did not receive NMBAs or only upon commencement of IMV (control). The primary objective in the PS-matched cohort was comparison between groups in 90-day in-hospital mortality, assessed through Cox proportional hazard modeling. Secondary objectives were comparisons in the numbers of ventilator-free days (VFD) between day 1 and day 28 and between day 1 and 90 through competing risk regression. Results: Data from 1953 patients were included. After propensity score matching, 210 cases from each group were well matched. In the PS-matched cohort, mean (± SD) age was 60.3 ± 13.2 years and 296 (70.5%) were male and the most common comorbidities were hypertension (56.9%), obesity (41.1%), and diabetes (30.0%). The unadjusted hazard ratio (HR) for death at 90 days in the NMBA treatment vs control group was 1.12 (95% CI 0.79, 1.59, p = 0.534). After adjustment for smoking habit and critical therapeutic covariates, the HR was 1.07 (95% CI 0.72, 1.61, p = 0.729). At 28 days, VFD were 16 (IQR 0–25) and 25 (IQR 7–26) in the NMBA treatment and control groups, respectively (sub-hazard ratio 0.82, 95% CI 0.67, 1.00, p = 0.055). At 90 days, VFD were 77 (IQR 0–87) and 87 (IQR 0–88) (sub-hazard ratio 0.86 (95% CI 0.69, 1.07; p = 0.177). Conclusions: In patients with COVID-19 and moderate-to-severe ARDS, short course of NMBA treatment, applied early, did not significantly improve 90-day mortality and VFD. In the absence of definitive data from clinical trials, NMBAs should be indicated cautiously in this setting. © 2022, The Author(s).
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页数:17
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