Comparison of Age-Based Formula and Ultrasound-Guided Subglottic Diameter Measurement for Endotracheal Tube Sizing
Comparison of Age-Based Formula and Ultrasound-Guided Subglottic Diameter Measurement for Endotracheal Tube Sizing in Single Ventricle Patients
調査の概要
詳細な説明
To compare the accuracy of ultrasound-guided subglottic diameter measurement versus age-based formulas in determining optimal ETT size in pediatric patients with single ventricle physiology to avoid post-extubation complications. All legal guardians will provide written informed consent after a full explanation of the study. During the pre-anesthetic evaluation, demographic data, ASA physical status, relevant comorbidities, and a recent echocardiogram confirming single ventricle physiology will be documented. In the operating room, patients will be monitored using standard ASA monitors including ECG, non-invasive blood pressure, pulse oximetry, and capnography, followed by preoxygenation with 100% oxygen. If intravenous access is available, anesthesia will be induced with ketamine, fentanyl, and rocuronium. If IV access is not available, inhalational induction with sevoflurane will be used until IV access is secured, after which fentanyl and rocuronium will be administered. Following induction, ventilation will continue with FiO₂ 100% and sevoflurane 1.5% for 3 minutes.
Patients will be divided into two groups:
Group A (Age-Based Formula):
In neonates and infants under 1 year, a weight-based sizing is used:
- Infants <1 kg (Preterm): 2.5 mm ETT
- Infants 1-2 kg: 3 mm ETT
- Infants 2-3 kg (Full Term): 3-3.5 mm ETT
- Infants >3 kg (3 months to 1 year): 3.5-4 mm ETT
In Infants > 1 year, ETT size will be selected based on the standard formula: Cole's Formula for uncuffed ETT.
ETT ID (mm) = (Age/4) + 4.
Group B (Ultrasound Group):
During mask ventilation, a trained anesthesiologist will perform transverse subglottic diameter measurement using a high-frequency linear ultrasound probe (7-15 MHz). The patient will be positioned supine with mild neck extension. The probe will be placed transversely just below the thyroid cartilage to identify the subglottic airway at the level of the cricoid cartilage. The measured diameter (in mm) will be recorded and used to determine ETT size from the equation:
ETT ID (mm) = Subglottic diameter (mm) × 0.8 To confirm appropriate ETT sizing, all patients will be placed on pressure-controlled mechanical ventilation and a leak test will be performed in both groups. Start with pressure 20-25 cm H₂O, if there is resistance to ETT passage into the trachea or no audible leak or ventilator-detected leak when the lungs are inflated, the tube will be exchanged for one that is 0.5 mm smaller. If a leak is detected, decrease the pressure to 10 cm H₂O. If there's still a detected leak at 10 cm H₂O, the ETT will be exchanged for one that is 0.5 mm larger. If there's no leak at 10 cm H₂O then the ETT is optimal. Tube size will be considered optimal when a tracheal leak is not detected at an inflation pressure between 10-20 cm H₂O with uncuffed tubes.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Nouran Nemr, M.B.B.Ch, M.Sc.
- 電話番号:01008558583
- メール:Nourannemr@med.asu.edu.eg
研究連絡先のバックアップ
- 名前:Mohamed Tolba, MD
- 電話番号:01156622298
研究場所
-
-
Abbasseya
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Cairo、Abbasseya、エジプト、00202
- 募集
- Ain Shams University
-
コンタクト:
- Nouran Nemr, M.B.B.Ch, M.Sc.
- 電話番号:01008558583
- メール:Nourannemr@med.asu.edu.eg
-
-
参加基準
適格基準
就学可能な年齢
- 子
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Pediatric patients (3 months to 8 years)
- Patients with single ventricle physiology
- Scheduled for Glenn or Fontan surgery or cardiac catheterization
- Patients with Glenn or Fontan shunt scheduled for surgery
Exclusion Criteria:
- Refusal of legal guardians
- Emergency surgery
- Patients with tracheostomy tubes
- Recent or active upper respiratory tract infection
- Airway anomalies (e.g. Pierre Robin, Treacher Collins)
- ICU stay due to complications other than that of airway
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:他の
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ:Age-Based Formula Group
In neonates and infants under 1 year, a weight-based sizing is used:
ETT ID (mm) = (Age/4) + 4. |
Subglottic diameter in mm x 0.8
|
|
アクティブコンパレータ:Ultrasound Group
During mask ventilation, a trained anesthesiologist will perform transverse subglottic diameter measurement using a high-frequency linear ultrasound probe (7-15 MHz). The patient will be positioned supine with mild neck extension. The probe will be placed transversely just below the thyroid cartilage to identify the subglottic airway at the level of the cricoid cartilage. The measured diameter (in mm) will be recorded and used to determine ETT size from the equation: ETT ID (mm) = Subglottic diameter (mm) × 0.8 |
Using Ultrasound for accuracy of ETT sizing
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Accuracy of ETT size selection
時間枠:During endotracheal intubation, immediately after induction of anesthesia and neuromuscular blockade (within 10 minutes after induction)
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Accuracy of endotracheal tube size selection measured by the number of ETT attempts required to achieve an appropriate leak test and successful airway placement.
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During endotracheal intubation, immediately after induction of anesthesia and neuromuscular blockade (within 10 minutes after induction)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of post-extubation stridor/croup
時間枠:From extubation until 24 hours post-extubation
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Occurrence of post-extubation stridor or croup assessed using the Westley croup score.
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From extubation until 24 hours post-extubation
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Severity of post-extubation croup
時間枠:At 30 minutes, 2 hours, and 24 hours after extubation
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Severity of post-extubation croup assessed using the Westley croup score
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At 30 minutes, 2 hours, and 24 hours after extubation
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Duration of ICU stay related to airway complications
時間枠:From ICU admission until ICU discharge, up to 30 days
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Length of ICU stay due to airway complications such as post-extubation stridor
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From ICU admission until ICU discharge, up to 30 days
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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