scholarly journals Emergency Department Echocardiography Demonstrates Large Pericardial Effusion and Pendulous Cardiac Motion in Patient with Shortness of Breath and Electrical Alternans

2008 ◽  
Vol 15 (7) ◽  
pp. 693-694
Author(s):  
Chandler Hill ◽  
Gavin Budhram
2004 ◽  
Vol 27 (12) ◽  
pp. 701-701
Author(s):  
Richard A. Kerensky ◽  
Jonica Calkins ◽  
Ezra Amsterdam

Circulation ◽  
2014 ◽  
Vol 130 (suppl_2) ◽  
Author(s):  
Cheng-Han Chen ◽  
Angela Kleiber ◽  
Christine Megerdichian ◽  
Gregg C Fonarow ◽  
Arnold S Baas

A 19-year-old female initially presented to an outside hospital with worsening shortness of breath over the course of hours. Echocardiogram revealed a large pericardial effusion with tamponade physiology. An urgent pericardiocentesis followed by a pericardial window yielded 600cc of cloudy fluid, and work-up for infectious, auto-immune, and malignant etiologies was unrevealing. She was discharged home, but over the next four weeks developed a repeat pericardial effusion requiring another pericardiocentesis yielding 750cc of cloudy fluid. She then presented to our hospital two weeks later with progressive shortness of breath. Echocardiogram revealed a large pericardial effusion with evidence of early tamponade physiology. Our differential diagnosis for her recurrent pericardial effusions remained broad, with infectious and malignant etiologies at the top of consideration. Computed tomography of the chest demonstrated the pericardial effusion and mild mediastinal adenopathy. She underwent another pericardial window with removal of 600cc of milky fluid, and fluid analysis was notable for a markedly elevated triglyceride level consistent with a diagnosis of chylopericardium. Work-up for malignancy as an etiology for recurrent chylopericardium was negative. A percutaneous lymphangiogram was then performed, which revealed a significant leak in the superior aspect of the thoracic duct into the pericardial space. Percutaneous embolization of the thoracic duct was performed using detachable coils along with embolic glue, resulting in resolution of the leak. She has since remained asymptomatic, and follow-up echocardiogram was without recurrence of any pericardial effusion. This case of idiopathic recurrent chylopericardium as the cause for pericardial effusion represents a rare manifestation of a relatively common cardiac condition. It illustrates the importance of routine pericardial fluid analysis for triglycerides, as this led to her correct diagnosis of chylopericardium. The use of percutaneous thoracic duct embolization has only recently been reported as a novel approach for treatment of chylous leak, and may emerge as a useful alternative to surgery for recurrent chylopericardium.


POCUS Journal ◽  
2016 ◽  
Vol 1 (3) ◽  
pp. 12
Author(s):  
Jeffrey Wilkinson, MD ◽  
Amer M. Johri, MD

Mr. DB was a 95 year old man who presented to the emergency department with dyspnea progressing over the last 3 months. Chest x-ray demonstrated an enlarged cardiac silhouette. He had a past medical history significant for coronary artery disease, hypertension and a lobectomy due to tuberculosis. A point of care cardiac ultrasound was conducted by an internal medicine resident as part of his physical examination in the emergency department. A large pericardial effusion was found. There were no clinical signs of tamponade. Video 1 (online supplement; Figure 1) demonstrates a parasternal long axis view with the pericardial effusion noted to be posterior to the left ventricle in this view. Video 2 (online supplement; Figure 2) is a short axis view of the heart which is showing that the effusion is surrounding the heart. Video 3 and 4 (online supplements; Figures 3 & 4) demonstrates that the pericardial effusion is present significantly surrounding the apex as well. An echocardiogram confirmed the POCUS findings and cardiology was consulted to conduct a pericardiocentesis, following which the patient’s symptoms resolved. The effusion was thought to be chronic and transudative. In this case, the use of POCUS at the bedside allowed for rapid detection of a large pericardial effusion and subsequent treatment.


1997 ◽  
Vol 15 (3) ◽  
pp. 371-372
Author(s):  
David E. Slattery ◽  
David W. Dickerson ◽  
Charles V. Pollack

2018 ◽  
Vol 27 (3) ◽  
pp. 224-225
Author(s):  
Niravkumar K Sangani ◽  
Santosh Mathew Naliath

A 37-year-old man underwent mechanical mitral valve replacement for rheumatic heart disease. One week after discharge, he presented with high-grade fever with chills, malaise, and shortness of breath. Echocardiography showed pericardial effusion with no evidence of vegetation. A blood malaria antigen test was positive for Plasmodium falciparum. One week after initiation of antimalarial medication, echocardiography revealed almost complete resolution of the pericardial effusion. Infective endocarditis is a common cause of fever after valvular heart surgery. Malaria can be considered in the differential diagnosis of fever and pericardial effusion after valvular surgery, especially in malaria-endemic countries.


Immunotherapy ◽  
2019 ◽  
Vol 11 (18) ◽  
pp. 1533-1540 ◽  
Author(s):  
Abdul Moiz Khan ◽  
Ayesha Munir ◽  
Vimala Thalody ◽  
Mohamed Khalid Munshi ◽  
Syed Mehdi

Immunotherapy drugs are associated with a multitude of immune-related adverse events. We describe a case of cardiac tamponade in a patient with stage IV lung adenocarcinoma, with almost 100% expression of PDL-1, treated with pembrolizumab. The patient is a 62-year-old male who developed worsening shortness of breath after five cycles of pembrolizumab. He was diagnosed with large pericardial effusion on computed tomography chest. Echocardiogram confirmed tamponade physiology. He was treated with discontinuation of pembrolizumab and urgent pericardial window followed by high dose prednisone with tapering. The patient responded very well to the treatment. We have comprehensively reviewed cases of pericardial effusion secondary to either immune mediated mechanisms or pseudoprogression.


2019 ◽  
Vol 12 (9) ◽  
pp. e229975 ◽  
Author(s):  
Charlotte Terry ◽  
Pascale Avery ◽  
Sarah Morton ◽  
Jon Aron

A 12-year-old boy presented with central chest pain, shortness of breath and type 1 respiratory failure. He had a background of graft versus host disease (GvHD), which was currently managed with imatinib therapy. A focused bedside ultrasound scan was performed revealing a large pericardial effusion. The child was referred to a tertiary paediatric cardiology centre where he underwent emergency pericardiocentesis, draining a total of 800 mL of pericardial fluid. Fluid analysis excluded infection, and with no other concerns for a GvHD flare the diagnosis of an imatinib-induced pericardial effusion was made. On terminating the therapy, the pericardial collection did not reaccumulate. Tyrosine kinase inhibitor-induced pericardial and/or pleural effusion should be considered as a differential diagnosis in paediatric patients on this therapy presenting in a similar manner.


QJM ◽  
2013 ◽  
Vol 107 (4) ◽  
pp. 305-307 ◽  
Author(s):  
M. A. R. Chamsi-Pasha ◽  
M. Bassiouny ◽  
E. S. H. Kim

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