This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
1. Introduction
Aortic stenosis is the most common valve disease in industrialised countries leading to surgery or catheter intervention [1, 2]. If severe symptomatic aortic stenosis is left untreated, prognosis is poor and mortality is up to 50% one year after onset of symptoms and more than 90% after five years [3]. Transcatheter aortic valve implantation (TAVI) is the standard treatment for patients with severe aortic stenosis at high and excessive risk for surgery [1, 4, 5]. Recently, guidelines were expanded, and TAVI is now also recommended as an alternative procedure to conventional surgery in intermediate-risk patients [6–8]. Clinical trials and registry data have demonstrated high procedural success and a significant improvement of survival [9]. However, comprehensive multimodality and multidisciplinary Heart Team assessment is pivotal to ensure best possible outcomes after TAVI [10]. Before patients are admitted for TAVI, they undergo thorough examinations, including functional and cognitive tests. The results are discussed at a multidisciplinary team conference, and risk-benefit analysis determines if TAVI procedure should be recommended. Additionally, the impact of the procedure on health status after TAVI is of importance to guide the patient-centred decision-making process. In the elderly, the consequences of health status after TAVI may be as or even more important than survival since they often express a preference for quality of life over quantity of life [11, 12]. The EQ-5D-5L questionnaire is a suitable instrument for evaluating patients’ health status after TAVI since it is a standardized test which has been used in previous studies [13–15]. In addition to health status, there are limited data on long-term complication rates and hospital readmissions following TAVI. Most studies report only one-year follow-up data with a maximum of 5 years [16–20]. In light of these facts, the main objective of this study was to investigate long-term perceived health status and self-reported outcomes at a minimum of 5 years after TAVI.
2. Methods
2.1. Study Population and Study Design
Between November 2006 and December 2012, a total of 452 patients with severe symptomatic aortic stenosis received TAVI at our institution. After checking survival status between October 2018 and January 2019, a trained professional contacted the patients still alive by telephone and asked a defined set of questions. In addition to some general health-related questions, the EQ-5D-5L questionnaire was conducted. Furthermore, questions about complications and rehospitalizations after TAVI were asked (A detailed list with all questions can be found in the supplementary data, Table S1 and S2 (available here)). All patients alive, who underwent TAVI more than 5 years ago, were included in our study regardless of access route or valve type. Patients were excluded from the study if they were cognitively impaired, unable to speak German, or too sick to answer the questions. No data on baseline health status were available. The study was approved by the local ethics committee of the Goethe University of Frankfurt, and it was conducted in accordance with the Declaration of Helsinki.
2.2. Procedure
Design features of the balloon-expandable and self-expanding prosthesis and technical details of the procedure have been previously described [21, 22]. The Edwards bioprosthesis, available in 23 mm, 26 mm, and 29 mm sizes, was implanted using the transfemoral or the transapical approach. The CoreValve prosthesis, available in 26 mm, 29 mm, and 31 mm sizes, was implanted using the transfemoral approach. Three patients received a JenaValve with the transapical approach. Two of them died before the follow-up, and only one patient with a 25 mm size JenaValve was included for further analysis. All procedures were performed under local anaesthesia or general anaesthesia with endotracheal intubation.
2.3. Health Status Assessment
Health status was measured with the generic European Quality of Life Five Dimensions Five Levels (EQ-5D-5L) questionnaire (Supplementary data, Table S2). The EQ-5D-5L is a standardized health utility Quality of Life (QoL) instrument and is qualified for measuring health status within an elderly population (EuroQoL Group, Germany) [23]. This descriptive system consists of five domains (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression). Each of these domains is divided into five levels of functioning (5L) indicating no problems (level 1), some problem (level 2), moderate problems (level 3), severe problem (level 4), and extreme problems (level 5). There are 3125 possible health states in the EQ-5D-5L questionnaire and each of them is referred to by a five-digit code. The health states can be converted to a utility score, ranging from −0.446 to 1 (a value of 1 indicating full health, while a value lower than 0 represents a status considered to be worse than death). In this study, health status was assessed using a validated German version of the EQ-5D-5L.
The second part of the EQ-5D includes a visual analogue scale (EQ-VAS), with numeric values from 0 (“worst imaginable health state”) to 100 (“best imaginable health state”) [24].
