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J Am Coll Cardiol, 2000; 35:1590-1598
© 2000 by the American College of Cardiology Foundation
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Hemodynamic effects of immunoadsorption and subsequent immunoglobulin substitution in dilated cardiomyopathy

Three-month results from a randomized study

Stephan B. Felix, MD*, Alexander Staudt, MD*, Wolf V. Dörffel, MD*, Verena Stangl, MD*, Kurt Merkel, MD{ddagger}, Manfred Pohl, PhD§, Wolf D. Döcke, MD||, Stanislao Morgera, MD§, Hans H. Neumayer, MD§, Klaus D. Wernecke, PhD, Gerd Wallukat, PhD#, Karl Stangl, MD* § and Gert Baumann, MD*

* Medizinische Klinik, Kardiologie Medizinische Klinik, Nephrologie Charité, Humboldt-Universtät zu Berlin, Berlin-Buch, Germany
{ddagger} Institut für Pathologie und Dermatohistologie, Diagnostisches Zentrum Berlin, Berlin-Buch, Germany
§ Institut für Medizinische Biophysik, Berlin-Buch, Germany
|| Immunologie, Berlin-Buch, Germany und
Biometrie, Charité, Humboldt-Universtät zu Berlin, Berlin-Buch, Germany
# Max Delbrück Zentrum für Molekulare Medizin, Berlin-Buch, Germany



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Figure 1 Time schedule of immunoadsorption (IA) and cardiovascular monitoring; IA was performed in four courses until the third month.

 


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Figure 2 Changes in hemodynamics in the immunoadsorption/immunoglobulin group (IA/IgG group, filled bars, n = 9) and in the control group (controls, open bars, n = 9). (A) Cardiac index. (B) Stroke volume index. (C) Systemic vascular resistance. (D) Changes in left ventricular ejection fraction, as assessed by echocardiography. *p < 0.05; **p < 0.01 significantly different from baseline; +p < 0.05; ++p < 0.01 significantly different from controls.

 


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Figure 3 Changes in beta-receptor antibody level in the immunoadsorption/immunoglobulin group (IA/IgG group, filled bars, n = 9) and in the control group (controls, open bars, n = 9). *p < 0.05; **p < 0.01 significantly different from baseline; +p < 0.05; ++p < 0.01 significantly different from controls.

 




 
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