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Genetic protein S (PS) deficiency caused by PROS1 gene mutation is an important risk factor for hereditary thrombophilia.Case introductionIn this case, we report a 28-year-old male patient who developed a severe pulmonary embolism during his visit. The patient had experienced one month of chestpains, coughing and hemoptysis symptoms.
He reports significant chestpain at the base of his scapula on the right side along with new shortness of breath. The estimated pulmonary artery systolic pressure is 27 mmHg + RA pressure. Wellen's waves indicate that, when the patient was having chestpain, there was occlusion. A 70-something y.o. Am Heart J.
Today’s patient presented to the ED not only with chestpain — but also with shortness of breath , therefore with a history potentially consistent with the diagnosis. When it is — this may greatly expedite clinical decision-making for anticoagulation and/or thrombolysis. The sensitivity of POC Echo is not perfect.
A middle-age woman with no previous cardiac history called 911 for chestpain. Chest X-ray also showed pulmonary edema. Primary VF in this study refers to fibrillation occurring in the absence of shock or pulmonary edema. This was her prehospital ECG: What do you think? She was given 2 mg Magnesium.
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