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Perioperative Atelectasis in Orthopaedic Surgery: a Prospective Study

Perioperative Atelectasis in Patients Undergoing Orthopaedic Surgery: Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05384795
Acronym
ATELHO
Enrollment
141
Registered
2022-05-20
Start date
2022-05-16
Completion date
2022-12-31
Last updated
2023-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atelectasis

Brief summary

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

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.

Interventions

OTHERLung ultrasound

Lung atelectasis score

Sponsors

Eric Albrecht
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Lung atelectasis scoreimmediately after the surgeryAtelectasis score based on validated ultrasound quantification (comparing different anesthesia techniques)

Secondary

MeasureTime frameDescription
Lung atelectasis scoreFour timepoints: at baseline, immediatly before surgery (after anesthesia induction), immediately after the surgery, and at the recovery roomAtelectasis score

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026