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1 the deep veins, one peripheral vein and one pulmonary embolism).
2 mboembolic events (deep venous thrombosis or pulmonary embolism).
3 e) and two PCC related (ischaemic stroke and pulmonary embolism).
4 ry angiography was performed to evaluate for pulmonary embolism.
5 ctor for deep vein thrombosis of the leg and pulmonary embolism.
6 ment of the pulmonary trunk to investigate a pulmonary embolism.
7 ired infections, venous thromboembolism, and pulmonary embolism.
8 ay of treatment for deep vein thrombosis and pulmonary embolism.
9 ciated with certain causes of arrest such as pulmonary embolism.
10 dentification of PH after exclusion of acute pulmonary embolism.
11 rotected mice from prostasome-induced lethal pulmonary embolism.
12 ombosis can lead to deep-vein thrombosis and pulmonary embolism.
13 venous thromboembolic events with or without pulmonary embolism.
14 nt travel history, there was suspicion for a pulmonary embolism.
15 nts, as well as for deep vein thrombosis and pulmonary embolism.
16 usceptible than Par4(-/-) mice to TF-induced pulmonary embolism.
17 with symptoms of acute coronary syndrome and pulmonary embolism.
18 g and life-threatening complication of acute pulmonary embolism.
19 ms suggestive of acute coronary syndrome and pulmonary embolism.
20 thrombosis can cause venous obstruction and pulmonary embolism.
21 normotensive patients with intermediate-risk pulmonary embolism.
22 as no evidence of an effect of statin use on pulmonary embolism.
23 med on pregnant patients suspected of having pulmonary embolism.
24 ith CTEPH have a history of clinically overt pulmonary embolism.
25 inclusion of patients with intermediate-risk pulmonary embolism.
26 icial in the treatment of some patients with pulmonary embolism.
27 d with deep-vein thrombosis, and 3319 with a pulmonary embolism.
28 t increased risk of deep vein thrombosis and pulmonary embolism.
29 thromboembolism, including those with severe pulmonary embolism.
30 decreases pulmonary embolism and symptomatic pulmonary embolism.
31 sis, device migration, caval penetration, or pulmonary embolism.
32 pulations for the prophylactic prevention of pulmonary embolism.
33 ce of PPCs, pleural effusion, pneumonia, and pulmonary embolism.
34 han those with left DVT to have a history of pulmonary embolism.
35 osing right ventricular dysfunction in acute pulmonary embolism.
36 uding 20 (61%) with no clinical suspicion of pulmonary embolism.
37 been shown not to be always the same as for pulmonary embolism.
38 py results in the accelerated lysis of acute pulmonary embolism.
39 approach may also simplify the treatment of pulmonary embolism.
40 cted from experimental cerebral ischemia and pulmonary embolism.
41 Adult in/outpatients diagnosed with acute pulmonary embolism.
42 VTE complication, including 51 patents with pulmonary embolism.
43 anticoagulant use was not a risk factor for pulmonary embolism.
44 s are available faster than CCTs and predict pulmonary embolism.
45 of the use of thrombolytic therapy in acute pulmonary embolism.
46 eeding were examined in a humanized model of pulmonary embolism.
47 esuscitation is particularly associated with pulmonary embolism.
48 tical care physicians in patients with acute pulmonary embolism.
49 lar size and function in patients with acute pulmonary embolism.
50 ating right ventricular dysfunction in acute pulmonary embolism.
51 d, deep-vein thrombosis in the arm or leg or pulmonary embolism.
52 lasmin, may have unique therapeutic value in pulmonary embolism.
53 alysis focuses on the included patients with pulmonary embolism.
54 with severe disease, have increased risk of pulmonary embolism.
55 er use did not reduce the risk of subsequent pulmonary embolism.
56 3319 patients had pulmonary embolism.
57 d to identify and treat patients at risk for pulmonary embolism.
58 pulmonary arterial system is referred to as pulmonary embolism.
59 r extremity thrombosis (0.77% versus 0.96%), pulmonary embolism (0.38% versus 0.96%), or urgent surge
62 43; 95% CI, 0.36-0.52; P<0.01; I(2)=34%) and pulmonary embolism (1.2% versus 2.8%; absolute risk redu
66 yed fixation suffered 2-fold higher rates of pulmonary embolism (2.6% versus 1.3%; rate ratio [RR] 2.
