Association of PC and AT levels in the early phase of STEMI treated with pPCI with LV systolic function and 6-month MACE.

Protein C ST-elevation myocardial infarction antithrombin III left Ventricle percutaneous coronary intervention

Journal

Acta clinica Belgica
ISSN: 2295-3337
Titre abrégé: Acta Clin Belg
Pays: England
ID NLM: 0370306

Informations de publication

Date de publication:
21 May 2020
Historique:
pubmed: 22 5 2020
medline: 22 5 2020
entrez: 22 5 2020
Statut: aheadofprint

Résumé

To examine a relationship between protein C (PC) and antithrombin III (AT III) activities with ejection fraction of left ventricle (EFLV), in the early phase of acute ST-elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (pPCI), and to investigate whether PC and AT III are associated with major adverse cardiovascular events (MACE) within 6 months following from pPCI. The research had a prospective character and included 357 patients who had, following the diagnosis of the STEMI, undergone pPCI at the Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, Belgrade, Serbia, from January 2010 until April 2019. The EFLV positively correlated with PC values (rho = 0.229). There was a statistically significant increase in the PC values between patients with MACE compared with those without MACE at 6 months' follow-up evaluation (p < 0.0001). Also, significant difference in PC values between patients who died in hospital and those who were alive at 6 months' follow-up (p < 0.01) was observed. PC values were different across different EFLV groups (p < 0.001), increasing from the 1 Increased PC activity in the early phase of STEMI is associated with higher EFLV 5 days after the pPCI as well as with MACE at 6 months after the pPCI.

Identifiants

pubmed: 32436782
doi: 10.1080/17843286.2020.1766850
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Auteurs

Slobodan Obradovic (S)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.
School of Medicine, University of Defense, Belgrade, Serbia.

Edin Begic (E)

Department of Cardiology, General Hospital "Prim.Dr. Abdulah Nakas", Sarajevo, Bosnia and Herzegovina.
Department of Pharmacology, Sarajevo Medical School, Sarajevo School of Science and Technology, Sarajevo, Bosnia and Herzegovina.

Slobodan Jankovic (S)

Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

Radoslav Romanovic (R)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.
School of Medicine, University of Defense, Belgrade, Serbia.

Nemanja Djenic (N)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.
School of Medicine, University of Defense, Belgrade, Serbia.

Boris Dzudovic (B)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.

Zoran Jovic (Z)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.
School of Medicine, University of Defense, Belgrade, Serbia.

Dragana Malovic (D)

Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy, University of Defense, Belgrade, Serbia.

Vesna Subota (V)

School of Medicine, University of Defense, Belgrade, Serbia.
Institute of Biochemistry, Military Medical Academy, University of Defense, Belgrade, Serbia.

Milena Stavric (M)

Institute of Biochemistry, Military Medical Academy, University of Defense, Belgrade, Serbia.

Farid Ljuca (F)

Department of Physiology, Faculty of Medicine Tuzla, Tuzla, Bosnia and Herzegovina.

Zumreta Kusljugic (Z)

Department for Science, Teaching and Clinical Trials, University Clinical Centre Tuzla, Tuzla, Bosnia and Herzegovina.

Classifications MeSH