H-FABP AS AN EXCELLENT BIOCHEMICAL CARDIAC MARKER FOR DIAGNOSING ACUTE NON ST ELEVATION MI (NSTEMI)...
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Transcript of H-FABP AS AN EXCELLENT BIOCHEMICAL CARDIAC MARKER FOR DIAGNOSING ACUTE NON ST ELEVATION MI (NSTEMI)...
![Page 1: H-FABP AS AN EXCELLENT BIOCHEMICAL CARDIAC MARKER FOR DIAGNOSING ACUTE NON ST ELEVATION MI (NSTEMI) IN FIRST 4 HOURS OF PRESENTATION TO AN ED.](https://reader038.fdocuments.in/reader038/viewer/2022110203/55d1fc93bb61eb7d5a8b4681/html5/thumbnails/1.jpg)
Background• AMI – The most serious
challenge in cardiology. • H – FABP – human heart
specific fatty acid binding protein , has a high potential as a marker for early diagnosis of AMI.
• H- FABP is released early to the blood stream.
• Useful for both rapid confirmation & exclusion of infarction.
• NSTEMI, unstable angina – diagnosis is difficult.
• A rapid qualitative test cardio detect test – H-FABP
• Fatty acid binding protein are members of cytosolic protein family.
• Tissue specific abundant in heart, liver & intestine and are named H-FABP, L-FABP, I-FABP respectively.
• H – FABP consist of 132 amino acid and is present mainly in heart and liver.
Advantages:• High myocardial content.• Low molecular weight.• Relative tissue specificity.• Early (within 2 hrs ) appearance
in plasma &urine after AMI.• Can detect reinfarction –
normalisation of HFABP, occurs within 24 hrs.
• To evaluate the diagnostic value of early h – FABP detection compared to other selected markers of myocardial injury such as Troponin – I , Troponin – T level .
• Measuring the H- FABP using the qualitative test CardioDetect med in acute myocardial infarction.
Aims & Objectives
Methods
Conclusion
H-FABP AS AN EXCELLENT BIOCHEMICAL CARDIAC MARKER FOR DIAGNOSING ACUTE NON ST ELEVATION MI (NSTEMI)
IN FIRST 4 HOURS OF PRESENTATION TO AN ED. Dr. Karthikeyan Sundaramurthy; Dr. Kesavardan Rddy Narsing*; Dr. Srihari Cattamanchi;
Dr. T.V. Ramakrishnan.Sri Ramchandra Medical College & Research Institute, Porur, Chennai – 600116. Tamil Nadu. India.
Results
Dr. Karthikeyan Subramanian; Mobile: +91-9843163160; Email id: [email protected]
Study Design: A prospective, diagnostic, analytical study Settings: Accident & Emergency Department at Sri Ramachandra Medical College & Research Institute, Porur, Chennai, Duration: Six Months from September 2009 to February 2010. Consecutive sampling technique employed. Methodology: Blood samples taken for Troponin T, Troponin I and H-FABPs as early as possible and sent for analysis. Instrument: A preformatted proforma was used as an instrument in the study. Inclusion Criteria: • ACS with out persistent ST
segment elevation in patients < 24 hr’s from the onset of chest pain .
• ECG features implying acute ischemia like ST segment depression, T wave pseudonormalisation, isolated T wave inversion .
• Without typical ischemic changes.
Exclusion Criteria:• ST elevation myocardial
infarction• Renal failure (creatinine >2mg/dl)• Skeletal muscle disorder.Data Collection: The patient's demographic data, presenting complaints past history, EKG changes and vitals are recorded. The values of Troponin T, Troponin I and H-FABPs are analyzed. Written informed consent was obtained Institutional Ethics Committee approval was obtained.Statistical analysis was done using SPSS software ver. 15.0.
• A total of 55 chest pain patients with equivocal ECG findings were enrolled in the study.
• There were 39 males and 16 females with mean age of 59.65 years.
• H-FABP had sensitivity of 83.63% and specificity of 98.18% compared with 62.21% and 98.46% for cTnT and 67.96% and 98.14% for cTnI in initial 4 hours after onset of chest pain.
• Altogether, 46 patients had acute myocardial infarction as confirmed by positive troponin levels (gold standard test).
• Qualitative h-FABP test (CardioDetect med) showed excellent sensitivity, higher than measurements of cTnI and cTnT in first 4 hours of hospital admission, and high specificity in patient group with NSTEMI.
• H-FABP is excellent biochemical cardiac marker for diagnosing NSTEMI, especially in its early phase, allowing exclusion of myocardial necrosis.
- : Negative+ : 20 to 40µg/L ++ : 80µg/L+++ : 160µg/L