2.4. Statistical Analysis
Descriptive statistics were summarized as mean ± SD for normally distributed continuous variables or otherwise as median and 25th to 75th percentile. Categorical variables are described by frequencies and percentages. Differences in paired samples were tested using the Wilcoxon signed-rank test or paired Student’s t-test. Categorical variables were compared using the chi-square or Fisher’s exact test. Statistical significance was defined at a level of
3. Results
From November 2006 to December 2012, 452 patients were consecutively treated with TAVI at our institution. 103 patients (22.8%) were still alive at a median follow-up period of 7 years (5.4–9.8). 335 (74.1%) patients died before the time of inclusion, 7 patients were lost to follow-up, and in 7 cases implantation was not successful (see Figure 1). 99 (96%) of the 103 patients were eligible for the study and agreed to participate in our survey. The mean age at follow-up was 86.5 years ± 8.0 years, and 56.6% were female. Baseline and procedural characteristics are presented in Tables 1 and 2. The devices used were in 58.8% balloon-expandable (Edwards) and in 40.2% self-expanding (CoreValve) prosthetic valves. Only one patient received a self-expanding JenaValve. The transfemoral approach was used in 65.0% of cases and the transapical in the remaining 35%. Early clinical outcome data are depicted in Table 3. In-hospital mortality was 9.2%, the need for a new pacemaker implantation (PPI) was 12.6%, and major bleeding occurred in 5.9% according to VARC-2 criteria [25].
[figure omitted; refer to PDF]
Table 1
Baseline characteristics before TAVI and at late follow-up.
Variable | Total (n = 103) |
---|---|
Before TAVI | |
Age, years at TAVI | 80.1 ± 7.9 (30–92), |
Female, n (%) | 58 (56.3) |
BMI (kg/m2) | 27.5 ± 4.3 |
STS score | 9.1 ± 5.6 |
Logistic EuroScore | 18.1 ± 11.7 |
NYHA functional class III to IV | 65 (67.0) |
Hypertension, n (%) | 92 (89.3) |
Diabetes mellitus, n (%) | 23 (22.3) |
CKD, (GFR <60 ml/min), n (%) | 63 (61.2) |
Previous MI, n (%) | 19 (18.4) |
Previous PCI, n (%) | 52 (51.5) |
Previous CABG, n (%) | 10 (9.7) |
Permanent pacemaker | 16 (15.5) |
COPD, n (%) | 15 (14.7) |
Prior CVA/TIA | 12 (11.6) |
Atrial fibrillation/atrial flutter | 36 (35.0) |
|
|
At late follow-up | |
Age, years | 86.5 ± 8.0 (37–98) |
Female, n (%) | 56 (56.6) |
Data are expected as absolute values (n) and percentages (%) or as mean ± standard deviation (SD). TAVI, transcatheter aortic valve implantation; n, number; BMI, body mass index; STS, society of thoracic surgery; NYHA, New York Heart Association; CKD, chronic kidney disease; MI, myocardial infarction; PCI, percutaneous coronary intervention; CABG, coronary artery bypass graft; COPD, chronic obstructive pulmonary disease; CVA; cerebrovascular accident; TIA, transient ischemic attack.
Table 2
Procedural characteristics.
Variable | n (%) |
---|---|
Valve type | |
Edward bioprosthesis | 60 (58.8) |
CoreValve | 41 (40.2) |
JenaValve | 1 (1.0) |
|
|
Access, n (%) | |
Transfemoral | 68 (65.0) |
Transapical | 35 (35.0) |
Prosthesis after dilatation, n (%) | 13 (12.7) |
Valve-in-valve, n (%) | 5 (5.0) |
|
|
Prosthesis diameter, n (%) | |
23 mm | 22 (21.6) |
25 mm | 1 (1.0) |
26 mm | 51 (50.0) |
29 mm | 26 (25.5) |
31 mm | 2 (2.0) |
|
|
Anaesthesia | |
Local | 64 (62.1) |
General | 39 (37.9) |
Data are expected as absolute values (n) and percentages (%).
Table 3
Early clinical outcomes.
