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QT Distance and P Dispersion in ECG in Patients Having Bronchoscopy in the ICU

Not Applicable
Conditions
Ventilator-Induced Lung Injury
Pulmonary Atelectasis
Interventions
Registration Number
NCT05434624
Lead Sponsor
Abant Izzet Baysal University
Brief Summary

Fiberoptic bronchoscopy (FOB) is one of the most useful procedures for diagnosing and treating respiratory illnesses to figure out symptoms like hemoptysis, wheezing, or cough. Furthermore, FOB is a frequent method, in intensive care units, for both diagnoses of ventilator-associated pneumonia (VAP) and treatment of atelectasis with bedside sedation.) Propofol is often used in anesthesia for endoscopic treatments. Using propofol for deep anesthesia may be indicated to prevent the patient from feeling discomfort before FOB and to reduce the chance of complications.

Although major complications of FOB such as hypoxia and pneumothorax are known, there are limited studies showing its effects on cardiac hemodynamics. The cardiac effects of laryngoscope and intubation were investigated by using different anesthetic agents. In this study, we evaluated the effect of bronchoscopy with BIS-controlled sedation on ECG in ICU patients by monitoring the QT interval and P interval.

Detailed Description

For this study, it was planned to recruit 40 patients who would have FOB in the ICU of Abant İzzet Baysal University Anesthesia department. All intubated patients over 18 years of age who do not meet the exclusion criteria will be included. Before the procedure, all patients were given i.v. 0:02 - 0:04 mg / kg midazolam (zolamide 15 mg / 3 mL, and medications, Turkey) will be administered. Volume-controlled ventilation modes will be preferred during FOB. The pre-trade-inspired FiO2 will be increased to 100%. During the procedure, mean blood pressure, heart rate, oxygen saturation, respiratory rate, CVP, airway pressure, and BIS will be closely monitored. Enteral feeding will be discontinued at least 6 hours before the procedure. At the end of the procedure, the endotracheal tube position will be checked.

FOB will be performed using mobile bronchoscopy (Storz FB; 5.0 mm outer diameter). All patients will be monitored with BIS (Bispectral Index A-2000, Aspect Medical Systems, Netherlands) to measure the depth of sedation. Patients will be randomly divided into two groups by an anesthesiologist blinded to the study. Propofol will not be given to Group I after midazolam, while propofol 0.5 mg/kg bolus dose will be administered to Group II. Maintenance will be provided with 60 mcg/kg/min propofol infusion, and the propofol infusion dose will be increased by 10 mcg/kg/min by titration until the BIS value is 40-60 during the procedure. Patients under the age of 18, pregnancy, using sedative drugs in the last 24 hours, hypersensitivity to the drugs used in the study, severe cardiac disorder (EF: \< 40), those who increase the QT interval (quinidine, lithium, procainamide, amiodarone, sotalol, phenothiazine, tricyclic Those who use antidepressants, disopyramide) or reducing (digitals) drugs, affecting QT such as hypomagnesemia- hypocalcemia - hypo or hyperthermia - hypo or hypercalcemia - hyperkalemia - hyper or hypothyroidism - myocarditis - mitral heart prolapse, etc. will be excluded from the study.

Patients will be randomly divided into 2 equal groups using the closed envelope method. Oral and written consent will be obtained from the first-degree relatives of all patients. All patients will be monitored with BIS to measure the depth of sedation. Age, weight - height, gender, medications used, comorbidities, hospitalization diagnosis, and duration of the procedure will be recorded for both groups. In addition, systolic blood pressure, diastolic blood pressure, mean blood pressure, heart rate, SpO2, BIS, respiratory rate, CVP, and airway pressure will be noted before and after the procedure of the first, fifth, tenth, and fifteenth minute. P wave dispersion, OTc, and OTd values will be calculated according to the max and min wavelengths as the primary outcomes.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
40
Inclusion Criteria

* All intubated patients over 18 years of age

Exclusion Criteria
  • Patients under the age of 18
  • Pregnancy
  • Patients using sedative drugs in the last 24 hours
  • Hypersensitivity to the drugs used in the study
  • Severe cardiac disorder (EF: < 40)
  • Patients using drugs that increase the QT interval (quinidine, lithium, procainamide, amiodarone, sotalol, phenothiazine, tricyclic antidepressants, disopyramide) or reduce the QT interval (digitals)
  • Patients who have hypomagnesemia- hypocalcemia - hypo or hyperthermia - hypo or hypercalcemia - hyperkalemia - hyper or hypothyroidism - myocarditis - mitral heart prolapsus

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group MMidazolamBronchoscopy group in which only midazolam will be used
Group PPropofolBronchoscopy group in which midazolam and propofol will be used
Primary Outcome Measures
NameTimeMethod
QTc (Corrected QT interval) and QTd (QT dispersion) valuesAfter the procedure of the fifteenth minute

The onset of the QRS complex and the descending T wave as the QT interval between the point where the arm cuts the isoelectric TP segment will be taken. QT dispersion (QTd) is the difference between the longest QT and the shortest QT interval. The heart rate-corrected value of the measurement of the QT interval will be used as the QTc. QTc \> 500 ms means increased.

P wave dispersion (PWD)After the procedure of the fifteenth minute

PWD in all leads will be measured manually with the X10 magnifying glass. The beginning of the P wave is the point where the isoelectric line and the P wave intersect. The endpoint was taken as the intersection of the isoelectric line and the end point of the P wave.ECG recordings of at least 6 QRS for each lead 1 mV at a rate of 20 mm/s, including the complex 3 channels in amplitude and standard 12 leads will be done simultaneously.

Secondary Outcome Measures
NameTimeMethod
Heart rate (HR)After the procedure of the fifteenth minute

The HR value will be measured from the monitor.

Peripheral oxygen saturationAfter the procedure of the fifteenth minute

This will be measured from the monitor.

Systolic blood pressure (SBP)After the procedure of the fifteenth minute

SBP will be measured from the monitor.

Airway pressure (P Peak)After the procedure of the fifteenth minute

This will be measured from the monitor.

Respiratory rateAfter the procedure of the fifteenth minute

This will be measured from the monitor.

HospitalizationBefore the procedure

The diagnosis of all patients will be noted on the first day of the ICU.

Bronchoscopy durationAt the end of the procedure

The duration of the procedure will be noted from the beginning of the bronchoscopy till the end of it.

Mean arterial pressure (MAP)After the procedure of the fifteenth minute

The MAP is the average of the systolic pressure and the diastolic pressure that is formulized as MAP = (SBP + \[2x DBP\]) / 3.

Diastolic blood pressure (DBP)After the procedure of the fifteenth minute

DBP will be measured from the monitor.

Central venous pressure (CVP)After the procedure of the fifteenth minute

The CVP value will be measured from the monitor.

Trial Locations

Locations (1)

Abant izzet baysal university

🇹🇷

Bolu, Turkey

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