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Missing rates ranged from 2.2%to13%3% in the private cohort, so mean substitution was not appropriate.
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Maximum item missing rates per domain ranged from 1.8%too 11.1% for the antenatal phase, from 5.3%too 31.6% for the birth phase, and from 5.3% to 14.6% for the post partum phase (see Additional file 1: Table S6 Appendix table for detailed description of all items).
Genotypes missing rates were low (range: 1 - 6%).
That is, we used the xor-genotypes from 50 individuals and replaced 30%and50%0% of the population with regular genotypes, and performed xor-haplotype inference under different missing data rates ranging from 0.5 % to 5%.
Ceiling effects (greatest severity of nausea and vomiting) were under minimal (according to well-accepted criteria: [34] 10.5% for number of days of vomiting or nausea, under 2.0% for number of episodes of vomiting, and under 3.5% for mean severity of nausea. Missing data rates ranged from a low of 2.5% (week 1) to to a high of 9.9% (week 2).
The missing rates varied substantially between studies during the entire follow-up, ranging from 0 to 67.0%.
The missing measurements appear in a random way which is governed by missing rates obeying a certain probability distribution.
In general, the missing rates were low.
Missing rates were calculated for each field.
Percentage rates of error and missing rates were calculated.
Prehospital intubation has been found to be somewhat challenging, and some authors have reported missed (esophageal) intubation rates ranging from 5.8% to 17%[1]-[4[1]-[4]
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