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Malaria Parasite Identification Test -
Identifies malaria parasites to diagnose malaria, causing fever or fatigue
Synonym Malaria Parasite Test
Test Code PART26040012
Test Type Parasitology
Pre-Test Condition No special
Report Availability 1–2 D(s)
# Test(s) 1
Test details Sample Report
Malaria Parasite Identification Test Sample Report Cowin-PathLab
Synonym Malaria Parasite Test
Test Code PART26040012
Test Category Malaria
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 1–2 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 24 H(s)
Stability @ 2-8 deg. C 48 H(s)
Stability @ Frozen Not frozen
# Test(s) 1
Processing Method Microscopy
Overview: Malaria Parasite Identification Test
Introduction: The Malaria Parasite Identification Test identifies malaria parasites to diagnose malaria, causing fever or fatigue. Following 2023 WHO guidelines, it uses microscopy for high specificity, supporting parasite screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in parasitology for patients with suspected malaria.
Other Names: Malaria Parasite Microscopy, Thick/Thin Smear Test.
FDA Status: Laboratory-developed test (LDT), meeting parasitology standards for diagnostic accuracy.
Historical Milestone: Malaria microscopy began in the 1900s with parasitology research. Staining techniques improved in the 2000s, enhancing diagnostic precision.
Purpose: Identifies malaria parasites to diagnose malaria, guides treatment, and evaluates patients with fever or fatigue.
Test Parameters: 1. Malaria Parasite Identification
Pretest Condition: No fasting required. Collect whole blood or peripheral blood smear. Report history of fever, fatigue, or travel to malaria-endemic areas.
Specimen: Whole Blood (EDTA, 2-5 mL), Peripheral Blood Smear (slide, 1-2 slides). Transport in a biohazard container.
Sample Stability at Room Temperature: 24 hours
Sample Stability at Refrigeration: 48 hours
Sample Stability at Frozen: Not frozen
Medical History: Document fever, fatigue, chills, or travel history to malaria-endemic areas. Include current medications, especially antimalarials.
Consent: Written consent required, detailing the tests purpose, malaria implications, and risks of blood collection.
Procedural Considerations: Uses microscopy to identify malaria parasites in blood smears. Results are available in 1-2 days, supporting rapid clinical decisions. Performed in laboratories, often for malaria diagnosis.
Factors Affecting Result Accuracy: Improper slide preparation or staining can affect results. Low parasite load may reduce sensitivity.
Clinical Significance: Identified malaria parasites confirm species-specific malaria, guiding antimalarial therapy. Negative results may require antigen testing or PCR.
Specialist Consultation: Consult an infectious disease specialist for result interpretation and treatment planning.
Additional Supporting Tests: Malaria antigen test, PCR, or rapid diagnostic test to confirm malaria diagnosis.
Test Limitations: Sensitivity depends on microscopist expertise; clinical correlation is needed. Low parasite loads may yield false negatives.
References: WHO Malaria Guidelines, 2023; The Lancet Infectious Diseases, White NJ, 2022.

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