Variable | n (%) |
---|---|
Procedural and in-hospital outcomes | |
In-hospital mortality | 44 (9.2) |
New-onset left bundle branch block | 21 (20.4) |
Need for pacemaker implantation | 13 (12.6) |
New-onset atrial fibrillation or flatter post-TAVI | 13 (12.6) |
Coronary obstruction | 0 (0) |
Ventricular perforation with tamponade | 3 (2.9) |
Need for second valve | 1 (1.0) |
Stroke, n (%) | 1 (1) |
Major vascular complication, n (%) |
2 (1.9) |
Minor vascular complication, n (%) |
13 (12.7) |
|
|
Bleeding, n (%)
|
|
Major |
6 (5.8) |
|
|
AKI, n (%)
|
|
Stage 1 | 2 (1.9) |
Stage 2 | 3 (2.9) |
Stage 3 | 2 (1.9) |
Data are expressed as absolute values (n) and percentages (%). AKI, acute kidney injury;
3.1. Health Status
Outcomes regarding health status including the EQ-5D-5L results and EQ-VAS scores are listed in Tables 4 and 5. Approximately, two-third (62.7%) of the interviewed patients stated that they are currently in a good general health condition. 93.4% of the patients described an improvement of their health status after receiving TAVI.
Table 4
Health status.
Variable | TAVI patients (n = 99) | German population |
---|---|---|
Current general health condition | ||
Good | 62 (62.6) | |
Okay | 31 (31.3) | |
Not good | 6 (6.0) | |
Better after TAVI | 93 (93.9) | |
|
||
EQ-5D (% of patients indicating a problem) | ||
Mobility | 85.4% | 54.2% |
Self-care | 26.1% | 16.0% |
Usual activities | 82.3% | 33.8% |
Pain/discomfort | 52.1% | 52.2% |
Anxiety/depression | 19.8% | 6.6% |
Utility score | 0.80 ± 0.20 | 0.84 ± 0.14 |
VAS | 58.49 ± 11.49 | 60.5 ± 20.3 |
|
||
NYHA functional class III to IV | 56 (58.3) | |
NYHA function ≤III | 40 (41.7) |
Data are expected as absolute values (n) and percentages (%) or as mean ± SD. TAVI, transcatheter aortic valve implantation; AP, angina pectoris; NYHA, New York Heart Association.
Table 5
Frequency of patients reporting problems in EQ-5D-3L domains at late follow-up.
Mobility | Self-care | Usual activities | Pain/discomfort | Anxiety/depression | |
---|---|---|---|---|---|
No problems | 14 (14.6) | 71 (74.0) | 17 (17.7) | 46 (47.9) | 77 (80.2) |
Slight to moderate problems | 57 (59.4) | 19 (19.8) | 71 (74.0) | 48 (50.0) | 19 (19.8) |
Severe to extreme problems | 25 (26.0) | 6 (6.3) | 8 (8.3) | 2 (2.1) | 0 (0) |
Data are expected as absolute values (n) and percentages (%).
With respect to EQ-5D-5L, mobility was found to be the most frequently reported limitation (85.4%), while anxiety/depression was the least frequently reported limitation (19.8%). The majority of the patients had slight to moderate limitations in most domains (Table 5). The mean utility index and EQ-VAS score were 0.80 ± 0.20 and 58.49 ± 11.49, respectively. Table 4 also shows a comparison of the health status in TAVI patients with the mean values of the age-adjusted German population older than 75 years.
With attention to functional New York Heart Association (NYHA) class, 67.0% were in NYHA class III or IV before TAVI and 64.9% at a median follow-up period of 7 years (
[figure omitted; refer to PDF]
3.2. Long-Term Outcome and Rehospitalization
Self-reported long-term outcomes revealed mainly low complication rates (Table 6, Figure 3). All-stroke rate was 3.3%, bleeding occurred in 5.5%, and acute coronary syndrome in 2.2% during the median time of 7 years after TAVI. PPI was necessary in 6 patients, and the overall pacemaker intervention rate including pacemaker replacement was 12.9%. In addition, 15.5% of patients reported events of new cardiac arrhythmias.
Table 6
Self-reported long-term outcome.
