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Left-ventricular function and autonomic cardiac responses after short-term inpatient cardiac rehabilitation: A prospective clinical trial

Left-ventricular function and autonomic cardiac responses after short-term inpatient cardiac rehabilitation following coronary artery bypass graft (CABG) surgery: A prospective clinical trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000559011
Enrollment
12
Registered
2010-07-12
Start date
2006-01-10
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

It is known that coronary artery bypass graft (CABG) leads to cardiac autonomic (CA) dysfunction and that cardiac rehabilitation (CR) involving physical exercise is associated with CA benefits. However, is not known whether differences in left ventricular function (LVF) interfere in CA responses after CR. The aim of this study was to assess the CA responses in normal and reduced LVF patients undergoing CABG and CR. The hypothesis of this study was that patients with the poorest LVF are likely to derive the greatest benefit in the cardiac autonomic activity from rehabilitation.

Interventions

Patients awaiting first-time CABG were invited to participate in the study, and enrolled after giving written informed consent. Participants were divided into left ventricular function (LVF) normal group (LVFN group) or left ventricular function (LVF) reduced group (LVFR group). Pre-operatively, the patient’s age, gender, weight, height, body mass index, risk factors, pharmacological treatment and other relevant medical history were documented. Additionally, a pulmonary function test was perform

Patients awaiting first-time CABG were invited to participate in the study, and enrolled after giving written informed consent. Participants were divided into left ventricular function (LVF) normal group (LVFN group) or left ventricular function (LVF) reduced group (LVFR group). Pre-operatively, the patient’s age, gender, weight, height, body mass index, risk factors, pharmacological treatment and other relevant medical history were documented. Additionally, a pulmonary function test was performed to investigate the presence of chronic obstructive pulmonary disease (COPD) and education about the effects of surgery on cardiorespiratory function, post-operative routines and cardiac rehabilitation programme were provided. Post-operatively, surgical and hospital data were recorded and all patients were engaged in cardiac rehabilitation supervised by one of three members of physiotherapy staff, specifically trained. All patients participated in a once-daily individual short-term supervised inpatient physiotherapy exercise protocol consisted of early mobilization plus respiratory exercises with approximate duration of daily physiotherapy sessions of 60 minutes per day starting on the first postoperative day until discharge Briefly, this protocol consisted of progressive exercises, range of movement (ROM) active-assistive movements to climbing flights of stairs. Estimated energy expenditure during this program was initially set at approximately 2 metabolic equivalent (MET)s and progressed to 4 METs. Exercise intensity was gauged by heart rate with an upper threshold set at standing resting heart rate +20bpm, monitored by a Polar S810i telemetry system. Moreover, the patients performed voluntary deep-breathing exercises from functional residual capacity to total lung capacity (40 deep breaths in four sets of 10, each breath included a 5 second hold at end inspiration) followed by coughs or huffs (with wound support) supervised once daily. Patients were instructed to perform these breathing and coughing exercises independently every waking hour. The outcome measures of heart rate (HR) and R-R intervals (R-Ri) were collected prior (pre-operative and first post-operative day - PO1) and after (day before discharge) to cardiac rehabilitation.

Sponsors

Renata Goncalves Mendes
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
42 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Patients undergoing first-time elective CABG surgery with LVF normal or reduced were included in this study

Exclusion criteria

Exclusion criteria were emergent or concomitant surgery, recent myocardial infarction (MI) (6 months), implanted pacemaker, unstable angina, chronic disturbances in heart rhythm, significant acute arrhythmias, valvular heart diseases, COPD, severe non-cardiac diseases and the inability to perform cardiac rehabilitation according to our protocol.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026