Charles Bowesman, O.B.E., B.A., M.D., F.R.C.S.E., F.A.C.S., D.T.M.&H., Editor. 1st edition, 1068 + viii pages, illustrated. Edinburgh and London, E. & S. Livingstone Ltd. (The Williams & Wilkins Co., Baltimore, exclusive U.S. agents), 1960. $22.50
* Division of Parasitic Diseases, Center for Infectious Diseases, Centers for Disease Control, Public Health Service, U.S. Department of Health and Human Services, 1600 Clifton Road, Atlanta, Georgia,30333
| † Center for Applied and Field Research, Qalyub Bilharziasis Project, Imbaba-Giza, Arab Republic of Egypt
| ‡ Department of Tropical Medicine and Parasitology, Tulane University School of Public Health and Tropical Medicine, 1430 Tulane Avenue, New Orleans, Louisiana 70112
The objective of this study was to determine a suitable method for quantitating Schistosoma haematobium eggs in urine specimens preserved in carbolfuchsin. Using a 0.002% carbolfuchsin-phenol-alcohol solution as a stain/preservative for urine obtained from 30 patients infected with S. haematobium, we compared egg counts obtained with four quantitative techniques: Nytrel filtration, Nuclepore filtration, suction filtration and centrifugation. Centrifugation gave statistically higher values than all other techniques for absolute number of eggs recovered in the preserved urine. We also measure a statistical difference between the counts obtained from Nuclepore filtration of fresh urine and those established on an equivalent volume of preserved urine by Nuclepore and Nytrel filtration. The preserved urine frequently caused obstruction of both Nuclepore filters and Whatman No. 1 filters (used in suction filtration), rendering them technically difficult to use and less satisfactory than other methods. From the techniques we examined, we conclude that in field studies where preservation of urine is necessary, preparation of Nuclepore filters with fresh urine, or centrifugation of a carbolfuchsin-preserved urine, are the methods of choice for quantitation of specimens.
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