Variable | n (%) |
---|---|
Hospitalization | 74 (78.7) |
Hospitalization for CVD | 32 (31.1) |
ACS | 2 (2.2) |
PCI | 6 (6.5) |
CABG | 0 (0) |
Cardiopulmonary resuscitation | 1 (1.1) |
PP implantation or replacement | 12 (12.9) |
All stroke | 3 (3.3) |
New cardiac arrhythmias | 16 (15.5) |
Syncope | 6 (5.8) |
Bleeding minor | 5 (5.4) |
Bleeding major | 0 (0) |
Cancer | 7 (7.5) |
Data are expected as absolute values (n) and percentages (%). CVD, cardiovascular disease; ACS, acute coronary syndrome; PCI, percutaneous coronary intervention; CABG, coronary artery bypass graft; PP, permanent pacemaker.
[figure omitted; refer to PDF]Furthermore, patients described 74 total hospitalizations after TAVI, and among them in 43% for cardiovascular reasons. Within cardiovascular rehospitalizations, requirement for PPI was the most frequently reported (18.9%), followed by cardiac decompensation and coronary heart disease (15.6%) (Table 7).
Table 7
Reasons for cardiovascular disease hospitalization.
Variable | n (%) |
---|---|
Cardiac decompensation | 5 (15.6) |
Coronary heart disease | 5 (15.6) |
New pacemaker implantation (4 ES, 1 CV, 1 unknown) | 6 (18.8) |
Pacemaker replacement | 4 (12.5) |
Prior CVA/TIA | 3 (9.4) |
Mitral valve surgery | 2 (6.3) |
Reoperation of aortic valve | 2 (6.3) |
Cardiac arrhythmias | 3 (9.4) |
Peripheral arterial disease | 1 (3.1) |
ICD implantation | 1 (3.1) |
Left atrial appendage closure | 1 (3.1) |
Data are expected as absolute values (n) and percentages (%). ES, Edwards sapiens; CV, CoreValve; CVA, cerebrovascular accident; TIA, transient ischemic attack; ICD, implantable cardioverter-defibrillator.
4. Discussion
The main finding of the present study analysing a selected group of patients more than five years after TAVI was a satisfactory health status, no significant change in functional (NYHA) class compared to before TAVI, and low self-reported complication and rehospitalization rates. Our study about self-reported health status and outcomes after TAVI is currently the only study with a very long follow-up time with a median duration of 7 years. A high proportion of the patients still alive could be included in the final analysis.
Over 90% of patients described an overall improvement of their health situation after TAVI. With regard to the standardized EQ-5D-5L questionnaire, the current health status showed satisfactory results at late follow-up. Mobility was found to be the most frequent limitation (85.4%), followed by limitation in usual activity (82.3%). Since we did not evaluate baseline EQ-5D-5L, we could not analyse any change in health status. The German TAVI registry evaluated the EQ-5D index after one year and found a significant improvement of health status [13]. Interestingly, however, our results showed a better EQ-5D index after a median follow-up time of 7 years compared to the one-year results of the German TAVI registry (0.80 ± 0.20 vs. 0.70 ± 0.24). In addition, the visual analogue health scale was similar in our study compared to the one-year results of the German TAVI registry (58.49 ± 11.49 vs. 57 ± 19.6). Previous studies focused mainly on the first postprocedural period up to one year after TAVI and most of them showed a substantial improvement in health status [14, 15, 28]. To our knowledge, only one Dutch study published recently data on quality of life data after TAVI with a mean follow-up time of 5.5 years [15]. All patients showed satisfactory quality of life data despite their age and multiple comorbidities. Nevertheless, their study revealed a lower utility score than the result in our analysis (0.69 ± 0.29 vs. 0.80 ± 0.20).
Moreover, our study showed a similar utility score and EQ-VAS score compared with the general age-adjusted German population (Table 4). Of note, the population norms for the EQ-5D were standardized to adults older than 75 years, whereas our patient population had a mean age of 86 years [23].
With respect to NYHA functional class, we revealed no improvement of NYHA class more than 5 years after TAVI, as NYHA class III/IV has been observed in two-third of our patients prior to TAVI and at late follow-up. In contrast to our results, short-term studies have described a sustained improvement of NYHA class in selected groups of survivors [15, 29, 30]. In these reports, most patients were in NYHA class I/II who were in NYHA class III/IV prior to TAVI up to five years after the procedure [31].
These findings may suggest that the initial benefit on functional gain which was described in the first years after TAVI may decline beyond 5 years. However, the advanced age of the population (mean age at follow-up was 86.5 years ± 8.0 years) and concomitant comorbidities may play an important impact on their functional status.