67 d possibly or probably related to treatment (pulmonary embolism [200 mg/day], respiratory failure [12
68 1, OR 0.85, 95% CI 0.72-1.01) and effects on pulmonary embolism (205 versus 222, OR 0.92, 95% CI 0.76
69 participants; OR, 0.25; 95% CI, 0.09-0.72), pulmonary embolism (3 studies, 237 participants; OR, 0.0
71 ne [2%]), asthenia (27 [5%] vs 17 [3%]), and pulmonary embolism (32 [6%] vs seven [1%]) occurred more
73 public awareness is substantially lower for pulmonary embolism (54%) and deep-vein thrombosis (44%)
74 thrombosis (12 more per 10 000 woman-years), pulmonary embolism (9 more per 10 000 woman-years), lung
76 s thromboembolism (which comprised events of pulmonary embolism and deep-vein thrombosis) was more co
78 63+/-14 years) with acute main or lower lobe pulmonary embolism and echocardiographic RV to left vent
79 rent venous thromboembolism in patients with pulmonary embolism and evidence of right ventricular dys
81 y for the initial and long-term treatment of pulmonary embolism and had a potentially improved benefi
83 es of pulmonary clots for differentiation of pulmonary embolism and postmortem organized thrombus wer
84 common were at significantly greater risk of pulmonary embolism and required longer hospital stay.
85 thrombolytic agents, but patients with acute pulmonary embolism and significant compromise in the abs
86 timates for both acute coronary syndrome and pulmonary embolism and suggested clinical actions design
87 ed with bid unfractionated heparin decreases pulmonary embolism and symptomatic pulmonary embolism.
88 nd readily available, the rapid diagnosis of pulmonary embolism and use of thrombolytics during cardi
89 infarction, stroke, deep vein thrombosis, or pulmonary embolism) and haemorrhagic events (symptomatic
90 nary embolism, one bronchopneumonia, and one pulmonary embolism) and one in the chemotherapy alone gr
91 h cancer who had recurrent VTE (particularly pulmonary embolism) and with bleeding on anticoagulation
92 y heart disease, invasive breast cancer, and pulmonary embolism), and raloxifene (venous thromboembol
93 ent), venous events (deep vein thrombosis or pulmonary embolism), and respiratory events (pneumonia,
100 d with pulmonary surgery, those who suffered pulmonary embolism, and those in the IGCCCG poor prognos
103 ion, stroke, transient ischemic attacks, and pulmonary embolism are major causes of morbidity and mor
105 ys of treatment for deep vein thrombosis and pulmonary embolism as well as for long-term (6 months) s
106 ys of treatment for deep vein thrombosis and pulmonary embolism as well as for long-term secondary pr
107 ospitalized patients with acute, symptomatic pulmonary embolism associated with lower-limb vein throm
113 esence or absence of deep vein thrombosis or pulmonary embolism at the time of IVC filter placement.
114 ism (which includes deep vein thrombosis and pulmonary embolism), but the evidence is uncertain.
115 rs with an opposite effect: a higher risk of pulmonary embolism, but little or no effect on DVT.
118 uscitation when cardiac arrest was caused by pulmonary embolism compared with hypoxia and primary arr
119 resuscitation from cardiac arrest caused by pulmonary embolism, compared with hypoxia and primary ar
120 rial thromboses and deep-vein thrombosis and pulmonary embolism comprise venous thromboembolism.
121 of symptomatic VTE (deep vein thrombosis and pulmonary embolism, confirmed by duplex ultrasonography
123 ty of DOACs were consistent in patients with pulmonary embolism, deep venous thrombosis, a body weigh
124 actionated heparin for preventing mortality, pulmonary embolism, deep venous thrombosis, bleeding out
125 WH) or unfractionated heparin and mortality, pulmonary embolism, deep venous thrombosis, thrombocytop
127 lism, proximal leg deep vein thrombosis, and pulmonary embolism developing during critical illness we
128 Of 176 included patients, 33 (18.7%) had pulmonary embolism diagnosed by computed tomography, inc
129 criteria, 35%; Prospective Investigation of Pulmonary Embolism Diagnosis study, 29%; no standardized
133 with deep-vein thrombosis (EINSTEIN-DVT) or pulmonary embolism (EINSTEIN-PE) were randomly assigned
135 he device is effective for the prevention of pulmonary embolism for at least 5 weeks after placement
136 omputed tomography pulmonary angiography for pulmonary embolism) for those with a high pretest probab
137 iterans from chronic rejection and by recent pulmonary embolism, for which she was undergoing anticoa
138 s suspected to be related to study drug were pulmonary embolism (four patients; 8%), vomiting (four;
139 ps for major bleeding, from 0.2% to 0.9% for pulmonary embolism, from 0.1% to 0.7% for periprocedural
140 m cardiac arrest with contributing reason of pulmonary embolism (grade 4, suspected to be study drug
144 ndary prevention of deep-vein thrombosis and pulmonary embolism has been shown in phase 3 trials.
