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   <subfield code="a">Effects of isradipine sustained release on platelet function and fibrinolysis in essential hypertensives with or without other risk factors</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[G. Ranieri, V. Filitti, A. Andriani, M. Bonfantino, G. Lamontanara, A. Cavallo, M. Milani, R. De Cesaris]</subfield>
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   <subfield code="a">Summary: The aim of this study was to assess the chronic effects of a highly selective dihydropiridine calcium channel blocker, israpidine, in its sustained release form (I-SRO), on platelet functions and fibrinolytic parameters in subjects with essential hypertension (EH) combined or not with other well-known cardiovascular risk factors, such as cigarette smoking (EH+S) and type II diabetes mellitus (EH+DM). Thirty-six patients with essential hypertension with sitting diastolic blood pressures of 96-104 mmHg without (EH, n=12) or with other risk factors (EH+S, n=12, EH+DM, n=12) were enrolled. After a 4-week, single-blind, placebo run-in period, the subjects received I-SRO 5 mg once daily for 18 weeks. After both placebo and 6 and 18 weeks of I-SRO treatment, the following parameters were measured: sitting blood pressure by mercury sphygmomanometer; platelet aggregation, plasma beta-thromboglobulin (BTG), platelet factor-4 (PF4), and plasminogen activator inhibitor 1 (PAI-1) by means of ELISA methods; and euglobulin lysis time before (ELT) and after standardized (10 min) venous occlusion (ELT-VO). In the group of patients as a whole compared with placebo, I-SRO significantly reduced SBP/DBP platelet aggregation, BTG, PF4, ELT, and ELT-VO. Significant reductions in these parameters were also observed in each group. In addition to the antihypertensive effect, I-SRO chronic treatment may favorably affect the platelet function and fibrinolytic system in essential hypertension with or without other cardiovascular risk factors.</subfield>
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   <subfield code="a">Kluwer Academic Publishers, 1996</subfield>
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   <subfield code="a">israpidine</subfield>
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   <subfield code="a">diabetes mellitus</subfield>
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   <subfield code="a">smoking</subfield>
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   <subfield code="a">platelet functions</subfield>
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   <subfield code="a">Ranieri</subfield>
   <subfield code="D">G.</subfield>
   <subfield code="u">Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine, Chair of Medical Therapy, University of Bari Medical School, Bari, Italy</subfield>
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   <subfield code="a">Filitti</subfield>
   <subfield code="D">V.</subfield>
   <subfield code="u">Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine, Chair of Medical Therapy, University of Bari Medical School, Bari, Italy</subfield>
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   <subfield code="a">Andriani</subfield>
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   <subfield code="u">Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine, Chair of Medical Therapy, University of Bari Medical School, Bari, Italy</subfield>
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   <subfield code="u">Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine, Chair of Medical Therapy, University of Bari Medical School, Bari, Italy</subfield>
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   <subfield code="D">R.</subfield>
   <subfield code="u">Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine, Chair of Medical Therapy, University of Bari Medical School, Bari, Italy</subfield>
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   <subfield code="t">Cardiovascular Drugs and Therapy</subfield>
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   <subfield code="g">10/2(1996-10-01), 119-123</subfield>
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