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Deep Breathing Exercise With Incentive Spirometer Started in the Preoperative Period

Primary Purpose

Breathing Exercises

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
deep breathing exercises with a incentive spirometer
Sponsored by
Ankara University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breathing Exercises focused on measuring Cardiac Surgical Procedures, Breathing Exercises, Postoperative Complications

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years and over,
  • Able to speak and understand Turkish,
  • Conscious, oriented and cooperative,
  • First time undergoing cardiac surgery,
  • In the Preoperative Chest Diseases Consultation, it was determined that there was no lung pathology and bronchodilator treatment was not started,
  • Coronary artery bypass graft (CABG), heart valve surgery or combined open cardiac surgery,
  • Having a score of 1 on the Medical Research Council Scale (MRCS),

Exclusion Criteria:

  • Emergency surgical intervention applied,
  • Complete (100%) occlusion of the left main coronary (LMCA) or right main coronary artery,
  • With concomitant vascular aneurysm,
  • Chronic respiratory system disease (Asthma, COPD, bronchiectasis, bullous lung, etc.),
  • Those who do not agree to participate in the study,
  • Died in the process of working,
  • Patients for whom data cannot be collected will be excluded.

Sites / Locations

  • Hatice ÖNER CENGİZ

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

deep breathing group

Control group

Arm Description

The intervention group is the group in which the investigators applied deep breathing exercises with incentive spirometer starting from the preoperative period.

The control group is the group that receives standard clinical care.

Outcomes

Primary Outcome Measures

Respiratory rate1
the respiratory rate will be counted by the research nurse the first day of hospitalization.
Respiratory rate2
the respiratory rate will be counted by the research nurse the day before surgery.
Respiratory rate3
the respiratory rate will be counted by the research nurse the day after surgery.
Respiratory rate4
the respiratory rate will be counted by the research nurse on the day of discharge.
SpO2 level1
the SpO2 level of patients will be evaluated the first day of hospitalization.
SpO2 level2
the SpO2 level of patients will be evaluated the day before surgery.
SpO2 level3
the SpO2 level of patients will be evaluated the day after surgery.
SpO2 level4
the SpO2 level of patients will be evaluated on the day of discharge.
Arterial blood gas parameters-pH1
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Arterial blood gas parameters-O2-1
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Arterial blood gas parameters-CO2-1
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Arterial blood gas parameters-saO2-1
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Arterial blood gas parameters-HCO3-1
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Arterial blood gas parameters-pH2
Arterial blood gas parameters of the patients before surgery will be evaluated .
Arterial blood gas parameters-O2-2
Arterial blood gas parameters of the patients before surgery will be evaluated
Arterial blood gas parameters-CO2-2
Arterial blood gas parameters of the patients before surgery will be evaluated
Arterial blood gas parameters-saO2-2
Arterial blood gas parameters of the patients before surgery will be evaluated
Arterial blood gas parameters-HCO3-2
Arterial blood gas parameters of the patients before surgery will be evaluated
Arterial blood gas parameters-pH-3
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Arterial blood gas parameters-pO2-3
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Arterial blood gas parameters-pCO2-3
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Arterial blood gas parameters-psaO2-3
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Arterial blood gas parameters-HCO3
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Arterial blood gas parameters-pH.4
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Arterial blood gas parameters-pO2.4
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Arterial blood gas parameters-pCO2.4
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Arterial blood gas parameters-psaO2.4
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Arterial blood gas parameters-HCO3.4
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Posteroanterior chest X-ray-1
All patients' first PA X-rays taken on the first day of hospitalization will be evaluated by the investigator.
Posteroanterior chest X-ray-2
All patients' last PA X-rays taken on the day of dischargewill be evaluated by the investigator.
Postoperative pulmonary complication
Defined as the occurrence of at least 1 pulmonary complication among atelectasis, pleural effusion, respiratory failure, pneumonia, pneumothorax, bronchospasm, or aspiration pneumonia. The presence of the developing condition, diagnosed by the doctor, was determined as the criterion. This will be evaluated by the Investigator physician and nurse.

