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1 spontaneous breathing or continuous positive airway pressure.
2 esity tolerate hemodynamically LRM with high airway pressure.
3 ay pressure, but can be controlled under low airway pressure.
4 less than 34 weeks under continuous positive airway pressure.
5 essure support on top of expiratory positive airway pressure.
6 ng CT scans were obtained at 5 and 45 cm H2O airway pressure.
7 irst hours of life under continuous positive airway pressure.
8 /- 7% (P < 0.0001) going from 5 to 45 cm H2O airway pressure.
9 ts who are intolerant to continuous positive airway pressure.
10 roduction of less invasive forms of positive airway pressure.
11 tomography measurements when increasing mean airway pressure.
12 reduced extravascular lung water and plateau airway pressure.
13 y small tidal volumes cycling at a high mean airway pressure.
14 -invasive ventilation or continuous positive airway pressure.
15 in the duration of nasal continuous positive airway pressure.
16 xia or respiratory acidosis and high plateau airway pressures.
17 ssessed at low (5 cmH2O) and high (45 cmH2O) airway pressures.
18 litude (50, 60, 70, 80, and 90 cm H2O), mean airway pressure (20, 30, and 40 cm H2O), test lung compl
19 kg predicted body weight, p < .001), in peak airway pressure (31-25 cm H2O, p < .001), and in the per
20 or the fraction of inspired oxygen 0.25/mean airway pressure 4 definition (i.e., increase in minimum
21 ng the fraction of inspired oxygen 0.25/mean airway pressure 4 thresholds to identify pediatric venti
22 derwent lung recruitment continuous positive airway pressure 40 cm H2O for 40 secs to normalize volum
23 e; the fraction of inspired oxygen 0.30/mean airway pressure 7 definition yielded ventilator-associat
24 ing the 75th to the 25th percentile for mean airway pressure; 95% CI, 1.10-1.74) after adjusting for
25 s, a group that has poor continuous positive airway pressure adherence and difficulty in achieving we
26 release ventilation of 0%, biphasic positive airway pressure/airway pressure release ventilation more
28 , and damage compared with biphasic positive airway pressure/airway pressure release ventilation more
31 distress syndrome in pigs, biphasic positive airway pressure/airway pressure release ventilation with
32 elease ventilation, 0%; 2) biphasic positive airway pressure/airway pressure release ventilation, > 0
33 e ventilation, > 0-30%; 3) biphasic positive airway pressure/airway pressure release ventilation, > 3
34 tilation, > 30-60%, and 4) biphasic positive airway pressure/airway pressure release ventilation, > 6
35 per group, 6 hr each): 1) biphasic positive airway pressure/airway pressure release ventilation, 0%;
43 S including preinduction continuous positive airway pressure and postextubation NRS for high-risk ind
44 scle pressure can be estimated from the peak airway pressure and the percentage of assistance (gain).
46 ntilator volumes lower in patients with high airway pressures and poor compliance (8.4-10.6 mL/kg int
48 f high frequency jet ventilation in reducing airway pressures and, perhaps, barotraumas are cited.
49 spiratory distress syndrome in whom airflow, airway pressure, and esophageal pressure were recorded d
50 ntilation treatment with continuous positive airway pressure, and other potential ocular and systemic
51 the managing clinician, the ventilator flow, airway pressure, and volume/time waveforms were continuo
52 pwise recruitment maneuver without sustained airway pressure appeared to associate with less biologic
54 ten pigs with acute lung injury at multiple airway pressures, as well as a theoretical model relatin
56 ve ventilation delivered as bilevel positive airway pressure (BiPAP) is often used to avoid reintubat
57 complex and costly than continuous positive airway pressure but might be advantageous because it pro
58 hepatic vein cannot be controlled under high airway pressure, but can be controlled under low airway
59 fraction of inspired oxygen by 0.25 or mean airway pressure by 4), rates ranged from 2.9 to 3.2 per
62 cm H2O) resulted in an increase in change in airway pressure, change in pleural pressure, change in p
63 .0001) after 3 months of continuous positive airway pressure, compared with standard care alone (7.5
64 .0001) after 3 months of continuous positive airway pressure, compared with standard care alone (9.2
66 and the clinical use of continuous positive airway pressure (CPAP) and positive end-expiratory press
67 an alternative to nasal continuous positive airway pressure (CPAP) as a means of respiratory support
69 Meta-analysis found that continuous positive airway pressure (CPAP) compared with sham was significan
70 ms Questionnaire (SASQ), continuous positive airway pressure (CPAP) compliance, and physician decisio
71 and economic benefits of continuous positive airway pressure (CPAP) for moderate to severe obstructiv
72 lar alternative to nasal continuous positive airway pressure (CPAP) for noninvasive respiratory suppo
74 rapy delivered by bubble continuous positive airway pressure (CPAP) improved outcomes compared with s
80 ients who cannot tolerate continous positive airway pressure (CPAP) machines or intraoral devices.
