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1 sources varied from 0.79 (diabetes) to 0.02 (dyspnea).
2 atients with PH-LHD or otherwise unexplained dyspnea.
3 ecome an efficient tool in the management of dyspnea.
4 pressures during exercise that contribute to dyspnea.
5 1 of 4 RFA animals (25%) developed fever and dyspnea.
6 ed urticaria and one developed urticaria and dyspnea.
7 tigue, neutropenia, alopecia, dizziness, and dyspnea.
8 uction and intermittent wheezing, cough, and dyspnea.
9 tical mechanical constraints and intolerable dyspnea.
10 associated with greater early improvement in dyspnea.
11 individuals undergoing evaluation of chronic dyspnea.
12 e syndrome including fever, hypotension, and dyspnea.
13 year smoking history presents with cough and dyspnea.
14 ock, acutely manifested with hypotension and dyspnea.
15 % of women; P = 0.59), mainly chest pain and dyspnea.
16 pper respiratory tract infection, cough, and dyspnea.
17 tients with poorly controlled disease and/or dyspnea.
18 tted to our hospital because of wheezing and dyspnea.
19 ignificantly associated with the presence of dyspnea.
20 illing pressure in patients with unexplained dyspnea.
21 od from the rectum, progressive fatigue, and dyspnea.
22 th holding of similar duration caused severe dyspnea.
23 aluated in the ED at a Mayo Clinic site with dyspnea.
24 oxygen levels incompatible with life without dyspnea.
25 erizing the burden of PH in individuals with dyspnea.
26 n, generalised muscle weakness, syncope, and dyspnea.
27 t with patient reports of moderate to severe dyspnea.
28 common cause of discontinuation followed by 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%).
31 eath, and 5 hospitalizations-1 chest pain, 2 dyspnea, 1 heart failure, and 1 syncope) over 368+/-156
32 atios (95% confidence intervals) as follows: dyspnea-1.31 (1.10-1.56), 2.20 (1.81-2.68), and 10.73 (8
34 pain (15%), 53 of 387 with chest pain and/or dyspnea (14%), and 49 of 433 with headache (11%) returne
44 .5% of patients, respectively; P < .001) and dyspnea (6.5%, 4.6%, and 0.8% of patients, respectively;
47 I], 1 to 12 percentage points) and help with dyspnea (78% v 70%; adjusted difference, 8 percentage po
49 6%), a 1.6-fold increased odds of exertional dyspnea (95% CI = 1.3-1.9), a 1.5-fold increased odds of
52 pping was the main determinant for decreased dyspnea after surgery (odds ratio, 1.2; 95% confidence i
56 management would be advantageous to improve dyspnea and clinical outcomes while minimizing the risks
57 dney transplant recipient who presented with dyspnea and cough and was diagnosed with COVID-19 pneumo
59 is a clinical syndrome marked by progressive dyspnea and cough with the absence of parenchymal lung d
60 with asthma may falsely attribute exertional dyspnea and esophageal reflux to asthma, leading to exce
65 dry cough, persistent fever, and progressive dyspnea and hypoxia, sometimes accompanied by diarrhea a
71 studied individuals with chronic exertional dyspnea and preserved ejection fraction who underwent ca
76 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 sputum production, pleuritic chest pain, and dyspnea) and no worsening of symptoms at 72 to 120 hours
84 italization within the previous 36 h, active dyspnea, and any of the following: 1) estimated glomerul
85 s cause abrupt onset of nonproductive cough, dyspnea, and chills with arthralgias or malaise usually
90 h left ventricular ejection fraction </=40%, dyspnea, and elevated plasma concentrations of natriuret
91 ), and body mass index, airflow obstruction, dyspnea, and exercise capacity index (adjusted beta = 0.
92 BODE (body mass index, airflow obstruction, dyspnea, and exercise capacity) index, -1.8 points (all
94 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 dyspnea ratings relative to patient-reported dyspnea, and the relationship between nurse-detected dys
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
107 s caring for patients with hypoxemia free of dyspnea are operating in the dark, placing vulnerable pa
109 ints included the clinical congestion score, dyspnea assessment, net urine output, and net weight cha
111 uration were associated with more persistent dyspnea at 24 h (>1 to 12 months, odds ratio [OR]: 1.20;
112 rollment predicted higher risk of persistent dyspnea at 6 hours (per 10 patient increase: odds ratio
113 es up to 5 years after surgery, for example, dyspnea at 6 months (MD 11, 95% CI 4-19) and global QOL
114 90 days; patient-reported thoracic pain and dyspnea at 7, 30, 90, and 180 days; health-related quali
115 dpoint was a 7-point change in self-assessed dyspnea at 8 and 16 h, using a novel standardized approa
118 tive heart failure, paraplegia, reoperation, dyspnea at rest, nongastric band surgery, age >/=60 year
121 dysgeusia (both incidence and severity) and dyspnea (both incidence and severity) in the second pati
122 ly proven HFpEF (n=50) and participants with dyspnea but no identifiable cardiac pathology (n=24).
