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1 644 9. 10. 11. 12. 13. VOL 60, No 7, DECEMBER 1979 CI RCULATION pulmonary hypertension following closure of ventricular and atrial septal defects. Circulation 17: 1167, 1958 Wagenvoort CA, Neufeld HN, Dushane JW, Edwards JE: The pulmonary arterial tree in ventricular septal defect. Circulation 23: 740, 1961 Gersony WM, Duc GV, Sinclair JC: "PFC" syndrome (persistence of the fetal circulation). Circulation 40 (suppl III): III87. 1969 Riemenschneider TA, Nielsen HC, Ruttenberg HD, Jaffe RB: Disturbances of the transitional circulation: spectrum of pulmonary hypertension and myocardial dysfunction. J Pediatr 89: 622, 1976 Goetzman BW, Sunshine P, Johnson JD, Wennberg RP, Hackel A, Merten DF, Bartoletti AL, Silverman NH: Neonatal hypoxia and pulmonary vasospasm: response to tolazoline. J Pediatr 89: 617, 1976 Levy RJ, Rosenthal A, Freed MD, Smith CD, Eraklis A, Nadas AS: Persistent pulmonary hypertension in a newborn with congenital diaphragmatic hernia: successful management with tolazoline. Pediatrics 60: 740. 1977 14. Boyle RJ, Oh W: Transcutaneous Po2 monitoring in infants with persistent fetal circulation who are receiving tolazoline therapy. Pediatrics 62: 605, 1978 15. Moodie DS, Telander RL, Kleinberg F, Feldt RH: Use of tolazoline in newborn infants with diaphragmatic hernia and severe cardiopulmonary disease. J Thorac Cardiovasc Surg 75: 725, 1978 16. Shah-Mirany J, Najafi H, Serrx C, Callaghan R, Yang J: Pathophysiological alterations in perfused and nonperfused lungs during cardiopulmonary bypass. Ann Thorac Surg 10: 402, 1970 17. Ellison LT, Ellison RG: Alteration in pulmonary surfactant associated with cardiopulmonary bypass. Ann Thorac Surg 10: 258, 1970 18. Eltringham WG, Schroder R, Jenny M, MatloffJM, Zollinger RM: Pulmonary arteriovenous admixture in cardiac surgical patients. Circulation 37 (suppl II): 11-207, 1968 19. Diament ML, Palmer KN: Venous/arterial pulmonary shunting as the principal cause of postoperative hypoxaemia. Lancet 1: 15, 1967 Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 Two-dimensional Echocardiography and B-mode Ultrasonography for the Diagnosis of Loculated Pericardial Effusion MARK J. FRIEDMAN, M.D., DAVID J. SAHN, M.D., AND KAI HABER, M.D. SUMMARY Two cases of loculated pericardial effusion resulting in cardiac tamponade are presented. The loculated nature and extent of the effusion was best defined by two-dimensional echocardiography or B-mode ultrasonography. Cross-sectional images should probably be obtained in all cases of suspected loculated pericardial effusion and in patients in whom the interpretation of the M-mode echocardiogram is equivocal as to the presence or absence of pericardial effusion. M-MODE ECHOCARDIOGRAPHY is a sensitive and specific technique for the detection of nonloculated pericardial effusion.1 2 Recent reports of two-dimensional echocardiography suggest that this method is also clinically useful for evaluating pericardial effusion.3 In contrast to the positive experience with these techniques for the detection of nonloculated pericardial effusion, loculated pericardial effusions have frequently resulted in false-negative M-mode echocardiographic studies.4 6 This report demonstrates the usefulness of two-dimensional echocardiography and B-mode ultrasonography in two patients with loculated pericardial effusion. From the Departm-lenit of Internal Medicine, Section of Cardiology, the Department of Pediatrics, Section of Cardiology, and the Department of Radiology, Arizona Health Sciences Center, Tucson, Arizona. Supported in part by Clinical Pharmacology Research Training grant 5T32GM07533-02, NIH. Address for correspondence: David J. Sahn, M.D., Department of Pediatrics, University of Arizona Health Sciences Center, Tucson, Arizona 85724. Received April 16, 1979; revision accepted July 2, 1979. Circulation 60, No. 7, 1979. Case 1 A 28-year-old Mexican male was admitted to the University of Arizona Health Sciences Center for evaluation of sharp, substernal chest pain, shortness of breath and cardiomegaly. On physical examination, the blood pressure was 92/70 mm Hg with 14 mm Hg pulsus paradoxus. The jugular veins were distended to the angle of the jaw with the patient sitting upright. The first and second heart sounds