Multicenter, Randomized, Double-Blind, Placebo-Controlled Study on the Effect of Oral Tolvaptan on Left Ventricular Dilation and Function in Patients With Heart Failure and Systolic Dysfunction
James E. Udelson, MD*,a,*,
Frank A. McGrew, MD ,
Enrique Flores, MD ,
Hassan Ibrahim, MD ,
Stewart Katz, MD¶,
Gregory Koshkarian, MD||,
Terrence OBrien, MD**,
Marvin W. Kronenberg, MD ,
Christopher Zimmer, MD ,b,
Cesare Orlandi, MD ,b and
Marvin A. Konstam, MD*,a
* Division of Cardiology, Tufts-New England Medical Center/Tufts University School of Medicine, Boston, Massachusetts
The Stern Cardiovascular Center, Memphis, Tennessee
Georgia Heart Specialists, Covington, Georgia
North Ohio Research Ltd., Sandusky, Ohio
¶ Yale University School of Medicine, New Haven, Connecticut
|| Desert Cardiology of Tucson, Tucson, Arizona
** Ralph H. Johnson VA Medical Center, Charleston, South Carolina
 Division of Cardiovascular Medicine, Vanderbilt University, Nashville, Tennessee
 Otsuka America Pharmaceutical, Inc., Rockville, Maryland.

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Figure 1 Effect of TLV on Time to Death or Heart Failure Hospitalization
Time-to-event analysis evaluating patients randomized to tolvaptan (TLV) (red line) versus placebo (PLC) (blue line) with regard to death or hospitalization for worsening heart failure. There was a favorable effect of TLV on this combined end point.
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Figure 2 Effect of Tolvaptan and Placebo on VP Levels During the Course of the Trial
Histogram of changes in vasopressin (VP) levels from baseline to week 54 (in pg/ml) for patients randomized to tolvaptan (open bars) or to placebo (cross-hatched bars). Group changes were significant (Table 7). The histogram of the changes in individual patients shows a shift to the right, which is consistent with the significant increase in the patients randomized to tolvaptan, as shown in Table 7.
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