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1 verse events clearly attributable to partial liquid ventilation.
2 mproved during total, but not during partial liquid ventilation.
3 is improved during total followed by partial liquid ventilation.
4 entially better approach to applying partial liquid ventilation.
5 ge, allowing successful performance of total liquid ventilation.
6 de, intratracheal pulmonary ventilation, and liquid ventilation.
7 ning, tracheal gas insufflation, and partial liquid ventilation.
8 s of lungs from animals treated with partial liquid ventilation.
10 = O.48 +/- 0.03 mL/cm H2O/kg, total/partial liquid ventilation = 0.50 +/- 0.17 mL/cm H2O/kg) were ob
11 with controls (pulmonary compliance: partial liquid ventilation, 0.43 +/- 0.04 mL/ cm H2O/kg; control
12 tilation = 0.43 +/- 0.03 mL/cm H2O/kg, total liquid ventilation = 1.13 +/- 18 mL/cm H2O/kg, p <.001;
13 al: gas ventilation 6 +/- 1 mL/cm H2O, total liquid ventilation 14 +/- 4 mL/cm H2O, p < .0001; surfac
14 ysiologic shunt after 50 mL/kg dose: partial liquid ventilation, 2 +/- 8%; control, 64 +/- 5%; p = .0
15 (gas ventilation = 89 +/- 7 mL/kg/min, total liquid ventilation = 22 +/- 10 mL/kg/min, p <.001; gas v
17 s ventilation = 91 +/- 12 mL/kg/min, partial liquid ventilation = 41 +/- 11 mL/kg/min, p < .001).
18 ompared with the gas ventilated group (total liquid ventilation 44 +/- 17 mL, gas ventilation 2 +/- 8
19 animals (gas ventilation = 93 +/- 8%, total liquid ventilation = 45 +/- 11%, p<.001; gas ventilation
20 volume observed with gas ventilation (total liquid ventilation 50 +/- 14 mL, gas ventilation 4 +/- 9
21 p<.001; gas ventilation = 95 +/- 3%, partial liquid ventilation = 61 +/- 12%, p<.001), while static c
22 (gas ventilation = 69 +/- 11%, total/partial liquid ventilation = 71 +/- 3%) and a decrease in static
24 al oxygen saturation after 50 mL/kg: partial liquid ventilation, 96 +/- 3%; control, 55 +/- 8%; p = .
25 ; d) CVF-PLV group, animals received partial liquid ventilation after cobra venom factor; e) CVF-PEEP
26 groups: surfactant alone (S; n = 8); partial liquid ventilation alone (PLV-only; n = 8); surfactant f
30 ventilator strategies, inhaled nitric oxide, liquid ventilation, and extracorporeal life support (ECL
31 After induction of lung injury, all partial liquid ventilation animals received intratracheal perflu
32 flammatory infiltration in the total/partial liquid ventilation animals when compared with the gas ve
33 ay pressure release ventilation, and partial liquid ventilation are potential protective ventilatory
35 nspiratory and expiratory phase during total liquid ventilation at low respiratory rates, apparently
37 ; b) PLV-CVF group, animals received partial liquid ventilation before the induction of lung injury;
38 information available from studies involving liquid ventilation, both laboratory-based and clinical t
40 s were lower in animals treated with partial liquid ventilation compared with conventionally ventilat
41 onary blood flow is preserved during partial liquid ventilation compared with gas ventilation in olei
42 rate achieved 58% versus 0% and 8% in total liquid ventilation, control, and conventional cooling gr
44 d significance (p < .05) only in the partial liquid ventilation-conventional ventilation animals.
46 d an oleic acid-induced lung injury: partial liquid ventilation during acute lung injury (OA-PLV) and
48 rate was significantly lower in the partial liquid ventilation-flow interruption group (p < .05).
