Newer Diagnostic Tests for MI ============================= þ Troponin - Consists of three subunits: Troponin-C, Troponin-T, Troponin-I - Found in skeletal muscle, too -- but the cardiac Troponin-T and -I are encoded by different genes, so can be distinguished from skeletal - Troponin-I most sensitive in early hours þ Troponin-T - more sensitive than CPK-MB; - peaks at 14 hours and 3-5 days in acute MI; - can be released from ischemic and not-yet infarcted tissue (reversible ischemic damage) [Hamm CW, et al. The prognostic value of single troponin T in unstable angina. N Engl Med J 1992;327(3):146-9.] - can last for 2-3 weeks. [Antman EM, Grudzien C, Sacks DB. Evaluation of a rapid bedside assaay for detection of serum cardiac troponin T.] - what level is positive? + 0.1 [Ohman EM, et al [for the Gusto-IIa investigators]. Cardiac Troponin T levels for risk stratification in acute myocardial ischemia. N Engl J Med 1996;335(18):1333-1341.] [Van de Werf F. Cardiac troponins in acute coronary syndromes [editorial]. N Engl J Med 1996;335(18):1388-1389.] + 0.2-0.4 (commmon clinical practice) - are bedside qualitative assays useful in the ED? + maybe (but this study has problems with selection bias; only patients admitted to CCU): [Antman EM, Grudzien C, Sacks DB. Evaluation of a rapid bedside assaay for detection of serum cardiac troponin T.] - Troponin T may be falsely elevated in those with renal failure. [Antoinette Mangione, MD, PharmD, FACEP, 1998 PaACEP conference] þ Mercy (and Mercy Prov) - used to use Troponin-T, revised 1/97 to detect level as low as 0.08 ng/ml, is a qualitative test. - now uses quantitive Troponin-I level (must go in red top or similar, purple top not acceptable) as of Dec 1 1998 þ Troponin-I - upslope similar to CPK-MB; usually positive starting about 4-8 hours after pain (per Mercy lab); both MB and cTnI (cardiac Troponin-I) peak at about 18 hours - stays elevated longer than CPK-MB (good substitute for LDH isos); CPK-MB usually gone in 48-72 hours but cTnI may stay elevated for up to 9 days (per Mercy lab) - not routinely elevated in dialysis patients - no "background level" as with CPK - Hennepin Co. Medical Center has converted to troponin-I [Antman EM, et al [including Eugene Braunwald]. Cardiac specific Troponin I levels to predict the risk of mortality in patients with acute coronary syndromes. New Engl J Med 1996;335(18):1342-1349.] þ Myoglobin - only present after MI for about 2 hours, so not very useful in ED. - found to be better than Troponin T or CPK-MB in one study [Bakker AJ, Koelemay MJW, Gorgels JPMC, van Vlies B, Smits R, Tussen JGP, Haagen FDM. Troponin T and myoglobin at admission; value of early diagnosis of acute myocardial infarction. Eur Heart J 1994;15:45-53.] Poor study; no gold standard: [Davis CP, Barrett K, Torre P, Wacasey K. Serial myoglobin levels for patients with possible myocardial infarction. Acad Emerg Med 1996;3(6):590-597.] - Need to do serial levels ("nurse, draw blood every 30 minutes"?!?): [Tucker JF, et al. Value of serial myoglobin levels in the early diagnosis of patients admitted for acute myocardial infarction. Ann Emerg Med 1994;24(4):704-708.] - elevated in trauma patients, those with renal failure. If exclude those patients, false + rate is acceptable. þ CPK-MB Isoforms - cleavage of CPK-MB results in isoforms CPK-MB1 and CPK-MB2. - ratio of 1/2 changes even before total CPK-MB elevates - research only at present (1998) þ Echos: - 93% sensitive, 57% specific; if discharged patients with normal echo and normal EKG would have missed 2 MIs out of 202 ED patients. [Sabia et al. Circ 1991;84(suppl):85.] þ Sestamibit imaging: - small study suggests normal scan rules out MI. [Varetto et al. J Amer Coll Cardiol 1993;22:1804.] - larger study seemed to confirm. [Tatum et al. Ann Emerg Med 1997;29:116/]