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1 were not significantly different compared to spontaneous breathing.
2 more rapid titration from the ventilator to spontaneous breathing.
3 tween total activity and diastolic BP during spontaneous breathing.
4 n between MSNA and diastolic pressure during spontaneous breathing.
5 ng pattern changed little after 2 minutes of spontaneous breathing.
6 ess during mechanical ventilation and during spontaneous breathing.
7 e lightly anesthetized with halothane during spontaneous breathing.
8 d retractor muscles could be measured during spontaneous breathing.
9 atients successfully completed the trials of spontaneous breathing.
10 hase, aimed to avoid derecruitment and allow spontaneous breathing.
11 n, mice were anesthetized and studied during spontaneous breathing.
12 ventilation during 7 days after the onset of spontaneous breathing.
13 range of the expiratory plume compared with spontaneous breathing.
14 g a proportional assist ventilator, PAV) and spontaneous breathing.
15 decreasing end-expiratory lung volume during spontaneous breathing.
16 the fine-scale modulations that occur during spontaneous breathing.
17 st that under supine resting conditions with spontaneous breathing: (1) R-R variability at all measur
18 dal volume during both T-piece breathing and spontaneous breathing 15 mins after extubation (p < .05)
19 expiratory diaphragmatic contraction during spontaneous breathing, 2) reduce expiratory flow and mak
20 r driving pressure (and tidal volume) versus spontaneous breathing (28.0 +/- 0.5 vs. 10.3 +/- 0.6 cm
21 flow velocity were measured during 5 min of spontaneous breathing, 30 mmHg lower body suction to sim
22 hs min-1) and volumes (0.5-1.0 l) and during spontaneous breathing across the physiological range of
23 ositive end-expiratory pressure both without spontaneous breathing activity (0.029 [0.027-0.030] vs 0
24 vs 0.044 [0.041-0.065]; p = 0.004) and with spontaneous breathing activity (0.032 [0.028-0.043] vs 0
25 e of four groups (n = 6/group; 12 hr): 1) no spontaneous breathing activity and positive end-expirato
26 ve end-expiratory pressure - 4 cm H2O, 2) no spontaneous breathing activity and positive end-expirato
27 itive end-expiratory pressure + 4 cm H2O, 3) spontaneous breathing activity and positive end-expirato
28 itive end-expiratory pressure + 4 cm H2O, 4) spontaneous breathing activity and positive end-expirato
32 stomy at ICU discharge was a faster start of spontaneous breathing after tracheotomy was performed.
33 g HF-SCS is similar to that occurring during spontaneous breathing and (b) differential descending sy
34 tor-supported patients who failed a trial of spontaneous breathing and 11 patients who tolerated a tr
35 tor-supported patients who failed a trial of spontaneous breathing and 14 patients who tolerated such
37 chlieren optical system were analyzed during spontaneous breathing and different nasal high-flow rate
38 nce (bias) ranging from -54 to 612 ms during spontaneous breathing and from -52 to 714 ms during mech
39 -expiration decreased from 24% to 16% during spontaneous breathing and from 32% to 18% during control
40 ventral portion of the 3rd interspace during spontaneous breathing and HF-SCS following C2 spinal sec
41 cal use of APRV has been shown to facilitate spontaneous breathing and is associated with decreased p
42 inspiratory lung conductance (G(Li)) during spontaneous breathing and quantitative radioisotope V/Q
43 intermittent mandatory ventilation, assisted spontaneous breathing, and biphasic positive airway pres
48 uld increase inspiratory tidal volume during spontaneous breathing, assessed using whole-body plethys
49 1 +/- 12 vs. -9 +/- 10 vs. -7 +/- 11 ml from spontaneous breathing at 30%, 60% and 80% W(max) , respe
51 ed with transpulmonary driving pressure from spontaneous breathing at lower (r = 0.850; p = 0.032) bu
52 overed from respiratory failure and achieved spontaneous breathing at the same rate as younger patien
53 transdiaphragmatic pressure decreased during spontaneous breathing by >10%, 2) expiratory flow was re
54 powder synthetic lung surfactant may assist spontaneous breathing by providing noninvasive surfactan
55 who had normal lung compliance values during spontaneous breathing (C(Lspont)), C(W)/C(Lspont) was si
56 CU, the interpretation of PPV is unreliable (spontaneous breathing, cardiac arrhythmias) or doubtful
59 groups: 1) acutely anesthetized control, 2) spontaneous breathing control, 3) spontaneously breathin
60 following ventilatory protocols for 4 hours: spontaneous breathing (control group), mechanical ventil
62 however, in animals with severe lung injury, spontaneous breathing could worsen lung injury, and musc
64 ansplantation, those supported via ECMO with spontaneous breathing demonstrated improved survival com
65 tor-supported patients who failed a trial of spontaneous breathing developed a progressive decrease i
66 eper understanding of the pathophysiology of spontaneous breathing during acute respiratory distress
67 t change in tidal volume) that was caused by spontaneous breathing during mechanical ventilation.
