There were 322 all-cause deaths in the bioprosthesis group vs 318 in the mechanical prosthesis group.
aP value calculated using a marginal Cox model with a robust sandwich variance estimator.
There were 68 strokes in the bioprosthesis group vs 71 in the mechanical prosthesis group; 79 reoperations in the bioprosthesis group vs 43 in the mechanical prosthesis group; and 58 major bleeding events in the bioprosthesis group vs 101 in the mechanical prosthesis group.
eTable 1. Definitions of Exclusion Criteria
eTable 2. Definitions of Baseline Characteristics
eTable 3. Definition of Secondary End Points
eTable 4. Definition of 30-Day Complications
eTable 5. Baseline Characteristics of Bioprosthetic Patients Who Did or Did Not Match
eTable 6. Repeat Analysis of Study End Points Using All 4,253 Patients
eFigure 1.Unadjusted Survival Curves for Overall Survival in Patients Aged 50 to 69 After Aortic Valve Replacement Before Propensity Score Matching
eFigure 2. Trend in Mechanical or Bioprosthetic Valve Usage for Aortic Valve Replacement in Patients Aged 50 to 69
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Chiang YP, Chikwe J, Moskowitz AJ, Itagaki S, Adams DH, Egorova NN. Survival and Long-term Outcomes Following Bioprosthetic vs Mechanical Aortic Valve Replacement in Patients Aged 50 to 69 Years. JAMA. 2014;312(13):1323–1329. doi:10.1001/jama.2014.12679
Copyright 2014 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.
The choice between bioprosthetic and mechanical aortic valve replacement in younger patients is controversial because long-term survival and major morbidity are poorly characterized.
To quantify survival and major morbidity in patients aged 50 to 69 years undergoing aortic valve replacement.
Design, Setting, and Participants
Retrospective cohort analysis of 4253 patients aged 50 to 69 years who underwent primary isolated aortic valve replacement using bioprosthetic vs mechanical valves in New York State from 1997 through 2004, identified using the Statewide Planning and Research Cooperative System. Median follow-up time was 10.8 years (range, 0 to 16.9 years); the last follow-up date for mortality was November 30, 2013. Propensity matching yielded 1001 patient pairs.
Main Outcomes and Measures
Primary outcome was all-cause mortality; secondary outcomes were stroke, reoperation, and major bleeding.
No differences in survival or stroke rates were observed in patients with bioprosthetic compared with mechanical valves. Actuarial 15-year survival was 60.6% (95% CI, 56.3%-64.9%) in the bioprosthesis group compared with 62.1% (95% CI, 58.2%-66.0%) in the mechanical prosthesis group (hazard ratio, 0.97 [95% CI, 0.83-1.14]). The 15-year cumulative incidence of stroke was 7.7% (95% CI, 5.7%-9.7%) in the bioprosthesis group and 8.6% (95% CI, 6.2%-11.0%) in the mechanical prosthesis group (hazard ratio, 1.04 [95% CI, 0.75-1.43). The 15-year cumulative incidence of reoperation was higher in the bioprosthesis group (12.1% [95% CI, 8.8%-15.4%] vs 6.9% [95% CI, 4.2%-9.6%]; hazard ratio, 0.52 [95% CI, 0.36-0.75]). The 15-year cumulative incidence of major bleeding was higher in the mechanical prosthesis group (13.0% [95% CI, 9.9%-16.1%] vs 6.6% [95% CI, 4.8%-8.4%]; hazard ratio, 1.75 [95% CI, 1.27-2.43]). The 30-day mortality rate was 18.7% after stroke, 9.0% after reoperation, and 13.2% after major bleeding.
Conclusions and Relevance
Among propensity-matched patients aged 50 to 69 years who underwent aortic valve replacement with bioprosthetic compared with mechanical valves, there was no significant difference in 15-year survival or stroke. Patients in the bioprosthetic valve group had a greater likelihood of reoperation but a lower likelihood of major bleeding. These findings suggest that bioprosthetic valves may be a reasonable choice in patients aged 50 to 69 years.
