Reducing length of stay after transfemoral transcatheter aortic valve implantation: the FAST-TAVI II trial
Author:
Durand Eric1ORCID, Beziau-Gasnier Delphine1, Michel Morgane234ORCID, Iung Bernard5, Tchetche Didier6, Bonnet Guillaume7ORCID, Lhermusier Thibault8ORCID, Gilard Martine9, Souteyrand Geraud10, Bouleti Claire11, Ohlmann Patrick12ORCID, Lefevre Thierry13, Beygui Farzin14ORCID, Chassaing Stephan15, Chevreul Karine234, Eltchaninoff Hélène1, , Alos Benjamin, Arnould Marc-Antoine, Bar Olivier, Barbey Christophe, Bertrand Bernard, Beygui Farzin, Bignon Mathieu, Bouchat Marine, Bouisset Frédéric, Bouleti Claire, Campelo-Parada Fransisco, Chassaing Stephan, Combaret Nicolas, Darodes Nicole, Delepine Stéphane, Didier Romain, Dongay Bruno, Dumonteil Nicolas, Fouassier David, Gallet de Saint Aurin Romain, Gilard Martine, Gouffran Guillaume, Himbert Dominique, Le Bivic Louis, Lefèvre Thierry, Lemaitre Adrien, Leroux Lionel, Levy Gilles, Lhermusier Thibaut, Lorgis Luc, Morelle Jean-François, Ohlmann Patrick, Piot Christophe, Pommier Thibaut, Rebouh Idir, Roule Vincent, Rusinaru Dan, Souteyrand Géraud, Spaulding Christian, Tchetche Didier, Teiger Emmanuel, Tribouilloy Christophe, , Eltchaninoff Hélène, Bellien Jérémy, Bertrand Benjamin, Beygui Farzin, Béziau-Gasnier Delphine, Brakenhielm Ebba, Caligiuri Giuseppina, Chevreul Karine, Debroucker Frédérique, Durand Eric, Fraschini Christophe, Gilard Martine, Iung Bernard, Kamel Said, Laschet Jamila, Manrique Alain, Messas Emmanuel, Messika-Zeitoun David, Pinet Florence, Richard Vincent, Saloux Eric, Thoenes Martin, Tribouilloy Christophe, Vézier Claire
Affiliation:
1. Univ Rouen Normandie , Inserm U1096, CHU Rouen, Department of Cardiology, F-76000 Rouen , France 2. Université Paris Cité , Paris , France 3. Inserm, ECEVE , Paris , France 4. Clinical Epidemiology Unit, Robert Debré Hospital, Assistance Publique-Hôpitaux de Paris , Paris , France 5. Cardiology Department, Bichat—Claude-Bernard Hospital Cardiology Service , Paris , France 6. Clinique Pasteur , Toulouse , France 7. Unité médico-chirurgicale des valvulopathies, CHU de Bordeaux , 33600 Pessac , France 8. CHU de Toulouse, Pôle Cardiovasculaire et Métabolique , Toulouse , France 9. Department of Cardiology, CHRU Brest , 29200 Brest , France 10. CHU de Clermont-Ferrand , Clermont-Ferrand , France 11. Clinical Investigation Center (INSERM 1204), Cardiology Department, ACTION and FACT study groups, University of Poitiers, Poitiers Hospital , France 12. Université de Strasbourg, Pôle d'Activité Médico-Chirurgicale Cardio-Vasculaire, Nouvel Hôpital Civil, Centre Hospitalier Universitaire , Strasbourg , France 13. Institut Cardiovasculaire Paris Sud, Hôpital Privé Jacques Cartier, Ramsay Générale de santé , Massy , France 14. Service de Cardiologie, ACTION Study Group, Centre Hospitalier Universitaire (CHU) de Caen Normandie, Normandie Univ, INSERM UMRS 1237, GIP Cyceron , Caen , France 15. Cardiology Department, Clinique NCT+-Saint Gatien-Alliance , Tours , France
Abstract
Abstract
Background and Aims
The length of stay (LOS) after transcatheter aortic valve implantation (TAVI) remains extremely variable whereas early discharge has been shown to be feasible and safe. The study objective was to evaluate the efficacy and safety of an intervention aimed at reducing LOS after transfemoral TAVI.
Methods
FAST-TAVI II is a prospective, multicentre, cluster, randomized, controlled study including patients with severe symptomatic aortic stenosis, who had transfemoral TAVI. The intervention consisted in a dedicated training programme to implement 10 quality of care measures to reduce LOS with an implementation phase of eight weeks. The primary endpoint was the proportion of patients discharged early within 3 days. Secondary endpoints included: LOS, 30-day mortality and 30-day incidence of readmission for cardiovascular events.
Results
During the study period, 969 patients were enrolled in the intervention group and 860 patients in the control group. Mean age was 81.9 ± 6.6 years and mean EuroSCORE II was 4.4 ± 4.5%. Early discharge was achieved in 563 (58.1%) patients in the intervention group vs. 364 (42.3%) patients in the control group (P < .0001). Median LOS was significantly reduced in the intervention group compared to the control group [3 (IQR: 3) vs. 4 days (IQR: 3), P < .0001]. Thirty-day mortality was low and similar in the two groups (0.5% vs. 0.9%, P = .30), as were 30-day readmissions (4.6% vs. 2.8%, P = .28).
Conclusions
The intervention was simple and fast to implement, and was effective and safe to reduce LOS and increase the proportion of patients discharged early after TAVI (NCT04503655).
Funder
French Government National Research Agency ANR
Publisher
Oxford University Press (OUP)
Cited by
5 articles.
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