Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery: A nationwide cohort study

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery : A nationwide cohort study. / Jørgensen, Mads E.; Sanders, Robert D.; Køber, Lars; Mehta, Kala; Torp-Pedersen, Christian; Hlatky, Mark A.; Pallisgaard, Jannik L.; Shaw, Richard E.; Gislason, Gunnar H.; Jensen, Per F.; Andersson, Charlotte.

I: European Heart Journal, Bind 38, Nr. 31, 2017, s. 2421-2428.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jørgensen, ME, Sanders, RD, Køber, L, Mehta, K, Torp-Pedersen, C, Hlatky, MA, Pallisgaard, JL, Shaw, RE, Gislason, GH, Jensen, PF & Andersson, C 2017, 'Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery: A nationwide cohort study', European Heart Journal, bind 38, nr. 31, s. 2421-2428. https://doi.org/10.1093/eurheartj/ehx214

APA

Jørgensen, M. E., Sanders, R. D., Køber, L., Mehta, K., Torp-Pedersen, C., Hlatky, M. A., Pallisgaard, J. L., Shaw, R. E., Gislason, G. H., Jensen, P. F., & Andersson, C. (2017). Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery: A nationwide cohort study. European Heart Journal, 38(31), 2421-2428. https://doi.org/10.1093/eurheartj/ehx214

Vancouver

Jørgensen ME, Sanders RD, Køber L, Mehta K, Torp-Pedersen C, Hlatky MA o.a. Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery: A nationwide cohort study. European Heart Journal. 2017;38(31):2421-2428. https://doi.org/10.1093/eurheartj/ehx214

Author

Jørgensen, Mads E. ; Sanders, Robert D. ; Køber, Lars ; Mehta, Kala ; Torp-Pedersen, Christian ; Hlatky, Mark A. ; Pallisgaard, Jannik L. ; Shaw, Richard E. ; Gislason, Gunnar H. ; Jensen, Per F. ; Andersson, Charlotte. / Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery : A nationwide cohort study. I: European Heart Journal. 2017 ; Bind 38, Nr. 31. s. 2421-2428.

Bibtex

@article{c0023837f0cc4ded9bc93f88b7223ac9,
title = "Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery: A nationwide cohort study",
abstract = "Aims Beta-blockers vary in pharmacodynamics and pharmacokinetic properties. It is unknown whether specific types are associated with increased perioperative risks. We evaluated perioperative risks associated with beta-blocker subtypes, overall and in patient subgroups. Methods and results We performed a Danish Nationwide cohort study, 2005-2011, of patients treated chronically with beta blocker (atenolol, bisoprolol, carvedilol, metoprolol, propranolol, or other) prior to non-cardiac surgery. Risks of 30-day all-cause mortality (ACM) and 30-day major adverse cardiovascular events (MACE) were estimated using adjusted logistic regression models and odds ratios with 95% confidence intervals. We identified 61 660 patients, most frequently treated with metoprolol (67% of patients, mean age 69 years, 49% males), atenolol (10% of patients, mean age 68 years, 36% males), or carvedilol (9% of patients, mean age 68 years, 60% males). The crude incidences of ACM and MACE were 4.1 and 3.5% in patients with metoprolol, 3.0 and 2.3% with atenolol, and 4.8 and 4.6% with carvedilol. In adjusted models, risks were not significantly different with atenolol (ACM; 1.10 [0.92-1.32], MACE; 1.08 [0.90-1.31]) or carvedilol (ACM; 0.99 [0.85-1.16], MACE; 1.07 [0.92-1.25]), compared with metoprolol. Risks of ACM were significantly lower in prior myocardial infarction patients treated with carvedilol (0.62 [0.43-0.87]) and no different in patients with uncomplicated hypertension (1.41 [0.83-2.40]). Risks did not differ in analyses stratified by age, surgery priority, duration of anaesthesia or surgery risk (all P for interaction >0.05). Conclusion Risks of ACM and MACE did not systematically differ by beta-blocker subtype. Findings may guide clinical practice and future trials.",
keywords = "Beta-blocker, Outcomes, Perioperative risks, Safety, Surgery",
author = "J{\o}rgensen, {Mads E.} and Sanders, {Robert D.} and Lars K{\o}ber and Kala Mehta and Christian Torp-Pedersen and Hlatky, {Mark A.} and Pallisgaard, {Jannik L.} and Shaw, {Richard E.} and Gislason, {Gunnar H.} and Jensen, {Per F.} and Charlotte Andersson",
year = "2017",
doi = "10.1093/eurheartj/ehx214",
language = "English",
volume = "38",
pages = "2421--2428",
journal = "European Heart Journal",
issn = "0195-668X",
publisher = "Oxford University Press",
number = "31",

}

RIS

TY - JOUR

T1 - Beta-blocker subtype and risks of perioperative adverse events following non-cardiac surgery

T2 - A nationwide cohort study

AU - Jørgensen, Mads E.

