Template:ICD10 Guideline Sepsis: Difference between revisions

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*As of January 2019, we are still using the SEPSIS-2 approach to diagnosis.  We may or may not switch over to the SEPSIS-3 definition.  SEPSIS-2 delineates 3 subtypes of sepsis:
**[[Sepsis (SIRS due to infection, without acute organ failure)]] -- defined as SIRS due to a known or presumed infection but NOT satisfying criteria for severe sepsis or septic shock (see SIRS critera, below)
**[[Severe sepsis]] -- defined as sepsis PLUS one or more acute organ failures
**[[Shock, septic]] -- defined as severe sepsis where an acute organ failure is the cardiovascular system (see criteria below)
*Note that an individual during a single episode of illness can evolve over time from a less advanced to a more advanced subtype of sepsis --- and as this occurs, make sure to code the more advanced subtypes as they occur
**e.g. admitted on Monday with '''[[Severe sepsis]]''' which is coded, but by Tuesday has progressed to '''[[Shock, septic]]''' which should then be added to the codes, in this case as an [[Acquired Diagnosis]].
**however, as a person improves there is NO NEED to "downcode" their sepsis


=== Identifying the Acute Organ Failure of Severe Sepsis ===
=== General Information ===
*There are many different scoring systems for this:  SOFA, LOD, MODS, Brussels score, others
*As of June 2024 we have modified our approach for identifying sepsis and related entities.  Prior to this we were using Sepsis-2 definitions, which depended on identifying SIRS (Systemic Inflammatory Response Syndrome). Instead, we are changing to the CDC Adult Sepsis Episode (ASE) criteria.
**They're all problematic for various reasons, but the biggest problem with them is the inability to distinguish acute vs. chronic organ dysfunction -- which is why the SEPSIS-3 definition uses the acute CHANGE in the SOFA score, not the score itselfHowever, while that makes sense, it's also VERY difficult to do, since we rarely know all the information needed to do the pre-sickness SOFA score.
*ASE defines two entities, which we will call [[Severe sepsis]], and [[Shock, septic]].  We are omitting what has been called "Sepsis", defined as SIRS due to infection.
*So, for our purposes we will be using the Brussels score:
**The terminology can be confusing. Since Sepsis-3 (which we are NOT using herein), what used to be called "Severe sepsis" is now just called "Sepsis"But in order to avoid confusion, and be consistent within ICD-10, we will use:
**Consider a patient to have severe sepsis if they meet criteria for sepsis AND have any one of the following 6 criteria:
***[[Severe sepsis]] = acute organ dysfunction due to proven or presumed infection
***Systolic BP <90 and iv fluids alone are not sufficient (e.g. on any vasoactive agents) ............AND THIS IS NOT KNOWN TO BE CHRONIC
***[[Shock, septic]] = severe sepsis which includes cardiovascular dysfunction (as defined by either elevated serum lactate, or use of iv vasopressors)
***PaO2/FIO2 ratio <300............AND THIS IS NOT KNOWN TO BE CHRONIC
 
***GCS<13.................................AND THIS IS NOT KNOWN TO BE CHRONIC
 
***Platelet count <80..................AND THIS IS NOT KNOWN TO BE CHRONIC
=== Identifying the Acute Organ Failure of [[Severe sepsis]] and [[Shock, septic]] ===
***Serum creatinine >180..........AND THIS IS NOT KNOWN TO BE CHRONIC
*As part of the June 2024 change from Sepsis-2 to ASE criteria for sepsis-related entities, our criteria for acute organ dysfunction are any of the 6 ASE criteria:
***Total bilirubin >34..................AND THIS IS NOT KNOWN TO BE CHRONIC
**(1) Serum lactate >=2.0 mmol/L
**(2) Use of any of the following vasopressors:  norepi, dopamine, epinephrine, phenylephrine or vasopressin
**(3) Use of invasive mechanical ventilation -- noninvasive ventilation does not count
**(4) Doubling of serum creatinine relative to baseline
***"baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization
***this criterion does not apply if the person had end-stage renal disease prior to hospitalization, i.e. chronically
**(5)Total bilirubin >=34.2 ''AND'' at least a doubling from baseline
***"baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization
**(6) Platelet count <100 ''AND'' >=50% fall from the baseline value
***"baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization


