High intraoperative inspiratory oxygen fraction and risk of major respiratory complications

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Standard

High intraoperative inspiratory oxygen fraction and risk of major respiratory complications. / Staehr-Rye, A K; Meyhoff, C S; Scheffenbichler, F T; Vidal Melo, M F; Gätke, M R; Walsh, J L; Ladha, K S; Grabitz, S D; Nikolov, M I; Kurth, T; Rasmussen, L S; Eikermann, M.

I: British Journal of Anaesthesia, Bind 119, Nr. 1, 2017, s. 140-149.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Staehr-Rye, AK, Meyhoff, CS, Scheffenbichler, FT, Vidal Melo, MF, Gätke, MR, Walsh, JL, Ladha, KS, Grabitz, SD, Nikolov, MI, Kurth, T, Rasmussen, LS & Eikermann, M 2017, 'High intraoperative inspiratory oxygen fraction and risk of major respiratory complications', British Journal of Anaesthesia, bind 119, nr. 1, s. 140-149. https://doi.org/10.1093/bja/aex128

APA

Staehr-Rye, A. K., Meyhoff, C. S., Scheffenbichler, F. T., Vidal Melo, M. F., Gätke, M. R., Walsh, J. L., Ladha, K. S., Grabitz, S. D., Nikolov, M. I., Kurth, T., Rasmussen, L. S., & Eikermann, M. (2017). High intraoperative inspiratory oxygen fraction and risk of major respiratory complications. British Journal of Anaesthesia, 119(1), 140-149. https://doi.org/10.1093/bja/aex128

Vancouver

Staehr-Rye AK, Meyhoff CS, Scheffenbichler FT, Vidal Melo MF, Gätke MR, Walsh JL o.a. High intraoperative inspiratory oxygen fraction and risk of major respiratory complications. British Journal of Anaesthesia. 2017;119(1):140-149. https://doi.org/10.1093/bja/aex128

Author

Staehr-Rye, A K ; Meyhoff, C S ; Scheffenbichler, F T ; Vidal Melo, M F ; Gätke, M R ; Walsh, J L ; Ladha, K S ; Grabitz, S D ; Nikolov, M I ; Kurth, T ; Rasmussen, L S ; Eikermann, M. / High intraoperative inspiratory oxygen fraction and risk of major respiratory complications. I: British Journal of Anaesthesia. 2017 ; Bind 119, Nr. 1. s. 140-149.

Bibtex

@article{1b151b7d60e7490792ac7e42bfff02b0,
title = "High intraoperative inspiratory oxygen fraction and risk of major respiratory complications",
abstract = "Background: High inspiratory oxygen fraction ( FIO2 ) may improve tissue oxygenation but also impair pulmonary function. We aimed to assess whether the use of high intraoperative FIO2 increases the risk of major respiratory complications.Methods: We studied patients undergoing non-cardiothoracic surgery involving mechanical ventilation in this hospital-based registry study. The cases were divided into five groups based on the median FIO2 between intubation and extubation. The primary outcome was a composite of major respiratory complications (re-intubation, respiratory failure, pulmonary oedema, and pneumonia) developed within 7 days after surgery. Secondary outcomes included 30-day mortality. Several predefined covariates were included in a multivariate logistic regression model.Results: The primary analysis included 73 922 cases, of whom 3035 (4.1%) developed a major respiratory complication within 7 days of surgery. For patients in the high- and low-oxygen groups, the median FIO2 was 0.79 [range 0.64-1.00] and 0.31 [0.16-0.34], respectively. Multivariate logistic regression analysis revealed that the median FIO2 was associated in a dose-dependent manner with increased risk of respiratory complications (adjusted odds ratio for high vs low FIO2 1.99, 95% confidence interval [1.72-2.31], P -value for trend <0.001). This finding was robust in a series of sensitivity analyses including adjustment for intraoperative oxygenation. High median FIO2 was also associated with 30-day mortality (odds ratio for high vs low FIO2 1.97, 95% confidence interval [1.30-2.99], P -value for trend <0.001).Conclusions: In this analysis of administrative data on file, high intraoperative FIO2 was associated in a dose-dependent manner with major respiratory complications and with 30-day mortality. The effect remained stable in a sensitivity analysis controlled for oxygenation.Clinical trial registration: NCT02399878.",
author = "Staehr-Rye, {A K} and Meyhoff, {C S} and Scheffenbichler, {F T} and {Vidal Melo}, {M F} and G{\"a}tke, {M R} and Walsh, {J L} and Ladha, {K S} and Grabitz, {S D} and Nikolov, {M I} and T Kurth and Rasmussen, {L S} and M Eikermann",
note = "{\textcopyright} The Author 2017. Published by Oxford University Press on behalf of the British Journal of Anaesthesia. All rights reserved. For Permissions, please email: journals.permissions@oup.com",
year = "2017",
doi = "10.1093/bja/aex128",
language = "English",
volume = "119",
pages = "140--149",
journal = "British Journal of Anaesthesia",
issn = "0007-0912",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - High intraoperative inspiratory oxygen fraction and risk of major respiratory complications

