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Mean haemoglobin at discharge was 10.3 ± 2.3 g/dl.
There was no difference in overall mean haemoglobin at the end of two trials with deworming (Analysis 1.7).
The mean haemoglobin at completion was 13.6 g dl -1) for r-HuEPO-treatedl -1ients compared with 11.0 g dl(-1) for control subjects (P = 0.0012).
The second trial also reported mean haemoglobin at baseline and eight months (with no difference between groups, Analysis 6.2), and various measures of nutrition and growth (see Appendix 4).
No trials reported the risk of mild anaemia, but two trials reported mean haemoglobin at delivery without clinically important differences between groups (MD 0.01 g/dL, 95% CI -0.23 to 0.24; two trials, 676 participants, Analysis 1.4).
Two trials reported mean haemoglobin at baseline and at six to eight months after treatment with no difference between groups (mean difference -0.08, 95% CI -0.24 to 0.09; 727 participants, two trials, Analysis 1.3).
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TI patients were occasionally transfused (0 6 blood transfusions/year and 93% of patients had at least 1 blood transfusion/year) and presented mean haemoglobin levels at 7 11 mg/dL.
In those using coumarin, the international normalized ratio (INR) at presentation was 4.87 ± 1.41 (mean ± SD) but the mean haemoglobin level at presentation did not differ from that in patients not taking coumarin, and neither did the number of units of blood administered during hospitalisation.
We compared mean haemoglobin levels at each haemoglobin cutoff point using student's t-test.
After thirty months, mean haemoglobin stabilised at 130.3 g/L, an increase of 8.2 g/L from baseline, and mean serum ferritin rose from 23.9 µg/L to 52 µg/L.
The mean haemoglobin level at presentation was 6.1 ± 1.9 mmol/l (mean ± SD; range 1.8 to 9.8).
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