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1 e) and two PCC related (ischaemic stroke and pulmonary embolism).
2 isk of VTE events (deep venous thrombosis or pulmonary embolism).
3 onfirmed symptomatic deep vein thrombosis or pulmonary embolism).
4 ve accuracy of 0.90 (95% CIs: 0.78-1.00) for pulmonary embolism.
5  interval [CI], 0.04 to 1.2); no patient had pulmonary embolism.
6  Seventeen of the 105 patients (16.2%) had a pulmonary embolism.
7 ography was not indicated to safely rule out pulmonary embolism.
8 of origin of human DVT associated with fatal pulmonary embolism.
9  fibrillation and those at risk of recurrent pulmonary embolism.
10  cannula-associated deep vein thrombosis and pulmonary embolism.
11 lar size and function in patients with acute pulmonary embolism.
12 lasmin, may have unique therapeutic value in pulmonary embolism.
13 ciated with certain causes of arrest such as pulmonary embolism.
14 ombosis can lead to deep-vein thrombosis and pulmonary embolism.
15 as no evidence of an effect of statin use on pulmonary embolism.
16 sis, device migration, caval penetration, or pulmonary embolism.
17 osing right ventricular dysfunction in acute pulmonary embolism.
18    Adult in/outpatients diagnosed with acute pulmonary embolism.
19 eeding were examined in a humanized model of pulmonary embolism.
20 esuscitation is particularly associated with pulmonary embolism.
21 tical care physicians in patients with acute pulmonary embolism.
22 ating right ventricular dysfunction in acute pulmonary embolism.
23 ected thrombolysis for submassive or massive pulmonary embolism.
24 d, deep-vein thrombosis in the arm or leg or pulmonary embolism.
25 nfarction, stroke, deep vein thrombosis, and pulmonary embolism.
26 alysis focuses on the included patients with pulmonary embolism.
27  with severe disease, have increased risk of pulmonary embolism.
28 er use did not reduce the risk of subsequent pulmonary embolism.
29                            3319 patients had pulmonary embolism.
30 lar diameter ratio in massive and submassive pulmonary embolism.
31 d to identify and treat patients at risk for pulmonary embolism.
32  pulmonary arterial system is referred to as pulmonary embolism.
33 al stemming from incompletely resolved acute pulmonary embolism.
34 ry angiography was performed to evaluate for pulmonary embolism.
35 ctor for deep vein thrombosis of the leg and pulmonary embolism.
36 ment of the pulmonary trunk to investigate a pulmonary embolism.
37 ired infections, venous thromboembolism, and pulmonary embolism.
38 oice for preventing deep vein thrombosis and pulmonary embolism.
39    Of 794 scans, 78 (9.8%) were positive for pulmonary embolism.
40  with and without contrast media to rule out pulmonary embolism.
41 the emergency department for suspected acute pulmonary embolism.
42 e outcomes in UK BioBank, most strongly with pulmonary embolism.
43 ng and does not suggest routine use in acute pulmonary embolism.
44 m the emergency department to rule out acute pulmonary embolism.
45 ary vasodilation in a porcine model of acute pulmonary embolism.
46 to approximate 2.3% among survivors of acute pulmonary embolism.
47 unprovoked events, deep vein thrombosis, and pulmonary embolism.
48  of pyrexia, cardiogenic pulmonary edema and pulmonary embolisms.
49 r extremity thrombosis (0.77% versus 0.96%), pulmonary embolism (0.38% versus 0.96%), or urgent surge
50 cluding 1 patient who died (relative risk of pulmonary embolism, 0; 95% CI, 0.00 to 0.55).
51 2.22, 95% CrI 1.78-2.89, p<0.0001) and fatal pulmonary embolism (1.58, 1.14-2.19, p=0.01), but less m
52  at least 5% of patients in either group was pulmonary embolism (13 [6%] vs seven [3%]).
