PMID- 3154320 OWN - NLM STAT- MEDLINE DCOM- 19910326 LR - 20201209 IS - 0920-3206 (Print) IS - 0920-3206 (Linking) VI - 1 IP - 2 DP - 1987 Aug TI - A multicenter study of a new inotropic agent, piperanometozine (OPC-8212) in congestive heart failure: clinical improvement during short-term treatment. PG - 169-75 AB - Piperanometozine (OPC-8212) is a new, orally effective inotropic agent. To evaluate the efficacy of this agent on systemic hemodynamics and clinical symptoms in patients with congestive heart failure, a multicenter study was performed. Thirty four patients with New York Heart Association (NYHA) functional classes II to IV and initially treated with digitalis were enrolled from ten centers. After a washout period of one or two weeks (placebo period), digitalis was replaced by piperanometozine (30 or 60 mg/day) for four weeks, while other drugs were continued. Clinical symptoms, routine physical findings, electrocardiogram, chest roentgenogram, echocardiogram, exercise tolerance time, and routine laboratory data were obtained in 34 patients. Four patients were withdrawn from the study before completion. After the withdrawal of digitalis, heart rate was increased and ejection fraction was decreased. Exercise tolerance time was increased while other parameters were unchanged. At the end of the treatment period with piperanometozine, ejection fraction significantly (p less than 0.05) increased with a decrease in LV end-systolic volume (p less than 0.05), whereas heart rate and blood pressure remained unchanged. Systolic blood pressure/LV end-systolic volume (P/V index) tended to decrease after the withdrawal of digitalis and increase during piperanometozine therapy. Exercise tolerance time was further increased (p less than 0.01) and NYHA functional class was improved in 11 patients, whereas it worsened in only one patient. No major adverse effects were observed. These results indicate that a short-term therapy of oral piperanometozine restored the depressed cardiac performance of the heart and improved clinical symptoms in patients with congestive heart failure. Thus, this promising agent deserves further clinical study in long-term trials. FAU - Inoue, M AU - Inoue M AD - First Department of Internal Medicine, Osaka University, School of Medicine, Japan. FAU - Hori, M AU - Hori M FAU - Yasuda, H AU - Yasuda H FAU - Takishima, T AU - Takishima T FAU - Sugimoto, T AU - Sugimoto T FAU - Sasayama, S AU - Sasayama S FAU - Sakurai, T AU - Sakurai T FAU - Nonogi, H AU - Nonogi H FAU - Kodama, K AU - Kodama K FAU - Kusukawa, R AU - Kusukawa R AU - et al. LA - eng PT - Clinical Trial PT - Journal Article PT - Multicenter Study PL - United States TA - Cardiovasc Drugs Ther JT - Cardiovascular drugs and therapy JID - 8712220 RN - 0 (Cardiotonic Agents) RN - 0 (Pyrazines) RN - 0 (Quinolines) RN - 5COW40EV8M (vesnarinone) SB - IM MH - Aged MH - Cardiotonic Agents/adverse effects/*therapeutic use MH - Female MH - Heart Failure/*drug therapy/physiopathology MH - Humans MH - Male MH - Middle Aged MH - Pyrazines MH - Quinolines/adverse effects/*therapeutic use EDAT- 1987/08/01 00:00 MHDA- 1987/08/01 00:01 CRDT- 1987/08/01 00:00 PHST- 1987/08/01 00:00 [pubmed] PHST- 1987/08/01 00:01 [medline] PHST- 1987/08/01 00:00 [entrez] AID - 10.1007/BF02125470 [doi] PST - ppublish SO - Cardiovasc Drugs Ther. 1987 Aug;1(2):169-75. doi: 10.1007/BF02125470.