| Literature DB >> 32937912 |
Daniel Hernandez-Vaquero1, Carlota Vigil-Escalera1, Yvan Persia2, Carlos Morales1, Isaac Pascual2, Alberto Domínguez-Rodríguez3, Emiliano Rodríguez-Caulo4, Manuel Carnero5, Rocío Díaz1, Pablo Avanzas2, Cesar Moris2, Jacobo Silva1.
Abstract
The Trifecta aortic valve has excellent hemodynamics characteristics. Moreover, the Perceval prosthesis may achieve better hemodynamics than the conventional valves; therefore, it has been proposed to reduce the incidence of patient-prosthesis mismatch. Our aim was to compare the prevalence of this complication between both prostheses. All patients who underwent valve replacement with a Perceval or a Trifecta from 2016 to 2020 at our institution were included. We calculated the prevalence of patient-prosthesis mismatch for each prosthesis and size and performed a multinomial logistic regression model to investigate the impact of choosing one prosthesis over the other. A total of 516 patients were analyzed. Moderate mismatch was present in 33 (8.6%) in the Trifecta group and 28 (21.4%) in the Perceval group, p < 0.001. Severe mismatch was present in 8 (2.1%) patients with Trifecta and 5 (3.8%) patients with Perceval, p = 0.33. Compared with the Perceval, the Trifecta prosthesis was shown to reduce moderate patient-prosthesis mismatch: OR = 0.5 (95% CI 0.3-0.9, p = 0.02). Both prostheses led to a similar risk of severe patient-prosthesis mismatch: OR = 0.9 (95% CI 0.3-2.8, p = 0.79). Both prostheses provide a very low risk of severe patient-prosthesis mismatch. Compared with the Perceval prothesis, the Trifecta prosthesis is able to reduce by 50% the risk of moderate mismatch.Entities:
Keywords: aortic valve replacement; bioprosthesis; patient–prosthesis mismatch
Year: 2020 PMID: 32937912 PMCID: PMC7563879 DOI: 10.3390/jcm9092964
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241
Baseline characteristics.
| Clinical Data | Trifecta | Perceval | |
|---|---|---|---|
| Women | 190 (46.6%) | 85 (60.7%) | 0.004 |
| Age, years | 76.7 ± 5.8 | 78.2 ± 6.4 | 0.008 |
| Weight, kg | 75.1 ± 12.5 | 73.4 ± 13.7 | 0.17 |
| Height, cms | 161.2 ± 8.9 | 159.2 ± 9.4 | 0.03 |
| Systemic hypertension | 326 (79.7%) | 107 (76.4%) | 0.40 |
| Diabetes | |||
| Non-insulin-dependent | 80 (19.6%) | 32 (22.9%) | |
| Insulin-dependent | 31 (7.6%) | 14 (10%) | 0.38 |
| Dyslipidemia | 220 (53.8%) | 93 (63.4%) | 0.01 |
| Body surface area (m2) | 1.8 ± 0.2 | 1.8 ± 0.2 | 0.22 |
| Body mass index (kg/m2) | 28.9 ± 4.5 | 29.1 ± 4.9 | 0.83 |
| Chronic obstructive pulmonary disease | 62 (15.2%) | 28 (20%) | 0.19 |
| Creatinine clearance (mL/min) | 63.3 ± 25.4 | 59.5 ± 28.5 | 0.17 |
| Previous stroke | 17 (4.2%) | 14 (10%) | 0.018 |
| Poor mobility | 8 (1.9%) | 3 (2.1%) | 1 |
| Extracardiac arteriopathy | 43 (10.5%) | 18 (12.9%) | 0.44 |
| Previous cardiac surgery | 18 (4.4%) | 10 (7.1%) | 0.26 |
| Critical preoperative state | 3 (0.7%) | 1 (0.7%) | 1 |
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| |||
| Active endocarditis | 21 (5.13%) | 6 (4.29%) | 0.82 |
| History of supraventricular arrhythmia | 83 (20.3%) | 26 (18.6%) | 0.71 |
| Concomitant coronary disease | 140 (34.2%) | 55 (39.3%) | 0.48 |
