Intradialytic Hypotension Clinical Trial
Official title:
Minimization of Intradialytic Hypotension Using Cardiography-Guided Intervention
This is a research study to test the application of FDA-approved, non-invasive device (NICaS) that measure the performance of your heart during HD treatment.
The incidence of intradialytic hypotension (IDH) events, reported to occur in 15% to 50% of
hemodialysis (HD) treatments, is still high despite major technical advances in HD
technology. By definition, excessive reduction in intravascular volume by ultrafiltration
and limited vascular refilling from tissues into the vascular space is the cause of IDH.
Chronic HD patients exhibit a high prevalence of peripheral vascular and cardiac
abnormalities. Specifically, hemodynamic instability during HD can occur due to insufficient
reduction in venous unstressed volume, poor diastolic filling under reduced atrial pressures
associated with diastolic dysfunction, altered cardiac contractility, and impaired vascular
reactivity. An IDH event can lead to myocardial cerebral and other organ ischemia. Long- and
short-term adverse outcomes have been associated with IDH, a common HD complication and
significant cause of morbidity.
Recent pilot studies suggest that in IDH-prone subjects, measurements of hemodynamic
variables during HD can be used to categorize the hemodynamic response into three subgroups:
cardiac power index (CPI) reduction with stable total peripheral resistance (TPR), TPR
reduction with stable CPI, and reduction in TPR and CPI groups. It is hypothesized that
targeted intervention for each subgroup can reduce IDH.
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