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Thrombocytopenia in children with vivax malaria: a study from north India
Chandra Mohan Kumar1, Shweta Singh, Rajnish Garg
1Department of Pediatrics, Hamdard Institute of Medical Sciences and Research, New Delhi, 110029, India, cmkumar1@rediffmail.com.
Insights
Children with vivax malaria often develop temporary thrombocytopenia (low platelet count). Platelet counts recover quickly with treatment, and significant bleeding is uncommon in pediatric cases.
Area of Science:
- Pediatric infectious diseases
- Hematology
Background:
- Vivax malaria is a significant global health concern, particularly affecting children.
- Thrombocytopenia is a common complication of malaria, but its clinical significance in pediatric vivax malaria requires further elucidation.
Purpose of the Study:
- To investigate the incidence, severity, and clinical implications of thrombocytopenia in children diagnosed with vivax malaria.
- To analyze the recovery patterns of platelet counts in this pediatric population.
Main Methods:
- A retrospective, hospital-based descriptive case series design was employed.
- Confirmed cases of vivax malaria in children were analyzed, with daily total platelet counts (TPC) recorded until recovery.
- Follow-up platelet counts were assessed one week post-treatment.
Main Results:
- Out of 39 children with vivax malaria, 22 experienced thrombocytopenia, with a mean admission platelet count of 48 × 10(9)/L.
- Platelet counts demonstrated rapid recovery with treatment, rising to 126.5 × 10(9)/L by day 3 without the need for platelet transfusion.
- In untreated cases, the lowest platelet counts occurred on days 5-6, with normalization by day 9. Younger children exhibited faster recovery than older children.
Conclusions:
- Vivax malaria is frequently associated with transient thrombocytopenia in children.
- This thrombocytopenia typically does not result in significant bleeding complications in pediatric patients.
Objectives:
To study incidence, severity and clinical significance of thrombocytopenia and to study recovery pattern of platelet counts in children with vivax malaria.
Methods:
This was a retrospective hospital based descriptive case series. Cases of confirmed vivax malaria were studied and their Total Platelet Counts (TPC) evaluated daily till recovery and again after 1 wk on follow up visit.
Results:
In this study out of 39 children of confirmed vivax malaria 22 had thrombocytopenia, having mean platelet count 48 × 10(9)/L on admission which showed a very quick recovery on treatment and by day 3 of treatment it rose to 126.5 × 10(9)/L without platelet transfusion. In untreated cases the lowest platelet counts was observed on day 5-6 and on treatment, platelet counts returned to normal without any platelet transfusion by 9th day. Even among children there are variations in different age groups and younger ones show more quicker recovery than older peers.
Conclusions:
Vivax malaria is associated with transient thrombocytopenia which does not lead to significant bleeding in children.
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