were normal and a three-component pericardial friction rub was heard over the anterior precordium. A chest radiograph showed marked enlargement of the cardiac silhouette, but was otherwise unremarkable. The diagnosis of pericarditis with cardiac tamponade was made and an M-mode echocardiogram was obtained using a SmithKline Ekoline 20A ultrasonoscope with a 2.25-MHz transducer. Standard sweeps from the aortic root to the left ventricle were attempted using previously described techniques,7 however, a limited echo window resulted in a suboptimal M-mode echocardiogram. The M-mode echocardiogram (fig. 1) demonstrated a large, echo-free space posterior to the left ventricular wall extending behind the left atrium. A small anterior 1645 DIAGNOSIS OF PERICARDIAL EFFUSION/Friedman et al. FIcGURE 1. M-mode echocardiograms from case 1. Panel A) Sweep from the mitral valve to the aortic root at a paper speed of 25 mm/sec. Panel B is taken from the mitral valve level, first at a paper speed of 25 mm/sec and then at 50 mm/sec. Adjustment of the gain allows identification of the pericardium. A large pericardial effusion located posterior to the left ventricle is identified. A small, echo-free space anterior to the heart is also seen. A O aortic root; EFF pericardial effusion; IVS interventricular septum; MV mitral valve; PERI pericardium. = = Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 effusion was also observed. A right-heart catheterization was performed that revealed equilibration of mean pulmonary wedge, right ventricular enddiastolic, and mean right atrial pressure, confirming the impression of cardiac tamponade (table 1). A pericardiocentesis under fluoroscopic guidance was attempted from the subxiphoid approach; however, only 2 ml of serosanguinous fluid could be extracted from the pericardial sac. A two-dimensional echocardiogram was performed using a high-resolution, 32element linear array ultrasound device (Toshiba SAL IOA). A large, echo-free space located posterior and lateral to the left ventricle was identified. The left ventricle appeared to be compressed by the posterior effusion and the right ventricle was compressed behind the sternum. No anterior fluid was found (fig. 2). These findings suggested a loculated pericardial effusion and a B-mode ultrasound examination of the mediastinum was performed using a water-delay multitransducer automated B scanner (Octoson).8 Pericardial fluid was identified posterior and lateral to the heart, but no effusion was identified anterior to the heart (fig. 3). At surgery, the chest was entered through a left lateral thoracotomy incision. A large mass was found behind TABLE 1. Hemodynamic Data From the Right-Heart Cat heterization. Pressure IlA ltVEI)P PA PAW (mm Jlg) 20 Case 1 20 20 25/20 16 14 Case 2 14 20/14 Abbreviations: PA = pulm-nonary artery; PAW mean rneani right atrial; ItVEI)P pulmoniary artery wedge; 11A m right venitricular enid-diastolic. = = ,LA Chest Wall - , LV-Papillary Muscle i 0, ;Effusion Ant R JL Post FIGURE 2. Short-axis view of the left ventricle from the two-dinmensional echocardiogram of case 1. The left ventricle is compressed by a large pericardial effusion located posterior and lateral to the left ventricle. L V left ventricle; RV right ventricle. = 1 646 CIRCULATION VOL 60, No 7, DECEMBER 1979 -Chest Wall RV PA2I -LV - Effusion Ant Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 Supp Inf Post FIGURE 3. Long-axis, B-mode ultrasound image from case 1. The left ventricle is compressed by the posterior effusion and the right ventricle is compressed behind the sternum. L V = left ventricle; PA pulmonary artery; RV = right ventricle. = the heart, which was compressing the heart against the sternum. The mass involved the pericardium and extended into the left chest. No extension into the anterior mediastinum was appreciated. Upon opening the mass and pericardium, a large amount of thick fluid as well as solid tumor was encountered. Pathologic analysis of the pericardium and tumor tissue revealed an undifferentiated seminoma as the etiology of the effusion. Case 2 A 21-year-old Mexican male was admitted to Tucson Medical Center with a history of chronic renal failure and recent onset of shortness of breath. On physical examination, the blood pressure was 140/80 mm Hg with 18-mm