Secondary Outcome Measures

Length of stay in mechanical ventilation
The time from the moment the patients are intubated until they are extubated will be recorded in "hours".
Length of stay in intencive care unit(ICU)
The time from the moment the patients are ICU. It will be recorded in "days".
Length of hospitalization
Postoperative stay will be calculated in days from the first postoperative day. This will be evaluated by the investigative nurse. It will be recorded in "days"

Full Information

First Posted
June 8, 2022
Last Updated
March 1, 2023
Sponsor
Ankara University
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1. Study Identification

Unique Protocol Identification Number
NCT05428722
Brief Title
Deep Breathing Exercise With Incentive Spirometer Started in the Preoperative Period
Official Title
The Effect of Deep Breathing Exercise With Incentive Spirometer Started in the Preoperative Period in Patients Undergoing Open Cardiac Surgery on Pulmonary Function and Complications: A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
June 25, 2022 (Actual)
Primary Completion Date
January 26, 2023 (Actual)
Study Completion Date
January 26, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ankara 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
Open cardiac surgery is an important treatment method that is frequently used in the treatment of complicated atherosclerotic ischemic heart disease and heart valve diseases. It is emphasized that respiratory functions decrease significantly after cardiac surgery, especially in the immediate post-operative period. Therefore, despite significant progress in the field of cardiopulmonary bypass and anesthesia technique, pulmonary complications after cardiac surgery are still seen as the main cause of other negative outcomes such as morbidity, mortality, and long-term hospitalization. Cardiac surgery patients are especially at high risk for the development of postoperative pulmonary complications (PPC). It has been reported that deep breathing exercises improve postoperative lung expansion and ventilation, resulting in a significant reduction in pulmonary complications. Postoperative respiratory physiotherapy techniques include techniques such as early mobilization, positioning, breathing exercises, active breathing techniques cycle, as well as the use of different mechanical devices such as incentive spirometry (IS), positive expiratory pressure mask therapy, and continuous positive airway pressure. Incentive spirometry (IS) is a mechanical breathing device that provides slow deep breathing and gives visual feedback and is used as one of the important interventions in the prevention of PPC in patients who have been undergoing open heart surgery for many years. In studies examining the effectiveness of deep breathing exercise with IS on the development of PPC in open cardiac surgery patients, it is seen that IS application is performed in the postoperative period , it is noteworthy that there is no study examining the effectiveness of preoperative IS application. In the light of this information, the aim of this study is to evaluate the effect of deep breathing exercise with incentive spirometry initiated in the preoperative period on pulmonary function and complications in patients undergoing open heart surgery.
Detailed Description
Open cardiac surgery is an important treatment method that is frequently used in the treatment of complicated atherosclerotic ischemic heart disease and heart valve diseases. Complications after cardiac surgery include; supraventricular tachycardia, atrial fibrillation, bradycardia, perioperative myocardial infarction, cardiac arrest, Postoperative pulmonary complications (PPC) such as pneumonia, atelectasis and pleural effusion . It is emphasized that respiratory functions decrease significantly after cardiac surgery, especially in the immediate post-operative period. Therefore, despite significant progress in the field of cardiopulmonary bypass and anesthesia technique, pulmonary complications after cardiac surgery are still seen as the main cause of other negative outcomes such as morbidity, mortality, and long-term hospitalization. Cardiac surgery patients are especially at high risk for the development of PPC. In approximately one-quarter of patients who undergo cardiac surgery without chronic respiratory dysfunction, a mild respiratory tract infection develops ranging from oxygen therapy to acute respiratory failure requiring invasive or non-invasive mechanical ventilation support. Among the factors that cause the development of PPC; surgical stress and anesthesia, cardiopulmonary bypass causing a systemic inflammatory response and oxidative stress that causes pulmonary ischemia-reperfusion injury, type of