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1 r atrophy in limb muscles when compared with respiratory muscle.
2 educing the metabolic demands of cardiac and respiratory muscles.
3 lve truncal, neck-flexor, facial, bulbar and respiratory muscles.
4 ic pressure and it increases the load on the respiratory muscles.
5 with activity related to the contractions of respiratory muscles.
6 ry control system or due to paralysis of the respiratory muscles.
7 rons, leading to atrophy of limb, axial, and respiratory muscles.
8 erception of increased work performed by the respiratory muscles.
9 itional/motor control, including that of the respiratory muscles.
10 ts primarily from the loss of innervation of respiratory muscles.
11 tory complications secondary to paralysis of respiratory muscles.
12 in the work output and metabolic rate of the respiratory muscles.
13 ary component in addition to the weakness of respiratory muscles.
14 uscles of vital organs including cardiac and respiratory muscles.
15 ventilator imposes too little stress on the respiratory muscles.
16 consideration when setting PSV to unload the respiratory muscles.
17 reflect in part structural attributes of the respiratory muscles; (2) that the variation of maximal t
19 exercise and associated effects on dyspnea, respiratory muscle activation, and pulmonary gas exchang
22 isease-specific differences in mechanics and respiratory muscle activity did not influence the key as
23 e vestibular system contributes to adjusting respiratory muscle activity during changes in posture, a
24 he vestibular system contributes to altering respiratory muscle activity during movement and changes
25 tatic pressure tests may not reveal specific respiratory muscle adaptations to disruptions in breathi
26 reathing, and thereby minimize activation of respiratory muscle afferents and motor command, subjects
27 lail chest, interfere with the action of the respiratory muscles-again in a manner unique to each dis
28 s using bioelectrical impedance, quadriceps, respiratory muscle and handgrip strength, and physical p
29 o-IMT) control group on weaning outcomes and respiratory muscle and pulmonary function 28 days after
31 %max), quantifies the mechanical load on the respiratory muscles and relates closely to breathlessnes
32 ed a suppression of tone in the postural and respiratory muscles and simultaneously caused a signific
34 ter fraction of whole-body VO2 towards their respiratory muscles, and demonstrate EIAH, suggesting wo
35 other tissues, including multiple accessory respiratory muscles, and of course the heart itself for
36 r muscles and, albeit to a lesser extent, in respiratory muscles, and they persisted during chronic t
37 lated by means of the recipient's airway and respiratory muscles, and they provided gas exchange in v
38 = 51-63) underwent comprehensive (invasive) respiratory muscle assessment and evaluation of dyspnea.
39 rmal values and in 293 patients referred for respiratory muscle assessment to compare the two measure
40 te that C-26 cancer cachexia causes profound respiratory muscle atrophy and weakness and ventilatory
42 dings suggest the presence of a pathological respiratory muscle blood flow steal phenomenon in PH and
43 rk at a given workload in PH commands higher respiratory muscle blood flow, impairing locomotory musc
45 ypothesis that reflexes arising from working respiratory muscle can elicit increases in sympathetic v
47 An imbalance between work of breathing and respiratory muscle capacity often results in rapid, shal
48 related to physiologic work of breathing and respiratory muscle capacity, should improve application
49 wever, fentanyl also paradoxically activates respiratory muscles causing a potentially lethal effect
50 nd exercise intolerance include skeletal and respiratory muscle contractile and metabolic disturbance
51 aled minute ventilation, and the duration of respiratory muscle contraction assessed by the ratio of
52 is a patient-ventilator interaction where a respiratory muscle contraction is triggered by a passive
53 l, pleural pressures generated during active respiratory muscle contraction, lung resistance and dyna
55 led at least 50 adult ICU patients, reported respiratory muscle (diaphragm or intercostal) ultrasound
57 urons or in coordinating the contractions of respiratory muscles during nonrespiratory responses (e.g
58 of the lung to increase ventilation and not respiratory muscle dysfunction a more attractive explana
59 r, a highly significant relationship between respiratory muscle dysfunction and symptoms of dyspnea.
