Volume 131, Issue 4 pp. E1380-E1382
Original Report

The Effect of Tonsillectomy and Adenoidectomy on Isolated Sleep Associated Hypoventilation in Children

Charles Saadeh MD

Charles Saadeh MD

Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, U.S.A.

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Seckin O. Ulualp MD

Corresponding Author

Seckin O. Ulualp MD

Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, U.S.A.

Division of Pediatric Otolaryngology, Children's Medical Center, Dallas, Texas, U.S.A.

Send correspondence to Seckin O. Ulualp, MD, 5323 Harry Hines Blvd, Dallas, TX, 75390-9035. E-mail: [email protected]

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First published: 02 September 2020
Citations: 3

Editor's Note: This Manuscript was accepted for publication on August 17, 2020.

The authors have no funding, financial relationships, or conflicts of interest to disclose.

This study was presented in part at the Annual Meeting of American Society of Pediatric Otolaryngology, April 20–22, 2018, National Harbor, MD.

Abstract

Objective

Sleep associated hypoventilation (SAH) is diagnosed when more than 25% of total sleep time (%TST) is spent with end tidal carbon dioxide (EtCO2) > 50 mmHg. SAH in children occurs as a single entity or combined with obstructive sleep apnea. Outcomes of surgical treatment for isolated SAH in children have not been reported.

Methods

The medical charts of children who were diagnosed with isolated SAH and did not have OSA at a tertiary children's hospital between January 2013 and December 2019 were reviewed. Data collection included information on history and physical examination, past medical history, polysomnography (PSG) findings, and surgical management.

Results

Seventeen children (10 male, 7 female, age range: 3–14 years) were diagnosed with isolated SAH. Comorbid conditions included asthma in four children, Down syndrome in one, and seizure in two. Eight children were normal weight, four were overweight, and five were obese. Children did not have obstructive or central sleep apnea. Three children (18%) had persistent SAH as documented by PSG. All normal weight children had resolution of SAH whereas two obese children and one overweight child had residual SAH. %TST with CO2 > 50 mmHg after upper airway surgery (3.4% ± 1.6%) was significantly less than that of before TA (59.1% ± 5.5%) (P < .001).

Conclusions

The majority of children with isolated SAH had normalization of hypercapnia after TA. Further studies in larger groups of children are needed to identify the risk factors for residual isolated SAH after TA.

Level of Evidence

4 Laryngoscope, 131:E1380–E1382, 2021

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