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  1. Article ; Online: Do non-vitamin K antagonist oral anticoagulants increase the risk of myocardial infarction?

    Grajek, Stefan / Kałużna-Oleksy, Marta

    Kardiologia polska

    2022  Volume 80, Issue 1, Page(s) 16–24

    Abstract: Non-vitamin K antagonist oral anticoagulants (NOACs), compared with warfarin, have a favorable risk-benefit profile. However, in the RE-LY study in patients with atrial fibrillation (AF), the number of patients with MI was higher in the dabigatran group ... ...

    Abstract Non-vitamin K antagonist oral anticoagulants (NOACs), compared with warfarin, have a favorable risk-benefit profile. However, in the RE-LY study in patients with atrial fibrillation (AF), the number of patients with MI was higher in the dabigatran group as compared to the warfarin group. Many meta-analyses showed that dabigatran treatment led to an increased risk of myocardial infarction (MI). Large real-world data (RWD) did not confirm an increase in the risk of MI during dabigatran treatment. In our meta-analysis we excluded RWD, and each of the four drugs was evaluated in two key-phase III randomized controlled trials: in patients with AF and patients with AF and chronic coronary syndrome or acute coronary syndrome treated with percutaneous coronary interventions. In each study, warfarin was the comparator for NOACs. In this homogeneous group of patients, dabigatran, in direct comparison with warfarin, significantly increased the risk of MI by about 30%. Moreover, the risk of MI was also significantly higher than the opposite effect of activated factor (F) X inhibitors (FXa inhibitors) vs. warfarin. In our network meta-analysis, considering individual NOACs in recommended doses, we found an increased risk of MI compared to warfarin only in patients treated with dabigatran 150 mg twice a day and, in particular, 110 mg twice a day. In this review we present evidence supporting our opinion that in patients with AF and coronary stenting, the choice of NOACs (direct FXa vs. thrombin inhibitors) is equally as important as choosing the optimal antiplatelet therapy (single or dual antiplatelet therapy).
    MeSH term(s) Administration, Oral ; Anticoagulants/adverse effects ; Atrial Fibrillation/drug therapy ; Dabigatran/adverse effects ; Humans ; Myocardial Infarction/drug therapy ; Stroke/drug therapy ; Warfarin/adverse effects
    Chemical Substances Anticoagulants ; Warfarin (5Q7ZVV76EI) ; Dabigatran (I0VM4M70GC)
    Language English
    Publishing date 2022-02-09
    Publishing country Poland
    Document type Journal Article ; Meta-Analysis ; Review
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    DOI 10.33963/KP.a2022.0017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Uwagi do stanowiska ekspertów w sprawie stosowania biwalirudyny u pacjentów z ostrym zawałem serca poddawanych przezskórnej interwencji wieńcowej w Polsce.

    Grajek, Stefan

    Kardiologia polska

    2014  Volume 72, Issue 8, Page(s) 768–770

    Language Polish
    Publishing date 2014
    Publishing country Poland
    Document type Comment ; Letter
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    DOI 10.5603/KP.2014.0161
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: List do "Kardiologii Polskiej" w sprawie optymalnego leczenia zawalu serca".

    Grajek, Stefan

    Kardiologia polska

    2012  Volume 70, Issue 2, Page(s) 213–214

    Title translation Letter to Kardiologia Polska concerning optimal treatment of myocardial infarction.
    MeSH term(s) Adenosine/analogs & derivatives ; Adenosine/therapeutic use ; Cost-Benefit Analysis ; Humans ; Models, Theoretical ; Myocardial Infarction/therapy ; Piperazines/therapeutic use ; Platelet Aggregation Inhibitors/therapeutic use ; Prasugrel Hydrochloride ; Purinergic P2Y Receptor Antagonists/therapeutic use ; Randomized Controlled Trials as Topic ; Thiophenes/therapeutic use ; Ticlopidine/analogs & derivatives ; Ticlopidine/therapeutic use
    Chemical Substances Piperazines ; Platelet Aggregation Inhibitors ; Purinergic P2Y Receptor Antagonists ; Thiophenes ; clopidogrel (A74586SNO7) ; Prasugrel Hydrochloride (G89JQ59I13) ; Ticagrelor (GLH0314RVC) ; Adenosine (K72T3FS567) ; Ticlopidine (OM90ZUW7M1)
    Language Polish
    Publishing date 2012
    Publishing country Poland
    Document type Letter
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: A Meta-Analysis Evaluating the Colchicine Therapy in Patients With Coronary Artery Disease.

    Grajek, Stefan / Michalak, Michał / Urbanowicz, Tomasz / Olasińska-Wiśniewska, Anna

    Frontiers in cardiovascular medicine

    2021  Volume 8, Page(s) 740896

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2021-12-09
    Publishing country Switzerland
    Document type Systematic Review
    ZDB-ID 2781496-8
    ISSN 2297-055X
    ISSN 2297-055X
    DOI 10.3389/fcvm.2021.740896
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Szczęki w oceanie sartanów.

