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Factors Associated With Late Extubation in Postoperative Patients in the Surgical Intensive Care Unit

2026年6月18日 更新者:Kaohsiung Armed Forces General Hospital

The Related Factors of Post Operation Patients With Late Extubation in Surgical Intensive Care Unit

Timely removal of a breathing tube after surgery is an important part of recovery for patients admitted to the intensive care unit (ICU). In some cases, patients may require longer use of mechanical ventilation, which can be associated with longer hospital stays and a higher risk of complications.

The purpose of this study is to examine clinical factors that may be associated with delayed removal of breathing tubes in postoperative ICU patients. This study will use information that has already been routinely collected during standard medical care, such as patient characteristics, breathing-related measurements, fluid balance, and laboratory test results.

This is a retrospective observational study and does not involve any additional treatments, procedures, or changes to routine clinical care. By analyzing these existing data, the study aims to improve understanding of factors related to extubation timing and support future efforts to enhance postoperative ICU care.

調査の概要

詳細な説明

Delayed extubation after surgery is a common clinical challenge in postoperative intensive care unit (ICU) patients and is associated with increased risks of pulmonary complications, prolonged mechanical ventilation, and extended hospitalization. Determining optimal extubation timing remains complex because respiratory mechanics, metabolic status, neurologic recovery, and perioperative stress responses must align for successful ventilator liberation.

This study is a retrospective observational study designed to identify clinical factors associated with delayed extubation in postoperative ICU patients and to develop predictive models using routinely collected clinical data. The institutional cohort includes adult postoperative patients admitted to the surgical ICU at Kaohsiung Armed Forces General Hospital who required invasive mechanical ventilation. An external cohort derived from the MIMIC-IV database is used to support model development and cross-domain learning. No additional interventions, procedures, or changes to standard clinical care are involved.

Delayed extubation is defined as removal of the endotracheal tube more than 24 hours after initiation of mechanical ventilation, while early extubation is defined as extubation within 24 hours. Demographic characteristics, disease severity scores, respiratory parameters, perioperative laboratory data, and fluid balance variables routinely documented in medical records are included for analysis.

Statistical analyses include univariable and multivariable regression models to identify factors independently associated with delayed extubation and hospital length of stay. In addition, machine learning and deep learning approaches are applied to explore complex interactions among clinical variables and to improve prediction performance. Transfer learning techniques are used to enhance model generalizability by integrating information from external ICU datasets while adapting to local institutional data.

The primary objective of this study is to improve understanding of physiologic, metabolic, and respiratory determinants of delayed extubation in postoperative ICU patients. The findings may support more individualized ventilator weaning strategies, reduce prolonged mechanical ventilation, and improve postoperative ICU care. This study involves secondary analysis of existing clinical data and poses no additional risk to patients.

研究の種類

観察的

入学 (実際)

204

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

    • 永康區
      • Kaohsiung City、永康區、台湾、802
        • Kaohsiung Armed Forces General 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

  • 子
  • 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 consists of adult postoperative patients admitted to the surgical intensive care unit who required invasive mechanical ventilation as part of routine postoperative care. This retrospective observational study analyzes existing clinical data collected during standard medical practice. No additional interventions, procedures, or changes to patient management were involved.

説明

Inclusion Criteria:

  1. Postoperative patients admitted to the surgical intensive care unit.
  2. Patients who required invasive mechanical ventilation after surgery.
  3. Patients with documented intubation and extubation events during the ICU stay.
  4. Patients with available routine clinical data, including demographic information, respiratory parameters, and laboratory results.

Exclusion Criteria:

  1. Patients without documented extubation information.
  2. Patients admitted to non-surgical intensive care units.
  3. Patients with incomplete or missing key clinical data required for analysis.
  4. Patients who did not receive invasive mechanical ventilation.

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
介入・治療
Early Extubation Group
This cohort includes postoperative intensive care unit patients who were extubated within 24 hours after initiation of invasive mechanical ventilation. No interventions were assigned as part of this study. Clinical data were analyzed retrospectively.
No intervention was administered or assigned in this study. This is a retrospective observational study based on secondary analysis of existing clinical data collected during routine clinical care. No changes to patient management, treatment decisions, or standard care were made as part of this study.
Delayed Extubation Group
This cohort includes postoperative intensive care unit patients who were extubated more than 24 hours after initiation of invasive mechanical ventilation. No interventions were assigned as part of this study. Clinical data were analyzed retrospectively.
No intervention was administered or assigned in this study. This is a retrospective observational study based on secondary analysis of existing clinical data collected during routine clinical care. No changes to patient management, treatment decisions, or standard care were made as part of this study.

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
Delayed Extubation
時間枠:Within 24 hours to 30 days after initiation of invasive mechanical ventilation
Delayed extubation is defined as removal of the endotracheal tube more than 24 hours after initiation of invasive mechanical ventilation during postoperative intensive care unit admission.
Within 24 hours to 30 days after initiation of invasive mechanical ventilation

二次結果の測定

結果測定
メジャーの説明
時間枠
Hospital Length of Stay
時間枠:From hospital admission through hospital discharge, up to 30 days
Hospital length of stay is defined as the total number of days from hospital admission to hospital discharge.
From hospital admission through hospital discharge, up to 30 days
Duration of Mechanical Ventilation
時間枠:From initiation of invasive mechanical ventilation to extubation, up to 30 days
Duration of mechanical ventilation is defined as the time from initiation of invasive mechanical ventilation to successful extubation.
From initiation of invasive mechanical ventilation to extubation, up to 30 days

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。

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)

2019年4月1日

一次修了 (実際)

2019年11月30日

研究の完了 (実際)

2019年12月31日

試験登録日

最初に提出

2026年4月20日

QC基準を満たした最初の提出物

2026年6月18日

最初の投稿 (実際)

2026年6月22日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月22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18日

最終確認日

2026年5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 because this is a retrospective observational study based on institutional clinical records. Data access is restricted by institutional policies and ethical approvals, and no consent for data sharing outside the study team was obtained.

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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