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SPAnish Aortic VALVE Multicentric Study

Retrospective Multicentric Study Spanish SPALVALVE: Follow-up to 15 Years of Patients Between 50-65 Years Undergoing Isolated Aortic Valve Replacement. Biological or Mechanical Prostheses

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03595423
Acronym
SPAVALVE
Enrollment
5000
Registered
2018-07-23
Start date
2018-07-10
Completion date
2019-06-30
Last updated
2018-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prosthesis Durability, Survival, Prosthesis, Valve Heart Disease

Keywords

long-term survival, bioprosthesis

Brief summary

Currently there is an increase in the use of bioprosthesis worldwide (\> 70% according to national data of the Spanish Society of Thoracic and Cardiovascular Surgery). There is conflicting evidence regarding the long-term survival of patients aged 50-65 years with mechanical (M) or biological (B) aortic prostheses. General consensus of greater complications associated with the use of long-life anticoagulation in M and of reoperation in B. Similar survival with lower MACCE complications in bioprosthesis could reconsider their choice in patients aged 50-65 years, specially in the current TAVI era. The investigators are going to perform a multicentric retrospective observational study (Registry) about 15 year-outcomes Following Bioprosthetic vs Mechanical Isolated Aortic Valve Replacement for Aortic Stenosis in Patients Aged 50 to 65 Years in 30 Cardiovascular Surgery Centers in Spain

Detailed description

Objectives The main objective is to analyze long-term survival (15 years) and major cardiovascular complications (MACE, (early 30-day death, stroke, any prosthesis reoperation, and major bleeding), in patients aged 50-65 years who underwent isolated aortic valve replacement (AVR) due to severe aortic stenosis . Secondary objectives were to analyze the evolution of transprosthetic gradients by echocardiography,, and degree of significant structural degeneration in bioprostheses. Material and Method: A retrospective analytical study of patients aged 50-65 years who underwent AVR surgery for stenosis between 2000-2015 in 30 centers with a Cardiovascular Surgery Dept. in SPAIN as an inclusion criterion. As exclusion criteria, autonomic change of residence, need for concomitant surgery, previous cardiac interventions and infective endocarditis. Survival analysis and clinical data records will be performed through the Public Health Care computed medical records , and direct telephone contact with family and / or relatives, in case of doubts. A crude analysis of the data and a posterior analysis by propensity score matching with SPSS or R software will be carried out using a 1: 1 or 2:1 nearest neighbour matching protocol based on the Number of total bioprosthesis. A total sample of more than 5000 cases is expected, of which about 1000 would be bioprostheses that would serve as a basis for the pairing. According to previous data(ANDALVALVE STUDY), to find a 4.8% difference in the primary endpoint, two groups of 1025 patients are required for a p = 0.05 and 80% for a bilateral contrast of two independent proportions. Subanalysis will be performed by subgroups of age (50-55 vs. 55-65 years) and another according to the mark of the 2 prostheses of each type most implanted. All statistical analyzes will be two-tailed with an alpha error of 0.05 to consider statistically significant data, and will be reviewed by IBIMA or Private biostatistics. Competing risks analysis will be performed to calculate the cumulative incidence of stroke, reoperation and major bleeding for each prosthesis type. Conclusions: A positive result (similar survival in group B, with lower complications) could change the current indications of AVR in our environment, allowing the age of indication for bioprostheses in European guidelines to be reduced below 60 years

Interventions

PROCEDURESurgical AVR with bioprosthetic or mechanical prosthesis

Surgical AVR with bioprosthetic or mechanical prosthesis

Sponsors

Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 50-65 years who underwent isolated aortic valve replacement (AVR) for severe aortic stenosis from years 2000-2015 both inclusive

Exclusion criteria

* Not reported Residency change (unreachable) * Need of concomitant surgery * Reoperations * Infective endocarditis

Design outcomes

Primary

MeasureTime frameDescription
Number of participants aliveFrom date of surgery until the date of death from any cause, assessed up to 18 yearsSurvival since surgery
Late postoperative combined endpoint of 4 Major Adverse Cardiovascular Events (MACE) complicationsFrom date of surgery until the date of first documented MACE (see description) or date of death from any cause, whichever came first, assessed up to 18 yearsEarly 30-day Mortality, major bleeding, stroke and need of any prosthesis reoperation

Secondary

MeasureTime frameDescription
Cumulative incidence of stroke at 15 years between groupsFrom date of surgery until the date of first documented stroke or date of death from any cause, whichever came first, assessed up to 18 yearsstroke cumulative incidence over time (competing risk analysis)
Cumulative incidence of prosthesis reoperation at 15 years between groupsFrom date of surgery until the date of first documented reoperation or date of death from any cause, whichever came first, assessed up to 18 yearsreoperation cumulative incidence over time (competing risk analysis)
Cumulative incidence of major bleeding at 15 years between groupsFrom date of surgery until the date of first documented major bleeding or date of death from any cause, whichever came first, assessed up to 18 yearsmajor bleeding cumulative incidence over time (competing risk analysis)

Countries

Spain

Contacts

Primary ContactEMILIANO A RODRIGUEZ CAULO, MD, PhD,FECTS
erodriguezcaulo@hotmail.com+34951032054

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026