surgery, pain management, anesthesia protocol, use of blood products, and diaphragmatic dysfunction. Despite advances in surgical technique and pre- and postoperative care practices in cardiac surgery, PPC is still an important problem. PPC, cost of patient care, increased morbidity and mortality and length of hospital stay elongation. Due to the absence of effective deep inspiration and coughing due to postoperative pain and anxiety, secretion accumulation and gas exchange are ineffective. In a study, it was determined that after coronary artery bypass graft (CABG), 1-20% of patients were hospitalized again in the first 30 days after discharge due to respiratory system complications and 0.4-22.5% of pleural effusion. Various respiratory physiotherapy methods are used for the prevention and treatment of PPC after cardiac surgery. The main purpose of respiratory physiotherapy is to improve ventilation-perfusion compatibility, increase lung volume, increase mucociliary clearance and reduce pain. It has been reported that deep breathing exercises improve postoperative lung expansion and ventilation, resulting in a significant reduction in pulmonary complications. Postoperative respiratory physiotherapy techniques include techniques such as early mobilization, positioning, breathing exercises, active breathing techniques cycle, as well as the use of different mechanical devices such as incentive spirometry (IS), positive expiratory pressure mask therapy, and continuous positive airway pressure. Incentive spirometry (IS) is a mechanical breathing device that provides slow deep breathing and gives visual feedback and is used as one of the important interventions in the prevention of PPC in patients who have been undergoing open heart surgery for many years. Deep breathing exercise training with IS is given to the patients in the preoperative period, and its application is started in the postoperative period. However, it has been reported that insufficiency of physical adaptation and respiratory muscle weakness in the preoperative period are closely related to PPC, which causes prolonged hospital stay and increased mortality. In a meta-analysis study examining the effectiveness of preoperative exercise training for the prevention of PPC in adults undergoing major surgery, it was found that preoperative exercise training minimizes the use of hospital resources, improves physical fitness, and reduces the risk of developing PPC, regardless of the type of surgery. In a meta-analysis study examining the effectiveness of preoperative and postoperative rehabilitation in patients with lung cancer, it was determined that preoperative rehabilitation was effective in reducing postoperative pulmonary complications and hospital stay associated with lung cancer surgery. In studies examining the effectiveness of deep breathing exercise with IS on the development of PPC in cardiac surgery patients, it is seen that IS application is performed in the postoperative period, it is noteworthy that there is no study examining the effectiveness of preoperative IS application. In the light of this information, the aim of this study is to evaluate the effect of deep breathing exercise with incentive spirometry initiated in the preoperative period on pulmonary function and complications in patients undergoing open heart surgery. Research Hypotheses H1: Oxygen saturation measured using the pulse oximeter TBY200 will be significantly higher in patients undergoing open heart surgery and initiating deep breathing exercise with IS in the preoperative period. H2: Arterial blood gas parameters (pH: 7.35-7.45, PaCO2:35-45 mmHg PaO2:80-100 mmHg, SaO2: 95-97%, HCO3:22-26 mEq/L) in patients who underwent open heart surgery and started deep breathing exercise with IS in the preoperative period will have significantly more normal values. H3: Postoperative pulmonary complications will develop significantly less in patients undergoing open heart surgery and initiating deep breathing exercise with IS in the preoperative period. H4: In patients undergoing open heart surgery and initiating deep breathing exercise with IS in the preoperative period, the duration of mechanical ventilation will be significantly shorter. H5: In patients undergoing open heart surgery and initiating deep breathing exercise with IS in the preoperative period, the length of stay in the intensive care unit will be significantly shorter. H6: In patients undergoing open heart surgery and initiating deep breathing exercise with IS in the preoperative period, the postoperative hospital stay will be significantly shorter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breathing Exercises
Keywords
Cardiac Surgical Procedures, Breathing Exercises, Postoperative Complications