145 p vein thrombosis (DVT) and its complication pulmonary embolism have high morbidity reducing quality
146 re were no consistent differences in risk of pulmonary embolism, hip fracture, or depression as a fun
147 (V/Q) scanning is often used to investigate pulmonary embolism; however, it has well-recognized limi
148 is (HR, 0.66; 95% CI, 0.47-0.92; P=0.01) and pulmonary embolism (HR, 0.66; 95% CI, 0.41-1.06; P=0.08)
149 ndomly assigned to cardiac arrest induced by pulmonary embolism, hypoxia, or primary arrhythmia.
150 ed a first episode of symptomatic unprovoked pulmonary embolism (ie, with no major risk factor for th
153 n [3%] in the control group), of which one-a pulmonary embolism in a 64-year-old male patient after 1
154 us thromboembolism, deep vein thrombosis, or pulmonary embolism in adults were included, as were inte
155 ophylaxis decreases deep vein thrombosis and pulmonary embolism in medical-surgical critically ill pa
157 e 3-month incidence of symptomatic UEDVT and pulmonary embolism in patients with a normal diagnostic
158 based guidelines for evaluation of suspected pulmonary embolism in pregnancy using the Grades of Reco
161 A studies but less heterogeneity for DVT and pulmonary embolism in TPKA studies and for VTE, DVT, and
162 (2%) patients died from adverse events; one (pulmonary embolism in treatment group A) was possibly re
163 postoperative mortality rate was 3% (due to pulmonary embolisms in 2 patients and hemorrhage after p
164 92; 95% confidence interval, 1.80-2.05), and pulmonary embolism (incidence rate ratio, 1.80; 95% conf
166 Following approval of rivaroxaban for the pulmonary embolism indication, patients with deep-vein t
167 lly treated with thrombolytic therapy during pulmonary embolism-induced cardiopulmonary arrest and di
168 ective analysis of 143 patients suspected of pulmonary embolism investigated with 3 different scanner
170 inical diagnosis of deep-vein thrombosis and pulmonary embolism is nonspecific, integrated diagnostic
174 y hypertension, a rare complication of acute pulmonary embolism, is characterized by fibrothrombotic
176 enefit" (all strokes, systemic embolism, MI, pulmonary embolism, major bleeding, and all-cause death)
178 ing during BAT in one [3%] patient each were pulmonary embolism, myocardial infarction, urinary obstr
183 igation); subsequent deep-vein thrombosis or pulmonary embolism occurred in 9.3% (5/54) and 8.9% (5/5
188 mab group (one interstitial lung disease and pulmonary embolism, one bronchopneumonia, and one pulmon
190 quently diagnosed in subjects with suspected pulmonary embolism or DVT and account for one-fourth to
192 ent of the composite, and death unrelated to pulmonary embolism or major bleeding, at 18 and 42 month
193 as associated with a lower risk of recurrent pulmonary embolism (OR, 0.40; 95% CI, 0.22-0.74; 1.17% [
195 was found between pulmonary tuberculosis and pulmonary embolism, or between extrapulmonary tuberculos
196 ohol consumption, acute pericardial disease, pulmonary embolism, or other acute pulmonary disease).
199 C), pulmonary hypertension (1B), symptomatic pulmonary embolism (PE) (1C), right ventricular (RV) inf
200 on-LR and LRnon-neonates, respectively), and pulmonary embolism (PE) (P < .001; 19.6% and 3.2% in Non
201 ed all patients who were suspected of having pulmonary embolism (PE) and who underwent CT pulmonary a
204 anguage processing (NLP) model in extracting pulmonary embolism (PE) findings from thoracic computed
206 d stroke, the treatment and outcome of acute pulmonary embolism (PE) have remained relatively unchang
207 mance of different diagnostic strategies for pulmonary embolism (PE) in patient subgroups is unclear.
216 tients with deep venous thrombosis (DVT) and pulmonary embolism (PE) were markedly higher than for th
217 The rates of deep vein thrombosis (DVT), pulmonary embolism (PE), and VTE within 30 days of the i
218 enous thrombosis (DVT) and its complication, pulmonary embolism (PE), and whether elevated fibrinogen
219 ostic strategy of clinically suspected acute pulmonary embolism (PE), but its clinical usefulness is
220 ), comprising deep vein thrombosis (DVT) and pulmonary embolism (PE), is a common, potentially lethal
221 ), comprising deep vein thrombosis (DVT) and pulmonary embolism (PE), is a significant source of mort
222 isk and the outcomes of all-cause mortality, pulmonary embolism (PE)-related mortality, and VTE rates
232 the vascular system (deep venous thrombosis/pulmonary embolism, peripheral vascular disease, hyperco
233 In patients with hemodynamically significant pulmonary embolism, physiological fibrinolysis fails to
234 The most frequently missed diagnoses were pulmonary embolism, pneumonia, secondary peritonitis, in
235 529 patients from the Prognostic Factors for Pulmonary Embolism (PREP) study (validation cohort).
