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Table 3 Per-protocol primary endpoint analysis of treatment responses in cases with Plasmodium falciparum or Plasmodium. vivax for PCR-corrected malaria

From: Efficacy of artemether–lumefantrine and dihydroartemisinin–piperaquine for the treatment of uncomplicated malaria in Papua New Guinea

 

AL

DHA-PPQ

Total

P-value

P. falciparum assessed at day 28, n

110

138

248

 

 Adequate clinical and parasitological response, n (%) [95% CI]

110 (100) [95.8–100]

138 (100) [96.6–100]

248 (100)

 Early treatment failure, %

0

0

0

 Late clinical failure, %

0

0

0

 Late parasitological failure, %

0

0

0

P. falciparum assessed at day 42, n

106

135

241

 

 Adequate clinical and parasitological response, n (%) [95% CI]

104 (98.1) [92–99.7]

135 (100) [96.6–100]

239 (99.2)

− 0.11

 Early treatment failure, %

0

0

0

 Late clinical failure, %

0

0

0

 Late parasitological failure, %

1.9

0

0.8

P. vivax assessed day 28, n

23

41

64

 Adequate clinical and parasitological response, n (%) [95% CI]

22 (95.7) [76.03–99.8]

41 (100) [89.3–100]

63 (98.4)

0.18

 Early treatment failure, %

0

0

0

 Late clinical failure, %

0

0

0

 Late parasitological failure, %

4.3

0

1.6

P. vivax assessed day 42, n

19

39

58

 Adequate clinical and parasitological response, n (%) [95% CI]

15 (78.9) [53.9–93.03]

36 (92.3) [78.03–98.0]

51 (87.9)

0.14

 Early treatment failure, %

0

0

0

 Late clinical failure, %

5.3

0

1.7

 Late parasitological failure, %

15.8

7.7

10.3