Aortic valve replacement is indicated for survival benefit, symptom relief, and preservation of left ventricular function in patients with severe aortic valve disease.1,2 Approximately 50 000 patients undergo aortic valve replacement annually in the United States alone.3 In older patients, bioprosthetic valves pose a low lifetime risk of reoperation for structural degeneration and avoid many of the major thrombotic and hemorrhagic complications associated with mechanical prostheses: bioprosthetic valves are therefore recommended in patients older than 70 years.1,2 The optimal prosthesis type for younger patients is less clear.1,2,4-7 This is primarily because structural valve degeneration of bioprostheses occurs earlier and progresses more rapidly in younger patients, resulting in a higher lifetime risk of reoperation.7 Prospective studies have been underpowered to detect differences in long-term mortality and major morbidity in this age group,8-10 and larger retrospective analyses are limited to single-center studies with follow-up dependent on patients returning to the same institution.11-13 We therefore analyzed a statewide administrative database to quantify differences in long-term survival, stroke, reoperation, and major bleeding episodes after aortic valve replacement according to prosthesis type among patients aged 50 to 69 years.
This was a retrospective cohort analysis comparing long-term outcomes after primary, isolated aortic valve replacement in New York State from January 1, 1997, through December 31, 2004, in patients aged 50 to 69 years, according to whether they received a bioprosthetic or mechanical prosthetic valve. Patients were identified using the International Classification of Diseases, Ninth Revision, Clinical Modification procedure code of bioprosthetic (35.21) or mechanical prosthetic (35.22) aortic valve replacement. The cohort was identified using the Statewide Planning and Research Cooperative System (SPARCS), an all-payer, administrative database that prospectively collects patient-level data on every hospital discharge, ambulatory surgery visit, and emergency department visit in New York State. SPARCS allocates each patient a unique identifier linking all such encounters, permitting longitudinal analysis. We also examined trends in prosthesis types implanted between 1997 and 2010.
Exclusion criteria were out-of-state residency, prior replacement of any valve, concomitant valve replacement, concomitant valve repair, coronary artery bypass graft surgery, or thoracic aortic surgery (see eTable 1 in the Supplement for definitions). Baseline comorbidities were identified using diagnosis codes from the index hospitalization and all hospitalizations up to 2 years prior to the index hospitalization (eTable 2 in the Supplement).
The study was approved by the data protection review board of the New York State Department of Health as well as the Program for Protection of Human Subjects at the Icahn School of Medicine at Mount Sinai. The approval included a waiver of informed consent.
The primary outcome measure was all-cause mortality. Secondary outcomes were stroke, reoperation, and major bleeding events. Deaths were identified using the Social Security Death Master File (current as of November 30, 2013) and by searching all hospital admissions and ambulatory or emergency department visits for patient deaths. Stroke was defined as cerebrovascular accident occurring during the index hospital admission as well as any subsequent hospital admission for which the primary diagnosis was recorded as a hemorrhagic or ischemic cerebrovascular event; transient ischemic attacks were excluded. Reoperation was defined as any repeat aortic valve replacement; subsequent cardiac surgical operations not involving the aortic valve were not included for the purposes of this analysis. Major bleeding events were defined as any subsequent hospitalization for which the primary diagnosis was intracerebral hemorrhage, hemopericardium, cardiac tamponade, gastrointestinal hemorrhage (including bleeding peptic ulcer), hematuria, hemarthrosis, or hemoptysis. The International Classification of Diseases, Ninth Revision, Clinical Modification codes used are listed in eTable 3 in the Supplement. Patients for whom no stroke, reoperation, or major bleeding event and no date of death were found were censored on December 31, 2012 (last date of follow-up by SPARCS).
Continuous variables are reported as mean (SD). Categorical variables are expressed as proportions. Baseline differences between patients receiving bioprosthetic or mechanical prosthetic valves were detected using t test for normally distributed continuous variables and Pearson χ2 test for categorical variables as well as standardized differences for both continuous and categorical variables.
