Comparison of a Urine Antigen Assay and Multiple Examinations with the Formalin-Ethyl Acetate Concentration Technique for Diagnosis of Opisthorchiasis

Author:

Worasith Chanika12,Techasen Anchalee23,Duenngai Kunyarat4,Intuyod Kitti25,Kopolrat Kulthida Y.6,Sithithaworn Jiraporn3,Loilome Watcharin27,Crellen Thomas89,Haswell Melissa R.101112,Sithithaworn Paiboon12

Affiliation:

1. Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;

2. Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand;

3. Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand;

4. Department of Thai Traditional Medicine, Faculty of Science and Technology, Phetchabun Rajabhat University, Phetchabun, Thailand;

5. Department of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;

6. Faculty of Public Health, Kasetsart University Chalermphrakiat Sakon Nakhon Province Campus, Sakon Nakhon, Thailand;

7. Department of Biochemistry, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;

8. School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom;

9. Big Data Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom;

10. Indigenous Strategy and Services, University of Sydney, Sydney, Australia;

11. School of Geosciences, University of Sydney, Sydney, Australia;

12. School of Public Health and Social Work, Queensland University of Technology, Brisbane, Australia

Abstract

ABSTRACT. Detection of worm antigen in urine is a sensitive diagnostic method for opisthorchiasis, particularly for light-intensity infections; however, the presence of eggs in feces is essential for validating results from the antigen assay. To address the issue of low sensitivity of fecal examination, we modified the protocol for the formalin-ethyl acetate concentration technique (FECT) and compared it against urine antigen measurements for detection of the parasite Opisthorchis viverrini. First, we optimized the FECT protocol by increasing the number of drops for examinations from the standard two drops to a maximum of eight. We were able to detect additional cases after examination of ≥ 3 drops, and the prevalence of O. viverrini saturated after examination of ≥ 5 drops. We then compared the optimized FECT protocol (examining five drops of suspension) against urine antigen detection for the diagnosis of opisthorchiasis in field-collected samples. The optimized FECT protocol detected O. viverrini eggs in 25 of 82 individuals (30.5%) who had positive urine antigen tests but were fecal egg negative by the standard FECT protocol. The optimized protocol also retrieved O. viverrini eggs in 2 of 80 antigen-negative cases (2.5%). In comparison with the composite reference standard (combined FECT and urine antigen detection), the diagnostic sensitivity of examining two and five drops of FECT and the urine assay was 58.2, 67, and 98.8%, respectively. Our results show that multiple examinations of fecal sediment increase the diagnostic sensitivity of FECT and thus provide further support for the reliability and utility of the antigen assay for diagnosis and screening of opisthorchiasis.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

Reference23 articles.

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