Coronary Artery bypass Graft patients.
Conditions
Interventions
Intervention 1: Intervention group: Homebased group. Intervention 2: Control group:Hospital Rehabilitation group.
Sponsors
Rajaie Cardiovascular, Medical and Research Institue
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: EuroSCORE 0-5 No major complications Cardiac surgery (need for reoperation after surgery due to bleeding or tamponade), the occurrence of mediastinitis, long-term hospitalization in ICU for more than 5 days, long-term intubation in ICU (more than 24 hours), long-term hospitalization in Hospital (more than 12 days) Lack of movement problems in upper and lower limbs due to previous CVA or following surgery Hemoglobin = 8.5 CABG patients The patient lives in Tehran All patients are required to have a caregiver at home The patient or the patient's companion must have the ability to learn to work with the Polar device Low and medium irsk patients base on AACVPR criteria The patient should be literate
Exclusion criteria
Exclusion criteria: Insulin-dependent diabetes Overt chronic respiratory insufficiency Major complication of Cardiac surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hemoglobin. Timepoint: : First postoperative Hemoglobin compared to Hemoglobin after the rehabilitation period. Method of measurement: Through testing the amount of hemoglobin in the laboratory of the institute with a specific kit.;Number of Hospital readmissions in period of the rehabilitation period. Timepoint: From the beginning of the rehabilitation period (4 weeks after heart surgery) until the end of the 24th rehabilitation session. Method of measurement: The rate of hospital visits based on the admission data.;Mileage in the 6-minute test. Timepoint: The first rehabilitation session after cardiac surgery and the end of the 24th rehabilitation session. Method of measurement: Refer the patient to the rehabilitation clinic and perform a 6-minute test at the institute.;LVEF (%). Timepoint: First postoperative echocardiography compared to echocardiography after the rehabilitation period. Method of measurement: Through echocardiography with Echo Philips device.;Patient’s satisfaction at the end of the rehabilitation period (0-10). Timepoint: After the rehabilitation period. Method of measurement: It is measured by a question from zero to ten.;Quality of life. Timepoint: Before starting the rehabilitation program and after the 24th session of rehabilitation. Method of measurement: SF36 questioner.;Spo2 rest& peak in 6MWD. Timepoint: Before the rehabilitation period at the rehabilitation clinic and after the end of the 24th rehabilitation session. Method of measurement: via 6MWT. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShiva Khaleghparast
Rajaie Cardiovascular Medical and Research Institue
Outcome results
None listed