To adjust for differences in baseline characteristics, propensity score matching was performed.14 To account for variation in practice between surgeons, a hierarchical logistic regression model was fit with bioprosthesis implantation as the outcome and with patients specified as being clustered within surgeons. For each patient, the proportion of aortic valve replacement operations performed by their surgeon using a bioprosthesis in the past year was entered as a covariate into the propensity score model. All baseline characteristics ( which included year of surgery, age, sex, race/ethnicity (self-reported; assessed as a confounding variable), admission urgency, active endocarditis, coagulation or platelet disorders, hypertension, diabetes, coronary artery disease, peripheral vascular disease, cerebrovascular disease, congestive heart failure, atrial fibrillation, chronic obstructive pulmonary disease, chronic kidney disease, liver disease, and cancer) were also included as covariates in the propensity score model. The area under the receiver operating curve for the model was 0.83. Patients were then matched on a 1:1 basis using a caliper width of 0.10 of the logit of the propensity score. After propensity score matching, differences in baseline characteristics and the incidence of 30-day complications between patients in each group were detected using paired t test for normally distributed continuous variables and McNemar test for categorical variables (see eTable 4 in the Supplement for definitions of 30-day complications) as well as standardized differences.
Survival curves for the primary end point of survival were constructed for the entire study population as well as the propensity-matched groups. Survival estimates at 15 years after surgery were derived from the life table. The difference in survival was assessed using a marginal Cox model with a robust sandwich variance estimator. Competing risk analysis of the secondary end points of stroke, reoperation, and major bleeding was performed by constructing cumulative incidence curves for the propensity-matched groups and comparing them using Gray test. Additionally, for each end point, Cox proportional hazards models with only prosthesis type entered as a covariate were fit to calculate hazard ratios. The proportional hazards assumption was valid in all models.
The baseline characteristics of patients in the bioprosthesis group who were not matched are listed in eTable 5 in the Supplement. To assess the validity of our results, analyses of all end points were repeated using all patients by fitting Cox models with prosthesis type, age, and sex entered as covariates (eFigure 1 in the Supplement) and then again with prosthesis type, propensity score, and all baseline characteristics entered as covariates (eTable 6 in the Supplement). There were no significant differences between the results obtained using these alternative analyses.
All tests were 2-tailed; an α level of .05 was considered statistically significant. All statistical analyses were performed using SAS version 9.3 (SAS Institute Inc).
A total of 10 981 patients aged 50 to 69 years were identified. Patients with 1 or more of the following characteristics were excluded: out-of-state residents (893 [8.1%]), prior replacement of any valve (587 [5.3%]), and concomitant valve replacement (1353 [12.3%]), valve repair (263 [2.4%]), coronary artery bypass graft surgery (4077 [37.1%]), or thoracic aortic surgery (1009 [9.2%]). After applying exclusion criteria, 4253 patients remained. Of these patients, 1466 (34.5%) received bioprosthetic valves and 2787 (65.5%) received mechanical prosthetic valves. Overall median follow-up time was 10.8 years (range, 0-16.9 years). Median follow-up times were 10.6 years (range, 0-16.9 years) in the bioprosthesis group and 10.9 years (range, 0-16.9 years) in the mechanical prosthesis group. Propensity score matching produced 1001 patient pairs.
The proportion of patients who underwent bioprosthetic aortic valve replacement increased from 15% in 1997 to 74% in 2012 (P < .001 [eFigure 2 in the Supplement]). In the study cohort of patients who underwent aortic valve replacement between 1997 and 2004, those who received a bioprosthetic valve were older (mean, 62.3 [SD, 5.4] vs 60.2 [SD, 5.6] years; P < .001) and more likely to have a history of diabetes (21% vs 18%, P = .01), cerebrovascular disease (7% vs 5%, P = .05), coagulation or platelet disorders (4% vs 3%, P = .01), liver disease (4% vs 2%, P = .01), and cancer (4% vs 3%, P = .03) (Table 1). After propensity score matching, age and all baseline comorbidities were balanced between the 2 groups (Table 2). There was no significant difference in 30-day mortality (3% in the bioprosthesis group vs 3% in the mechanical prosthesis group, P = .49) or other short-term outcomes (Table 3).
No difference in long-term survival was observed (P = .74). Figure 1 displays the survival curves for overall survival in the propensity-matched cohort (survival curves for the unmatched patients are shown in eFigure 2 in the Supplement). There were 322 deaths in the bioprosthesis group and 318 deaths in the mechanical prosthesis group during a maximum of 16.9 years of follow-up. Actuarial 15-year survival was 60.6% (95% CI, 56.3%-64.9%) in the bioprosthesis group compared with 62.1% (95% CI, 58.2%-66.0%) in the mechanical prosthesis group. The hazard ratio for death for mechanical prostheses vs bioprostheses was 0.97 (95% CI, 0.83-1.14).
