- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02364427
Arterial Stiffness and AKI Post-CABG (Heart-AKI)
Arterial Stiffness and Acute Kidney Injury Post-Coronary Artery Bypass Graft Surgery
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Acute kidney injury (AKI) affects around 20% of all hospitalised patient. Previously it was believed that recovery from an episode of AKI resulted in full renal recovery and return to normal function in the long term. However this assumption may reflect the fact that many of these patients did not receive long term follow-up and a failure to return to their baseline renal function was not identified. It is now recognised that AKI has both major long-term health and socioeconomic impacts. Studies have demonstrated that an episode of AKI can significantly increase both risk of development of chronic kidney disease and early mortality.
Episodes of dialysis-requiring AKI in patients with previously normal renal function who were not dialysis-dependent on discharge resulted in a 28-fold increase in risk of developing severe chronic kidney disease (CKD) stage 4 or 5 and a 2-fold increase in the risk of death at one year when compared to non-AKI controls. This was also observed over a 5-year follow-up period, during which patients who had suffered an episode of AKI were at a 6-fold increased risk of developing both CKD stage 4 or end stage renal failure (ESRF).
There is also an increased risk of death in patients who have experienced an episode of non-dialysis requiring AKI, which remains apparent even with mild AKI stage 1. AKI has a long-term impact on patient morbidity and mortality, an effect that appears to persist despite 'biochemical resolution'. The size of this impact is dependent upon the degree of severity and duration of AKI experienced. However, there is some controversy regarding the link of AKI to CKD. At the present time there is no specific therapy for AKI and the management of patients is completely supportive. Furthermore, in the absence of more sensitive biomarkers, it would appear that even a non-severe episode of AKI already confers a worse prognosis with regards to the risk of development of CKD and long term survival in patients. Thus perhaps focus should be on prevention of AKI as opposed to cure. This is even more pertinent when one considers that the National Confidential Enquiry into Patient Outcomes and Death (NCEPOD) report in 2009 identified 30% of cases as being 'preventable' and a deficiency of care in 50% of cases. The median length of stay for patients diagnosed with AKI was 17.8 days, which was 4.7 days longer than for those without AKI. Marion Kerr, a health economist, reported that by avoiding 'preventable' cases a potential saving of £130-186 million per year could be made.
The difficulty lies in identification of patients that are at risk of AKI. Although factors such as diabetes, older age and low estimated glomerular filtration rate (eGFR) are all associated with increased risk, there is no standardized scoring method for risk. In addition, it is not fully clear why some patients suffer AKI while others, with similar co-morbidities, do not.
Arterial stiffness (AS) is defined as 'the unit of pressure required to generate a change in volume of one unit' within a specified arterial segment. Clinically it can be assessed non-invasively by measurement of pulse wave velocity (PWV. AS varies significantly with age, gender and race, and it is only in the last few years that studies have been undertaken to attempt to quantify a 'normal' or reference value within various populations. Arterial stiffness is also increased in numerous clinical conditions such as diabetes and hypertension and there is now increasing evidence that AS may be an important predictor of disease progression and potential recovery in a wide spectrum of conditions including cardiovascular risk, development of dementia, functional recovery from strokes and in renal disease. Increased AS has been shown to be associated with decreased kidney function and to be an independent risk factor for cardiovascular events in ESRF and in renal transplant recipients.
The mechanism of injury in CKD from increased AS is thought to be related to barotrauma inflicted on glomeruli in a "stiff" vascular system. However, there is little data with regards to the effects of AS in AKI.
For this initial pilot study, we have selected the cohort of patients who are undergoing elective coronary artery bypass graft surgery (CABG) to see if this type of event is associated with increased risk of AKI. On average 450 patients per year undergo CABG surgery at King's College Hospital (KCH) and of these over 200 are elective operations. All elective patients will attend a pre-assessment clinic, which is run weekly with about 20 patients per clinic. Many of these patients will have co-morbidities associated with both an increased risk of AKI and of AS. We have performed a retrospective analysis of incidence of AKI in patients undergoing elective, isolated CABG surgery at KCH from January to December 2012. Of a total of 219 patients, 42 patients were classified as having post-operative AKI according to serum AKI criteria.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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London, United Kingdom, SE5 9RS
- King's College Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients undergoing pure (non-valvular repair) CABG surgery
- Male or female
- Aged >18 years
- Written informed consent
Exclusion Criteria:
- Patients who have aortic grafts or renal stents
- Patients at CKD stage 4 or 5 or on dialysis
- Bilateral amputee
- Unable to lie supine for 10-15 mins
- Psychiatric illness, including anxiety, mood and untreated eating disorders
- Infection or course of antibiotics within the last month
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Arterial stiffness
Arterial stiffness - Vicorder to measure pulse wave velocity
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Pulse wave velocity (PWV)measures the stiffness of the arteries.
This provides a simple and quick noninvasive method of obtaining the PWV for an arterial segment.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pulse Wave Velocity (arterial stiffness)
Time Frame: Baseline visit
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Baseline visit
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Kidney function measured by renal blood profile
Time Frame: baseline
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baseline
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Collaborators and Investigators
Investigators
- Principal Investigator: Sharlene A Greenwood, PhD, Consultant renal physiotherapist
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KCH heart-AKI
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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