81 gy study performed using continuous positive airway pressure (CPAP) manipulations indicated that the
83 determine the effect of continuous positive airway pressure (CPAP) of patients with OSA on renal hem
84 ive ventilation (NIV) or continuous positive airway pressure (CPAP) on cardiac structure and function
85 ence about the effect of continuous positive airway pressure (CPAP) on glycemic control in patients w
86 n premature infants with continuous positive airway pressure (CPAP) preserves surfactant and keeps th
87 irway pressure (PAP), 3) continuous positive airway pressure (CPAP) rather than noninvasive ventilati
90 to examine the effect of continuous positive airway pressure (CPAP) therapy on atrial fibrillation (A
92 rm studies indicate that continuous positive airway pressure (CPAP) therapy reduces blood pressure in
93 ents had been prescribed continuous positive airway pressure (CPAP) therapy to manage OSA and were id
95 ood pressure response to continuous positive airway pressure (CPAP) treatment is highly variable and
96 ence about the effect of continuous positive airway pressure (CPAP) treatment on blood pressure in pa
97 n women, and the role of continuous positive airway pressure (CPAP) treatment on this association.
98 apeutic decision-making, continuous positive airway pressure (CPAP) treatment or a healthy habit asse
99 A who were intolerant to continuous positive airway pressure (CPAP) treatment, submitted to DISE betw
100 ve ventilation (NIV) and continuous positive airway pressure (CPAP) use in patients with OHS, informa
101 pressure associated with continuous positive airway pressure (CPAP) use, with smaller or uncontrolled
102 of early treatment with continuous positive airway pressure (CPAP) versus early surfactant treatment
103 similar to that of nasal continuous positive airway pressure (CPAP) when used as postextubation suppo
104 am) on morning BP, after continuous positive airway pressure (CPAP) withdrawal in patients with moder
105 We aimed to determine if continuous positive airway pressure (CPAP), a form of non-invasive ventilati
106 o receive treatment with continuous positive airway pressure (CPAP), a weight-loss intervention, or C
107 t for symptomatic OSA is continuous positive airway pressure (CPAP), but its value in patients withou
108 rough the application of continuous positive airway pressure (CPAP), which remains a primary therapeu
109 tilation (IPPV) or nasal continuous positive airway pressure (CPAP)--at the time of the first use of
112 Noninvasive ventilation (continuous positive airway pressure [CPAP] or noninvasive intermittent posit
115 and regression analyses were performed among airway pressure, CVP, and pneumoperitoneum pressure.
118 n predicting 90-day mortality, baseline mean airway pressure demonstrated similar discriminative abil
120 ume loop [in Joules]) and stress relaxation (airway pressure drop during an end-inspiratory pause [in
121 Pmusc/Eadi index was also calculated from airway pressure drop during end-expiratory occlusions.
123 tubation risk factors included lower maximum airway pressure during airway occlusion (aPiMax) preextu
124 vation of the Pmusc/Eadi index from Eadi and airway pressure during an expiratory occlusion enables a
125 ntaneous breathing trials, and the change in airway pressure during an occlusion maneuver to measure
127 glets to investigate the continuous positive airway pressure failure rate with nebulized poractant al
128 for 2 hours (phase 2) or continuous positive airway pressure for 2 hours (phase 3), and then crossove
129 ve treatment of OSA with continuous positive airway pressure for 3 months significantly reduced sever
130 ressure of 30 cm H2O: 1) continuous positive airway pressure for 30 seconds (CPAP-30); 2) stepwise ai
131 alternative treatment to continuous positive airway pressure for patients with obstructive sleep apne
132 spiratory muscle strength (maximal change in airway pressure generated during airway occlusion [PiMax
133 t compensation for more negative inspiratory airway pressures generated during heavy exercise occurs
134 re 1.63 (SD 3.74) in the continuous positive airway pressure group and 1.44 (3.07) in the non-invasiv
135 olic blood pressure occurred in the positive airway pressure group than in the usual care group (-3.5
136 ion group and 107 in the continuous positive airway pressure group were included in the analysis.
137 ed (one allocated to the continuous positive airway pressure group) and all were unrelated to the int
138 years (4.36-6.32) in the continuous positive airway pressure group, and 5.55 years (4.53-6.50) in the
139 ion group and 115 to the continuous positive airway pressure group, of which 97 patients in the non-i
140 rthermore, unlike in the continuous positive airway pressure group, there were no cases of respirator
143 asal cannula therapy and continuous positive airway pressure had similar efficacy (RR, 1.11; 95% CI,
145 ntilation treatment with continuous positive airway pressure have an increased risk of second eye inv
146 ositive airway pressure and bilevel positive airway pressure have been actively introduced in clinica
147 invasive ventilation and continuous positive airway pressure have similar long-term effectiveness.
