Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants. / Holt, Anders; Blanche, Paul; Zareini, Bochra; Rasmussen, Peter Vibe; Strange, Jarl Emanuel; Rajan, Deepthi; Jensen, Mads Hashiba; El-Sheikh, Mohammed; Schjerning, Anne-Marie; Schou, Morten; Gislason, Gunnar; Torp-Pedersen, Christian; McGettigan, Patricia; Lamberts, Morten.

In: Heart, Vol. 108, No. 8, 2022, p. 626-632.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Holt, A, Blanche, P, Zareini, B, Rasmussen, PV, Strange, JE, Rajan, D, Jensen, MH, El-Sheikh, M, Schjerning, A-M, Schou, M, Gislason, G, Torp-Pedersen, C, McGettigan, P & Lamberts, M 2022, 'Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants', Heart, vol. 108, no. 8, pp. 626-632. https://doi.org/10.1136/heartjnl-2021-319503

APA

Holt, A., Blanche, P., Zareini, B., Rasmussen, P. V., Strange, J. E., Rajan, D., Jensen, M. H., El-Sheikh, M., Schjerning, A-M., Schou, M., Gislason, G., Torp-Pedersen, C., McGettigan, P., & Lamberts, M. (2022). Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants. Heart, 108(8), 626-632. https://doi.org/10.1136/heartjnl-2021-319503

Vancouver

Holt A, Blanche P, Zareini B, Rasmussen PV, Strange JE, Rajan D et al. Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants. Heart. 2022;108(8):626-632. https://doi.org/10.1136/heartjnl-2021-319503

Author

Holt, Anders ; Blanche, Paul ; Zareini, Bochra ; Rasmussen, Peter Vibe ; Strange, Jarl Emanuel ; Rajan, Deepthi ; Jensen, Mads Hashiba ; El-Sheikh, Mohammed ; Schjerning, Anne-Marie ; Schou, Morten ; Gislason, Gunnar ; Torp-Pedersen, Christian ; McGettigan, Patricia ; Lamberts, Morten. / Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants. In: Heart. 2022 ; Vol. 108, No. 8. pp. 626-632.

Bibtex

@article{6b91012b6bc543c880123f0dc975969a,
title = "Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants",
abstract = "Objective Gastrointestinal bleeding (GIB) risk in relation to concomitant treatment with non-vitamin K oral anticoagulants (NOAC) and oral glucocorticoids is insufficiently explored. We aimed to investigate the short-term risk following coexposure.Methods This is a register-based, nationwide Danish study including patients with atrial fibrillation on NOACs during 2012–2018. Patients were defined as exposed to oral glucocorticoids if they claimed a prescription within 60 days prior to GIB. We investigated the associations between GIB and oral glucocorticoid exposure, reporting HRs via a nested case–control design and absolute risk via a cohort design. Matching terms were age, sex, calendar year, follow-up time and NOAC agent.Results 98 376 patients on NOACs (median age: 75 years (IQR: 68–82), 44% female) were included, and 16% redeemed at least one oral glucocorticoid prescription within 3 years. HRs of GIB were increased comparing exposed with non-exposed patients (<20 mg daily dose, HR 1.54 (95% CI 1.29 to 1.84); ≥20 mg daily dose, HR 2.19 (95% CI 1.81 to 2.65)). 60-day standardised absolute risk of GIB following first claimed oral glucocorticoid prescription increased compared with non-exposed: 60-day absolute risk: 0.71% (95% CI 0.58% to 0.85%) vs 0.38% (95% CI 0.32% to 0.43%). The relative risk was elevated as well: risk ratio of 1.89 (95% CI 1.43 to 2.36).Conclusions Concomitant treatment with NOACs and oral glucocorticoids was associated with a short-term rate and risk increase of GIB compared with patients only on NOACs. This could have implications for clinical management, necessitating closer monitoring or other risk mitigation strategies during episodes of cotreatment with oral glucocorticoids.",
keywords = "atrial fibrillation, drug interactions, pharmacology, epidemiology",
author = "Anders Holt and Paul Blanche and Bochra Zareini and Rasmussen, {Peter Vibe} and Strange, {Jarl Emanuel} and Deepthi Rajan and Jensen, {Mads Hashiba} and Mohammed El-Sheikh and Anne-Marie Schjerning and Morten Schou and Gunnar Gislason and Christian Torp-Pedersen and Patricia McGettigan and Morten Lamberts",
year = "2022",
doi = "10.1136/heartjnl-2021-319503",
language = "English",
volume = "108",
pages = "626--632",
journal = "Heart",
issn = "1355-6037",
publisher = "B M J Group",
number = "8",