53 yed fixation suffered 2-fold higher rates of pulmonary embolism (2.6% versus 1.3%; rate ratio [RR] 2.
54 is was associated with a lower occurrence of pulmonary embolism (2/18; 11%) than standard regimen (11
55 d possibly or probably related to treatment (pulmonary embolism [200 mg/day], respiratory failure [12
56 ith COVID-19 have an increased prevalence of pulmonary embolisms (26%), and most (78.7%) have moderat
57                            Six patients with pulmonary embolism (46%) and 14 patients without pulmona
58 1 minutes, P = 0.001), and increased rate of pulmonary embolism (5.4% vs 0.9%, P = 0.007) in comparis
59 onary embolism (46%) and 14 patients without pulmonary embolism (52%) died at ICU discharge (odds rat
60  public awareness is substantially lower for pulmonary embolism (54%) and deep-vein thrombosis (44%)
61 Thrombolysis Procedure for Intermediate-Risk Pulmonary Embolism; 8 mg/2 hours, 8 mg/4 hours, 12 mg/6
62 endpoint of this study was the occurrence of pulmonary embolism according to the use of standard thro
63 950 921; among individuals aged 15-55 years, pulmonary embolism accounted for 8-13 per 1000 deaths in
64 for the treatment of critical limb ischemia, pulmonary embolism, acute ischemic stroke, and acute aor
65 onary complications including development of pulmonary embolism, acute respiratory distress syndrome,
66 he occurrence of deep vein thrombosis alone, pulmonary embolism alone.
67             Both scores successfully exclude pulmonary embolism, although YEARS has a better negative
68                            The prevalence of pulmonary embolism among patients hospitalized for synco
69 modynamics were evaluated at baseline, after pulmonary embolism and after each dose by biventricular
70 ts were evaluated in vivo at baseline, after pulmonary embolism and after each dose by invasive hemod
71  Eligible patients had submassive or massive pulmonary embolism and an RV/LV diameter ratio >=0.9 on
72 ll-established risk factor for VTEs, such as pulmonary embolism and deep vein thrombosis.
73    Venous thromboembolism (VTE), composed of pulmonary embolism and deep venous thrombosis, is a sign
74 s thromboembolism (which comprised events of pulmonary embolism and deep-vein thrombosis) was more co
75 rent venous thromboembolism in patients with pulmonary embolism and evidence of right ventricular dys
76        Two dose-limiting toxicities (grade 2 pulmonary embolism and grade 4 hypocellular marrow) occu
77 08 [95% CrI 0.00-1.76]), but the results for pulmonary embolism and major bleeding are highly uncerta
78                           The results of the pulmonary embolism and major bleeding meta-analyses are
79 us adverse events occurred during the study (pulmonary embolism and myocarditis while taking amantadi
80 ion of a low pretest clinical probability of pulmonary embolism and negative d-dimer assay.
81 the eltrombopag group: one treatment-related pulmonary embolism and one vertigo.
82 common were at significantly greater risk of pulmonary embolism and required longer hospital stay.
83 nd readily available, the rapid diagnosis of pulmonary embolism and use of thrombolytics during cardi
84 dilation in a porcine in vivo model of acute pulmonary embolism and vasorelaxation in isolated pulmon
85                              The location of pulmonary embolisms and the degree of elevation of D-dim
86  large intestine perforation, pneumonia, and pulmonary embolism) and two (1%) in the lenalidomide and
87 y heart disease, invasive breast cancer, and pulmonary embolism), and raloxifene (venous thromboembol
88 ents are hemodynamically unstable with acute pulmonary embolism, and a minority of them have proximal
89 ished VTE risk factors), and unprovoked VTE, pulmonary embolism, and deep-vein thrombosis.
90 mary endpoint, and pulmonary embolism, fatal pulmonary embolism, and major bleeding as secondary endp
91 n thrombosis (symptomatic and asymptomatic), pulmonary embolism, and major bleeding.
