1A? No way. KDOQI has lost its way

It started with a tweet. It always does.

Daniel Coyne is one of my heroes in nephrology. Starting in fellowship and for the first decade of being a nephrologist, I was suckered into the normalization of hemoglobin delusion. The idea that we could heal our patients’ hearts by treating the ubiquitous anemia of CKD was seductive. The theory made sense. The retrospective data looked amazing. Many really smart nephrologists promoted the idea. Living through the medical reversal of CHOIR, CREATE, and finally TREAT was both academically traumatic and a profoundly formative moment in my career. One of the major components of the CKD-anemia delusion was the role that KDOQI played in promoting the high hemoglobin targets before the clinical data showed the folly of this strategy. Dr. Coyne is one of the first nephrologists to ring the warning bells. We highlighted his story in NephMadness 2016. So when Dr. Coyne criticized the nutrition guideline my ears were perked.

The thread highlighted above is convincing and I amplified it.

Subsequently,` I received a polite email from one of the guideline authors suggesting I may have gone too far in criticizing the guideline. Time to put up or shut up. Here are my thoughts, at longer than tweet-length, regarding the protein restriction guideline. Much of this comes from Dr Coyne’s thread, so read that first, so you know where the smart stuff comes from.

Guidelines should only express certainty when there is certainty. When guidelines flip-flop with each new edition doctors lose credibility while taking care of patients. Consistency is important. Because of this I want guidelines to be late adopters rather than on the cutting edge, and for guidelines to be humble about the frailties of human knowledge. 

This puts me in opposition to many guidelines but this 1A guideline on low protein diet seems particularly egregious. The guideline I’m focused on is:

The Detailed Justification of this guideline provides this guidance

Research reports a beneficial effect of protein restriction (0.55-0.6 g/kg per day) on ESKD/death in adults with CKD. In adults with CKD, 5 RCTs reported findings on the effect of protein restriction on survival/deaths. Three studies clearly indicated a beneficial effect of moderate restriction in dietary protein on the development of ESKD/death.153,164,168


So there are 5 RCT that looked at protein restriction for the development of ESRD/Death. Of these 5 studies (of which I could only find 4), 3 were positive, but one of them, Locatelli, is only positive if you consider a P value of 0.06 as significant.

It is so strange to see this reported as a positive trial, because when I would answer questions about low protein diets for my patients with relatively early kidney disease, I would say, this has been looked at in a number of studies but there were two big studies, one in Italy (this one) and one in the US (MDRD) and neither were able to show improvement in outcomes. But here, I guess, this is good enough to qualify for “clearly indicated a beneficial effect.”

The second reference is a small 82 person study by Henrik Hansen. I find this troubling because even though the KDOQI guideline specifically excludes people with diabetes, Hansen restricted enrollment to patients with diabetic nephropathy.

The last of the triplets is Rosman. I could not find Reference 168. This sounds like a study that was presented at a conference, Proceedings of the European Dialysis and Transplant Associations, European Renal Association 1985. Here is the pubmed listing. The abstract is pretty thin. I am particularly concerned because a later publication that seems to be long-term follow-up this cohort (no I don’t know how they picked up an additional 50 patients) and it spins a different tale. The title says it all:

I also highlighted a concerning line from the abstract, “The diet appeared to have a selective effect on the progression rate of renal failure: only patients with primary glomerular disease responded to the diet.” If this is the case this is something that should have given pause to the authors trying to generalize this recommendation for all people without diabetes and CKD 3-5 not on dialysis.

The three “positive” trials were published in 1991, 2002, and 1989. This means the cohorts were pre-ACEi/ARB. In fact, Locatelli’s study actively discouraged the use of ACEi.

Lastly, of the two negative trials (of the five that looked at ESRD/death) the authors brush off Cianciaruso for being, “a relatively small sample size.” Let’s take a look at the trials.

Cianciaruso had an N of 423, twice the size of Rosman’s study and five times the size of Hansen’s. The only study in the group of 5 larger was Locatelli with 456. Relatively small sample size? Come on.
We are currently in the midst of a revolution in evidence based nephrology with the data emerging about the effects of SGLT2i. One of the compelling findings with each subsequent blockbuster study is how consistent the data is regardless of how the outcome is assessed:

  • Change in GFR? Yup, the SGLT2i is better
  • Change in GFR slope? Check, SGLT2i again
  • Fraction of patients that reach death or dialysis? SGLT2i still got you covered.

