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Biomedical subjects

C Almog

Publications and source records attributed to C Almog.

At least 37 records · Page 2Linked to original sources

Concealed bigeminy in acute myocardial infarction.

Concealed bigeminy represents a rhythm disorder in which bigeminy is ever-present, but the ventricular premature beats are not always detectable and there is an odd number of interectopic sinus beats. Retrospective examination of the ECG tracings of patients with acute myocardial infarction and ventricular premature beats demonstrated a statistically significant predominance of odd numbers of interectopic sinus beats. There were 20 cases of concealed bigeminy and in 10 of these the probability that this was a chance finding was less than 0.01. In 1 case with 79 consecutive odd series of interectopic beats the chance of such an occurrence was 2(-79). These results indicate that a predictable pattern may exist in the arrhythmias associated with some cases of acute myocardial infarction.

Cardiac Complexes, Premature↗

The effect of oral treatment with beta blockers on the tear secretion.

Tear secretion was examined in 194 patients treated with oral beta blockers, mainly with propranolol, oxprenolol, pindolol, and atenolol, and metaprolol and in 185 healthy control subjects. Statistical analysis included the Student's t test used to compare the mean values of tear secretion and the chi square test used to compare the percentage of eyes with tear hyposecretion between treated and control groups. This statistical study showed clearly that oral beta blockers significantly reduce the tear secretion.

Administration, Oral↗

Legionnaires' disease: a case acquired in Israel.

What is probably the first case of presumably nosocomial Legionnaires' Disease (LD) in Israel is described in a 56-yr-old man hospitalized for acute myocardial infarction. The patient developed bilateral pneumonia and hemorrhagic pleural effusion. The diagnosis of LD was confirmed by serological examinations that showed a significant increase and decrease in IgM- and IgG-type antibodies to Legionella pneumophila serogroups 1 and 3. The patient recovered on antibiotic treatment which included erythromycin.

Anti-Bacterial Agents↗

Usefulness of myoglobin radioimmunoassay determintion in CCU.

In 112 patients with an acute coronary event, admitted to the CCU of Assaf-Harofeh Hospital, myoglobin radioimmunoassay was determined at 0 (time of admission), 12 and 24 hours. In 77 patients with acute myocardial infarction (M.I.) (64 patients with acute transmural and 13 with acute subendocardial M.I.), the myoglobin values were significantly increased. Appearing in blood 3-4 hours after the onset of chest pains, myoglobin represents the earliest marker of acute M.I. known until know. In 12 of 23 cases diagnosed at first as acute coronary insufficiency according to clinical, biological and E.C.G. criteria, significantly increased values of myoglobin were found, as an expression of micro-necroses which were not detected by conventional methods (SGOT, CPK, LDH). This finding has important practical, prognostic and therapeutical implications, showing that myoglobin radioimmunoassay may detect myocardial micronecroses which are not discovered by usual methods. Myoglobin radioimmunoassay assessment offers a valuable indication of necrosis extent. Values above 800 ng/ml were accompanied in 65% of our cases with symptoms and signs of left heart failure, the highest values of myoglobin being found in extensive anterior M.I. associated with acute pulmonary edema. In 9 non cardiac patients with repeated intra-muscular injections with antibotics, the myoglobin was at the upper normal limit, demonstrating that intra-muscular injections, at least with antibiotics, have no influence on myoglobin values. From our experience it appears that the myoglobin radioimmunoassay determination is a useful tool for the early establishment of M.I. diagnosis and the assessment of myocardial necrosis extent.

Adult↗

Right myocardial infarction with predominant right ventricular dysfunction.

Two patients with right ventricular myocardial infarction are described. In both cases, the hemodynamic criteria established for this diagnosis were fulfilled, namely, right-side pressure values (central venous pressure and right atrial pressure) equal to or higher than left-side pressure values (pulmonary capillary wedge pressure and left ventricular end-diastolic pressure). ECG tracings showed acute diaphragmatic myocardial infarction. The lungs were clear both clinically and radiologically. The diagnosis of right ventricular myocardial infarction was confirmed in the first patient by hemodynamic studies and at autopsy, and in the second patient, by hemodynamic and echocardiographic studies. Only in the second care was the administration of massive quantities of fluids and dopamine followed by good results. The importance of establishing a precise diagnosis of right ventricular myocardial infarction is emphasized, since therapy for this condition is different than that for left ventricular myocardial infarction.

Aged↗

Autosomal recessive lipid storage myopathy (probable carnitine deficiency).

Two sisters died at the age of 17 and 19, respectively, of a myopathy with exacerbations and remissions characterised by pain and weakness of muscles which ended fatally with lactic acidosis and respiratory failure. The clinical picture was very similar to that described in some cases of carnitine deficiency and the histochemical finding of many lipid-filled vacuoles in muscle fibres and the electron microscopical findings were identical to those reported in that disease. The finding of affected sisters supports autosomal recessive mode of inheritance.

Adolescent↗

Acute intoxication with ajmaline.

A 57-year-old man ingested 1,000 mg of ajmaline with suicidal intent. He was unconscious, hypotensive and showed serious disturbances in cardiac conduction on admission. High serum and urine levels of ajmaline were found. Although only 4% of the ingested dose was excreted following forced diuresis, all evidence of toxicity disappeared within 21 h.

Acute Disease↗

Inflammatory fibrous histiocytoma of the bronchus.

A 33 year-old woman underwent lobectomy of the middle and lower lobes of the right lung because of inflammatory fibrous histiocytoma of the bronchus. To our knowledge, this is the first description of such a tumor originating in the bronchus.

Adult↗

Regression of malignant thymoma with metastases after treatment with adrenocortical steroids.

A patient with a malignant lymphoepithelial thymoma and pleural metastases is described. Incidental treatment with adrenocortical steroids after an allergic reaction resulted in a marked regression of the masses for a period of 18 months. A second course of treatment resulted in complete radiological regession of the tumors, and the patient has remained symptom free with normal chestX-rays for a further period of 18 months.

Female↗

Thymolipoma simulating cardiomegaly: a clinicopathological rarity.

This report describes a 19-year-old girl with a chest radiograph strongly suggestive of cardiomegaly. Although she did not consent to haemodynamic studies, cardiomegaly wasru led out on the basis of the clinical course. Careful radiological study proved the existence of a large mass in the anterior mediastinum, simulating cardiomegaly. At thoracotomy a thymolipoma weighing 450 g was resected. The pathogenesis of thymolipoma is discussed.

Adult↗