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Article: Prognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome

TitlePrognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome
Authors
KeywordsAcute coronary syndrome
Monomorphic ventricular tachycardia
Mortality
Polymorphic ventricular tachycardia
Ventricular fibrillation
Issue Date2018
Citation
Heart Rhythm, 2018, v. 15 n. 6, p. 822-829 How to Cite?
AbstractBackground: 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 Identifierhttp://hdl.handle.net/10722/262199
ISSN
2021 Impact Factor: 6.779
2020 SCImago Journal Rankings: 2.768
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHai, SHJJ-
dc.contributor.authorUn, KC-
dc.contributor.authorWong, CK-
dc.contributor.authorWong, KL-
dc.contributor.authorZhang, ZY-
dc.contributor.authorChan, PHM-
dc.contributor.authorLau, CP-
dc.contributor.authorSiu, DCW-
dc.contributor.authorTse, HF-
dc.date.accessioned2018-09-28T04:55:02Z-
dc.date.available2018-09-28T04:55:02Z-
dc.date.issued2018-
dc.identifier.citationHeart Rhythm, 2018, v. 15 n. 6, p. 822-829-
dc.identifier.issn1547-5271-
dc.identifier.urihttp://hdl.handle.net/10722/262199-
dc.description.abstractBackground: 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.languageeng-
dc.relation.ispartofHeart Rhythm-
dc.subjectAcute coronary syndrome-
dc.subjectMonomorphic ventricular tachycardia-
dc.subjectMortality-
dc.subjectPolymorphic ventricular tachycardia-
dc.subjectVentricular fibrillation-
dc.titlePrognostic implications of early monomorphic and non–monomorphic tachyarrhythmias in patients discharged with acute coronary syndrome-
dc.typeArticle-
dc.identifier.emailHai, SHJJ: haishjj@hku.hk-
dc.identifier.emailChan, PHM: phmchan@hku.hk-
dc.identifier.emailLau, CP: cplau@hkucc.hku.hk-
dc.identifier.emailSiu, DCW: cwdsiu@hkucc.hku.hk-
dc.identifier.emailTse, HF: hftse@hkucc.hku.hk-
dc.identifier.authorityHai, SHJJ=rp02047-
dc.identifier.authorityChan, PHM=rp01864-
dc.identifier.authoritySiu, DCW=rp00534-
dc.identifier.authorityTse, HF=rp00428-
dc.identifier.doi10.1016/j.hrthm.2018.02.016-
dc.identifier.pmid29454138-
dc.identifier.scopuseid_2-s2.0-85047137626-
dc.identifier.hkuros293234-
dc.identifier.volume15-
dc.identifier.issue6-
dc.identifier.spage822-
dc.identifier.epage829-
dc.identifier.isiWOS:000433427200008-

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