- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07658456
Factors Associated With Late Extubation in Postoperative Patients in the Surgical Intensive Care Unit
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.
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
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永康區
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Kaohsiung City, 永康區, Taiwan, 802
- Kaohsiung Armed Forces General Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
- Postoperative patients admitted to the surgical intensive care unit.
- Patients who required invasive mechanical ventilation after surgery.
- Patients with documented intubation and extubation events during the ICU stay.
- Patients with available routine clinical data, including demographic information, respiratory parameters, and laboratory results.
Exclusion Criteria:
- Patients without documented extubation information.
- Patients admitted to non-surgical intensive care units.
- Patients with incomplete or missing key clinical data required for analysis.
- Patients who did not receive invasive mechanical ventilation.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
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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.
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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.
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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.
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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.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Delayed Extubation
Lasso di tempo: Within 24 hours to 30 days after initiation of invasive mechanical ventilation
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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.
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Within 24 hours to 30 days after initiation of invasive mechanical ventilation
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Hospital Length of Stay
Lasso di tempo: From hospital admission through hospital discharge, up to 30 days
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Hospital length of stay is defined as the total number of days from hospital admission to hospital discharge.
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From hospital admission through hospital discharge, up to 30 days
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Duration of Mechanical Ventilation
Lasso di tempo: From initiation of invasive mechanical ventilation to extubation, up to 30 days
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Duration of mechanical ventilation is defined as the time from initiation of invasive mechanical ventilation to successful extubation.
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From initiation of invasive mechanical ventilation to extubation, up to 30 days
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Collaboratori e investigatori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- KAFGHIRB 108-006
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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