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Table 2 Demographic and baseline clinical characteristics of participants who took all the three doses of Eurartesim® and completed study procedures

From: Prospective observational study to evaluate the clinical safety of the fixed-dose artemisinin-based combination Eurartesim® (dihydroartemisinin/piperaquine), in public health facilities in Burkina Faso, Mozambique, Ghana, and Tanzania

 

Main study

Nested cohort

Total n (%)

Variable

N = 9,589

1,002

10,591

Country (n (%))

   

Burkina Faso

2,718 (28. 3)

299 (29. 8)

3,017 (28. 5)

Ghana

4,119 (43. 0)

444 (44. 3)

4,563 (43. 1)

Mozambique

1,876 (19. 6)

89 (8. 9)

1,965 (18. 6)

Tanzania

876 (9. 1)

170 (17. 0)

1,046 (9. 9)

Gender (n (%))

   

Female

5,068 (52. 8)

519 (51. 8)

5,587 (52. 7)

Male

4,521 (47. 2)

483 (48. 2)

5,004 (47. 3)

Age group (n (%))

   

<6

4,654 (48. 5)

331 (33. 0)

4,985 (47. 1)

6 - <13

2,612 (27. 2)

398 (37. 7)

3,010 (28. 4)

13- <18

753 (7. 8)

112 (11. 2)

865 (8. 2)

>18

1,570 (16. 4)

161 (16. 1)

1,731 (16. 3)

Plasmodium positivity (n (%))

   

RDT only

3,170 (33. 0)

-

3,170(29. 9)

Microscopy only

1,405 (14. 6)

274 (27. 4)

1,679 (15. 9)

Both RDT and microscopy

4,984 (52. 0)

728 (72. 6)

5,712(53. 9)

Presumptive diagnosis

30 (0. 3)

-

30 (0. 3)

*Parasite density (/μL) ( P. falciparum) * (n (%))

   

No parasite observed

37 (0. 6)

8 (0. 8)

45 (0. 6)

<50

421 (6. 6)

80 (8. 0)

501 (6. 8)

50- < 500

1,282 (20. 1)

214 (21. 5)

1,496 (20. 3)

500- < 5,000

1,800 (28. 3)

265 (26. 6)

2,065 (28. 0)

5000- < 50,000

1,477 (23. 2)

268 (26. 9)

1,745 (23. 7)

≥50,000

1,354 (21. 2)

160 (16. 1)

1,514 (20. 6)

  1. *25 patients had other species of Plasmodium that was not falciparum.