=== Identifying the organism responsible ===
=== Identifying the organism responsible ===
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*The rule now is that you make all efforts to identify the specific organism, even if blood cultures never grow anything
*The rule now is that you make all efforts to identify the specific organism, even if blood cultures never grow anything
*At the same time, however, if the person IS bacteremic, then you must ALSO code the '''[[Bacteremia]]''' -- see that article for information on whether or not to link the bacteremia code to others.
*At the same time, however, if the person IS bacteremic, then you must ALSO code the '''[[Bacteremia]]''' -- see that article for information on whether or not to link the bacteremia code to others.
*In the presence of bacteremia or fungemia, with or without other infection(s) (e.g. pneumonia) ALL showing the same bug, consider that bug to be the agent for the sepsis
*Without bacteremia or fungemia, with one or more other infections occurring around the same time that all have the same bug, consider that bug to be the agent for the sepsis
*With multiple infections occurring around the same time as the sepsis, having DIFFERENT bugs, the bug responsible for the sepsis is not clear (even if one of those infections is bacteremia it’s still not clear), so in this case choose [[Infectious organism, unknown]].
{{Ex|
{{Ex|
*e.g. Patient has severe sepsis with the acute organ failure being acute renal failure due to ATN --- and it's felt to be due to a pseudomonas pneumonia.  So in this case the pseudomonas is the bug that should be combined with the severe sepsis (and with with the pneumonia, of course)
*e.g. Patient has [[Severe sepsis]] with the acute organ failure being acute renal failure due to ATN --- and it's felt to be due to a pseudomonas pneumonia.  So in this case the pseudomonas is the bug that should be combined with the [[Severe sepsis]] (and with with the pneumonia, of course)
**e.g. Patient with septic shock has an E.coli UTI and a pseudomonas pneumonia.  The team is not certain which of those two bacteria is causing the septic shock, but of course is treating them both.  In this case the bug is known to be a bacterium, but not clear which, so the bug to combine with the Septic shock is [[Bacteria, NOS]] }}
**e.g. Patient with septic shock has an E.coli UTI and a pseudomonas pneumonia.  The team is not certain which of those two bacteria is causing the septic shock, but of course is treating them both.  In this case the bug is known to be a bacterium, but not clear which, so the bug to combine with the Septic shock is [[Bacteria, NOS]] }}


=== Combining a sepsis code with a specific infection code ===  
=== Combining a sepsis code with a specific infection code ===  
*Guidelines for such combination to include (this is a new rule, changed Feb 19, 2020):
*Guidelines for such combination to include (this changed Feb 19, 2020, prior rule was to not combine sepsis codes with any specific infection):
**Combine if it is reasonably clear that the specific infection is the source of the sepsis episode.  But if it is NOT clear then do not combine.
**Combine if it is reasonably clear that the specific infection is the source of the sepsis episode.  But if it is NOT clear then do not combine.
***Clear example, so DO combine:  Sepsis and the only evident infection is pneumonia
***Clear example, so DO combine:  Sepsis and the only evident infection is pneumonia
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***Clear example, so DO combine.  Sepsis with pneumonia developing around the same time, and then 5 days later a UTI occurs.  Here it’s appropriate to combine the sepsis + pneumonia but not with the UTI.
***Clear example, so DO combine.  Sepsis with pneumonia developing around the same time, and then 5 days later a UTI occurs.  Here it’s appropriate to combine the sepsis + pneumonia but not with the UTI.
***Clear example, so DO combine:  Sepsis with pneumonia and bacteremia, with the same bug isolated from the lungs and blood.  Here it’s reasonable to conclude that all 3 are causally related and combine all 3, with the same bug as cause in all 3.
***Clear example, so DO combine:  Sepsis with pneumonia and bacteremia, with the same bug isolated from the lungs and blood.  Here it’s reasonable to conclude that all 3 are causally related and combine all 3, with the same bug as cause in all 3.
*Regarding identifying the bug responsible for sepsis -- this also can be unclear, here is some guidance:
**In the presence of bacteremia, with or without other  infection(s) (e.g. pneumonia) ALL showing the same bug, consider that bug to be the agent for the sepsis
**Without bacteremia, with one or more other infections occurring around the same time that all have the same bug, consider that bug to be the agent for the sepsis
**With multiple infections occurring around the same time as the sepsis, having DIFFERENT bugs, the bug responsible for the sepsis is not clear (even if one of those infections is bacteremia it’s still not clear), so in this case choose [[Infectious organism, unknown]].  Allan has added to that Wiki page to clarify this.
=== Criteria for SIRS ===
*SIRS is defined as 2 or more of the following things:
**Fever of more than 38°C (100.4°F) or less than 36°C (96.8°F)
**Heart rate of more than 90 beats per minute
**Respiratory rate of more than 20 breaths per minute or arterial carbon dioxide tension (PaCO 2) of less than 32 mm Hg
**Abnormal white blood cell count (>12,000/µL or <4,000/µL or >10% immature [band] forms)
===Criteria for the SHOCK in Septic Shock===
*Persisting hypotension requiring vasopressors to maintain MAP>65mmHg ''AND'' serum lactate>2 mmol/L -- both despite adequate volume resuscitation.
*The CAUSE is proven infection OR '''presumed''' infection -- thus positive cultures are not required.
{{Ex | if someone has another obvious cause of shock (e.g. massive hemorrhage) and ''also'' has infection, that does not mean it is combined hemorrhagic and septic shock. Basically, septic shock '''should not be called''' if there '''is another obvious cause for shock'''.}}
*Also recognize that not all vasodilatory (aka distributive) shock is due to infection.  When it is due to infection then use THIS code, when it's not due to infection, then use one of the other appropriate codes, such as:  '''[[Anaphylactic reaction (anaphylaxis)]]''', or '''[[Shock, NOS]]'''
*Also recognize that not all vasodilatory (aka distributive) shock is due to infection.  When it is due to infection then use THIS code, when it's not due to infection, then use one of the other appropriate codes, such as:  '''[[Anaphylactic reaction (anaphylaxis)]]''', or '''[[Shock, NOS]]'''


