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Biomedical subjects

D H Fitchett

Publications and source records attributed to D H Fitchett.

34 records · Page 2Linked to original sources

Torsade de pointes. A cause of syncope with atrioventricular block.

Two patients with syncope due to an atypical ventricular tachycardia are described. In both, undulation of the QRS axis during episodes of tachycardia, a prolonged QT interval, the initiation of the tachycardia by a late ventricular premature depolarization, and the association with high-degree atrioventricular block suggested a diagnosis of "torsade de pointes" (twisting of the points). Therapy with conventional antiarrhythmic drugs did not control the arrhythmia, but increasing the heart rate by transvenous pacing completely suppressed the tachycardia. In one patient, the QT interval became normal with ventricular pacing alone, while in the second, the QT interval remained abnormal until correction of coexisting hypokalemia. Torsade de pointes is a recognized complication of bradyarrhythmias, hypokalemia, and therapy with quinidine-like and psychotropic drugs. The ideal treatment is to recognize and correct the underlying cause, as antiarrhythmic drugs can exacerbate the arrhythmia.

Aged↗

Ventricular aneurysm: false or True? An important distinction.

A case of ventricular false aneurysm withe the typical clinical, radiological, electrocardiographic, and angiographic features of this entity is presented. The distinction between false ventricular aneurysm and true aneurysm is discussed. This distinction is important because of the propensity of false aneurysms to rupture. An early diastolic murmur was present prior to, but not after, resection of the aneurysmal sac. A theory as to the origin of this murmur is offered.

Cardiac Catheterization↗

Cardiac involvement in secondary haemochromatosis: a catheter biopsy study and analysis of myocardium.

Although high blood transfusion regimens have improved the life expectancy of the patient with Thalassemia Major, cardiac failure and arrhythmias remain a cause of early death. It is not certain whether the massive myocardial iron deposition found in such patients is preventable by intensive chelation therapy. This study evaluates endomyocardial biopsy as a method of assessing myocardial iron deposition. Of four patients with clinical and biochemical evidence of severe haemochromatosis, only one had a myocardial iron content comparable to that found in severe haemochromatotic myocardium. The one patient with cardiac failure had an endomyocardial iron content within the normal range. Studies of the iron distribution in haemochromatotic myocardium demonstrate that the subendocardial myocardium contains only half the iron content of the subepicardial layer, and there is a large sampling variation. It is concluded that catheter endomyocardial biopsy is an insensitive method of determining early myocardial deposition because of the location of iron and the variability of the sampling. Studies of the nature of the myocardial iron protein with CM32 cation exchange resin chromatography show that there is a large increase in the haemosiderin: ferritin ratio (5:1) in iron overload myocardium as compared with the normal heart (2:1). Similar results have been observed in the liver with iron overload, where the increase in hepatic haemosiderin was associated with greater lysosomal fragility. It is possible that myocardial cell damage may also occur by the rupture of iron engorged lysosomes.

Adolescent↗

Myocardial subcellular fractionation studies on cardiomyopathic Syrian hamsters.

Myocardial homogenates from control animals and from hamsters with hereditary cardiomyopathy were subjected to analytical subcellular fractionation and enzymic microanalysis. Animals without ventricular hypertrophy or overt heart failure were used in this study. The principal subcellular organelles were characterised by density gradient centrifugation. Apart from evidence of enhanced lysosomal and peroxisomal fragility, probably secondary to the intracellular oedema, the intracellular organelles investigated in this study were unaffected by the myopathic process. Highly significant increases in 5'-nucleotidase activity, a marker for the sarcolemma, and an increased equilibrium density of this organelle were found in the myopathic tissue. Ultrastructural studies revealed patchy myocytolysis associated with lysosomes and with more extensive invaginations of the sarcolemma. It is suggested that a primary defect in membrane composition, leading to increased cation permeability, is the underlying abnormality in the myopathic hamster.

Animals↗

Aneurysm of left ventricle secondary to bacterial endocarditis.

Three cases are described of aneurysms of the area of fibrous continuity between the aortic and mitral valves, each associated with infective endocarditis of the aortic valve. In two cases surgical treatment was successful, one of these having been diagnosed by angiography prior to operation. The other case was discovered only at autopsy, but the histologic findings showed the lesion to be a true aneurysm. Although some cases have been successfully managed by operation, most have proved fata. These cases and the previous successes illustrate the potential value of urgent operation.

Adult↗

"Torsade de pointes" initiated by electrical ventricular stimulation.

