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Observational Study
. 2021 Nov;8(2):e001742.
doi: 10.1136/openhrt-2021-001742.

Predictors and clinical outcomes of poor symptomatic improvement after transcatheter aortic valve replacement

Affiliations
Observational Study

Predictors and clinical outcomes of poor symptomatic improvement after transcatheter aortic valve replacement

Nobuhiro Yoshijima et al. Open Heart. 2021 Nov.

Abstract

Objective: Transcatheter aortic valve replacement (TAVR) improves clinical symptoms in most patients with severe aortic stenosis (AS). However, some patients do not benefit from the symptom-reducing effects of TAVR. We assessed the predictors and clinical outcomes of poor symptomatic improvement (SI) after TAVR.

Methods: A total of 1749 patients with severe symptomatic AS undergoing transfemoral TAVR were evaluated using the Japanese multicentre TAVR registry. Poor SI was defined as readmission for heart failure (HF) within 1 year after TAVR or New York Heart Association (NYHA) class ≥3 after 1 year. A logistic regression model was used to identify predictors of poor SI. One-year landmark analysis after TAVR was used to evaluate the association between poor SI and clinical outcomes.

Results: Among the overall population (mean age, 84.5 years; female, 71.3%; mean STS score, 6.3%), 6.6% were categorised as having poor SI. Atrial fibrillation, chronic obstructive pulmonary disease, Clinical Frailty Scale ≥4, chronic kidney disease and moderate to severe mitral regurgitation were independent predictors of poor SI. One-year landmark analysis demonstrated that poor SI had a higher incidence of all-cause death and readmission for HF compared with SI (p<0.001). Poor SI with preprocedural NYHA class 2 had a worse outcome than SI with preprocedural NYHA class ≥3.

Conclusions: Poor SI was associated with worse outcomes 1 year after the procedure. It had a greater impact on clinical outcomes than baseline symptoms. TAVR may be challenging for patients with many predictors of poor SI.

Trial registration number: This registry, associated with the University Hospital Medical Information Network Clinical Trials Registry, was accepted by the International Committee of Medical Journal Editors (UMIN-ID: 000020423).

Keywords: aortic valve stenosis; heart failure; transcatheter aortic valve replacement.

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Conflict of interest statement

Competing interests: MY, NT, TN, SS, KM, MT, HU, YW and KH are clinical proctors for Edwards Lifesciences and Medtronic. HS and KT are clinical proctors for Edwards Lifesciences.

Figures

Figure 1
Figure 1
Distribution of preprocedural and postprocedural New York Heart Association (NYHA-pre) classes and postprocedural readmission for heart failure (HF) each number shows the number of patients with a pair of scores for the NYHA class before and 1 year (NYHA-1y) after transcatheter aortic valve replacement (TAVR) or readmission for HF within 1 year after TAVR. The overall population was divided into two groups: symptomatic improvement (SI), (green +blue) and a poor SI (red +yellow) or four groups, with the subgroups of SI with NYHA-pre 2 (blue), SI with NYHA-pre ≥3 (green), poor SI with NYHA-pre 2 (yellow) and poor SI with NYHA-pre ≥3 (red).
Figure 2
Figure 2
Cumulative incidence of all-cause death and readmission for heart failure from the first postprocedural year according to symptomatic improvement (SI) time-to-event curves are shown from 1 to 2 years for all-cause death (A) and readmission for heart failure (B). Event rates were calculated using the Kaplan-Meier method and compared with the log-rank test.
Figure 3
Figure 3
Cumulative incidence of all-cause death and readmission for heart failure from the first postprocedural year according to preprocedural New York Heart Association (NYHA) functional class and symptomatic improvement (SI) time-to-event curves are shown from 1 to 2 years for all-cause death (A) and readmission for heart failure (B). Event rates were calculated using the Kaplan-Meier method and compared with the log-rank test.

References

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