{{Collapsable
=== When to code an [[Admit Diagnosis]] vs [[Acquired Diagnosis]] ===
| always=background about 2016 sepsis consensus
*There are sometimes subtle issues here, especially for diagnoses that use lab test results. 
| full=*Even though as of November 2017 ICD-10 has not yet been modified to reflect it, we are using the 2016 consensus definition of sepsis and septic shock (JAMA 315(8):801-10, 2016). These new definitions completely do away with talking about the Systemic Inflammatory Response Syndrome (SIRS). }}
*An example is patient comes in to ED with shock presumed due to pneumonia and a lactate=1.7 --> this doesn't meet the requirement for [[Shock, septic]], but by 3 hours later the next lactate checked in the ICU is 2.7, so that threshold for septic shock IS met.  Clearly this person was "brewing" septic shock at admission and it seems logical to include that diagnosis as an admit diagnosis.  THUS -- in such cases where it seems pretty clear, in retrospect, that a diagnosis was brewing/present at admission but only became fully evident after admission, that diagnosis SHOULD be coded as an [[Admit Diagnosis]] IF it becomes fully evident within 6 hours of admission.
*Note that an individual during a single episode of illness can evolve over time from [[Severe sepsis]] to [[Shock, septic]] -- if this occurs, make sure to also code the more advanced subtype
**e.g. admitted on Monday with '''[[Severe sepsis]]''' which is coded, but by Tuesday has progressed to '''[[Shock, septic]]''' which should then be added to the codes, in this case as an [[Acquired Diagnosis]].
**however, as a person improves there is NO NEED to "downcode" their sepsis

Latest revision as of 09:06, 2024 June 13

This template info about coding sepsis to keep it consistent across pages.

To use:

{{ICD10 Guideline Sepsis}}


General Information

  • As of June 2024 we have modified our approach for identifying sepsis and related entities. Prior to this we were using Sepsis-2 definitions, which depended on identifying SIRS (Systemic Inflammatory Response Syndrome). Instead, we are changing to the CDC Adult Sepsis Episode (ASE) criteria.
  • ASE defines two entities, which we will call Severe sepsis, and Shock, septic. We are omitting what has been called "Sepsis", defined as SIRS due to infection.
    • The terminology can be confusing. Since Sepsis-3 (which we are NOT using herein), what used to be called "Severe sepsis" is now just called "Sepsis". But in order to avoid confusion, and be consistent within ICD-10, we will use:
      • Severe sepsis = acute organ dysfunction due to proven or presumed infection
      • Shock, septic = severe sepsis which includes cardiovascular dysfunction (as defined by either elevated serum lactate, or use of iv vasopressors)


