Analgesia, sedation, and neuromuscular blocking agents: A standardized protocol of analgosedation in COVID-19.

Publication date: May 30, 2025

Primary: To evaluate the level of sedation, use, daily doses, and duration of analgosedative drugs in COVID-19 patients on mechanical ventilation (MV) using a standardized protocol, comparing survivors and non-survivors. Secondary: To identify independent predictors of hospital mortality. Retrospective cohort study. Medical-surgical ICU. Adults with SARS-CoV-2 infection requiring invasive MV and continuous infusion of analgosedation and/or neuromuscular blocking agents (NMBAs) for at least 48 h. None. Level of sedation, use, daily doses, and duration of analgosedative drugs; hospital mortality and associated factors. Among 198 patients (nurse-to-patient ratio 1:2. 4; 65% staff turnover), median global RASS was -4. 5. Kaplan-Meier analysis showed lower survival with deeper sedation. Fentanyl (99%) and midazolam (97%) were the most used, followed by NMBAs (81%), propofol and dexmedetomidine (48%). Non-benzodiazepine sedatives were precribed more in survivors (88%) than non-survivors (53%) (p 

Concepts Keywords
48h Agentes bloqueantes neuromusculares
Daily Analgesic drugs
Dexmedetomidine ARDS
Invasive COVID-19 pandemic
Nurse Critical care
Cuidados críticos
Guías
Guidelines
Neuromuscular blocking agents
Pandemia de COVID-19
Protocolos
Protocols
SDRA
Sedantes
Sedatives

Semantics

Type Source Name
disease MESH COVID-19
pathway REACTOME SARS-CoV-2 Infection
drug DRUGBANK Etoperidone
drug DRUGBANK Fentanyl
drug DRUGBANK Midazolam
drug DRUGBANK Propofol
drug DRUGBANK Dexmedetomidine
drug DRUGBANK Benzodiazepine

Original Article

(Visited 1 times, 1 visits today)