    Grajek, Stefan

    Kardiologia polska

    2010  Volume 68, Issue 10, Page(s) 1186–1188

    Title translation Comment to article "Szczęki" w oceanie sartanów.
    Language Polish
    Publishing date 2010-10
    Publishing country Poland
    Document type Comment ; Journal Article
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The impact of left circumflex coronary artery ostium stenosis on outcomes for patients after percutaneous coronary intervention for unprotected left main disease.

    Skorupski, Wojciech Jan / Kałużna-Oleksy, Marta / Mitkowski, Przemysław / Araszkiewicz, Aleksander / Skorupski, Włodzimierz / Grajek, Stefan / Pyda, Małgorzata / Lesiak, Maciej / Grygier, Marek

    Kardiologia polska

    2023  Volume 81, Issue 9, Page(s) 903–908

    Abstract: Background: The impact of left circumflex coronary artery (LCX) ostium atherosclerosis in left main coronary artery (LM) bifurcation disease is not well-known.: Aim: The study aimed to assess whether the involvement of LCX ostium carries prognostic ... ...

    Abstract Background: The impact of left circumflex coronary artery (LCX) ostium atherosclerosis in left main coronary artery (LM) bifurcation disease is not well-known.
    Aim: The study aimed to assess whether the involvement of LCX ostium carries prognostic implications in patients undergoing unprotected LM percutaneous coronary intervention (PCI).
    Methods: Consecutive 564 patients with unprotected LM (ULMCA) disease who underwent LM PCI between January 2015 and February 2021, with at least 1 year of available follow-up were included in the study. The first group was composed of 145 patients with ULMCA disease with LCX ostium stenosis, and the second group consisted of 419 patients with ULMCA disease without LCX ostium stenosis.
    Results: Patients in the group with ULMCA disease with LCX ostium stenosis were significantly older and had more comorbidities. The two-stent technique was used more often in the group with LCX ostium stenosis (62.8% vs. 14.6%; P <0.001). During 7-year follow-up, all-cause mortality did not differ significantly between groups with and without LCX ostium stenosis (P = 0.50). The use of one-stent or two-stent technique also did not impact mortality in patients with LCX ostial lesions (P = 0.75). Long-term mortality subanalysis for three groups of patients: (1) patients with LM plus LCX ostium stenosis; (2) LM plus left anterior descending artery (LAD) ostium stenosis; (3) LM plus LCX ostium plus LAD ostium stenosis also did not differ significantly (P = 0.63).
    Conclusions: LCX ostium involvement in LM disease PCI is not associated with adverse long-term outcomes, which is highly beneficial for the Heart Team's decision-making process.
    MeSH term(s) Humans ; Coronary Artery Disease/complications ; Coronary Artery Disease/surgery ; Coronary Vessels/surgery ; Percutaneous Coronary Intervention/adverse effects ; Constriction, Pathologic/etiology ; Constriction, Pathologic/pathology ; Coronary Angiography ; Treatment Outcome ; Drug-Eluting Stents ; Coronary Stenosis/surgery ; Coronary Stenosis/etiology
    Language English
    Publishing date 2023-07-25
    Publishing country Poland
    Document type Journal Article
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    DOI 10.33963/KP.a2023.0156
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Inhibitory enzymu konwertujacego w ostrym zawale serca z uniesieniem odcinka ST w 2008 r. Czy wobec powszechnego stosowania przezskórnej angioplastyki leki te musza być nadal stosowane w ostrej fazie zawału serca?

    Grajek, Stefan

    Kardiologia polska

    2008  Volume 66, Issue 7, Page(s) 781–785

    Title translation ACE-I in acute myocardial infarction. State of art - 2008 year.
    MeSH term(s) Angiotensin-Converting Enzyme Inhibitors/therapeutic use ; Humans ; Myocardial Infarction/drug therapy
    Chemical Substances Angiotensin-Converting Enzyme Inhibitors
    Language Polish
    Publishing date 2008-07
    Publishing country Poland
    Document type Journal Article ; Review
    ZDB-ID 411492-9
    ISSN 0022-9032
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Czy inhibitory receptora angiotensyny zwiekszaja ryzyko zawału serca? Krajobraz po badaniu ONTARGET.

