Manifestations of malaria: a clinical experience

Authors

  • Prabhu S. Department of General Medicine, BMCRI, Bengaluru, Karnataka, India
  • Prashanth V. N. Department of General Medicine, BMCRI, Bengaluru, Karnataka, India

DOI:

https://doi.org/10.18203/2349-3933.ijam20184210

Keywords:

ACT (Artemesinin combination therapy), Atypical manifestations, Malaria, Severe malaria

Abstract

Background: Malaria is fast emerging as a number one infectious disease with high morbidity and mortality across the globe. It’s being transmitted across 108 countries containing 3 billion populations (40% of world’s populations) with more than 3 million deaths per year. India is an endemic country for malaria with an estimated 70-100 million1 cases per year. 45-50% of them are due to Plasmodium falciparum (Pf). Pf is responsible for majority of severe and fatal malaria though death due to Plasmodium vivax mono infection have also been reported. Symptoms and sign are highly non-specific in malaria making it more of a clinical diagnosis more than a laboratory diagnosis. Presentation may vary at times and can be quite confusing as malaria is a multisystem disease. Authors’ idea was to study the variable manifestations in confirmed cases of malaria patients at our hospital

Methods: A hospital based cross sectional study was conducted for a period of one year-from 01-08-2015 to 31-07-2016 based on authors’ hospitals records (case sheets with demography profile, clinical features, investigations and treatment outcome).

Results: A total of 369 patients positive for malaria parasite were included in the study. 369 were smear positive-219 positive for Plasmodium vivax, 127 were P. falciparum type and 23 were for both. Majority were males (64.50%) and belonged to the age group of 21-50 years (58.84%). They were admitted in post monsoon months (60.43%). Of them 46.44% had classical symptoms of malaria. All the patients had received mainly artemisinin combination therapy (ACT) and 91.87% patients recovered in 7-28 days. The mortality rate was nearly 5.69%.

Conclusions: The present study was useful to know the varied manifestations of malaria and hence will be useful in making a clinical diagnosis of malaria.

References

Greenwood B, Mutabingwa T. Malaria in 2002. Nature. 2002 Feb 7;415(6872):670.

Sharma A, Khanduri U. How benign is benign tertian malaria?. J Vector Borne Dis. 2009 Jun 1;46(2):141.

Rao A, Kumar MK, Joseph T, Bulusu G. Cerebral malaria: insights from host-parasite protein-protein interactions. Malaria journal. 2010 Dec;9(1):155.

Sharma VP. Hidden burden of malaria in Indian women. Malaria J. 2009 Dec;8(1):281.

Murthy GL, Sahay RK, Srinivasan VR, Upadhaya AC, Shantaram V, Gayatri K. Clinical profile of falciparum malaria in a tertiary care hospital. J Indian Med Assoc. 2000 Apr;98(4):160-2.

Beale PJ, Cormack JD, Oldrey TB. Thrombocytopenia in malaria with immunoglobulin (IgM) changes. Br Med J. 1972 Feb 5;1(5796):345-9.

Harris VK, Richard VS, Mathai E, Sitaram U, Kumar KV, Cherian AM, et al. A study on clinical profile of falciparum malaria in a tertiary care hospital in south India. Indian J Malariol. 2001;38(1-2):19-24.

Mehta SR, Naidu G, Chandar V, Singh IP, Johri S, Ahuja RC. Falciparum malaria -present day problems. An experience with 425 cases. J Assoc Physicians India. 1989 Apr;37(4):264-7.

Palyfair JHL. Immunity to malaria. Br Med Bull. 1982;38(2):153-60.

Sharma SK, Das RK, Das BK, Das PK. Haematological and coagulation profile in acute falciparum malaria. J Assoc Physicians India. 1992 Sep;40(9):581-3.

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Published

2018-11-22

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Section

Original Research Articles