92 tion, thyrotoxicosis, alcohol, pericarditis, pulmonary embolism, and myocarditis).
93 ictegravir group and one unknown causes, one pulmonary embolism, and one lymphoma in the dolutegravir
94 hrombosis, two patients (15.4%) had isolated pulmonary embolism, and one patient (7.7%) had both cann
95 ficiency or failure, venous thromboembolism, pulmonary embolism, and operative complications.
96 myocardial infarction, deep vein thrombosis, pulmonary embolism, and pneumonia).
97                  Of these, 3 events-syncope, pulmonary embolism, and serum creatinine increase-in 3 p
98 complications, such as deep vein thrombosis, pulmonary embolism, and stroke.
99 d with pulmonary surgery, those who suffered pulmonary embolism, and those in the IGCCCG poor prognos
100  rs10886430-G in increasing risk for stroke, pulmonary embolism, and venous thromboembolism through i
101 ailure, atrial fibrillation, cardiac arrest, pulmonary embolism, and/or stroke).
102               Deep vein thrombosis (DVT) and pulmonary embolism are collectively known as venous thro
103 ion, stroke, transient ischemic attacks, and pulmonary embolism are major causes of morbidity and mor
104  European estimates of the burden imposed by pulmonary embolism are not available to this date.
105 gns of deep-vein thrombosis, hemoptysis, and pulmonary embolism as the most likely diagnosis) and mea
106 f deep vein thrombosis or non-fatal or fatal pulmonary embolism at 12 months.
107 esence or absence of deep vein thrombosis or pulmonary embolism at the time of IVC filter placement.
108 lment; a secondary end point was symptomatic pulmonary embolism between day 8 and day 90 in the subgr
109 ary arteries done in patients with suspected pulmonary embolisms between March 15 and April 30, 2020
110 erences in D-dimer levels or the location of pulmonary embolisms between the two groups.
111 ism (which includes deep vein thrombosis and pulmonary embolism), but the evidence is uncertain.
112 d hemodynamically stable patients with acute pulmonary embolism can be safely managed as outpatients.
113   Deep venous thrombosis (DVT) and secondary pulmonary embolism cause approximately 100,000 deaths pe
114                                              Pulmonary embolism caused a four-fold increase in pulmon
115                                         When pulmonary embolism coexists with a patent foramen ovale,
116                     Deep vein thrombosis and pulmonary embolism, collectively defined as venous throm
117 global index" (these end points plus stroke, pulmonary embolism, colorectal cancer, and hip fracture)
118 embolism was 6.4% in those with subsegmental pulmonary embolism compared with 6.0% in those with more
119 uscitation when cardiac arrest was caused by pulmonary embolism compared with hypoxia and primary arr
120  resuscitation from cardiac arrest caused by pulmonary embolism, compared with hypoxia and primary ar
121 rial thromboses and deep-vein thrombosis and pulmonary embolism comprise venous thromboembolism.
122 of symptomatic VTE (deep vein thrombosis and pulmonary embolism, confirmed by duplex ultrasonography
123 , but primary noncardiac conditions, such as pulmonary embolism, critical illness, and sepsis, probab
124                      Finally, complications (pulmonary embolism, deep vein thrombosis, acute respirat
125 infarction, stroke, surgical site infection, pulmonary embolism, deep venous thrombosis, and death.
126 wer LOEs were observed for interventions for pulmonary embolism/deep vein thrombosis (A 0%, B 24%, C
127 ter specificity than CT angiography alone in pulmonary embolism detection.
128  anticoagulation within 7 days after injury, pulmonary embolism developed in none of those in the ven
129                   In our case, we found both pulmonary embolism due to DVT and paradoxical embolism d
130 entified a group of patients at low risk for pulmonary embolism during follow-up.
