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1.
Arch Intern Med ; 148(8): 1725-8, 1988 Aug.
Article in English | MEDLINE | ID: mdl-3041936

ABSTRACT

Previous studies have indicated that some hypertensive patients, following a period of effective treatment with certain antihypertensive drugs, may experience prolonged normotension after drug withdrawal. We have studied the ability of carteolol, a nonselective beta-adrenoceptor antagonist with intrinsic sympathomimetic activity, to produce such remissions of hypertension. Thirty-four patients whose diastolic blood pressure was controlled at 90 mm Hg or less with carteolol monotherapy (2.5 to 5.0 mg/d for an average of 328 days) were randomized to a nine-month, double-blind, placebo-controlled drug-withdrawal trial. Those patients randomized to continue carteolol therapy had initially responded to carteolol treatment with reduction in blood pressure from 151 +/- 4/99 +/- 2 to 132 +/- 4/80 +/- 2 mm Hg. Those randomized to treatment with placebo had initially responded with blood pressure reductions from 154 +/- 4/97 +/- 2 to 137 +/- 4/81 +/- 2 mm Hg. Changes in mean systolic and diastolic blood pressure (mm Hg +/- SEM) from baseline during carteolol therapy to the final visit at nine months were not different for patients receiving placebo (13 +/- 5/6 +/- 4 mm Hg, recumbent; 11 +/- 6/4 mm Hg, standing) or carteolol (11 +/- 5/7 +/- 3 mm Hg, recumbent; 12 +/- 6/7 +/- 3 mm Hg, standing). The final mean recumbent diastolic blood pressure (86.9 mm Hg) was the same in both groups. Prolonged normotension may follow a period of carteolol treatment, again suggesting the potential importance of periodic withdrawal of antihypertensive medication.


Subject(s)
Carteolol/therapeutic use , Hypertension/drug therapy , Propanolamines/therapeutic use , Sympathomimetics , Blood Pressure/drug effects , Clinical Trials as Topic , Double-Blind Method , Female , Humans , Hypertension/physiopathology , Male , Middle Aged , Random Allocation
2.
JAMA ; 256(16): 2214-21, 1986.
Article in English | MEDLINE | ID: mdl-3531560

ABSTRACT

We compared verapamil and propranolol hydrochloride for monotherapy of hypertension. Verapamil lowered blood pressure (BP) more effectively than propranolol in black and white patients. Verapamil was equally effective in blacks and whites, whereas propranolol was more effective in whites. Heart rate was reduced by 6.0 beats per minute by verapamil, and by 13.6 beats per minute by propranolol. In blacks, verapamil lowered systolic BP 16.9 vs 8.1 mm Hg for propranolol; verapamil reduced diastolic BP 12.8 vs 8.6 mm Hg for propranolol. In whites, verapamil lowered systolic BP 19.0 vs 12.7 mm Hg for propranolol; verapamil reduced diastolic BP 16.7 vs 12.3 mm Hg for propranolol. Increases in systolic BP were observed in 22% and 3.4% of patients receiving propranolol and verapamil, respectively. The PR interval was increased from 163.5 to 174.9 ms for verapamil vs 160.3 to 164.4 ms for propranolol. Constipation (15%) and headaches (10%) were most frequent complaints for verapamil vs fatigue (18%) and dizziness (7%) for propranolol. Changes in blood biochemistry values were of small magnitude. We conclude that verapamil monotherapy is a safe and effective means of achieving BP control in patients with essential hypertension.


Subject(s)
Hypertension/drug therapy , Propranolol/therapeutic use , Verapamil/therapeutic use , Adult , Black or African American , Clinical Trials as Topic , Dose-Response Relationship, Drug , Double-Blind Method , Humans , Hypertension/ethnology , Propranolol/adverse effects , Random Allocation , Verapamil/adverse effects , White People
3.
Clin Pharmacol Ther ; 37(1): 61-5, 1985 Jan.
Article in English | MEDLINE | ID: mdl-3880686

