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Association between β-blocker dose and cardiovascular outcomes after myocardial infarction : insights from the SWEDEHEART registry

Mars, Katarina (författare)
Karolinska Institutet
Wallert, John (författare)
Karolinska Institutet
Held, Claes, 1956- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR),Kardiologi
visa fler...
Humphries, Sophia (författare)
Uppsala universitet,Klinisk psykologi i hälso- och sjukvård
Pingel, Ronnie, 1978- (författare)
Uppsala universitet,Statistiska institutionen
Jernberg, Tomas (författare)
Karolinska Institutet
Olsson, Erik M. G., 1967- (författare)
Uppsala universitet,Klinisk psykologi i hälso- och sjukvård
Hofmann, Robin (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
2020-09-01
2020
Engelska.
Ingår i: European Heart Journal. - : Oxford University Press (OUP). - 2048-8726 .- 2048-8734. ; 10:4, s. 372-379
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • AimsDose-dependent effects of β-blockers on survival and cardiovascular outcomes after myocardial infarction (MI) are not well understood. We investigated the long-term risk of cardiovascular events in patients with different doses of β-blockers after MI.Methods and resultsThis was a nationwide observational study linking morbidity, mortality, socioeconomic, and medication data from Swedish national registries. Between 2006 and 2015, 97 575 unique patients with first-time MI were included. In total, 33 126 (33.9%) patients were discharged with ≥50% of the target β-blocker dose and 64 449 (66.1%) patients with <50% of the target β-blocker dose used in previous randomized trials. The primary composite endpoint was re-infarction or all-cause death within 1 year from discharge. Multivariable adjusted 1-year follow-up estimates using mixed effects Cox regression [HR (95% CI)] showed that patients treated with ≥50% of the target dose had a similar risk of the composite endpoint [1.03 (0.99–1.08)] and a somewhat higher risk when stroke, atrial fibrillation, or heart failure hospitalization were added to the composite endpoint [1.08 (1.04–1.12)], compared with patients on <50% of the target β-blocker dose. Results remained similar up to 5 years of follow-up and consistent across relevant patient subgroups, including patients who developed heart failure during the index hospitalization.ConclusionsIn contrast to doses of β-blockers used in previous trials, ≥50% of the target β-blocker dose was not associated with superior cardiovascular outcomes up to 5 years as compared with <50% of the target dose. Contemporary randomized clinical trials are needed to clarify the optimal dose of β-blockers after MI.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Myocardial infarction
Adrenergic beta-antagonist
Mortality
Nationwide register data
Prognosis

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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