PPI in Weaning Prediction

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGaziosmanpasa Research and Education Hospital

About this trial

The aim of this study is to evaluate the predictive role of the Peripheral Perfusion Index (PPI) in forecasting extubation success during the weaning process in intensive care unit (ICU) patients. The study will investigate the ability of PPI to predict extubation failure by comparing it with traditional weaning criteria, including the Rapid Shallow Breathing Index (RSBI), PaO₂/FiO₂ ratio, and respiratory rate.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who have been on mechanical ventilation for at least 48 hours

Patients over 18 years of age who are planned to undergo extubation following a spontaneous breathing trial (SBT)

Patients or their legal representatives who provide informed consent to participate in the study

Disqualifiers

Patients for whom extubation is not planned due to hemodynamic instability

Patients with peripheral vascular disease or a history of hand surgery

Patients who die or cannot be followed up during the study period

Trial population

Patients who have been on mechanical ventilation for at least 48 hours and Patients over 18 years of age who are planned to undergo extubation following a spontaneous breathing trial (SBT) Patients or their legal representatives who provide informed consent to participate in the study

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • patients were monitored for reentubation for 48 hours.

    Other intervention

    patients were monitored for reentubation for 48 hours.

  • weaning group

    Other intervention

    patients were monitored for reentubation for 48 hours.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

• The ability of Peripheric Perfusion Index(PPI) measured 1 hour after extubation to predict extubation failure within 48 hours following extubation.

Time frame
48 hours

Secondary outcomes

1

• The predictive power of Peripheric Perfusion Index(PPI) measured at the beginning of the spontaneous breathing trial (SBT), at the 15th minute, at the end of SBT, and 2 hours after extubation in determining extubation success.

Time frame
3 hours
2

• Correlation of Peripheric Perfusion Index(PPI) measurements between cardiac patients(Patients with at least one diagnosis of cardiac disease) and non-cardiac patients.

Time frame
48 hours
3

Changes in Peripheric Perfusion Index(PPI) values in patients who experience spontaneous breathing trial(SBT) failure.

Time frame
48 hours

Other outcomes

Sponsors and contacts

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