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Preoperative Incentive Spirometer Breathing Exercise to Prevent Postoperative Pulmonary Complications

Effectiveness of Incentive Spirometer on The Prevention of Postoperative Pulmonary Complications following Cardiac Surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211224053503N1
Enrollment
128
Registered
2022-01-04
Start date
2022-01-05
Completion date
Unknown
Last updated
2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative pulmonary complications.

Interventions

Intervention 1: Intervention group: The starting point of the intervention phase will start by instructing patients undergoing open heart surgeries to use Incentive Spirometer (IS) which is a mechanic

Sponsors

College of Nursing, University of Baghdad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 79 Years

Inclusion criteria

Inclusion criteria: Patients who will agree to participate in the study based on their informed consent . Subjects with age >50 years. Patients who undergo open heart surgery including ( coronary and valvular) procedures

Exclusion criteria

Exclusion criteria: Patients who refuse to participate in the study. Patients who have thoracic, abdominal, or cerebral aneurysms recent cardiothoracic or abdominal surgery.

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative pulmonary complications. Timepoint: Subjects response to the intervention will be within one week of the first meeting to examine the effectiveness of the intervention on preventing pulmonary complications. Method of measurement: Diagnosis of pulmonary complications from patients' records, results of Peak Expiratory Flow Rate and Arterial Blood Gases.

Secondary

MeasureTime frame
Peak Expiratory Flow Rate (PEFR). Timepoint: Secondary outcome is measured before and after the application of intervention within one week. Method of measurement: Data will be obtained from patient's records.;Arterial Blood Gases. Timepoint: Secondary outcome is measured before and after the application of intervention within one week. Method of measurement: Data will be obtained from patient's records.;Hospital length of stay. Timepoint: Secondary outcome is measured after the application of intervention within one week. Method of measurement: Data will be obtained from patient's records.;Oxygen dependency. Timepoint: Secondary outcome is measured after the application of intervention during the postoperative phase. Method of measurement: Observation, medical records.;Intensive Care Unit stay. Timepoint: Secondary outcome is measured after the application of intervention during the postoperative phase in the intensive care unit. Method of measurement: Data will be obtained from patient's records.;Prolonged ventilation. Timepoint: Secondary outcome is measured after the application of intervention during the postoperative phase in the intensive care unit. Method of measurement: Data will be obtained from patient's records.

Countries

Iraq

Contacts

Public ContactJadeel Al-Tuwaij

College of Nursing, University of Baghdad

jadeel.nour1202a@conursing.uobaghdad.edu.iq+964 1 521 1494

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026