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S Merchant

Publications and source records attributed to S Merchant.

49 records · Page 3Linked to original sources

Frequency of inferior vena caval abnormalcy due to a juxtaposed pathology.

Radionuclide inferior vena cavagrams were done in 135 patients who had hepatomegaly, splenomegaly or a mass in the vicinity of the inferior vena cava (I.V.C.). 2-5mCi 66mTc phytate, 99mTc S colloid, 99mTc O4-, 99mTc-LIDA, 99mTc pyridoxyledene glutamate or 113mIn colloid were injected directly and rapidly into either a malleolar or a femoral vein while the patient lay supine under the 13.5'' detector head of a scinticamera. Rapid sequential scintiphotos were manually taken at approximately 1 sec. interval for 20-30 sec. Thus iliac vein, I.V.C., cardiopulmonary zone in infants, aorta and the arterial phase were visualized. 48% of these subjects had an abnormal I.V.C. and the depictions were interestingly varied, indicating that different patients responded in a different manner even to grossly similar pathologies. It became evident that this soft walled vessel could be compressed by both fluids and neoplastic tissue (Fig. 1, 2); the long I.V.C. channel could also be segmentally pushed away by a mass in its vicinity. (Fig. 2, 3, 4). An abnormal arterial flush usually differentiated between benign (Fig. 2) and malignant (Fig. 3) lesions, even when the mass was extra-hepatic (Fig. 4) and retiroperitoneal (Fig. 5). Such a systematic study of I.V.C. had not been possible earlier since the classical x-ray contrast inferior vena cavagram necessitates venous dissection, passage of a catheter, and the injection of large volume of fluid under an unphysiologically high pressure. The simplified radionuclide technique, however, permitted the study of neonates and critically ill subjects with massive ascites, while retaining a satisfactory reproducability.

Abdominal Muscles

Radiorespirometric study of carbohydrate metabolism in childhood liver disease.

The need for a suitable parameter to evaluate patients with chronic liver disease has been felt for some time, especially in order to judge the response to surgical shunts and the influence of certain drugs and diets on the liver. Since the liver is a major organ for carbohydrate metabolism, it was decided to analyze the in vivo oxidation of such substrates as glucose and galactose labeled with 14C. Moderately advanced "Indian childhood cirrhosis" and idiopathic fatty hepatic infiltration were selected to represent diffuse chronic liver disease. Oral administration of 14C-U-glucose or 14C-1-galactose was followed by analyses of 14CO2 in breath by liquid scintillation counting. Conversion of 14C-glucose to 14CO2 was accelerated by both diseases. On the other hand, oxidation of 14C-galactose was slowed in fatty infiltration and was markedly subnormal in Indian childhood cirrhosis.

Carbon Dioxide

Quality control in pulmonary function testing. A help or a hindrance?

The results of 120 sets of ventilatory capacity, lung volume (LV) and carbon monoxide transfer factor (TCOSB) measurements, 40 sets from each of three pulmonary function laboratories in one city, were examined retrospectively. Vital capacity (VC) was estimated by a forced expiratory manoeuvre (FVC), a relaxed expiratory manoeuvre (VCR) and an inspiratory manoeuvre (VCI) in the three different tests. Differences between VCR and FVC ranged from--88 ml to + 1 400 ml with a mean of + 47 ml. VCI differed from the largest estimate of expiratory VC by--1 800 ml to + 300 ml with a mean of--480 ml. Such differences, which were observed in all three laboratories, affect the calculations in each test and thus the final results quoted. Adequate quality control therefore requires comparison of estimates of VC not only within a test but also between tests. Although more time must be spent with some patients, technical errors and poor patient performance can be distinguished from true changes in pulmonary function, thus better enabling the clinician to assess the relationship between the results and the clinical condition of the patient.

Female