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A study on intestinal helminths causing human anaemia in Cairo
Journal of the Egyptian Society of Parasitology
|June 1, 1989
Summary
This study examined parasitic infections in Egyptians, finding anemia in all cases. Ancylostomiasis showed the most severe anemia and highest eosinophilia compared to other infections.
Area of Science:
- Clinical Medicine
- Infectious Diseases
- Hematology
Background:
- Parasitic infections are prevalent in Egypt, affecting both urban and rural populations.
- Common helminthic infections include Ancylostoma duodenale, Ascaris lumbricoides, Enterobius vermicularis, Hymenolepis nana, Schistosoma mansoni, and Taenia saginata.
- These infections can lead to various clinical manifestations, including anemia.
Purpose of the Study:
- To investigate the hematological and biochemical profiles of Egyptians infected with common helminthic parasites.
- To compare the severity of anemia and associated hematological changes among different parasitic infections.
Main Methods:
- Hematological and biochemical analyses were performed on 50 Egyptian patients with confirmed parasitic infections.
- Parameters assessed included hemoglobin (Hb%), hematocrit, eosinophil count, total blood protein, blood cholesterol, and blood urea.
- Patients were categorized based on the specific parasitic infection identified.
Main Results:
- All infected individuals exhibited anemia of varying degrees.
- Ancylostomiasis cases presented with the lowest Hb% and hematocrit values, alongside severe hypochromia and the highest eosinophilia.
- Total blood protein levels were generally normal, with a slight elevation observed in two cases of Schistosoma mansoni infection. Blood cholesterol and urea levels remained unaffected.
Conclusions:
- Ancylostomiasis is associated with the most significant hematological disturbances, particularly severe anemia and hypochromia.
- While most parasitic infections studied did not cause major biochemical deviations, hematological monitoring is crucial for managing anemia in infected individuals.