Abstract
OBJECTIVE:
We sought to ascertain predictors of Patient Prosthesis Mismatch, an independent predictor of mortality, in patients with aortic stenosis using bioprosthetic valves.
METHOD:
We analyzed 2,107 sequential surgeries. Patient Prosthesis Mismatch was calculated using the effective orifice area of the prosthesis divided by the patient's body surface area. We defined nonsignificant, moderate, and severe Patient Prosthesis Mismatch as effective orifice area indexes of >0.85 cm2/m, 0.85-0.66 cm2/m2, and ≤0.65 cm2/m2, respectively.
RESULTS:
A total of 311 bioprosthetic patients were identified. The incidence of nonsignificant, moderate, and severe Patient Prosthesis Mismatch was 41%, 42, and 16%, respectively. Severe Patient Prosthesis Mismatch was significantly more prevalent in females (82%). In severe Patient Prosthesis Mismatch, the perfusion and the cross-clamp times were considerably lower when compared with nonsignificant Patient Prosthesis Mismatch and moderate Patient Prosthesis Mismatch. Patients with severe Patient Prosthesis Mismatch had a significantly higher likelihood of spending time in the intensive care unit and a significantly longer length of stay in the hospital. Body surface area was not different in severe Patient Prosthesis Mismatch when compared with nonsignificant Patient Prosthesis Mismatch. In-hospital mortality in patients with nonsignificant, moderate, and severe Patient Prosthesis Mismatch was 2.3%, 6.1%, and 8%, respectively. Minimally invasive surgery was significantly associated with moderate Patient Prosthesis Mismatch in 49% of the patients, but not with severe Patient Prosthesis Mismatch.
CONCLUSION:
Severe Patient Prosthesis Mismatch is more common in females, but not in those with minimal available body surface area. Though operative times were shorter in these patients, intensive care unit and hospital lengths of stay were longer. Surgeons and cardiologists should be cognizant of these clinical predictors and complications prior to valve surgery.
Keywords: Aortic Stenosis, Patient Prosthesis Mismatch, Bioprosthesis Female, Gender Clinical Predictors
INTRODUCTION
Aortic valve stenosis affects 2% to 4% of older adults and is the most common reason for valve surgery. An estimated 50,000 aortic valve procedures are performed each year in the United States (1). However, once the aortic valve is replaced, issues related to prosthesis-patient mismatch (PPM) may emerge.
PPM was first described by Rahimtoola in 1978 (2). PPM is considered to be present when the prosthetic valve used in the patient is smaller than the normal native valve. As a consequence of the smaller prosthetic valve, the left ventricle has to produce higher pressures to overcome the mechanical resistance produced by the new device. This is transmitted in higher transvalvular pressure gradients as measured by Doppler (2). It has been demonstrated that the high-pressure gradients through the prosthesis are associated with higher morbidity and impact both short- and long-term mortality, when compared with prostheses of adequate size, based on the patient's body surface area (4-5).
It has been shown that PPM is a common problem in patients undergoing AVR, occurring in up to 70% of aortic valve replacements (3). At the same time, this problem can be prevented through the use of a systematic approach prior to surgery (3). This may result in enhanced recovery with lower morbidity and mortality. The aim of this study was to determine the prevalence, clinical predictors, and short-term impact of severe PPM.
METHODS
Patient population: After obtaining approval from the independent review board, we retrospectively reviewed 2,107 consecutive heart surgeries performed at our institution between January 2005 and June 2009. Of these, 964 were coronary artery bypass surgeries, 683 involved single-valve surgeries, 411 were concomitant valve and bypass surgeries, and 144 were multivalve surgeries. From this group, patients with a diagnosis of severe aortic stenosis (AVA≤1 cm2) were included in the study, along with those in whom a bioprosthetic valve was used for the aortic valve replacement. Patients with concomitant valve or coronary artery bypass surgery were also included in the study, but patients with a diagnosis of aortic insufficiency as the reason for AVR were excluded. Baseline preoperative and operative variables were used based on the information provided by the Society of Thoracic Surgeons database in Tables 1 and 2.
