Determining The Effects Of Nasopharyngeal Suction
Aspiration, Respiratory, Pain, Mucosal Irritation
About this trial
This is an interventional health services research trial for Aspiration, Respiratory
Eligibility Criteria
Inclusion Criteria: Existence of secretion Exclusion Criteria: Being premature without family consent
Sites / Locations
- Istanbul Medeniyet University Goztepe Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Experimental group (Positive Pressure Group)
Control group (Negative Pressure Group)
The nasopharyngeal suction with positive pressure method was employed in the sample group. In this method, the infant's head is turned to the side, to the nostril on the other side 1-2 ml of physiological saline (PS- Mustela trademark), is injected with a 2,5-milliliter syringe (Can Medikal trademark), and then positive pressure is exerted with the help of the end of the oxygen connection hose (CGR Medikal trademark) from the same nostril, with oxygen or air supply at 5-8 lt/min (liter/minute) (if the baby requires oxygen, using an oxygen source) and the nasopharyngeal secretions are removed from the nostril into which physiological saline (PS) has been not injected. The oxygen connection hose is held one centimeter away from the infant's nostril. The researchers prepared a guideline for nasopharyngeal suction with positive pressure based on the literature.
The nasopharyngeal suction with negative pressure method was employed in the control group in this study. In this method, the nasal secretions were softened with 1-2 ml of physiological saline (PS- Mustela trademark) like experimental group, and then negative pressure suction was performed using a pine-tipped suction set (Bıcakcılar trademark). The suction pressure was kept between 60 and 80 mmHg, and no suction lasted for more than 15 seconds