Integrated Pulmonary Index in Gastroscopic Procedures

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

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-02-06

Study Completion Date

2023-11-05

Brief Summary

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Various complications are the leading cause of morbidity in sedation practices in endoscopic procedures, and guidelines recommend continuous monitoring of circulation, respiratory function, and ventilation. Integrated Pulmonary Index (IPI), one of the methods that can be used in this monitoring, gives a single numerical value obtained by continuous and simultaneous joint mathematical analysis of Oxygen saturation, End-tidal carbon dioxide concentration, respiratory rate, and heart rate values and is a good monitorization in these interventions. and provides tracking. In this study, the aim is to determine the role of IPI in the diagnosis and follow-up of respiratory complications in patients who were sedated during gastroscopy procedures.

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Detailed Description

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IPI EtCO2 is a monitoring method consisting of respiratory rate, SPO2 and heart rate parameters. While EtCO2 is measured with nasal capnography, SPO2, heart rate, respiratory rate are measured with finger probe and it will show instant measurement of respiratory status. IPI takes values between 1-10. An IPI value of 8 and above will indicate normal values, a value between 5-7 will indicate that the respiratory status of the patient should be carefully examined and intervened if necessary, values of 4 and below will definitely indicate that the patient's respiratory status should be intervened.

Blood pressure measurement will be made with a sphingmomanometer noninvasively at certain time intervals with the help of a cuff that will be placed on the patient's arm area.

Conditions

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Endoscopy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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ketaprop

At the beginning of anesthesia, 0.25 mg/kg ketamine and 0.75 mg/kg propofol will be administered.

gastroscopy

Intervention Type PROCEDURE

anaesthetic management of ambulatory endoscopic procedures

remiprop

At the beginning of anesthesia, 1 mcg/kg of remifentanil and 0.75 mg/kg propofol will be administered.

gastroscopy

Intervention Type PROCEDURE

anaesthetic management of ambulatory endoscopic procedures

Interventions

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gastroscopy

anaesthetic management of ambulatory endoscopic procedures

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* ASA 1-2-3 risk scored patients,
* patients over the age of 18 who will undergo endoscopic intervention

Exclusion Criteria

* Patients who need mechanical ventilator support,
* patients who need emergency endoscopic intervention,
* patients with a history of substance abuse,
* patients with a history of allergy to the drugs to be used,
* pregnant women will be excluded from the study.

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No