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3.
J Am Coll Cardiol ; 10(2): 246-52, 1987 Aug.
Article in English | MEDLINE | ID: mdl-2955019

ABSTRACT

Determination of the restenosis rate after multilesion percutaneous transluminal coronary angioplasty is an important consideration in defining expanded indications for the procedure. Of 209 patients who underwent successful multilesion coronary angioplasty, 55 symptomatic and 74 asymptomatic patients were restudied an average of 7 +/- 4 months after dilation. The restenosis rate was 82% (45 of 55) in the symptomatic patients and 30% (22 of 74) in the asymptomatic patients (p less than 0.001). Only 4% of the asymptomatic patients had restenosis at more than one dilation site. When only patients who developed a restenosis were considered, the restenosis occurred at more than one dilation site in 47% (21 of 45) of the symptomatic group versus 14% (3 of 22) of the asymptomatic group (p less than 0.05). When all recurrent stenoses were examined, the severity of the luminal narrowing was greater than or equal to 70% in 64% (45 of 70) of the stenotic lesions in the symptomatic patients versus 31% (8 of 26) of the stenotic lesions in the asymptomatic patients (p less than 0.05). Proximal left anterior descending coronary artery disease, increased length of the stenotic narrowing, male gender and diabetes were associated with an increased incidence of restenosis by multivariate analysis. Patient-related variables were not predictive of multilesion restenosis. In conclusion, the majority of patients are clinically improved after multilesion coronary angioplasty. Recurrent symptoms after multilesion coronary angioplasty are frequently associated with multilesion restenosis and a more severe degree of restenotic narrowing. Restenosis at more than one dilation site is uncommon in the asymptomatic patient.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Angioplasty, Balloon , Coronary Disease/therapy , Adult , Aged , Cardiac Catheterization , Coronary Angiography , Female , Follow-Up Studies , Humans , Male , Middle Aged , Recurrence , Sex Factors
5.
Cancer ; 59(10): 1713-6, 1987 May 15.
Article in English | MEDLINE | ID: mdl-3103904

ABSTRACT

The safety and efficacy of buserelin, a luteinizing hormone-releasing hormone (LH-RH) agonist, was tested in 33 evaluable patients with Stages C or D adenocarcinoma of the prostate. With a minimum follow-up duration of 10 months, there was one complete response and 22 partial responses (69%) by National Prostatic Cancer Project criteria, with a median duration greater than 18 months. Six patients (18%) had stable disease, median duration greater than 25 months, and only 12 patients have progressed. Performance status improved in 67%, patient-scored pain improved in 75%, and quality of life improved in 58%. Symptoms occurring during treatment consisted of hot flashes, loss of libido, and impotence. Buserelin produces a high frequency of durable objective and subjective responses in patients with advanced prostatic carcinoma.


Subject(s)
Adenocarcinoma/drug therapy , Buserelin/therapeutic use , Prostatic Neoplasms/drug therapy , Adenocarcinoma/pathology , Aged , Follow-Up Studies , Humans , Male , Prostatic Neoplasms/pathology , Quality of Life
7.
J Cancer Educ ; 2(4): 229-31, 1987.
Article in English | MEDLINE | ID: mdl-3274980

ABSTRACT

A pilot cancer education program for Boy Scouts in grades six through nine was developed. Motivation to complete requirements was provided by awarding a "Cancer Awareness Patch." Content of the program included health issues related to smoking and tobacco use, diet, and sun exposure, plus education about the practice of testicular self-examination, and sunscreen usage. Retention of factual material was good up to 18 months post-program. Participants developed positive attitudes toward lifestyle development and volunteerism. The program is recommended for supplementation of school health promotion curricula.


Subject(s)
Health Education/methods , Neoplasms/prevention & control , Adolescent , American Cancer Society , California , Child , Follow-Up Studies , Humans , Male , Pilot Projects , United States
10.
Can J Cardiol ; 1(4): 259-62, 1985.
Article in English | MEDLINE | ID: mdl-2996729

ABSTRACT

Intravenous labetalol was evaluated in 10 patients with stable angina without heart failure. Mean dose was 1.75 mg/kg (range 1.5-2 mg/kg). Measurements were taken within one minute after the injection, and at 1, 5 and 15 minutes thereafter. Labetalol significantly decreased blood pressure and increased heart rate. Peak aortic flow velocity increased only significantly at 1 minute; dP/dt+ max. was significantly decreased during all the measurements. Left ventricular end diastolic pressure did not change. Thus in patients without failure left ventricular function remained stable despite the negative inotropic effects of labetalol.