131                     Deep Vein Thrombosis and pulmonary embolism (DVT/PE) is one of the most common ca
132 overall mortality as a primary endpoint, and pulmonary embolism, fatal pulmonary embolism, and major
133 n a porcine model of acute intermediate-risk pulmonary embolism, fluid loading increased right ventri
134 he device is effective for the prevention of pulmonary embolism for at least 5 weeks after placement
135 sease is associated with a high incidence of pulmonary embolisms, generally peripherally distributed
136                         All patients in whom pulmonary embolism had not been ruled out underwent CT p
137 ndary prevention of deep-vein thrombosis and pulmonary embolism has been shown in phase 3 trials.
138 p vein thrombosis (DVT) and its complication pulmonary embolism have high morbidity reducing quality
139 3; 95% CI 0.349-0.783, P = 0.002) and not in pulmonary embolism (HR 0.882; 95% CI 0.511-1.521, P = 0.
140 ndomly assigned to cardiac arrest induced by pulmonary embolism, hypoxia, or primary arrhythmia.
141  Classification of Disease-10 code for acute pulmonary embolism (I26) or any code for deep or superfi
142                           Pulmonary surgery, pulmonary embolism, IGCCCG poor prognosis, and smoking i
143                        CTPA was positive for pulmonary embolism in 16 of 60 (26.7%).
144 o Action to Prevent Deep Vein Thrombosis and Pulmonary Embolism in 2008 has been lower than expected
145 6.9%), pulmonary infection in 80 (6.5%), and pulmonary embolism in 47 (3.8%) patients.
146 n [3%] in the control group), of which one-a pulmonary embolism in a 64-year-old male patient after 1
147 us thromboembolism, deep vein thrombosis, or pulmonary embolism in adults were included, as were inte
148         We performed a systematic workup for pulmonary embolism in patients admitted to 11 hospitals
149 m clinical outcomes of incidentally detected pulmonary embolism in patients with cancer.
150                             Risk factors for pulmonary embolism in patients with coronavirus disease
151                                 Diagnosis of pulmonary embolism in pregnancy is challenging, with sym
152 inical diagnostic pathways for evaluation of pulmonary embolism in pregnancy that show conflicting re
153  recommended by guidelines for evaluation of pulmonary embolism in pregnancy, reviews current evidenc
154 ded for informed decision making to diagnose pulmonary embolism in pregnancy.
155 ts, and imaging widely used for diagnosis of pulmonary embolism in the non-pregnant population show l
156  little attention to a diagnostic workup for pulmonary embolism in these patients.
157 (2%) patients died from adverse events; one (pulmonary embolism in treatment group A) was possibly re
158                            The prevalence of pulmonary embolisms in the same period in 2019 was 13.2%
159 92; 95% confidence interval, 1.80-2.05), and pulmonary embolism (incidence rate ratio, 1.80; 95% conf
160                                              Pulmonary embolism increased mean pulmonary arterial pre
161    Following approval of rivaroxaban for the pulmonary embolism indication, patients with deep-vein t
162  patients who did not receive a diagnosis of pulmonary embolism initially and did not receive anticoa
163 ective analysis of 143 patients suspected of pulmonary embolism investigated with 3 different scanner
164 .3% of patients, whereas a strategy in which pulmonary embolism is considered to be ruled out with a
165                                              Pulmonary embolism is incidentally diagnosed in up to 5%
166                                              Pulmonary embolism is one of the leading causes of mater
167                         Pregnancy-associated pulmonary embolism is one of the leading causes of mater
168          Retrospective analyses suggest that pulmonary embolism is ruled out by a d-dimer level of le
169 tic imaging in pregnant women with suspected pulmonary embolism is unknown.
170 ich includes both deep venous thrombosis and pulmonary embolism, is a common and potentially fatal co
171 TE), which includes deep vein thrombosis and pulmonary embolism, is a common complication of cancer a
172 hrombosis (DVT) with its major complication, pulmonary embolism, is a global health problem.
