Asthma, Asthma Acute, Asthma Attack, Asthma in Children
Conditions
Keywords
Asthma attack, Child, Nurse, Nebulization, Chest Pain
Brief summary
The purpose of this study was to establish the effect on pulse rate, oxygen saturation, respiratory rate, pain and anxiety levels of Fowler's and the forward-leaning positions during nebulization in children experiencing asthma attacks.
Detailed description
In the first stage, data on the children who agreed to participate in the study were recorded on the Patient Identification Form 10 minutes before the procedure by the researcher during a face-to-face interview. The children's body temperature, oxygen saturation, pulse rate and respiratory rate were measured. Upon explaining the FPS-R, the children were asked whether they had experienced pain before treatment, and to point at the pain level felt from among the faces on the scale. Then, CSA was explained and the children, and their level of anxiety on the scale was recorded. The pre-nebulization findings were recorded. In the second stage, the salbutamol therapy prescribed by the physician was administered to the participating children with a nebulizer three times at 20-minute intervals. During nebulization, the study group patients were placed in forward-leaning position, placing a pillow on their knees, while the control group was placed in Fowler's position on a chair. Nebulization took an average of 10 minutes for each child. Oxygen saturation, pulse and respiratory rate were recorded immediately after the mask was removed. The children were allowed to rest for 20 minutes in Fowler's position. In the third stage, oxygen saturation, pulse and respiratory rate were determined immediately after the mask was removed following a 10-minute second nebulization. The values determined were recorded, and the children were allowed to rest for 20 minutes in Fowler's position. In the fourth stage, oxygen saturation, pulse and respiratory rate were determined immediately after the mask was removed following the 10-minute third nebulization. The children were asked whether they had pain, and to point at the pain level represented by the faces on the scale. The patients then marked their level of anxiety on the CSA. The post-nebulization findings were recorded.
Interventions
OTHERA Randomized Controlled Study
For forward-leaning position, the child is first placed on a suitable chair with a soft pillow on their knees. The child will remain in the same position for the duration of the nebulization, and the pillow provides support, ensuring the child does not get tired. The child leans forward at an angle of 45°, places their arms on the pillow as shown in the figure and holds their head upright with their eyes facing forward (slight hyperextension). The upright head position of the child prevents spillage of the liquid medicine from the nebulizer chamber.
Sponsors
Istanbul University - Cerrahpasa
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
A randomized controlled study
Eligibility
Sex/Gender
ALL
Age
6 Years to 11 Years
Healthy volunteers
No
Inclusion criteria
* To be between 6-11 ages, * Having a body temperature below 37.2°C at admission, * Having been prescribed nebulized salbutamol by the physician during data collection, * Having not using bronchodilators or corticosteroid drugs within the last 6 hours, * Having no other respiratory system disease, * Verbal and written consent of the child and parent to participate in the study.
Exclusion criteria
* Administering drugs other than nebulized salbutamol to the child during data collection, * Having an obstacle for positioning (Lordosis, kyphosis, scoliosis, chest wall deformities, previous surgical procedure, etc.), * Child and parent not knowing Turkish.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Pulse Rate | 90 minute | Heart rate will be monitored |
| Change in chest pain score | 90 minute | Pain score will be evaluated with The faces pain scale-revised (FPS-R). |
| Change in anxiety score | 90 minute | Anxiety score will be evaluated with The children state anxiety scale (CSA). |
| Change in Oxygen Saturation | 90 minute | Oxygen saturation will be monitored |
| Change in respiratory rate | 90 minute | Respiratory rate will be monitored |
Countries
Turkey (Türkiye)
Outcome results
None listed