Hg pulsus paradoxus. The jugular veins were distended to the angle of the jaw with the patient sitting upright. The first and second heart sounds were diminished in intensity. A pericardial friction rub was not heard. A chest radiograph revealed a right pleural effusion, obscuring the right heart border, and cardiomegaly. An M-mode echocardiogram was obtained using a Smith Kline Ekoline 20A ultrasonoscope with a 2.25-MHz transducer. The M-mode echocardiogram (fig. 4) showed a large, echo-free space between the anterior chest wall and A EFF¾ EFF RV IVs IVs LV = MV PERI PERt ~ ~ ~ ~~~,, FIGURE 4. M-mode echocardiogram from case 2. Panel A is at the mitral valve level and panel B is at the level of the left ventricle. A large, echo-free space is identified anterior to the heart. No effusion is identified posterior to the left ventricle. EFF = effusion; I VS = interventricular septum; L V = left ventricle, MV = mitral valve, PERI = pericardium, P W = posterior wall; RV right ventricle; R VA W =-right ventricular anterior wall. PERI DIAGNOSIS OF PERICARDIAL EFFUSION/Friedman et al. Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 the right ventricular anterior wall. The right ventricle appeared to be compressed and paradoxical septal motion was noted. An echo-free space posterior to the left ventricle was not identified. A two-dimensional echocardiogram was performed using a dynamically focused, phased-array, wide-angle sector scanner. This study demonstrated a large, echo-free space located between the chest wall and the right ventricle that resulted in marked compression of the right ventricle (fig. 5). Several septations were noted within the anterior echo free space. No space between the left ventricle and posterior pericardium was noted. A Bmode ultrasound examination of the mediastinum was performed using the Octoson B-scanner.8 A large multiloculated anterior pericardial effusion, compressing the right ventricle, and a right pleural effusion were found (fig. 6). No posterior pericardial effusion was detected. A right-heart catheterization revealed equilibration of the mean pulmonary wedge, right ventricular end-diastolic and mean right atrial pressure confirming the impression of cardiac tamponade (table 1). At surgery, the chest was opened through a median sternotomy incision. A tense, distended pericardial sac was encountered which was incised, yielding 300 ml of hemorrhagic fluid and degenerating clot. The pericardium was markedly thickened with adhesions between the visceral and parietal pericardium. The posterior aspect of the heart was free of pericardial fluid, but some thickening of the pericardium was appreciated. Pathologic analysis of the pericardium revealed only chronic inflammation. 1647 Effusion RV Septum LA MV Ant Inf + Sup Post Discussion Using ultrasound techniques, most large pericardial effusions have fluid demonstrated in the anterior as well as posterior pericardial spaces.1 3Case I had a large pericardial effusion located posterior and lateral to the heart with little fluid present in the anterior pericardial space, while case 2 had a large multiloculated pericardial effusion localized to the anterior surface of the heart with no effusion present posterior to the left ventricle. The M-mode echocardiogram from case 1 demonstrated a large, posterior, echo-free space that extended behind the left atrium and a small anterior clear space. The inability to obtain fluid by pericardiocentesis, in the presence of pericardial tamponade, necessitated further evaluation which was accomplished noninvasively using two-dimensional echocardiography and B-mode ultrasonography. These studies confirmed that the major portion of the pericardial effusion was located posterior Papillary Muscle , FIGURE 5. Long-axis (A) and short-axis (B) views from the two-dimensional echocardiogram from case 2. A large, anterior pericardial effusion is identified. No posterior effusion is noted. A single septation is evident in the short-axis view. A o aortic root; LA left atrium; L V - left ventricle; M V = m i t ral val ve; R V = righ t ven tricle; s ep ta = septation. = = RV- Ant R+L Post 1648 VOL 60, No 7, DECEMBER 1979 ClIRCU LATION _'- Chest Wall Peri Eff- -RV -LV PilEff Ant L R Post Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 FIGURE 