124 eous disease, often manifesting with wheeze, dyspnea, chest tightness, and cough as prominent symptom
125 ined as no plan to restore sinus rhythm) and dyspnea classified as New York Heart Association class I
126 lated missing data by omitting the predictor dyspnea cohort-wide, and we present 6 methods for handli
127 The geographical, anthropometrics, FEV1, dyspnea, comorbidities, and health status scores were me
128 nce and relief of common symptoms (ie, pain, dyspnea), concordance with patients' wishes for EOL care
129 ential diagnosis of patients presenting with dyspnea, congestion, and a normal ejection fraction.
130 ted high rates of severe symptoms, including dyspnea, constipation, low appetite, fatigue, depression
131 with COPD who experience advanced refractory dyspnea despite otherwise optimal therapy.Conclusions: T
137 toms (eg, odynophagia, dysphagia, dysphonia, dyspnea, earache, nasal obstruction) occurred in 48 (98%
138 tolvaptan to a background diuretic improved dyspnea early in patients selected for an enhanced vasop
139 ically meaningful benefits in lung function, dyspnea, exercise tolerance, and quality of life, with a
141 arging cervical lymphadenopathy, progressive dyspnea, fatigue, night sweats, and an unintentional wei
143 try included normal adjusted mean values for dyspnea grade (0.8), St. George's Respiratory Questionna
144 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),
148 tory of heart disease, symptoms of angina or dyspnea, hemoglobin <12 mg/dl, vascular surgery, and eme
150 A 56-year-old man who developed hypotension, dyspnea, hypoxia, and pulseless electrical activity 10 d
151 FTR was independently associated with more dyspnea, impaired kidney function, and lower cardiac out
155 and patients experiencing moderate or marked dyspnea improvement on day 1 were classified as early re
156 ul CTO PCI was associated with more frequent dyspnea improvement than failure, even after adjustment
159 nous OM did not meet the primary endpoint of dyspnea improvement, but it was generally well tolerated
160 the use of V/Q scanning in the evaluation of dyspnea in adult SCD patients given the important implic
161 ine, to induce sensations of palpitation and dyspnea in healthy individuals (n=23) during arterial sp
165 lling 788 patients hospitalized for AHF with dyspnea, increased plasma concentrations of natriuretic
166 atching (increased dead space) and resultant dyspnea, independent of markers of cardiac function.
167 t (SLS-I and II) using 2 anchors: Transition Dyspnea Index (>/=change of 1.5 units for improvement an
168 ose FEV1, 2-h post-dose FEV1, and Transition Dyspnea Index (TDI) focal score, all measured at week 26
170 ory Questionnaire total score and transition dyspnea index total score and reduction in daily rescue
171 Medical Research Council scale and baseline dyspnea index), quality of life (QoL), mood disorders, e
172 a, wheezing, worsening bronchitis, worsening dyspnea, influenza, pneumonia, other respiratory infecti
173 re, helmet NIV improves oxygenation, reduces dyspnea, inspiratory effort, and simplified pressure-tim
174 entilation efficiency (VE/VCO(2) ratio), and dyspnea intensity (Borg scale) in HF and healthy subject
176 id not influence the key association between dyspnea intensity and inspiratory neural drive to the di
185 PE, 2-pillow orthopnea, paroxysmal nocturnal dyspnea, left and right ventricular structure and functi
187 ncil [mMRC] scale 0 to 4; 4 represents worse dyspnea; MCID, 0.7 units), baseline 6-minute walk distan
188 16, 95% CI 5-26), pain (MD 18, 95% CI 7-30), dyspnea (MD 15, 95% CI 2-27), insomnia (MD 20, 95% CI 8-
189 of life (QOL) (MD -10, 95% CI -18 to -2) and dyspnea (MD 16, 95% CI 5-27) from 3 years onwards, compa
190 Secondary outcomes were baseline measures of dyspnea (modified Medical Research Council [mMRC] scale
191 , 44.3 pack-years), we evaluated spirometry, dyspnea (modified Medical Research Council grade, >/=2),
192 pic diseases), symptoms (chronic bronchitis, dyspnea-modified Medical Research Council scale and base
193 llow-up examination of survivors, persistent dyspnea (mostly mild) or functional limitation was repor
196 common clinical presentation was exertional dyspnea (n=17; 65%), whereas 8 (31%) patients had no wor
197 consecutive patients with chronic exertional dyspnea (New York Heart Association class II to IV) and
198 NOCA subjects (n=185; 47%) had more limiting dyspnea (New York Heart Association classification III/I
199 ubjects (age 67 +/- 9 years) with exertional dyspnea (New York Heart Association functional class II
200 with stage C heart failure (HF) (exertional dyspnea, New York Heart Association functional class II
201 erval [CI], 1.30-2.12), paroxysmal nocturnal dyspnea (odds ratio 1.95; 95% CI, 1.55-2.44), and abnorm
202 he developed a nonproductive cough and mild dyspnea on exertion (Modified Medical Research Council d
209 apy with LABA/LAMA in patients with COPD and dyspnea or exercise intolerance who have experienced one
210 r LAMA monotherapy in patients with COPD and dyspnea or exercise intolerance; 2) a conditional recomm
211 lure is a clinical syndrome characterized by dyspnea or exertional limitation due to impairment of ve
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,
224 he accuracy of nurses and personal caregiver dyspnea ratings relative to patient-reported dyspnea, an
226 difference in the primary endpoint of day 1 dyspnea reduction, despite significantly greater weight
227 Versus the comparators, the relative risk of dyspnea-related discontinuation during follow-up was 6.4
228 Objectives: To determine the frequency of dyspnea relative to pain, the accuracy of nurses and per
229 , OM did not improve the primary endpoint of dyspnea relief (3 OM dose groups and pooled placebo: pla
230 e temporal relationship between diuresis and dyspnea relief and a possible clinical role for tolvapta
231 independently associated with greater early dyspnea relief and improved post-discharge survival comp
232 However, the association between short-term dyspnea relief and postdischarge clinical outcomes and h
233 e-specified analyses, OM resulted in greater dyspnea relief at 48 h (placebo, 37% vs. OM, 51%; p = 0.
