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ADAPT Protocol for Cardiac Event Risk
ADAPT Protocol for Cardiac Event Risk
ADAPT Protocol
Assesses chest pain patients at 2 hours for risk of cardiac event.
2-hour rule out for low risk chest pain.
adapt-protocol-cardiac-event-risk
The ADAPT Protocol for Cardiac Event Risk uses a 2-hour accelerated diagnostic protocol to assess patients with chest pain for 30 day risk of cardiac event.
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[ "Chest Pain" ]
Addition of the selected points: *cTnI level at 0 and 2 hours above institutional cutoff for elevated troponin.**ST-segment depression of at least 0.05 mV in ≥2 contiguous leads (including reciprocal changes), T-wave inversion of at least 0.1 mV, or Q waves ≥30 ms in width and ≥0.1 mV in depth in at least 2 contiguous leads.
[]
|
Risk group |
Risk of major adverse cardiac event (MACE) in 30 days |
|
|
Normal troponin, normal EKG and TIMI 0 |
Low |
0-0.3%* |
|
Normal troponin, normal EKG and TIMI 1 |
Intermediate |
0.8%** |
|
Abnormal troponin or abnormal EKG and any TIMI |
High |
15.3%*** |
*Per Than 2012.
**Per Cullen 2013. The study examined patients with TIMI 0 or 1, with no reported data for patients with TIMI >1 (presuming according to TIMI data, risk of MACE increases with increasing TIMI Score).
***Per Than 2012. In the original paper, 15.3% of patients studied (302 of 1,975 total) had a MACE, and only 1 patient was identified as low risk.
{ "Clinical Practice Guidelines": [ { "href": "", "text": "" } ], "Manufacturer Website": [ { "href": "", "text": "" } ], "Original/Primary Reference": [ { "href": "https://www.ncbi.nlm.nih.gov/pubmed/22578923", "text": "Than M, et. al. 2-Hour Accelerated Diagnostic Protocol to Assess Patients With Chest Pain Symptoms Using Contemporary Troponins as the Only Biomarker : The ADAPT Trial. J Am Coll Cardiol. 2012 Jun 5;59(23):2091-8. doi: 10.1016/j.jacc.2012.02.035. Epub 2012 May 9." } ], "Other References": [ { "href": "", "text": "" } ], "Outcomes": [ { "href": "", "text": "" } ], "Validation": [ { "href": "https://www.ncbi.nlm.nih.gov/pubmed/23583250", "text": "Cullen L, Mueller C, Parsonage WA, Wildi K, Greenslade JH, Twerenbold R,Aldous S, Meller B, Tate JR, Reichlin T, Hammett CJ, Zellweger C, Ungerer JP, Rubini Gimenez M, Troughton R, Murray K, Brown AF, Mueller M, George P, Mosimann T, Flaws DF, Reiter M, Lamanna A, Haaf P, Pemberton CJ, Richards AM, Chu K, Reid CM, Peacock WF, Jaffe AS, Florkowski C, Deely JM, Than M. Validation of high-sensitivity troponin I in a 2-hour diagnostic strategy to assess 30-day outcomes in emergency department patients with possible acute coronary syndrome. J Am Coll Cardiol. 2013 Oct 1;62(14):1242-9. doi: 10.1016/j.jacc.2013.02.078. Epub 2013 Apr 10. PubMed PMID: 23583250." } ], "Validations": [] }
The ADAPT Score and Accelerated Diagnostic Protocol can be used to evaluate patients with chest pain and potentially identify 20% of patients who are low-risk and can be evaluated with a 0-hour and 2-hour troponin test along with EKG and TIMI Risk Scores (for
Up to 20% of chest pain patients may be able to be safely ruled out for MI and ACS within 2 hours of arrival in the ED, reducing length of stay dramatically without adverse outcome.
Barring other concerning features for acute coronary syndrome or other life-threatening causes of chest pain (pneumothorax, pulmonary embolism, cardiac tamponade, aortic dissection, esophageal rupture, etc.), patients that meet the low-risk criteria can be considered for discharge with close follow-up with their primary care physician after negative 0h and 2h troponin testing.
Patients who do not meet the low-risk criteria should be ruled-out for myocardial infarction with serial EKGs and biomarkers and risk stratified as per normal chest pain guidelines and protocols.
[ "Acute Coronary Syndrome", "Myocardial Infarction" ]
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2022-04-21T20:29:03.096Z
[ "Algorithm", "Prognosis", "Rule Out" ]
[ "acs", "troponin", "cp", "chest pain" ]
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[ "Cardiology", "Emergency Medicine", "Hospitalist Medicine", "Internal Medicine" ]
[ "Cardiac" ]
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