148 s ventilatory consequences include increased airway pressures, hypercarbia, and decreased pulmonary c
149 months of treatment with continuous positive airway pressure improved the quality of life in patients
150 r whether treatment with continuous positive airway pressure improves daytime function in these patie
151 ructive sleep apnea with continuous positive airway pressure improves not only patient-reported outco
152 the main alternative to continuous positive airway pressure, improves endothelial function in patien
154 improved after starting continuous positive airway pressure in asthmatics with moderate to severe ob
155 al recruitment, but decreased at the maximum airway pressure in nine patients, indicative of a reduct
156 analysis of the ISAACC (Continuous Positive Airway Pressure in Patients with ACS and OSA) study, inc
157 linical effectiveness of continuous positive airway pressure in patients with mild obstructive sleep
158 ntilation treatment with continuous positive airway pressure in patients with severe OSAS increased t
159 tilation was superior to continuous positive airway pressure in preventing extubation failure (RR, 0.
161 similar to that of CPAP-30; and 3) stepwise airway pressure increase (5 cm H2O/step, 5 s at each ste
162 essure for 30 seconds (CPAP-30); 2) stepwise airway pressure increase (5 cm H2O/step, 8.5 s at each s
163 ve intra-abdominal pressure 5 mm Hg, plateau airway pressure increased linearly by ~ 50% of the appli
164 ificantly improved at 24 hours, as were peak airway pressures, intrinsic positive end-expiratory pres
169 proved allograft lung function based on peak airway pressure, less infiltrates/consolidation on micro
170 +10, +15) in a randomized order, with a mean airway pressure level determined by adding 5, 10, or 15
172 ies that use lower end-inspiratory (plateau) airway pressures, lower tidal volumes (VT), and higher p
174 ter; both plans included continuous positive airway pressure, mandibular advancement splints, or cons
175 bjects were treated with continuous positive airway pressure (mean duration of 26 weeks), after which
176 wer complexity and cost, continuous positive airway pressure might be the preferred first-line positi
177 ients were switched to the bi-level positive airway pressure mode with 1 second of 24 cm H2O high pre
180 sal cannula >2 L/min or noninvasive positive airway pressure (n = 617); and grade 3, invasive mechani
181 ort noninferior to nasal continuous positive airway pressure (nCPAP) or bilevel nCPAP (BiPAP) as a pr
182 is optimal: noninvasive continuous positive airway pressure (NCPAP) or intubate-surfactant-extubate
184 fidence interval, 0.96-0.99; p = .017), peak airway pressure (odds ratio per 5-cm H2O increase: 1.11;
186 ticipants who died compared to a median mean airway pressure of 12 cm H2O (interquartile range, 10-14
187 ontrol) lung was kept on continuous positive airway pressure of 20 cm H2O, and CO2 was partially remo
188 ilator settings were an inspiratory positive airway pressure of 24 (IQR, 22-26) cm H2O, an expiratory
189 t recruitment maneuvers, targeted to maximal airway pressure of 30 cm H2O: 1) continuous positive air
190 (IQR, 22-26) cm H2O, an expiratory positive airway pressure of 4 (IQR, 4-5) cm H2O, and a backup rat
191 airway occlusion and on continuous positive airway pressure of 5 and pressure support of 10 above po
193 cording to the protocol of Webb and Tierney (airway pressures of 14/0, 30/0, 45/10, 45/0 cm H2O).
