Neonatal Screening
Conditions
Interventions
Intervention group: 20 hospitalized newborns will be submitted to the collection of the foot test using the puncture in the hand.
Control group: 20 newborns hospitalized, will be submitted to the coll
Other
E02.800
Sponsors
Universidade de Brasília
Secretaria de estado de Saúde do Distrito Federal
Eligibility
Age
1 Days to 28 Days
Inclusion criteria
Inclusion criteria: Newborns (<28 days), of both genders, independent of gestational age admitted to the hospital unit studied.
Exclusion criteria
Exclusion criteria: Babies with cerebral anatomical abnormality; injury or bone fracture; Apnea history less than 72h; Venous access infiltrates or lost at the time of research; baby who were undergoing painful invasive procedures such as punctures and passing of a nasogastric tube or vesical cathetein less than 1 hour of the study intervention; involvements of the CNS as cerebral hemorrhages, syndromes with neurological impairment, seizure history and hypertension; and also the presence of congenital heart disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that the pain levels found in newborns during blood collection for newborn screening, are lower in venipuncture of the hand group.Parameter evaluated from the NFCS neonatal pain scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is hoped that the painful sensation level during the blood collection procedure are lower in newborns at term. Parameter evaluated from the NFCS neonatal pain scale. It is expected that the group submitted to venipuncture in hand, occurs less changes in vital signs during the procedure. Evaluation of heart rate and oxygen saturation measured before, during and after the procedure. It is expected that the number of punctures to the appropriate blood collection for newborn screening is less venipuncture group at hand. | — |
Countries
Brazil
Contacts
Public ContactSimone Marques
Universidade de Brasília
Outcome results
None listed