Importantly, all patients alive reported very low incidence of complications in the following years after TAVI. All-stroke rate was 3.3%, which was similar to a previous study published by Barbanti et al. [18]. In this report, neurological event rate was 7.5% at 5 years; however, approximately 5% occurred in the first 6 months after the procedure. Another study by Tarantini et al. observed a stroke rate of 2.5% with the CoreValve and 3.7% with the Edwards Sapiens bioprosthesis at 5 years [30]. In the same report, the incidence of acute coronary syndrome was 2.4% which was in line with our result (2.2%). Recently, data from the FRANCE-2 registry showed that the majority of cardiovascular events occurred in the first months after valve replacement [31]. Our analysis revealed similar outcome data, and most complications including bleeding and pacemaker implementation occurred mainly in the earlier period after TAVI and were described at late follow-up only in 5.4% and 6%, respectively. The high incidence of new cardiac arrhythmias may be due to the fact that the prevalence of many cardiac arrhythmias increases with older age [32, 33]. Larger studies are needed to assess if there is any association between TAVI and late onset of cardiac arrhythmias.
In the present study, there were in total 74 rehospitalizations reported during the median time period of 7 years after TAVI. Cardiovascular reasons accounted for 43.2% with new PPI, heart failure, and coronary heart disease as the most frequent indications. Interestingly, the majority of patients who received a new PPI had a balloon-expandable (four out of six patients) and not self-expanding bioprosthesis. However, larger studies have to evaluate if there is any association between valve type and long-term PPI rate. In general, data on long-term hospital readmissions after TAVI are very limited [16–18, 34]. In a one-year follow-up study, Franzone et al. observed hospital admission in one out of four patients. Cardiovascular rehospitalization was reported in 46.1%, with heart failure as the most frequent reason [34]. Similar to our study, Barbanti et al. observed a rehospitalization rate for cardiovascular reasons in 46% in a 5-year follow-up period [18]. Among all rehospitalizations, acute heart failure was the most frequently reported (42.7%), followed by requirement of permanent pacemaker implantation (17.4%).
4.1. Limitations
Our study was performed as a single-centre investigation with a fairly limited number of patients. Second, the study design leads to the exclusion of patients with early death and those who were too ill or cognitively impaired to participate. Selection bias may have occurred. Third, patient self-reported data can be subject to error as the result of a variety of factors, including recall and patients’ health knowledge and awareness, possibly leading to underestimation of the true event rates [35–37]. Fourth, medical records or health insurance data may be a better alternative to survey data in order to collect information about health services. However, both data sources also have their limitations. Medical records may be inaccurate due to errors in recording data, and it can be difficult to access them from different hospitals and physicians [38, 39]. Health insurance data do not include health service information from people covered by private insurance or self-payers [40]. Lastly, and most importantly, we did not conduct the survey with the EQ-5D-5L questionnaire before and directly after TAVI. Consequently, we cannot report whether and how much the patients’ health status changed from baseline.
5. Conclusion
In the present study, about one-fourth of the patients after TAVI survived at a median follow-up period of 7 years. Most of these patients reported about a satisfactory health status at late follow-up. The initial benefits of functional status seemed to be reduced more than 5 years after TAVI. According to the patients’ reported outcome, incidence of clinical events and hospitalization was very low in the survival cohort within the first five to ten years after TAVI.
[1] H. Baumgartner, V. Falk, J. J. Bax, "2017 ESC/EACTS Guidelines for the management of valvular heart disease," European Heart Journal, vol. 38 no. 36, pp. 2739-2791, DOI: 10.1093/eurheartj/ehx391, 2017.
[2] R. J. Everett, M.-A. Clavel, P. Pibarot, M. R. Dweck, "Timing of intervention in aortic stenosis: a review of current and future strategies," Heart, vol. 104 no. 24, pp. 2067-2076, DOI: 10.1136/heartjnl-2017-312304, 2018.
[3] R. Bonow, M. Leon, D. Doshi, N. Moat, "Management strategies and future challenges for aortic valve disease," The Lancet, vol. 387 no. 10025, pp. 1312-1323, 2019.