Table 1.
Preoperative Data.
| Patients | Non PPMn = 129 (41%) | Moderate PPMn = 132 (42%) | SeverePPM n = 50(16%) | p-value |
| Age (years) | 75±11 | 73±9 | 77±7 | 0.6 |
| Female | 45 (34.9%) | 42 (32.1%) | 41 (82%) | <0.001 |
| Body surface area (m2) | 1.80±0.2 | 1.97±0.2 | 1.75±0.25 | 0.155*) |
| Body mass index (Kg/m2) | 26.6±4.27 | 29.4±5.4 | 27.8±6.2 | 0.120*) |
| NYHA class ≥ III | 49 (38%) | 49 (37%) | 28 (56%) | 0.05 |
| Diabetes mellitus | 34 (26%) | 59 (44%) | 17 (34%) | 0.008 |
| Renal failure | 3 (2.3%) | 4 (3%) | 6 (12%) | 0.01 |
| Hypertension | 111 (86%) | 125 (95%) | 47 (94%) | 0.04 |
| Cerebrovascular disease | 12 (9.3%) | 10 (7.6%) | 6 (12%) | 0.64 |
| Smoker | 33 (25%) | 37 (28%) | 17 (34%) | 0.53 |
| Chronic lung disease | 79 (61%) | 86 (65%) | 34 (68%) | 0.65 |
| Peripheral vascular disease | 14 (11%) | 7 (5.3%) | 4 (8%) | 0.25 |
| Prior coronary artery bypass grafting | 11 (8.5%) | 16 (12%) | 6 (12%) | 0.60 |
| Myocardial infarction | 11 (8.5%) | 16 (12%) | 10 (20%) | 0.10 |
| Left ventricular ejection fraction ≤55% | 45 (35%) | 47 (36%) | 14 (28%) | 0.60 |
| Mean ejection fraction | 52±12 | 52±13 | 54±12 | 0.62 |
| Preoperative aortic valve gradient (mmHg) | 53±19 | 53±22 | 51±18 | 0.38 |
| Severe mitral insufficiency | 13 (10%) | 18 (14%) | 14 (28%) | 0.009 |
| Preoperative Medical TherapyBeta-blockers | 74 (57%) | 85 (64%) | 30 (60%) | 0.50 |
| Angiotensin converting enzyme inhibitors | 43 (33%) | 59 (45%) | 15 (30%) | 0.08 |
| Aspirin | 46 (36%) | 55 (42%) | 19 (38%) | 0.60 |
| Lipid lowering medications | 66 (51%) | 75 (57%) | 32 (64%) | 0.30 |
represents the p-value of severe PPM vs. no PPM.
NYHA: New York Heart Association heart failure class.
Table 2.
Operative Data.