194 raphy (CT) during breath-holding sessions at airway pressures of 5, 15, and 45 cm H2O and Cine-CTs on
195 the beneficial effect of continuous positive airway pressure on quality of life, mood, and work absen
198 rst 72 hours (the use of continuous positive airway pressure or high-flow nasal cannula for at least
199 is commonly treated with continuous positive airway pressure or non-invasive ventilation during sleep
200 high-flow nasal cannula, continuous positive airway pressure, or bilevel noninvasive ventilation in t
201 uired a mask, continuous or bilevel positive airway pressure, or mechanical ventilation were classifi
202 s include weight loss and exercise, positive airway pressure, oral appliances that hold the jaw forwa
203 respiratory system dynamic compliance, mean airway pressure, PaO2/FiO2 ratio, and oxygenation index
204 mbulatory patients with OHS receive positive airway pressure (PAP), 3) continuous positive airway pre
205 toms, adherence to using continuous positive airway pressure, patient satisfaction, and health care c
207 th at least 8 cm H2O positive end-expiratory airway pressure (PEEP), and bilateral infiltrates consis
209 ntilation as a 35 cm H2O continuous positive airway pressure period lasting 3-4 seconds at different
210 ratio, tidal volume, respiratory rate, mean airway pressure, plateau pressure, and hemodynamic varia
211 0.3 +/- 0.1, and 0.3 +/- 0.1 mm Hg/mL/kg for airway pressure, pleural pressure, pericardial pressure,
212 1) to either 3 months of continuous positive airway pressure plus standard care (sleep counselling),
213 uscle pressure, estimated in cm H2O as (peak airway pressure-positive end-expiratory pressure)x[(100-
214 culated from airway pressures alone (plateau airway pressure--positive end-expiratory pressure) did n
215 icted body weight with corresponding plateau airway pressures (PPlat) less than or equal to 30 cm H2O
216 spontaneous breathing or continuous positive airway pressure; pressure support ventilation 5-12 cm H2
217 show that important qualitative features of airway pressure-radius hysteresis loops are highly depen
218 ed by adding 5, 10, or 15 cm H2O to the mean airway pressure recorded during conventional mechanical
219 o a "reference" P0.1 (P0.1ref) measured from airway pressure recording during an occlusion.Methods: A
221 ventional mechanical ventilation (n = 15) or airway pressure release ventilation (n = 12) for 48 hrs
228 ation for acute hypoxic respiratory failure, airway pressure release ventilation is associated with a
229 release ventilation was conducted using the airway pressure release ventilation mode with an inspira
235 mode to prevent intubation and then go on to airway pressure release ventilation, high-frequency osci
236 caused by severe smoke inhalation in swine, airway pressure release ventilation-treated animals deve
239 ation index (p < .05); and 1/PaO2/Fio2, mean airway pressure, serum pH, and Paco2 were associated wit
241 eight, positive end-expiratory pressure, and airway pressure), subjects with an overweight fluid-bala
242 Eadi index obtained during an occlusion from airway pressure swing was tightly correlated with that d
243 ic bifurcations also exhibit higher proximal airway pressures than symmetric ones, but the improvemen
244 ife support, when combined with lower Vt and airway pressures than the current standard of care, may
245 the chest wall allows for calculation of an airway pressure that would place the lung at a desired v
247 icant in those who were adherent to positive airway pressure therapy (-4.4 mm Hg vs. -1.6 mm Hg; P =
248 re previously prescribed continuous positive airway pressure therapy (CPAP) but were dissatisfied wit
251 d at baseline and after 3 months of positive airway pressure therapy in a heterogeneous group of 52 c
252 tiation of autotitrating continuous positive airway pressure therapy in the home has greatly reduced
257 However, it is not known whether positive airway pressure therapy results in improvements in the n
260 ction in children after 3 months of positive airway pressure therapy, even in developmentally delayed
262 expenditure (effort), arterial blood gases, airway pressure, tidal volume and its coefficient of var
264 and inflammation were assessed based on the airway pressure-time index, bronchoalveolar lavage (BAL)
265 nt of confirmed OSA with continuous positive airway pressure to reduce driving risk, rather than no t
267 d by repeatedly lowering continuous positive airway pressure to subtherapeutic levels for 3 minutes d
269 DATION 2: ACP recommends continuous positive airway pressure treatment as initial therapy for patient
271 n alternative therapy to continuous positive airway pressure treatment for patients diagnosed with OS
273 e might be the preferred first-line positive airway pressure treatment modality until more studies be
275 Patients who received continuous positive airway pressure treatment were significantly less likely
276 idences of both OSA (AHI of >/=5 or positive airway pressure treatment) and OSA concomitant with habi
280 ive sleep apnea refusing continuous positive airway pressure treatment.Methods: In an international,
282 spiratory distress syndrome, using high mean airway pressure under high-frequency oscillatory ventila
283 o, 0.98; 0.97-0.99, p = 0.018), initial mean airway pressure (unit odds ratio, 1.13; 1.02-1.28, p = 0
284 h-flow nasal cannula and continuous positive airway pressure use in a monitored setting to prevent re
285 were randomized to three continuous positive airway pressure-ventilated groups: 1) nebulized surfacta
286 We tested whether a continuous positive airway pressure ventilation strategy mitigates ventilato
289 ulticenter prospective cohort, baseline mean airway pressure was independently associated with 90-day
292 of respiratory mechanics based on unmodified airway pressure were misleading regarding lung behavior
294 ar mechanics (derived from alveolar size and airway pressure) were determined in noninjured (n = 9) a
295 was measured 3 times at each of 9 levels of airway pressure, which was increased in increments of 5
296 others were examined over a range of static airway pressures, which varied the extents of regional P
297 y, chronic alcohol abuse, shock, higher peak airway pressure while being mechanically ventilated, cur
298 = 1,500), 65 (4%) were missing baseline mean airway pressure, while 352 (23.5%) were missing baseline
299 infants were ventilated, continuous positive airway pressure without ventilation increased from 7% (1
300 onsiveness during transient manipulations of airway pressure, zolpidem did not alter pharyngeal muscl