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BMJ Open logoLink to BMJ Open
. 2023 Feb 6;13(2):e070715. doi: 10.1136/bmjopen-2022-070715

Spatial analysis and factors associated with transcatheter aortic valve implantation in Portugal: a retrospective analysis from 2015 to 2017

Fernando Genovez Avelar 1,2,, Isabel Emmerick 3, Joana Alves 4
PMCID: PMC9906166  PMID: 36746542

Abstract

Objectives

To identify the factors associated with transcatheter aortic valve implantation (TAVI) use of TAVI in inpatients with aortic stenosis (AS) in Portugal and its geographical distribution.

Methods

A quantitative, observational and retrospective study using the Portuguese National Health Service inpatient discharge database from 2015 to 2017. Surgical aortic valve replacement (SAVR) and TAVI procedures were selected using the International Classification of Diseases. First, we mapped the yearly age-standardised rate for each procedure using QGIS. Then, we performed χ2 tests, independent t-tests and logistic regressions to study the factors associated with TAVI use.

Results

From 2015 to 2017, 8398 hospitalisations were selected, 88.5% SAVR and 11.5% TAVI. From 2015 to 2017, SAVR use increased in the Northern region and decreased in the Lisbon region, while the opposite was observed for TAVI. TAVI was performed among the most complex (p<0.001) and older patients (the mean (SD) age for SAVR was 70 (±11) years old and 81 (±7) years old for TAVI, p<0.001). The results for the logistic regressions showed that, more recent hospitalisations, being older, living in the Lisbon region and having a higher Charlson Comorbidity Index was associated with an increased likelihood of undergoing TAVI (p<0.001).

Conclusions

TAVI increased over the years. TAVI is more often performed in more severe patients as an alternative to SAVR with similar discharge outcomes. These results suggest the existence of geographic disparities in the availability and access to healthcare services and technologies.

Keywords: Epidemiology, PUBLIC HEALTH, Valvular heart disease


Strengths and limitations of this study.

  • This study is highly representative of the national real practice as it used a large database of all inpatient data for the Portuguese National Health Service hospitals, from 2015 to 2017.

  • Identifying geographical differences in aortic stenosis (AS) treatment might contribute to designing informed policies to improve the healthcare systems.

  • This is a secondary database, collected for administrative purposes, which was not intended for academic research and excludes the private settings.

  • We cannot infer causality with the present study design and data.

  • The Charlson Comorbidity Index is represented by a specific group of comorbidities commonly used in observational studies; other important comorbidities, which might influence AS severity and medical decision on therapeutic choice, might not be considered.

Introduction

Aortic Stenosis (AS) is a pathological condition characterised by the narrowing of the cardiac aortic valve, which has severe consequences for a patient’s quality of life, including loss of mobility, decreased productivity and limitations in daily living activities.1 2 It is a significant public health problem worldwide, particularly in developed countries, due to increasing life expectancy, and it affects 2.3% of the world population.3 4 The prevalence of AS in the Portuguese population varies from 3% to 23%,1 and the estimated number of patients eligible for treatment is of 32 000 patients.5

This condition can result in death if not appropriately treated, particularly in most severe cases. Without treatment, approximately half of patients would die within 1–2 years.6 Also, half to one-third of patients might be asymptomatic at the time of diagnosis.7 Additionally, the survival prognosis for every three out of four patients is generally of 3 years, after symptoms onset.8 Although asymptomatic patients usually present a low rate of complications, when symptoms are already installed, the absence of follow-up would result in a very adverse prognosis.9

Until the beginning of the 21st century, surgical aortic valve replacement (SAVR) was the standard procedure for AS treatment, and it was the only available surgical intervention.8 Nevertheless, this therapeutic option was not possible in high-risk surgical cases, due to patient frailty and numerous comorbidities.2 5 In 2002, transcatheter aortic valve implantation (TAVI) emerged as a solution for individuals not eligible for SAVR, since it was a less invasive procedure. This technology represented an important innovation in the treatment of AS patients with high-risk surgical. TAVI has been shown in various clinical trials1 10 to reduce all-cause mortality, cardiovascular disease and readmissions.11 In Portugal, the records of the beginning of the use of this procedure date from 2007.12

In the forthcoming years, the use of TAVI is expected to increase. The reasons are: (1) AS is expected to become more prevalent due to the demographic transition and the ageing population observed worldwide.3 4 Therefore, the need for treatment will also increase; (2) It is also likely that the technology will be used more extensively, expanding of the criteria for TAVI use (eg, for medium-risk or low-risk surgical patients). Thus, the number of individuals eligible for treatment will also increase.13

Despite the predictable rise in the use of technology, scientific evidence tells us that the incorporation of technologies is usually not done homogeneously.14 Although technologies may improve people’s health, lack of equitable access might perpetuate health disparities. Even in countries with universal access to healthcare, disparities in access may exist at the regional level. Hence, it is important to study the determinants of access to treatment and incorporation of technology to reduce this effect. This study aims to identify the geographical patterns and sociodemographic and clinical factors associated with TAVI use in inpatients diagnosed with AS in the Portuguese National Health Service (NHS) from 2015 and 2017.

