Perioperative Atelectasis in Orthopaedic Surgery: a Prospective Study

NCT ID: NCT05384795

Last Updated: 2023-04-05

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

141 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-16

Study Completion Date

2022-12-31

Brief Summary

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This study aims at comparing a perioperative pulmonary atelectasis score, measured by pulmonary ultrasound, in patients operated undergoing orthopedic surgery under general anesthesia, spinal anesthesia or peripheral nerve block. The association between the atelectasis score and previously identified risk factors will be studied.

Detailed Description

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Atelectasis is one of the most common pulmonary complications in the perioperative period, occurring in 85% to 90% of patients under general anesthesia. It can be responsible for hypoxemia and be associated with postoperative pulmonary complications such as pneumonia. The consequences are a prolongation of the hospital stay and an increase in mortality.

The appearance of perioperative atelectasis is mainly secondary to the induction of general anesthesia with an incidence up to 90%. The different causes are, for example, the administration of muscle relaxants, mechanical ventilation and the position of the patient.

In orthopedic surgery, many procedures are performed under spinal anesthesia or under peripheral nerve block. At present, there are no studies measuring the incidence of atelectasis in patients operated under these two techniques of locoregional anesthesia, with the exception of parturients undergoing cesarean section.

This study aims at comparing a perioperative pulmonary atelectasis score, measured by pulmonary ultrasound, in patients operated undergoing orthopedic surgery under general anesthesia, spinal anesthesia or peripheral nerve block. The association between the atelectasis score and previously identified risk factors will be studied.

Conditions

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Atelectasis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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General anesthesia

Lung ultrasound

Intervention Type OTHER

Lung atelectasis score

Spinal anesthesia

Lung ultrasound

Intervention Type OTHER

Lung atelectasis score

Peripheral nerve block

Lung ultrasound

Intervention Type OTHER

Lung atelectasis score

Interventions

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Lung ultrasound

Lung atelectasis score

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients over the age of 18;
* Patients scheduled for an elective operation at the Orthopedic Hospital of CHUV;
* Signature of the study consent

Exclusion Criteria

* Thoracic deformities preventing the performance of pulmonary ultrasound (dressings, drains, fractures, etc.);
* Refusal to participate;
* Patient does not speak French.
* Inability to discern
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eric Albrecht

OTHER

Sponsor Role lead

Responsible Party

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Eric Albrecht

Prof. Dr. med

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Centre Hospitalier Universitaire Vaudois

Lausanne, Canton of Vaud, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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CER-VD 2022-00712

Identifier Type: -

Identifier Source: org_study_id

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