This is not the case for this guideline. The authors trumpet guideline 3.0.1 claiming a reduction in need for dialysis, but this benefit appears to be fragile because if instead we look at low protein diets (LPD) through the lens of the change in GFR, the data no longer points to a benefit. From the guideline:

This mismatch between the 1A conclusions about development of ESRD or death and the lack of biologic plausibility that one can prevent ESRD without preventing loss of GFR should be addressed in the guideline mentioned and probably should have forced the guideline committee to rethink the 1A grade they awarded to protein restriction. 

Coyne’s first tweet was in response to this

Dr Fouque expresses outrage that someone would question the safety of low protein diets. Well safety is a concern. As I wrote on this blog (see this and the follow up here). These posts are regarding long term follow-up of the MDRD cohort. MDRD is famous for not showing any difference in ESRD or death with either a low or very low protein diet, the long term follow up revealed that among people that did progress to dialysis, the patients randomized to the very low protein had nearly a two times higher risk of death (HR 1.92). So Dr. Fouque, with all due respect, I do think it is quite reasonable to question the risks of a low protein diet.

Dr. Fouque comment also highlights what is so dangerous about the 1A grade for protein restriction, it says this is settled science, we no longer need to investigate this. A 1A guideline insulates protein restriction from questions that need to be asked. This is not settled science. Not even close.

When the KDIGO Diabetic Kidney Disease Guidelines were published a lot of people went nuts over the fact that ACEi did not warrant a 1A recommendation.

If you find this curious, I advise you to listen to Freely Filtered #27 where Ian de Boer describes the logic for that 1B grade. Whether or not you find that admirable or absurd it is clear that the authors of the diabetic kidney disease guideline respect a score of 1A. They hold it in reverence and reserve it for only the most rigorous evidence. This argument came from the mind of Nayan Arora:

I can’t find the same respect for grading the evidence in the KDOQI nutrition guidelines.

The agony and ecstasy of of secondary hyperparathyroidism

Managing secondary hyperparathyroidism in dialysis patients should be a rewarding aspect of nephrology. I thrive on complex management that involves balancing various numbers with clever treatment strategies. It is exactly what I find so exhilarating about a juicy electrolyte case in the ICU.

The principle variables in secondary hyperparathyroidism are:

  • PTH
  • Phosphorous
  • Calcium
And I use one additional lab that is generally ignored in the guidelines, alkaline phosphatase.
To bend these numbers we have a variety of tools with interesting effects, mechanisms of action and side-effects. The principle therapeutics:
  • low phosphorous diet
  • calcium containing binders
  • non-calcium binders
  • calcitriol
  • paricalcitol and doxercalciferol
  • cinacalcet
And additional therapeutics that can be brought to bear in difficult cases or in unusual circumstances
  • dialysate calcium concentration
  • parathyroidectomy

And K/DOQI provided cleanly laid out treatment goals:

  • PTH 150-300
  • Caclium 8.4-9.5
  • Phosphorous 3.5-5.5
  • Calcium x phosphorous product < 55
Patients that achieve those targets have a lower mortality risk than patients that miss these targets:

The numbers (0 of 3, 1 of 3, etc) refer to the number of months a patient is at the K/DOQI target in the quarter, PTH was measured only once a quarter

The problem is that no one has performed a prospective randomized controlled trial showing these targets improve outcomes. We want to believe that the retrospective data showing a survival advantage with cinacalcet and paricalcitol are real and that the observational data showing better calcium and phosphorous (and to a smaller degree, PTH) results in better patient outcomes.

Teng et al. Survival of patients undergoing hemodialysis with paricalcitol or calcitriol therapy. N Engl J Med (2003) vol. 349 (5) pp. 446-56

Block et al. Mineral metabolism, mortality, and morbidity in maintenance hemodialysis. J Am Soc Nephrol (2004) vol. 15 (8) pp. 2208-18
But given nephrology’s previous relationships with retrospective data (see anemia, Kt/V, and statins, and homocysteine) I can’t accept that data. I can’t take these treatment goals seriously. I appreciate that the fresh KDIGO guidelines readily admit that the emperor has no clothes and that the best they can recommend is to generally keep the calcium and phosphorous close to normal (evidence level 2D) and the PTH anywhere from 150 to 600 (evidence level 2c) or roughly wherever the hell you want it.

