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Two patients were excluded from the analysis because of sample hemolysis.
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Of the 45 patients evaluated, two were excluded from the analysis because sample hemolysis prevented NSE measurement.
A total of 14 subjects were excluded: 5 samples due to sample hemolysis and 9 samples due to sample DNA degradation.
In the CFT, 4.4% of the samples yielded uninterpretable result, because of either hemolysis or anticomplementary activity.
Twenty-two of the 201 initially recruited mother-newborn dyads were excluded because of hemolysis or insufficient blood sample (n = 16), or inappropriate storage or transportation (n = 6), therefore, the study sample comprised 179 mother-newborn dyads.
We excluded one individual from this analysis because of hemolysis in the plasma sample for PON1 testing.
Some values were missing for biomarkers other than suPAR (samples failed because of hemolysis or because they were lost).
On day 19, hemoglobin level decreased to 5.3 g/dL because of persistent hemolysis (LDH 672 U/L); he was again given transfusions of packed erythrocytes.
Furthermore, all blood samples were collected in the same way on a dedicated arterial line that also excluded common errors of blood sampling, including hemolysis and sample contamination.
(A few plasma samples were excluded because of hemolysis).
Remaining samples contained insufficient volumes or could not be tested because of hemolysis.
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