No difference in stroke rates was observed (P = .84) (Figure 2). A total of 68 strokes in the bioprosthesis group and 71 strokes in the mechanical prosthesis group occurred during a maximum follow-up of 16.9 years. The cumulative incidence of stroke at 15 years was 7.7% (95% CI, 5.7%-9.7%) for patients who received a bioprosthetic valve, compared with 8.6% (95% CI, 6.2%-11.0%) for those who received a mechanical prosthetic valve. The hazard ratio for stroke for mechanical prostheses vs bioprostheses was 1.04 (95% CI, 0.75-1.43). The 30-day mortality after stroke was 18.7%.
Bioprostheses were associated with a significantly higher rate of aortic valve reoperation than mechanical prostheses (P = .001) (Figure 2). During a maximum follow-up time of 16.9 years, 79 patients in the bioprosthesis group and 43 patients in the mechanical prosthesis group underwent reoperation. The cumulative incidence of aortic valve reoperation at 15 years was 12.1% (95% CI, 8.8%-15.4%) in the bioprosthesis group compared with 6.9% (95% CI, 4.2%-9.6%) in the mechanical prosthesis group. The hazard ratio for aortic valve reoperation for mechanical prostheses vs bioprostheses was 0.52 (95% CI, 0.36-0.75). The 30-day mortality after aortic valve reoperation was 9.0%.
Mechanical prostheses were associated with a significantly higher rate of major bleeding compared with bioprostheses (P = .001) (Figure 2). There were 58 major bleeding events in the bioprosthesis group vs 101 in the mechanical prosthesis group during a maximum of 16.9 years of follow-up. The cumulative incidence of major bleeding events at 15 years was 6.6% (95% CI, 4.8%-8.4%) for the bioprosthesis group compared with 13.0% (95% CI, 9.9%-16.1%) for the mechanical prosthesis group. The hazard ratio for major bleeding in the mechanical prosthesis group was 1.75 (95% CI, 1.27-2.43). The 30-day mortality after a major bleeding event was 13.2%.
Current consensus guidelines state that choice of either a bioprosthetic or mechanical prosthetic aortic valve is reasonable in patients aged 60 to 70 years, and that a mechanical valve replacement is reasonable in patients younger than 60 years without contraindications to coumadin.1,2 These class IIa recommendations are based on the results of 3 randomized clinical trials,8-10 2 of which enrolled patients nearly 4 decades ago and evaluated prostheses since superseded by more durable and less thrombogenic models.8,9 Consequently, the findings of these studies may no longer reflect outcomes in current clinical practice. Our analysis of a large, contemporary patient cohort supports the view that either prosthesis type is a reasonable choice in patients aged 60 to 69 years and suggests that this recommendation could reasonably be extended to include patients aged 50 to 59 years.
There are conflicting data from recent single-center retrospective studies comparing long-term outcomes in this age group. Brown et al11 reported a 10-year survival benefit in 250 matched pairs aged 50 to 70 years favoring mechanical prostheses. This may reflect the authors’ inability to control for a systematic treatment bias arising from the tendency to implant mechanical prosthetic valves in healthier patients with better life expectancy: even after propensity matching, the patients who received bioprosthetic valves in their study were older, more symptomatic, more likely to have major comorbidities such as lung disease and peripheral vascular disease, and had a significantly higher 30-day mortality. McClure et al13 compared groups that were more closely matched (30-day mortality was the same) and in their single-center analysis of 310 propensity matched pairs younger than 65 years saw no significant survival difference up to 18 years following surgery.
