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

18 de junho de 2026 atualizado por: 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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Observacional

Inscrição (Real)

204

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • 永康區
      • Kaohsiung City, 永康區, Taiwan, 802
        • Kaohsiung Armed Forces General Hospital

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

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.

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Delayed Extubation
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Hospital Length of Stay
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de abril de 2019

Conclusão Primária (Real)

30 de novembro de 2019

Conclusão do estudo (Real)

31 de dezembro de 2019

Datas de inscrição no estudo

Enviado pela primeira vez

20 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

18 de junho de 2026

Primeira postagem (Real)

22 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

18 de junho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

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.

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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