Risk of Respiratory Complications Following Gastrointestinal Endoscopy Under Monitored Anesthesia Care

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

10313 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-01

Study Completion Date

2025-02-28

Brief Summary

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The purpose of this study is to investigate the incidence of respiratory complications after gastroenteroscopy, and establish a Logistic regression model to analyze the related risk factors of respiratory complications.

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Detailed Description

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Gastrointestinal endoscopy is currently the most widely used and reliable technique for diagnosing digestive tract diseases.With the increasing need for pain relief and the improvement of anesthesiology technology, more and more patients prefer to undergo gastroenteroscopy under sedation or anesthesia.The painless technique of gastroenteroscopy is an anesthetic method , and like other anesthesia techniques, it brings risks as well as comfort.However, current studies mainly focus on respiratory and circulation-related adverse events during the examination , while little attention is paid to delayed respiratory complications after examination.

Conditions

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Pneumonia, Aspiration

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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M group

Gratrointestinal endoscopy is undergone with moderate sedation.

No interventions assigned to this group

D/G group

Gratrointestinal endoscopy is undergone without deep sedation/general anesthsia.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Age ≥18 years old;
2. Qualified gastrointestinal tract preparation in strict accordance with the preparation requirements related to gastroenteroscopy;