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Long-term follow-up of complete versus lesion-only revascularization in STEMI and multivessel disease: The CvLPRIT trial

Long-term follow-up of complete versus lesion-only revascularization in STEMI and multivessel disease: The CvLPRIT trial
Long-term follow-up of complete versus lesion-only revascularization in STEMI and multivessel disease: The CvLPRIT trial

BACKGROUND: Randomized trials have shown that complete revascularization in patients with ST-segment elevation myocardial infarction (MI) with multivessel disease results in lower major adverse cardiovascular events (MACE) (all-cause death, MI, ischemia-driven revascularization, heart failure).

OBJECTIVES: The goal of this study was to determine whether the benefits of complete revascularization are sustained long-term and their impact on hard endpoints.

METHODS: CvLPRIT (Complete versus Lesion-only Primary PCI Trial) was a randomized trial of complete inpatient revascularization versus infarct-related artery revascularization only at the index admission. Randomized patients have been followed longer-term. The components of the original primary endpoint were collected from physical and electronic patient records, and from local databases for all readmissions.

RESULTS: The median follow-up (achieved in >90% patients) from randomization to first event or last follow-up was 5.6 years (0.0 to 7.3 years). The primary MACE endpoint rate at this time point was 24.0% in the complete revascularization group but 37.7% of the infarct-related artery-only group (hazard ratio: 0.57; 95% confidence interval: 0.37 to 0.87; p = 0.0079). The composite endpoint of all-cause death/MI was 10.0% in the complete revascularization group versus 18.5% in the infarct-related artery-only group (hazard ratio: 0.47; 95% confidence interval: 0.25 to 0.89; p = 0.0175). In a landmark analysis (from 12 months to final follow-up), there was no significant difference between MACE, death/MI, and individual components of the primary endpoint.

CONCLUSIONS: Long-term follow-up of the CvLPRIT trial shows that the significantly lower rate of MACE in the complete revascularization group, previously seen at 12 months, is sustained to a median of 5.6 years. A significant difference in composite all-cause death/MI favoring the complete revascularization was also observed. (Complete versus Lesion-only Primary PCI Trial; ISRCTN70913605).

0735-1097
3083-3094
Gershlick, Anthony H.
5beb7f92-68f7-41df-ba72-ef3d2cdf20b9
Banning, Amerjeet S.
8c5d4cd8-42f9-4df7-bc17-a55d48eecbfd
Parker, Emma
fb1f220e-8edf-48c1-a00a-c87bd05bd9a8
Wang, Duolao
deae0e52-e682-47d6-af54-4aa41afbc386
Budgeon, Charley A.
3c42d1da-16b6-4de1-b444-e65d58484561
Kelly, Damian J.
2dc363f6-884a-4f82-a4d7-bfadf72f9533
Kane, Peter O.
42387f42-1c88-47f1-8856-5987849d8441
Dalby, Miles
0296ef2f-0e85-41da-974c-2e709b9494c6
Hetherington, Simon L.
cab8fada-9654-4417-ae2f-c04838e52e77
McCann, Gerry P.
8e61a5f4-0764-4adf-bc9c-5abba82425fc
Greenwood, John P.
af864161-94e9-4094-9c1f-85d696682fb7
Curzen, Nicholas
70f3ea49-51b1-418f-8e56-8210aef1abf4
Gershlick, Anthony H.
5beb7f92-68f7-41df-ba72-ef3d2cdf20b9
Banning, Amerjeet S.
8c5d4cd8-42f9-4df7-bc17-a55d48eecbfd
Parker, Emma
fb1f220e-8edf-48c1-a00a-c87bd05bd9a8
Wang, Duolao
deae0e52-e682-47d6-af54-4aa41afbc386
Budgeon, Charley A.
3c42d1da-16b6-4de1-b444-e65d58484561
Kelly, Damian J.
2dc363f6-884a-4f82-a4d7-bfadf72f9533
Kane, Peter O.
42387f42-1c88-47f1-8856-5987849d8441
Dalby, Miles
0296ef2f-0e85-41da-974c-2e709b9494c6
Hetherington, Simon L.
cab8fada-9654-4417-ae2f-c04838e52e77
McCann, Gerry P.
8e61a5f4-0764-4adf-bc9c-5abba82425fc
Greenwood, John P.
af864161-94e9-4094-9c1f-85d696682fb7
Curzen, Nicholas
70f3ea49-51b1-418f-8e56-8210aef1abf4