Material and methods

Quantitative, observational and retrospective study using the inpatient discharge database for the Portuguese NHS hospitals, from 2015 to 2017.

Data source

The Central Administration of Health Services and the Shared Services of the Ministry of Health jointly managed the inpatient database. All entries in the database had a unique identifier that was anonymised to ensure the confidentiality of the patients analysed. The database had information about primary and secondary diagnosis, age, gender, interventions performed, in-patient length of stay and area of residence.

This study was a secondary analysis of an existing database; thus, it does not fall within the definition of research involving human subjects. Nonetheless, the ethical principles governing health research were considered and anonymised information guaranteed data confidentiality.

The dependent variable was intervention type, and it was defined using the International Statistical Classification of Diseases and Related Health Problems (ICD), versions 9 (ICD-9) and 10 (ICD-10). The codes used to select SAVR procedure were the following: ICD-9—3521 and 3522; ICD-10—02RF07Z, 02RF08Z, 02RF0JZ, 02RF0KZ and X2RF032. For TAVI, we used the following ICD codes: ICD-9—3505 and 3506; ICD-10—02RF37H, 02RF37Z, 02RF38H, 02RF38Z, 02RF3JH, 02RF3JZ, 02RF3KH, 02RF3KZ, 02RF47Z, 02RF48Z, 02RF4JZ, 02RF4KZ, X2RF332 and X2RF432.15 Then, it was dichotomised (SAVR=0 and TAVI=1).

The sociodemographic characterisation included variables, such as gender, age and place of residence. Additionally, inpatient clinical information, such as and type of admission (elective or non-elective admission), length of stay, destination after discharge, severity level (minor, moderate, major or extreme) and main and secondary diagnosis were considered in the analysis.

The primary and secondary diagnoses were used to compute the Charlson Comorbidity Index (CCI),16 as presented in online supplemental appendix 1. The CCI is widely used in clinical practice to assess patient comorbidity level, as a proxy of patients’ severity. According to the literature, it predicts long-term17 and in-hospital18 mortality. It can also be used to evaluate differences in diagnosis and prognosis between groups of patients sharing the same clinical diagnosis.18 The CCI is a validated instrument, allowing the assessment of the burden of comorbidities and the measurement of patients’ outcomes, particularly among AS patients.19 20 Online supplemental appendix 2 presents the weights used to calculate the CCI. The CCI was analysed in two ways: as an index, and as a categorical variable (cut-off point≥3).19 21 22 Additionally, the relation between procedures and the pathologies that compose the index were evaluated separately, as many of the pathologies that comprise the index are common among AS patients.

Supplementary data

bmjopen-2022-070715supp001.pdf (281.8KB, pdf)

Spatial analysis

The age-standardised hospitalisation rate per year was then calculated using the direct method to compare population groups with different age structures23 (online supplemental appendix 3). For standardisation, the total Portuguese population stratified by age was used. From the absolute number of each procedure, the procedure’s prevalence per district and age group was calculated. This value was subsequently used to estimate the value of expected hospitalisations by age group. The standardised rate resulted from dividing the total number of expected cases by the standard population and multiplying by 100 000 inhabitants.

The age-standardised rate was mapped for the years analysed using QGIS Desktop V.3.22.724 software, using the shapefiles of the administrative map of Portugal available at http://dados.gov.pt,25 to characterise the spatial distribution of TAVI and SAVR procedures, and their trends from 2015 to 2017.

For the spatial analysis, the TAVI and SAVR procedures were analysed according to the district of residence.26 For the remaining statistical analysis, the place of residence was aggregated according to Nomenclature of Territorial Units for Statistics II classification,26 due to the low number of district-level observations.

Statistical analysis

In the first stage, the χ2 test, Fisher’s exact test and independent t-tests were performed to measure the association between the procedures performed and the remaining variables. In the second stage, the adjusted and unadjusted OR using logistic regressions were computed to identify the association between TAVI and the explanatory factors, using significance level of 5% (two-tailed test). The analyses were performed using the Statistical Package for the Social Sciences (IBM SPSS Statistics) V.28.

Patient and public involvement

None.