61 develop respiratory muscle weakness and that respiratory muscle dysfunction may contribute to the une
65 ometer captures chest wall vibrations due to respiratory muscle effort, known as high-frequency mecha
67 reas MV-RDOS score, esophageal pressure, and respiratory muscle EMG did not change as compared with f
68 -RDOS] scores), P(0.1), esophageal pressure, respiratory muscle EMG, and arterial blood gas were comp
70 pogonadal and eugonadal patients had similar respiratory muscle endurance times (302 +/- 29 and 313 +
74 tricular or sinus block requiring pacemaker, respiratory muscle failure requiring mechanical ventilat
75 e: time to severe arrhythmia, heart failure, respiratory muscle failure, and/or cardiomyotoxicity-rel
78 PV in children with acute severe asthma with respiratory muscle fatigue and failure of medical treatm
80 keletal muscle MR deficiency led to improved respiratory muscle force generation and less deleterious
81 eakness (Pdi(sniff) < 30 cm H(2)O), abnormal respiratory muscle function (lesser rise in Pdi) and a l
83 ing several bedside indicators of bulbar and respiratory muscle function can aid in evidence-based ri
84 virus (HIV), the effects of HIV infection on respiratory muscle function have not been well character
86 rage clinicians from having a closer look at respiratory muscle function in critically ill patients.
87 ring and possible implications of monitoring respiratory muscle function in critically ill patients.
88 To test this postulate, we measured limb and respiratory muscle function in nine clinically stable lu
89 uggest a new therapeutic approach to improve respiratory muscle function in patients with respiratory
90 : Inspiratory muscle training (IMT) improves respiratory muscle function in patients with weaning dif
92 nsation of dyspnea was related to indices of respiratory muscle function including respiratory rate a
96 ormal subjects, however, these decrements in respiratory muscle function may result in symptoms of sh
97 s an intact cough reflex as well as adequate respiratory muscle function to generate elevated intrath
99 ance, reducing ventilatory demand, improving respiratory muscle function, and altering central percep
100 LVRS improves not only lung recoil, but also respiratory muscle function, and reduces dynamic hyperin
101 hyperinflation, air trapping, and improving respiratory muscle function, enables the lung and chest
106 muscles, the diaphragm, and heart; limb and respiratory muscle functional improvement; and reduction
108 Heart failure is characterised by limb and respiratory muscle impairments that limit functional cap
109 and imbalance within the diaphragm and other respiratory muscles in emphysema has been considered the
110 s of studying neuronal circuits that control respiratory muscles in humans with better spatial and te
111 enic strains of PRV were injected into these respiratory muscles in nine ferrets; the strain injected
115 siological drivers, the impact of obesity on respiratory muscles-in particular, the diaphragm-has not
116 ientific understanding of ventilator-induced respiratory muscle injury has not reached the stage wher
119 itis indicated that systematic screening for respiratory muscle involvement, coupled with active vent
120 two-step process: the time from diagnosis to respiratory muscle involvement, followed by the time fro
122 nderstanding of disease states affecting the respiratory muscles is necessary for every physician who
123 ition to the diaphragm's role as the primary respiratory muscle, it also plays an under-recognized ro
124 lusion, whilst the diaphragm is an important respiratory muscle, it is likely that dystrophin needs t
126 s and administration of pharmacotherapy, the respiratory muscles may be rendered almost (or completel
127 ung injury, regional forces generated by the respiratory muscles may lead to injurious effects on a r
131 The arterial blood pressure response to the respiratory muscle metaboreflex is greater in older male
133 etically mediated pressor reflex, termed the respiratory muscle metaboreflex, in which young females
134 sed state-dependent changes in breathing and respiratory muscle modulation under urethane anesthesia
135 sses the latest developments in the field of respiratory muscle monitoring and possible implications
136 which include reflex responses recorded from respiratory muscle nerves of the thorax and abdomen.
137 of vestibular-evoked responses recorded from respiratory muscle nerves of the upper airway. as well a
138 ion of airflow (e.g. neuromuscular junction, respiratory muscles or respiratory mechanics) and is not
139 ion, albuterol relieves dyspnea and enhances respiratory muscle output in patients with COPD primaril
142 also led to morbidity and mortality owing to respiratory muscle paralysis and paralysis in the face o
143 a potential nanotherapy for the treatment of respiratory muscle paralysis resulted from cervical SCI.
144 ith muscle fatigue, n = 11) displayed weaker respiratory muscles (Pdi(max) 61 versus 115 cm H(2)O; p
145 y reported that hypogonadism does not affect respiratory muscle performance and exercise capacity in
149 tment algorithm was defined to target a peak respiratory muscle pressure between 5 and 10 cm H2O.
