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Mechanical Ventilation Based on Driving Pressure in Lateral Position

Primary Purpose

Fracture of Hip, Osteoarthritis, Hip, Congenital Hip Deformity

Status
Recruiting
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
routine lung protective, conventional mechanical ventilation
Sponsored by
Akdeniz University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fracture of Hip focused on measuring Driving Pressure, lung protective ventilation, PEEP, total hip replacement, lateral position

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients planned to have total hip replacement

Exclusion Criteria:

High intracranial pressure Bronchopleural fistula Hypovolemic shock Right ventricular failure Left ventricular failure(Ejection fraction lower than 50%) Arrythmia

Sites / Locations

  • Akdeniz University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

conventional mechanical ventilation

mechanical ventilation adjusted according to driving pressure

Arm Description

routine mechanical ventilation will be adjusted based on conventional mechanical ventilation settings with tidal volume of 8 ml/kg and PEEP level of 5

routine mechanical ventilation adjusted based on driving pressure during lateral position. After patients are put to lateral position incremental increase in PEEP will be applied and the driving pressures will be recorded for each PEEP level and the patients will be ventilated with this PEEP during anesthesia. the other setting will be same with conventional group. tidal volume of 8 ml/kg

Outcomes

Primary Outcome Measures

volume of intraoperative fluid administration
the patients will receive intraoperative fluids according to a protocol based on PVI.
intraoperative etCO2 levels
et CO2 levels will be recorded form the anesthesia machine monitor
lactate levels
lactate levels will be obtained from the serial blood gas analysis

Secondary Outcome Measures

postoperative mechanical ventilation duration
The patient's need for mechanical ventilation, after the surgery, will be assessed
postoperative intensive care stay
after the end of surgery the patients need for intensive care will be assessed
length of hospital stay after the operation
the effects of mechanical ventilation on the days of hospital stay will be assessed

Full Information

First Posted
June 25, 2020
Last Updated
July 26, 2022
Sponsor
Akdeniz University
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1. Study Identification

Unique Protocol Identification Number
NCT04455789
Brief Title
Mechanical Ventilation Based on Driving Pressure in Lateral Position
Official Title
Mechanical Ventilation in Lateral Position During Total Hip Replacement Surgery : Comparison of Driving Pressure With Conventional Ventilation
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2019 (Actual)
Primary Completion Date
August 1, 2022 (Anticipated)
Study Completion Date
August 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Akdeniz University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Previous studies showed that, best lung protective strategies of ventilation parameters are based on driving pressure in damaged lungs. But there are few studies concerning the effects of different positions during different types of surgery on driving pressure with normal lungs.So the investigators decided to compare mechanical ventilation based on driving pressure with conventional mechanical ventilation in patients with lateral decubitus position during total hip replacement surgery. The investigators hypothesised that, there will be better intraoperative hemodynamic and respiratory parameters with better early postoperative results in patients whom mechanical ventilation parameters are adjusted according to driving pressure. In this randomised, controlled, double blind study, 60 patients who will have total hip replacement surgery will be recruited to the study. 30 patients will be ventilated by 8 ml/kg tidal volume and 5 cmH20 PEEP, in conventional lung protective group. And the other 30 patients will be ventilated by 8 ml/kg tidal volume and PEEP level with the lowest driving pressure. The investigators primary goal in this study study is to compare the effects of conventional lung protective ventilation with ventilation based on driving pressure on hemodynamic and respiratory parameters. And secondly, the investigators aim to compare the effects of these two techniques s on early postoperative outcome. The investigators primary result parameters are intra operative fluid consumption, lactate, etC02 and mix venous oxygen saturation levels.The investigators secondary result parameters are postoperative mechanical ventilation, ICU stay and discharge times.
Detailed Description
There may be physiologic and pathologic pulmonary changes because of inflammatory cytokine release during total hip replacement surgery due to surgical invasivity or advanced age, comorbidities, perioperative immobility of patients. Also intraoperative mechanical ventilation can cause volutrauma, barotrauma or atelectrauma risk because of lateral position during hip replacement surgery. All these factors can cause pulmonary complications and vascular permeability increase in dependent and independent regions due to neutrophil response increase. Intraoperative hypovolemia is often observed in this group patients because of preoperative prolonged fasting periods, insufficient fluid intake due to preoperative delirium and depression. Also mechanical ventilation with positive pressure slightly decreases venous return to the heart resulting decrease in cardiac output. It is more obvious in the presence of hypovolemia. Providing continuous sufficient intravascular volume is necessary for prevention of tissue hypoxia and providing optimal cardiac output. It is known that intra operative hemodynamic optimisation, has positive effects on mortality ratio. But proper intravascular volume is not always easy to maintain, and it is not always easy for anaesthetists to identify deficiency or overload of intra operative intravascular volume. In recent years, intravascular volume therapies are goal directed by the reflections of respiratory mechanics on arterial pressure and pulse oximetry. Plethysmographic wave changes observed in pulse oximetry induced by positive pressure ventilation is accepted as indicator of hypovolemia. Hemodynamic changes induced by respiratory mode can be measured by invasive arterial monitorization. This dynamic variable is called as pulse pressure variation index and is correlated with amplitude changes observed in pulse oximetry signals. These variations are based on changes observed in pulse wavelength due to the changes in intrathoracic pressure. In some pulse oximetry devices, this is done as standard function as path variability index (PVI). PVI is measurement of dynamic changes of perfusion index during a whole respiratory cycle. Pulse oximetry wave length changes enables the evaluate hypovolemia noninvasively. PVI is gaining importance as a dynamic parameter in evaluating fluid treatment during surgery. Goal directed fluid therapy has shown positive effects on results on patient survival. In a study which fluid therapy was guided by PVI changes and it was reported that, goal directed fluid therapy had positive results.The investigators also, use some invasive and noninvasive monitorization techniques, including PVI and CVP, to monitor static and dynamic hemodynamic parameters during hip replacement surgery and we apply fluids according to our fluid therapy protocols. The investigators use blood gas analysis to monitor the efficiency of this treatment. In this study, in both groups the investigators will apply fluid according to PVI values, so if any difference detected is observed between groups will be because of the differences of respiratory parameters between groups. And the investigators can detect, PVI stability and less fluid needs differences between groups. PETCO2 is, another parameter which will be evaluated in this study, is a factor of tissue CO2 production (VCO2), alveolar ventilation and cardiac output (mainly pulmonary blood flow). It is known that, when CO2 produced at the tissues and formed in lungs are constant, the changes of etCO2 are due to the blood flow differences and it is related to changes of cardiac output. For this reason, PETCO2 is suggested as a noninvasive measure for continuous assessment of cardiac output. At the same time, it is possible to comment about changes of dead space by measuring arterial CO2 pressure. Decrease of PETCO2, resulted from cardiac output decrease, can not be explained only with the decrease rate of excretion of CO2, but also can be explained by the changes of production of CO2 caused by dependency to oxygen supply. On the contrary, when cardiac output is high, pulmonary blood flow is no longer a limiting factor for PETCO2 formation, and PETCO2 is related to sufficiency of alveolar ventilation. As a result, etCO2 measurement has some advantages; it is simple noninvasive and does not require a invasive hemodynamic measurement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fracture of Hip, Osteoarthritis, Hip, Congenital Hip Deformity
Keywords
Driving Pressure, lung protective ventilation, PEEP, total hip replacement, lateral position

