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Bedside Ultrasound for Confirmation of Endotracheal Tube Placement in the Emergency Department

2026年6月20日 更新者:Antalya Health Sciences University

The Role of Bedside Ultrasound in Confirming Endotracheal Tube Placement in Patients Undergoing Endotracheal Intubation in the Emergency Department

This prospective observational study evaluated the role of bedside ultrasound in confirming endotracheal tube placement in adult patients who underwent endotracheal intubation in the emergency department. Correct placement of the endotracheal tube is critical because unrecognized incorrect placement may cause hypoxemia, hypoxic brain injury, or death.

In this study, bedside ultrasound was performed during or immediately after endotracheal intubation without interfering with the intubation procedure. Ultrasound findings were compared with capnographic end-tidal carbon dioxide measurement, which was used as the reference method for confirming tube placement. The main aim was to assess whether bedside ultrasound is a useful and reliable method for confirming endotracheal tube position in emergency department patients.

調査の概要

詳細な説明

This single-center, prospective observational diagnostic accuracy study was conducted in the Emergency Department of Antalya Training and Research Hospital. Adult patients who underwent endotracheal intubation in the emergency department after ethics committee approval were included.

Endotracheal intubation was performed as part of routine emergency care by the most senior emergency medicine resident or an experienced emergency physician. Bedside ultrasound assessment was performed during or immediately after intubation by trained emergency physicians without interrupting or delaying the intubation procedure. The ultrasound examination was performed from the suprasternal notch region to assess the position of the endotracheal tube.

The physicians who performed bedside ultrasound had at least two years of emergency medicine experience and had completed accredited ultrasound training. Before study data collection, they received additional theoretical and practical training focused on ultrasound confirmation of endotracheal tube placement.

Ultrasound findings were compared with capnometric end-tidal carbon dioxide measurement, which was used as the reference method for confirmation of endotracheal tube placement. Ultrasound images were stored in the hospital computer system and reviewed by two qualified, independent radiology specialists. Images or measurements with insufficient quality were excluded from analysis. Agreement between ultrasound assessments was evaluated statistically.

The study aimed to determine whether bedside ultrasound can be used as a rapid, reliable, and practical method for confirming endotracheal tube placement in emergency department patients.

研究の種類

観察的

入学 (実際)

70

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • konyaaltı
      • Antalya、konyaaltı、トルコ(Türkiye)、07100
        • University of Health Sciences, Antalya Training and Research Hospital

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

The study population consisted of adult patients aged 18 years or older who presented to the Emergency Department of Antalya Training and Research Hospital and underwent endotracheal intubation as part of routine emergency care. Patients were included after ethics committee approval if bedside ultrasound and capnometric end-tidal carbon dioxide assessment were performed for confirmation of endotracheal tube placement.

説明

Inclusion Criteria:

  • Patients aged 18 years or older
  • Patients who underwent endotracheal intubation in the emergency department as part of routine emergency care
  • Patients in whom bedside ultrasound and capnometric end-tidal carbon dioxide assessment were performed for confirmation of endotracheal tube placement

Exclusion Criteria:

  • Patients younger than 18 years of age
  • Patients with missing or incomplete study data
  • Patients with ultrasound images of insufficient quality for evaluation

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
Patients Undergoing Endotracheal Intubation in the Emergency Department
Adult patients who underwent endotracheal intubation in the emergency department were included in this cohort. Endotracheal intubation was performed as part of routine emergency care. Bedside ultrasound was performed during or immediately after intubation by trained emergency physicians without interrupting the procedure. Ultrasound findings were compared with capnometric end-tidal carbon dioxide measurement, which was used as the reference method for confirming endotracheal tube placement.

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
Diagnostic Accuracy of Bedside Ultrasound for Confirmation of Endotracheal Tube Placement
時間枠:During or immediately after endotracheal intubation, within a maximum of 20 seconds
The diagnostic accuracy of bedside ultrasound for confirming endotracheal tube placement will be evaluated by comparing ultrasound findings with capnometric end-tidal carbon dioxide measurement, which will be used as the reference method. Diagnostic performance will be assessed using sensitivity, specificity, positive predictive value, negative predictive value, overall accuracy, and agreement with the reference method.
During or immediately after endotracheal intubation, within a maximum of 20 seconds

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:MURAT DUYAN, ASSOCIATE PROFESSOR、University of Health Sciences, Antalya Training and Research Hospital
  • スタディディレクター:HALIT EKICI, MEDICAL DOCTOR、University of Health Sciences, Antalya Training and Research Hospital
  • スタディディレクター:CEMIL KAVALCI, PROFESSOR、University of Health Sciences, Antalya Training and Research Hospital
  • スタディディレクター:ENGIN DENIZ ARSLAN, ASSOCIATE PROFESSOR、University of Health Sciences, Antalya Training and Research Hospital
  • スタディディレクター:FEVZI YILMAZ、University of Health Sciences, Antalya Training and Research Hospital

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年1月10日

一次修了 (実際)

2026年6月10日

研究の完了 (実際)

2026年6月10日

試験登録日

最初に提出

2026年6月20日

QC基準を満たした最初の提出物

2026年6月20日

最初の投稿 (実際)

2026年6月25日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月25日

QC基準を満たした最後の更新が送信されました

2026年6月20日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data will not be shared publicly because the study includes clinical data from emergency department patients and there may be confidentiality and institutional restrictions. De-identified aggregate results will be reported in scientific publications.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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