Four cases are described in which electrical stimulation of the right ventricle produced the ventricular arrhythmia known as "torsade de pointes". This arrhythmia has previously been described as classically occurring in the context of the chronic bradycardias, particularly when there is also hypokalemia and a long QT interval, being most frequently initiated by a ventricular extrasystole occurring relatively late during ventricular repolarization. One patient had suffered a recent anterior myocardial infarction and developed the arrhythmia during rapid pacing for atrial flutter, when the electrode catheter had inadvertently entered the right ventricle. In the other three patients the arrhythmia was produced during the ventricular extrastimulus test performed during routine diagnostic electrophysiological investigation.

Adult↗

Practolol peritonitis presenting as a pelvic mass.

A case of sclerosing fibro-peritonitis occurring as a result of practolol therapy is presented. This may occur months after cessation of the practolol because of other side effects and may present to the gynaecologists as a pelvic mass.

Adult↗

Granulomatous mitral valve obstruction.

Acquired non-rheumatic valvular mitral valve obstruction is extremely rare. A case of mitral valve obstruction is described which resulted from a granulomatous mass replacing the valve cusps. The problems in diagnosis and probable aetiology are discussed.

Adult↗

Intravenous salbutamol in management of status asthmaticus.

After the administration of intravenous salbutamol (100-300 mug) to 11 patients admitted to hospital with a severe exacerbation of asthma there was a mean increase in peak expiratory flow of 44% accompanied by a rise in pulse rate of 24 beats/min. Blood gas tensions showed a trend to improvement and there were no serious side effects. It is concluded that intravenous salbutamol is an effective and apparently safe bronchodilator in the management of acutely ill patients with severe asthma.

Acute Disease↗

A Canadian multicentre study of a 48 h infusion of milrinone in patients with severe heart failure.

Milrinone is a nonglycoside, nonsympathomimetic bipyridine with positive inotropic and systemic vasodilator properties. In order to evaluate the efficacy and safety of a short term infusion of milrinone, 105 patients with stable New York Heart Association (NYHA) class III or IV heart failure received a loading dose (50 micrograms/kg) and a 48 h continuous infusion (0.5 micrograms/kg/min). Administration of the loading dose resulted in a 28% decrease in pulmonary capillary wedge pressure (PCWP) (P less than 0.001), a 38% increase in cardiac index (P less than 0.001), and a 34% increase in stroke volume index (P less than 0.001) within 15 mins. Milrinone infusion maintained an average 27% and 24% reduction in PCWP during the first and second days, respectively (P less than 0.001). Cardiac index was 32% and 34% above baseline during the same intervals (P less than 0.001). There were no clinically significant changes in heart rate or mean arterial blood pressure during the study period. In a subset of 47 patients who underwent Holter monitoring before and during infusion, a significant increase in ventricular arrhythmias (premature ventricular complexes per hour, ventricular couplets per hour and ventricular runs greater than or equal to three) was demonstrated (P less than 0.0001). In general, milrinone was well tolerated. Of the 105 patients entered, one died of an acute myocardial infarction after premature termination of the infusion, and the infusion rate was decreased in two others because of supraventricular arrhythmias. In patients with severe heart failure, intravenous milrinone has significant beneficial hemodynamic effects. ECG monitoring for arrhythmias is recommended during milrinone infusion.

Adult↗

Dyslipoproteinemias after heart and heart-lung transplantation: potential relation to accelerated graft arteriosclerosis.

Plasma lipid, lipoprotein lipid, and low-density lipoprotein (LDL) apolipoprotein B (Apo B) levels were measured in 34 patients who had undergone heart transplantation and in two patients who had undergone heart-lung transplantation. In contrast to initial reports, atherogenic dyslipoproteinemias were common, with 14% of patients having increased LDL cholesterol levels, 16.7% increased triglyceride levels, 8.3% decreased high-density lipoprotein (HDL) cholesterol levels, and 22.2% increased LDL Apo B levels. Of interest, 14% of patients had an HDL cholesterol level greater than the 95th percentile of the general population. In four patients coronary arteriosclerosis developed after transplantation. All had an atherogenic dyslipoproteinemia. One had type II hypercholesterolemia, and one had isolated low HDL cholesterol levels. Two had hyperapobetalipoproteinemia, one of whom also had low HDL cholesterol levels. The results establish that atherogenic dyslipoproteinemias are frequent in patients after heart transplantation and suggest that these dyslipoproteinemias, along with rejection, may play a role in the pathogenesis of arteriosclerosis after transplantation.

Adult↗