173 y hypertension, a rare complication of acute pulmonary embolism, is characterized by fibrothrombotic
174 iography in the diagnostic approach to acute pulmonary embolism, it has a major role in the evaluatio
175 <1%] on upadacitinib 30 mg), one adjudicated pulmonary embolism (&lt;1%; upadacitinib 15 mg), and one de
176 ells, and suggest that prevention of DVT and pulmonary embolism may be improved by mechanical devices
177          Patients with more life-threatening pulmonary embolism may derive the greatest benefit from
178 n pregnancy is challenging, with symptoms of pulmonary embolism mimicking those of pregnancy.
179 d survival in a collagen/epinephrine-induced pulmonary embolism model of in vivo platelet activation
180 ing during BAT in one [3%] patient each were pulmonary embolism, myocardial infarction, urinary obstr
181 , multiple organ dysfunction syndrome (n=2), pulmonary embolism (n=2), sepsis (n=1), and small intest
182 oside group (death, febrile neutropenia, and pulmonary embolism [n=2 each]; enterocolitis, general ph
183  the deep vein thrombosis network, 12 in the pulmonary embolism network (13 interventions; n=15 555),
184 lactic dose, 28-35 days) ranked first in the pulmonary embolism network (RR 0.02 [95% CrI 0.00-3.86])
185                                           No pulmonary embolism occurred.
186                                              Pulmonary embolism often causes cardiac arrest.
187 ere enrolled and evaluated, of whom 7.4% had pulmonary embolism on initial diagnostic testing.
188                      Venous thromboembolism (pulmonary embolism or any lower-limb deep-vein thrombosi
189 t result in a lower incidence of symptomatic pulmonary embolism or death at 90 days than no placement
190 ary end point was a composite of symptomatic pulmonary embolism or death from any cause at 90 days af
191 nferior vena cava filter reduces the risk of pulmonary embolism or death in severely injured patients
192 significantly lower incidence of symptomatic pulmonary embolism or death than no placement of a filte
193 current venous thromboembolism manifested as pulmonary embolism or deep vein thrombosis.
194 mbolism was defined as deep vein thrombosis, pulmonary embolism, or both, diagnosed greater than 24 h
195 tic distal or proximal deep-vein thrombosis, pulmonary embolism, or venous thromboembolism-related de
196 us thromboembolism, deep vein thrombosis, or pulmonary embolism outcomes.
197 relevance and optimal therapy for incidental pulmonary embolism, particularly distal clots, is unclea
198 C), pulmonary hypertension (1B), symptomatic pulmonary embolism (PE) (1C), right ventricular (RV) inf
199 on-LR and LRnon-neonates, respectively), and pulmonary embolism (PE) (P < .001; 19.6% and 3.2% in Non
200 nts of follow-up within 1 y in patients with pulmonary embolism (PE) and the factors predictive of co
201 ed all patients who were suspected of having pulmonary embolism (PE) and who underwent CT pulmonary a
202  Medicare fee-for-service beneficiaries with pulmonary embolism (PE) between 1999 and 2015 to assess
203                                   Asthma and pulmonary embolism (PE) can present with overlapping sym
204  data from the EMR to automatically classify Pulmonary Embolism (PE) cases.
205                                        While pulmonary embolism (PE) causes approximately 100 000-180
206 ice of the imaging modality for diagnosis of pulmonary embolism (PE) could be influenced by provider,
207               Intermediate-risk (submassive) pulmonary embolism (PE) describes normotensive patients
208 anguage processing (NLP) model in extracting pulmonary embolism (PE) findings from thoracic computed
209 t is not clear whether mortality after acute pulmonary embolism (PE) has decreased over time.
210 d stroke, the treatment and outcome of acute pulmonary embolism (PE) have remained relatively unchang
211 mance of different diagnostic strategies for pulmonary embolism (PE) in patient subgroups is unclear.