70 e lung protective and injurious potential of spontaneous breathing effort during positive pressure ve
71 d higher plateau pressure and more excessive spontaneous breathing effort, resulting in the highest t
73 nce on endogenous NK1 activation depended on spontaneous breathing frequency and the modulatory state
76 echanical ventilation, followed by trials of spontaneous breathing in appropriate patients and notifi
77 Although these results support the use of spontaneous breathing in patients with acute respiratory
79 ul tests were followed by two-hour trials of spontaneous breathing in those who met the criteria.
82 n endotracheal catheter during CPAP-assisted spontaneous breathing (intervention group) or after conv
86 ositive end-expiratory pressure and enhanced spontaneous breathing may increase the proportion of tid
88 by minimally invasive methods that allow for spontaneous breathing might be safer and more effective
91 pread was 0.99, 2.18, 2.92, and 4.1 m during spontaneous breathing, nasal high-flow of 20 L/min, nasa
94 ure spread to the amygdala may cause loss of spontaneous breathing of which patients are unaware, and
95 est that amygdala seizures may cause loss of spontaneous breathing of which patients are unaware-a co
96 ded after a weaning readiness test involving spontaneous breathing on a T-piece or low levels of vent
97 ntilation was categorized into four classes: spontaneous breathing or continuous positive airway pres
98 sure support ventilation, +2.3% (9.5) during spontaneous breathing or continuous positive airway pres
101 with 4-hr low tidal volume ventilation with spontaneous breathing or without spontaneous breathing (
104 noninvasive ventilation sessions than during spontaneous breathing periods (p < 0.05) as a result of
106 cm H2O continuous positive airway pressure, spontaneous breathing, preextubation trial when associat
107 lation with spontaneous breathing or without spontaneous breathing (prevented by a neuromuscular bloc
112 We used the reduction in PET(CO2) below spontaneous breathing required to produce apnea (DeltaPE
113 without respiratory complications or without spontaneous breathing, resulting in rebreathing of gases
114 aphragm pacing and a 45-min period of loaded spontaneous breathing, separated by a 20-min recovery pe
115 cord was clamped when infants showed regular spontaneous breathing, stable heart rates greater than 1
117 e movement greater during HF-SCS compared to spontaneous breathing, stimulus amplitude during HF-SCS
118 ction, ratings of effort were greater during spontaneous breathing than during mechanical ventilation
119 al carbon dioxide pressure (PET(CO2)) during spontaneous breathing, the apnea-hypopnea threshold for
121 in; p = 0.0001) and the change in VO(2) from spontaneous breathing to mechanical ventilation was sign
122 H2O, and reduced the contribution of patient spontaneous breathing to total driving pressure by 57.0%
123 peptic ulcer prophylaxis (0.46 [0.38-0.57]), spontaneous breathing trial (0.81 [0.76-0.86]), family c
124 ed shorter ventilation times until the first spontaneous breathing trial (1 [0-15] vs. 9 [1-51] h; P
125 tly shorter median times to first successful spontaneous breathing trial (1.0 vs. 4.0 d; P < 0.0001),
126 e rate ratio, 1.57; 95% CI, 1.45-1.71) and a spontaneous breathing trial (incidence rate ratio, 1.24;
128 nzodiazepine dose was associated with failed spontaneous breathing trial (p<.01) and delirium (p=.05)
130 management, and patient perception during a spontaneous breathing trial (SBT) might be related to ex
131 eaning failure was defined as failure of the spontaneous breathing trial (SBT) or the need for MV wit
133 erable controversy exists regarding the best spontaneous breathing trial (SBT) technique to use.
