Drug-Eluting versus Bare-Metal Stents in Saphenous Vein Grafts Compared to Native Coronary Vessels: The Norwegian Coronary Stent Trial Study

Background: Drug-eluting stents (DES) reduce target lesion revascularization (TLR) with no effect on mortality or myocardial infarction (MI) compared to bare-metal stents (BMS) in native vessels. Randomized stent studies in saphenous vein grafts (SVG) are few and the reported effects are ambiguous....

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Veröffentlicht in:Cardiology 2022-01, Vol.147 (1), p.14-22
Hauptverfasser: Mølstad, Per Morten, Nordrehaug, Jan Erik, Steigen, Terje K., Wilsgaard, Tom, Wiseth, Rune, Rotevatn, Svein, Mannsverk, Jan, Larsen, Tommy, Larsby, Kristina Elisabet, Skarstad, Sigrun Ådnegard, Fosse, Eivind Øygard, Dahl-Eriksen, Øystein, Bønaa, Kaare Harald
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container_end_page 22
container_issue 1
container_start_page 14
container_title Cardiology
container_volume 147
creator Mølstad, Per Morten
Nordrehaug, Jan Erik
Steigen, Terje K.
Wilsgaard, Tom
Wiseth, Rune
Rotevatn, Svein
Mannsverk, Jan
Larsen, Tommy
Larsby, Kristina Elisabet
Skarstad, Sigrun Ådnegard
Fosse, Eivind Øygard
Dahl-Eriksen, Øystein
Bønaa, Kaare Harald
description Background: Drug-eluting stents (DES) reduce target lesion revascularization (TLR) with no effect on mortality or myocardial infarction (MI) compared to bare-metal stents (BMS) in native vessels. Randomized stent studies in saphenous vein grafts (SVG) are few and the reported effects are ambiguous. The Norwegian Coronary Stent Trial study is the first to randomize lesions to percutaneous coronary intervention in native vessels and SVG. Aims: The aim of this study was to compare the rate of mortality, MI, and TLR across stent and vessel types. Methods: In this substudy, 6,087 patients with a single lesion in native vessels and 164 in SVG were followed for 5 years. Results: MI was more frequent in SVG (subdistributional hazard ratio [SHR] 4.95 (3.75–6.54, p < 0.001), but not affected by stent type. In the first 500 days, DES reduced TLR in native vessels (SHR 0.21 (0.15–0.30) p < 0.001) and SVG (SHR 0.18 (0.04–0.80) p = 0.02). Thereafter, DES and BMS were equivalent in native vessels, but DES had a higher TLR rate than BMS in SVG (SHR 3.31 (1.23–8.94) p = 0.02). After 5 years, the TLR rate was still significantly lower for DES in native vessels (3.2% vs. 7.8%, p < 0.001) but not in SVG (21.4% vs. 18. 4%). Conclusion: In SVG, no difference in TLR between DES and BMS was observed after 5 years in contrast to persistent benefit in native vessels. The high rate of TLR and MI in SVG makes treatment of native vessels a preference whenever feasible and better treatment options for SVG are warranted.
doi_str_mv 10.1159/000521085
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Randomized stent studies in saphenous vein grafts (SVG) are few and the reported effects are ambiguous. The Norwegian Coronary Stent Trial study is the first to randomize lesions to percutaneous coronary intervention in native vessels and SVG. Aims: The aim of this study was to compare the rate of mortality, MI, and TLR across stent and vessel types. Methods: In this substudy, 6,087 patients with a single lesion in native vessels and 164 in SVG were followed for 5 years. Results: MI was more frequent in SVG (subdistributional hazard ratio [SHR] 4.95 (3.75–6.54, p &lt; 0.001), but not affected by stent type. In the first 500 days, DES reduced TLR in native vessels (SHR 0.21 (0.15–0.30) p &lt; 0.001) and SVG (SHR 0.18 (0.04–0.80) p = 0.02). Thereafter, DES and BMS were equivalent in native vessels, but DES had a higher TLR rate than BMS in SVG (SHR 3.31 (1.23–8.94) p = 0.02). After 5 years, the TLR rate was still significantly lower for DES in native vessels (3.2% vs. 7.8%, p &lt; 0.001) but not in SVG (21.4% vs. 18. 4%). Conclusion: In SVG, no difference in TLR between DES and BMS was observed after 5 years in contrast to persistent benefit in native vessels. The high rate of TLR and MI in SVG makes treatment of native vessels a preference whenever feasible and better treatment options for SVG are warranted.</description><identifier>ISSN: 0008-6312</identifier><identifier>ISSN: 1421-9751</identifier><identifier>EISSN: 1421-9751</identifier><identifier>DOI: 10.1159/000521085</identifier><identifier>PMID: 34879374</identifier><language>eng</language><publisher>Basel, Switzerland: Karger Publishers</publisher><subject>CAD and AMI: Research Article ; Coronary Vessels ; Drug-Eluting Stents ; Humans ; Metals ; Percutaneous Coronary Intervention ; Pharmaceutical Preparations ; Prosthesis Design ; Risk Factors ; Saphenous Vein - transplantation ; Stents ; Treatment Outcome</subject><ispartof>Cardiology, 2022-01, Vol.147 (1), p.14-22</ispartof><rights>2021 S. Karger AG, Basel</rights><rights>2021 S. Karger AG, Basel.