| Variables | Non PPM n = 129 (41%) | Moderate PPM n = 132 (42%) | Severe PPM n = 50 (16%) | p-value |
| Elective | 129 (100%) | 129 (98%) | 50 (100%) | 0.12 |
| Coronary artery bypass grafting | 53 (41%) | 48 (36%) | 21 (42%) | 0.67 |
| Left main disease | 4 (3.1%) | 8 (6.0%) | 4 (8%) | 0.34 |
| Mitral valve surgery | 16 (12%) | 23 (17%) | 17 (34%) | 0.003 |
| Tricuspid valve surgery | 0 | 1 (0.8%) | 4 (8%) | 0.01 |
| Aortic annular enlargement | 2 (1.6%) | 1 (0.8%) | 3 (6%) | 0.06 |
| Intra-aortic balloon pump use | 19 (15%) | 27 (20%) | 13 (26%) | 0.19 |
| Intraoperative blood use | 68 (52.7%) | 78 (59.1%) | 28 (56%) | 0.58 |
| Perfusion time (minutes) | 118±38 | 114±40 | 100±42 | 0.0091 |
| Cross-clamp time (minutes) | 87.2±32 | 83.3±33 | 72.2±28 | 0.0052 |
| Minimally invasive surgery | 38 (32%) | 37 (28%) | 0 | <0.001 |
| Complications | ||||
| Total intensive care unit length of stay (hours) | 146±339 | 130±137 | 203±250 | 0.0123 |
| Prolonged ventilation (hours) | 73±268 | 48±100 | 112±304 | 0.08 |
| Permanent neurologic complications | 5 (3.9%) | 3 (2.3%) | 2 (4%) | 0.72 |
| Transient neurologic complications | 0 | 1 (0.8%) | 1 (2%) | 0.31 |
| Pneumonia | 10 (7.8%) | 6 (4.5%) | 3 (6%) | 0.13 |
| Renal failure | 10 (7.8%) | 10 (7.6%) | 5 (10%) | 0.9 |
| Short-term mortality | 3 (2.3%) | 8 (6.1%) | 4 (8%) | 0.19 |
| Length of hospital stay (days) | 15±16 | 14±10 | 20±13 | 0.04 |
1p-value between severe PPM versus no PPM. p = 0.05 between severe PPM versus moderate PPM.
2p-value between severe PPM versus no PPM. p = 0.04 between severe PPM vs. moderate PPM.
3p-value between severe PPM versus moderate PPM. p = 0.27 between severe PPM and no PPM.
Measurements: The effective orifice area (EOA) of each valve was obtained from a list that the American Society of Echocardiography published in their 2009 Recommendations for the Evaluation of Prosthetic Valves with Echocardiography and Doppler Ultrasound (6), which was based on a published report of normally functioning aortic valve prostheses (7). The effective orifice area values obtained from in vivo measurements for the different bioprosthetic aortic valves used during this analysis are given in Table 3. PPM was calculated using the EOA of the aortic valve prosthesis, which was divided by the patient's body surface area to obtain the indexed EOA. We defined nonsignificant, moderate, and severe PPM as an indexed EOA of >0.85 cm2/m2, 0.66 cm2/m2 to ≤0.85 cm2/m2, and ≤0.65 cm2/m2, respectively (12). We defined the nonsignificant PPM group as our control because they received the optimal therapy. Mortality was analyzed at the time of discharge from the hospital.
Table 3.
Reference values of effective orifice area for bioprosthetic aortic valves.
| Size, mm | Prosthetic | Valve | |||||
| 19 | 21 | 23 | 25 | 27 | 29 | ||
| No. of Patients | 54 | 98 | 90 | 51 | 17 | 1 | |
| Mosaic Porcine | 121 | 1.4 | 1.5 | 1.8 | 1.9 | 2.1 | |
| Freestyle | 4 | 1.4 | 1.7 | 2.1 | 2.5 | ||
| Mitroflow | 1 | 1.1 | 1.3 | 1.5 | 1.8 | ||
| Carpentier Edwards Standard | 166 | 0.9 | 1.5 | 1.7 | 1.9 | 2.3 | 2.8 |
| stented porcine | |||||||
| Carpentier Edwards Pericardial | 19 | 1.2 | 1.5 | 1.8 | |||
| stented bovine pericardial | |||||||
Statistical Analysis: Continuous variables are expressed as the mean ±1 SD; comparisons were conducted by t-tests/ANOVAs or nonparametric Mann-Whitney/Kruskal-Wallis tests if the normality assumption was violated when comparing severe PPM with no PPM or severe PPM with moderate PPM. Discrete variables are presented as percentages and relatives frequencies; comparisons were conducted by chi-squared statistics or Fisher's exact test, as appropriate. A p-value <0.05 was considered statistically significant. A stepwise logistic regression analysis (backward Wald) was used for the variables with a p-value <0.05 to assess the independent predictors of PPM and length of stay in the intensive care unit. We used a software system (Statistical Package for the Social Sciences, SPSS version 17 Chicago, Illinois) for all analyses.
