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Table 2 Per-protocol secondary endpoint analysis of treatment responses in cases with Plasmodium falciparum or Plasmodium vivax for PCR-uncorrected 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]

108 (98.2) [92.9–99.7]

138 (100) [96.6–100]

246 (99.2)

− 0.28

 Early treatment failure, %

0

0

0

 Late clinical failure, %

0.9

0

0.4

 Late parasitological failure, %

0.9

0

0.4

P. falciparum assessed at day 42, n

106

135

241

 

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

102 (96.2) [90.07–98.8]

132 (97.8) [93.2–99.4]

234 (97.1)

0.48

 Early treatment failure, %

0

0

0

 Late clinical failure, %

0

0

0

 Late parasitological failure, %

3.8

2.2

2.9

P. vivax assessed day 28, n

23

41

64

 

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

20 (87.0) [65.3–96.6]

41 (100) [89.3–100]

61 (95.3)

0.06

 Early treatment failure, %

0

0

0

 Late clinical failure, %

4.3

0

1.6

 Late parasitological failure, %

8.7

0

3.1

P. vivax assessed day 42, n

19

39

58

 

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

13 (68.4) [43.5–86.4]

34 (87.2) [71.8–95.2]

47 (81.03)

0.23

 Early treatment failure, %

0

0

0

 Late clinical failure, %

10.5

5.1

6.9

 Late parasitological failure, %

21.1

7.7

5.3