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1 r atrophy in limb muscles when compared with respiratory muscle.
2 ic pressure and it increases the load on the respiratory muscles.
3 with activity related to the contractions of respiratory muscles.
4 ry control system or due to paralysis of the respiratory muscles.
5 rons, leading to atrophy of limb, axial, and respiratory muscles.
6 erception of increased work performed by the respiratory muscles.
7 itional/motor control, including that of the respiratory muscles.
8 ts primarily from the loss of innervation of respiratory muscles.
9 tory complications secondary to paralysis of respiratory muscles.
10 in the work output and metabolic rate of the respiratory muscles.
11 ary component in addition to the weakness of respiratory muscles.
12 ventilator imposes too little stress on the respiratory muscles.
13 consideration when setting PSV to unload the respiratory muscles.
14 educing the metabolic demands of cardiac and respiratory muscles.
15 lve truncal, neck-flexor, facial, bulbar and respiratory muscles.
16 reflect in part structural attributes of the respiratory muscles; (2) that the variation of maximal t
18 exercise and associated effects on dyspnea, respiratory muscle activation, and pulmonary gas exchang
21 isease-specific differences in mechanics and respiratory muscle activity did not influence the key as
22 e vestibular system contributes to adjusting respiratory muscle activity during changes in posture, a
23 he vestibular system contributes to altering respiratory muscle activity during movement and changes
24 reathing, and thereby minimize activation of respiratory muscle afferents and motor command, subjects
25 lail chest, interfere with the action of the respiratory muscles-again in a manner unique to each dis
26 s using bioelectrical impedance, quadriceps, respiratory muscle and handgrip strength, and physical p
28 %max), quantifies the mechanical load on the respiratory muscles and relates closely to breathlessnes
29 ed a suppression of tone in the postural and respiratory muscles and simultaneously caused a signific
31 ter fraction of whole-body VO2 towards their respiratory muscles, and demonstrate EIAH, suggesting wo
32 other tissues, including multiple accessory respiratory muscles, and of course the heart itself for
33 lated by means of the recipient's airway and respiratory muscles, and they provided gas exchange in v
34 rmal values and in 293 patients referred for respiratory muscle assessment to compare the two measure
35 te that C-26 cancer cachexia causes profound respiratory muscle atrophy and weakness and ventilatory
37 ypothesis that reflexes arising from working respiratory muscle can elicit increases in sympathetic v
39 An imbalance between work of breathing and respiratory muscle capacity often results in rapid, shal
40 related to physiologic work of breathing and respiratory muscle capacity, should improve application
41 aled minute ventilation, and the duration of respiratory muscle contraction assessed by the ratio of
42 l, pleural pressures generated during active respiratory muscle contraction, lung resistance and dyna
45 urons or in coordinating the contractions of respiratory muscles during nonrespiratory responses (e.g
46 of the lung to increase ventilation and not respiratory muscle dysfunction a more attractive explana
47 r, a highly significant relationship between respiratory muscle dysfunction and symptoms of dyspnea.
49 develop respiratory muscle weakness and that respiratory muscle dysfunction may contribute to the une
53 pogonadal and eugonadal patients had similar respiratory muscle endurance times (302 +/- 29 and 313 +
57 PV in children with acute severe asthma with respiratory muscle fatigue and failure of medical treatm
59 eakness (Pdi(sniff) < 30 cm H(2)O), abnormal respiratory muscle function (lesser rise in Pdi) and a l
61 virus (HIV), the effects of HIV infection on respiratory muscle function have not been well character
63 rage clinicians from having a closer look at respiratory muscle function in critically ill patients.
64 ring and possible implications of monitoring respiratory muscle function in critically ill patients.
65 To test this postulate, we measured limb and respiratory muscle function in nine clinically stable lu
66 uggest a new therapeutic approach to improve respiratory muscle function in patients with respiratory
68 nsation of dyspnea was related to indices of respiratory muscle function including respiratory rate a
72 ormal subjects, however, these decrements in respiratory muscle function may result in symptoms of sh
73 s an intact cough reflex as well as adequate respiratory muscle function to generate elevated intrath
75 ance, reducing ventilatory demand, improving respiratory muscle function, and altering central percep
76 LVRS improves not only lung recoil, but also respiratory muscle function, and reduces dynamic hyperin
77 hyperinflation, air trapping, and improving respiratory muscle function, enables the lung and chest
82 and imbalance within the diaphragm and other respiratory muscles in emphysema has been considered the
83 s of studying neuronal circuits that control respiratory muscles in humans with better spatial and te
84 enic strains of PRV were injected into these respiratory muscles in nine ferrets; the strain injected
88 ientific understanding of ventilator-induced respiratory muscle injury has not reached the stage wher
90 two-step process: the time from diagnosis to respiratory muscle involvement, followed by the time fro
92 nderstanding of disease states affecting the respiratory muscles is necessary for every physician who
93 lusion, whilst the diaphragm is an important respiratory muscle, it is likely that dystrophin needs t
95 s and administration of pharmacotherapy, the respiratory muscles may be rendered almost (or completel
96 ung injury, regional forces generated by the respiratory muscles may lead to injurious effects on a r
97 sed state-dependent changes in breathing and respiratory muscle modulation under urethane anesthesia
98 sses the latest developments in the field of respiratory muscle monitoring and possible implications
99 which include reflex responses recorded from respiratory muscle nerves of the thorax and abdomen.
