2018
DOI: 10.1016/j.repce.2017.06.020
|View full text |Cite
|
Sign up to set email alerts
|

Effect of beta-blocker dose on mortality after acute coronary syndrome

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
5
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(5 citation statements)
references
References 23 publications
0
5
0
Order By: Relevance
“…10,23 The true impact of beta-blocker therapy in current post-MI patients has been questioned, and a new investigation regarding beta-blocker therapy is frequently sought. 10,11,19,[24][25][26] In the current paper, post-ACS mrEF patients seem to represent an intermediate risk group, regarding past clinical history, coronary anatomy and inhospital mortality rate. This is in line with previously published studies regarding this population.…”
Section: Discussionmentioning
confidence: 75%
See 2 more Smart Citations
“…10,23 The true impact of beta-blocker therapy in current post-MI patients has been questioned, and a new investigation regarding beta-blocker therapy is frequently sought. 10,11,19,[24][25][26] In the current paper, post-ACS mrEF patients seem to represent an intermediate risk group, regarding past clinical history, coronary anatomy and inhospital mortality rate. This is in line with previously published studies regarding this population.…”
Section: Discussionmentioning
confidence: 75%
“…In this trial, beta-blocker dosage was not registered, but recent trials in European populations have identified no difference in higher versus lower doses. 11 The benefit of being started on a therapy de novo may be greater than the effect calculated by the model, as improvements may have already occurred 32our multivariate model included previous medication information in order to attenuate this difference.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…When 50 patients who died due to CV events are distributed according to their diagnoses, 13 (3.8%) of 339 patients were diagnosed with UAP (mean follow-up of 30.02 ± 7.41 months), 19 (9,2%) of 206 patients with NSTEMI (mean follow-up of 30 ± 9.21 months), and 18 (5.1%) of 356 patients with STEMI (mean follow-up of 29.86 ± 8.62 months). During follow-up, 26% (13) of CVrelated deaths were seen in the UAP group, 38% (19) in the NSTEMI group, and 36% (18) In hospital Mortality of Acute Coronary Syndrome worse in the NSTEMI group. The frequency of death, re-infarction, stroke and CABG was found to be higher in the NSTEMI group (p < 0.0001).…”
Section: Discussion Discussionmentioning
confidence: 97%
“…However, there are also publications in the literature showing that there may not be a long-term reduction in mortality with the use of high-dose titrated betablockers after ACS. 18 Given the lack of strong randomized controlled trial on the duration of beta-blocker usage in post-MI patients, a more personalized approach should be adopted (based on the LVEF, arrhythmias, etc). If the LVEF is low (< 40%), beta-blockers should be used for longer periods of time.…”
Section: Discussion Discussionmentioning
confidence: 99%