</rights><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c353t-74afa5df92eb36159c81df557c93d50e11892d72772549b80e0a23c0d83b1d5b3</cites><orcidid>0000-0002-1216-3718 ; 0000-0002-2709-9472 ; 0000-0001-6988-1123 ; 0000-0002-3040-6410 ; 0000-0001-6933-5712</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,2427,26566,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34879374$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mølstad, Per Morten</creatorcontrib><creatorcontrib>Nordrehaug, Jan Erik</creatorcontrib><creatorcontrib>Steigen, Terje K.</creatorcontrib><creatorcontrib>Wilsgaard, Tom</creatorcontrib><creatorcontrib>Wiseth, Rune</creatorcontrib><creatorcontrib>Rotevatn, Svein</creatorcontrib><creatorcontrib>Mannsverk, Jan</creatorcontrib><creatorcontrib>Larsen, Tommy</creatorcontrib><creatorcontrib>Larsby, Kristina Elisabet</creatorcontrib><creatorcontrib>Skarstad, Sigrun Ådnegard</creatorcontrib><creatorcontrib>Fosse, Eivind Øygard</creatorcontrib><creatorcontrib>Dahl-Eriksen, Øystein</creatorcontrib><creatorcontrib>Bønaa, Kaare Harald</creatorcontrib><title>Drug-Eluting versus Bare-Metal Stents in Saphenous Vein Grafts Compared to Native Coronary Vessels: The Norwegian Coronary Stent Trial Study</title><title>Cardiology</title><addtitle>Cardiology</addtitle><description>Background: Drug-eluting stents (DES) reduce target lesion revascularization (TLR) with no effect on mortality or myocardial infarction (MI) compared to bare-metal stents (BMS) in native vessels. Randomized stent studies in saphenous vein grafts (SVG) are few and the reported effects are ambiguous. The Norwegian Coronary Stent Trial study is the first to randomize lesions to percutaneous coronary intervention in native vessels and SVG. Aims: The aim of this study was to compare the rate of mortality, MI, and TLR across stent and vessel types. Methods: In this substudy, 6,087 patients with a single lesion in native vessels and 164 in SVG were followed for 5 years. Results: MI was more frequent in SVG (subdistributional hazard ratio [SHR] 4.95 (3.75–6.54, p &lt; 0.001), but not affected by stent type. In the first 500 days, DES reduced TLR in native vessels (SHR 0.21 (0.15–0.30) p &lt; 0.001) and SVG (SHR 0.18 (0.04–0.80) p = 0.02). Thereafter, DES and BMS were equivalent in native vessels, but DES had a higher TLR rate than BMS in SVG (SHR 3.31 (1.23–8.94) p = 0.02). 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Randomized stent studies in saphenous vein grafts (SVG) are few and the reported effects are ambiguous. The Norwegian Coronary Stent Trial study is the first to randomize lesions to percutaneous coronary intervention in native vessels and SVG. Aims: The aim of this study was to compare the rate of mortality, MI, and TLR across stent and vessel types. Methods: In this substudy, 6,087 patients with a single lesion in native vessels and 164 in SVG were followed for 5 years. Results: MI was more frequent in SVG (subdistributional hazard ratio [SHR] 4.95 (3.75–6.54, p &lt; 0.001), but not affected by stent type. In the first 500 days, DES reduced TLR in native vessels (SHR 0.21 (0.15–0.30) p &lt; 0.001) and SVG (SHR 0.18 (0.04–0.80) p = 0.02). Thereafter, DES and BMS were equivalent in native vessels, but DES had a higher TLR rate than BMS in SVG (SHR 3.31 (1.23–8.94) p = 0.02). After 5 years, the TLR rate was still significantly lower for DES in native vessels (3.2% vs. 7.8%, p &lt; 0.001) but not in SVG (21.4% vs. 18. 4%). Conclusion: In SVG, no difference in TLR between DES and BMS was observed after 5 years in contrast to persistent benefit in native vessels. The high rate of TLR and MI in SVG makes treatment of native vessels a preference whenever feasible and better treatment options for SVG are warranted.</abstract><cop>Basel, Switzerland</cop><pub>Karger Publishers</pub><pmid>34879374</pmid><doi>10.1159/000521085</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1216-3718</orcidid><orcidid>https://orcid.org/0000-0002-2709-9472</orcidid><orcidid>https://orcid.org/0000-0001-6988-1123</orcidid><orcidid>https://orcid.org/0000-0002-3040-6410</orcidid><orcidid>https://orcid.org/0000-0001-6933-5712</orcidid><oa>free_for_read</oa></addata></record>
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ispartof Cardiology, 2022-01, Vol.147 (1), p.14-22
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source MEDLINE; NORA - Norwegian Open Research Archives; Karger Journals
subjects CAD and AMI: Research Article
Coronary Vessels
Drug-Eluting Stents
Humans
Metals
Percutaneous Coronary Intervention
Pharmaceutical Preparations
Prosthesis Design
Risk Factors
Saphenous Vein - transplantation
Stents
Treatment Outcome
title Drug-Eluting versus Bare-Metal Stents in Saphenous Vein Grafts Compared to Native Coronary Vessels: The Norwegian Coronary Stent Trial Study
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