[4] S. R. Kapadia, M. B. Leon, R. R. Makkar, "5-year outcomes of transcatheter aortic valve replacement compared with standard treatment for patients with inoperable aortic stenosis (PARTNER 1): a randomised controlled trial," The Lancet, vol. 385 no. 9986, pp. 2485-2491, DOI: 10.1016/s0140-6736(15)60290-2, 2015.
[5] M. J. Mack, M. B. Leon, C. R. Smith, "5-year outcomes of transcatheter aortic valve replacement or surgical aortic valve replacement for high surgical risk patients with aortic stenosis (PARTNER 1): a randomised controlled trial," The Lancet, vol. 385 no. 9986, pp. 2477-2484, DOI: 10.1016/s0140-6736(15)60308-7, 2015.
[6] M. B. Leon, C. R. Smith, M. J. Mack, "Transcatheter or surgical aortic-valve replacement in intermediate-risk patients," New England Journal of Medicine, vol. 374 no. 17, pp. 1609-1620, DOI: 10.1056/NEJMoa1514616, 2016.
[7] V. H. Thourani, S. Kodali, R. R. Makkar, "Transcatheter aortic valve replacement versus surgical valve replacement in intermediate-risk patients: a propensity score analysis," The Lancet, vol. 387 no. 10034, pp. 2218-2225, DOI: 10.1016/s0140-6736(16)30073-3, 2016.
[8] M. J. Reardon, N. M. Van Mieghem, J. J. Popma, "Surgical or transcatheter aortic-valve replacement in intermediate-risk patients," New England Journal of Medicine, vol. 376 no. 14, pp. 1321-1331, DOI: 10.1056/nejmoa1700456, 2017.
[9] L. Voigtländer, M. Seiffert, "Expanding TAVI to low and intermediate risk patients," Frontiers in Cardiovascular Medicine, vol. 5,DOI: 10.3389/fcvm.2018.00092, 2018.
[10] C. M. Otto, D. J. Kumbhani, K. P. Alexander, "2017 ACC expert consensus decision pathway for transcatheter aortic valve replacement in the management of adults with aortic stenosis," Journal of the American College of Cardiology, vol. 69 no. 10, pp. 1313-1346, DOI: 10.1016/j.jacc.2016.12.006, 2017.
[11] A. Bowling, S. Ebrahim, "Measuring patients’ preferences for treatment and perceptions of risk," Quality and Safety in Health Care, vol. 10 no. I,DOI: 10.1136/qhc.0100002, 2001.
[12] M. R. Reynolds, E. A. Magnuson, K. Wang, "Health-related quality of life after transcatheter or surgical aortic valve replacement in high-risk patients with severe aortic stenosis (placement of aortic transcatheter valve) trial (cohort A)," Journal of the American College of Cardiology, vol. 60 no. 6, pp. 548-558, DOI: 10.1016/j.jacc.2012.03.075, 2012.
[13] J. Biermann, M. Horack, P. Kahlert, "The impact of transcatheter aortic valve implantation on quality of life: results from the German transcatheter aortic valve interventions registry," Clinical Research in Cardiology, vol. 104 no. 10, pp. 877-886, DOI: 10.1007/s00392-015-0857-9, 2015.
[14] A. Stańska, D. Jagielak, M. Kowalik, "Health-related quality of life following transcatheter aortic valve implantation using transaortic, transfemoral approaches and surgical aortic valve replacement—a single-center study," Journal of Geriatric Cardiology, vol. 15 no. 11, pp. 657-665, 2018.
[15] M. J. De Ronde-Tillmans, T. A. de Jager, J. A. Goudzwaard, "Long-term follow-up of quality of life in high-risk patients undergoing transcatheter aortic valve implantation for symptomatic aortic valve stenosis," Journal of Geriatric Cardiology, vol. 15 no. 4, pp. 261-267, 2018.
[16] T. Arai, F. Yashima, R. Yanagisawa, "Hospital readmission following transcatheter aortic valve implantation in the real world," International Journal of Cardiology, vol. 269, pp. 56-60, DOI: 10.1016/j.ijcard.2018.07.073, 2018.
[17] A. Czarnecki, P. Austin, S. Fremes, "Predictors of hospital readmission after trans-catheter aortic valve implantation," Canadian Journal of Cardiology, vol. 33 no. 10, pp. 118-119, DOI: 10.1016/j.cjca.2017.07.038, 2017.
