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Table 2 Number of RDT information inserts (n = 40) addressing critical steps in procedure and interpretation

From: Malaria rapid diagnostic kits: quality of packaging, design and labelling of boxes and components and readability and accuracy of information inserts

Items addressed in procedure section

Number (%)

Bring the RDT device and buffer to room temperature

32 (80.0)

Check the integrity of the device package

9 (22.5)

Check expiry date

27 (67.5)

Use the device immediately after opening

28 (70.0)

Place the device on a level surface

0 (0.0)

Check the desiccant for signs of exposure to humidity

11 (27.5)

Write down sample identification

3 (7.5)

Wipe finger with alcohol

26 (65.0)

Allow the finger to dry before pricking

12 (30.0)

Hold the transfer device (loop, straw) vertical

8 (20.0)

Hold the buffer vial vertical

12 (30.0)

Do not to use another buffer than the one provided with the kit

9 (22.5)

Use an adequate light source for reading

3 (7.5)

Items addressed in interpretation section

Number (%)

All possible line combinations for invalid test results are mentioned

12 (30.0)

All possible test line combinations for positive test results are mentioned

31 (77.5)

Interpretation of a faint test line as positive is mentioned

8 (20.0)

Causes of false negative results are mentioned, in particular low parasite densities

11 (27.5)

Causes of false positive results are mentioned, e.g. presence of the rheumatoid factor

3 (7.5)

Persistence of HRP-2 is mentioned

19 (47.5)

To repeat the test in case of a negative RDT result and persistent suspicion of malaria is mentioned

1 (2.5)