Template:ICD10 Guideline KDIGO Guidelines for Acute Renal Failure: Difference between revisions

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</noinclude>=== KDIGO Guidelines for Acute Kidney Injury (AKI) ===
</noinclude>=== KDIGO Guidelines for Acute Kidney Injury (AKI) ===
*Starting January 1, 2019 when we began using ICD10 for diagnosis coding and CCI for procedure coding, we shifted to using the KDIGO criteria for defining Acute Kidney Injury -- which also goes by the names AKI, Acute Renal Failure and Acute Renal Insufficiency
*We use the KDIGO criteria for defining Acute Kidney Injury (aka AKI, Acute Renal Failure and Acute Renal Insufficiency) (starting January 1, 2019)
*The main thing here is identifying that the observed problem with kidney function is acute, rather than chronic --- and THIS is the reason that identifying AKI requires trying to find a past/baseline value of serum creatinine
*The main thing here is identifying that the observed problem with kidney function is acute, rather than chronic - and THIS is the reason that identifying AKI requires trying to find a past/baseline value of serum creatinine
*The KDIGO guidelines delineate several different "levels/degrees" of AKI.  You'll note that (at its lowest level) AKI is present even with pretty small rises in serum creatinine.  While one MIGHT think that such small rises are inconsequential, indeed they are not.  As indicated in the paper [https://doi.org/10.1164/rccm.201311-2097OC  "Small Acute Increases in Serum Creatinine Are Associated with Decreased Long-Term Survival in the Critically Ill"], even rises in creatinine of 27 mcg/L in ICU patients are associated with higher rates of death.  Thus in this new schema we are not ''overcounting'' those with significant AKI, but before we probably were ''undercounting'' them.
*The KDIGO guidelines delineate several different "levels/degrees" of AKI.  You'll note that (at its lowest level) AKI is present even with pretty small rises in serum creatinine.  While one MIGHT think that such small rises are inconsequential, indeed they are not.  As indicated in the paper [https://doi.org/10.1164/rccm.201311-2097OC  "Small Acute Increases in Serum Creatinine Are Associated with Decreased Long-Term Survival in the Critically Ill"], even rises in creatinine of 27 mcg/L in ICU patients are associated with higher rates of death.  Thus in this new schema we are not ''overcounting'' those with significant AKI, but before we probably were ''undercounting'' them.
*These criteria will apply everywhere we need to identify ARF/AKI -- including:
*These criteria will apply everywhere we need to identify ARF/AKI -- including:
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**[[Kidney, acute tubular necrosis (ATN)]]
**[[Kidney, acute tubular necrosis (ATN)]]
**[[Kidney, acute renal failure, postprocedural]]
**[[Kidney, acute renal failure, postprocedural]]
*But NOT for [[Kidney, renal failure/insufficiency/uremia, unspecified as acute or chronic]] -- since as stated this code is for kidney failure or insufficiency when you don't know whether it's acute or chronic.
*But NOT for [[Kidney, renal failure/insufficiency/uremia, unspecified as acute or chronic]] - since as stated this code is for kidney failure or insufficiency when you don't know whether it's acute or chronic.


*In order to reduce the workload for identifying ARF/AKI, we will implement a first stage screening process to try and filter out the majority of people, who will NOT have AKI/ARF.
*In order to reduce the workload for identifying ARF/AKI, we will implement a first stage screening process to try and filter out the majority of people, who will NOT have AKI/ARF.
**We expect that this screening will misclassify a few people who do have AKI as not having it, but we also expect that most of those who are missed will continue to experience declining renal function and their AKI/ARF will be identified in the following days.
**We expect that this screening will misclassify a few people who ''do'' have AKI as not having it, but we also expect that most of those who are missed will continue to experience declining renal function and their AKI/ARF will be identified in the following days.


==== First stage - screening ====
==== First stage - screening ====

Revision as of 16:20, 2020 January 31

This template contains the KDIGO guideline definition so it can be applied consistently everywhere it is used.

To use:

{{ICD10 Guideline KDIGO Guidelines for Acute Renal Failure}}

KDIGO Guidelines for Acute Kidney Injury (AKI)

  • In order to reduce the workload for identifying ARF/AKI, we will implement a first stage screening process to try and filter out the majority of people, who will NOT have AKI/ARF.
    • We expect that this screening will misclassify a few people who do have AKI as not having it, but we also expect that most of those who are missed will continue to experience declining renal function and their AKI/ARF will be identified in the following days.

First stage - screening

Second stage - Full assessment

  • Acute Kidney Injury (AKI) is present if ANY ONE OR MORE of the following are true (these are the KDIGO guidelines):
  • (a) Urine output < 0.5 mL/kg/hour for 6 hours
    • so, obviously, you can't make this determination until there has been at least 6 hours of observation of urine output
    • also you need a weight -- if there isn't one already measured you have the following options: Wait for one to be done; Ask the nurse to do one; Do your best to estimate the weight, remembering that if the person appears to be of average size, then you could use default values based on average values in the Canadian population, i.e. 85 kg for men and 70 kg for women
  • (b) Increase in serum creatinine by 27 micromoles/L or more within 48 hours
    • so, while this may happen quickly and thus this criterion be met before 48 hrs, you cannot make a full determination that it is NOT true until you have at least 2 serum creatinine values separated by at least 48 hours
    • in the case that the creatinine rises by >27, say in the first 12 hours, but then declines back down so that at the end of 48 hrs the net rise is <27, THEN THIS DOES QUALIFY AS AKI
  • (c) Increase in serum creatinine to 1.5 times baseline or more within the last 7 days
    • this criterion is important because since many people have some degree of CHRONIC renal insufficiency or failure, a solitary serum creatinine can't tell you if the high value is acute or chronic
    • thus, to evaluate this criterion, seek a serum creatinine value at least 7 days old -- use whatever is the most recent value more than 7 days old that is available, even if it's years old
    • if there ARE NO values >7 days old, then you can use the sex-specific normal value as follows:
      • Men: 100 micromoles/L
      • Women: 85 micromoles/L