Evaluation of Protective Pulmonary Ventilation by Pulmonary Ultrasound

NCT ID: NCT04991727

Last Updated: 2021-08-05

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

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-21

Study Completion Date

2023-12-23

Brief Summary

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Peri - operative ultrasonography was used to evaluate the effects of protective lung ventilation on the postoperative lungs of obese patients.The purpose of this study was to apply ultrasound lung ventilation area score to the monitoring of pulmonary complications in patients with postoperative obesity.To verify the reliability and practicability of perioperative lung ultrasound quantitative scoring.

Detailed Description

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Ultrasound lung ventilation area score was applied to monitor the pulmonary complications of patients after obesity operation to verify the perioperative period.

The reliability and practicability of quantitative lung ultrasound score to clarify the effect of protective lung ventilation under perioperative pulmonary ultrasound monitoring on obesity patients.To guide the management of mechanical ventilation under general anesthesia and the prevention and treatment of postoperative pulmonary complications

Conditions

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Assessment

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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PEEP

The patient was admitted to the operating room, and routine ECG monitoring was performed. The patient was placed in supine position, and ultrasound lung examination was performed. The images of the patient were saved and the score of lung ventilation area was recorded. The induction of general anesthesia was started, and endotracheal intubation was performed after 3min of preoxygenation (100% O2) to establish a safe and effective artificial airway.Mechanical ventilation was performed after endotracheal intubation, and a second time was performed immediately after endotracheal intubation was completed.Pulmonary ultrasound was performed. The PEEPgroup was given the first RM (pulmonary retraction) with pressure maintained at 40cmH2O for 30s, followed by a 7cmH2O PEEP to maintain mechanical ventilation, and the RMS was repeated every 30 minutes until the end of surgery

recruitment maneuvers

Intervention Type BEHAVIORAL

Immediately after endotracheal intubation is completed

First RM (pulmonary retraction), maintain pressure at 40cmH2O for 30s, and then

Mechanical ventilation was maintained with 7cmH2O PEEP, and the RMS was repeated every 30 minutes until the end of surgery

ZEEP

The patient was admitted to the operating room, and routine ECG monitoring was performed. The patient was placed in supine position, and ultrasound lung examination was performed. The images of the patient were saved and the score of lung ventilation area was recorded. The induction of general anesthesia was started, and endotracheal intubation was performed after 3min of preoxygenation (100% O2) to establish a safe and effective artificial airway. Mechanical ventilation was performed after endotracheal intubation, and a second time was performed immediately after endotracheal intubation was completed

On pulmonary ultrasound, patients in the ZEEP group maintained normal mechanical ventilation throughout the operation without PEEP or RMS

recruitment maneuvers

Intervention Type BEHAVIORAL

Immediately after endotracheal intubation is completed

First RM (pulmonary retraction), maintain pressure at 40cmH2O for 30s, and then

Mechanical ventilation was maintained with 7cmH2O PEEP, and the RMS was repeated every 30 minutes until the end of surgery

Interventions

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recruitment maneuvers

Immediately after endotracheal intubation is completed

First RM (pulmonary retraction), maintain pressure at 40cmH2O for 30s, and then

Mechanical ventilation was maintained with 7cmH2O PEEP, and the RMS was repeated every 30 minutes until the end of surgery

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* enrollment of patients aged 18 years or above;
* Eligible adult patients had an American Society of Anesthesiologists (ASA) physical status classification of I to IV
* undergoing elective or expedited nonurgent, noncardiac surgery with general anesthesia

Exclusion Criteria

* patient refusal;
* morbid obesity (BMI \>40 kg/ m²);
* American Society of Anesthesiologists (ASA) physical status categories IV-V;
* previous intrathoracic procedure;
* severechronic obstructive pulmonary disease (forced expiratory volume in 1 s \<30% of the predicted value;
* a contraindication to radial artery cannulation.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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General Hospital of Ningxia Medical University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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General Hospital of Ningxia Medical University

Yinchuan, Ningxia, China

Site Status RECRUITING

Countries

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China

Facility Contacts

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Ma Hanxiang

Role: primary

+86-13519591508

References

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Wanguemert Perez AL. Clinical applications of pulmonary ultrasound. Med Clin (Barc). 2020 Apr 10;154(7):260-268. doi: 10.1016/j.medcli.2019.11.001. Epub 2020 Jan 8. English, Spanish.

Reference Type BACKGROUND
PMID: 31926654 (View on PubMed)

Costamagna A, Pivetta E, Goffi A, Steinberg I, Arina P, Mazzeo AT, Del Sorbo L, Veglia S, Davini O, Brazzi L, Ranieri VM, Fanelli V. Clinical performance of lung ultrasound in predicting ARDS morphology. Ann Intensive Care. 2021 Mar 29;11(1):51. doi: 10.1186/s13613-021-00837-1.

Reference Type BACKGROUND
PMID: 33779834 (View on PubMed)

Other Identifiers

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KYLL-2021-277

Identifier Type: -

Identifier Source: org_study_id

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