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Volume 25, Issue 1, Pages 3-9 (March 2010)


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Risk factors for the deterioration of oxygenation ratio in ventilated intensive care unit patients: A retrospective cohort study

Ilma W.F. Fick, MSca, Myrthe M. Tijdink, MSca, Feico J.J. Halbertsma, MD, PhDb, Johannes G. van der Hoeven, MD, PhDb, Peter Pickkers, MD, PhDbCorresponding Author Informationemail address

published online 10 July 2009.

Abstract 

Purpose

The aim of the study is to determine which factors are associated with the deterioration of Pao2/fraction of inspired oxygen (Fio2) ratio in patients with normal oxygenation at admission and ventilated according to a lung protective ventilation strategy.

Materials and Methods

Retrospective cohort study of ventilated (≥3 days) intensive care unit patients with an admission Pao2/Fio2 ratio of 300 mm Hg or higher (n = 105). Patients who developed lung injury (Pao2/Fio2 ratio, <300 mm Hg) on day 7 (n = 37) were compared to those who did not (n = 68), with regard to ventilator settings, gas exchange variables, and lung injury risk factors.

Results

Mean ± SD of administered tidal volume was 7.9 ± 1.3 mL/kg. Patients who developed lung injury were older (P = .019), had lower Pao2 (P = .009), higher Paco2 (P = .045), and lower Pao2/Fio2 ratio (P = .002) at admission. Postoperative state (Hazard risk [HR], 5.1) and controlled ventilation mode (HR, 4.3) were identified as independent risk factors. Lung injury-free time was shorter in patients with low initial Pao2/Fio2 ratio (odds ratio, 1.7; P = .039). This effect was not only caused by the baseline difference, as the decrease in Pao2/Fio2 ratio was more pronounced in patients who developed lung injury compared to those who did not (P = .008).

Conclusions

Lung injury exacerbates during mechanical ventilation. In patients treated with a mean tidal volume of 7.9 mL/kg, controlled ventilation is a major risk factor.

a Radboud University Nijmegen Medical Center, PO-Box 9101, 6500HB Nijmegen, The Netherlands

b Department of Intensive Care Medicine, Radboud University Nijmegen Medical Center, PO-Box 9101, 6500HB Nijmegen, The Netherlands

Corresponding Author InformationCorresponding author. Tel.: +31 24 3617273; fax: +31 24 3541612.

PII: S0883-9441(09)00116-6

doi:10.1016/j.jcrc.2009.04.007


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