TY - JOUR
T1 - Incidence of postoperative opioid-induced respiratory depression episodes in patients on room air or supplemental oxygen
T2 - a post-hoc analysis of the PRODIGY trial
AU - The Prediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphY (PRODIGY) Group Investigators
AU - Doufas, Anthony G.
AU - Laporta, Mariana L.
AU - Driver, C. Noelle
AU - Di Piazza, Fabio
AU - Scardapane, Marco
AU - Bergese, Sergio D.
AU - Urman, Richard D.
AU - Khanna, Ashish K.
AU - Weingarten, Toby N.
AU - Jungquist, Carla R.
AU - Morimatsu, Hiroshi
AU - Uezono, Shoichi
AU - Lee, Simon
AU - Ti, Lian Kah
AU - McIntyre, Robert
AU - Tornero, Carlos
AU - Dahan, Albert
AU - Saager, Leif
AU - Wittmann, Maria
AU - Auckley, Dennis
AU - Brazzi, Luca
AU - Le Guen, Morgan
AU - Soto, Roy
AU - Schramm, Frank
AU - Buhre, Wolfgang
AU - Overdyk, Frank J.
N1 - Publisher Copyright:
© 2023, BioMed Central Ltd., part of Springer Nature.
PY - 2023/12
Y1 - 2023/12
N2 - Background: Supplemental oxygen (SO) potentiates opioid-induced respiratory depression (OIRD) in experiments on healthy volunteers. Our objective was to examine the relationship between SO and OIRD in patients on surgical units. Methods: This post-hoc analysis utilized a portion of the observational PRediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphY (PRODIGY) trial dataset (202 patients, two trial sites), which involved blinded continuous pulse oximetry and capnography monitoring of postsurgical patients on surgical units. OIRD incidence was determined for patients receiving room air (RA), intermittent SO, or continuous SO. Generalized estimating equation (GEE) models, with a Poisson distribution, a log-link function and time of exposure as offset, were used to compare the incidence of OIRD when patients were receiving SO vs RA. Results: Within the analysis cohort, 74 patients were always on RA, 88 on intermittent and 40 on continuous SO. Compared with when on RA, when receiving SO patients had a higher risk for all OIRD episodes (incidence rate ratio [IRR] 2.7, 95% confidence interval [CI] 1.4–5.1), apnea episodes (IRR 2.8, 95% CI 1.5–5.2), and bradypnea episodes (IRR 3.0, 95% CI 1.2–7.9). Patients with high or intermediate PRODIGY scores had higher IRRs of OIRD episodes when receiving SO, compared with RA (IRR 4.5, 95% CI 2.2–9.6 and IRR 2.3, 95% CI 1.1–4.9, for high and intermediate scores, respectively). Conclusions: Despite oxygen desaturation events not differing between SO and RA, SO may clinically promote OIRD. Clinicians should be aware that postoperative patients receiving SO therapy remain at increased risk for apnea and bradypnea. Trial registration: Clinicaltrials.gov: NCT02811302, registered June 23, 2016.
AB - Background: Supplemental oxygen (SO) potentiates opioid-induced respiratory depression (OIRD) in experiments on healthy volunteers. Our objective was to examine the relationship between SO and OIRD in patients on surgical units. Methods: This post-hoc analysis utilized a portion of the observational PRediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphY (PRODIGY) trial dataset (202 patients, two trial sites), which involved blinded continuous pulse oximetry and capnography monitoring of postsurgical patients on surgical units. OIRD incidence was determined for patients receiving room air (RA), intermittent SO, or continuous SO. Generalized estimating equation (GEE) models, with a Poisson distribution, a log-link function and time of exposure as offset, were used to compare the incidence of OIRD when patients were receiving SO vs RA. Results: Within the analysis cohort, 74 patients were always on RA, 88 on intermittent and 40 on continuous SO. Compared with when on RA, when receiving SO patients had a higher risk for all OIRD episodes (incidence rate ratio [IRR] 2.7, 95% confidence interval [CI] 1.4–5.1), apnea episodes (IRR 2.8, 95% CI 1.5–5.2), and bradypnea episodes (IRR 3.0, 95% CI 1.2–7.9). Patients with high or intermediate PRODIGY scores had higher IRRs of OIRD episodes when receiving SO, compared with RA (IRR 4.5, 95% CI 2.2–9.6 and IRR 2.3, 95% CI 1.1–4.9, for high and intermediate scores, respectively). Conclusions: Despite oxygen desaturation events not differing between SO and RA, SO may clinically promote OIRD. Clinicians should be aware that postoperative patients receiving SO therapy remain at increased risk for apnea and bradypnea. Trial registration: Clinicaltrials.gov: NCT02811302, registered June 23, 2016.
KW - Apnea
KW - Capnography
KW - Continuous monitoring
KW - Pulse oximetry
KW - Respiratory depression
KW - Room air
KW - Spot check monitoring
KW - Supplemental oxygen
UR - https://www.scopus.com/pages/publications/85173636402
U2 - 10.1186/s12871-023-02291-x
DO - 10.1186/s12871-023-02291-x
M3 - Article
C2 - 37794334
AN - SCOPUS:85173636402
SN - 1471-2253
VL - 23
JO - BMC Anesthesiology
JF - BMC Anesthesiology
IS - 1
M1 - 332
ER -