Reasoning around moving to ICD10 and our subset of it

From CCMDB Wiki
Jump to navigation Jump to search

This article explains our choice of ICD10 as a coding schema and of the subset of codes we include.

Why are we moving to a new diagnostic coding schema?

Our old diagnosis list was made in-house designed mostly for the Critical Care setting where our database started out. We are moving to a new diagnosis set primarily to make our data set more comparable to other data sets, and to include more diagnoses that are relevant to Internal Medicine physicians outside of the ICU setting.

Why are we moving to ICD10 rather than a different coding schema?

ICD10 is one of the most widely used diagnosis coding standards. It is the diagnosis coding schema used in all hospitals in Canada, including those in Manitoba. Using the same system as used elsewhere means that diagnoses don't need to be translated to another system, where often a 1-to-1 translation is not possible. It also means that our definitions are more likely to be equivalent to those used by other data sets.

Another benefit of moving to ICD10 will be that it should eliminate diagnoses for which we don't have a code, since ICD10 includes codes for diagnoses that have no specific code.

Why are we including the subset of diagnoses that we do

We are seeing increased interest by Internal Medicine physicians in our data set. Since they fund our program to a large extent, we need to make sure our data includes what they are interested in, in a format that is usable for them.

Why are we including some codes that are not part of ICD10-CA

Non-standard ICD10 Diagnoses lists these and provides reasons.

Why do we not include the entire set of ICD10 codes

The full ICD10 includes over 16000 diagnosis codes. We decided to only use a subset of this to make it easier to learn the new list. Any diagnoses whose codes we omitted can be assigned to the next more general NOS code.

Should we remove some?

Some diagnoses such as Alopecia (nonscarring hair loss), Albinism (albino), disorder of the nails do not initially seem significant enough to code. However, they should be retained so that they can be used as comorbidities, especially for medicine patients. For example, albinism is a condition associated with other genetic abnormalities.

Concerns

Pathogen issues

more general coding

Template:Discussion Just leaving this for now so all can check it; this section can be deleted 2018-04-15 or after.

limit to list?

  • A. set a limit to pathogen list
  • B. We need to be quite specific in our database in order to properly code VAP criteria, CLI etc. I don’t think the pathogen list for bacteria is extensive enough. No mixed option so would need to put in each pathogen separately. Is Dr Kumar OK with this list?
  • SMW


  • Cargo


  • Categories

Template:DiscussAllan

From: Rob Ariano - Subject: RE: VAP organisms 
Sent: Thursday, February 15, 2018 8:32 AM
To: Laura Kolesar, Cc: Trish Ostryzniuk

Hi Laura, Yes, Dr. Allan Garland had asked me about that; but I hadn’t noticed all the missing ones that you have identified below.      I just mentioned that I felt that S.maltophilia should be tracked. 
Looking at your listing below I would now suggest that we also add:
*All Klebsiella - ICD10 reduced to just Klebsiella species
*All Serratia - ICD10, reduced to just species
*All Citrobacter - ICU10, reduced to just Citrobacter species
*All Enterobacter- ICU10, reduced to just Enterobacter species
*All Acinetobacter - ICU10, reduced to just Acinetobacter species
Those are all important Gram-negative rods causing serious pneumonia as seen in the critical care / infectious diseases literature. ESBL’s are an especially important problem with all Klebsiella species, and Amp-C beta-lactamases have been found commonly with the remaining ones listed above.  
I would not list Candida, nor Enterococcus.
Can you let Allan know that I had not noticed these missing? Thanks,Rob
  • Allan agreed we should add these however, we must be careful as the list of pathogen is endless! I do not think we should collect all sub species related to a specific pathogen. For example, we collected Klebsiella oxytoca and pnuemoniae before and any other species was just put under Klebsiella SPP. We will take this to Steering meeting. 18:56, 2018 February 22 (CST)

What exactly are we taking to steering, then, and has it been added to the agenda? Ttenbergen 22:18, 2018 March 20 (CDT)

  • SMW


  • Cargo


  • Categories

Diagnosis issues

Diagnoses without specific codes missing in ICD10

Template:DiscussAllan

Template:DiscussAllan

Template:DiscussAllan

Template:DiscussAllan

Template:DiscussAllan

Diagnoses where it is questionable whether we need them

Please put those right into the offending dxs. That way if we decide to keep them we can put the reason there, and if we decide to remove them we are already there.

APACHE/Charlson in ICD10

Completeness / Do we need to add codes?

Template:DiscussAllan