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1 pper respiratory tract infection, cough, and dyspnea.
2 tients with poorly controlled disease and/or dyspnea.
3 tted to our hospital because of wheezing and dyspnea.
4 ed urticaria and one developed urticaria and dyspnea.
5 ignificantly associated with the presence of dyspnea.
6 illing pressure in patients with unexplained dyspnea.
7 od from the rectum, progressive fatigue, and dyspnea.
8 th holding of similar duration caused severe dyspnea.
9 nts presenting to the ED with chest pain and dyspnea.
10 nts presenting to the ED with chest pain and dyspnea.
11 spital stay for patients with chest pain and dyspnea.
12 ed reflexes and sensations such as cough and dyspnea.
13 filling pressures with resultant symptoms of dyspnea.
14 patient required treatment for self-limited dyspnea.
15 rea were independently associated with worse dyspnea.
16 ith chemotherapy were fatigue, alopecia, and dyspnea.
17 ents with either condition may be limited by dyspnea.
18 emotions, to +0.96 (95% CI = 0.57-1.35) for dyspnea.
19 lc pleurodesis at relieving patient-reported dyspnea.
20 o update the 1999 ATS Consensus Statement on dyspnea.
21 uction and intermittent wheezing, cough, and dyspnea.
22 tical mechanical constraints and intolerable dyspnea.
23 associated with greater early improvement in dyspnea.
24 e syndrome including fever, hypotension, and dyspnea.
25 pressures during exercise that contribute to dyspnea.
26 year smoking history presents with cough and dyspnea.
27 ock, acutely manifested with hypotension and dyspnea.
28 % of women; P = 0.59), mainly chest pain and dyspnea.
29 lushes (0.8% v 0.4%), myalgia (0.8% v 0.7%), dyspnea (0.8% v 0.5%), and depression (0.8% v 0.6%).
30 atios (95% confidence intervals) as follows: dyspnea-1.31 (1.10-1.56), 2.20 (1.81-2.68), and 10.73 (8
31 pain (15%), 53 of 387 with chest pain and/or dyspnea (14%), and 49 of 433 with headache (11%) returne
35 plus-exemestane group), anemia (6% vs. <1%), dyspnea (4% vs. 1%), hyperglycemia (4% vs. <1%), fatigue
40 .5% of patients, respectively; P < .001) and dyspnea (6.5%, 4.6%, and 0.8% of patients, respectively;
43 I], 1 to 12 percentage points) and help with dyspnea (78% v 70%; adjusted difference, 8 percentage po
45 ); nocturnal cough (33% vs. 26%; P = 0.005); dyspnea (8% vs. 4%; P = 0.011); and use of medication (i
46 6%), a 1.6-fold increased odds of exertional dyspnea (95% CI = 1.3-1.9), a 1.5-fold increased odds of
47 a 1-week history of chest pain, progressive dyspnea, abdominal swelling, bipedal edema, and anorexia
55 management would be advantageous to improve dyspnea and clinical outcomes while minimizing the risks
57 is a clinical syndrome marked by progressive dyspnea and cough with the absence of parenchymal lung d
59 gns and symptoms of heart failure, including dyspnea and edema due to inability of the severely disea
60 with asthma may falsely attribute exertional dyspnea and esophageal reflux to asthma, leading to exce
66 Furthermore, since he developed progressive dyspnea and hypoxemia, he was admitted to our hospital.
77 1.5%), fatigue (51.5%), pyrexia (42.4%), and dyspnea and thrombocytopenia (each 39.4%) were the most
80 t Pain), patients with stable chest pain (or dyspnea) and intermediate pretest probability for obstru
81 rrhea, loss of sense of smell, wheezing, and dyspnea) and on quality-of-life scores, irrespective of
82 spiratory tract (cough, wheeze, stridor, and dyspnea), and/or the gastrointestinal tract (persistent
85 italization within the previous 36 h, active dyspnea, and any of the following: 1) estimated glomerul
88 te walk distance, progression-free survival, dyspnea, and death from any cause or from idiopathic pul
89 h left ventricular ejection fraction </=40%, dyspnea, and elevated plasma concentrations of natriuret
90 higher Body Mass Index, Airflow Obstruction, Dyspnea, and Exercise Capacity (BODE) index (0.31 [0.19
92 ), and body mass index, airflow obstruction, dyspnea, and exercise capacity index (adjusted beta = 0.
