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Updated: Aug 20, 2025

Novel and Innovative Hybrid Technique for Type A Aortic Dissection
Published on: March 28, 2025
Pharmacological treatment in patients with aortic dissection
Christian Smedberg1,2, Rebecka Hultgren3,4, Karin Leander5
1Department of Clinical Science and Education Södersjukhuset, Karolinska Institutet, Stockholm, Sweden christian.smedberg@ki.se.
Insights
Statin therapy improved long-term survival in medically managed aortic dissection (AD) patients. Beta-blockers benefited surgically managed AD patients, while antithrombotics showed no survival association.
Area of Science:
- Cardiovascular Medicine
- Medical Management
- Pharmacological Interventions
Background:
- Aortic dissection (AD) is a life-threatening condition requiring careful medical management.
- Understanding the long-term impact of various pharmacological agents on survival is crucial for optimizing patient outcomes.
Purpose of the Study:
- To describe the medical management of patients with aortic dissection (AD).
- To analyze the association between antihypertensive, antithrombotic, anticoagulant, and statin agents and long-term survival in AD patients.
Main Methods:
- Retrospective analysis of Swedish medical registers for AD patients diagnosed between 2006-2015.
- Examined prescription data prior to admission and within one year post-discharge for patients alive at 30 days.
- Utilized Cox proportional hazards models to assess the association between medications and long-term survival.
Main Results:
- Statin treatment was associated with significantly higher long-term survival (HR 0.74).
- This positive association for statins persisted in medically managed patients but not in surgically managed ones.
- Beta-blockers improved survival in surgically managed patients (HR 0.58) but not in medically managed patients.
Conclusions:
- Statin therapy is linked to better long-term outcomes in medically managed AD.
- Beta-blocker therapy is associated with improved survival specifically in surgically managed AD patients.
- Further research, including randomized controlled trials, is needed to confirm the roles of statins and optimal antihypertensive therapy in chronic AD management.
Objectives:
To describe medical management in aortic dissection (AD) and to analyse the possible associations between antihypertensive, antithrombotic, anticoagulant and statin agents, respectively, and long-term survival.
Methods:
From Swedish medical registers, all patients diagnosed with AD in 2006-2015 were identified. Filled prescriptions prior to admission and within 1 year from discharge in patients discharged and alive at 30 days were registered. Associations between pharmacological treatment and long-term survival were analysed using Cox proportional hazards models.
Results:
Of 3951 patients hospitalised with acute AD, 3046 (77%) were discharged and alive at 30 days. In hospitalised patients, mean age was 66 years (SD 13), and 36% (n=1098) were women. Within 1 year from discharge, 96% (n=2939) had at least one antihypertensive drug. Beta blocker was the most commonly used drug type (90%, n=2741). Statin treatment (47%, n=1418) was associated with higher long-term survival; HR 0.74 (95% CI 0.63 to 0.87, p<0.001). The positive association between statins and long-term survival remained, in subgroup analysis, in medically managed patients (HR 0.72 (95% CI 0.60 to 0.86, p<0.001)), but not in patients undergoing surgical repair (HR 0.82 (95% CI 0.58 to 1.14, p=0.230)). Beta blockers were associated with favourable long-term survival in surgically managed patients (HR 0.58 (95% CI 0.35 to 0.97, p=0.038)) but not in medically managed patients (HR 0.93 (95% CI 0.72 to 1.12, p=0.057)). Neither antiplatelet therapy nor anticoagulants were associated with long-term survival.
Conclusions:
Statin treatment was associated with favourable long-term outcome in medically managed AD patients, whereas treatment with beta blocker was associated with higher survival only in surgically managed AD patients. Statin use as well as optimal antihypertensive therapy in the chronic stage of the disease need to be further analysed, preferably in randomised controlled trials.
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