ABSTRACT

Effects of once-daily doses of 50 mg triamterene with 25 mg hydrochlorothiazide and 5 mg amiloride with 50 mg hydrochlorothiazide were compared in a randomized, multicenter study of 84 adult subjects with mild to moderate hypertension (diastolic blood pressure 90 to 114 mm Hg). After a 3-wk placebo lead-in period, the subjects entered a 6-wk treatment period. The two drug regimens were compared with respect to antihypertensive effects and effects on serum potassium and magnesium levels during the final week of drug therapy, with the use of the last week of placebo therapy as a covariate. Both drug regimens substantially reduced mean supine systolic and diastolic blood pressures to well within normal limits; there was no significant difference the two groups. Twenty-four of the 41 subjects receiving triamterene-hydrochlorothiazide (59%) and 29 of the 43 patients receiving amiloride-hydrochlorothiazide (67%) had diastolic blood pressure less than 90 mm Hg at week 9. Five subjects receiving amiloride-hydrochlorothiazide (12%) and two subjects receiving triamterene-hydrochlorothiazide (5%) had hypokalemia (serum potassium level less than 3.5 mEq/l) at week 9. The average decrease in serum potassium levels during amiloride-hydrochlorothiazide therapy (-0.33 +/- 0.08 mEq/l) was greater than that after triamterene-hydrochlorothiazide (- 0.08 +/- 0.07 mEq/l). Serum magnesium levels were not changed by either regimen. Weight loss was greater in the amiloride-hydrochlorothiazide group than in the triamterene-hydrochlorothiazide group.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Amiloride/therapeutic use , Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Potassium/metabolism , Pyrazines/therapeutic use , Triamterene/therapeutic use , Adult , Aged , Blood Pressure/drug effects , Clinical Trials as Topic , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Potassium/blood , Random Allocation
4.
JAMA ; 252(21): 2957-8, 1984 Dec 07.
Article in English | MEDLINE | ID: mdl-6502851
7.
Group Pract J ; 30(6): 11-4, 1981 Jul.
Article in English | MEDLINE | ID: mdl-10251934
8.
Cutis ; 26(5): 503-5, 1980 Nov.
Article in English | MEDLINE | ID: mdl-7460620

ABSTRACT

Elastosis perforans serpiginosa (EPS) is a cutaneous connective tissue disorder featuring transepidermal elimination of altered elastic tissue. Morphologically and histologically EPS presents characteristic patterns; the case reported herein classically illustrates these patterns. In approximately one-fourth of reported cases, EPS has been associated with systemic connective tissue disorders and may thus be a useful clue in the early recognition of diseases such as Down's syndrome or pseudoxanthoma elasticum.


Subject(s)
Connective Tissue Diseases/pathology , Skin Diseases/pathology , Skin/pathology , Adolescent , Diagnosis, Differential , Humans , Male
9.
N Engl J Med ; 302(14): 817, 1980 Apr 03.
Article in English | MEDLINE | ID: mdl-7354831
10.
J Clin Psychiatry ; 39(8): 679-82, 1978 Aug.
Article in English | MEDLINE | ID: mdl-28313

ABSTRACT

In this multi-clinic double-blind study, patients suffering from insomnia were treated with triazolam 0.5 mg (Halcion) or placebo for 14 days. Four investigators treated 239 patients, 122 on triazolam and 117 on placebo. Thirty-nine patients, 10 on triazolam and 29 on placebo, dropped out for ineffectiveness of the medication and 32 patients, 16 in each group, dropped out for side effects. Analysis of pooled efficacy data showed that triazolam was significantly better than placebo on all efficacy parameters measured, including how much the medication helped the patients sleep, onset of sleep, duration of sleep, duration compared to usual, number of nocturnal awakenings, and feeling of restfulness in the morning. Triazolam did not produce evidence of tolerance development after 2 weeks of treatment. The same variety of side effects occurred on each treatment and primarily included drowsiness, grogginess, headaches, impaired coordination nausea, and dizziness.


Subject(s)
Anti-Anxiety Agents/therapeutic use , Sleep Initiation and Maintenance Disorders/drug therapy , Triazolam/therapeutic use , Adolescent , Adult , Clinical Trials as Topic , Double-Blind Method , Humans , Middle Aged , Sleep/drug effects , Triazolam/administration & dosage
11.
JAMA ; 238(15): 1628, 1977 Oct 10.
Article in English | MEDLINE | ID: mdl-578235
12.
Group Pract ; 25(2): 22-3, 1976.
Article in English | MEDLINE | ID: mdl-1024050
16.
J Med Soc N J ; 66(5): 202-3, 1969 May.
Article in English | MEDLINE | ID: mdl-4239097
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