136 ; p = 0.004) and decreased odds of passing a spontaneous breathing trial (soluble suppression of tumo
138 determined before and at the end of a 60-min spontaneous breathing trial and 4 hrs after extubation.
139 thing trial, a primary analysis included all spontaneous breathing trial and a secondary analysis inc
140 ose was independently associated with failed spontaneous breathing trial and extubation, and subseque
141 an extubation readiness testing bundle and a spontaneous breathing trial as part of the bundle met Mo
142 To assess whether lung derecruitment during spontaneous breathing trial assessed by lung ultrasound
143 t <or=25% of patients successfully completed spontaneous breathing trial but did not proceed to immed
144 ocol (n=154) underwent daily screening and a spontaneous breathing trial by respiratory and nursing s
145 patients receiving mechanical ventilation, a spontaneous breathing trial consisting of 30 minutes of
146 er extubation immediately after a successful spontaneous breathing trial is associated with clinical
147 Postextubation distress after a successful spontaneous breathing trial is associated with increased
149 tion of aeration changes during a successful spontaneous breathing trial may accurately predict poste
151 ot occurred despite successful completion of spontaneous breathing trial on >or=1 occasion, a rate th
152 oped acute respiratory failure (failure of a spontaneous breathing trial or successful breathing tria
154 ty, and feasibility of protocols using daily spontaneous breathing trial plus pressure support ventil
155 Adoption and implementation of a common spontaneous breathing trial protocol across multiple int
156 oring of esophageal pressure swings during a spontaneous breathing trial provides additional guidance
157 ltrasound performed at the end of the failed spontaneous breathing trial showed a pattern consistent
158 er failed or were not yet ready to undergo a spontaneous breathing trial to automated or protocolized
159 Most respondents (96.1%) reported relying on spontaneous breathing trial to guide decision for extuba
161 o undertake a spontaneous breathing trial, a spontaneous breathing trial to test ventilator liberatio
162 ung ultrasound and echocardiography during a spontaneous breathing trial uncovered an unexpected caus
163 : Prompt extubation after a first successful spontaneous breathing trial was associated with more ven
164 Loss of lung aeration during the successful spontaneous breathing trial was observed only in group 2
165 or and not by the patient until a successful spontaneous breathing trial was performed or for up to 7
167 hen first meeting established criteria for a spontaneous breathing trial was significantly greater du
168 groups, and the median time to pass a 2-hour spontaneous breathing trial was similar between both the
171 The percentage of patients undergoing a spontaneous breathing trial when first meeting establish
172 ontaneous breathing trials were analyzed, 21 spontaneous breathing trial with weaning-induced pulmona
175 1) withholding extubation after a successful spontaneous breathing trial, 2) extubation failure withi
177 Because some patients performed several spontaneous breathing trial, a primary analysis included
178 daily screening for readiness to undertake a spontaneous breathing trial, a spontaneous breathing tri
179 patients, identifies patients earlier for a spontaneous breathing trial, and shortens the duration o
183 for ideal body weight, 0.97 (0.93-1.01) for spontaneous breathing trial-induced changes in plasma pr
195 ty-six patients were assessed at their first spontaneous breathing trial: 63% had diaphragm dysfuncti
196 ts had 3,486 safety screens for conducting a spontaneous breathing trial; 2072 (59%) patients failed
197 d extubation within 7 days after the initial spontaneous-breathing trial, as well as reintubation wit
199 ress syndrome (47% vs 52%; p = 0.28) and for spontaneous breathing trials (55% vs 51%; p = 0.27).
