Citations

1. The results of closure of atrial septal defects in 155 patients over 45 years of age have been reviewed. 2. The over-all operative mortality rate was 6.5%; the operative mortality rate in the last 48 patients was 2.1%. 3. The late results of operation were considered excellent in 83% and good in 13% of the patients. 4. Long-term follow-up studies suggest that patients have significantly longer survival with closure of their defects. 5. It is concluded that operation for atrial septal defect in the older patient may be done at a low risk with an excellent prospect of a good, long-term result in almost all cases.

Ventricular performance was assessed before and after angiocardiography in 22 patients with normal left ventricle, mitral stenosis, aortic stenosis, and myocardial disease. The increased circulating blood volume known to occur after angiocardiography is a determinant of the increased ventricular pre-load. The after-load is unchanged. Patients with normal left ventricle and some patients with valve stenosis responded by an increase in the work performed and some had only a minimal or no increase. A group of patients with serious heart disease performed less work. If the ventricular response can be considered on the basis of the Frank-Starling principle, then the abnormal response of such patients is due to an altered length-tension relationship.

Data on 11 patients with orthostatic hypotension and primary systemic amyloidosis have been presented. Dizziness and light-headedness or syncope significantly hampered the involved patients. Three were incapacitated by orthostatic hypotension. Diarrhea, nausea, vomiting, and loss of weight were common, and adrenal insufficiency was seriously considered in the differential diagnosis of six of the 11 patients. Abnormal sweating was found in all six in whom this test was done. The drug 9-α-fluorohydrocortisone showed promise in symptomatic therapy of the condition. The possibility of primary systemic amyloidosis should be considered in the presence of orthostatic hypotension. Rectal biopsy and bone-marrow aspiration are recommended as initial biopsy procedures unless another organ suitable for biopsy is obviously involved.

The atrioventricular conduction system was studied by a technique of selected serial histological sections in examples of tetralogy of Fallot and ventricular septal defect to correlate the anatomic findings observed with the electrophysiological findings as manifested by the vectorcardiographic pattern. Eight hearts were studied; two examples of each anomaly had electrocardiographic and VCG patterns in the frontal plane similar to A-V canal defects and two examples of each had ECG and VCG patterns usually associated with these lesions. Of the four examples of tetralogy, the two examples with VCG patterns similar to the A-V canal pattern differed from the other examples in that the distance between the A-V node and the origin of left bundle branching was shorter and the fibers destined to become the right bundle branch took an elongated course. The VSD examples offered less striking differences. A short distance from the A-V node to the onset of left bundle branching was seen in both examples with VCG patterns similar to the A-V canal pattern, but one example of VSD with a representative VCG pattern had a similar anatomic configuration. When measurement ratios were compared, the right bundle took its origin at a relatively greater distance from the A-V node in the examples with VCG patterns similar to the A-V canal pattern. The anatomic configuration of those examples of tetralogy and VSD with VCG patterns similar to the A-V canal pattern was such that relatively early conduction to the left bundle branch system could occur.

Triamterene (2,4,7-triamino-6-phenylpteridine) was employed alone and in combination with hydrochlorothiazide in the treatment of patients with group 1 and 2 hypertension. In 21 patients, triamterene alone had an inconsistent antihypertensive effect on the systolic blood pressure, which was minimal in most patients. In 16 patients the combination of triamterene and hydrochlorothiazide (2:1 by weight) reduced the systolic blood pressure slightly more than did hydrochlorothiazide alone. Triamterene alone or in combination with hydrochlorothiazide produced an increase in the concentration of potassium in serum. Side effects due to triamterene were similar to those noted with thiazide diuretics. In addition, five patients had a decrease in blood hemoglobin concentration, and two patients had reversible alterations in liver function during triamterene therapy. Triamterene may be a useful adjunct for thiazidetreated hypertensive patients by decreasing the likelihood of complicating hypokalemia.

The pharmacological and biochemical tests available for the diagnosis of pheochromocytoma were evaluated among 28 patients with proved tumors and 148 other patients in whom the diagnosis was suspected. Of the biochemical tests on urine, determinations of total metanephrines (MN) and of vanilmandelic acid (VMA) were much less subject to false-positive results than was determination of catecholamines (CA). Since urinary MN values changed the most in tumor patients, MN determination is preferred as the current screening test. Of the pharmacological tests, the histamine test continues to be the most valuable, especially when combined with determination of plasma CA concentration. The phentolamine (Regitine) test has not proved to be of any distinct value as a primary diagnostic aid. Any of the chemical or pharmacological tests occasionally may give a false-positive result. The urinary output of excessive amounts of homovanillic acid (HVA) was an indication of the presence of pheochromocytoma with some features histologically similar to other neural crest tumors but was not an indication of malignancy. Reliable diagnosis of pheochromocytoma still must be based on multiple studies in an appropriate clinical setting.

Cardiac output, stroke volume, and atrial, pulmonary arterial, left ventricular, and systemic arterial pressures were measured preoperatively, during operation, and for 48 hours thereafter in 14 patients undergoing prosthetic replacement of the mitral valve. Cardiac output was usually abnormally low after repair, being lowest 3 to 6 hours after operation. This pattern was different from that in a patient undergoing plication of the posterior leaflet and very different from that in a patient undergoing removal of a left atrial myxoma, who served as controls. Ventricular filling pressure was high, there was no significant diastolic pressure difference across the Starr-Edwards prosthesis, and there was no pressure difference across the left ventricular outflow tract. Blood gas levels and pH were within satisfactory range. The data are interpreted as indicating that impairment of ventricular performance, particularly left, usually contributes significantly to the low cardiac output in these patients. This is probably related in part to preoperative ventricular function. Possible additional contributing factors are discussed.

Data from 43 patients with common ventricle for whom satisfactory hemodynamic data are available are presented; these form 3.2% of the patients with congenital heart disease studied by means of catheterization at the Mayo Clinic. Selective biplane angiocardiography is essential for diagnosis of common ventricle. Associated cardiovascular anomalies are common, with transposition of the great vessels occurring in 84% of the patients. The right-to-left shunt present in all 43 patients results in desaturation of systemic arterial blood. The common ventricle receives all the systemic and pulmonary venous blood [see table in the PDF file] flows; yet complete mixing is uncommon in this chamber, for it occurred in only 16% of the patients who did not have severe pulmonary stenosis. Fifty-eight per cent had oxygenated blood directed preferentially to the systemic circuit ("favorable streaming"). This occurred most commonly with L-transposition and resulted in a higher oxygen saturation of systemic arterial blood. Obstruction to pulmonary flow (from pulmonary stenosis or pulmonary vascular disease) results in a larger right-to-left shunt and lower oxygen saturation of systemic arterial blood.

Seventeen of 44 patients undergoing operation for complete correction of transposition of the great arteries survived operation and were dismissed to return home. Three late deaths followed. Mortality remains high among infants less than one year old and among patients of all ages who have severely elevated pulmonary vascular resistance. Nine of the last 13 patients, in whom repair was accomplished by the Mustard technique, have survived. Late results in all surviving patients have generally been excellent.