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The 2015 KDOQI Hemodialysis Adequacy Guideline Update—What’s New

The 2015 Hemodialysis Adequacy Guideline Update from KDOQI is the next iteration of guidelines from the 2006 report. The document covers a number of important topics to guide clinicians in the management of patients with kidney disease. These include:

It is accompanied by a systematic review by Slinin et al entitled, “Timing of Dialysis Initiation, Duration and Frequency of Hemodialysis Sessions, and Membrane Flux: A Systematic Review for a KDOQI Clinical Practice Guideline.” Let’s take a look at each of these issues and review what the guidelines state.

The guidelines are graded for strength of recommendation as either

Level 1: Strong Recommendation (We Recommend)
Level 2: Conditional Recommendation/Suggestion (We Suggest)

Furthermore, the quality of evidence is graded from

A: High quality of evidence
B: Moderate quality of evidence
C: Low quality of evidence
D: Very low quality of evidence

Each of these 5 guidelines are summarized in Box 2.

1. Timing of Hemodialysis Initiation

2. Frequent and Long Duration Hemodialysis (note: not in 2006 guideline)

In-center Frequent HD

Home Long HD

 Pregnancy

3. Measurement of Dialysis: Urea Kinetics

4. Volume and Blood Pressure Control: Treatment Time and Ultrafiltration Rate

– Consider longer session or extra session if large weight gains, high BP, high UF rates, metabolic complications, or inability to achieve dry weight. No change from 2006. No grade given for this.

– Prescribe a UF rate balancing risk of hemodynamic instability with benefit of volume removal. No change from 2006. No grade given for this.

5. New Hemodialysis Membranes for HD

Overall, the 2015 HD Adequacy Guideline is move streamlined than the 2006 version, and covers topics such as frequent in-center, home HD, and pregnancy. These topics didn’t get much attention in 2006, and reflect a shift in practice. However, the literature review only rose to the level of garnering a “suggest” for frequent in-center and “no grade given” to home HD from the work group. However, it does represent a shift. Hopefully more research will emerge on these topics to bolster the guidelines. The other major change is the removal of an eGFR cutoff suggestion for initiating RRT, focusing more on signs and symptoms, a result of data from the IDEAL trial demonstrating no clinical benefit from the earlier initiation of HD. Overall, the document provides a comprehensive review of the topic but it is sobering to realize how little evidence we truly have.

Matthew Sparks, MD
AJKD Blog Advisory Board member

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