AU - Staehr-Rye, A K

AU - Meyhoff, C S

AU - Scheffenbichler, F T

AU - Vidal Melo, M F

AU - Gätke, M R

AU - Walsh, J L

AU - Ladha, K S

AU - Grabitz, S D

AU - Nikolov, M I

AU - Kurth, T

AU - Rasmussen, L S

AU - Eikermann, M

N1 - © The Author 2017. Published by Oxford University Press on behalf of the British Journal of Anaesthesia. All rights reserved. For Permissions, please email: journals.permissions@oup.com

PY - 2017

Y1 - 2017

N2 - Background: High inspiratory oxygen fraction ( FIO2 ) may improve tissue oxygenation but also impair pulmonary function. We aimed to assess whether the use of high intraoperative FIO2 increases the risk of major respiratory complications.Methods: We studied patients undergoing non-cardiothoracic surgery involving mechanical ventilation in this hospital-based registry study. The cases were divided into five groups based on the median FIO2 between intubation and extubation. The primary outcome was a composite of major respiratory complications (re-intubation, respiratory failure, pulmonary oedema, and pneumonia) developed within 7 days after surgery. Secondary outcomes included 30-day mortality. Several predefined covariates were included in a multivariate logistic regression model.Results: The primary analysis included 73 922 cases, of whom 3035 (4.1%) developed a major respiratory complication within 7 days of surgery. For patients in the high- and low-oxygen groups, the median FIO2 was 0.79 [range 0.64-1.00] and 0.31 [0.16-0.34], respectively. Multivariate logistic regression analysis revealed that the median FIO2 was associated in a dose-dependent manner with increased risk of respiratory complications (adjusted odds ratio for high vs low FIO2 1.99, 95% confidence interval [1.72-2.31], P -value for trend <0.001). This finding was robust in a series of sensitivity analyses including adjustment for intraoperative oxygenation. High median FIO2 was also associated with 30-day mortality (odds ratio for high vs low FIO2 1.97, 95% confidence interval [1.30-2.99], P -value for trend <0.001).Conclusions: In this analysis of administrative data on file, high intraoperative FIO2 was associated in a dose-dependent manner with major respiratory complications and with 30-day mortality. The effect remained stable in a sensitivity analysis controlled for oxygenation.Clinical trial registration: NCT02399878.

AB - Background: High inspiratory oxygen fraction ( FIO2 ) may improve tissue oxygenation but also impair pulmonary function. We aimed to assess whether the use of high intraoperative FIO2 increases the risk of major respiratory complications.Methods: We studied patients undergoing non-cardiothoracic surgery involving mechanical ventilation in this hospital-based registry study. The cases were divided into five groups based on the median FIO2 between intubation and extubation. The primary outcome was a composite of major respiratory complications (re-intubation, respiratory failure, pulmonary oedema, and pneumonia) developed within 7 days after surgery. Secondary outcomes included 30-day mortality. Several predefined covariates were included in a multivariate logistic regression model.Results: The primary analysis included 73 922 cases, of whom 3035 (4.1%) developed a major respiratory complication within 7 days of surgery. For patients in the high- and low-oxygen groups, the median FIO2 was 0.79 [range 0.64-1.00] and 0.31 [0.16-0.34], respectively. Multivariate logistic regression analysis revealed that the median FIO2 was associated in a dose-dependent manner with increased risk of respiratory complications (adjusted odds ratio for high vs low FIO2 1.99, 95% confidence interval [1.72-2.31], P -value for trend <0.001). This finding was robust in a series of sensitivity analyses including adjustment for intraoperative oxygenation. High median FIO2 was also associated with 30-day mortality (odds ratio for high vs low FIO2 1.97, 95% confidence interval [1.30-2.99], P -value for trend <0.001).Conclusions: In this analysis of administrative data on file, high intraoperative FIO2 was associated in a dose-dependent manner with major respiratory complications and with 30-day mortality. The effect remained stable in a sensitivity analysis controlled for oxygenation.Clinical trial registration: NCT02399878.

U2 - 10.1093/bja/aex128

DO - 10.1093/bja/aex128

M3 - Journal article

C2 - 28974067

VL - 119

SP - 140

EP - 149

JO - British Journal of Anaesthesia

JF - British Journal of Anaesthesia

SN - 0007-0912

IS - 1

ER -

ID: 196042606