6. Short-axis, B-mode ultrasound image from case 2. A large, multiloculated, anterior pericardial effusion conmpressing the right ventricle is identified. A right pleural effusion is also visible. No effusion posterior to the left ventricle is identified. L V left ventricle; Peri. Eff pericardial effusion; Pl. Eff pleural effusion; RV = right ventricle. = = = and lateral to the left ventricle. This aided in the planning for the prompt surgical evacuation and relief of the cardiac tamponade. Other possible explanations for the posterior echo-free space noted on the M-mode echocardiogram include the misdiagnosis of a left pleural effusion as a pericardial effusion,9 a giant left atrium simulating a pericardial effusion,1 or tumor,"1 13 or fibrosis'2 simulating pericardial effusion. The two-dimensional echocardiograms and B-mode ultrasound examination excluded most of these possibilities. The small anterior clear space identified on the Mmode echocardiogram (fig. 1) was not detected by the other ultrasound techniques. This is probably because M-mode echocardiography is primarily an axial technique and damping controls can be used effectively to image structures in the near field. Although the pericardial effusion and tumor mass was not noted to extend anteriorly at the time of surgery, the anterior pericardial space was not fully explored once the cardiac tamponade was relieved and the malignant nature of the tumor was identified. Thus, a small amount of pericardial fluid may have been present in the anterior pericardial space. The M-mode echocardiogram from case 2 demonstrated a large, echo-free space anterior to the right ventricular wall with no echo free space behind the left ventricle. This M-mode echo pattern is considered to be nonspecific for pericardial effusion; it has been reported with pericardial cysts'4 and noncardiac mediastinal cysts" and tumors.5 16 Tajik'7 speculated that an echocardiogram demonstrating a large, anterior, echo-free space without any significant posterior echo-free space might be found in a patient with loculated anterior pericardial effusion. However, he had not seen such an example. We believe this case demonstrates that an echo-free space isolated to the anterior surface of the heart may be related to a loculated pericardial effusion. The etiology of the effusion in the second case is probably related to chronic pericarditis secondary to the patient's chronic renal failure. Although pericardial effusion is common in patients with chronic renal failure on hemodialysis,18-20 pericardial tamponade is unusual2' and many of the effusions are silent.'9 We believe this is the first documented case of pericardial tamponade secondary to a loculated pericardial effusion in a patient with chronic renal failure diagnosed by ultrasound. The distinction by ultrasound between pericardial cysts, noncardiac mediastinal cysts and loculated pericardial effusion is not always possible. The multiloculated nature of the effusion in patient 2 helped distinguish it from a pericardial cyst since pericardial cysts are rarely multiloculated.2 However, this finding would not be helpful in distinguishing pericardial effusion from thymic cysts, which are frequently multiloculated.23 We recently used ultrasound to assist in the differential diagnosis between pericardial effusion, tumor and mediastinal (bronchogenic) cyst in a patient who had the latter diagnosis. Even with thickened intracystic fluid, the boundaries and extent of the cystic mass could be localized with both the Bscan and real-time, cross-sectional echo systems. We believe that two-dimensional echocardiography or B-mode ultrasonography should be used in all cases of suspected loculated pericardial effusion and in all cases where the interpretation of the Mmode echocardiogram is equivocal as to the presence or absence of pericardial effusion. DIAGNOSIS OF PERICARDIAL EFFUSION/Friedman et al. References Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 1. Feigenbaum H: Echocardiography. Philadelphia, Lea and Febiger, 1976, p 419 2. Horowitz MS, Schultz CS, Stinson E, Harrison DC, Popp RL: Sensitivity and specificity of echocardiographic diagnosis of pericardial effusion. Circulation 50: 239, 1974 3. Martin RP, Rakowski H, French J, Popp RL: Localization of pericardial effusion with