The absence of a significant survival benefit associated with one prosthesis type over another focuses decision making on lifestyle considerations, including the burden of anticoagulation medication and monitoring, and the relative risks of major morbidity—primarily stroke, reoperation, and major bleeding events. In our study cohort, long-term stroke risk did not appear to be affected by choice of prosthesis, which is consistent with the findings of previous studies.11,13 We observed significant differences in reoperation and major bleeding rates according to prosthesis type. By 15 years after surgery, 12.1% of patients with bioprostheses had undergone aortic valve reoperation, compared with 6.9% with mechanical prostheses. The observed 30-day mortality after reoperation (9.0%) could perhaps be reduced. High-volume valve centers report mortality of 2% to 5% for reoperative aortic valve replacement,15-17 and there may consequently be a case for targeted referrals of selected patients requiring reoperation to reference centers. In a small number of high-risk patients with an aortic bioprosthesis requiring reoperation, transcatheter valve-in-valve implantation has been used18: this technique may eventually represent a reasonable alternative to open reoperation.
Mechanical prostheses were associated with a lower reoperation rate, but this was at the expense of more major bleeding events, experienced by 6.6% of patients with bioprostheses compared with 13.0% of patients with mechanical prostheses by 15 years after surgery. The 30-day mortality after a major bleeding event in this cohort was 13.2%. Two randomized trials comparing low-intensity, self-monitored anticoagulation regimens with standard anticoagulation in patients with mechanical valves have not shown a significant reduction in major bleeding or thromboembolic events.19,20 These outcomes, together with the well-recognized patient dissatisfaction with the prospect of a lifetime of anticoagulation,21 may partially explain the increasing use of bioprostheses that we observed during the last decade, which follows national trends previously reported in an analysis of the Society of Thoracic Surgeons cardiac surgery database.22
SPARCS is a prospectively collected statewide, mandatory database containing detailed demographic, diagnostic, and procedural information. Despite the use of statistical methods to reduce imbalance, several potential confounding variables could not be included in the model, including frailty, etiology of aortic valve dysfunction, severity of other valve lesions, extent of coronary artery disease, and ventricular dysfunction. This potentially introduces a bias in favor of mechanical valves because surgeons tend to implant bioprosthetic valves in patients that they consider to have reduced life expectancy based on these and other factors. If this bias were significant, one would expect a survival difference between the 2 groups in the overall study population after adjusting for age and sex and no other comorbidities; however, this was not the case (eFigure 2 in the Supplement). A second potential bias in favor of mechanical prostheses is the greater tendency for deaths to be missing in the Social Security Death Master File for younger patients, who were more likely to receive mechanical prostheses. Last, we were unable to determine when patients were hospitalized out of state, potentially causing us to underestimate the rate of the secondary end points: we believe that movement out of state would affect both groups equally and note that the rates of stroke, reoperation, and major bleeding we observed were similar to those reported in other series.7,23
Among propensity-matched patients aged 50 to 69 years who underwent aortic valve replacement with bioprosthetic compared with mechanical prosthetic valves, there was no significant difference in 15-year survival or stroke. Patients in the bioprosthetic valve group had a greater likelihood of reoperation but a lower likelihood of major bleeding. These findings suggest that bioprosthetic valves may be a reasonable choice in patients aged 50 to 69 years.
Corresponding Author: Joanna Chikwe, MD, Department of Cardiovascular Surgery, Mount Sinai Medical Center, 1190 Fifth Ave, New York, NY 10029 (email@example.com).
Author Contributions: Mr Chiang had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Chiang, Chikwe, Moskowitz, Adams, Egorova.
Acquisition, analysis, or interpretation of data: Chiang, Chikwe, Itagaki, Adams, Egorova.
Drafting of the manuscript: Chiang, Chikwe.
Critical revision of the manuscript for important intellectual content: Chiang, Chikwe, Moskowitz, Itagaki, Adams, Egorova.
Statistical analysis: Chiang, Itagaki, Egorova.
Administrative, technical, or material support: Chikwe.
Study supervision: Chikwe, Moskowitz, Adams, Egorova.
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Mr Chiang reported receiving a research stipend from the Icahn School of Medicine at Mount Sinai Patient Oriented Research Training and Leadership (PORTAL) Program. Dr Adams reported that the Icahn School of Medicine at Mount Sinai receives royalties payments from Edwards Lifesciences and Medtronic for intellectual property related to his involvement in the development of 2 mitral valve repair rings and 1 tricuspid valve repair ring and that he is National Co-Principal Investigator of the CoreValve United States Pivotal Trial, which was supported by Medtronic. No other authors reported disclosures.