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  • 1
    ISSN: 1432-1041
    Keywords: Felodipine ; β-blocker ; combination therapy ; essential hypertension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary We have studied the efficacy and tolerability of felodipine plus a β-adrenoceptor blocker in 79 patients with essential hypertension previously treated with a combination of three or more anti-hypertensive agents, one of which was a β-adrenoceptor blocker. After a 4-week run-in period on the same β-blocker plus placebo (as a substitute for the other agents in the regimen), felodipine was added and its dose titrated to achieve a supine diastolic blood pressure or less than 90 mm Hg. This was followed by a 12-week maintenance phase in all patients, and 47 patients entered an optional long-term follow-up for an additional 9 months. The mean supine blood pressure was 149/88 mm Hg at entry and 174/108 mm Hg after the run-in phase. Felodipine significantly reduced the blood pressure to 142/85 mm Hg after dose titration and to 141/84 mm Hg after 12 weeks, 94% of patients achieving a supine diastolic blood pressure of 90 mm Hg or below. This reduction was maintained in the patients who were followed for 12 months. The adverse events recorded were usually mild, transient, and typical for an effective precapillary vasodilator. Nine of 74 patients (11%) were withdrawn in the first phase of the study because of adverse events and 5 of 47 patients were withdrawn during the long-term follow-up. These results show that the efficacy and tolerability of a combination of felodipine with a β-blocker allow a simplified regimen for hypertensive patients who were previously taking three or more drugs for satisfactory blood pressure control.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 1970-03-01
    Description: The safety and effectiveness of a standard dosage schedule of streptokinase was evaluated in 50 patients with thromboembolic disease. A streptokinase resistance test was performed, and each patient was then treated with 250,000 units of streptokinase infused over 30 minutes followed by 100,000 units per hour. The results of serial tests of fibrinolytic activity were then correlated with the streptokinase resistance in each patient. Forty six of the fifty patients had a resistance of 250,000 units or lower and all these developed an active thrombolytic state with rapid plasminogen depletion. The four patients with a streptokinase resistance in excess of 250,000 units showed a delayed fibrinolytic response; however, once obtained, the fibrinolytic effects were similar to those found in the other 46 patients. It is concluded that an active thrombolytic state would be obtained most consistently if the inducing dose of streptokinase is individualized for each patient. The thrombolytic effects of a standard dose schedule are less predictable, but its routine use may be an acceptable alternative in a particular community if the range and distribution of the streptokinase resistance have been determined and have been shown to be relatively low in a large percentage of the community.
    Print ISSN: 0006-4971
    Electronic ISSN: 1528-0020
    Topics: Biology , Medicine
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