Integrated Pulmonary Index Monitoring for Thoracic Surgery Patients

Completed

• Conditions: Postoperative Complications; Monitoring
• Interventions: Device: integrated pulmonary index monitor

• Registration Number: NCT05368740
• Lead Sponsor: Cukurova University

Brief Summary

The aim of this study was to investigate the effect of postoperative Integrated Pulmonary Index (IPI) scores on postoperative complications, blood gas analysis, mortality and morbidity in the patients undergoing thoracic surgery.

Detailed Description

This prospective observational clinical study was performed between August 1, 2020 and January 31, 2021. After faculty ethics committee approval (Cukurova University, decision number: 111, date 02.10.2020) and written informed patient consent, 97 patients with American Society of Anesthesiologists (ASA) physical status I-II, over 18 years, volunteer to participate study, scheduled for elective VATS and thoracotomy surgery under general anesthesia were included in this study. Exclusion criteria were the presence of neuromuscular disorder, serious respiratory, cardiovascular, renal, and hepatic disease, ASA score \> II, pneumonectomy surgery, morbid obesity with body mass index (BMI) \> 40 kg/m2, younger than 18 years old, pre-determined need for postoperative intensive care.

Routine monitoring (electrocardiogram, noninvasive arterial blood pressure, heart rate and oxygen saturation) were applied before the induction of anesthesia to all patients. The induction was with intravenously (iv) 1.5-2 mg/kg propofol and 0.6 mg/kg rocuronium. After adequate muscle relaxation, female patients were intubated with a 35-37 F, male patients were intubated with a 39-41 F double-lumen tube. Anesthesia was maintained by repeated rocuronium doses if needed, 1.5-2% sevoflurane and an oxygen-air mixture. One lung ventilation was started just before the thorax was opened.

At the end of the surgery, neuromuscular block was antagonised with neostigmine (0.05 mg/kg) and atropine (0.015 mg/kg). Following extubation, patients were brought to the postanesthetic care unit (PACU) for 2 hours. For postoperative analgesia, regional techniques were used if the patients agreed, otherwise, iv opioid and nonsteroidal anti-inflammatory drugs (NSAIDs) were applied. All patients were given 2 L/minute oxygen as a standard with a nasal cannula. Postoperative pain was assessed by Visual Analog Scale (VAS), if the patients complained of pain (VAS ≥ 4), iv 0.5 mg/kg meperidine was given as a rescue analgesia.

Age, height, body weight, BMI, ASA physical status, comorbidity, and respiratory function test values were recorded as demographic data. Surgery type, duration of anesthesia, duration of surgery, and complications also were recorded. Systolic, diastolic, and mean blood pressure, SpO2, EtCO2, IPI values (monitored with the CapnostreamTM35 portable respiratory monitor), and arterial blood gas analyzes (evaluated with the ABL800 BASIC blood gas device) were recorded at the 15, 30, 60 and 120th minutes at the PACU. After 2 hours, when patients met standard PACU discharge criteria (fully awake, stable hemodynamic and respiratory parameters, satisfaction analgesia) they were transferred to the thoracic surgery ward.

All patients were evaluated in three groups according to their IPI score: high IPI (score level 8-10) group, medium IPI (score level 5-7) group, and low IPI (score level 1-4) group. Required attention was defined as SpO2 was between 88% and 92%, RR ≤ 8 breath/minute or IPI score level was between 5 and 7. The required intervention was defined as SpO2 ≤ 88% and IPI score level was ≤ 4. Postoperatively, at 6, 12, 18 and 24th hours, hemodynamic values and arterial blood gas analyses, length of hospital stay, complications, need for intensive care and 28-day mortality were evaluated and recorded.

Study Timeline

• Study Start: 2020-08-01
• Primary Completion: 2021-01-31
• Study Completion: 2021-02-01
• Study First Submitted: 2022-04-22
• Status Verified: 2022-05
• Study First Submitted QC: 2022-05-06
• Study First Posted: 2022-05-10
• Last Update Submitted: 2022-05-10
• Last Update Posted: 2022-05-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 97

Inclusion Criteria

1. American Society of Anesthesiologists (ASA) physical status I-II,
2. Over 18 years,
3. Scheduled for elective VATS and thoracotomy surgery under general anesthesia

Exclusion Criteria

1. Neuromuscular disorder,
2. Serious respiratory disease,
3. Serious cardiovascular disease,
4. Renal failure,
5. Hepatic failure,
6. ASA score > II,
7. Pneumonectomy surgery,
8. Morbid obesity with body mass index (BMI) > 40 kg/m2,
9. Younger than 18 years old,
10. Pre-determined need for postoperative intensive care.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
high IPI group	integrated pulmonary index monitor	IPI score level was between 8-10
median IPI group	integrated pulmonary index monitor	IPI score level was between 5-7

Primary Outcome Measures

Name	Time	Method
number of participants with postoperative complications	postoperative first 24 hours	The patients were visited in the thoracic surgery service and postoperative complications were recorded.
arterial blood pH values in the first 24 hours postoperatively	postoperative first 24 hours	The patients were visited in the thoracic surgery service, blood gas analyses were analysis and arterial blood pH values were recorded.

Secondary Outcome Measures

Name	Time	Method
length of hospital stay	through study completion, an average of 1 week"	Postoperatively, the patients were visited in the thoracic surgery service everyday and length of hospital stay was recorded.

Trial Locations

Locations (1)

Mediha Türktan; 🇹🇷 Adana, Turkey