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. 2014 Apr 23;59(3):446–453. doi: 10.1093/cid/ciu286

Table 3.

Efficacy Outcomes Following Treatment With Artemisinin-Based Combination Therapies

Efficacy Outcomes PROMOTE
TCC
AL (n = 572) AL (n = 201) DP (n = 165)
Fever clearancea, No. (%)
 Fever on day 1 200 (35.2) 106 (53.0) 46 (40.6)
 Fever on day 2 39 (7.0) 16 (8.0) 7 (4.2)
 Fever on day 3 17 (3.1) 3 (1.5) 5 (3.0)
Parasite clearance, No. (%)
 Parasitemia on day 2 31 (5.6) 32 (16.1) 5 (3.0)
 Parasitemia on day 3 5 (0.9) 3 (1.5) 1 (0.6)
WHO 28-day outcome, No. (%)
 Lost to follow-up 4 (0.7) 2 (1.0) 2 (1.2)
 Early treatment failure 4 (0.7) 0 0
 Late clinical failure 42 (7.3) 19 (9.5) 3 (1.8)
 Late parasitological failure 123 (21.5) 53 (26.4) 11 (6.7)
 Adequate clinical and parasitological response 399 (69.8) 127 (63.2) 149 (90.3)
Gametocytes detected during 28-day follow-up, No. (%) 97 (17.0) 15 (7.5) 30 (18.2)
Hemoglobin recoveryb, g/dL, mean (SD) 0.6 (1.2) 0.6 (1.5) 1.0 (1.4)

Abbreviations: AL, artemether-lumefantrine; DP, dihydroartemisinin-piperaquine; SD, standard deviation; TCC, Tororo Child Cohort; WHO, World Health Organization.

a Subjective fever over previous 24 hours or temperature ≥38.0°C.

b Change in hemoglobin from day 0 to day 28 or day of clinical failure.