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Published on: November 6, 2019
Hypopharyngeal packing during adenotonsillectomy by cold dissection in children: a randomized controlled trial
Luciana Pimentel Oppermann1, José Faibes Lubianca Neto2, Renata Loss Drummond3
1Department of Pediatric Otolaryngology of Hospital da Criança Santo Antônio/Postgraduate Program in Pediatrics, Irmandade da Santa Casa de Misericórdia de Porto Alegre/Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil. luopp24@hotmail.com.
Insights
Hypopharyngeal packing (HP) did not reduce nausea and vomiting after pediatric adenotonsillectomy. This study found no significant benefit of HP in preventing postoperative nausea and vomiting (PONV) in children undergoing this common surgery.
Area of Science:
- Pediatric Otolaryngology
- Anesthesiology
- Surgical Outcomes Research
Background:
- Postoperative nausea and vomiting (PONV) affects up to 70% of children after adenotonsillectomy.
- Ingested blood during the procedure is a potential cause of emesis.
- Hypopharyngeal packing (HP) is used to prevent blood swallowing, but its efficacy in pediatric adenotonsillectomy is unstudied.
Purpose of the Study:
- To evaluate the effectiveness of hypopharyngeal packing (HP) in preventing postoperative nausea and vomiting (PONV) in children undergoing adenotonsillectomy.
- To address the lack of research on HP's impact on PONV in pediatric adenotonsillectomy patients.
Main Methods:
- A randomized, double-blinded, controlled trial was conducted with children aged 4-16 years undergoing adenotonsillectomy.
- 129 participants were randomized to receive either HP or no packing during surgery.
- Postoperative nausea and vomiting (PONV) occurrence was assessed within 24 hours, with relative risk calculated.
Main Results:
- The incidence of PONV was 20.3% in the hypopharyngeal packing (HP) group and 23.1% in the control group.
- The relative risk for PONV with HP was 0.88 (95% CI 0.46-1.70), indicating no significant difference.
- Baseline characteristics and surgical variables were similar between the groups.
Conclusions:
- Hypopharyngeal packing (HP) does not provide a significant benefit in preventing postoperative nausea and vomiting (PONV) in children undergoing adenotonsillectomy.
- The findings suggest that HP is not an effective strategy for reducing PONV in this pediatric surgical population.
Purpose:
Nausea and vomiting occur in up to 70% of children after adenotonsillectomy, ingested blood during procedure being one of the reasons for emesis. Hypopharyngeal packing (HP) is a common practice among otolaryngologists to prevent blood from being swallowed, but studies in nasal surgeries in adults failed to show efficacy of this technique in reducing postoperative nausea and vomiting (PONV). There are no studies evaluating the effect of HP in adenotonsillectomy in children. The aim of this study is to evaluate the efficacy HP during adenotonsillectomy in children in the prevention of PONV.
Methods:
This is a randomized, double-blinded, controlled trial. Children aged 4-16 years, scheduled for adenotonsillectomy due to sleep-disordered breathing were enrolled in Hospital da Criança Santo Antônio (Brazil). 192 participants were screened, while 129 were enrolled and completed follow-up for primary outcome. Patients were randomized in a consecutive manner to receive HP or not during adenotonsillectomy. PONV occurrence was assessed in the first 24 h after surgery in HP and control group and relative risk with 95% confidence interval was calculated.
Results:
There were 129 patients randomized, 64 in the HP and 65 in the control group. Female were 40.3% and mean ± SD age was 7.3 ± 2.9. Baseline characteristics and surgery variables were distributed similarly between the groups. Incidence of PONV was 20.3% in the HP and 23.1% in the control group. The relative risk for PONV was 0.88 (95% CI 0.46-1.70).
Conclusion:
Our results suggest that there is no benefit of HP during adenotonsillectomy in children for the prevention of PONV.
Trial Registration:
Brazilian Register of Randomized Trials (REBEC) identifier: RBR-3zjn27; Universal Trial Number U1111-1197-7461.
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