PMID- 32576233 OWN - NLM STAT- MEDLINE DCOM- 20210111 LR - 20210111 IS - 1471-2261 (Electronic) IS - 1471-2261 (Linking) VI - 20 IP - 1 DP - 2020 Jun 23 TI - Usefulness of ECG to differentiate apical hypertrophic cardiomyopathy from non-ST elevation acute coronary syndrome. PG - 306 LID - 10.1186/s12872-020-01592-0 [doi] LID - 306 AB - BACKGROUND: Apical hypertrophic cardiomyopathy (ApHCM) is a phenotypic variant of nonobstructive HCM. ApHCM is characterized by left ventricular hypertrophy involve the distal apex. The electrocardiographic character of ApHCM can mimic non-ST elevation acute coronary syndrome (NSTEACS), triggering a series of studies and treatments that may be unnecessary. This study aimed to clarify the electrocardiogram (ECG) differences between the two diseases. METHODS: Initial ECG recordings of 41 patients with ApHCM and 72 patients with NSTEACS were analyzed retrospectively. We analyzed the voltage of negative T (neg T) and R wave, the change of ST-segment as well as the number of leads with neg T wave in the 12-lead ECGs. RESULTS: Across the 12-lead ECGs, the magnitude of R wave significantly differed between ApHCM and NSTEACS in 10 leads excluding leads aVR and V1. ApHCM was associated with a greater maximal amplitude of R wave in lead V5 (3.13 +/- 1.08 vs. 1.38 +/- 0.73 mV, P < 0.001). The magnitude of T wave significantly differed between ApHCM and NSTEACS in 10 leads excluding leads II and V1. ApHCM was associated with a greater maximal amplitude of neg T wave in lead V4 (0.85 +/- 0.69 vs. 0.35 +/- 0.23 mV, P < 0.001). The frequency of giant neg T (1mv or more) wave was higher in ApHCM (36.5% vs. 0%, P < 0.001). The magnitude of ST-segment deviation significantly differed between ApHCM and NSTEACS in 10 leads excluding leads aVF and V2. ApHCM was associated with a greater maximal amplitude of ST-segment depression in lead V5 (0.19 +/- 0.07 vs. 0.03 +/- 0.06 mV, P < 0.001). The number of leads with neg T wave also differed between ApHCM and NSTEACS (6.75 +/- 1.42 vs. 6.08 +/- 1.51, P = 0.046). The sum of R wave in lead V5, neg T wave in lead V6 and ST-segment depression in lead V4 > 2.585 mV identified ApHCM with 90.2% sensibility and 87.5% specificity, representing the highest diagnostic accuracy. CONCLUSIONS: Compared with NSTEACS patients, ApHCM patients presented higher R and neg T wave voltage as well as a greater ST-segment depression in the 12-lead ECG. The ECG characteristics can help to differentiate ApHCM from NSTEACS in clinical setting. FAU - Tao, Yirao AU - Tao Y AD - Department of Cardiology, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China. FAU - Xu, Jing AU - Xu J AD - Department of Cardiology, Shanghai East Hospital, Shanghai Tongji University School of Medicine, Shanghai, China. FAU - Bako, Samira Yerima AU - Bako SY AD - Department of Cardiology, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China. FAU - Yao, Xiaobo AU - Yao X AD - Department of Cardiology, Shanghai East Hospital, Shanghai Tongji University School of Medicine, Shanghai, China. FAU - Yang, Donghui AU - Yang D AUID- ORCID: 0000-0003-4640-357X AD - Department of Cardiology, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China. yangdonghui1@126.com. LA - eng PT - Journal Article DEP - 20200623 PL - England TA - BMC Cardiovasc Disord JT - BMC cardiovascular disorders JID - 100968539 SB - IM MH - *Action Potentials MH - Acute Coronary Syndrome/*diagnosis/physiopathology MH - Aged MH - Aged, 80 and over MH - Cardiomyopathy, Hypertrophic/*diagnosis/physiopathology MH - Diagnosis, Differential MH - *Electrocardiography MH - Female MH - *Heart Rate MH - Humans MH - Male MH - Middle Aged MH - Non-ST Elevated Myocardial Infarction/*diagnosis/physiopathology MH - Predictive Value of Tests MH - Retrospective Studies PMC - PMC7310283 OTO - NOTNLM OT - Apical hypertrophic cardiomyopathy OT - Electrocardiogram OT - Non-ST elevation acute coronary syndrome COIS- The authors declare that they have no competing interests. EDAT- 2020/06/25 06:00 MHDA- 2021/01/12 06:00 PMCR- 2020/06/23 CRDT- 2020/06/25 06:00 PHST- 2020/03/31 00:00 [received] PHST- 2020/06/17 00:00 [accepted] PHST- 2020/06/25 06:00 [entrez] PHST- 2020/06/25 06:00 [pubmed] PHST- 2021/01/12 06:00 [medline] PHST- 2020/06/23 00:00 [pmc-release] AID - 10.1186/s12872-020-01592-0 [pii] AID - 1592 [pii] AID - 10.1186/s12872-020-01592-0 [doi] PST - epublish SO - BMC Cardiovasc Disord. 2020 Jun 23;20(1):306. doi: 10.1186/s12872-020-01592-0.