​Malaria/PF.PV Rapid Test Cassette For Clinical and Field Use in Africa

Product Specification

Description

The Malaria/PF.PV Rapid Test Cassette is a critical in-vitro diagnostic tool designed for the qualitative detection of malaria parasites in human whole blood. ​Malaria/PF.PV Rapid Test Cassette is engineered to not only identify the presence of any malaria infection but also to provide a differential diagnosis by specifically detecting the antigens for Plasmodium falciparum(PF) and Plasmodium vivax(PV). These two species are among the most common and dangerous parasites causing malaria, making this test vital for accurate diagnosis and subsequent treatment decisions.

​​Primary Function​:

​

The core function of this rapid test is to provide a clear, visual result indicating whether a patient is infected with malaria. Crucially, it distinguishes between a Plasmodium falciparum-specific infection, a Plasmodium vivax-specific infection, or an infection caused by other malaria species. This differentiation is essential for healthcare providers, as the treatment protocols for P. falciparum—the species most associated with severe complications and death—can differ from those for other species. The test works by capturing specific parasite antigens (HRP-II for Pf and aldolase for Pan-species) present in a blood sample from a finger prick.

​​Key Advantages and Features​:

​

​Malaria/PF.PV Rapid Test Cassette offers numerous significant advantages in the fight against malaria. It delivers results in just 15-20 minutes, which is a critical speed advantage over laboratory microscopy, especially in remote and resource-limited settings. This speed enables immediate diagnosis and allows for treatment to begin during the same clinical visit.

The test is designed for extreme ease of use. The procedure requires minimal training, making it suitable for use by community health workers and in clinics without advanced laboratory facilities. The clear visual readout—lines appear on the cassette to indicate a positive or negative result—minimizes interpretation errors.

Furthermore, the test demonstrates high sensitivity and specificity, meaning it is very effective at correctly identifying true positive cases and true negative cases, reducing the risk of misdiagnosis. Its stability at room temperature makes it perfectly suited for the challenging climatic conditions often found in malaria-endemic regions. The long shelf life ensures the product remains effective for a substantial period, which is vital for supply chain logistics.

​​Application Scenarios​​

This diagnostic test is indispensable in a wide range of settings across Africa and other malaria-endemic regions. Its primary application is in remote and rural clinics where access to electricity, advanced laboratory equipment, and trained microscopists is limited or non-existent. It empowers community health workers to provide diagnostic confidence directly in the village, bringing lifesaving testing closer to where people live.

It is also extensively used in larger health centers and hospitals as a first-line rapid screening tool to triage patients quickly, even when microscopy is available. This helps to reduce the workload on laboratory staff and ensures positive cases are identified without delay. Furthermore, the test is invaluable in emergency departments, during outbreak surveillance campaigns, and for screening in cross-border areas to help monitor and control the spread of malaria across regions.

​​Important Usage Considerations​:

​

For optimal performance, it is imperative to strictly follow the manufacturer's instructions. The test must be used within its stated expiration date and stored in a cool, dry place, protected from direct sunlight. While the test is highly accurate, the results should be interpreted within the exact time window specified in the instructions guide (typically 15-20 minutes) to avoid inaccurate readings. As with all diagnostic tests, clinical symptoms and patient history should be considered alongside the rapid test result for a comprehensive diagnosis.

Specification