I mean if I have more than 85 litres of blood pumped through the kidney. I'm not sure of the medical term for it.
The problem(s) start with realizing that kt/V is for UREA clearance. However, urea is not really the "uremic toxin" that makes people ill with kidney failure. The nice thing about urea is that it is cheap to measure, and is very small. We use it as a marker of the other stuff that builds up with kidney failure that actually would make someone ill. Urea is very rapidly cleared with todays high-flux membranes (F-160, 180, etc...), since it is very small. Most of the clearance of urea takes place in the first hour or two (..."zero order kinetics, for the chemists out there). This is a CONCENTRATION dependent clearance (the higher the concentration, the faster the clearance...thus the first hour is where most of the urea is removed, because your urea is actually higher at the start of the treatment.)However, we think that many of the toxins in renal failure are bigger than urea....this is the "middle molecule" theory. These bigger molecules (...those into the data might have heard of beta2-macroglobulins as a marker of this size stuff), are not so eaisly cleared. These larger compounds are removed in a more linear (or "first order" kinetics) fashion. In other words, this is more TIME dependent. The amount of these middle molecules removed is THE SAME for each hour of dialysis...the first hr is the same as the last hr. The problem is that we don't measure theses things.So, just by solely focusing on urea modeling (kt/V for urea), we can miss a whole bunch of stuff....so just because your Kt/V is above goal, maybe cutting your time is not a good idea, because you will have less clearance of larger molecules (but we don't measure this). Over time, perhaps this is why ESRD pts have other medical problems faster than other people (vascular disease, etc...).
....I wish some of ya'll where my patients....someone actually posted that they want MORE time on the machine. Clearly not one of my patients!
However, we think that many of the toxins in renal failure are bigger than urea....this is the "middle molecule" theory. These bigger molecules (...those into the data might have heard of beta2-macroglobulins as a marker of this size stuff), are not so eaisly cleared. These larger compounds are removed in a more linear (or "first order" kinetics) fashion. In other words, this is more TIME dependent. The amount of these middle molecules removed is THE SAME for each hour of dialysis...the first hr is the same as the last hr. The problem is that we don't measure these things.So, just by solely focusing on urea modeling (kt/V for urea), we can miss a whole bunch of stuff....so just because your Kt/V is above goal, maybe cutting your time is not a good idea, because you will have less clearance of larger molecules (but we don't measure this). Over time, perhaps this is why ESRD pts have other medical problems faster than other people (vascular disease, etc...).
If anyone is interested about the next big thing in dialysis, I think it may be Hemodiafiltration (hemodialysis + hemofiltration).It is used in some countries in Europe. Some data is starting to come out, and it seems promising.If anyone is interested, post a reply and i will dive into it.
Is this why 8 hour treatments (nocturnal), six days a week is thought of as one of the better forms of hemodialysis? ... Because it also removes the "middle molecules?"
So, just by solely focusing on urea modeling (kt/V for urea), we can miss a whole bunch of stuff....so just because your Kt/V is above goal, maybe cutting your time is not a good idea, because you will have less clearance of larger molecules (but we don't measure this). Over time, perhaps this is why ESRD pts have other medical problems faster than other people (vascular disease, etc...).
Since Kt/V is, in part, a function of time, what would you suppose is the minimum (Kt/V) per treatment to remove some of those middle molecules? In other words, does it take at least 3 hours of a single treatment to remove a significant amount of the larger molecules?And of course, it also depends on the type of filter that is used.
does kt/V vary by the size of the patient for what the goal should be?? (Sorry if this is a dumb question. I am still learning)
The V in Kt/V is volume of the patient, so the larger the patient, the longer treatment time is necessary (or better filter) to reach the 1.2 Kt/V.