Hemodynamic Monitoring
Conditions
Interventions
This is an open, non-randomized, crossover controlled clinical trial, where 16 premature newborns were selected and comprised the two groups at two different times, separated into a control group (CG)
Sponsors
Obras Sociais e Educacionais de Luz
Instituto de Responsabilidade Social Sirio Libanes
Eligibility
Age
28 Weeks to 37 Weeks
Inclusion criteria
Inclusion criteria: Premature newborns, whose guardians agreed to the research and signed the informed consent form (ICF); premature newborns of both sexes, with more than 72 hours of life who do not meet the minimum handling criteria; premature newborns who are indicated for nasotracheal aspiration according to the criteria indicated in the literature; premature newborns aged up to 37 gestational weeks, who are hemodynamically stable on room air, using oxygen therapy or non-invasive ventilation
Exclusion criteria
Exclusion criteria: Full-term newborns; newborns using sedation and/or vasoactive drugs, presenting hemodynamic instability; newborns presenting severe neurological alterations; newborns on invasive ventilatory support under orotracheal intubation; newborns who meet the criteria for minimal manipulation; newborns who have composed the initial collection, and after that do not present indication for nasotracheal aspiration in the other care
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postural nesting is expected to promote more comfort for premature newborns, reducing hemodynamic changes and the level of pain during nasotracheal aspiration, which is considered an invasive and potentially painful procedure | — |
Secondary
| Measure | Time frame |
|---|---|
| Postural nesting is expected to help reduce the time for stabilization and reorganization of the premature newborn after the procedure | — |
Countries
Brazil
Contacts
Public ContactNathália Monteiro
Universidade do Vale do Sapucaí
Outcome results
None listed