50 quid ventilation (S-PLV; n = 8); and partial liquid ventilation-followed by surfactant (PLV-S; n = 8)
51 n=5) over the ensuing 2.5 hrs, or with total liquid ventilation for 1 hr, followed by partial liquid
52 id ventilation for 1 hr, followed by partial liquid ventilation for 1.5 hrs (total/partial liquid ven
55 was significantly lower in the total/partial liquid ventilation group when compared with that of the
56 a induced by total liquid ventilation (total liquid ventilation group) or by combination of cold sali
58 0 minutes of total liquid ventilation (total liquid ventilation group, n = 12) or IV cold saline (con
62 ) liquid, such as perflubron, during partial liquid ventilation improves lung function and also reduc
63 nuous positive-pressure ventilation (partial liquid ventilation) improves lung function in animals wi
67 ased from baseline (before injury or partial liquid ventilation) in the most dependent areas of the l
73 eatments or no treatment (control): modified liquid ventilation (MLV), intramuscular ampicillin, MLV
74 mals were assigned to receive either partial liquid ventilation (n = 16) with perflubron (18 mL/kg vi
77 groups: a normal group that received partial liquid ventilation (Normal-PLV) and two acute lung injur
78 to decipher the effect of hypothermic total liquid ventilation on the systemic and cerebral response
79 f) PLV only group, animals received partial liquid ventilation only; g) GV only group, animals recei
83 y oscillatory ventilation (HFOV) and partial liquid ventilation (PLV) also decrease lung injury and i
84 g opacification by perflubron during partial liquid ventilation (PLV) and extracorporeal membrane oxy
88 onary neutrophil accumulation during partial liquid ventilation (PLV) in the setting of acute lung in
90 evaluated the safety and efficacy of partial liquid ventilation (PLV) with perflubron in adult patien
92 mpared the effects of surfactant and partial liquid ventilation (PLV), and the impact of administrati
93 Animals were assigned to receive partial liquid ventilation (PLV, n = 15) with perflubron (18 mL/
96 only; n = 8); surfactant followed by partial liquid ventilation (S-PLV; n = 8); and partial liquid ve
99 haled nitric oxide, almitrine, prostacyclin, liquid ventilation, surfactant, and immune-modulating th
102 ce of perflubron-filled lungs during partial liquid ventilation to treat acute respiratory distress s
103 3 hours of mild hypothermia induced by total liquid ventilation (total liquid ventilation group) or b
104 hermia induced by either 30 minutes of total liquid ventilation (total liquid ventilation group, n =
105 -phosphatidylcholine activity in the partial liquid ventilation treated- vs. control rabbits demonstr
106 The phospholipid content of the partial liquid ventilation treated- vs. the control rabbits demo
111 nsion of normal atelectatic lungs with total liquid ventilation was associated with an 11-fold increa
119 ications potentially associated with partial liquid ventilation were limited to pneumothoraces in two
120 onary compliance was observed during partial liquid ventilation when compared with controls (pulmonar
121 which gas exchange is improved during total liquid ventilation when compared with gas ventilation in
122 y following attempted reexpansion with total liquid ventilation when compared with gas ventilation in
123 gnificantly reduced during total and partial liquid ventilation when compared with physiologic shunt
124 d beyond 28 days after initiation of partial liquid ventilation whereas 5 patients survived to discha
126 entional gas ventilation (n = 8); b) partial liquid ventilation with conventional ventilation (n = 7)
127 requency oscillation (n = 7); and e) partial liquid ventilation with high-frequency flow interruption
128 conventional ventilation (n = 7); c) partial liquid ventilation with high-frequency jet ventilation (
129 requency jet ventilation (n = 7); d) partial liquid ventilation with high-frequency oscillation (n =
130 requency oscillatory ventilation and partial liquid ventilation with perfiubron was well tolerated he
131 nventional mechanical ventilation or partial liquid ventilation with Perflubron (18 mL/kg by bolus fi
137 flammatory activity and suggest that partial liquid ventilation with PFC may be considered in future
138 d whole-body cooling can be induced by total liquid ventilation with temperature-controlled perfluoro
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