Key result
Same-day discharge after TAVI appears safe and effective in carefully selected low-risk patients.
Why the study?
Increasing TAVI procedure volumes place growing demands on hospital resources, prompting the need for guidance on safely and effectively implementing same-day discharge after TAVI.
Is same-day discharge after TAVI safe and effective in selected patients?
Is same-day discharge after TAVI safe and effective in selected patients?
Same-day discharge after TAVI is a promising strategy for carefully selected low-risk patients to improve healthcare efficiency, though randomized trials are needed.
May support SDD after TAVI to reduce bed occupancy; leaves open safety confirmation in prospective trials.
The burden of severe aortic stenosis requiring treatment is growing due to ageing populations. This places increased demands on health resources due to the growing number of transcatheter aortic valve implantation (TAVI) procedures and hospital bed occupancy. There are several studies of same-day discharge (SDD) after coronary angioplasty demonstrating its safety, particularly in transfemoral cases. There has been significant evolution in techniques and technologies underpinning TAVI, which have reduced its risk profile over time. As a result, several observational studies have demonstrated that SDD after TAVI is safe and effective. Careful selection of low-risk patients and a minimalist TAVI approach, with appropriate post-procedure review and follow-up, are crucial for successful SDD after TAVI. However, there is a need for randomised trials to validate this practice. This article provides a state-of-the-art overview and guidance to safely and effectively implement a SDD-TAVI service to improve the healthcare system efficiency while enhancing patient satisfaction and recovery.
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Khan et al. (2026) conducted a review in Severe aortic stenosis. Same-day discharge after transcatheter aortic valve implantation (TAVI) was evaluated. Same-day discharge after transcatheter aortic valve implantation appears safe and effective in carefully selected low-risk patients, though randomized trials are needed to validate this practice.
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