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Fragmented QRS may predict new onset atrial fibrillation in patients with ST-segment elevation myocardial infarction

Authors :
Macit Kalçık
Metin Çağdaş
Yavuz Karabağ
Süleyman Karakoyun
Mahmut Yesin
İbrahim Rencüzoğulları
Mustafa Ozan Gürsoy
Süleyman Çağan Efe
Hitit Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
Source :
Journal of electrocardiology. 51(1)
Publication Year :
2017

Abstract

Background Fragmented QRS (fQRS) has been shown to be a marker of local myocardial conduction abnormalities, cardiac fibrosis in previous studies. It was also reported to be a predictor of sudden cardiac death and increased morbidity and mortality in selected populations. However, there is no study investigating the role of fQRS in the development of atrial fibrillation in patients with ST segment elevation myocardial infarction (STEMI). In this study we aimed to investigate the relationship between the presence of fQRS after primary percutaneous coronary intervention (pPCI) and in-hospital development of new-onset atrial fibrilation (AF) in patients with STEMI. Material and methods This study enrolled 171 patients undergoing pPCI for STEMI. Among these patients 24 patients developed AF and the remaining 147 patients were designated as the controls. All clinical, demographical and laboratory parameters were entered into a dataset and compared between AF group and the controls. Results The presence of fQRS was higher in the AF group than in the controls (P = 0.001). Diabetes mellitus and fQRS was significantly more common in the AF group (P = 0.003 and P = 0.001 respectively) Logistic regression analysis demonstrated that the presence of fQRS was the independent determinant of AF (OR: 3.243, 95% CI 1.016–10.251, P = 0.042). Conclusions Increased atrial fibrillation was observed more frequently in STEMI patients with fQRS than in patients without fQRS. fQRS is an important determinant of AF in STEMI after pPCI.

Details

ISSN :
15328430
Volume :
51
Issue :
1
Database :
OpenAIRE
Journal :
Journal of electrocardiology
Accession number :
edsair.doi.dedup.....2b133cc952d599ff08ab25cc77d092be