HFNC for Postoperative Atelectasis After Laparoscopic Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBursa Yuksek Ihtisas Training and Research Hospital

About this trial

Pneumoperitoneum and Trendelenburg positioning during laparoscopic surgery promote atelectasis development, which has been reported in up to 90% of patients under general anesthesia and increases the risk of postoperative pulmonary complications. High-flow nasal cannula (HFNC) oxygen therapy may reduce post-extubation atelectasis through alveolar recruitment. This prospective observational cohort study aims to evaluate the role of HFNC in postoperative atelectasis monitored by lung ultrasonography (LUS) in patients undergoing elective laparoscopic surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients aged 18 years and older

Patients scheduled for elective laparoscopic surgery (general surgery, urology, gynecology)

Patients undergoing mechanical ventilation under general anesthesia

ASA physical status I-III

Disqualifiers

Severe or uncontrolled chronic obstructive pulmonary disease, asthma, or other chronic pulmonary diseases

Patients with atelectasis or pleural effusion detected on preoperative lung ultrasonography

Patients requiring intraoperative recruitment maneuver

ASA physical status IV or above

Trial population

Adult patients aged 18-75 years scheduled for elective laparoscopic surgery (general surgery, urology, and gynecology) under general anesthesia.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • High-Flow Nasal Cannula (HFNC)

    Other intervention

    HFNC Group

  • Conventional Oxygen Therapy

    Other intervention

    Standard oxygen therapy administered via face mask or nasal cannula after extubation following elective laparoscopic surgery.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: HFNC Group1 intervention
Group B: Control Group1 intervention

Trial outcomes

Primary outcomes

1

Total Lung Ultrasonography Score (LUS Score)

Total lung ultrasonography score assessed using the Monastesse modified LUS scoring system. Each hemithorax is divided into 6 segments along parasternal, anterior axillary, and posterior axillary lines, evaluating a total of 12 thoracic regions with a total score ranging from 0 to 36 points. Scores are compared between HFNC and conventional oxygen therapy groups.

Time frame
T0: preoperative; T1: 5th minute after extubation; T2: 30th minute in the recovery unit; T3: discharge from the recovery unit

Secondary outcomes

1

Incidence of Significant Atelectasis

Proportion of patients with at least one lung region scoring ≥2 on the LUS scoring system (coalescing B-lines/irregular pleura or consolidation \>1×2cm) at each time point.

Time frame
T0: preoperative; T1: 5th minute after extubation; T2: 30th minute in the recovery unit; T3: discharge from the recovery unit
2

Minimum SpO₂ in the Post-Anesthesia Care Unit (PACU)

Minimum oxygen saturation recorded during the entire post-anesthesia care unit stay.

Time frame
From extubation to PACU discharge, up to 2 hours
3

Incidence of Hypoxemia

Proportion of patients with SpO₂ below 95% during the post-anesthesia care unit stay.

Time frame
From extubation to PACU discharge, up to 2 hours
4

Incidence of Severe Hypoxemia

Proportion of patients with SpO₂ below 90% during the post-anesthesia care unit stay.

Time frame
From extubation to PACU discharge, up to 2 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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