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1.
Am J Cardiol ; 77(12): 1037-44, 1996 May 15.
Article in English | MEDLINE | ID: mdl-8644654

ABSTRACT

The occurrence of an autonomic disturbance early in acute myocardial infarction (AMI) has been reported: signs of sympathetic activation were mainly observed in relation to an anterior localization, whereas signs of vagal overactivity were more frequent in inferior wall AMI. Information is limited in relation to the persistence of these alterations during the early hours of AMI. We studied 33 patients with an AMI within 188 +/- 16 minutes from the onset of symptoms and 1 week after hospital admission. From a 20-minute Holter recording, we computed with autoregressive methodology, time and frequency domain indexes of heart rate variability. At admission, patients with an anterior wall AMI exhibited a smaller RR variance (593 +/- 121 ms2) than did those with an inferior wall AMI (1,122 +/- 191 ms2). In both groups the spectral profile was characterized by a predominant (73 +/- 4 and 61 +/- 4 normalized units) low frequency and by a small (13 +/- 2 and 22 +/- 3 normalized units) high-frequency component, indicating the presence of a sympathetic excitation and of a diminished vagal modulation. Although signs of sympathetic activation were more evident in patients with anterior wall AMI, no evidence of a vagal hyperactivity was observed in patients with inferior wall AMI. In the latter group, we noticed 1 week after the acute event an increase in the low-frequency component, which reached the values observed in patients with anterior wall AMI. Thrombolysis did not affect heart rate variability parameters. Thus, this study suggests the presence of an autonomic disturbance characterized by signs of sympathetic excitation and of a reduced vagal modulation, which was more evident in patients with an anterior localization early after AMI.


Subject(s)
Heart Rate , Myocardial Infarction/physiopathology , Electrocardiography, Ambulatory , Heart Rate/physiology , Humans , Middle Aged , Sympathetic Nervous System/physiopathology , Time Factors
2.
Minerva Cardioangiol ; 40(7-8): 293-6, 1992.
Article in Italian | MEDLINE | ID: mdl-1470395

ABSTRACT

The paper describes the case of a patients suffering from a pre-excitation syndrome who underwent numerous episodes of reciprocal tachycardia during pregnancy. The clinical implications and various methods of therapy used are discussed.


Subject(s)
Pregnancy Complications, Cardiovascular/diagnosis , Tachycardia, Paroxysmal/diagnosis , Wolff-Parkinson-White Syndrome/diagnosis , Acute Disease , Adult , Combined Modality Therapy , Electrocardiography , Female , Humans , Pregnancy , Pregnancy Complications, Cardiovascular/therapy , Tachycardia, Paroxysmal/therapy , Wolff-Parkinson-White Syndrome/therapy
3.
Cardiovasc Drugs Ther ; 4 Suppl 1: 119-22, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2285641

ABSTRACT

The aim of the study was to evaluate whether the combination of ketanserin with captopril exerts an additive antihypertensive effect, as compared with single drug treatment. Twelve patients with uncomplicated moderate essential hypertension received, according to a randomized, double-blind, crossover design, ketanserin (40 mg twice daily), captopril (50 mg twice daily), the combination of the two drugs at these dosages, and the corresponding placebo, each treatment being given for 1 month. Both ketanserin and captopril as monotherapy similarly and significantly reduced blood pressure as compared with placebo (p less than 0.001). The combination treatment of ketanserin plus captopril further and significantly reduced blood pressure when compared with single drug treatment (p less than 0.001). Moreover, the percentage of responders and patients whose blood pressure was normalized were significantly greater under the combined treatment than under ketanserin or captopril monotherapy (p less than 0.001). These data indicate that the combination of ketanserin plus captopril exerts a clear additive antihypertensive effect when compared with each treatment as monotherapy, a finding that suggests this combination can be usefully employed in the treatment of hypertensive patients.


Subject(s)
Captopril/therapeutic use , Hypertension/drug therapy , Ketanserin/therapeutic use , Adult , Aldosterone/blood , Blood Pressure/drug effects , Body Weight/drug effects , Captopril/adverse effects , Double-Blind Method , Drug Therapy, Combination , Female , Heart Rate/drug effects , Humans , Hypertension/physiopathology , Ketanserin/adverse effects , Male , Middle Aged , Potassium/blood , Sodium/blood
8.
Clin Endocrinol (Oxf) ; 15(6): 555-65, 1981 Dec.
Article in English | MEDLINE | ID: mdl-6276052

ABSTRACT

To study effects on pituitary-adrenocortical activity of a sustained block of angiotensin II formation, six 'drug-resistant' patients with essential hypertension were studied before and during treatment with an inhibitor of the angiotensin-converting enzyme (Captopril, SQ 14,225). The drug was given in increasing doses (100-400 mg/day) for 2 weeks whilst patients received a moderately restricted sodium intake (60-80 mmol/day). Immunoreactive ACTH, cortisol, aldosterone, plasma renin activity (PRA) and the activity of the angiotensin-converting enzyme (ACE) were measured in blood samples drawn at 0800-0900 h. Urinary excretion of cortisol and aldosterone were measured in 24-h urine collections. Further information on pituitary-adreno-cortical function was obtained by measuring serial plasma corticosteroid levels after submaximal stimulation with a synthetic ACTH preparation. ACTH and cortisol did not change an observation which does not support the hypothesis that glucocorticoid activity is influenced by a decrease in plasma angiotensin II concentrations.


Subject(s)
Captopril/therapeutic use , Hypertension/drug therapy , Pituitary-Adrenal System/drug effects , Proline/analogs & derivatives , Adrenocorticotropic Hormone , Adult , Aldosterone/metabolism , Female , Humans , Hydrocortisone/metabolism , Hypertension/metabolism , Hypertension/physiopathology , Male , Middle Aged , Pituitary-Adrenal Function Tests , Pituitary-Adrenal System/physiopathology , Sodium/metabolism
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