軽度の睡眠呼吸障害児の手術は受診や投薬の減少につながる(Surgery in kids with mild sleep-disordered breathing tied to fewer doctor visits, meds)

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2025-03-17 アメリカ国立衛生研究所 (NIH)

米国国立衛生研究所(NIH)の支援を受けた臨床研究により、軽度の睡眠呼吸障害(SDB)を有する子供に対するアデノイド切除術と扁桃摘出術(アデノトンシレクトミー)が、医療機関への受診回数と処方薬の使用を大幅に減少させることが明らかになりました。 この研究では、手術を受けた子供たちが、32%の受診回数減少と48%の処方薬使用減少を示しました。SDBは、睡眠中のいびきや呼吸停止を特徴とし、米国の子供の約6~17%が影響を受けています。中等度から重度のSDBには手術が一般的な治療法ですが、軽度のSDBに対する手術の有効性はこれまで明確ではありませんでした。今回の研究結果は、軽度のSDBを持つ子供に対するアデノトンシレクトミーが、医療リソースの使用を減少させる可能性を示唆しています。

<関連情報>

いびきと軽度の睡眠時無呼吸を有する小児における腺扁桃摘出術と医療利用 無作為臨床試験 Adenotonsillectomy and Health Care Utilization in Children With Snoring and Mild Sleep Apnea A Randomized Clinical Trial

Jessie P. Bakker, MS, PhD; Fang Zhang, PhD; Raouf Amin, MD; et al
JAMA Pediatrics  Published:March 17, 2025
DOI:10.1001/jamapediatrics.2025.0023

Key Points

Question Among children who snore without frequent obstructive events, does early adenotonsillectomy compared with watchful waiting with supportive care reduce health care utilization over 12 months of follow-up?

Findings In this randomized clinical trial including 459 children with mild sleep-disordered breathing (SDB), adenotonsillectomy compared with watchful waiting resulted in reductions in both total health care encounters and prescriptions. The clinical categories demonstrating the greatest difference between surgery and no surgery were encounters related to respiratory and sleep conditions.

Meaning In children with mild SDB, adenotonsillectomy resulted in reduced health care utilization.

Abstract

Importance The literature indicates that health care utilization (HCU) of children with untreated moderate-to-severe obstructive sleep apnea is greater than that of matched controls before diagnosis, and treatment is associated with a decline in HCU not observed in those who remain untreated. Research on this topic has been limited to retrospective analyses and observational cohort studies; little is known about HCU among the many children with snoring and mild sleep-disordered breathing (SDB).

Objective To determine whether adenotonsillectomy in comparison with watchful waiting with supportive care is associated with fewer health care encounters and prescriptions.

Design, Setting, and Participants This randomized clinical trial, Pediatric Adenotonsillectomy Trial for Snoring (PATS), was a 12-month, parallel-arm trial conducted from 2016 to 2022 in tertiary care centers in the United States. Participants were recruited from otolaryngology, sleep, pulmonary, or general pediatric clinics; aged 3 to 13 years; diagnosed with mild SDB; had a tonsillar hypertrophy grade of 2 or more; and had a body mass index z score less than 3. Children referred from a clinician outside of the local electronic medical record system were excluded. Data analysis was conducted from June 2022 to April 2024.

Intervention Early adenotonsillectomy.

Main Outcomes and Measures Evaluation of HCU was a prespecified secondary aim of PATS. Total encounters and total prescriptions over the 12 months after randomization were analyzed.

Results Among 459 children who were randomized, the analytic sample included 381 children, after excluding those referred from outside the local electronic medical record system. The median (IQR) age was 6 (4-8) years; 192 participants (50%) were female and 189 (50%) male. Adenotonsillectomy was associated with a 32% reduction in total health care encounters (mean difference, -1.25 per participant per year; 95% CI, -1.96 to -0.53) and a 48% reduction in prescriptions (mean difference, -2.53 per participant per year; 95% CI, -4.12 to -0.94). The difference in encounters was primarily driven by fewer office visits and outpatient procedures rather than by reduced hospitalizations or urgent care visits.

Conclusions and Relevance This study found that adenotonsillectomy was associated with reduced all-cause HCU in children with mild SDB, supporting early intervention for children with mild SDB. Future research focused on the cost effectiveness of adenotonsillectomy for pediatric SDB is warranted.

Trial Registration ClinicalTrials.gov Identifier: NCT02562040

医療・健康
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