236 osite of symptomatic deep-vein thrombosis or pulmonary embolism, progression or recurrence of superfi
237 terms of symptomatic deep-vein thrombosis or pulmonary embolism, progression or recurrence of superfi
238 inal bleeding (1.4% versus 1.8%; P=0.35), or pulmonary embolism rates (18.4% versus 17.9%; P=0.72).
240 ons (nonfatal myocardial infarction, stroke, pulmonary embolism, renal failure, or bowel infarction)
241 ons (nonfatal myocardial infarction, stroke, pulmonary embolism, renal failure, or bowel infarction)
242 prognostic and therapeutic plan is through a Pulmonary Embolism Response Team, which combines experti
244 tionated heparin) thromboprophylaxis lowered pulmonary embolism risk (hazard ratio, 0.51; 95% CI, 0.2
245 1 [95% CI, 0.41, 0.63]; p<0.0001; I=77%) and pulmonary embolism (risk ratio, 0.52 [95% CI, 0.28, 0.97
246 0.39, 1.00]; p=0.05; I=53%) and symptomatic pulmonary embolism (risk ratio, 0.58 [95% CI, 0.34, 0.97
247 ow-molecular-weight heparin reduced rates of pulmonary embolism (risk ratio, 0.62 [95% CI, 0.39, 1.00
250 rate/low risk of embolism according to Wells pulmonary embolism score, selected from the emergency se
253 -causality grade 3 and 4 adverse events were pulmonary embolism (seven [3%]), prolonged electrocardio
255 The final model included the simplified Pulmonary Embolism Severity Index, cardiac troponin I, b
256 rude comparison of patients with and without pulmonary embolism shows no difference in length of stay
258 autonomic (sympathetic) reflexes, can cause pulmonary embolism, stroke, and, in severe cases, death.
260 r and fewer had active cancer or concomitant pulmonary embolism than those in the standard anticoagul
261 ned as patients with deep vein thrombosis or pulmonary embolism) that occurred during the patient's i
262 mong hospitalized patients with severe acute pulmonary embolism, the use of a retrievable inferior ve
263 o [8%]), dyspnoea (three [12%] vs one [4%]), pulmonary embolism (three [12%] vs 0), fatigue (one [4%]
264 in the palbociclib plus letrozole group were pulmonary embolism (three [4%] patients), back pain (two
269 ion (two of eight), diarrhea (two of eight), pulmonary embolism (two of eight), pulmonary hypertensio
271 of thrombin generation in a murine model of pulmonary embolism using our protease-activated peptide
272 many patients with deep vein thrombosis and pulmonary embolism (venous thromboembolism, VTE), biomar
273 , pneumonia, sepsis, deep venous thrombosis, pulmonary embolism, venous thromboembolism, and myocardi
274 In the entire cohort, the prevalence of pulmonary embolism was 17.3% (95% confidence interval, 1
283 urces; no subsequent deep-vein thrombosis or pulmonary embolism was observed in fondaparinux patients
286 rombosis, but not risk for death or nonfatal pulmonary embolism, was reduced with factor Xa inhibitor
288 ts with deep-vein thrombosis and concomitant pulmonary embolism were also eligible; however, those wi
289 vival following collagen/epinephrine-induced pulmonary embolism were also observed in Dicer1-deficien
291 and pooled incidence rates of VTE, DVT, and pulmonary embolism were estimated using random-effects m
293 th cancer or with intermediate- to high-risk pulmonary embolism, were underrepresented in the Phase I
294 d rhythm analysis: 32 mm (95% CI, 29-36) for pulmonary embolism which was significantly larger than b
295 ver, findings may not apply to patients with pulmonary embolism who are hemodynamically stable withou
296 patients with a first episode of unprovoked pulmonary embolism who received 6 months of anticoagulan
298 ic deep-vein thrombosis or acute symptomatic pulmonary embolism (with or without deep-vein thrombosis
299 ented proximal deep vein thrombosis (DVT) or pulmonary embolism, with a life expectancy greater than
300 e hypothesis that filters reduce the risk of pulmonary embolism, with a point estimate suggesting inc
301 ified stroke, transient ischemic attack, and pulmonary embolism) yielded a 44% higher annual risk tha
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