Reasoning around moving to ICD10 and our subset of it: Difference between revisions

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** What do you mean by that? Ttenbergen 23:08, 2018 March 20 (CDT)
** What do you mean by that? Ttenbergen 23:08, 2018 March 20 (CDT)
{{Discussion}}
{{Discussion}}
*Previous conditions refers to comorbids.  We need to know if all previous conditions that a patient has had in their lifetime (their history) must be documented in the comorbids.  Many conditions are old and irrelevant to the current admission.  What is our guideline here as our comorbid list is much broader now that our original comorbid list. Please clarify.   
*Previous conditions refers to comorbids.  We need to know if all previous conditions that a patient has had in their lifetime (their history) must be documented in the comorbids.  Many conditions are old and irrelevant to the current admission.  What is our guideline here as our comorbid list is much broader now than our original comorbid list. Please clarify.   


* Do we need methamphetamine added?
* Do we need methamphetamine added?

Revision as of 12:21, 2018 April 9

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

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Does ICD10 meet our goals?

  • Goals for our database should be: Data must be easily, efficiently and consistently entered. The data must be readily identifiable to retrieve for statistical purposes. The data must meet the needs of most users of the data.

Do we really compare our data to other data sets

  • What is the rationale for converting to the ICD10 system? Is it so that we can compare data to a universal system? How much is this going to be done and how will this bring value to our database?
  • I want to propose that other alternatives exist. Another idea would be to fix our old system to include the list we already have of codes that are missing...
    • That would not make it any more comparable to other data sets.
  • Have all the people who use the database been given a list of the new codes and examples of the CCI codes to see if this data is sufficient for what they need?

Use of wiki for documentation

  • The idea to look on the wiki when trying to determine the best code is not an efficient system and wifi is not available at all times in all locations.
    • And yet, the wiki is our documentation tool. The kind of detail we have become used to in documentation would be quite impossible to maintain in paper. Also, the number of places without wifi is getting smaller all the time. See Wireless networking. Besides, we have been using the wiki for documentation for almost 10 years, do we really still need to be talking about this or can we finally consider this a decision made? Ttenbergen 22:35, 2018 March 20 (CDT)

Pathogen issues

  • Klebsiella: only have K.pneumoniae, not K. Oxytoca
  • Serratia: no sub categories
  • Candida: no sub categories
  • Enterococcus: no sub categories
  • Corynebacterium species: not in list.
  • 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?

set a limit to pathogen list

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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
*All Serratia
*All Citrobacter
*All Enterobacter
*All Acinetobacter
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


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Diagnosis issues

Template:Discussion

Diagnosis codes missing in ICD10

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coding Medication/therapy non-compliance

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  • Medication/therapy non-compliance...I see the need for some reflection of this issue in a diagnostic code as I have frequent admission/ re-admissions for non-compliance with medications and/or therapies especially dialysis.--Llemoine 14:31, 2018 February 22 (CST)
  • Septic Emboli: no specific code even though it is a very significant problems with endocarditis patients which can cause widespread clotting to any blood vessels which causes strokes, ischemia to many organs, etc.
  • Vasculitis: only options are limited to skin, NOS or necrotizing vasculopthy/vasculitis NOS
  • Intra-abdominal abscess: only options are intestine, anus, liver, peritonitis. No pancreatic abscess (do have pancreatitis and pseudocyst).
  • Cardiac arrest - Does not differentiate between witnessed or unwitnessed arrest.

APACHE/Charlson in ICD10

Completeness / Do we need to add codes?

  • Are all previous conditions being put in this list? If so, this is a significant increase in numbers of codes required.
    • What do you mean by that? Ttenbergen 23:08, 2018 March 20 (CDT)

Template:Discussion

  • Previous conditions refers to comorbids. We need to know if all previous conditions that a patient has had in their lifetime (their history) must be documented in the comorbids. Many conditions are old and irrelevant to the current admission. What is our guideline here as our comorbid list is much broader now than our original comorbid list. Please clarify.
  • Do we need methamphetamine added?
  • ( I recently had this on one of my patients and I ended up using psychoactive substance NOS, chronic abuse/dependence/addiction. When I googled meth, it came up as a psychoactive drug.)--LKolesar 11:52, 2018 February 13 (CST)