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Updated: Feb 9, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Cardiovascular Outcomes Reported in Hemodialysis Trials
Emma O'Lone1, Andrea K Viecelli2, Jonathan C Craig3
1Sydney School of Public Health, The University of Sydney, Sydney, New South Wales, Australia; Centre for Kidney Research, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.
Insights
Patients undergoing long-term hemodialysis face high cardiovascular disease risks. Standardized core outcome measures are needed for clinical trials to improve evidence-based decision-making for this population.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Clinical Trials Methodology
Background:
- Patients on long-term hemodialysis have a significantly elevated risk of cardiovascular disease.
- They are frequently excluded from general and at-risk population clinical trials.
- There is a lack of consensus on universally agreed cardiovascular outcomes for hemodialysis-specific trials.
Purpose of the Study:
- To review the current reporting of cardiovascular outcomes in clinical trials involving hemodialysis patients.
- To highlight the challenges posed by short trial durations, small sample sizes, and heterogeneous outcome measures.
- To emphasize the need for standardized core outcome sets in this high-risk population.
Main Methods:
- Review of existing literature on cardiovascular outcomes in hemodialysis clinical trials.
- Analysis of trial duration, participant numbers, and outcome reporting heterogeneity.
- Discussion of the development of core outcome sets, specifically the Standardized Outcomes in Nephrology-Hemodialysis (SONet-HD) initiative.
Main Results:
- Cardiovascular trials in hemodialysis patients are typically short (median 3-6 months) and small (59% <100 participants).
- Reported cardiovascular outcomes are highly heterogeneous, often using surrogates with uncertain clinical importance.
- Inconsistent outcome reporting hinders meta-analysis and evidence interpretation.
Conclusions:
- Establishing a core outcome measure for cardiovascular disease in hemodialysis is crucial.
- Involving patients, caregivers, and health professionals in defining these outcomes is essential.
- Consistent reporting will strengthen the evidence base for this vulnerable patient group.
Abstract:
Patients on long-term hemodialysis are at very high risk for cardiovascular disease but are usually excluded from clinical trials conducted in the general population or in at-risk populations. There are no universally agreed cardiovascular outcomes for trials conducted specifically in the hemodialysis population. In this review, we highlight that trials reporting cardiovascular outcomes in hemodialysis patients are usually of short duration (median 3 to 6 months) and are small (59% of trials have <100 participants). Overall, the cardiovascular outcomes are very heterogeneous and may not reflect outcomes that are meaningful to patients and clinicians in supporting decision making, as they are often surrogates of uncertain clinical importance. Composite outcomes used in different trials rarely share the same components. In a field in which a single trial is often insufficiently powered to fully assess the clinical and economic impact of interventions, differences in outcome reporting across trials make the task of meta-analysis and interpretation of all the available evidence challenging. Core outcome sets are now being established across many specialties in health care to prevent these problems. Through the global Standardized Outcomes in Nephrology-Hemodialysis initiative, cardiovascular disease was identified as a critically important core domain to be reported in all trials in hemodialysis. Informed by the current state of reporting of cardiovascular outcomes, a core outcome measure for cardiovascular disease is currently being established with involvement of patients, caregivers, and health professionals. Consistent reporting of cardiovascular outcomes that are critically important to hemodialysis patients and clinicians will strengthen the evidence base to inform care in this very high-risk population.
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