RESULTS
A total of 311 patients (128 females and 183 males) with a diagnosis of severe aortic stenosis who underwent AVR with a bioprosthetic valve were identified. Based on the severity of the PPM, the cohort was divided in three groups: non-significant PPM (n = 129), 41%; moderate PPM (n = 132), 42%; and severe PPM, (n = 50) 16%. PPM was present in 58% of the total population, in 42% as moderate PPM and in 16% as severe PPM.
Patient characteristics: The baseline characteristics are presented in Table 1. The mean age was 75±11, 73±9, and 77±7 years for nonsignificant, moderate, and severe PPM, respectively (p = 0.6). Females represented 82% of the severe PPM group compared with 34% and 32% of the nonsignificant and moderate PPM groups, respectively (p<0.001) (Figure 1). There was no discrepancy in age between the different groups of PPM, (p = 0.6). The body surface area was lowest in the severe PPM group (1.75±0.5 m2) compared with 1.97±0.2 m2 of the moderate PPM (p<0.001), but this was not significantly different when compared with the nonsignificant PPM group value of 1.80±0.2 m2 (p = 0.155).
Figure 1.
Percentage of prosthesis-patient mismatch by gender.
Body mass index did not differ between the severe (27.8±6.2 Kg/m2) and moderate groups (29.4±5.4 Kg/m2), (p = 0.10), or when comparing nonsignificant (26.6±4.27 Kg/m2) and severe mismatch groups, (p = 0.12). Advanced heart failure (based on the New York Heart Association criteria) was found in 56% of patients in the severe group (p = 0.05). Diabetes mellitus was more prevalent in patients with moderate PPM (p = 0.008). Hypertension was prevalent in all of the groups, in particular, in those with moderate and severe mismatch (p = 0.04). Renal failure (serum creatinine >2 mg/dl) was higher in the severe PPM group, (p = 0.01). Coronary artery disease, with previous coronary artery bypass grafting (CABG) was similar in all groups as well, (p = 0.6).
The echocardiographic basal characteristics of the study population presented no differences in the mean ejection fraction: no PPM, 52±12%; moderate PPM, 52±13%; and severe PPM, 54±12%, (p = 0.62). Likewise, the aortic valve gradient was not significantly different: 53±19 mmHg, 53±22 mmHg, and 51±18 mmHg, in that order, (p = 0.38).
Surgical data: Most of the procedures were elective. Coronary artery bypass graft surgery was performed in 41% (nonsignificant PPM), 36% (moderate PPM), and 42% (severe PPM), respectively, (p = 0.67). Concomitant mitral valve surgery was performed in 34% of the severe PPM group, 17% of the moderate PPM group, and 12% in the no-PPM group (p = 0.003). Tricuspid valve surgery was completed in 8% of the severe PPM cases. A total of six (6) aortic annular enlargement procedures was performed; two in the no PPM, one in the moderate PPM, and three in the severe PPM groups.
Interestingly, the operative data in Table 2 show that patients in the severe PPM group had the shortest perfusion (p = 0.009) and cross-clamp times (p = 0.005) (Figure 2). However, the same group had the highest total intensive care unit length of stay with a mean value of 203 hours compared with 146 and 130 hours in the nonsignificant and moderate PPM groups, respectively (Figure 3). This was statistically significant (p = 0.012) when comparing severe and moderate PPM. No other factors were associated with the amount of intensive care unit hours except for the PPM difference. However, there was a statistical trend (p = 0.08) for prolonged mechanical ventilation in hours in the severe mismatch group (Figure 4). Along with these findings, patients with severe mismatch had the longest hospital stay with a mean value of 20 days compared with 15 and 14 days in the nonsignificant and moderate PPM groups, respectively (p = 0.04) (Figure 5). Fifteen cases of in-hospital mortality were identified, three in nonsignificant PPM, eight in moderate PPM, and four in the severe PPM groups (p = 0.19). Seventy-five minimally invasive surgeries were performed, 38 (50%) had nonsignificant PPM and 37 (50%) had moderate PPM. No case of severe PPM was found to be associated with minimally invasive surgery.