93 BODE (body mass index, airflow obstruction, dyspnea, and exercise capacity) index, -1.8 points (all
95 cores, Body-mass index, airflow Obstruction, Dyspnea, and Exercise index, or Global Initiative for Ch
98 ients with abdominal pain, chest pain and/or dyspnea, and headache; P < .0001); median post-CT confid
99 hese 5 patients had a history of progressive dyspnea, and the anomalous cord, which was intact at ope
100 es after ingestion, he experienced coughing, dyspnea, and wheezing and had to be treated by anti-hist
104 Attention to symptoms of weight gain and dyspnea are central tenets of patient education in heart
108 ssification schema based on patient-reported dyspnea assessed both pre- and post-ultrafiltration, in
110 ints included the clinical congestion score, dyspnea assessment, net urine output, and net weight cha
112 uration were associated with more persistent dyspnea at 24 h (>1 to 12 months, odds ratio [OR]: 1.20;
113 rollment predicted higher risk of persistent dyspnea at 6 hours (per 10 patient increase: odds ratio
114 dpoint was a 7-point change in self-assessed dyspnea at 8 and 16 h, using a novel standardized approa
116 failure, systolic blood pressure >125 mm Hg, dyspnea at rest or with mild exertion, intravenous diure
118 tive heart failure, paraplegia, reoperation, dyspnea at rest, nongastric band surgery, age >/=60 year
120 dysgeusia (both incidence and severity) and dyspnea (both incidence and severity) in the second pati
121 ced CT group], two patients with progressive dyspnea [both in the contrast-enhanced CT group], and on
122 ly proven HFpEF (n=50) and participants with dyspnea but no identifiable cardiac pathology (n=24).
123 equently present with exertional fatigue and dyspnea, but the hemodynamic basis for exercise limitati
125 lated missing data by omitting the predictor dyspnea cohort-wide, and we present 6 methods for handli
126 The geographical, anthropometrics, FEV1, dyspnea, comorbidities, and health status scores were me
127 nce and relief of common symptoms (ie, pain, dyspnea), concordance with patients' wishes for EOL care
128 ential diagnosis of patients presenting with dyspnea, congestion, and a normal ejection fraction.
129 ted high rates of severe symptoms, including dyspnea, constipation, low appetite, fatigue, depression
130 se HRQoL with respect to cognitive function, dyspnea, constipation, thirst, leg swelling, numbness, d
135 elor significantly enhanced the sensation of dyspnea during adenosine infusion, and the effects were
137 ction are strongly related to an increase in dyspnea during bronchial provocation with methacholine.
140 toms (eg, odynophagia, dysphagia, dysphonia, dyspnea, earache, nasal obstruction) occurred in 48 (98%
141 tolvaptan to a background diuretic improved dyspnea early in patients selected for an enhanced vasop
143 ically meaningful benefits in lung function, dyspnea, exercise tolerance, and quality of life, with a
145 arging cervical lymphadenopathy, progressive dyspnea, fatigue, night sweats, and an unintentional wei
147 ly respiratory (five patients with new-onset dyspnea [four in contrast-enhanced CT group and one in u
148 try included normal adjusted mean values for dyspnea grade (0.8), St. George's Respiratory Questionna
149 R, 4.80; 95% CI, 1.68-13.69; P = 0.003), MRC dyspnea grade (OR, 2.57; 95% CI, 1.44-4.59; P = 0.001),
150 ; P = 0.015), Medical Research Council (MRC) dyspnea grade (OR, 4.57; 95% CI, 2.62-7.95; P < 0.001),
153 A 56-year-old man who developed hypotension, dyspnea, hypoxia, and pulseless electrical activity 10 d
157 -h PEFR change related to moderate or marked dyspnea improvement by DI (adjusted odds ratio: 1.04 for
158 and patients experiencing moderate or marked dyspnea improvement on day 1 were classified as early re
159 ul CTO PCI was associated with more frequent dyspnea improvement than failure, even after adjustment
162 nous OM did not meet the primary endpoint of dyspnea improvement, but it was generally well tolerated
164 ding lung function (100 ml for trough FEV1), dyspnea (improvement of >/= 1 unit in the Transition Dys
166 ine, to induce sensations of palpitation and dyspnea in healthy individuals (n=23) during arterial sp
171 adenosine-induced CBFV and the sensation of dyspnea in these healthy male subjects via an adenosine-
172 atching (increased dead space) and resultant dyspnea, independent of markers of cardiac function.
