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1 g wet and dry weights and decreased specific lung compliance.
2 s including airway obstruction and increased lung compliance.
3 eration on computed tomography, and impacted lung compliance.
4 e activity, cytokine contents, and decreased lung compliance.
5 ation and lung histology) and improvement in lung compliance.
6 lar apoptosis and a decrease in quasi-static lung compliance.
7 eased the respiratory compliance by reducing lung compliance.
8 iratory distress syndrome was related to low lung compliance.
9 m inducing perivascular cuffs and decreasing lung compliance.
10  also protected from LPS-induced decrease in lung compliance.
11 nd airway resistance as well as decreases in lung compliance.
12 t alveolar edema, are sufficient to decrease lung compliance.
13 ll tolerated with minimal effects on dynamic lung compliance.
14 , diffuse pulmonary infiltrates, and altered lung compliance.
15 id not change gas exchange, hemodynamics, or lung compliance.
16 hese responses likely contribute to impaired lung compliance.
17 and exhibited normal oxygenation and dynamic lung compliance.
18 e shifted upward and to the left) and higher lung compliance (0.21 vs 00.9 L/cm H(2) O; P < .05) comp
19 irway pressure (20, 30, and 40 cm H2O), test lung compliance (10, 30, and 50 mL/cm H2O), endotracheal
20  +/- 35 vs. 267 +/- 98; p = .15), and static lung compliance (30.9 +/- 13.5 vs. 38.5 +/- 11.7; p = .2
21 g of face mask, manikin head, training lung (lung compliance, 50 mL/cm H2O; airway resistance, 5 cm H
22 f survival and quality of life influenced by lung compliance, albeit while accelerating disease progr
23                                              Lung compliance, alveolar-arterial oxygen difference, an
24  group (406+/-63 vs 148+/-33 mm Hg, P=0.01); lung compliance and airway resistance did not differ sig
25 ma, as evidenced by attenuation of increased lung compliance and alveolar size.
26                      Survivors had increased lung compliance and decreased elastance.
27  injury, with preserved gas exchange, better lung compliance and histology scores, and decreased lung
28 cute lung injury, is associated with reduced lung compliance and hypoxemia.
29 ry in WT mice was characterized by decreased lung compliance and increased protein and cytokine conce
30 and a decrease in PaO2, a decrease in static lung compliance and inhibition of surfactant function.
31                     PG490-88 improved static lung compliance and injury scores, reduced bronchioalveo
32  certain phospholipids had similar activity (lung compliance and lung pressure-volume behavior) to ra
33 healing response, as it results in worsening lung compliance and oxygenation.
34 at resulted in significant decreases in both lung compliance and oxygenation.
35 opterin was associated with better preserved lung compliance and PaO2/FIO2 ratio, which were associat
36 gous mice (Hhip(+/-)), we observed increased lung compliance and spontaneous emphysema in Hhip(+/-) m
37                      Beta-Ac alone increased lung compliance and surfactant concentration in the feta
38                                              Lung compliance and the oxygenation index were measured
39                                  The dynamic lung compliance and the postventilatory expansion of lun
40 ved lung function (specifically quasi-static lung compliance and tissue elastance) and reduced mucus
41 ow, and tidal volume, and calculated dynamic lung compliance and total lung resistance.
42                    We measured the effect on lung compliance and whether positive end-expiratory pres
43 monary function (lung resistance and dynamic lung compliance), and inflammatory cell infiltration.
44 y resistance and decreases in minute volume, lung compliance, and alveolar function.
45 siveness, alveolar simplification, decreased lung compliance, and decreased lung angiogenesis.
46 xchange, increased pulmonary edema, abnormal lung compliance, and extensive airway obstruction.
47  positive end-expiratory pressures), reduced lung compliance, and high lung injury scores.
48 characterized by severe hypoxemia, decreased lung compliance, and high vascular permeability.
49 l animals include airspace collapse, reduced lung compliance, and impaired gas exchange.
50 reduced morbidity and viral burden, improved lung compliance, and increased CD8(+) T cell numbers in
51 mation and injury, decreased oxygenation and lung compliance, and increased respirations.
52 ses mortality, promotes lung injury, reduces lung compliance, and increases degradation of lung elast
53 -expiratory pressure, the decrease in static lung compliance, and the extent of infiltrates on the ch
54 monary function, including Pao2/Fio2, static lung compliance, and time to meeting weaning criteria.
55       However, the loss of static expiratory lung compliance appears partly ameliorated by applicatio
56          SURF without PEEP further decreased lung compliance as compared with PMA only.
57 a series of different airway resistances and lung compliances as would be seen in different types of
58 rious combinations of airway resistances and lung compliances, auto-PEEP can be generated to substant
59 e most predictive of lung volume: a) dynamic lung compliance; b) the slope of phase 3; c) the slope o
60 predictive of lung volume change: a) dynamic lung compliance; b) the slope of phase III; c) the slope
61 with reduced minute ventilation, a result of lung compliance below design parameters.
62 ctant, a lipoprotein complex which increases lung compliance by reducing alveolar surface tension.
