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1.
Heart Views. 2014; 15 (1): 16-18
en Inglés | IMEMR | ID: emr-147233

RESUMEN

Afibrinogenemia is a rare autosomal recessive bleeding disorder with an estimated prevalence of 1:1,000,000. Usual presentation of this disorder is spontaneous bleeding, bleeding after minor trauma and excessive bleeding during interventional procedures. Paradoxically, few patients with afibrinogenemia may also suffer from severe thromboembolic complications. The management of these patients is particularly challenging because they are not only at risk of thrombosis but also of bleeding. We are presenting a case of 33-year-old male patient of congenital afibrinogenemia who had two episodes myocardial infarction in a span of two years. The patient was managed conservatively with antiplatelet therapy and thrombolytic therapy was not given due to high risk for bleeding

2.
JCVTR-Journal of Cardiovascular and Thoracic Research. 2012; 4 (4): 119-122
en Inglés | IMEMR | ID: emr-139758

RESUMEN

Thrombosis of Inferior Vena Cava [IVC] following filter insertion can occur in up to 30% of the cases. The optimal management of such cases is unknown. We describe a simple and less expensive method of achieving successful recanalization of the IVC in a 40 year old hypertensive man who developed recurrent pulmonary embolism after his orthopedic treatment. An IVC filter was inserted, which developed extensive thrombosis of the whole IVC and venous system of the lower limbs. Catheter directed thrombolysis using a multiple side-hole multipurpose catheter and balloon angioplasty was carried out in order to [crush and lyse] the IVC thrombi


Asunto(s)
Humanos , Masculino , Terapia Trombolítica/métodos , Trombosis de la Vena/terapia , Embolia Pulmonar/prevención & control , Cateterismo , Resultado del Tratamiento
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