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Bioabsorbable polym...
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Buccheri, SergioUppsala universitet,Uppsala University,Fondazione Mediterranea G.B. Morgagni,Kardiologi,Uppsala kliniska forskningscentrum (UCR)
(author)
Bioabsorbable polymer everolimus-eluting stents in patients with acute myocardial infarction : A report from the Swedish Coronary Angiography and Angioplasty Registry
- Article/chapterEnglish2018
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LIBRIS-ID:oai:lup.lub.lu.se:9c9fd4a6-a432-4d23-aff8-b0fc51179095
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https://lup.lub.lu.se/record/9c9fd4a6-a432-4d23-aff8-b0fc51179095URI
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https://doi.org/10.4244/EIJ-D-18-00392DOI
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-355163URI
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http://kipublications.ki.se/Default.aspx?queryparsed=id:138915683URI
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Language:English
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Summary in:English
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Subject category:art swepub-publicationtype
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Subject category:ref swepub-contenttype
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Aims: The clinical performance of the SYNERGY drug-eluting stent (DES) in patients with acute myocardial infarction (MI) has not been investigated in detail. We sought to report on the outcomes after SYNERGY DES (Boston Scientific, Marlborough, MA, USA) implantation in patients with MI undergoing percutaneous revascularisation (PCI). Methods and results: We included all consecutive patients with MI undergoing PCI with the SYNERGY DES and newer-generation DES (n-DES group) in Sweden. From March 2013 to September 2016, a total of 36,292 patients, of whom 39.7% presented with ST-elevation MI, were included. As compared to patients in the n-DES group (n=31,403), patients in the SYNERGY group (n=4,889) were older and presented more often with left main or three-vessel disease involvement, as well as with restenotic lesions (p<0.001 for all parameters). The Kaplan-Meier estimates of ST at two years in the SYNERGY and n-DES groups were 0.69% and 0.81%, respectively (adjusted HR 1.00, 95% CI: 0.69-1.46; p=0.99). Clinically relevant restenosis was encountered in 1.48% and 1.25% of patients in the SYNERGY and n-DES groups, respectively (adjusted HR 1.05, 95% CI: 0.81-1.37; p=0.72). No differences in the risk of all-cause death and recurrent MI were found between the two groups after adjustment (adjusted HR 1.12, 95% CI: 0.98-1.28; p=0.10, and adjusted HR 0.95, 95% CI: 0.82-1.10; p=0.49, respectively). Conclusions: In a large and unselected cohort of patients with MI undergoing percutaneous revascularisation with the SYNERGY DES, stent performance and clinical outcomes did not differ compared with other n-DES up to two years.
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Sarno, GiovannaUppsala universitet,Uppsala University,Uppsala kliniska forskningscentrum (UCR),Kardiologi(Swepub:uu)giosa853
(author)
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Lagerqvist, Bo,1952-Uppsala universitet,Uppsala University,Kardiologi,Uppsala kliniska forskningscentrum (UCR)(Swepub:uu)bolager
(author)
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Olivecrona, GöranLund University,Lunds universitet,Kardiologi,Sektion II,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Cardiology,Section II,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital(Swepub:lu)kard-gol
(author)
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Hambraeus, KristinaFalun Central Hospital
(author)
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Witt, NilsKarolinska Institutet,Karolinska Institute
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Lindholm, Daniel,1982-Uppsala universitet,Uppsala University,Kardiologi,Uppsala kliniska forskningscentrum (UCR)(Swepub:uu)danli945
(author)
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Erlinge, DavidLund University,Lunds universitet,Molekylär kardiologi,Forskargrupper vid Lunds universitet,Molecular Cardiology,Lund University Research Groups,Skåne University Hospital(Swepub:lu)kard-der
(author)
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Angerås, OskarSahlgrenska University Hospital
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James, Stefan K,1964-Uppsala universitet,Uppsala University,Kardiologi,Uppsala kliniska forskningscentrum (UCR)(Swepub:uu)stjam367
(author)
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Uppsala UniversityFondazione Mediterranea G.B. Morgagni
(creator_code:org_t)
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In:EuroIntervention14:5, s. 562-5691774-024X1969-6213
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