    Grajek, Stefan

    Kardiologia polska

    2008  Volume 66, Issue 12, Page(s) 1313–1324

    Title translation Do angiotensin receptor blockers increased the risk of myocardial infarction? The landscape after ONTARGET study.
    MeSH term(s) Angiotensin II Type 1 Receptor Blockers/adverse effects ; Angiotensin Receptor Antagonists ; Animals ; Antihypertensive Agents/adverse effects ; Humans ; Myocardial Infarction/chemically induced ; Randomized Controlled Trials as Topic ; Risk Factors
    Chemical Substances Angiotensin II Type 1 Receptor Blockers ; Angiotensin Receptor Antagonists ; Antihypertensive Agents
    Language Polish
    Publishing date 2008-12
    Publishing country Poland
    Document type Journal Article ; Review
    ZDB-ID 411492-9
    ISSN 0022-9032
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Non-Vitamin K Antagonist Oral Anticoagulants and Risk of Myocardial Infarction in Patients with Atrial Fibrillation with or without Percutaneous Coronary Interventions: A Meta-Analysis.

    Grajek, Stefan / Kałużna-Oleksy, Marta / Siller-Matula, Jolanta M / Grajek, Maksymilian / Michalak, Michał

    Journal of personalized medicine

    2021  Volume 11, Issue 10

    Abstract: The study aimed to assess the risk of myocardial infarction (MI) and major adverse cardiac events during non-vitamin K antagonist oral anticoagulants (NOAC) compared to warfarin therapy in patients with atrial fibrillation (AF), both treated and not ... ...

    Abstract The study aimed to assess the risk of myocardial infarction (MI) and major adverse cardiac events during non-vitamin K antagonist oral anticoagulants (NOAC) compared to warfarin therapy in patients with atrial fibrillation (AF), both treated and not treated with percutaneous coronary interventions (PCI). In a systematic search, we selected eight randomized clinical trials with a total of 81,943 patients. Dabigatran, compared to warfarin, significantly increased the risk of MI (relative risk [RR] 1.38, 95% CI 1.14-1.67), while the FXa inhibitors' effect did not differ significantly from warfarin (RR 0.96, 95% CI 0.86-1.09). The RR comparison between analyzed subgroups (dabigatran vs. FXa inhibitors) showed a significant difference (Chi
    Language English
    Publishing date 2021-10-09
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662248-8
    ISSN 2075-4426
    ISSN 2075-4426
    DOI 10.3390/jpm11101013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Peri-Procedural Troponin Elevation after Percutaneous Coronary Intervention for Left Main Coronary Artery Disease.

    Skorupski, Wojciech Jan / Kałużna-Oleksy, Marta / Mitkowski, Przemysław / Skorupski, Włodzimierz / Grajek, Stefan / Pyda, Małgorzata / Araszkiewicz, Aleksander / Lesiak, Maciej / Grygier, Marek

    Journal of clinical medicine

    2022  Volume 12, Issue 1

    Abstract: Left main (LM) percutaneous coronary interventions (PCI) are challenging and highly invasive procedures. Periprocedural myocardial injury (Troponin (Tn) elevation > 99th percentile) is frequently detected after LM PCI, being identified even in up to 67% ... ...

    Abstract Left main (LM) percutaneous coronary interventions (PCI) are challenging and highly invasive procedures. Periprocedural myocardial injury (Troponin (Tn) elevation > 99th percentile) is frequently detected after LM PCI, being identified even in up to 67% of patients. However, the prognostic implications of periprocedural Tn elevation after LM PCI remain controversial. We aim to assess the impact and prognostic significance of the periprocedural troponin elevation on long-term outcomes in patients undergoing LM PCI in a real-world setting. Consecutive 673 patients who underwent LM PCI in our department between January 2015 to February 2021 were included in a prospective registry. The first group consisted of 323 patients with major cardiac Troponin I elevation defined as an elevation of Tn values > 5× the 99th percentile in patients with normal baseline values or post-procedure Tn rise by >20% in patients with elevated pre-procedure Tn in whom the Tn level was stable or falling (based on the fourth universal definition of myocardial infarction). The second group consisted of patients without major cardiac Troponin I elevation. Seven-year long-term all-cause mortality was not higher in the group with major Tn elevation (36.9% vs. 40.6%; p = 0.818). Naturally, periprocedural myocardial infarction was diagnosed only in patients from groups with major Tn elevation (4.9% of all patients). In-hospital death and other periprocedural complications did not differ significantly between the two study groups. The adjusted HRs for mortality post-PCI in patients with a periprocedural myocardial infarction were not significant. Long-term mortality subanalysis for the group with criteria for cardiac procedural myocardial injury showed no significant differences (39.5% vs. 38.8%; p = 0.997). The occurrence of Tn elevation (>1×; >5×; >35× and >70× URL) after LM PCI was not associated with adverse long-term outcomes. The results of the study suggest that the isolated periprocedural troponin elevation is not clinically significant.
    Language English
    Publishing date 2022-12-28
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm12010244
    Database MEDical Literature Analysis and Retrieval System OnLINE

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