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Published on: June 11, 2019
Severe Disseminated Intravascular Coagulopathy Associated With Biventricular Massive Mural Thrombi in Newly Diagnosed
Muhammad Ghallab1,2, Mahmoud Khairy3, Allison Foster1
1Internal Medicine, Icahn School of Medicine at Mount Sinai, New York City (NYC) Health and Hospitals, Queens, New York, USA.
Insights
This case highlights a rare instance of disseminated intravascular coagulopathy (DIC) in a patient with non-ischemic cardiomyopathy and extensive cardiac thrombi. Early recognition and management of DIC and heart failure are crucial for improved patient outcomes.
Area of Science:
- Cardiology
- Hematology
- Critical Care Medicine
Background:
- Hemostatic system abnormalities are linked to congestive heart failure (CHF).
- Disseminated intravascular coagulopathy (DIC) is a rare but serious complication.
Observation:
- A 55-year-old female presented with biventricular heart failure, marked thrombocytopenia, coagulopathy, and elevated D-dimer.
- Transthoracic echocardiogram revealed right atrial and biventricular thrombi.
- CT scan showed extensive pulmonary emboli, and venous duplex confirmed deep vein thrombosis.
Findings:
- This case presents a rare association of DIC with non-ischemic cardiomyopathy, biventricular thrombus, deep vein thrombosis, and pulmonary embolism.
- Unlike prior reports, this patient had both right atrial and biventricular thrombi.
Implications:
- Early identification of DIC and cardiac thrombi in heart failure patients is vital.
- Prompt management including thrombectomy, optimized heart failure medications, and anticoagulation can improve outcomes.
Abstract:
Hemostatic system abnormalities have been previously associated with congestive heart failure (CHF). Here, we report a rare case of disseminated intravascular coagulopathy (DIC) in the setting of non-ischemic cardiomyopathy with right atrial and biventricular thrombus. We present a 55-year-old female with a past medical history of bronchial asthma who presented with a six-day history of bilateral leg swelling and dry cough. Her physical examination on admission was significant for signs of biventricular heart failure. Initial workup was significant for elevated pro-brain natriuretic peptide (ProBNP), elevated transaminases, marked thrombocytopenia (19,000/mcL), and coagulopathy with international normalized ratio (INR) of 2.5 and D-dimer of 15,585 ng/mL. Transthoracic echocardiogram (TTE) showed a large mobile right atrial thrombus protruding into the right ventricle and a more adherent left ventricular (LV) thrombus with severely reduced biventricular contractility. Pan CT was done and was significant for multifocal multilobar pulmonary emboli. A lower limb venous duplex was done and revealed extensive bilateral lower limb deep venous thrombosis (DVT). This rare case demonstrates an unusual association between DIC with non-ischemic cardiomyopathy, biventricular thrombus, extensive deep vein thrombosis, and pulmonary embolism (PE). In comparison, there are multiple prior reports for DIC with CHF and LV thrombus. However, our case differs from prior reports in terms of the presence of right atrial and biventricular thrombus. The patient received antibiotics, diuretics, and cryoprecipitate in the setting of persistent low fibrinogen levels. The patient underwent Interventional radiology-guided thrombectomy for extensive pulmonary emboli followed by inferior vena cava (IVC) filter insertion, resulting in the resolution of the right atrial thrombus and extensive decrease of the pulmonary emboli burden. The patient was then given apixaban after normalization of the platelet count and fibrinogen level. Hypercoagulability workup was inconclusive. The patient was then discharged after improvement of symptoms. Early recognition of DIC and cardiac thrombi in patients with new-onset heart failure is crucial for the implementation of the correct management by thrombectomy, optimizing heart failure medications, and anticoagulation to achieve better outcomes.
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