I love this figure from KDIGO, essentially once the PTH rises over 150 it provides no information. PTH > 300 has a positive predictive value of only 65% for high turnover disease. And don’t miss the laughably small numbers. We are basing global guidelines off of a study of less than 100 patients. From Barreto and Barreto.

It is shameful that Abbott has not done an RCT with survival as an endpoint on Zemplar or Calcijex. They have had 20+ years to do this. Both of the other players in CKD-MBD have taken a chance at building RCT data to support there products:

  • Genzyme took a poke with DCOR (RCT of sevelamer versus calcium based binders) 
  • Amgen is in the final countdown of EVOLVE (RCT of sensipar + usual care vs usual care)
Abbott the oldest player is sitting on the sidelines.
The lack of data, the lack of clarity, and the reliance on observational data muddles the issue enough that I don’t enjoy taking care of secondary hyperparathyroidism. But recently I had a great case, a situation where treating secondary hyperparathyroidism did more than loaded the dice in my patients favor but actually really made a difference.
I have a young dialysis patient who suffers from a horrific trauma a number of years ago. As a result he has profound chronic pain. Much of the pain is back pain but he also complained of diffuse body aches. Earlier this year his PTHs were consistently over a thousand with some over two thousand.
We added 90 mg of cinacalcet daily and the the PTH plummeted to goal. This was in a patient who had not responded to doxercalciferol 10 mcg three times a week. It was nice to see the PTH come down but what made this case standout was that his body aches melted away. We had been sending him to pain clinics and switching narcotics trying to get his pain tolerable and all of a sudden, done. Pain dramatically improved with a log reduction in PTH. 
Sometimes I get so carried away worrying about total mortality that I forget about the direct toxicity of high PTH. 

KDIGO


bill goodman talking on KDIGO. Goodman wrote the article that interested me in the topic of vascular calcification and binder choice.

What is KDIGO
Kidney Disease Improving Global Outcomes
established in 2003

Independent non-profit, established by the NKF
The concept was to take K/DOQI and generalize the guidelines for a global audience.

The KDIGO mission is to provide:

  • Clinical Practice Guidelines
  • Guideline database
  • Work groups
  • Controversy conferences
  • Mineral and bone inititative (in draft)
  • Hepatitis C in kidney disease (coming)
  • Care of transplant patient (coming)
  • Acute kidney disease (coming)

CKD Mineral and Bone Disease
A rose from the perception that international perspective needed to define renal osteodystrophy

use the phrase ROD exclusively to define: alterations in bone morphology in patients with CKD
classification based on bone histology, bone turnover, mineralization and volume.

CKD-MBD is a systemic disorder of mineral and bone metabolism due to ckd manifested by either one or a combination of the following:

  • abnormalities of Ca, Phos, PTH, Vitamin D
  • abnormal bone turnover, mineralization, volume, linear growth or strength
  • vascular or soft tissue calcification

KDIGO revisited the concept of guidelines
They graded evidence and created their guidelines by limitting the data to:

  • RCT of at least six months in duration
  • N>50 excepts for pediatrics and bone biopsy
  • Intermediate endpoints including: BMD, bone biopsy, vascular calcification and biochemical endpoints are not considered unless they have been validated prospectively [unclear if any surrogates have been validated]
  • Observational studies acceptable if a clinical outcome examined conducted with a high methodological quality and had a relative risk of >2.0 or <0.5

treatment of CKD-MBD

  • lowering high phos
  • abnormal PTH levels in CKD-MBD
  • treatment of bone and bisphosphonates, other osteoporosis medication and growth hormone
  • evaluation and treatment of kidney transplant bone disease

there is little evidence to provide guidance for a specific therapeutic target range for any biochemical parameter

  • extreme values are associated with greater mortality risk
  • little evidence to support preferred treatments

KDIGO concluded that PTH guidelines are mainly opinion based and not informed by randomized clinical trials

150-300 is based on evidence just not rct and outdated

phos and calcium guidelines are loose

repeated emphasis through out document on the lack of evidence from RCT with hard outcomes

Data Gaps

Evolve is really important, largest prospective clinical trial on dialysis population