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Artemisinin-based combination therapy for ... - The Cochrane Library

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5.1 Mean haemoglobin (g/dl)<br />

at baseline<br />

5.2 Mean change in<br />

haemoglobin (g/dl) from<br />

baseline to day 14<br />

5.3 Mean change in<br />

haemoglobin (g/dl) from<br />

baseline to Day 28<br />

5.4 Mean haemoglobin (g/dl)<br />

at Day 28<br />

6 Serious adverse events (including<br />

deaths)<br />

4 Mean Difference (IV, Fixed, 95% CI) Not estimable<br />

1 Mean Difference (IV, Fixed, 95% CI) Not estimable<br />

2 Mean Difference (IV, Fixed, 95% CI) Not estimable<br />

1 Mean Difference (IV, Fixed, 95% CI) Not estimable<br />

7 4200 Risk Ratio (M-H, Fixed, 95% CI) 0.61 [0.36, 1.03]<br />

Comparison 14. Dihydroartemisinin-piperaquine dose analysis: 3 dose vs 4 dose regimen<br />

Outcome or subgroup title<br />

No. of<br />

studies<br />

No. of<br />

participants Statistical method Effect size<br />

1 Total Failure PCR unadjusted 1 318 Risk Ratio (M-H, Fixed, 95% CI) 1.72 [0.84, 3.53]<br />

1.1 Day 63 1 318 Risk Ratio (M-H, Fixed, 95% CI) 1.72 [0.84, 3.53]<br />

2 Total Failure PCR adjusted 1 292 Risk Ratio (M-H, Fixed, 95% CI) 0.56 [0.05, 6.09]<br />

2.1 Day 63 1 292 Risk Ratio (M-H, Fixed, 95% CI) 0.56 [0.05, 6.09]<br />

Comparison 15. Dihydroartemisinin-piperaquine dose analysis (versus Artesunate plus mefloquine)<br />

Outcome or subgroup title<br />

No. of<br />

studies<br />

No. of<br />

participants Statistical method Effect size<br />

1 Total Failure Day 63 PCR<br />

unadjusted<br />

4 1784 Risk Ratio (M-H, Random, 95% CI) 0.83 [0.49, 1.38]<br />

1.1 DHA-P 4 doses 3 1019 Risk Ratio (M-H, Random, 95% CI) 0.81 [0.59, 1.10]<br />

1.2 DHA-P 3 doses 2 765 Risk Ratio (M-H, Random, 95% CI) 1.44 [0.09, 22.81]<br />

2 Total Failure Day 63 PCR<br />

adjusted<br />

4 1634 Risk Ratio (M-H, Random, 95% CI) 0.48 [0.18, 1.31]<br />

2.1 DHA-P 4 doses 3 908 Risk Ratio (M-H, Random, 95% CI) 0.42 [0.17, 1.04]<br />

2.2 DHA-P 3 doses 2 726 Risk Ratio (M-H, Random, 95% CI) 1.27 [0.03, 48.28]<br />

3 Total Failure Day 42 PCR<br />

unadjusted<br />

5 2126 Risk Ratio (M-H, Random, 95% CI) 0.77 [0.43, 1.35]<br />

3.1 DHA-P 4 doses 3 957 Risk Ratio (M-H, Random, 95% CI) 0.80 [0.50, 1.28]<br />

3.2 DHA-P 3 doses 3 1169 Risk Ratio (M-H, Random, 95% CI) 0.88 [0.20, 3.81]<br />

4 Total Failure Day 42 PCR<br />

adjusted<br />

5 2043 Risk Ratio (M-H, Random, 95% CI) 0.62 [0.20, 1.91]<br />

4.1 DHA-P 4 doses 3 903 Risk Ratio (M-H, Random, 95% CI) 0.62 [0.14, 2.82]<br />

4.2 DHA-P 3 doses 3 1140 Risk Ratio (M-H, Random, 95% CI) 0.70 [0.08, 5.87]<br />

5 Total Failure Day 28 PCR<br />

unadjusted<br />

6 2191 Risk Ratio (M-H, Random, 95% CI) 0.74 [0.20, 2.65]<br />

5.1 DHA-P 4 doses 4 1075 Risk Ratio (M-H, Random, 95% CI) 0.56 [0.10, 3.14]<br />

<strong>Artemisinin</strong>-<strong>based</strong> <strong>combination</strong> <strong>therapy</strong> <strong>for</strong> treating uncomplicated malaria (Review)<br />

Copyright © 2009 <strong>The</strong> <strong>Cochrane</strong> Collaboration. Published by John Wiley & Sons, Ltd.<br />

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