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1 es of predetermined combinations of PEEP and fraction of inspired oxygen.
2 aps were generated in rat eyes under varying fractions of inspired oxygen.
4 visory board of the study proposed using the fraction of inspired oxygen 0.25/mean airway pressure 4
5 0 ventilator days depending on ICU type; the fraction of inspired oxygen 0.30/mean airway pressure 7
7 the effects of 2 weeks of cIH (1-min cycle, fraction of inspired oxygen 21-5%, 8 h/day) on whole-bod
8 96%) but similar mean (SD) ratios of PaO2 to fraction of inspired oxygen (304.40 [65.7] vs 312.97 [68
9 e partial pressure of arterial oxygen to the fraction of inspired oxygen at 72 hours was 88 mm Hg hig
10 definition (i.e., increase in minimum daily fraction of inspired oxygen by 0.25 or mean airway press
11 of thresholds for increases in daily minimum fraction of inspired oxygen (by 0.20, 0.25, and 0.30) an
13 y (less than 16 hours) improvement in Pa(O2)/fraction of inspired oxygen compared with the convention
14 published in regard to the effect of a high fraction of inspired oxygen concentration (FiO(2)) durin
15 y the partial pressure of arterial oxygen to fraction of inspired oxygen concentration ratio (DeltaPa
16 cal shunt and the ratio between PaO2 and the fraction of inspired oxygen enable estimation of CT shun
18 0 d age, HFOV animals had consistently lower fraction of inspired oxygen (FI(O(2))) and higher a/ A r
22 ial pressure of arterial oxygen (PaO) to the fraction of inspired oxygen (FiO) of 200 mm Hg (26.7 kPa
25 40 mm Hg, despite ventilatory support with a fraction of inspired oxygen (Fio2) of 1.0 and a positive
26 e partial pressure of arterial oxygen to the fraction of inspired oxygen (FiO2) of less than 150 mm H
27 lateral infiltrates on chest x-ray, and PaO2/fraction of inspired oxygen (FiO2) ratio < or =100 or A-
28 aneous partial pressure of oxygen (Ptco2) to fraction of inspired oxygen (Fio2) ratio, alveolar-arter
29 even hypoxic which were exposed to decreased fraction of inspired oxygen (FiO2) to achieve varying ph
31 brain tissue oxygen, mean arterial pressure, fraction of inspired oxygen (FiO2), partial pressure of
32 rk in KE; (2) greater work rates with higher fraction of inspired oxygen (FIO2); (3) an even greater
34 sly through a nasal cannula (flow, 50 L/min; fraction of inspired oxygen [FiO2], 50%) (n = 414) or Bi
35 t were a Silverman score of 5 or higher or a fraction of inspired oxygen higher than 0.3 for a target
36 e end-expiratory pressure of </=5 cm H2O and fraction of inspired oxygen </=40% for at least 3 days w
37 of less than 60 mm Hg (or ratio of PaO(2) to fraction of inspired oxygen <300); and normoxia, not cla
38 acute respiratory distress syndrome (Pa(O2)/fraction of inspired oxygen <or= 200 mm Hg on 10 or more
39 e partial pressure of arterial oxygen to the fraction of inspired oxygen of 300 mm Hg or less to high
41 at least 2 hours, supplemental oxygen with a fraction of inspired oxygen of at least 0.30 for at leas
43 ory index scores (mean airway pressure x the fraction of inspired oxygen) of 52.4 at two weeks of age
44 tor, defined by changes in the daily minimum fraction of inspired oxygen or positive end-expiratory p
45 io of arterial partial pressure of oxygen to fraction of inspired oxygen: P/F) after the initial chan
46 s death, partial pressure of arterial oxygen/fraction of inspired oxygen ratio </=55, cardiac index <
47 001) and partial pressure of arterial oxygen/fraction of inspired oxygen ratio (p < 0.0001) were asso
48 he mean partial pressure of oxygen, arterial/fraction of inspired oxygen ratio (PaO(2)/FIO(2)) was 19
51 mean partial pressure of arterial oxygen to fraction of inspired oxygen, shunt fraction, and pulmona
52 sitive end-expiratory pressure, 5-10 cm H2O; fraction of inspired oxygen titrated to maintain SpO2 >/
53 ex ([mean airway pressure x the ratio of the fraction of inspired oxygen to the partial pressure of a
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