| Previous acute myocardial infarction < 3 months | 10 (2.4%) | 3 (2.1%) | 1 |
| Functional class NYHA | |||
| NYHA I | 20 (4.9%) | 1 (0.7%) | |
| NYHA II | 160 (39.1%) | 81 (57.9%) | |
| NYHA III | 206 (50.4%) | 53 (37.9%) | |
| NYHA IV | 23 (5.6%) | 5 (0.04%) | 0.005 |
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| |||
| Left ventricular ejection fraction | |||
| >50% | 345 (84.4%) | 116 (82.9%) | |
| >30% y ≤50% | 48 (11.7%) | 16 (11.4%) | |
| ≤30% y >20% | 16 (3.9%) | 8 (5.71%) | |
| ≤20% | 0 (0%) | 0 (0%) | 0.63 |
| Interventricular septum > 17mm | 73 (17.8%) | 44 (31.4%) | 0.001 |
| Left ventricular outflow tract diameter, mm | 22 ± 2.3 | 20.5 ± 2.4 | <0.001 |
| Systolic pulmonary pressure > 55 mmHg | 48 (11.9%) | 9 (6.43%) | 0.004 |
| Aortic pathology | |||
| Pure stenosis | 312 (76.5%) | 107 (76.9%) | |
| Pure insufficiency | 48 (11.8%) | 8 (5.76%) | |
| Double lesion | 48 (11.8%) | 24 (17.3%) | 0.046 |
| Mean gradient, mmHg | 47.3 ± 14.8 | 44.7 ± 14.5 | 0.11 |
| Peak gradient, mmHg | 79.5 ± 21.4 | 75.9 ± 22.9 | 0.16 |
Operation characteristics and postoperative complications
| Operation Characteristics | Trifecta | Perceval | |
|---|---|---|---|
| Non-elective surgery | 90 (22.3%) | 33 (23.6%) | 0.76 |
| Prosthetic size | * | ||
| 19 mm/S | 76 (18.6%) | 33 (23.6%) | |
| 21 mm/M | 151 (36.9%) | 53 (37.9%) | |
| 23 mm/L | 132 (32.3%) | 29 (20.7%) | |
| 25/XL | 38 (9.3%) | 25 (17.9%) | |
| 27 | 12 (2.9%) | ||
| Mitral surgery | 63 (15.4%) | 13 (9.3%) | 0.09 |
| Tricuspid surgery | 9 (2.2%) | 3 (2.1%) | 0.63 |
| Proximal aortic surgery | 18 (4.4%) | 1 (0.7%) | 0.06 |
| Number of aortocoronary grafts | 0.38 | ||
| None | 90 (70%) | 278 (67.9%) | |
| 1 | 27 (19.3%) | 72 (17.6%) | |
| 2 | 9 (6.4%) | 38 (9.3%) | |
| 3 | 6 (4.3%) | 18 (4.4%) | |
| 4 or more | 0 (0%) | 3 (0.7%) | |
| Cardiopulmonary bypass time | 95.7 ± 37.9 | 81.3 ± 34.9 | <0.001 |
| Cross-clamping time | 77.2 ± 30.3 | 65.3 ± 29.1 | <0.001 |
| Aortic root enlargement | 12 (2.9%) | 0 (0%) | 0.04 |
| EuroSCORE II | 5.4 ± 5.8 | 4.5 ± 4.6 | 0.17 |
| Logistic EuroSCORE | 12.9 ± 11.3 | 11.3 ± 9.3 | 0.21 |
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| |||
| Pre-discharge mortality or <30 days | 24 (5.9%) | 9 (6.4%) | 0.47 |
| Oro-tracheal intubation > 24 h | 57 (13.9%) | 23 (16.4%) | 0.49 |
| Stroke | 11 (2.7%) | 4 (2.9%) | 1 |
| Acute myocardial infarction | 6 (4.3%) | 32 (7.8%) | 0.18 |
| New need of permanent pacemaker | 8 (2%) | 15 (10.7%) | 0.002 |
| Supraventricular arrhythmia without effective cardioversion | 18 (12.9%) | 66 (16.1%) | 0.42 |
| Peri-valvular regurgitation | <0.001 | ||
| I | 8 (1.9%) | 6 (4.3%) | |
| II | 2 (0.5%) | 5 (3.6%) | |
| III | 1 (0.2%) | 3 (2.1%) | |
| IV | 0 (0%) | 0 (0%) | |
| Intra-valvular regurgitation | <0.001 | ||
| I | 11 (2.7%) | 14 (10%) | |
| II | 1 (0.2%) | 3 (2.1%) | |
| III | 0 (0%) | 0 (0%) | |
| IV | 0 (0%) | 0 (0%) |
* Size S of Perceval is for aortic annulus of 19–21 mm. Size M for 21–23 mm. Size L for 23–25 mm and size XL for 25–27 mm [6]. Therefore, the size of a Perceval does not match the size of any Trifecta. Accordingly, p-value was not calculated, since a direct comparison may be misleading.