[18] M. Barbanti, A. S. Petronio, S. Gulino, "5-year outcomes after transcatheter aortic valve implantation with CoreValve prosthesis," JACC: Cardiovascular Interventions, vol. 8 no. 8, pp. 1084-1091, DOI: 10.1016/j.jcin.2015.03.024, 2015.
[19] S. Toggweiler, K. H. Humphries, M. Lee, "5-year outcome after transcatheter aortic valve implantation," Journal of the American College of Cardiology, vol. 61 no. 4, pp. 413-419, DOI: 10.1016/j.jacc.2012.11.010, 2013.
[20] V. Bianco, A. Kilic, T. G. Gleason, "Long-term hospital readmissions after surgical versus transcatheter aortic valve replacement," The Annals of Thoracic Surgery,DOI: 10.1016/j.athoracsur.2019.03.077, 2019.
[21] A. Cribier, H. Eltchaninoff, C. Tron, "Treatment of calcific aortic stenosis with the percutaneous heart valve," Journal of the American College of Cardiology, vol. 47 no. 6, pp. 1214-1223, DOI: 10.1016/j.jacc.2006.01.049, 2006.
[22] C. Tamburino, S. Mule, B. Cammalleri, "Procedural success and 30-day clinical outcomes after percutaneous aortic valve replacement using current third—generation self—expanding CoreValve prosthesis," Journal of Invasive Cardiology, vol. 21 no. 3, pp. 93-98, 2009.
[23] M. Huber, P. Reitmeir, M. Vogelmann, R. Leidl, "EQ-5D-5L in the general German population: comparison and evaluation of three yearly cross-section surveys," International Journal of Environmental Research and Public Health, vol. 13 no. 3,DOI: 10.3390/ijerph13030343, 2016.
[24] T. Sénage, T. Le Tourneau, Y. Foucher, "Early structural valve deterioration of mitroflow aortic bioprosthesis: mode, incidence, and impact on outcome in a large cohort of patients," Circulation, vol. 130 no. 23, pp. 2012-2020, DOI: 10.1161/circulationaha.114.010400, 2014.
[25] A. P. Kappetein, S. J. Head, P. Généreux, "Updated standardized endpoint definitions for transcatheter aortic valve implantation," Journal of the American College of Cardiology, vol. 60 no. 15, pp. 1438-1454, DOI: 10.1016/j.jacc.2012.09.001, 2012.
[26] A. Szende, B. Janssen, J. Cabasés, Self-Reported Population Health: An International Perspective based on EQ-5D, pp. 85-90, 2014.
[27] K. Ludwig, J.-M. Graf von der Schulenburg, W. Greiner, "German value set for the EQ-5d-5L," PharmacoEconomics, vol. 36 no. 6, pp. 663-674, DOI: 10.1007/s40273-018-0615-8, 2018.
[28] R. L. Osnabrugge, S. V. Arnold, M. R. Reynolds, "Health status after transcatheter aortic valve replacement in patients at extreme surgical risk: results from the CoreValve U.S. Trial ruben," JACC: Cardiovascular Interventions, vol. 8 no. 2, pp. 315-323, DOI: 10.1016/j.jcin.2014.08.016, 2015.
[29] P. Avanzas, I. Pascual, A. J. Muñoz-García, "Long-term follow-up of patients with severe aortic stenosis treated with a self-expanding prosthesis," Revista Española de Cardiología (English Edition), vol. 70 no. 4, pp. 247-253, DOI: 10.1016/j.rec.2016.09.024, 2017.
[30] G. Tarantini, P. A. M. Purita, A. D’Onofrio, "Long-term outcomes and prosthesis performance after transcatheter aortic valve replacement: results of self-expandable and balloon-expandable transcatheter heart valves," Annals of Cardiothoracic Surgery, vol. 6 no. 5, pp. 473-483, DOI: 10.21037/acs.2017.08.02, 2017.
[31] R. Didier, H. Eltchaninoff, P. Donzeau-Gouge, "Five-year clinical outcome and valve durability after transcatheter aortic valve replacement in high-risk patients," Circulation, vol. 138 no. 23, pp. 2597-2607, DOI: 10.1161/circulationaha.118.036866, 2018.