150 tion with load-adjustable gain factors, peak respiratory muscle pressure can be estimated from the pe
151 rements and Main Results: Inflation volumes, respiratory muscle pressure generation, and transpulmona
152 istance to maintain a predefined boundary of respiratory muscle pressure is feasible, simple, and oft
154 .7-1.8) times per day, according to the peak respiratory muscle pressure target range in 91% of cases
156 ning, forced expiratory volumes, and maximum respiratory muscle pressure, leisure-time physical activ
159 ion, exercise performance, gas exchange, and respiratory muscle recruitment (estimated by esophageal
160 comotion to minimize antagonistic loading of respiratory muscles, reduce work of breathing and minimi
161 ing factors such as recruitment of accessory respiratory muscles, reduction in REM sleep, and loss of
162 Mead-Whittenberger technique was used, with respiratory muscle relaxation provided by brief manual v
164 in posture can affect the resting length of respiratory muscles, requiring alterations in the activi
170 with severe COPD occurs as a consequence of respiratory muscle (RM) weakness or fatigue, we would ex
171 pulmonary endpoints that allow assessment of respiratory muscle status, especially in nonambulatory s
173 27, 95% confidence interval 0.02, 0.52), and respiratory muscle strength (g = 0.51, 95% confidence in
174 sure during an occlusion maneuver to measure respiratory muscle strength (maximal change in airway pr
176 c lateral sclerosis (ALS) and measurement of respiratory muscle strength (RMS) has been shown to have
179 sts (PFTs), arterial blood gases (ABGs), and respiratory muscle strength as estimated by maximum stat
181 predictive power of invasive and noninvasive respiratory muscle strength assessments for survival or
182 effect of oral magnesium supplementation on respiratory muscle strength by using manuvacuometry and
183 ith significant bulbar involvement, tests of respiratory muscle strength do not predict hypercapnia.
186 at it could usefully be included in tests of respiratory muscle strength in ALS and will be helpful i
187 neuromuscular disease develop reductions in respiratory muscle strength in association with URI.
188 ntation helped improve both the SK score and respiratory muscle strength in pediatric patients with C
189 n COPD is multifactorial, changes in DCO and respiratory muscle strength may contribute to its intens
194 y, body plethysmography, diffusion capacity, respiratory muscle strength, 6-min walk test, and increm
195 ovement in lung function, exercise capacity, respiratory muscle strength, and ventilatory efficiency.
196 of spontaneous breathing trials, measures of respiratory muscle strength, assessment of risk of poste
197 y of life, physical function, peripheral and respiratory muscle strength, increasing ventilator-free
198 ents with COPD performed pulmonary function, respiratory muscle strength, six-minute walk and cardiop
199 owed a linear decline for direct measures of respiratory muscle strength, whereas VC showed little to
201 ratory problems, including: (1) reduction in respiratory muscle strength; (2) airways hyperresponsive
202 cal evaluations of extremity, hand grip, and respiratory muscle strength; anthropometrics (height, we
203 ate O2 supply and O2 demand in locomotor and respiratory muscles, subjects performed both maximal con
204 nation, complete pulmonary function testing, respiratory muscle testing, cardiopulmonary exercise tes
206 e airways interferes with the ability of the respiratory muscles to generate subatmospheric pressure
207 thing depends on coordinated activity of the respiratory muscles to generate subatmospheric pressure.
209 ss of intercostal muscles, reorganization of respiratory muscles to the ventral side of the ribs, (su
211 ned but respond to aggressive whole-body and respiratory muscle training with an improvement in stren
212 Significant variations exist in the use of respiratory muscle ultrasound in intensive care with no
213 ercise endurance improvements accompanied by respiratory muscle unloading and dyspnea reductions in p
215 (S1): 5 min of normal breathing (NB), 5 min respiratory muscle unloading with a ventilator, and 5 mi
219 alpha causes atrophy and loss of function in respiratory muscle, we asked whether transgenic mice dev
221 2) 67 versus 104% predicted; p < 0.0001) and respiratory muscle weakness (PI(max) 77 versus 115% pred
222 Patient 1 had cervical, limb girdle, and respiratory muscle weakness and died of respiratory fail
224 pothesized that HIV+ individuals may develop respiratory muscle weakness and that respiratory muscle
225 ssociated with relevant axial, proximal, and respiratory muscle weakness but without vocal cord palsy
227 g function tests revealed progressive global respiratory muscle weakness detectable from the time of
229 nale: A model for stratifying progression of respiratory muscle weakness in amyotrophic lateral scler
231 e and early treatment for cardiomyopathy and respiratory muscle weakness is advocated because early t
233 agm atrophy and contractile dysfunction, and respiratory muscle weakness is thought to contribute sig
234 had mucocutaneous involvement, skeletal and respiratory muscle weakness, and myalgia that negatively
241 ow, as well as electromyographic activity in respiratory muscles were recorded in combination with lo
242 heart failure, pulmonary factors, including respiratory muscle work and airflow turbulence, contribu
243 or [2] clinical signs suggestive of intense respiratory muscle work and/or labored breathing) if it
245 blood flow; and reducing the normal level of respiratory muscle work during heavier intensity exercis