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Does Frailty Help Predict Postoperative Outcomes in Cardiac Surgery?

Assessment of the Frailty Score in Cardiac Surgery and Its Correlation to Cardiac Postoperative Morbidity and Disability - a Prospective Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02749149
Acronym
FOCuS
Enrollment
120
Registered
2016-04-22
Start date
2016-01-31
Completion date
2017-06-30
Last updated
2016-04-22

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

Conditions

Coronary Heart Disease, Heart Valve Diseases

Keywords

Cardiac, Surgery, Frailty, Frail, Patients, Recovery, Morbidity, Outcomes, Mortality, Heart, Perioperative, Disability, WHODAS

Brief summary

This study will assess the benefit in using a frailty score to quantify accurate risk pre-operatively in patients undergoing major cardiac surgery in order to predict morbidity and disability-free survival post-operatively.

Detailed description

Increasingly, the group of patients undergoing cardiac surgery are older. Patients that are more elderly and frail are known to have an increase risk of injury to major organs following surgery including the heart, kidneys, and brain, all of which are associated with worse survival or diminished quality of life. It is becoming more important to be able to predict how well patients will fair in cardiac surgery, including predicting risk of complications (such as stroke or heart attacks) as well as long-term survival and quality of life. Currently, scores such as EUROscore can be used with good effect in predicting survival and major complications in cardiac surgery patients. However, frailty - the severity of a patient's weakness or fragility - has emerged as a potential candidate in predicting risk. Recent research has shown frailty score to predict risk of survival and complications following cardiac surgery and suggested to be possibly superior to pre-existing scores. The investigators wish to investigate the possible link between frailty and outcomes following cardiac surgery, in addition to current risk scores. The investigators also wish to determine whether frailty can effectively predict longer-term outcomes such as 'disability-free survival' - a patient-centred score that measures the ability of a patient to lead normal life activities. Patients undergoing major cardiac surgery at King's College Hospital will be recruited, following consent. The study will mainly involve questionnaires at various stages, starting at a pre-operative clinic. After surgery, follow up of patient's progress will be carried out at 3 days in hospital; and at 1 month, 3 months, and 6 months and 1 year via telephone. The investigators expect the results of this observational study to influence further research into the use of frailty risk scoring prior to clinical decisions, and add to the evidence in assessing risk-related outcomes in cardiac surgery.

Interventions

None listed

Sponsors

King's College Hospital NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 years or over * Due to undergo elective cardiac surgery: coronary artery bypass graft (CABG); valve replacement/repair; or transcatheter aortic valve implantation (TAVI) surgery * Able to give informed consent * Fluency in English

Exclusion criteria

* Emergency cardiac surgery and non-cardiac surgery * Inadequate knowledge of English that will prevent patients from completing the consent or undertaking study assessments * Severe visual, auditory, or motor handicap * Concurrent diseases of the central nervous system, * Patients at the extremes of frailty, in whom it would be unethical to perform a full assessment.

Design outcomes

Primary

MeasureTime frameDescription
Disability-free survival1 yearDefined as percentage of participants alive and with a disability score (using World Health Organisation Disability Assessment Schedule 2.0, WHODAS) of less than 25%.

Secondary

MeasureTime frameDescription
Mortality1 month postoperative
Delirium3 days postoperativeUsing Confusion Assessment Method (CAM).
In hospital complications1 monthIncidence of major adverse cardiac or cerebrovascular events, and/or acute renal injury.
Return to theatre1 month
Length of hospital stay1 month

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026