Subject(s)
Coronary Disease/drug therapy , Labetalol/therapeutic use , Myocardial Contraction/drug effects , Receptors, Adrenergic, alpha/drug effects , Receptors, Adrenergic, beta/drug effects , Angina Pectoris/drug therapy , Blood Flow Velocity/drug effects , Blood Pressure/drug effects , Cardiac Output/drug effects , Heart Rate/drug effects , Humans , Infusions, Parenteral , Male , Middle Aged
11.
Am J Cardiol ; 49(5): 1267-9, 1982 Apr 01.
Article in English | MEDLINE | ID: mdl-7064851

ABSTRACT

Labetalol, an alpha and beta receptor blocking agent, was evaluated in 11 patients with documented coronary artery disease and stable angina. The mean dose of labetalol was 1.5 (range 1 to 2) mg/kg. Cardiovascular effects began within 1 minute after injection and were maximal within 10 minutes. Mean arterial pressure decreased from 105 +/- 13 to 81 +/- 10 mm Hg (p less than 0.0001), heart rate from 70 +/- 10 to 66 +/- 7 beats/min (p less than 0.05) and the pressure-rate product from 10,322 +/- 2,344 to 7,171 +/- 1,650 (p less than 0.001). Cardiac output and pulmonary wedge pressure did not change significantly. Mean pulmonary arterial pressure decreased from 20 +/- 3 to 16 +/- 2 mm Hg (p less than 0.005). Systemic and pulmonary resistances also decreased significantly (p less than 0.0001 and p less than 0.01, respectively). Coronary sinus flow increased from 107 +/- 26 to 118 +/- 25 ml/min (p less than 0.01) and coronary vascular resistance decreased from 1.0 +/- 0.2 to 0.77 +/- 0.1 mm Hg/ml per min (p less than 0.001). Labetalol may be a useful adjunct in the treatment of angina not only because it diminishes myocardial oxygen requirements but also because it improves coronary hemodynamics. Thus, labetalol appears to have some advantage compared with the usual beta blocking agents with their potentially detrimental effects on coronary hemodynamics.


Subject(s)
Coronary Disease/drug therapy , Ethanolamines/therapeutic use , Labetalol/therapeutic use , Adult , Blood Pressure/drug effects , Cardiac Output/drug effects , Coronary Circulation/drug effects , Female , Heart Rate/drug effects , Humans , Injections, Intravenous , Labetalol/administration & dosage , Male , Middle Aged , Pulmonary Artery/drug effects , Vascular Resistance/drug effects
12.
Cathet Cardiovasc Diagn ; 8(4): 393-7, 1982.
Article in English | MEDLINE | ID: mdl-6812962

ABSTRACT

Myocardial infarction is usually caused by a thrombus occurring on a significant coronary lesion. A 60-year-old male was admitted with an acute evolving anterior myocardial infarction. Three hours after the beginning of chest pain, the electrocardiogram showed ST-segment elevation in the anterior and lateral leads which persisted despite intravenous nitroglycerin (100 mcg/min). One hour later, an angiogram showed complete obstruction at the origin of the left anterior descending artery (LAD). After intracoronary streptokinase (250,000 units) the LAD opened and a 90% obstruction was seen at its origin. However, an anterior myocardial infarction occurred. One month later, an angiogram showed a slight irregularity at the origin of the LAD. Thus, this case demonstrates that 1) a myocardial infarction may occur with a near normal coronary artery, and 2) a thrombus may occur at the site of a slight coronary irregularity.


Subject(s)
Coronary Circulation/drug effects , Coronary Disease/drug therapy , Myocardial Infarction/drug therapy , Streptokinase/therapeutic use , Cardiac Catheterization , Coronary Angiography , Coronary Disease/diagnostic imaging , Coronary Vasospasm/complications , Coronary Vasospasm/diagnostic imaging , Humans , Male , Middle Aged , Myocardial Infarction/diagnostic imaging , Nitroglycerin/therapeutic use
13.
Can Med Assoc J ; 113(10): 966-7, 1975 Nov 22.
Article in English | MEDLINE | ID: mdl-1192314

ABSTRACT

A patient with methadone-induced pulmonary edema had increased extravascular water in the lungs and a reduced total vascular albumin space. Diuresis resulted in hypotension. These observations suggest that the appropriate treatment of this condition should be ventilatory support and restoration of plasma oncotic pressure with albumin. Diuretic therapy should be used with caution.


Subject(s)
Methadone , Pulmonary Edema/chemically induced , Substance-Related Disorders , Adult , Body Water , Capillary Permeability/drug effects , Diuretics/adverse effects , Diuretics/therapeutic use , Humans , Hypotension/chemically induced , Male , Pulmonary Edema/therapy , Respiration, Artificial , Serum Albumin/analysis
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