Figure 2.
Total amount of intensive care unit hours distributed according to patient-prosthesis mismatch.
Figure 3.
Hours of mechanical ventilation according to the severity of patient-prosthesis mismatch.
Figure 4.
Total amount of mechanical ventilation in hours distributed according to patient-prosthesis mismatch.
Figure 5.
Total length of in-hospital stay in days distributed according to patient-prosthesis mismatch.
Table 3 shows the different types of bioprosthetic valves used. The Carpentier Edwards Standard (Edwards Lifesciences, Irvine, CA), and the Mosaic Porcine (Medtronic, Minneapolis, MN) were the most commonly used, 53% and 39% of the time, respectively. A valve size of 21 mm was implanted in 31% of the surgeries, making it the most frequently used, while a valve size of 23 mm was the second most common, being used 29% of the time.
Independent Risk Factors: Univariate analysis from preoperative data showed that female gender and renal failure were statistically associated with severe PPM. Diabetes mellitus and ACE inhibitors use were associated with the moderate PPM group but not with the severe PPM group. Further multivariable analysis demonstrated that female gender was associated with severe mismatch (p<0.001), even when compared with the nonsignificant as well as the moderate PPM groups.
DISCUSSION
In patients undergoing AVR, PPM is a commonly encountered problem that leads to worsened hemodynamic function, less regression of left ventricular hypertrophy, and more cardiac events with lower survival rates (4,11,12). Other studies have demonstrated an association between female gender and higher operative mortality after valvular heart surgery (15).
Our results indicate that female gender is an independent risk factor for severe prosthesis-patient mismatch. This association was observed after the body surface area of the severe mismatch group proved not to be significantly different when compared with the group without any mismatch. When compared with men, women in general have a smaller body surface area and a smaller aortic annulus. Accordingly, PPM has proven to be more common in older females with concomitant coronary artery disease (16-18).
Our study demonstrated that 82 percent of severe mismatches corresponded to females without differences in age or any other baseline characteristics. Interestingly, this particular group had the shortest operative times. It is our impression that the use of smaller prosthetic valves for small and severely calcified annuli may have shortened the surgical times. It is possible that the reason is associated with the fact that surgeons did not have to enlarge the aortic root. PPM is therefore more frequently encountered in females, and the discrepancy between the inadequate size of both the prosthesis and the patient have proven to be risk factors for mortality (4,12,13). At the same time, the female heart responds differently than the male heart does for the same degree of left ventricular outflow obstruction, resulting in smaller end-systolic chamber size and higher pressures in the female heart response (18). This is particularly common with elderly patients with an excessive or inappropriate degree of hypertrophy; wall thickness is greater than necessary to counterbalance the high intracavitary pressures. As a result, the systolic wall stress is lower, and the ejection fraction is higher; such inappropriate LV hypertrophy has been associated with higher perioperative morbidity and mortality (17-19).
We found a significant impact of severe PPM on the intensive care unit length of stay and on the total hospital length of stay. Because of the nature of the study, we cannot establish a causal relationship between the degree of PPM and the findings. However, it has been demonstrated that abnormal intracavitary flow accelerations (defined as the presence of a dagger-shaped intracavitary flow signal on continuous-wave Doppler) after aortic valve replacement for severe aortic stenosis are associated with concentric left ventricular hypertrophy and supernormal systolic function. The abnormal intracavitary flow acceleration and concentric left ventricular hypertrophy were associated with higher in-hospital mortality, morbidity and prolonged intubation (17-20). Although not directly investigated in our study, this may have played a role in our patients.
