Rationale: Patients undergoing cardiac surgery are at risk of developing perioperative complications and major adverse cardiac events, mainly related to both their preoperative status and type of surgical procedure. Postoperative exercise based cardiac rehabilitation (CR) is an effective therapy to prolong survival and improve quality of life. However, little is known about the effect on post-operative complications, quality of life and return to work of a combined pre- and post-operative CR program encompassing physical therapy, dietary counseling, psychological support and life style management compared to a CR program, which is provided only after cardiac surgery. Objective: to determine whether a pre- and postoperative (PRE+POST) CR program improves the short (up to three months) and long term outcomes (up to one year) of the cardiac surgery (i.e. reduction in postoperative surgical complications, readmissions to hospital and major adverse cardiac events in conjunction with improvements in the physical component of health related quality of life), when compared to postoperative CR only (POST). Study design: A Prospective Randomized Open controlled trial, Blinded End-point. Patients are randomized between two standard care CR programs. One group will start a the POST CR program after surgery. The other group will be randomized to a combined PRE+POST CR program. Study population: Patients (age \> 18 years) admitted for elective coronary bypass surgery, valve surgery and/or aortic surgery Main study parameters/endpoints: The primary outcome is a composite weighted endpoint of postoperative surgical complications, re-admissions to hospital, major adverse cardiac events and health related quality of life (two domains: physical functioning and physical problem), at three months and one year after surgery. Endpoints are determined by an independent endpoint committee, blinded to the group allocation. Secondary, the study focuses on physical health (cardiorespiratory fitness, muscle strength and functional status), psychological health (feelings of anxiety and depression), work participation, economics, lifestyle risk factors (physical activity and smoking behavior), self-efficacy and illness representations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
350
CR has the aim to influence favorably the underlying cause of cardiovascular disease, as well as to provide the best possible physical, mental and social conditions (BACPR, 2012).
CR has the aim to influence favorably the underlying cause of cardiovascular disease, as well as to provide the best possible physical, mental and social conditions (BACPR, 2012).
University Medical Center Groningen
Groningen, Netherlands
RECRUITINGa composite weighted score of functional status, postoperative surgical complications, re-admissions to hospital and major adverse cardiac events
Each event, complication or worsening in functional status are considered as a score of 1 to 3 points. These points are summed to calculate the total score.
Time frame: Up to one year post-surgery
Atrial fibrillation
Time frame: up to one year post-surgery
prolonged stay at the intensive care unit
Time frame: up to one year post-surgery
re-thoracotomy
Time frame: up to one year post-surgery
re-admissions to intensive care unit
Time frame: up to one year post-surgery
re-admissions to hospital
Time frame: up to one year post-surgery
All-cause mortality
Time frame: up to five year post-surgery
six minutes walking test
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year post-surgery
muscle strength
This will include grip strength and knee extension
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year post-surgery
functional status (KATZ)
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year post-surgery
Quality of life (Rand-36-v2)
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year post-surgery
Depression (PHQ-9)
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year post-surgery
Anxiety (GAD)
Depression (PHQ-9), anxiety (GAD), Quality of life (Rand-36-v2)
Time frame: Baseline, one day before surgery, 4-7 days, 3-4 months and one year after surgery
iMTA Productivity Cost Questionnaire (PCQ)
Time frame: Baseline, 3-4, 7-8 and 12 months post-surgery
iMTA Medical Cost Questionnaire (MCQ)
Time frame: Baseline, 3-4, 7-8 and 12 months post-surgery
Lifestyle risk factors
Physical activity is assessed using the Sensewear GECKO mini-armband (SWA) and the long version (27 questions) of the International Physical Activity Questionnaire (iPAQ)
Time frame: Baseline, 3-4 months and one year post-surgery
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.