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
conventional mechanical ventilation
Arm Type
Experimental
Arm Description
routine mechanical ventilation will be adjusted based on conventional mechanical ventilation settings with tidal volume of 8 ml/kg and PEEP level of 5
Arm Title
mechanical ventilation adjusted according to driving pressure
Arm Type
Experimental
Arm Description
routine mechanical ventilation adjusted based on driving pressure during lateral position. After patients are put to lateral position incremental increase in PEEP will be applied and the driving pressures will be recorded for each PEEP level and the patients will be ventilated with this PEEP during anesthesia. the other setting will be same with conventional group. tidal volume of 8 ml/kg
Intervention Type
Procedure
Intervention Name(s)
routine lung protective, conventional mechanical ventilation
Other Intervention Name(s)
routine lung protective, conventional mechanical ventilation with PEEP adjusted to the lowest Driving Pressure level
Intervention Description
routine lung protective, conventional mechanical ventilation with stabil PEEP
Primary Outcome Measure Information:
Title
volume of intraoperative fluid administration
Description
the patients will receive intraoperative fluids according to a protocol based on PVI.
Time Frame
during intraoperative period
Title
intraoperative etCO2 levels
Description
et CO2 levels will be recorded form the anesthesia machine monitor
Time Frame
during mechanical ventilation
Title
lactate levels
Description
lactate levels will be obtained from the serial blood gas analysis
Time Frame
during intraoperative period
Secondary Outcome Measure Information:
Title
postoperative mechanical ventilation duration
Description
The patient's need for mechanical ventilation, after the surgery, will be assessed
Time Frame
From end of surgery to the end of mechanical ventilation duration in the intensive care unit until the patient is extubated, up to 3 days
Title
postoperative intensive care stay
Description
after the end of surgery the patients need for intensive care will be assessed
Time Frame
From end of operation to the end of intensive care stay, up to 1 week
Title
length of hospital stay after the operation
Description
the effects of mechanical ventilation on the days of hospital stay will be assessed
Time Frame
form end of surgery to the end of hospital stay, up to 10 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients planned to have total hip replacement Exclusion Criteria: High intracranial pressure Bronchopleural fistula Hypovolemic shock Right ventricular failure Left ventricular failure(Ejection fraction lower than 50%) Arrythmia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nesil coskunfırat, Ass Prof
Phone
00902422496257
Ext
6260
Email
nesildgr@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yesim Cetintas, specialist
Phone
00902422496257
Ext
6260
Email
yesimcetintas@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zekiye Bigat, Prof
Organizational Affiliation
Akdeniz University Medical School Anesthesiology and Reanimation Department
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
İlker O Aycan, Ass Prof
Organizational Affiliation
Akdeniz University Medical school Anesthesiology and Reanimation Departmnet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Akdeniz University Hospital
City
Antalya
ZIP/Postal Code
07070
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nesil Coskunfırat, Ass. Prof
Phone
00902422496257
Ext
6260
Email
nesildgr@yahoo.com
First Name & Middle Initial & Last Name & Degree
Yesim Cetintas, Specialist
Phone
00902422496257
Ext
6260
Email
yesimcetintas@yahoo.com
First Name & Middle Initial & Last Name & Degree
Zekiye Bigat, Prof
First Name & Middle Initial & Last Name & Degree
Ilker O Aycan, Ass.Prof

12. IPD Sharing Statement

Plan to Share IPD
No

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Mechanical Ventilation Based on Driving Pressure in Lateral Position

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