Move over MACE
and say hello to CRACE!
These high profile authors from the USA sought to determine
the incidence of short term life threatening events in low risk chest pain
patients admitted to hospital.
Their concern was a lack of benefit from admission balanced with the potential harm (false
positives, over-diagnosis, hospital acquired infections, VTE, iatrogenic etc.).
They reviewed a large database from 3 hospitals in the US
Midwest from 2008-2013. They identified admitted patients that had negative serial biomarkers (old school troponins), normal vital signs and non-ischemic ECGs.
Interestingly, these authors picked a different outcome
measure for this study from the traditional MACE that we have seen in many previous studies. They created “CRACE” defined
as:
- Life-threatening arrhythmia (VF, symptomatic bradycardia, or treated brady or tachy arrhythmias)
- Inpatient STEMI
- Cardiac or respiratory arrest
- Death
(Noticeably
absent from CRACE is non-STEMI or longer term outcomes beyond hospitalization.)
What did they find?
Of
course this group was very low risk… but could you have guessed a CRACE rate of only 0.06% (4 of 7266
patients)!
As
is usually the case, there were some methodological issues with this study and the reported rate is probably not a
complete reflection of the truth. However this makes a compelling argument that this is an extremely low risk group that may
derive more net harm from admission.
The
authors are careful to mention that this study does not mean patients derive no
utility from further investigation and management after the ED evaluation. But
suggest this may be done as an outpatient and might provide a framework for shared decision making.
My
guess is the Australians would never admit many of these low risk patients
anyway. In addition, these patients would be even lower risk with the high
sensitive troponin assays.
Take home? Perhaps we can sleep a
little better knowing that low risk patients truly are very low risk. Hope this doesn’t
seem to CRACEy…
Covering:
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