212                            The prevalence of pulmonary embolism (PE) in patients presenting with sync
213 investigated rates of diagnostic testing for pulmonary embolism (PE) in US emergency departments (EDs
214                                              Pulmonary embolism (PE) is a leading cause of maternal m
215                                              Pulmonary embolism (PE) is a potentially fatal cardiopul
216                                              Pulmonary embolism (PE) is a serious and prevalent cause
217                                        Acute pulmonary embolism (PE) is associated with high morbidit
218                                              Pulmonary embolism (PE) is associated with increased ris
219 ong-term effect of thrombolytic treatment of pulmonary embolism (PE) is unknown.
220         Vena cava filter (VCF) placement for pulmonary embolism (PE) prophylaxis in trauma is controv
221                                              Pulmonary embolism (PE) represents the third leading cau
222 ual-energy CT iodine maps are used to detect pulmonary embolism (PE) with CT angiography but require
223 hich includes deep vein thrombosis (DVT) and pulmonary embolism (PE), is the third most common cause
224 BEC in patients with acute intermediate-risk pulmonary embolism (PE).
225 C) filters are widely used for prevention of pulmonary embolism (PE).
226 phy and may result in proximal thrombosis or pulmonary embolism (PE).
227  caval filters (IVCFs) may prevent recurrent pulmonary embolism (PE).
228 In patients with hemodynamically significant pulmonary embolism, physiological fibrinolysis fails to
229 st prognostication, cardiac arrest caused by pulmonary embolism, postresuscitation oxygenation and ve
230 osite of symptomatic deep-vein thrombosis or pulmonary embolism, progression or recurrence of superfi
231 terms of symptomatic deep-vein thrombosis or pulmonary embolism, progression or recurrence of superfi
232  A contrast material-enhanced CT angiography pulmonary embolism protocol and cardiac MRI were perform
233  A contrast material-enhanced CT angiography pulmonary embolism protocol and cardiac MRI were perform
234 , we assessed patients with acute submassive pulmonary embolism randomly assigned to 1 of 4 tPA dosin
235                 Complications of CRT include pulmonary embolism, recurrent deep venous thrombosis, lo
236  between 2013 and 2015, an average of 38 929 pulmonary embolism-related deaths occurred annually in t
237                       Deaths were considered pulmonary embolism-related if International Classificati
238                           We aimed to assess pulmonary embolism-related mortality and time trends in
239            The observed decreasing trends in pulmonary embolism-related mortality might reflect impro
240 tween 2000 and 2015, age-standardised annual pulmonary embolism-related mortality rates decreased lin
241 ons (nonfatal myocardial infarction, stroke, pulmonary embolism, renal failure, or bowel infarction)
242  myocardial infarction, ischemic stroke, and pulmonary embolism, represent an important source of adv
243 prognostic and therapeutic plan is through a Pulmonary Embolism Response Team, which combines experti
244                             In patients with pulmonary embolism, right ventricular dysfunction is ass
245      In patients with cancer with incidental pulmonary embolism, risk of recurrent venous thromboembo
246          Patients in control groups had more pulmonary embolism (RR 2.22, 95% CrI 1.78-2.89, p<0.0001
247                   Patients with subsegmental pulmonary embolism seemed to have a risk of recurrent ve
248 mechanical ventilation, respiratory failure, pulmonary embolism, sepsis, or death.
