Mechanical Power in One-lung Ventilation

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAnkara University

About this trial

Thoracic surgery usually necessitates one-lung ventilation (OLV) to provide surgical access while maintaining adequate gas exchange. However, OLV is associated with an increased risk of PPCs , a major cause of morbidity and mortality. Mechanical power, a composite parameter incorporating tidal volume, respiratory rate, driving pressure, and flow resistance, has been proposed as a key factor influencing ventilator-induced lung injury (VILI) and postoperative outcome. Understanding the association between mechanical power during OLV and PPCs could provide insights for optimizing intraoperative ventilatory strategies and reducing the burden of PPCs. As OLV inherently alters normal lung mechanics by decreasing functional residual capacity and introducing inequalities in ventilation-perfusion ratio, the complexity of managing mechanical power becomes even more pronounced. Under these altered conditions, the risk of PPC-including atelectasis, pneumonia, and respiratory failure-can be significantly elevated. Factors such as ventilatory settings, lung protection strategies, and the duration of OLV play pivotal roles in influencing mechanical power delivery and thereby impacting lung function recovery post-surgery. Current literature indicates a correlation between inappropriate mechanical ventilation strategies during OLV and increased incidence of PPCs. However, there remains a gap in understanding how precisely mechanical power, as a quantifiable measure, influences patient outcomes following OLV. Therefore, this study aims to investigate the relationship between mechanical power during OLV and the subsequent risk of PPC. By elucidating these dynamics, the findings may inform clinical practices surrounding OLV management, ultimately improving patient safety and outcomes in thoracic surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18 years or older,

ASA physical status I-IV

All thoracic surgeries

One lung ventilation period >1 hour

Disqualifiers

None

Trial population

hospital

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Number of PPCs during the first five postoperative days, defined according to standard criteria

Postoperative pulmonary complications ;(e.g., pneumonia, acute respiratory distress syndrome \[ARDS\], or prolonged mechanical ventilation).According to StEP-COMPAC group definition \[Abbott et al. 2018 Br J Anaesth 2018 May;120(5):1066-1079.\]

Time frame
From enrollment to the end of postoperative 5 th day

Secondary outcomes

1

Threshold mechanical power (J/min)associated with PPCs

Time frame
From enrollment to postoperative 5 th day
2

Unscheduled ICU admission rates

Time frame
From enrollment to postoperative 5 th day
3

Extra-pulmonary postoperative complications(number of complications)

Time frame
From enrollment to postoperative 5 th day
4

Length of ICU stay(day)

Time frame
up to 5 th day

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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