200 r testing extubation readiness or conducting spontaneous breathing trials (B) were reported in 57%, w
201 ct of transitions of care on compliance with spontaneous breathing trials (odds ratio, 1.00; 95% CI,
202 eaning protocol incorporating daily screens, spontaneous breathing trials (SBT), and prompts to careg
203 at included a daily screen (DS) coupled with spontaneous breathing trials (SBTs) and physician prompt
205 rding physicians for the completion of daily spontaneous breathing trials (SBTs) in three academic ho
206 ional parameters to determine the success of spontaneous breathing trials (SBTs) may fail to detect i
207 ated spontaneous awakening trials (SATs) and spontaneous breathing trials (SBTs) might prevent VAEs.
210 extraction were measured immediately before spontaneous breathing trials and at 60 minutes after spo
211 ng protocols should be in place that include spontaneous breathing trials and criteria for initiating
212 that daily sedation interruption paired with spontaneous breathing trials improved 1-year survival, w
217 s (ie, interruption of sedatives) with daily spontaneous breathing trials results in better outcomes
218 ements were made before and 30 minutes after spontaneous breathing trials that lasted up to 60 minute
220 venous oxygen saturation (DeltaScvO2) during spontaneous breathing trials were independently associat
222 akening trials (daily sedation vacation plus spontaneous breathing trials) as a quality improvement p
224 trategies with spontaneous awakening trials, spontaneous breathing trials, and early mobility and sle
225 management to spontaneous awakening trials, spontaneous breathing trials, and ICU early mobility and
226 , and 21.1% for lung-protective ventilation, spontaneous breathing trials, and neuromuscular blockade
227 prophylaxis, stress ulcer prophylaxis, daily spontaneous breathing trials, and sedative interruptions
228 edian values of respiratory variables during spontaneous breathing trials, and the change in airway p
230 le consists of spontaneous awakening trials, spontaneous breathing trials, coordination of awakening
231 , daily screens for weaning readiness, daily spontaneous breathing trials, early resuscitation in sep
232 ther evidence-based ICU practices, including spontaneous breathing trials, ICU early mobility program
233 with three evidence-based processes of care (spontaneous breathing trials, lung-protective ventilatio
234 tions related to the methods and duration of spontaneous breathing trials, measures of respiratory mu
235 Both groups used pressure support, included spontaneous breathing trials, used a common positive end
236 and central venous oxygen saturation, during spontaneous breathing trials, were independent predictor
245 B" for Both Spontaneous Awakening Trials and Spontaneous Breathing Trials; "C" for Choice of Analgesi
247 tly more ventilator-free days at day 28 than spontaneous-breathing trials performed with a T-piece.
248 s who had a high risk of extubation failure, spontaneous-breathing trials performed with PSV did not
249 c cardiac or respiratory disease) to undergo spontaneous-breathing trials performed with the use of e
250 d into 3 groups and followed up for 6 hours: spontaneous breathing ventilation (SBV, n = 5), continuo
251 phragm thickening fraction during unassisted spontaneous breathing was +17% and -14%, respectively, P
257 te to tidal volume in spinally injured rats, spontaneous breathing was measured in anesthetized C2 he
259 chanical ventilation, expiratory time during spontaneous breathing was prolonged less than 20% of tha
261 at the level of support we imposed, assisted spontaneous breathing was the most comfortable mode of v
263 hout acute lung injury, and the influence of spontaneous breathing with continuous positive airway pr
264 % during four breathing patterns compared to spontaneous breathing, with the greatest changes during