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- Publisher Website: 10.1016/j.hrthm.2018.02.016
- Scopus: eid_2-s2.0-85047137626
- PMID: 29454138
- WOS: WOS:000433427200008
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Article: Prognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome
Title | Prognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome |
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Authors | |
Keywords | Acute coronary syndrome Monomorphic ventricular tachycardia Mortality Polymorphic ventricular tachycardia Ventricular fibrillation |
Issue Date | 2018 |
Citation | Heart Rhythm, 2018, v. 15 n. 6, p. 822-829 How to Cite? |
Abstract | Background: The prognostic implication of early ventricular tachyarrhythmias (VTs) after acute coronary syndrome (ACS) remains unclear. Objective: We sought to investigate the clinical outcomes of early monomorphic and non–monomorphic VTs that occur within 48 hours in patients after ACS. Methods: We retrospectively reviewed the clinical outcomes of 2033 [mean age 67.0 ± 13.4 years; 1486 (73.1%) men] consecutive patients who presented with ACS from 2004 to 2015. Results: A total of 67 (3.3%) and 90 (4.4%) patients developed early monomorphic or non–monomorphic VT, respectively. Killip class IV (odds ratio [OR] 3.05; 95% confidence interval [CI] 1.47–6.36; P <.01), creatine kinase level (OR 1.01; 95% CI 1.00–1.02 per 100 IU/L; P =.01), and left ventricular ejection fraction (OR 0.96; 95% CI 0.94–0.99; P <.01) were independently associated with early monomorphic VT, whereas age (OR 0.98; 95% CI 0.97–0.99; P =.04), ST elevated myocardial infarction (OR 3.53; 95% CI 1.71–7.27; P <.01), Killip class IV (OR 4.91; 95% CI 2.76–8.74; P <.01), diabetes mellitus (OR 0.48; 95% CI 0.28–0.81; P <.01), and left ventricular ejection fraction (OR 0.97; 95% CI 0.95–0.99; P <.01) were independently associated with early non–monomorphic VT. More patients with early monomorphic VT (n = 22 [32.8%]) died in hospital than those with non–monomorphic VT (n = 16 [17.8%]) or without early VT (n = 133 [7.1%]; P <.01). After a mean follow-up of 67.8 ± 43.2 months, 21 patients with early monomorphic VT (46.7%), 22 patients with early non–monomorphic VT (29.7%), and 552 patients without early VT (31.7%) died. Both early monomorphic and non–monomorphic VTs were associated with a long-term increase in sudden arrhythmic deaths and recurrent VTs. Nevertheless, only early monomorphic VT was shown to independently predict overall survival (hazard ratio 1.62; 95% CI 1.03–2.55; P =.04). Conclusion: Early monomorphic VT, but not early non–monomorphic VT, independently predicted all-cause mortality in patients with ACS who survived to hospital discharge. |
Persistent Identifier | http://hdl.handle.net/10722/262199 |
ISSN | 2023 Impact Factor: 5.6 2023 SCImago Journal Rankings: 2.072 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hai, SHJJ | - |
dc.contributor.author | Un, KC | - |
dc.contributor.author | Wong, CK | - |
dc.contributor.author | Wong, KL | - |
dc.contributor.author | Zhang, ZY | - |
dc.contributor.author | Chan, PHM | - |
dc.contributor.author | Lau, CP | - |
dc.contributor.author | Siu, DCW | - |
dc.contributor.author | Tse, HF | - |
dc.date.accessioned | 2018-09-28T04:55:02Z | - |
dc.date.available | 2018-09-28T04:55:02Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Heart Rhythm, 2018, v. 15 n. 6, p. 822-829 | - |
dc.identifier.issn | 1547-5271 | - |
dc.identifier.uri | http://hdl.handle.net/10722/262199 | - |
dc.description.abstract | Background: The prognostic implication of early ventricular tachyarrhythmias (VTs) after acute coronary syndrome (ACS) remains unclear. Objective: We sought to investigate the clinical outcomes of early monomorphic and non–monomorphic VTs that occur within 48 hours in patients after ACS. Methods: We retrospectively reviewed the clinical outcomes of 2033 [mean age 67.0 ± 13.4 years; 1486 (73.1%) men] consecutive patients who presented with ACS from 2004 to 2015. Results: A total of 67 (3.3%) and 90 (4.4%) patients developed early monomorphic or non–monomorphic VT, respectively. Killip class IV (odds ratio [OR] 3.05; 95% confidence interval [CI] 1.47–6.36; P <.01), creatine kinase level (OR 1.01; 95% CI 1.00–1.02 per 100 IU/L; P =.01), and left ventricular ejection fraction (OR 0.96; 95% CI 0.94–0.99; P <.01) were independently associated with early monomorphic VT, whereas age (OR 0.98; 95% CI 0.97–0.99; P =.04), ST elevated myocardial infarction (OR 3.53; 95% CI 1.71–7.27; P <.01), Killip class IV (OR 4.91; 95% CI 2.76–8.74; P <.01), diabetes mellitus (OR 0.48; 95% CI 0.28–0.81; P <.01), and left ventricular ejection fraction (OR 0.97; 95% CI 0.95–0.99; P <.01) were independently associated with early non–monomorphic VT. More patients with early monomorphic VT (n = 22 [32.8%]) died in hospital than those with non–monomorphic VT (n = 16 [17.8%]) or without early VT (n = 133 [7.1%]; P <.01). After a mean follow-up of 67.8 ± 43.2 months, 21 patients with early monomorphic VT (46.7%), 22 patients with early non–monomorphic VT (29.7%), and 552 patients without early VT (31.7%) died. Both early monomorphic and non–monomorphic VTs were associated with a long-term increase in sudden arrhythmic deaths and recurrent VTs. Nevertheless, only early monomorphic VT was shown to independently predict overall survival (hazard ratio 1.62; 95% CI 1.03–2.55; P =.04). Conclusion: Early monomorphic VT, but not early non–monomorphic VT, independently predicted all-cause mortality in patients with ACS who survived to hospital discharge. | - |
dc.language | eng | - |
dc.relation.ispartof | Heart Rhythm | - |
dc.subject | Acute coronary syndrome | - |
dc.subject | Monomorphic ventricular tachycardia | - |
dc.subject | Mortality | - |
dc.subject | Polymorphic ventricular tachycardia | - |
dc.subject | Ventricular fibrillation | - |
dc.title | Prognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome | - |
dc.type | Article | - |
dc.identifier.email | Hai, SHJJ: haishjj@hku.hk | - |
dc.identifier.email | Chan, PHM: phmchan@hku.hk | - |
dc.identifier.email | Lau, CP: cplau@hkucc.hku.hk | - |
dc.identifier.email | Siu, DCW: cwdsiu@hkucc.hku.hk | - |
dc.identifier.email | Tse, HF: hftse@hkucc.hku.hk | - |
dc.identifier.authority | Hai, SHJJ=rp02047 | - |
dc.identifier.authority | Chan, PHM=rp01864 | - |
dc.identifier.authority | Siu, DCW=rp00534 | - |
dc.identifier.authority | Tse, HF=rp00428 | - |
dc.identifier.doi | 10.1016/j.hrthm.2018.02.016 | - |
dc.identifier.pmid | 29454138 | - |
dc.identifier.scopus | eid_2-s2.0-85047137626 | - |
dc.identifier.hkuros | 293234 | - |
dc.identifier.volume | 15 | - |
dc.identifier.issue | 6 | - |
dc.identifier.spage | 822 | - |
dc.identifier.epage | 829 | - |
dc.identifier.isi | WOS:000433427200008 | - |