249 -causality grade 3 and 4 adverse events were pulmonary embolism (seven [3%]), prolonged electrocardio
250                                              Pulmonary embolism still imposes a relevant medical and
251  defibrillator, acute myocardial infarction, pulmonary embolism, stroke/transient ischemic attack, in
252 mpared with 6.0% in those with more proximal pulmonary embolism (subdistribution hazard ratio, 1.1; 9
253 oximal deep-vein thrombosis in a lower limb, pulmonary embolism, symptomatic deep-vein thrombosis in
254 r and fewer had active cancer or concomitant pulmonary embolism than those in the standard anticoagul
255           To evaluate the frequency of acute pulmonary embolism, the use of clinical probability scor
256 five [6%]), febrile neutropenia (five [6%]), pulmonary embolism (three [4%]), bronchitis (two [2%]),
257                                             (Pulmonary Embolism Thrombolysis study [PEITHO]; NCT00639
258                                  The PEITHO (Pulmonary Embolism Thrombolysis) trial was a randomized
259 ental acute proximal deep-vein thrombosis or pulmonary embolism to receive oral apixaban (at a dose o
260 r System and Activase for Treatment of Acute Pulmonary Embolism) to identify clinical characteristics
261 ated thrombophlebitis, deep vein thrombosis, pulmonary embolism, transitory ischemic attacks to arter
262 ion (two of eight), diarrhea (two of eight), pulmonary embolism (two of eight), pulmonary hypertensio
263 imer test, all pregnant women with suspected pulmonary embolism undergo computed tomographic (CT) pul
264                Risk stratification for acute pulmonary embolism using imaging presence of right ventr
265  be reasonably explained by a combination of pulmonary embolism, ventilation-perfusion mismatching in
266 2019 mechanically ventilated patients have a pulmonary embolism visible on CT pulmonary angiography.
267      In the entire cohort, the prevalence of pulmonary embolism was 17.3% (95% confidence interval, 1
268                       The frequency of acute pulmonary embolism was 23.0% and the Wells Score was exp
269    We performed a prospective study in which pulmonary embolism was considered to be ruled out withou
270                                              Pulmonary embolism was diagnosed in 20 patients (4.0%) a
271                                            A pulmonary embolism was found in three patients (23.1%).
272                                              Pulmonary embolism was identified in 45 of the 355 patie
273            Among the remaining 230 patients, pulmonary embolism was identified in 97 (42.2%).
274                                              Pulmonary embolism was identified in nearly one of every
275                               Survival after pulmonary embolism was increased in diabetic DKO mice re
276                                        Acute pulmonary embolism was induced by administration of thre
277                                              Pulmonary embolism was induced by jugular vein infusion
278                                        Acute pulmonary embolism was induced by large emboli made from
279                                           If pulmonary embolism was not diagnosed, patients did not r
280                                              Pulmonary embolism was ruled out if none of the three cr
281                               A diagnosis of pulmonary embolism was ruled out in 330 of the 560 patie
282                             The diagnosis of pulmonary embolism was ruled out in patients who had a l
283                                              Pulmonary embolism was safely ruled out by the pregnancy
284 omboembolism was not suspected before death; pulmonary embolism was the direct cause of death in 4 pa
285                            The prevalence of pulmonary embolisms was higher in patients with COVID-19
286 tudy involving pregnant women with suspected pulmonary embolism, we assessed three criteria from the
287 ts with deep-vein thrombosis and concomitant pulmonary embolism were also eligible; however, those wi
288 vival following collagen/epinephrine-induced pulmonary embolism were also observed in Dicer1-deficien
289 ch risk factors for deep vein thrombosis and pulmonary embolism were assessed.
290  cancer and a recent diagnosis of incidental pulmonary embolism were eligible.
291 ts with massive (n=31) or submassive (n=119) pulmonary embolism were enrolled.
292  also eligible; however, those with isolated pulmonary embolism were not included.
293 r ischemia) and VTE (deep vein thrombosis or pulmonary embolism) were assessed.
294 th cancer or with intermediate- to high-risk pulmonary embolism, were underrepresented in the Phase I
295 milar results for all endpoints except fatal pulmonary embolism, where evidence of an effect was weak
296 d rhythm analysis: 32 mm (95% CI, 29-36) for pulmonary embolism which was significantly larger than b
297    Thirteen patients (33%) were diagnosed of pulmonary embolism, which was bilateral in six patients
298 ous thromboembolism (deep vein thrombosis or pulmonary embolism) who were new users of apixaban or ri
299  I endometrial cancer with tamoxifen and one pulmonary embolism with placebo.
300 ic deep-vein thrombosis or acute symptomatic pulmonary embolism (with or without deep-vein thrombosis

 
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