Massive pulmonary embolism with a large thrombus stuck in patent foramen ovale - an impending paradoxical embolism.

Patent foramen ovale is a persisting communication between the left and right atrium, present in approximately 25% of population, usually asymptomatic. Under normal conditions there is either no blood flow or a hemodynamically nonsignificant left-to-right shunt between the atria. However, increased right atrium pressure, as it is in pulmonary embolism, can make PFO a right-to-left shunt and poses a risk of paradoxical systemic embolism, including the risk of ischemic stroke. Here we report a case of a patient presenting with venous thromboembolism provoked by a recent polytrauma. We identified a large thrombus stuck in patent foramen ovale - an impending paradoxical embolism. Both surgical intervention and systemic thrombolysis were contraindicated so the patient was administered an anticoagulation treatment with unfractionated heparin and warfarin. By frequent echocardiography we were able to monitor complete resolution of the thrombus by 6 months from the diagnosis, with no systemic embolism.

Edoxaban vs. warfarin in vitamin K antagonist experienced and naive patients with atrial fibrillation†.

AIMS: Edoxaban is an oral, once-daily factor Xa inhibitor that is non-inferior to well-managed warfarin in patients with atrial fibrillation (AF) for the prevention of stroke and systemic embolic events (SEEs). We examined the efficacy and safety of edoxaban vs. warfarin in patients who were vitamin K antagonist (VKA) naive or experienced. METHODS AND RESULTS: ENGAGE AF-TIMI 48 randomized 21 105 patients with AF at moderate-to-high risk of stroke to once-daily edoxaban vs. warfarin. Subjects were followed for a median of 2.8 years. The primary efficacy endpoint was stroke or SEE. As a pre-specified subgroup, we analysed outcomes for those with or without prior VKA experience (>60 consecutive days). Higher-dose edoxaban significantly reduced the risk of stroke or SEE in patients who were VKA naive [hazard ratio (HR) 0.71, 95% confidence interval (CI) 0.56-0.90] and was similar to warfarin in the VKA experienced (HR 1.01, 95% CI 0.82-1.24; P interaction = 0.028). Lower-dose edoxaban was similar to warfarin for stroke or SEE prevention in patients who were VKA naive (HR 0.92, 95% CI 0.73-1.15), but was inferior to warfarin in those who were VKA experienced (HR 1.31, 95% 1.08-1.60; P interaction = 0.019). Both higher-dose and lower-dose edoxaban regimens significantly reduced the risk of major bleeding regardless of prior VKA experience (P interaction = 0.90 and 0.71, respectively). CONCLUSION: In patients with AF, edoxaban appeared to demonstrate greater efficacy compared with warfarin in patients who were VKA naive than VKA experienced. Edoxaban significantly reduced major bleeding compared with warfarin regardless of prior VKA exposure.

Variability of aortic blood flow predicts fluid responsiveness in spontaneously breathing healthy volunteers.

BACKGROUND: Assessment of fluid responsiveness is an important topic in acute cardiology. Echocardiographic measurement of respiratory variations of aortic blood velocity in ventilated shock patients can accurately predict the effect of volume expansion. On the other hand, it remains unclear whether this respiratory variability is a common physiological reaction to hypovolaemia and whether its measurement is applicable also in spontaneously breathing patients. AIM: To assess whether respiratory variability of peak aortic blood flow velocity (DVpeakao) and of aortic velocity time integral (DVTIao) reflects preload-dependent changes of cardiac index (CI) and whether it predicts fluid responsiveness in healthy spontaneously breathing volunteers. METHODS: DVpeakao, DVTIao and CI were measured by transthoracic echocardiography in 20 volunteers at baseline and after intravenous administration of furosemide (0.5 mg/kg). Afterwards, volunteers were randomised to rapid intravenous volume expansion (group A) or no expansion (group B) and assessed finally. RESULTS: Hypovolaemia induction was associated with a decrease of CI (from 3.25 +/- 0.50 to 2.28 +/- 0.43 l/min/m2, p < 0.001) which correlated with an increase of DVpeakao (r = -0.490, p = 0.028) and DVTIao (r = -0.554, p = 0.011) in both groups. In group A, volume expansion was followed by a drop of DVpeakao (from 16.04 +/- 1.99 to 2.97 +/- 1.65 %, p < 0.001) and DVTIao (from 20.43 +/- 5.13 to 3.43 +/- 1.68 %, p < 0.001) and CI increase (from 2.14 +/- 0.47 to 3.29 +/- 0.57 l/min/m2, p < 0.001). This increase strongly correlated with the value of DVpeakao (r = 0.782, p = 0.008) and DVTIao (r = 0.770, p = 0.009) before volume expansion. Conversely, there was no change of measured parameters in group B. Threshold values of 14% for DVaopeak and 17% for DVTIao were identified to predict fluid responsiveness (increase of CI > 15%) with a sensitivity of 89% and specificity of 100%. CONCLUSIONS: DVpeakao and DVTIao reflect preload-dependent changes of CI in healthy spontaneously breathing volunteers and predict fluid responsiveness.