Table 4. ORS impact on the study outcomes during the follow-up.
IRR or ORa | 95% CI | |
---|---|---|
Biting rate | ||
Month 0 to Month 3 | 0.28 | 0.21–0.37 |
Month 4 to Month 6 | 0.21 | 0.12–0.38 |
Proportion of parous females | ||
Month 0 to Month 3 | 0.65 | 0.48–0.87 |
Month 4 to Month 6 | 1.15 | 0.67–1.98 |
Vivax malaria incidence | ||
Month 0 to Month 6 | 0.46 | 0.13–1.43 |
Month 7 to Month 12 | 0.09 | 0.01–0.63 |
Proportion of lambda-cyhalothrin resistant phenotypes | ||
Month 0 to Month 3 | 2.70 | 2.00–3.65 |
Month 4 to Month 6 | 3.58 | 2.11–6.03 |
CI, confidence interval; IRR, incidence rate ration, OR, odds ratio.
a Coefficient estimate for the interaction term between the ORS group and the follow-up period, considering the control as the reference.