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized conrolled trial in the parallel group
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
deep breathing group
Arm Type
Experimental
Arm Description
The intervention group is the group in which the investigators applied deep breathing exercises with incentive spirometer starting from the preoperative period.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
The control group is the group that receives standard clinical care.
Intervention Type
Behavioral
Intervention Name(s)
deep breathing exercises with a incentive spirometer
Intervention Description
Deep breathing exercise will be explained to the patients with an incentive spirometer (IS), it will be demonstrated in practice and it will be applied from the first day of hospitalization in addition to routine treatment and care. The patient will be informed about whether they are doing it right and their questions will be answered. It will be ensured that the patients start after breakfast in the morning and make 5-10 inspirations, hold her/his breath for 3 seconds and 5-10 expirations per hour with IS until they fall asleep. The research nurse will warn the patients that they should do the exercise every hour, and the alarms of the patients' mobile phones will be set to ring every hour to be a warning. The start and end time of the exercise will be decided together with the patient, and usually the time of waking and going to bed will be taken into account.
Primary Outcome Measure Information:
Title
Respiratory rate1
Description
the respiratory rate will be counted by the research nurse the first day of hospitalization.
Time Frame
within 24 hours of hospitalization
Title
Respiratory rate2
Description
the respiratory rate will be counted by the research nurse the day before surgery.
Time Frame
up to 24 hours before surgery
Title
Respiratory rate3
Description
the respiratory rate will be counted by the research nurse the day after surgery.
Time Frame
up to 24 hours
Title
Respiratory rate4
Description
the respiratory rate will be counted by the research nurse on the day of discharge.
Time Frame
up to 24 hours
Title
SpO2 level1
Description
the SpO2 level of patients will be evaluated the first day of hospitalization.
Time Frame
within 24 hours of hospitalization
Title
SpO2 level2
Description
the SpO2 level of patients will be evaluated the day before surgery.
Time Frame
up to 24 hours
Title
SpO2 level3
Description
the SpO2 level of patients will be evaluated the day after surgery.
Time Frame
up to 24 hours
Title
SpO2 level4
Description
the SpO2 level of patients will be evaluated on the day of discharge.
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pH1
Description
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Time Frame
within 24 hours of hospitalization
Title
Arterial blood gas parameters-O2-1
Description
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Time Frame
within 24 hours of hospitalization
Title
Arterial blood gas parameters-CO2-1
Description
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Time Frame
within 24 hours of hospitalization
Title
Arterial blood gas parameters-saO2-1
Description
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Time Frame
within 24 hours of hospitalization
Title
Arterial blood gas parameters-HCO3-1
Description
Arterial blood gas parameters of the patients on the first day of hospitalization will be evaluated
Time Frame
within 24 hours of hospitalization
Title
Arterial blood gas parameters-pH2
Description
Arterial blood gas parameters of the patients before surgery will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-O2-2
Description
Arterial blood gas parameters of the patients before surgery will be evaluated
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-CO2-2
Description
Arterial blood gas parameters of the patients before surgery will be evaluated
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-saO2-2
Description
Arterial blood gas parameters of the patients before surgery will be evaluated
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-HCO3-2
Description
Arterial blood gas parameters of the patients before surgery will be evaluated
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pH-3
Description
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pO2-3
Description
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pCO2-3
Description
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-psaO2-3
Description
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-HCO3
Description
Arterial blood gas parameters of the patients postoperative first day will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pH.4
Description
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pO2.4
Description
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-pCO2.4
Description
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-psaO2.4
Description
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Time Frame
up to 24 hours
Title
Arterial blood gas parameters-HCO3.4
Description
Arterial blood gas parameters of the patients on the day of discharge will be evaluated .
Time Frame
up to 24 hours
Title
Posteroanterior chest X-ray-1
Description
All patients' first PA X-rays taken on the first day of hospitalization will be evaluated by the investigator.
Time Frame
within 24 hours of hospitalization
Title
Posteroanterior chest X-ray-2
Description
All patients' last PA X-rays taken on the day of dischargewill be evaluated by the investigator.
Time Frame
up to 24 hours
Title
Postoperative pulmonary complication
Description
Defined as the occurrence of at least 1 pulmonary complication among atelectasis, pleural effusion, respiratory failure, pneumonia, pneumothorax, bronchospasm, or aspiration pneumonia. The presence of the developing condition, diagnosed by the doctor, was determined as the criterion. This will be evaluated by the Investigator physician and nurse.
Time Frame
Before discharge (up to 14 days)
Secondary Outcome Measure Information:
Title
Length of stay in mechanical ventilation
Description
The time from the moment the patients are intubated until they are extubated will be recorded in "hours".
Time Frame
up to 24 hours
Title
Length of stay in intencive care unit(ICU)
Description
The time from the moment the patients are ICU. It will be recorded in "days".
Time Frame
Before discharge ICU (up to 1 day)
Title
Length of hospitalization
Description
Postoperative stay will be calculated in days from the first postoperative day. This will be evaluated by the investigative nurse. It will be recorded in "days"
Time Frame
Before discharge (up to 14 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years and over, Able to speak and understand Turkish, Conscious, oriented and cooperative, First time undergoing cardiac surgery, In the Preoperative Chest Diseases Consultation, it was determined that there was no lung pathology and bronchodilator treatment was not started, Coronary artery bypass graft (CABG), heart valve surgery or combined open cardiac surgery, Having a score of 1 on the Medical Research Council Scale (MRCS), Exclusion Criteria: Emergency surgical intervention applied, Complete (100%) occlusion of the left main coronary (LMCA) or right main coronary artery, With concomitant vascular aneurysm, Chronic respiratory system disease (Asthma, COPD, bronchiectasis, bullous lung, etc.), Those who do not agree to participate in the study, Died in the process of working, Patients for whom data cannot be collected will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hatice ÖNER CENGİZ, PhD.
Organizational Affiliation
Ankara University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Zeynep ULUŞAN ÖZKAN, MD
Organizational Affiliation
university of health sciences ankara education and research hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eylem GANİ, Nurse
Organizational Affiliation
university of health sciences ankara education and research hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hatice ÖNER CENGİZ
City
Altındağ
State/Province
Ankara
Country
Turkey

12. IPD Sharing Statement

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Deep Breathing Exercise With Incentive Spirometer Started in the Preoperative Period

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