238 with other potentially noncardiac causes of dyspnea reported less dyspnea improvement after CTO PCI.
239 6MWD), the Modified Medical Research Council Dyspnea Scale (mMRC), the COPD Assessment Test (CAT), St
241 82%) were assessed for dyspnea with the Rose Dyspnea Scale at baseline and 1 month after CTO PCI.
244 PF, breathlessness (Medical Research Council dyspnea scale score >1), and impaired lung function (for
245 exertion (Modified Medical Research Council dyspnea scale score of 2 [ie, he had to stop for breath
246 mptomatic (modified Medical Research Council dyspnea scale score, >=2; or COPD Assessment Test score,
247 predicted; modified Medical Research Council dyspnea scale score, 2.2 +/- 0.7; COPD Assessment Test s
249 -reported outcomes (Medical Research Council dyspnea scale, 5-level EuroQol 5-dimension questionnaire
250 e 12-Item Short Form Health Survey, the Rose Dyspnea Scale, the Patient Health Questionnaire-8, and t
251 1.2 to -0.2; P=0.009), and postexercise Borg dyspnea score (-2.0; 95% CI, -3.7 to -0.3; P=0.04), but
252 correlated with the Medical Research Council dyspnea score (r = 0.34; P < 0.0001), FEV1% predicted (r
254 .5 points; modified Medical Research Council dyspnea score, -0.6 points; and BODE (body mass index, a
258 echanical inspiratory constraints and higher dyspnea scores for a given work rate leading to poorer e
262 pirometry and multiple phenotypes, including dyspnea severity (Modified Medical Research Council grad
263 l, role, and social functioning and fatigue, dyspnea, sleep, and financial problems were severely and
264 c, reported a complete lack of awareness for dyspnea, suggestive of impaired respiratory interoceptio
265 alpitations, orthopnea, paroxysmal nocturnal dyspnea, swelling of the legs or feet, abdominal pain, n
266 e nonmajor, and 86% of adverse events due to dyspnea that led to discontinuation of treatment with ti
267 everity of lung impairment, symptoms such as dyspnea, the amount of cough and sputum production, and
269 ression defined by 48-week worsening of FVC, dyspnea (University of California, San Diego Shortness o
270 hospitalized for acute heart failure and had dyspnea, vascular congestion on chest radiography, incre
271 examine whether triggering palpitations and dyspnea via stimulation of non-chemosensory interoceptiv
272 [43-138] vs. 200 [168-335]; P = 0.001), and dyspnea (visual analog scale 3 [2-5] vs. 8 [6-9]; P = 0.
273 notably of respiratory status at admission (dyspnea-Visual Analogic Scale and PaCO2 >= 45 mm Hg).
278 Control Test (ACT) score <20 (n = 287), and dyspnea was defined as a modified Medical Research Counc
281 Physician-assessed and patient-reported dyspnea was not independently associated with HRQOL, all
282 tal physician-assessed, and patient-reported dyspnea was not independently associated with postdischa
283 wever, nurse detection of moderate to severe dyspnea was not significantly associated with any assess
284 in 97 (61%), cough was observed in 88 (56%), dyspnea was observed in 52 (33%), lymphocytopenia was ob
288 raters, the frequency of moderate to severe dyspnea was similar or greater than that of pain (P < 0.
290 t, minor allergic symptoms of urticarial and dyspnea were observed on two occasions, but they disappe
292 a, diarrhea, fatigue, pain, paresthesia, and dyspnea were translated into Italian and rephrased.
293 tive heart failure, acute renal failure, and dyspnea) were analyzed in terms of agreement between adm
294 selected patients presenting to the ED with dyspnea when analyzed with artificial intelligence and o
296 s attributable to an increased perception of dyspnea, which, during exercise, is mainly associated wi
297 led ECG to identify patients presenting with dyspnea who have left ventricular systolic dysfunction (
300 CI (procedure success 82%) were assessed for dyspnea with the Rose Dyspnea Scale at baseline and 1 mo