63      Respiratory system compliance (Crs) and lung compliance (C(L)) were calculated from airway openi
64 g pressure (DP(TP))-the quotient of V(T) and lung compliance (C(L)), in response to intra-abdominal h
65 cessfully extubated had significantly better lung compliance (Cdyn: 0.59 +/- 0.91 versus 0.39 +/- 0.1
66 e dismutase (SOD) treatment on gas exchange, lung compliance (CL), and pulmonary vascular resistance
67 ed substantial and significant impairment in lung compliance compared with control littermates receiv
68 exaggerated lung fibrosis and reduced static lung compliance compared with controls.
69 erial pulmonary function tests, blood gases, lung compliance, computed tomography (CT) imaging, and q
70  final plateau pressure (Pp), and peripheral lung compliance (Cp).
71     Airway opening pressure (P-Flex), static lung compliance (Crs), and trapped gas volume (TGV) were
72                            When total static lung compliance decreased to 0.15 mL (cm H2O)(-1) x kg(-
73                                              Lung compliance did not differ between groups at the pos
74 cture is destroyed, which leads to decreased lung compliance, disrupted gas exchange, and ultimately
75                                              Lung compliance dose-dependently decreased after thapsig
76                           Changes in dynamic lung compliance during inspiration and expiration cannot
77                                              Lung compliance during mechanical ventilation was impair
78 90% O2 resulted in the restoration of normal lung compliance, elastance, and pressure-volume loops (t
79 (6) CFU) rapidly lost weight, had diminished lung compliance, experienced lung hemorrhage, and respon
80 coil pressure at total lung capacity, static lung compliance, expiratory flow rates, and lung volumes
81                                              Lung compliance, hemodynamics, right ventricular heart m
82 and is characterized by a virtual absence of lung compliance, highly disorganized lamellar bodies, an
83 O-exposed mice with ML335 or BL1249 improved lung compliance, histological lung injury scores, bronch
84                                       Static lung compliance improved over time in the prone group (3
85 es was indicated by improved oxygenation and lung compliance in FG-4095-treated newborns.
86 tation lung, and significantly reduced total lung compliance in late gestation embryos that lack lymp
87 phospholipid pool sizes and composition, and lung compliance in SP-A(-/-) mice were unaltered.
88 lthough prone positioning improved posterior lung compliance in the early acute respiratory distress
89 n gas exchange and a significant decrease in lung compliance in the juvenile rabbit model.
90                                      Dynamic lung compliance increased from 38 (24-64) mL/cm H2O at b
91 o tidal volume (VD/VT) decreased, and static lung compliance increased with PEEP at LIP +1 cm H2O (p
92 l volume to DeltaPes (an estimate of dynamic lung compliance) increased (P < 0.05); finally, ventilat
93 a), lung pathology, pulmonary edema, reduced lung compliance, increased basal airway resistance, and
94 ncluded decreased pulmonary gas exchange and lung compliance, increased pulmonary edema, and extensiv
95 ncluded decreased pulmonary gas exchange and lung compliance, increased pulmonary edema, and inflamma
96 me, respiratory rate, minute volume, dynamic lung compliance, inspiratory resistance, and blood gases
97 here was no difference in lung resistance or lung compliance measured by body plethysmography between
98 tion, but they demonstrated neither abnormal lung compliance nor increased respiratory rate and displ
99  and absence of plasma inhibitors, but whole lung compliance of the SP-A(-/-,D/A) animals was not dif
100 e.g., increased airway resistance, decreased lung compliance, or both.
101 okines (interleukin [IL] 6 and IL-8), static lung compliance, or lung histology.
102 al lung resistance and a decrease in dynamic lung compliance (P < 0.05).
103                                 Final static lung compliance (p =.0002) and Pao2/Fio2 (p =.001) decre
104                    Outcome measures included lung compliance, Pao /Fio ratio, wet/dry lung weight, an
105 creased capillary permeability, and improved lung compliance, particularly at 12-hr storage times.
106 IIai dramatically protected gas exchange and lung compliance, prevented lung edema and pulmonary hype
107  capacity was associated with a reduction in lung compliance (r(2) = 0.43; p = 0.03) and isotime esop
108                                       Static lung compliance significantly increased postrandomizatio
109 most dramatically characterized by decreased lung compliance that was associated with an intense mono
110 ulmonary function (total lung volume, static lung compliance, tissue damping, and tissue elastance).
111 ic responses (airway hyperresponsiveness and lung compliance) to Mp infection were more severely affe
112 13 to increase lung size, alveolar size, and lung compliance, to stimulate pulmonary inflammation, hy
113 ctant proteins SpC, SpB, and SpA, decline of lung compliance, transient fibrosis, and eventually emph
114 eduction in movement, and a fall in specific lung compliance unseen in conventional mouse asthma mode
115                   In subjects who had normal lung compliance values during spontaneous breathing (C(L
116 asurements included physiological variables (lung compliance, vascular resistance, oxygenation capaci
117 ility to modify lipid properties and restore lung compliance was investigated with circular dichroism
118                                              Lung compliance was measured during ventilation througho
119                                     Specific lung compliance was significantly increased in lungs of
120                     Indirect measurements of lung compliance were consistent with a stiffening of the
121      Pulmonary inflammation and quasi-static lung compliance were largely unaffected by neutralizatio
122 e, pulmonary vascular resistance, and static lung compliance were measured at baseline and after mode
123 after PMA injury causes marked reductions in lung compliance when no PEEP is coadministered.
124 r bundle and the lung parenchyma, decreasing lung compliance without impacting central venous pressur

 
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