100 of vestibular-evoked responses recorded from respiratory muscle nerves of the upper airway. as well a
101 ion of airflow (e.g. neuromuscular junction, respiratory muscles or respiratory mechanics) and is not
102 ion, albuterol relieves dyspnea and enhances respiratory muscle output in patients with COPD primaril
105 also led to morbidity and mortality owing to respiratory muscle paralysis and paralysis in the face o
106 a potential nanotherapy for the treatment of respiratory muscle paralysis resulted from cervical SCI.
107 ith muscle fatigue, n = 11) displayed weaker respiratory muscles (Pdi(max) 61 versus 115 cm H(2)O; p
108 y reported that hypogonadism does not affect respiratory muscle performance and exercise capacity in
112 tment algorithm was defined to target a peak respiratory muscle pressure between 5 and 10 cm H2O.
113 tion with load-adjustable gain factors, peak respiratory muscle pressure can be estimated from the pe
114 istance to maintain a predefined boundary of respiratory muscle pressure is feasible, simple, and oft
116 .7-1.8) times per day, according to the peak respiratory muscle pressure target range in 91% of cases
118 ning, forced expiratory volumes, and maximum respiratory muscle pressure, leisure-time physical activ
120 ion, exercise performance, gas exchange, and respiratory muscle recruitment (estimated by esophageal
121 comotion to minimize antagonistic loading of respiratory muscles, reduce work of breathing and minimi
122 ing factors such as recruitment of accessory respiratory muscles, reduction in REM sleep, and loss of
123 Mead-Whittenberger technique was used, with respiratory muscle relaxation provided by brief manual v
125 in posture can affect the resting length of respiratory muscles, requiring alterations in the activi
131 with severe COPD occurs as a consequence of respiratory muscle (RM) weakness or fatigue, we would ex
132 pulmonary endpoints that allow assessment of respiratory muscle status, especially in nonambulatory s
134 27, 95% confidence interval 0.02, 0.52), and respiratory muscle strength (g = 0.51, 95% confidence in
136 c lateral sclerosis (ALS) and measurement of respiratory muscle strength (RMS) has been shown to have
138 sts (PFTs), arterial blood gases (ABGs), and respiratory muscle strength as estimated by maximum stat
140 predictive power of invasive and noninvasive respiratory muscle strength assessments for survival or
141 effect of oral magnesium supplementation on respiratory muscle strength by using manuvacuometry and
142 ith significant bulbar involvement, tests of respiratory muscle strength do not predict hypercapnia.
145 at it could usefully be included in tests of respiratory muscle strength in ALS and will be helpful i
146 neuromuscular disease develop reductions in respiratory muscle strength in association with URI.
147 ntation helped improve both the SK score and respiratory muscle strength in pediatric patients with C
148 n COPD is multifactorial, changes in DCO and respiratory muscle strength may contribute to its intens
153 y, body plethysmography, diffusion capacity, respiratory muscle strength, 6-min walk test, and increm
154 ovement in lung function, exercise capacity, respiratory muscle strength, and ventilatory efficiency.
155 y of life, physical function, peripheral and respiratory muscle strength, increasing ventilator-free
156 owed a linear decline for direct measures of respiratory muscle strength, whereas VC showed little to
158 cal evaluations of extremity, hand grip, and respiratory muscle strength; anthropometrics (height, we
159 ate O2 supply and O2 demand in locomotor and respiratory muscles, subjects performed both maximal con
160 nation, complete pulmonary function testing, respiratory muscle testing, cardiopulmonary exercise tes
162 e airways interferes with the ability of the respiratory muscles to generate subatmospheric pressure
163 thing depends on coordinated activity of the respiratory muscles to generate subatmospheric pressure.
165 ss of intercostal muscles, reorganization of respiratory muscles to the ventral side of the ribs, (su
167 ned but respond to aggressive whole-body and respiratory muscle training with an improvement in stren
168 ercise endurance improvements accompanied by respiratory muscle unloading and dyspnea reductions in p
170 (S1): 5 min of normal breathing (NB), 5 min respiratory muscle unloading with a ventilator, and 5 mi
173 alpha causes atrophy and loss of function in respiratory muscle, we asked whether transgenic mice dev
175 2) 67 versus 104% predicted; p < 0.0001) and respiratory muscle weakness (PI(max) 77 versus 115% pred
176 Patient 1 had cervical, limb girdle, and respiratory muscle weakness and died of respiratory fail
177 pothesized that HIV+ individuals may develop respiratory muscle weakness and that respiratory muscle
178 ssociated with relevant axial, proximal, and respiratory muscle weakness but without vocal cord palsy
180 g function tests revealed progressive global respiratory muscle weakness detectable from the time of
183 e and early treatment for cardiomyopathy and respiratory muscle weakness is advocated because early t
185 agm atrophy and contractile dysfunction, and respiratory muscle weakness is thought to contribute sig
192 ow, as well as electromyographic activity in respiratory muscles were recorded in combination with lo
193 heart failure, pulmonary factors, including respiratory muscle work and airflow turbulence, contribu
194 or [2] clinical signs suggestive of intense respiratory muscle work and/or labored breathing) if it
195 blood flow; and reducing the normal level of respiratory muscle work during heavier intensity exercis
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