Gershlick, Anthony H., Banning, Amerjeet S., Parker, Emma, Wang, Duolao, Budgeon, Charley A., Kelly, Damian J., Kane, Peter O., Dalby, Miles, Hetherington, Simon L., McCann, Gerry P., Greenwood, John P. and Curzen, Nicholas (2019) Long-term follow-up of complete versus lesion-only revascularization in STEMI and multivessel disease: The CvLPRIT trial. Journal of the American College of Cardiology, 74 (25), 3083-3094. (doi:10.1016/j.jacc.2019.10.033).

Record type: Article

Abstract

BACKGROUND: Randomized trials have shown that complete revascularization in patients with ST-segment elevation myocardial infarction (MI) with multivessel disease results in lower major adverse cardiovascular events (MACE) (all-cause death, MI, ischemia-driven revascularization, heart failure).

OBJECTIVES: The goal of this study was to determine whether the benefits of complete revascularization are sustained long-term and their impact on hard endpoints.

METHODS: CvLPRIT (Complete versus Lesion-only Primary PCI Trial) was a randomized trial of complete inpatient revascularization versus infarct-related artery revascularization only at the index admission. Randomized patients have been followed longer-term. The components of the original primary endpoint were collected from physical and electronic patient records, and from local databases for all readmissions.

RESULTS: The median follow-up (achieved in >90% patients) from randomization to first event or last follow-up was 5.6 years (0.0 to 7.3 years). The primary MACE endpoint rate at this time point was 24.0% in the complete revascularization group but 37.7% of the infarct-related artery-only group (hazard ratio: 0.57; 95% confidence interval: 0.37 to 0.87; p = 0.0079). The composite endpoint of all-cause death/MI was 10.0% in the complete revascularization group versus 18.5% in the infarct-related artery-only group (hazard ratio: 0.47; 95% confidence interval: 0.25 to 0.89; p = 0.0175). In a landmark analysis (from 12 months to final follow-up), there was no significant difference between MACE, death/MI, and individual components of the primary endpoint.

CONCLUSIONS: Long-term follow-up of the CvLPRIT trial shows that the significantly lower rate of MACE in the complete revascularization group, previously seen at 12 months, is sustained to a median of 5.6 years. A significant difference in composite all-cause death/MI favoring the complete revascularization was also observed. (Complete versus Lesion-only Primary PCI Trial; ISRCTN70913605).

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More information

Accepted/In Press date: 6 October 2019
e-pub ahead of print date: 16 December 2019
Published date: 24 December 2019

Identifiers

Local EPrints ID: 438684
URI: http://eprints.soton.ac.uk/id/eprint/438684
ISSN: 0735-1097
PURE UUID: f59bd736-c727-4923-ba8a-c5814088ecb7
ORCID for Nicholas Curzen: ORCID iD orcid.org/0000-0001-9651-7829

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Date deposited: 20 Mar 2020 17:37
Last modified: 17 Mar 2024 03:02

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Contributors

Author: Anthony H. Gershlick
Author: Amerjeet S. Banning
Author: Emma Parker
Author: Duolao Wang
Author: Charley A. Budgeon
Author: Damian J. Kelly
Author: Peter O. Kane
Author: Miles Dalby
Author: Simon L. Hetherington
Author: Gerry P. McCann
Author: John P. Greenwood
Author: Nicholas Curzen ORCID iD

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