Comparison of polyvinyl alcohol fixative with three less hazardous fixatives for detection and identification of intestinal parasites. 2000

B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
Veterans Affairs Medical Center, Atlanta, GA 30033, USA.

Polyvinyl alcohol (PVA) containing the fixative mercuric chloride is considered the "gold standard" for the fixation of ova and parasites in the preparation of permanently stained smears of stool specimens. However, mercuric chloride is potentially hazardous to laboratory personnel and presents disposal problems. We compared three new alternative, nontoxic fixatives with PVA, analyzing ease of sample preparation and quality of smears. Sixty-eight fresh stool specimens were divided into aliquots and placed in each of four different fixatives: PARASAFE (PS) (Scientific Devices Laboratory, Inc., Des Plaines, Ill.), ECOFIX (EC) (Meridian Diagnostics, Inc., Cincinnati, Ohio), Proto-Fix (PF) (Alpha-Tec Systems, Inc., Vancouver, Wash.), and low-viscosity PVA fixative (PVA) (Meridian). Specimens were processed and stained according to each manufacturer's directions. Parasites were found in 31 of 68 slide preparations with PVA, 31 with PF, 30 with EC, and 30 with PS. Blastocystis hominis and Iodamoeba bütschlii were preserved in a readily identifiable state by all methods of fixation. However, some parasites were more easily identified with some of the fixatives because of differences in parasite distortion. For example, Entamoeba histolytica (Entamoeba dispar) was detected in 13 stools fixed with PF, 7 with PVA, and 6 with EC but none with PS. Likewise, Chilomastix mesnili was identified in 13 specimens fixed with PF, 8 with EC, and 5 with PVA but only 1 with PS, while Entamoeba coli was seen much less frequently with PS than with the other three fixatives. A dirty background was observed in 41% of specimens prepared with PS, whereas background quality was acceptable with other fixatives. Sample preparation was most rapid with PS, although the EC method involved the fewest steps. In conclusion, PVA and PF produced the least parasite distortion, while PS proved unsatisfactory for the identification of E. histolytica, E. coli, and C. mesnili. Both PF and EC appear to be acceptable, environmentally safe substitutes for PVA.

UI MeSH Term Description Entries
D007411 Intestinal Diseases, Parasitic Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS. Parasitic Intestinal Diseases,Disease, Parasitic Intestinal,Diseases, Parasitic Intestinal,Intestinal Disease, Parasitic,Parasitic Intestinal Disease
D010274 Parasitology The study of parasites and PARASITIC DISEASES. Medical Parasitology,Parasitology, Medical
D011142 Polyvinyl Alcohol A polymer prepared from polyvinyl acetates by replacement of the acetate groups with hydroxyl groups. It is used as a pharmaceutic aid and ophthalmic lubricant as well as in the manufacture of surface coatings artificial sponges, cosmetics, and other products. Liquifilm Tears,Polyviol,Alcohol, Polyvinyl,Tears, Liquifilm
D011528 Protozoan Infections Infections with unicellular organisms formerly members of the subkingdom Protozoa. Histomoniasis,Infections, Protozoan,Histomoniases,Infection, Protozoan,Protozoan Infection
D005243 Feces Excrement from the INTESTINES, containing unabsorbed solids, waste products, secretions, and BACTERIA of the DIGESTIVE SYSTEM.
D005404 Fixatives Agents employed in the preparation of histologic or pathologic specimens for the purpose of maintaining the existing form and structure of all of the constituent elements. Great numbers of different agents are used; some are also decalcifying and hardening agents. They must quickly kill and coagulate living tissue. Fixative,Pickling Agents,Agents, Pickling
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D015386 Hazardous Substances Elements, compounds, mixtures, or solutions that are considered severely harmful to human health and the environment. They include substances that are toxic, corrosive, flammable, or explosive. Biohazard,Hazardous Chemical,Hazardous Chemicals,Hazardous Material,Hazardous Materials,Hazardous Substance,Toxic Environmental Substance,Toxic Substances, Environmental,Biohazards,Chemicals, Hazardous,Environmental Substances, Toxic,Toxic Environmental Substances,Chemical, Hazardous,Environmental Substance, Toxic,Environmental Toxic Substances,Material, Hazardous,Materials, Hazardous,Substance, Hazardous,Substance, Toxic Environmental,Substances, Environmental Toxic,Substances, Hazardous,Substances, Toxic Environmental
D056890 Eukaryota One of the three domains of life (the others being BACTERIA and ARCHAEA), also called Eukarya. These are organisms whose cells are enclosed in membranes and possess a nucleus. They comprise almost all multicellular and many unicellular organisms, and are traditionally divided into groups (sometimes called kingdoms) including ANIMALS; PLANTS; FUNGI; and various algae and other taxa that were previously part of the old kingdom Protista. Eukaryotes,Eucarya,Eukarya,Eukaryotas,Eukaryote

Related Publications

B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
January 1973, Boletin chileno de parasitologia,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
January 1954, Boletin chileno de parasitologia,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
December 1981, Journal of clinical microbiology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
June 1983, Journal of clinical microbiology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
March 1967, Stain technology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
February 1993, Journal of clinical microbiology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
August 1967, Technical bulletin of the Registry of Medical Technologists. American Society of Clinical Pathologists. Registry of Medical Technologists,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
January 1993, Journal of clinical microbiology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
July 1953, American journal of clinical pathology,
B Jensen, and W Kepley, and J Guarner, and K Anderson, and D Anderson, and J Clairmont, and W De L'aune, and E H Austin, and G E Austin
January 1970, Revista de la Facultad de Ciencias Medicas de Cordoba,
Copied contents to your clipboard!