Nose-close and Abdomen-compression in Pediatric Flexible Bronchoscopy (NPO-NC-AC)
Bradycardia, Hypoxemia
About this trial
This is an interventional supportive care trial for Bradycardia focused on measuring CPR, flexible bronchoscope, resuscitation, ventilation
Eligibility Criteria
Inclusion Criteria:
- body weight (BW) less than 5.0 kg;
- receiving nasal approach flexible bronchoscopy.
Exclusion Criteria:
- cannot nasal approach flexible bronchoscopy.
Sites / Locations
- Taipei-Veterans General Hospital
Arms of the Study
Arm 1
Experimental
outcome
Cardiopulmonary parameters were measured and recorded at baseline, just before and at every minute during NC-AC, and at the end of the FB session. In infants who already had an arterial line, arterial blood gas (ABG) analyses were taken for study. Data was represented as mean ± SD. The results obtained from the baseline and different stages. The values were considered statistically significant only when p < 0.05. Technique failure was defined as: any vital signs of hypoxia did not return to accepted levels(HR>100 beat/min, SpO2>90%, mean BP>50 mmHg)within 2 minutes of the experimental CPR technique. Then traditional CPR procedures involving bag-mask ventilation, endotracheal intubation, Ambu bag ventilation or even chest compressions were substituted.