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Cross Sectional Study of Severe and Mixed Malaria Infections : Experience of a Tertiary Care Hospital in South-West Coastal Karnataka

Ruchee Khanna, Akshita Gupta, Asem Ali Ashraf, Vinay Khanna, Gauri Kumar, Seemitr Verma

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Indian Journal of Forensic Medicine and Pathology 14(1):p 27-33, JAN-MARCH 2021. | DOI: https://doi.org/10.21088/ijfmp.0974.3383.14121.3

How Cite This Article:

AkshitaGupta,RucheeKhanna,AsemAliAshrafetal./CrossSectionalStudyofSevereandMixedMalariaInfections:Experience ofaTertiaryCareHospitalinSouth-WestCoastalKarnataka/IndianJ.ForensicMedPathol.2021;14(1):27-33.

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Received : September 16, 2020         Accepted : January 13, 2021          Published : March 30, 2025

Abstract

Background: India launched the National Framework for Malaria Elimination to encourage surveillance and strategies towards ‘elimination’ rather than control by 2030. Considering the significant challenges on this path, regional variations in clinical and haematological manifestations are useful parameters to help shape national elimination strategies. Our study aims to compare the demographic, clinical and haematological parameters among severe malaria casesandhighlightmixedmalariainfection. Methods: A cross sectional study was carried out between January 2015 and May 2018. Diagnosis was done by peripheral smear microscopy, followed by immunochromatographicrapid test and finally quantitative buffy coat test. Patients were classified as severe and non-severe disease according to WHO major criteria. The relevant data of the study subjects was collected from inpatient case records and analysed. Results: A total of 403 inpatients with confirmed malaria were included in our study. Severe malaria was observed in 21.5% and these patients had a significantly longer stay in hospital of 6.08±3.78days.InfectionscausedbyP.falciparum(48.6%)andP.vivax(46.9%)werealmost equalinnumber.Acuterespiratorydistresssyndromewasobservedmorein21.4%(9/42)ofP. vivaxinfections.Mixedmalarialinfectionswereobservedin4.5%(18/403)oftotalpatientsand 33%ofmixedmalarialcasespresentedwithseveremanifestations. Conclusions: AttributingseveremalariatoP.falciparumorP.vivaxalonecanbemisleading especially in regions with complicated epidemiology, like India. Identification of malarial coinfectionsinfection are difficult without molecular diagnostic tools. Incorrect diagnosis may directly affect appropriate antimalarial therapy selection. Highlights • Clinical and haematological manifestations have not been observed as a malaria burden metric in all regions. • Identification of malarial coinfectionsinfection are difficult without molecular diagnostic tools. • Appropriatelaboratorydiagnosisofmixedmalarialinfectionsaidsinselectingantimalarial therapy. • Study of regional variations in malaria presentations can improve public health


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AkshitaGupta,RucheeKhanna,AsemAliAshrafetal./CrossSectionalStudyofSevereandMixedMalariaInfections:Experience ofaTertiaryCareHospitalinSouth-WestCoastalKarnataka/IndianJ.ForensicMedPathol.2021;14(1):27-33.


Licence:

Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.



Received Accepted Published
September 16, 2020 January 13, 2021 March 30, 2025

DOI: https://doi.org/10.21088/ijfmp.0974.3383.14121.3

Keywords

Malaria co-infectionPlasmodium;IndiaEndemic;Eradication.

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Received September 16, 2020
Accepted January 13, 2021
Published March 30, 2025

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Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.



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