We demonstrated that minimally invasive surgery may be related to a higher frequency of moderate PPM, but also to a lower rate of severe PPM; we believe that if this is confirmed, it is likely to have clinical implications with respect to the selection of a particular surgical technique. For this reason, we are currently prospectively exploring this possibility in our institution.
This study highlights the importance of avoiding PPM, particularly in females who react differently from a pathophysiologic standpoint. Aortic PPM can be avoided through optimal prosthesis selection in the individual patient by calculating the necessary indexed EOA prior to surgery (3). This is particularly important in patients with left ventricular dysfunction and/or severe left ventricular hypertrophy (3).
Study Limitations: The current study was based on data obtained from a patient registry with retrospective analysis and was not able to establish a causal relationship. The postoperative intracavitary flow accelerations were not available but may have helped to confirm our hypothesis. The assessment of these parameters along with the patient's outcome may have an impact on selecting the appropriate therapy.
Footnotes
No potential conflict of interest was reported.
REFERENCES
- 1.Freeman RV, Otto CM. Spectrum of calcific aortic valve disease. Pathogenesis, disease progression, and treatment strategies. Circulation. 2005;111:3316–26. doi: 10.1161/CIRCULATIONAHA.104.486738. [DOI] [PubMed] [Google Scholar]
- 2.Rahimtoola SH. The problem of valve prosthesis-patient mismatch. 1978;58:20–4. doi: 10.1161/01.cir.58.1.20. Circulation. [DOI] [PubMed] [Google Scholar]
- 3.Pibarot P, Dumesnil JG. Prosthetic Heart Valves. Selection of the optimal prosthesis and long-term management. Circulation. 2009;119:1034–48. doi: 10.1161/CIRCULATIONAHA.108.778886. [DOI] [PubMed] [Google Scholar]
- 4.Blais C, Dumesnil JG, Baillot R, Simard S, Doyle D, Pibarot P. Impact of valve prosthesis-patient mismatch on short-term mortality after aortic valve replacement. Circulation. 2003;108:983–8. doi: 10.1161/01.CIR.0000085167.67105.32. [DOI] [PubMed] [Google Scholar]
- 5.Mohty D, Malouf JF, Girard SE, Schaff HV, Grill DE, Enriquez-Sarano ME, et al. Impact of prosthesis-patient mismatch on long-term survival in patients with small St. Jude medical mechanical prosthesis in the aortic position. Circulation. 2006;113:420–6. doi: 10.1161/CIRCULATIONAHA.105.546754. [DOI] [PubMed] [Google Scholar]
- 6.Zoghbi WA, Chambers JB, Dumesnil JG, Foster E, Gottdiener JS, Grayburn PA, et al. Recommendations for evaluation of prosthetic valves with echocardiography and doppler ultrasound: a report From the American Society of Echocardiography's Guidelines and Standards Committee and the Task Force on Prosthetic Valves, developed in conjunction with the American College of Cardiology Cardiovascular Imaging Committee, Cardiac Imaging Committee of the American Heart Association, the European Association of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography and the Canadian Society of Echocardiography, endorsed by the American College of Cardiology Foundation, American Heart Association, European Assocation of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography, and Canadian Society of Echocardiography. J Am Soc Echo. 2009;22:975–1014. doi: 10.1016/j.echo.2009.07.013. [DOI] [PubMed] [Google Scholar]