Prevalence of PPM and other parameters for patients at discharge.
| Variables | Trifecta ( | Perceval ( |
|---|---|---|
|
| ||
| Prevalence of PPM | ||
| No PPM | 54 (73.2%) | 16 (50%) |
| Moderate PPM | 13 (17.8%) | 12 (37.5%) |
| Severe PPM | 6 (8.2%) | 4 (12.5%) |
| Mean gradient, mmHg | 14.4 ± 5.1 | 14.6 ± 4.6 |
| EOA, cm2 | 1.6 ± 0.4 | 1.5 ± 0.3 |
| IEOA, cm2/m2 | 0.9 ± 0.2 | 0.9 ± 0.2 |
|
| ||
| Prevalence of PPM | ||
| No PPM | 128 (91.4%) | 41 (78.9%) |
| Moderate PPM | 10 (7.1%) | 11 (21.2%) |
| Severe PPM | 2 (1.4%) | 0 (0%) |
| Mean gradient, mmHg | 11.9 ± 4.8 | 12.4 ± 5.5 |
| EOA, cm2 | 2 ± 0.3 | 1.7 ± 0.3 |
| IEOA, cm2/m2 | 1.2 ± 0.2 | 1 ± 0.2 |
|
| ||
| Prevalence of PPM | ||
| No PPM | 115 (92%) | 24 (85.7%) |
| Moderate PPM | 10 (8%) | 3 (10.7%) |
| Severe PPM | 0 (0%) | 1 (3.6%) |
| Mean gradient, mmHg | 9.4 ± 3.9 | 9.9 ± 3.8 |
| EOA, cm2 | 2.3 ± 0.4 | 1.8 ± 0.3 |
| IEOA, cm2/m2 | 1.2 ± 0.2 | 1 ± 0.2 |
|
| ||
| Prevalence of PPM | ||
| No PPM | 47 (100%) | 17 (79.5%) |
| Moderate PPM | 0 (0%) | 2 (10.5%) |
| Severe PPM | 0 (0%) | 0 (0%) |
| Mean gradient, mmHg | 6.7 ± 2.5 | 8.4 ± 2.9 |
| EOA, cm2 | 2.5 ± 0.4 | 2.1 ± 0.2 |
| IEOA, cm2/m2 | 1.4 ± 0.2 | 1.1 ± 0.2 |
EOA: effective orifice area. IEOA: indexed effective orifice area. PPM: patient–prosthesis mismatch. Size S of Perceval is for aortic annulus of 19–21 mm. Size M for 21–23 mm. Size L for 23–25 mm and size XL for 25–27 mm [6]. Therefore, the size of a Perceval does not match the size of any Trifecta. Accordingly, p-value was not calculated since a direct comparison can be misleading.
Figure 1Mean transaortic gradients according to the type of prosthesis and size. Both types of prosthesis are presented together for visual inspection. However, size S of the Perceval is for an aortic annulus of 19–21 mm. Size M: 21–23 mm. Size L: 23–25 mm. Size XL: 25–27 mm [6]. Therefore, the size of a Perceval does not match the size of any Trifecta.
Figure 2Indexed effective orifice area according to the type of prosthesis and size. Both types of prosthesis are presented together for visual inspection. However, size S of the Perceval is for an aortic annulus of 19–21 mm. Size M: 21–23 mm. Size L: 23–25 mm. Size XL: 25–27 mm [6]. Therefore, the size of a Perceval does not match the size of any Trifecta.
Figure 3Relationship between effective orifice area and body surface area. Green line separates patients with and without PPM. The sizes of circles vary according to size of the prostheses. (19 Trifecta similar to S Perceval, 21–M, 23–L, and 25/27–XL). PPM: patient–prosthesis mismatch.
Figure 4Predicted probability of PPM according to different body surface area in our sample. Lines are formed by a lowess function. PPM: patient–prosthesis mismatch.