173 t (SLS-I and II) using 2 anchors: Transition Dyspnea Index (>/=change of 1.5 units for improvement an
174 ose FEV1, 2-h post-dose FEV1, and Transition Dyspnea Index (TDI) focal score, all measured at week 26
176 ory Questionnaire total score and transition dyspnea index total score and reduction in daily rescue
177 (improvement of >/= 1 unit in the Transition Dyspnea Index total score or 5 units in the University o
178 ratory Questionnaire total score, transition dyspnea index total score, and reduction in rescue medic
179 Medical Research Council scale and baseline dyspnea index), quality of life (QoL), mood disorders, e
182 id not influence the key association between dyspnea intensity and inspiratory neural drive to the di
190 PE, 2-pillow orthopnea, paroxysmal nocturnal dyspnea, left and right ventricular structure and functi
191 ncil [mMRC] scale 0 to 4; 4 represents worse dyspnea; MCID, 0.7 units), baseline 6-minute walk distan
192 Secondary outcomes were baseline measures of dyspnea (modified Medical Research Council [mMRC] scale
193 , 44.3 pack-years), we evaluated spirometry, dyspnea (modified Medical Research Council grade, >/=2),
194 pic diseases), symptoms (chronic bronchitis, dyspnea-modified Medical Research Council scale and base
195 llow-up examination of survivors, persistent dyspnea (mostly mild) or functional limitation was repor
197 common clinical presentation was exertional dyspnea (n=17; 65%), whereas 8 (31%) patients had no wor
198 ubjects (age 67 +/- 9 years) with exertional dyspnea (New York Heart Association functional class II
199 with stage C heart failure (HF) (exertional dyspnea, New York Heart Association functional class II
201 y more patient complaints of acute transient dyspnea occurred after gadoxetate disodium administratio
202 nt were low in both groups, though transient dyspnea occurred significantly more frequently with cang
205 erval [CI], 1.30-2.12), paroxysmal nocturnal dyspnea (odds ratio 1.95; 95% CI, 1.55-2.44), and abnorm
206 he developed a nonproductive cough and mild dyspnea on exertion (Modified Medical Research Council d
213 er cough, sputum, fever/chills/night sweats, dyspnea or pleuritic chest pain) or with Pneumonia-in-Pl
214 928 of 2395 (38.8%) with available data had dyspnea or respiratory distress, and hospitalizations oc
220 tion of fever, higher morbidity of tachypnea/dyspnea, pleural effusion, diarrhea, hepatosplenomegaly,
221 most common treatment-emergent SAEs included dyspnea, pneumonia, febrile neutropenia, dehydration, an
227 difference in the primary endpoint of day 1 dyspnea reduction, despite significantly greater weight
228 ompanied by respiratory muscle unloading and dyspnea reductions in patients with severe hypoxemic COP
229 Hg) and the percentage of patients achieving dyspnea relief (17.7%, 24.6%, 32.2%, 36.2%, 37.8%, 47.4%
230 , OM did not improve the primary endpoint of dyspnea relief (3 OM dose groups and pooled placebo: pla
231 e temporal relationship between diuresis and dyspnea relief and a possible clinical role for tolvapta
232 independently associated with greater early dyspnea relief and improved post-discharge survival comp
233 However, the association between short-term dyspnea relief and postdischarge clinical outcomes and h
234 e-specified analyses, OM resulted in greater dyspnea relief at 48 h (placebo, 37% vs. OM, 51%; p = 0.
