Mimicking platelet indices in patients with malaria and dengue hemorrhagic fever: characteristics and clinical applications
Issued Date
2022-12-01
Resource Type
ISSN
13488945
eISSN
13494147
Scopus ID
2-s2.0-85139678391
Journal Title
Tropical Medicine and Health
Volume
50
Issue
1
Rights Holder(s)
SCOPUS
Bibliographic Citation
Tropical Medicine and Health Vol.50 No.1 (2022)
Suggested Citation
Mon N.T.S., Tangpukdee N., Charunwatthana P., Boonnak K., Krudsood S., Kano S., Wilairatana P., Leowattana W. Mimicking platelet indices in patients with malaria and dengue hemorrhagic fever: characteristics and clinical applications. Tropical Medicine and Health Vol.50 No.1 (2022). doi:10.1186/s41182-022-00467-8 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/87174
Title
Mimicking platelet indices in patients with malaria and dengue hemorrhagic fever: characteristics and clinical applications
Other Contributor(s)
Abstract
Background: Although platelet indices are routinely available using automated blood cell counters, the clinical applications of these parameters for malaria and dengue hemorrhagic fever (DHF) have not been substantially implemented. We conducted this study to investigate the potential role of platelet indices as a prognostic marker in adult patients with Plasmodium vivax malaria, Plasmodium falciparum malaria, and DHF admitted to the Hospital for Tropical Diseases, Bangkok, Thailand. Methods: We enrolled 219 eligible patients, comprising 96 with P. falciparum malaria, 71 with P. vivax malaria, and 52 with DHF. We evaluated the study groups’ baseline clinical features and alterations of platelet indices during the first 4 days of admission. Results: Upon admission, the initial laboratory findings showed no statistically significant difference in platelet count (PC), plateletcrit (PCT), or platelet distribution width (PDW) between patients with P. vivax and P. falciparum; however, mean platelet volume (MPV) was significantly higher in patients with P. falciparum. Comparisons of the initial platelet indices in malaria and DHF showed that only PC and PCT were significantly lower in DHF. Although MPV in DHF tended to be lower than in malaria, a statistically significant difference was observed only with P. falciparum. Moreover, the results also showed no significant alterations in the platelet indices among the study groups during the first 4 days of admission. Conclusions and recommendations: Clinical presentations of DHF and malaria are nonspecific and may overlap with other common tropical diseases. Alterations of initial platelet indices may be investigated in P. vivax and P. falciparum malaria mimicking DHF. Although a significant reduction in PC and PCT in DHF might be a clue for differential diagnosis of malaria, the use of MPV and PDW might be impractical. We suggest that appropriate laboratory diagnoses for malaria and dengue infections are still needed for the differential diagnosis of acute febrile patients who have a risk of malaria or dengue infections. To clarify the clinical utility of platelet indices in patients with dengue and malaria, further studies are required that particularly include patients with different severities, geographical areas, and levels of health care settings.