Extubation Guided by Bedside Ultrasound

NCT05674812 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 130

Last updated 2025-09-03

No results posted yet for this study

Summary

The aging of the global population has led to an increased number of surgical procedures being performed on elderly patients. However, with aging, the main structure and function of the lungs undergo progressive changes involving lung elasticity , impaired defense mechanisms, weakened respiratory muscle strength, and lessened responsiveness of the lungs to anesthesia . Smetana showed that nearly 33% of patients older than 65 years of age who undergo surgical procedures develop postoperative pulmonary complications. It can be seen that elderly patients are themselves at high risk of pulmonary complications .Common postoperative pulmonary complications include pleural effusion, atelectasis, pneumonia, acute respiratory distress syndrome, cardiogenic pulmonary edema, and postoperative need for mechanical ventilation.This can lead to prolonged hospitalization, increased economic burden on patients, and increased long-term mortality . Therefore, accurately determining factors influencing successful postoperative weaning and extubation in elderly patients is crucial to reduce complications.

Clinical practice guidelines for critically ill patients in general recommend a well-defined, albeit imperfect, protocolized weaning and extubation procedure, including the evaluation of weaning readiness, spontaneous breathing trial (SBT) assessment, extubation, and consideration of prophylactic noninvasive ventilation or high-flow nasal oxygen.However, even if the SBT is successful, 3%-30% of patients still need to be reintubated due to respiratory distress after removal of the endotracheal tube . Predicting successful extubation in these patients is difficult. Predicting successful extubation remains difficult even after a successful SBT. The decision often relies on SBT results and clinical judgment, which can be unreliable. Identifying objective factors associated with extubation failure is therefore essential.

Lung ultrasound score (LUS)has been shown to accurately predict extubation failure by detecting significant pulmonary edema during SBT,and diaphragm excursion (DE)can be used to quantitatively assess diaphragm activity to assess extubation success. However, these studies primarily involved ICU patients with mixed medical and surgical conditions. Data specifically focusing on elderly surgical patients in the Post-Anesthesia Care Unit (PACU) are limited.Given this background, we conducted this multicenter prospective observational study to investigate the association between lung ultrasound parameters (LUS, DE), oxygenation index (OI), and other clinical and laboratory factors with extubation failure specifically in elderly surgical patients recovering in the PACU.

Conditions

  • Respiratory Insufficiency
  • Ventilator Weaning
  • Postoperative Complications

Interventions

DIAGNOSTIC_TEST

Multimodal pre-extubation risk assessment in elderly surgical patients

This observational cohort study evaluates risk factors for extubation failure in elderly surgical patients. All participants receive standard pre-extubation clinical assessments per institutional protocol, including LUS、DE and oxygenation index (PaO₂/FiO₂), arterial blood gas analysis, and the patients'laboratory results before and after surgery. The association between these parameters and extubation failure will be analyzed.

Sponsors & Collaborators

  • Tianjin Forth Central Hospital

    collaborator UNKNOWN
  • Tianjin Fifth Central Hospital

    collaborator UNKNOWN
  • Tianjin TEDA Hospital

    collaborator UNKNOWN
  • The First Affiliated Hospital of Shanxi Medical University

    collaborator OTHER
  • Shanxi Province Cancer Hospital

    collaborator OTHER
  • Lili Jia

    lead OTHER

Principal Investigators

  • Wenli Yu · Tian Jin First Center Hospital

Eligibility

Min Age
65 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2024-06-30
Completion
2024-08-01
FDA Device
Yes

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05674812 on ClinicalTrials.gov