[32] A. B. Curtis, R. Karki, A. Hattoum, U. C. Sharma, "Arrhythmias in patients ≥80 years of age," Journal of the American College of Cardiology, vol. 71 no. 18, pp. 2041-2057, DOI: 10.1016/j.jacc.2018.03.019, 2018.
[33] G. V. Chow, J. E. Marine, J. L. Fleg, "Epidemiology of arrhythmias and conduction disorders in older adults," Clinics in Geriatric Medicine, vol. 28 no. 4, pp. 539-553, DOI: 10.1016/j.cger.2012.07.003, 2012.
[34] A. Franzone, T. Pilgrim, N. Arnold, "Rates and predictors of hospital readmission after transcatheter aortic valve implantation," European Heart Journal, vol. 38 no. 28, pp. 2211-2217, DOI: 10.1093/eurheartj/ehx182, 2017.
[35] P. Raina, V. Torrance-Rynard, M. Wong, C. Woodward, "Agreement between self-reported and routinely collected health-care utilization data among seniors," Health Services Research, vol. 37 no. 3, pp. 751-774, DOI: 10.1111/1475-6773.00047, 2002.
[36] M. Hunger, L. Schwarzkopf, M. Heier, A. Peters, R. Holle, K. S. Group, "Official statistics and claims data records indicate non-response and recall bias within survey-based estimates of health care utilization in the older population," BMC Health Services Research, vol. 13 no. 1,DOI: 10.1186/1472-6963-13-1, 2013.
[37] P. L. Ritter, A. L. Stewart, H. Kaymaz, D. S. Sobel, D. A. Block, K. R. Lorig, "Self-reports of health care utilization compared to provider records," Journal of Clinical Epidemiology, vol. 54 no. 2, pp. 136-141, DOI: 10.1016/s0895-4356(00)00261-4, 2001.
[38] J. Starlinger, M. Kittner, O. Blankenstein, U. Leser, "How to improve information extraction from German medical records," It-Information Technology, vol. 59 no. 4, pp. 171-179, DOI: 10.1515/itit-2016-0027, 2017.
[39] K. C. Stange, S. J. Zyzanski, T. F. Smith, "How valid are medical records and patient questionnaires for physician profiling and health services research ? A comparison with direct observation of patients visits," Medical Care, vol. 36 no. 6, pp. 851-867, DOI: 10.1097/00005650-199806000-00009, 1998.
[40] I. Schubert, I. Köster, J. Küpper-Nybelen, P. Ihle, "Health services research based on routine data generated by the SHI. Potential uses of health insurance fund data in health services research," Bundesgesundheitsblatt—Gesundheitsforschung—Gesundheitsschutz, vol. 51 no. 10, pp. 1095-1105, DOI: 10.1007/s00103-008-0644-0, 2008.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Copyright © 2019 Marie-Isabel K. Murray et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0/
Abstract
Background. Transcatheter aortic valve implantation (TAVI) is currently recommended for patients with severe aortic stenosis at intermediate or high surgical risk. The decision process during TAVI evaluation includes a thorough benefit-risk assessment, and knowledge about long-term benefits and outcomes may improve patients’ expectation management. Objective. To evaluate patients’ perceived health status and self-reported long-term outcome more than 5 years after TAVI. Methods and Results. Demographic and procedure data were obtained from all patients treated with TAVI at our institution from 2006 to 2012. A cross-sectional survey was conducted on the patients alive, measuring health status, including the EQ-5D-5L questionnaire, and clinical outcomes. 103 patients (22.8%) were alive at a median follow-up period of 7 years (5.4–9.8). 99 (96%) of the 103 patients were included in the final analysis. The mean age at follow-up was 86.5 years ± 8.0 years, and 56.6% were female. Almost all patients (93.9%) described an improvement of their quality of life after receiving TAVI. At late follow-up, the mean utility index and EQ-VAS score were 0.80 ± 0.20 and 58.49 ± 11.49, respectively. Mobility was found to be the most frequently reported limitation (85.4%), while anxiety/depression was the least frequently reported limitation (19.8%). With respect to functional class, 64.7% were in New York Heart Association (NYHA) class III or IV, compared to 67.0% prior to TAVI (
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details


1 Department of Cardiology, University Hospital Frankfurt, Frankfurt am Main, Germany
2 Department of Cardiac Surgery, University Hospital Frankfurt, Frankfurt am Main, Germany