- 7.Rajani R, Mukherjee D, Chambers JB. Doppler echocardiography in normally functioning replacement aortic valves: a review of 129 studies. J Heart Valve Dis. 2007;16:521–35. [PubMed] [Google Scholar]
- 8.Oakley RE, Kleine P, Bach DS. Choice of prosthetic heart valve in today's practice. Circulation. 2008;117:253–6. doi: 10.1161/CIRCULATIONAHA.107.736819. [DOI] [PubMed] [Google Scholar]
- 9.Pibarot P, Dumesnil JG. Hemodynamic and clinical impact of prosthesis patient mismatch in the aortic valve position and its prevention. J Am Coll Cardiol. 2000;36:1131–41. doi: 10.1016/s0735-1097(00)00859-7. [DOI] [PubMed] [Google Scholar]
- 10.Rahimtoola SH. Choice of prosthetic heart valve for adult patients. J Am Coll Cardiol. 2003;41:893–904. doi: 10.1016/s0735-1097(02)02965-0. [DOI] [PubMed] [Google Scholar]
- 11.Rubio Alvarez J, Sierra Quiroga J, Vega Fernandez M, Adrio Nazar B, Gude Sampedro F, Martinez Comendador JM, et al. Up to twenty-five-year survival after aortic valve replacement with size 19 mm valves. Inter Cardiovasc and Thorac Surg. 2010;10:32–6. doi: 10.1510/icvts.2009.209197. [DOI] [PubMed] [Google Scholar]
- 12.Pibarot P, Dumesnil JG. Prosthesis-patient mismatch: definition, clinical impact, and prevention. Heart. 2006;92:1022–9. doi: 10.1136/hrt.2005.067363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Walther T, Rastan A, Falk V, Lehmann S, Garbade J, Funkat AK, et al. Patient prosthesis mismatch affects short and long term outcomes after aortic valve replacement. Eur J Cardiothorac Surg. 2006;30:15–9. doi: 10.1016/j.ejcts.2006.04.007. [DOI] [PubMed] [Google Scholar]
- 14.Pai RG, Kapoor N, Bansal RC, Varadarajan P. Malignant natural history of asymptomatic severe aortic stenosis: benefit of aortic valve replacement. Ann Thorac Surg. 2006;82:2116–22. doi: 10.1016/j.athoracsur.2006.07.043. [DOI] [PubMed] [Google Scholar]
- 15.Edwards FH, Peterson ED, Coombs LP, DeLong ER, Jamieson WR, Shroyer ALW, et al. Prediction of operative mortality after valve replacement surgery. J Am Coll Cardiol. 2001;37:885–92. doi: 10.1016/s0735-1097(00)01202-x. [DOI] [PubMed] [Google Scholar]
- 16.Taggart DP. Prosthesis patient mismatch in aortic valve replacement: possible but pertinent. Eur Heart J. 2006;27:644–6. doi: 10.1093/eurheartj/ehi757. [DOI] [PubMed] [Google Scholar]
- 17.Aurigemma G, Battista S, Orsinelli D, Sweeney A, Pape L, Cuenoud H. Abnormal left ventricular intracavitary flow acceleration in patients undergoing aortic valve replacement for aortic stenosis: a marker for high postoperative morbidity and mortality. Circulation. 1992;86:926–36. doi: 10.1161/01.cir.86.3.926. [DOI] [PubMed] [Google Scholar]
- 18.Carroll JD, Carroll EP, Feldman T, Ward DM, Lang RM, McGaughey D, et al. Sex-associated differences in left ventricular function in aortic stenosis of the elderly. Circulation. 1992;86:1099–107. doi: 10.1161/01.cir.86.4.1099. [DOI] [PubMed] [Google Scholar]
- 19.Orsinelli DA, Aurigemma GP, Battista S, Krendel S, Gaasch WH. Left ventricular hypertrophy and mortality after aortic valve replacement for aortic stenosis: a high risk subgroup identified by preoperative relative wall thickness. J Am Coll Cardiol. 1993;22:1679–83. doi: 10.1016/0735-1097(93)90595-r. [DOI] [PubMed] [Google Scholar]
- 20.Duncan AI, Lowe BS, Garcia MJ, Xu M, Gillinov AM, Mihaljevic T, et al. Influence of concentric left ventricular remodeling on early mortality after aortic valve replacement. Ann Thorac Surg. 2008;85:2030–9. doi: 10.1016/j.athoracsur.2008.02.075. [DOI] [PubMed] [Google Scholar]