Identifying the Acute Organ Failure of Severe sepsis and Shock, septic

  • As part of the June 2024 change from Sepsis-2 to ASE criteria for sepsis-related entities, our criteria for acute organ dysfunction are any of the 6 ASE criteria:
    • (1) Serum lactate >=2.0 mmol/L
    • (2) Use of any of the following vasopressors: norepi, dopamine, epinephrine, phenylephrine or vasopressin
    • (3) Use of invasive mechanical ventilation -- noninvasive ventilation does not count
    • (4) Doubling of serum creatinine relative to baseline
      • "baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization
      • this criterion does not apply if the person had end-stage renal disease prior to hospitalization, i.e. chronically
    • (5)Total bilirubin >=34.2 AND at least a doubling from baseline
      • "baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization
    • (6) Platelet count <100 AND >=50% fall from the baseline value
      • "baseline" can be a value prior to hospitalization, or if that's not available, use the BEST value from the entire current hospitalization

Identifying the organism responsible

  • Until Jan 2019, the rule was that you only identify the responsible organism if it was present in blood culture. THIS RULE HAS CHANGED AS OF 1/1/2019 -- because in fact the majority of even septic shock cases never grow anything from the blood and most derive from localized infections (pneumonia, UTI, etc)
  • The rule now is that you make all efforts to identify the specific organism, even if blood cultures never grow anything
  • At the same time, however, if the person IS bacteremic, then you must ALSO code the Bacteremia -- see that article for information on whether or not to link the bacteremia code to others.
  • In the presence of bacteremia or fungemia, with or without other infection(s) (e.g. pneumonia) ALL showing the same bug, consider that bug to be the agent for the sepsis
  • Without bacteremia or fungemia, with one or more other infections occurring around the same time that all have the same bug, consider that bug to be the agent for the sepsis
  • With multiple infections occurring around the same time as the sepsis, having DIFFERENT bugs, the bug responsible for the sepsis is not clear (even if one of those infections is bacteremia it’s still not clear), so in this case choose Infectious organism, unknown.
Example:   
  • e.g. Patient has Severe sepsis with the acute organ failure being acute renal failure due to ATN --- and it's felt to be due to a pseudomonas pneumonia. So in this case the pseudomonas is the bug that should be combined with the Severe sepsis (and with with the pneumonia, of course)
    • e.g. Patient with septic shock has an E.coli UTI and a pseudomonas pneumonia. The team is not certain which of those two bacteria is causing the septic shock, but of course is treating them both. In this case the bug is known to be a bacterium, but not clear which, so the bug to combine with the Septic shock is Bacteria, NOS

Combining a sepsis code with a specific infection code

  • Guidelines for such combination to include (this changed Feb 19, 2020, prior rule was to not combine sepsis codes with any specific infection):
    • Combine if it is reasonably clear that the specific infection is the source of the sepsis episode. But if it is NOT clear then do not combine.
      • Clear example, so DO combine: Sepsis and the only evident infection is pneumonia
      • Unclear example, so do NOT combine: Sepsis with both pneumonia and a UTI.
      • Clear example, so DO combine. Sepsis with pneumonia developing around the same time, and then 5 days later a UTI occurs. Here it’s appropriate to combine the sepsis + pneumonia but not with the UTI.
      • Clear example, so DO combine: Sepsis with pneumonia and bacteremia, with the same bug isolated from the lungs and blood. Here it’s reasonable to conclude that all 3 are causally related and combine all 3, with the same bug as cause in all 3.
  • Also recognize that not all vasodilatory (aka distributive) shock is due to infection. When it is due to infection then use THIS code, when it's not due to infection, then use one of the other appropriate codes, such as: Anaphylactic reaction (anaphylaxis), or Shock, NOS

When to code an Admit Diagnosis vs Acquired Diagnosis

  • There are sometimes subtle issues here, especially for diagnoses that use lab test results.
  • An example is patient comes in to ED with shock presumed due to pneumonia and a lactate=1.7 --> this doesn't meet the requirement for Shock, septic, but by 3 hours later the next lactate checked in the ICU is 2.7, so that threshold for septic shock IS met. Clearly this person was "brewing" septic shock at admission and it seems logical to include that diagnosis as an admit diagnosis. THUS -- in such cases where it seems pretty clear, in retrospect, that a diagnosis was brewing/present at admission but only became fully evident after admission, that diagnosis SHOULD be coded as an Admit Diagnosis IF it becomes fully evident within 6 hours of admission.
  • Note that an individual during a single episode of illness can evolve over time from Severe sepsis to Shock, septic -- if this occurs, make sure to also code the more advanced subtype
    • e.g. admitted on Monday with Severe sepsis which is coded, but by Tuesday has progressed to Shock, septic which should then be added to the codes, in this case as an Acquired Diagnosis.
    • however, as a person improves there is NO NEED to "downcode" their sepsis