wide angle phased array echocardiography. Am J Cardiol 42: 904, 1978 4. Goldschlager AW, Freeman LM, Davis PJ: Pericardial effusions and echocardiography. False results with ultrasound reflection method. NY State J Med 67: 1854, 1967 5. Casarella WJ, Schneider BO: Pitfalls in the ultrasonic diagnosis of pericardial effusion. Am J Roentgenol 110: 760, 1970 6. Feigenbaum H, Zaky A, Waldhouser JA: Use of reflected ultrasound in detecting pericardial effusion. Am J Cardiol 19: 84, 1967 7. Abbasi AS, Ellis N, Flynn JJ: Echocardiographic M-scan technique in the diagnosis of pericardial effusion. J Clin Ultrasound 1: 300, 1973 8. Kossoff G, Carpenter DA, Radovanovich G, Robinson DE, Garrett WJ: Octason: a new rapid multitransducer general purpose water coupling echoscope. Excerpta Med Int Cong Series 363: 90, 1975 9. Goldberg BB, Strum BJ, Isard HJ: Ultrasonic determination of pericardial effusion. JAMA 202: 927, 1967 10. Ratshin RA, McKamy S, Hood W: Possible false-positive diagnosis of pericardial effusion by echocardiography in presence of large left atrium. Chest 65: 112, 1974 11. Foote WC, Jefferson CM, Price H: False positive echocardiographic diagnosis of pericardial effusion. Result of tumor encasement of the heart simulating constrictive pericarditis. Chest 71: 546, 1977 1649 12. Millman A, Meller J, Motro M, Blank HS, Horowitz I, Herman MV, Teichholz LE: Pericardial tumor or fibrosis mimicking pericardial effusion by echocardiography. Ann Intern Med 86: 434, 1977 13. Lin TK, Stech JM, Eckert WG, Lin JL, Farha SJ, Hagan CT: Pericardial angio sarcoma simulating pericardial effusion by echocardiography. Chest 73: 881, 1978 14. Felner JM, Fleming WH, Franch RH: Echocardiographic identification of a pericardial cyst. Chest 68: 386, 1975 15. Child JS, Abbasi AS, Pearce ML: Echocardiographic differentiation of mediastinal tumors from primary cardiac disease. Chest 67: 108, 1975 16. Tingelstad JB, McWilliams NB, Thomas CE: Confirmation of a retrosternal mass by echocardiogram. J Clin Ultrasound 4: 129, 1976 17. Tajik AJ: Echocardiography in pericardial effusion. Am J Med 63: 29, 1977 18. Winney RJ, Wright N, Sumerleng MD, Lambie AT: Echocardiography in uraemic pericarditis with effusion. Nephron 18: 201, 1977 19. Goldstein DJ, Nagar C, Srivastava N, Schact RA, Ferris FZ, Flowers NC: Clinically silent pericardial effusions in patients on long-term hemodialysis. Chest 72: 744, 1977 20. Klerman JH, Motta J, London E, Pennell JP, Popp RL: Pericardial effusions in patients with end stage renal disease. Br Heart J 40: 190, 1978 21. Hager EB; clinical observations on five patients with uremic pericardial tamponade. N Engl J Med 273: 304, 1965 22. Wychulis AR, Connally DC, McGoon DC: Pericardial cysts, tumors, and fat necrosis. J Thorac Cardiovasc Surg 62: 294, 1971 23. Wychulis AR, Payne WS, Clagett OT, Woolner. LB: Surgical treatment of mediastinal tumors. J Thorac Cardiovasc Surg 62: 379, 1971 Two-dimensional echocardiography and B-mode ultrasonography for the diagnosis of loculated pericardial effusion. M J Friedman, D J Sahn and K Haber Downloaded from http://circ.ahajournals.org/ by guest on April 29, 2017 Circulation. 1979;60:1644-1649 doi: 10.1161/01.CIR.60.7.1644 Circulation is published by the American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231 Copyright © 1979 American Heart Association, Inc. All rights reserved. Print ISSN: 0009-7322. Online ISSN: 1524-4539 The online version of this article, along with updated information and services, is located on the World Wide Web at: http://circ.ahajournals.org/content/60/7/1644 Permissions: Requests for permissions to reproduce figures, tables, or portions of articles originally published in Circulation can be obtained via RightsLink, a service of the Copyright Clearance Center, not the Editorial Office. Once the online version of the published article for which permission is being requested is located, click Request Permissions in the middle column of the Web page under Services. Further information about this process is available in the Permissions and Rights Question and Answer document. Reprints: Information about reprints can be found online at: http://www.lww.com/reprints Subscriptions: Information about subscribing to Circulation is online at: http://circ.ahajournals.org//subscriptions/