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. Author manuscript; available in PMC: 2006 Mar 6.
Published in final edited form as: Clin Infect Dis. 2005 Aug 23;41(7):948–957. doi: 10.1086/432941

Table 3.

Predictors of mortality via multiple logistic regression in African children with malaria, by site.

Characteristic Blantyre, Malawi(n = 2159) Kilifi, Kenya(n = 4670) Kumasi, Ghana(n = 3730)
Weight-for-age Z score (per unit increase) 0.84 (0.71–1.01) 0.75 (0.68–0.82) 0.90 (0.81–0.99)
Deep breathing 3.78 (1.76–8.14) 1.53 (0.99–2.36) 2.26 (1.57–3.27)
Blantyre coma score ≤2 2.29 (1.05–5.03) 1.93 (1.25–2.99) 3.15 (2.18–4.56)
Unable to sit 3.64 (1.73–7.63) 2.65 (1.68–4.17) 1.83 (1.17–2.85)
Hypoglycemiaa 2.17 (0.77–6.12) 2.48 (1.57–3.92) 2.10 (1.34–3.29)
Lactate (per mmol/l increase) 1.05 (0.99–1.12) 1.02 (0.98–1.07)
Base excess (per unit decrease) 1.14 (1.08–1.21) 1.13 (1.09–1.17) 1.11 (1.07–1.15)
c Statistic 0.88 0.87 0.83

NOTE. Data are OR (95% CI), unless otherwise indicated. There were a total of 59 deaths in Blantyre, 156 deaths in Kilifi, and 183 deaths in Kumasi. P values were <.05 whenever an OR of 1.0 was excluded from the 95% CI. Also, P = .06 for weight-for-age Z score, P= .14 for hypoglycemia, and P = .14 for lactate concentration in Blantyre; P = 06 for deep breathing in Kilifi; and P = .31 for lactate concentration in Kumasi.

a

Glucose level, ≤2.2 mmol/L.