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J Thorac Cardiovasc Surg 1998;115:1215-1216
© 1998 Mosby, Inc.


BRIEF COMMUNICATIONS

Echocardiographic and surgical correlation of pericardial effusions in patients with malignant disease

F. Ida Hsu, BAa, Deborah Keefe, MDb,c, Dawn Desiderio, MDc, Robert J. Downey, MDa,c

New York, N.Y.

From the Divisions of Thoracic Surgerya and Cardiologyb and the Department of Anesthesia and Critical Care,c Memorial Sloan-Kettering Cancer Center, New York, N.Y.

Received for publication Sept. 5, 1997. Accepted for publication Dec. 5, 1997. Address for reprints: Robert J. Downey, MD, Division of Thoracic Surgery, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, NY 10021.

Malignant disease is present in the pericardium of 15% to 20% of patients dying of cancer and examined post mortem,Go 1 and malignancy is the most common cause of cardiac tamponade in patients without previously suspected cancer.Go 2 Currently, the most sensitive and the least invasive method for detecting pericardial effusions is echocardiography, which can detect effusions as small as 15 ml, characterize total volume, and demonstrate the presence of fibrin bands, pericardial masses, loculations, thickened pericardial membranes, chamber compression, and dilatation of the inferior vena cava.Go Go 2,3 However, it has not been clearly established whether such echocardiographically obtained information can characterize a pericardial effusion as being malignant or benign. Similarly, although needle pericardiocentesis is effective in draining pericardial effusions, it is unknown whether the additional information gained by histologic examination of pericardial tissue obtained during the performance of a pericardial window will increase the frequency of detection of malignant effusions. Defining the disease processes leading to an effusion is critical, because both overall prognosis and the treatment choice may be altered,Go 4 and for a marginally stable patient with a potentially limited outlook, extensively invasive intervention may be inappropriate. Therefore, this retrospective study attempts (1) to correlate various echocardiographic signs with pathologic specimens to determine whether echocardiography may reliably characterize an effusion as malignant or benign and (2) to examine the sensitivity and specificity of pericardial fluid cytology and pericardial tissue histology in establishing the presence of intrapericardial malignant disease.

The records of 25 patients seen at Memorial Sloan-Kettering Cancer Center during the period of January 1, 1993, to December 30, 1994, with a history of malignant disease, transthoracic echocardiograms demonstrating pericardial fluid, and subsequent pericardial fluid and tissue submitted for analysis were reviewed. All patients were grouped into one of two categories: those with malignant effusions and those with benign effusions. Intrapericardial malignancy was diagnosed when cytologic examination of pericardial fluid and/or pathologic examination of pericardial tissue demonstrated malignant cells. In addition, patient records were reviewed for age, sex, primary cancer diagnosis, prior thoracic irradiation, cardiac function, and relevant laboratory findings. All echocardiograms were again reviewed by one author (D.K.), blinded to cytologic and pathologic data, for the following: size of effusion; degree of collapse of the right atrium; right ventricle, or left atrium, dilatation of the inferior vena cava; and the presence of fibrin bands, loculations, or pericardial masses.

Ten men and 15 women, with a median age of 59 years (range 28 to 72 years), were studied. Effusions were confirmed by pericardial sac histology or pericardial fluid cytology as malignant in 13 of 25 patients (52%). The distribution of primary malignant tumors and the causes of the effusions are listed in Table I. Of patients with intrapericardial malignant disease, eight had positive cytology but negative pathology (lung carcinoma, n = 5; esophageal carcinoma, n = 1; sarcoma, n = 1; adenocarcinoma of unknown primary, n = 1), two had negative cytology but positive pathology (metastatic breast carcinoma, n  = 1; mesothelioma, n = 1), and three had both positive cytology and pathology (lung carcinoma, n = 1; breast carcinoma, n = 1; adenocarcinoma of unknown primary, n = 1). Only one patient had received prior thoracic irradiation, and this patient was found to have both benign cytology and benign pathology. Cultures were performed on pericardial fluid from five patients with malignant effusions and three with benign effusions: none of the cultures were positive for bacterial or fungal infection.


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Table I. Primary malignant tumors and etiology of effusions
 
Echocardiographic findings and their distribution between the benign and malignant effusions are listed in Table II. In addition, the average volume was estimated to be 287 ml (median 250 ml) in the 19 patients for whom complete data were available. Nine of the malignant effusions (69%) were classified as large, as were six of the benign effusions (50%). Right atrial collapse was severe in one patient with malignant effusion, moderate in six patients (malignant, n = 5; benign, n = 1), mild in eight (malignant, n = 3; benign, n = 5), and not present in nine (malignant, n = 3; benign, n = 6). Right ventricular collapse was severe in one patient with a malignant effusion, moderate in four (malignant, n = 2; benign, n = 2), mild in seven (malignant, n = 5; benign, n = 2), and not present in 12 (malignant, n = 4; benign, n = 8). Left atrial collapse was moderate in one patient with benign effusion, mild in four with malignant effusion, and not present in 18 (malignant, n = 7; benign, n = 11). Left ventricular function was normal in 22 patients, hypocontractile in one patient with benign effusion, and could not be characterized in two. Overall, cardiac tamponade, as evidenced by moderate to severe collapse of one or more chambers, was more common in patients with malignant effusions than benign effusions ({chi}2 = 4.44, 0.02 < p < 0.05, n = 24). The median survival of patients with benign effusions was 219 days (range 8 days to 3.5 years) and for patients with malignant effusions 81 days (range 5 days to 3.8 years); two patients with benign effusions were alive at the end of the follow-up period.


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Table II. Echocardiographic findings
 
Overall, echocardiographic evidence for the presence or absence of fibrin bands, loculations, pericardial masses, or inferior vena caval dilatation could not be correlated with the presence of malignancy, although moderate to severe chamber collapse did correlate with the diagnosis of malignant pericardial effusion. Pericardial fluid cytology and pericardial sac pathology are complementary tests, with the latter often informative when the former is negative; thus obtaining both pericardial tissue and fluid will increase the frequency of detection of intrapericardial malignant disease.

References

  1. Hawkins JW, Vacek JL. What constitutes definitive therapy of malignant pericardial effusion? "Medical" versus surgical treatment. Am Heart J 1989;118:428-32.[Medline]
  2. Groeger JS, Keefe D. Cardiac tamponade. In: Groeger JS, editor. Critical care of the cancer patient. 2nd ed. St. Louis: Mosby, 1991;250-60.
  3. Horowitz MS, Schultz CS, Stinson EB, Harrison DC, Popp RL. Sensitivity and specificity of echocardiographic diagnosis of pericardial effusion. Circulation 1974;50:239-47.[Abstract/Free Full Text]
  4. Posner MR, Cohen GI, Skarin AT. Pericardial disease in patients with cancer. Am J Med 1981;71:407-13. [Medline]



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