241 PCWP quartile, the adjusted odds ratios for dyspnea relief were 0.92 (95% confidence interval [CI],
242 ssure quartile, the adjusted odds ratios for dyspnea relief were 2.0 (95% CI, 1.41-2.82), 2.23 (95% C
245 with other potentially noncardiac causes of dyspnea reported less dyspnea improvement after CTO PCI.
246 ergometer exercise and associated effects on dyspnea, respiratory muscle activation, and pulmonary ga
247 6MWD), the Modified Medical Research Council Dyspnea Scale (mMRC), the COPD Assessment Test (CAT), St
248 82%) were assessed for dyspnea with the Rose Dyspnea Scale at baseline and 1 month after CTO PCI.
251 exertion (Modified Medical Research Council dyspnea scale score of 2 [ie, he had to stop for breath
253 n, body mass index, Medical Research Council dyspnea scale, disease severity, and demographic data we
254 ime to clinical worsening, score on the Borg dyspnea scale, quality-of-life variables, and safety.
255 e 12-Item Short Form Health Survey, the Rose Dyspnea Scale, the Patient Health Questionnaire-8, and t
257 correlated with the Medical Research Council dyspnea score (r = 0.34; P < 0.0001), FEV1% predicted (r
258 ospital admissions, Medical Research Council dyspnea score greater than or equal to 4, FEV1 < 30% pre
259 .5 points; modified Medical Research Council dyspnea score, -0.6 points; and BODE (body mass index, a
260 onal class, time to clinical worsening, Borg dyspnea score, quality-of-life variables, and safety.
261 s no significant between-group difference in dyspnea scores (P=0.16) or in rates of death from any ca
262 ry and impulse oscillometry, as well as Borg dyspnea scores at baseline and during a methacholine pro
264 echanical inspiratory constraints and higher dyspnea scores for a given work rate leading to poorer e
265 g-swallowing synchronization, and Borg Scale dyspnea scores improved significantly with noninvasive m
266 as associated with a higher increase in Borg dyspnea scores in subjects with asymptomatic BHR, but no
270 pirometry and multiple phenotypes, including dyspnea severity (Modified Medical Research Council grad
271 c, reported a complete lack of awareness for dyspnea, suggestive of impaired respiratory interoceptio
272 e disodium can result in acute self-limiting dyspnea that can have a deleterious effect on arterial p
273 e nonmajor, and 86% of adverse events due to dyspnea that led to discontinuation of treatment with ti
275 ression defined by 48-week worsening of FVC, dyspnea (University of California, San Diego Shortness o
276 examine whether triggering palpitations and dyspnea via stimulation of non-chemosensory interoceptiv
281 Control Test (ACT) score <20 (n = 287), and dyspnea was defined as a modified Medical Research Counc
284 Physician-assessed and patient-reported dyspnea was not independently associated with HRQOL, all
285 tal physician-assessed, and patient-reported dyspnea was not independently associated with postdischa
292 t, minor allergic symptoms of urticarial and dyspnea were observed on two occasions, but they disappe
293 a, diarrhea, fatigue, pain, paresthesia, and dyspnea were translated into Italian and rephrased.
294 o leads to background symptomatology such as dyspnea, which can mask the clinical diagnosis of cardia
295 normal breathing-swallowing interactions and dyspnea, which improved with noninvasive mechanical vent
296 s attributable to an increased perception of dyspnea, which, during exercise, is mainly associated wi
299 consists of unexplained fever, weight gain, dyspnea with pulmonary infiltrates, pleuropericardial ef
300 CI (procedure success 82%) were assessed for dyspnea with the Rose Dyspnea Scale at baseline and 1 mo
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