}

RIS

TY - JOUR

T1 - Gastrointestinal bleeding risk following concomitant treatment with oral glucocorticoids in patients on non-vitamin K oral anticoagulants

AU - Holt, Anders

AU - Blanche, Paul

AU - Zareini, Bochra

AU - Rasmussen, Peter Vibe

AU - Strange, Jarl Emanuel

AU - Rajan, Deepthi

AU - Jensen, Mads Hashiba

AU - El-Sheikh, Mohammed

AU - Schjerning, Anne-Marie

AU - Schou, Morten

AU - Gislason, Gunnar

AU - Torp-Pedersen, Christian

AU - McGettigan, Patricia

AU - Lamberts, Morten

PY - 2022

Y1 - 2022

N2 - Objective Gastrointestinal bleeding (GIB) risk in relation to concomitant treatment with non-vitamin K oral anticoagulants (NOAC) and oral glucocorticoids is insufficiently explored. We aimed to investigate the short-term risk following coexposure.Methods This is a register-based, nationwide Danish study including patients with atrial fibrillation on NOACs during 2012–2018. Patients were defined as exposed to oral glucocorticoids if they claimed a prescription within 60 days prior to GIB. We investigated the associations between GIB and oral glucocorticoid exposure, reporting HRs via a nested case–control design and absolute risk via a cohort design. Matching terms were age, sex, calendar year, follow-up time and NOAC agent.Results 98 376 patients on NOACs (median age: 75 years (IQR: 68–82), 44% female) were included, and 16% redeemed at least one oral glucocorticoid prescription within 3 years. HRs of GIB were increased comparing exposed with non-exposed patients (<20 mg daily dose, HR 1.54 (95% CI 1.29 to 1.84); ≥20 mg daily dose, HR 2.19 (95% CI 1.81 to 2.65)). 60-day standardised absolute risk of GIB following first claimed oral glucocorticoid prescription increased compared with non-exposed: 60-day absolute risk: 0.71% (95% CI 0.58% to 0.85%) vs 0.38% (95% CI 0.32% to 0.43%). The relative risk was elevated as well: risk ratio of 1.89 (95% CI 1.43 to 2.36).Conclusions Concomitant treatment with NOACs and oral glucocorticoids was associated with a short-term rate and risk increase of GIB compared with patients only on NOACs. This could have implications for clinical management, necessitating closer monitoring or other risk mitigation strategies during episodes of cotreatment with oral glucocorticoids.

AB - Objective Gastrointestinal bleeding (GIB) risk in relation to concomitant treatment with non-vitamin K oral anticoagulants (NOAC) and oral glucocorticoids is insufficiently explored. We aimed to investigate the short-term risk following coexposure.Methods This is a register-based, nationwide Danish study including patients with atrial fibrillation on NOACs during 2012–2018. Patients were defined as exposed to oral glucocorticoids if they claimed a prescription within 60 days prior to GIB. We investigated the associations between GIB and oral glucocorticoid exposure, reporting HRs via a nested case–control design and absolute risk via a cohort design. Matching terms were age, sex, calendar year, follow-up time and NOAC agent.Results 98 376 patients on NOACs (median age: 75 years (IQR: 68–82), 44% female) were included, and 16% redeemed at least one oral glucocorticoid prescription within 3 years. HRs of GIB were increased comparing exposed with non-exposed patients (<20 mg daily dose, HR 1.54 (95% CI 1.29 to 1.84); ≥20 mg daily dose, HR 2.19 (95% CI 1.81 to 2.65)). 60-day standardised absolute risk of GIB following first claimed oral glucocorticoid prescription increased compared with non-exposed: 60-day absolute risk: 0.71% (95% CI 0.58% to 0.85%) vs 0.38% (95% CI 0.32% to 0.43%). The relative risk was elevated as well: risk ratio of 1.89 (95% CI 1.43 to 2.36).Conclusions Concomitant treatment with NOACs and oral glucocorticoids was associated with a short-term rate and risk increase of GIB compared with patients only on NOACs. This could have implications for clinical management, necessitating closer monitoring or other risk mitigation strategies during episodes of cotreatment with oral glucocorticoids.

KW - atrial fibrillation

KW - drug interactions

KW - pharmacology

KW - epidemiology

U2 - 10.1136/heartjnl-2021-319503

DO - 10.1136/heartjnl-2021-319503

M3 - Journal article

C2 - 34389550

VL - 108

SP - 626

EP - 632

JO - Heart

JF - Heart

SN - 1355-6037

IS - 8

ER -

ID: 286299290