AU - Sanders, Robert D.

AU - Køber, Lars

AU - Mehta, Kala

AU - Torp-Pedersen, Christian

AU - Hlatky, Mark A.

AU - Pallisgaard, Jannik L.

AU - Shaw, Richard E.

AU - Gislason, Gunnar H.

AU - Jensen, Per F.

AU - Andersson, Charlotte

PY - 2017

Y1 - 2017

N2 - Aims Beta-blockers vary in pharmacodynamics and pharmacokinetic properties. It is unknown whether specific types are associated with increased perioperative risks. We evaluated perioperative risks associated with beta-blocker subtypes, overall and in patient subgroups. Methods and results We performed a Danish Nationwide cohort study, 2005-2011, of patients treated chronically with beta blocker (atenolol, bisoprolol, carvedilol, metoprolol, propranolol, or other) prior to non-cardiac surgery. Risks of 30-day all-cause mortality (ACM) and 30-day major adverse cardiovascular events (MACE) were estimated using adjusted logistic regression models and odds ratios with 95% confidence intervals. We identified 61 660 patients, most frequently treated with metoprolol (67% of patients, mean age 69 years, 49% males), atenolol (10% of patients, mean age 68 years, 36% males), or carvedilol (9% of patients, mean age 68 years, 60% males). The crude incidences of ACM and MACE were 4.1 and 3.5% in patients with metoprolol, 3.0 and 2.3% with atenolol, and 4.8 and 4.6% with carvedilol. In adjusted models, risks were not significantly different with atenolol (ACM; 1.10 [0.92-1.32], MACE; 1.08 [0.90-1.31]) or carvedilol (ACM; 0.99 [0.85-1.16], MACE; 1.07 [0.92-1.25]), compared with metoprolol. Risks of ACM were significantly lower in prior myocardial infarction patients treated with carvedilol (0.62 [0.43-0.87]) and no different in patients with uncomplicated hypertension (1.41 [0.83-2.40]). Risks did not differ in analyses stratified by age, surgery priority, duration of anaesthesia or surgery risk (all P for interaction >0.05). Conclusion Risks of ACM and MACE did not systematically differ by beta-blocker subtype. Findings may guide clinical practice and future trials.

AB - Aims Beta-blockers vary in pharmacodynamics and pharmacokinetic properties. It is unknown whether specific types are associated with increased perioperative risks. We evaluated perioperative risks associated with beta-blocker subtypes, overall and in patient subgroups. Methods and results We performed a Danish Nationwide cohort study, 2005-2011, of patients treated chronically with beta blocker (atenolol, bisoprolol, carvedilol, metoprolol, propranolol, or other) prior to non-cardiac surgery. Risks of 30-day all-cause mortality (ACM) and 30-day major adverse cardiovascular events (MACE) were estimated using adjusted logistic regression models and odds ratios with 95% confidence intervals. We identified 61 660 patients, most frequently treated with metoprolol (67% of patients, mean age 69 years, 49% males), atenolol (10% of patients, mean age 68 years, 36% males), or carvedilol (9% of patients, mean age 68 years, 60% males). The crude incidences of ACM and MACE were 4.1 and 3.5% in patients with metoprolol, 3.0 and 2.3% with atenolol, and 4.8 and 4.6% with carvedilol. In adjusted models, risks were not significantly different with atenolol (ACM; 1.10 [0.92-1.32], MACE; 1.08 [0.90-1.31]) or carvedilol (ACM; 0.99 [0.85-1.16], MACE; 1.07 [0.92-1.25]), compared with metoprolol. Risks of ACM were significantly lower in prior myocardial infarction patients treated with carvedilol (0.62 [0.43-0.87]) and no different in patients with uncomplicated hypertension (1.41 [0.83-2.40]). Risks did not differ in analyses stratified by age, surgery priority, duration of anaesthesia or surgery risk (all P for interaction >0.05). Conclusion Risks of ACM and MACE did not systematically differ by beta-blocker subtype. Findings may guide clinical practice and future trials.

KW - Beta-blocker

KW - Outcomes

KW - Perioperative risks

KW - Safety

KW - Surgery

U2 - 10.1093/eurheartj/ehx214

DO - 10.1093/eurheartj/ehx214

M3 - Journal article

C2 - 28472245

AN - SCOPUS:85032724302

VL - 38

SP - 2421

EP - 2428

JO - European Heart Journal

JF - European Heart Journal

SN - 0195-668X

IS - 31

ER -

ID: 189462840