TY - JOUR
T1 - Variation in Sedative and Analgesic Use During the COVID-19 Pandemic and Associated Outcomes
AU - Society of Critical Care Medicine Discovery Viral Infection and Respiratory Illness Universal Study COVID-19 Registry Investigator Group
AU - Rucci, Justin M.
AU - Law, Anica C.
AU - Bolesta, Scott
AU - Quinn, Emily K.
AU - Garcia, Michael A.
AU - Gajic, Ognjen
AU - Boman, Karen
AU - Yus, Santiago
AU - Goodspeed, Valerie M.
AU - Kumar, Vishakha
AU - Kashyap, Rahul
AU - Walkey, Allan J.
AU - Mesland, Jean Baptiste
AU - Henin, Pierre
AU - Petre, Hélène
AU - Buelens, Isabelle
AU - Gerard, Anne Catherine
AU - Markotić, Dragana
AU - Bošnjak, Ivana
AU - Garza, Ruben
AU - Chu, Eric
AU - Chan, Victoria
AU - Gavidia, Oscar Y.
AU - Pachon, Felipe
AU - El Kassas, Mohamed
AU - Tawheed, Ahmed
AU - Matsuda, Wataru
AU - Itagaki, Yuki
AU - Kodate, Akira
AU - Suzuki, Reina
AU - Kodate, Akira
AU - Takahashi, Yuki
AU - Moriki, Koyo
AU - Amer, Marwa Ridha
AU - Bawazeer, Mohammed Abdullah
AU - Dahhan, Talal I.
AU - Kseibi, Eiad
AU - Butt, Abid Shahzad
AU - Khurshid, Syed Moazzum
AU - Rabee, Muath
AU - Abujazar, Mohammed
AU - Alghunaim, Razan
AU - Abualkhair, Maal
AU - AlFirm, Abeer Turki
AU - Kseibi, Eiad
AU - Khurshid, Syed Moazzum
AU - Reilkoff, Ronald A.
AU - Heneghan, Julia A.
AU - Goertzen, Lexie
AU - McGonagill, Patrick W.
N1 - Publisher Copyright:
© 2024
PY - 2024/3
Y1 - 2024/3
N2 - Background: Providing analgesia and sedation is an essential component of caring for many mechanically ventilated patients. The selection of analgesic and sedative medications during the COVID-19 pandemic, and the impact of these sedation practices on patient outcomes, remain incompletely characterized. Research Question: What were the hospital patterns of analgesic and sedative use for patients with COVID-19 who received mechanical ventilation (MV), and what differences in clinical patient outcomes were observed across prevailing sedation practices? Study Design and Methods: We conducted an observational cohort study of hospitalized adults who received MV for COVID-19 from February 2020 through April 2021 within the Society of Critical Care Medicine Discovery Viral Infection and Respiratory Illness Universal Study (VIRUS) COVID-19 Registry. To describe common sedation practices, we used hierarchical clustering to group hospitals based on the percentage of patients who received various analgesic and sedative medications. We then used multivariable regression models to evaluate the association between hospital analgesia and sedation cluster and duration of MV (with a placement of death [POD] approach to account for competing risks). Results: We identified 1,313 adults across 35 hospitals admitted with COVID-19 who received MV. Two clusters of analgesia and sedation practices were identified. Cluster 1 hospitals generally administered opioids and propofol with occasional use of additional sedatives (eg, benzodiazepines, alpha-agonists, and ketamine); cluster 2 hospitals predominantly used opioids and benzodiazepines without other sedatives. As compared with patients in cluster 2, patients admitted to cluster 1 hospitals underwent a shorter adjusted median duration of MV with POD (β-estimate, –5.9; 95% CI, –11.2 to –0.6; P =.03). Interpretation: Patients who received MV for COVID-19 in hospitals that prioritized opioids and propofol for analgesia and sedation experienced shorter adjusted median duration of MV with POD as compared with patients who received MV in hospitals that primarily used opioids and benzodiazepines.
AB - Background: Providing analgesia and sedation is an essential component of caring for many mechanically ventilated patients. The selection of analgesic and sedative medications during the COVID-19 pandemic, and the impact of these sedation practices on patient outcomes, remain incompletely characterized. Research Question: What were the hospital patterns of analgesic and sedative use for patients with COVID-19 who received mechanical ventilation (MV), and what differences in clinical patient outcomes were observed across prevailing sedation practices? Study Design and Methods: We conducted an observational cohort study of hospitalized adults who received MV for COVID-19 from February 2020 through April 2021 within the Society of Critical Care Medicine Discovery Viral Infection and Respiratory Illness Universal Study (VIRUS) COVID-19 Registry. To describe common sedation practices, we used hierarchical clustering to group hospitals based on the percentage of patients who received various analgesic and sedative medications. We then used multivariable regression models to evaluate the association between hospital analgesia and sedation cluster and duration of MV (with a placement of death [POD] approach to account for competing risks). Results: We identified 1,313 adults across 35 hospitals admitted with COVID-19 who received MV. Two clusters of analgesia and sedation practices were identified. Cluster 1 hospitals generally administered opioids and propofol with occasional use of additional sedatives (eg, benzodiazepines, alpha-agonists, and ketamine); cluster 2 hospitals predominantly used opioids and benzodiazepines without other sedatives. As compared with patients in cluster 2, patients admitted to cluster 1 hospitals underwent a shorter adjusted median duration of MV with POD (β-estimate, –5.9; 95% CI, –11.2 to –0.6; P =.03). Interpretation: Patients who received MV for COVID-19 in hospitals that prioritized opioids and propofol for analgesia and sedation experienced shorter adjusted median duration of MV with POD as compared with patients who received MV in hospitals that primarily used opioids and benzodiazepines.
KW - COVID-19
KW - acute respiratory failure
KW - analgesia
KW - mechanical ventilation
KW - sedation
UR - https://www.scopus.com/pages/publications/105000814198
UR - https://www.scopus.com/pages/publications/105000814198#tab=citedBy
U2 - 10.1016/j.chstcc.2024.100047
DO - 10.1016/j.chstcc.2024.100047
M3 - Article
C2 - 38576856
AN - SCOPUS:105000814198
SN - 2949-7884
VL - 2
JO - CHEST Critical Care
JF - CHEST Critical Care
IS - 1
M1 - 100047
ER -