P61
Conditions
Interventions
Group 1: 200 patients in three groups:
1)(30-33 woche (wk)) 100 per group
2) (34-35 wk), 50 per group
3) (36–40 wk), 50 per group
We will take a blood sample of the umbilical cord of every child bo
Sponsors
Universitätsklinik für Anästhesie, Allgmeine Intensivmedizin und Schmerztherapie
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: preterms
Exclusion criteria
Exclusion criteria: parenteral refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| reverence values of coagulation function in preterms | — |
Secondary
| Measure | Time frame |
|---|---|
| correlation between the measuremtent of Rotem and standard coagulation tests after 50 patients per group ( 200 patients) Comparison of age groups will be analyzed with ANOVA and correction for multiple testing will be performed with Tukey’s post hoc test. Correlations will be analyzed with Pearson’s and Spearman’s correlation coefficient. | — |
Countries
Austria
Contacts
Public ContactLydia Triffterer
AKH Wien
Outcome results
None listed