Results

Procedures distribution

Between 2015 and 2017, 2 199 933 inpatients were admitted to NHS hospitals. From this, 8398 hospitalisations were analysed, corresponding to 0.38% of the total, 2722 (32.41%), 2832 (33.72%) and 2844 (33.87%), respectively, in 2015, 2016 and 2017 (figure 1). SAVR was performed in 7433 admissions (88.51%) and TAVI in 965 admissions (11.49%). TAVI showed an increasing trend, from 7.1% in 2015 to 15.6% in 2017. By contrast, the number of patients undergoing SAVR decreased by more than eight percentage points over the analysed period.

Figure 1.

Figure 1

Annual number of hospitalisations, and procedures, in the Portuguese National Health Service, from 2015 to 2017. SAVR, surgical aortic valve replacement; TAVI, transcatheter aortic valve implantation.

Spatial analysis

Figure 2 presents the geographical distribution of the age-adjusted hospitalisation rate by district, from 2015 to 2017. When analysing SAVR, the colour becomes darker in the Northern region over the years and becomes lighter in the Lisbon region. The opposite trend was observed among TAVI, where the colour became darker in the region around Lisbon.

Figure 2.

Figure 2

Age-adjusted hospitalisation rates for SAVR and TAVI in Portuguese National Health Service hospitals by patients’ district of residence, from 2015 to 2017. The standardised rate resulted from dividing the total number of expected cases by the standard population and multiplying by 100,000 inhabitants. SAVR, surgical aortic valve replacement; TAVI, transcatheter aortic valve implantation.

Regarding TAVI, there was both a growth and a concentration of procedures performed. Most districts had an increase in TAVI use. The Lisbon district had the highest absolute difference (3.98), from 3.80 per 100 000 inhabitants in 2015 to 7.78 per 100 000 inhabitants in 2017. Lisbon and Setubal were among the three districts with the highest rates of TAVI per 100 000 inhabitants (3.91, 5.57 and 8.01 for Lisbon and 3.37, 4.34 and 5.18 for Setubal in 2015, 2016 and 2017, respectively). During this period, Viana do Castelo, Guarda and Braga districts had a negative absolute difference for TAVI.

SAVR increased in 11 districts and decreased in the other nine districts. From 2015 to 2017, the autonomous region of Madeira presented the highest absolute difference (17.25) and Santarem had the highest absolute reduction (−7.18) in SAVR procedures. Braga and Viana do Castelo are two of the three districts with the highest SAVR rates (Viana do Castelo: 37.19: 35.17 and 31.53 per 1000 inhabitants; and Braga: 33.56; 33.17 and 30.20 per 1000 inhabitants). Braga and Viana do Castelo showed the highest SAVR standardised rate in 2017, and these same districts showed a higher reduction in TAVI.

Study population characteristics

SAVR patients were mostly men (56.9%), while TAVI patients were mostly women (55.4%) (p<0.001). The mean age among TAVI patients was higher than among SAVR (81 years old vs 70 years old, p<0.001). Most admissions were elective for both procedures, but non-elective hospitalisations were higher among TAVI than SAVR (13.1% vs 9.4%) (table 1). The Northern Region had the highest percentage of SAVR (41.20%), while the Lisbon region had the highest percentage of TAVI (46.30%). Both procedures had a comparable length of stay (13 days, p=0.602). The mortality was also similar for both procedures, with more than 80% of patients discharged home. Most admissions had moderate severity level (53.0% for SAVR and 47.6% for TAVI), but the minor severity was more expressive among SAVR (31.8%) than TAVI (27.8%). The CCI was higher among TAVI than SAVR (1.80 vs 1.33, p<0.001). Most individuals had between 0 and 2 points of the CCI (TAVI 83.8% vs SAVR 69.8%). The patients undergoing TAVI had more comorbidities or severe clinical conditions, represented by a higher percentage of individuals with CCI>3 (30.2% compared with 16.2% in SAVR, p<0.001). A distribution of the CCI by procedure is available in online supplemental appendix 4.

Table 1.

Study population characteristics by SAVR and TAVI in Portuguese National Health Service hospitals admissions database from 2015 to 2017.

Characteristics SAVR n=7433 TAVI n=965 Total P value (SAVR vs TAVI)
Sex Male n (%) 4226 (56.9) 430 (44.6) 4656 (55.4) <0.001
Age Years Mean (SD) 70 (11) 81 (7) 8398 (100.0) <0.001
Year of hospitalisation 2015 n (%) 2530 (34.0) 192 (19.9) 2722 (32.4) <0.001
2016 n (%) 2503 (33.7) 329 (34.1) 2832 (33.7)
2017 n (%) 2400 (32.3) 444 (46.0) 2844 (33.9)
Type of admission Elective n (%) 6737 (90.6) 829 (85.9) 7566 (90.1) <0.001
Non-elective n (%) 696 (9.4) 136 (13.1) 832 (9.9)
Country region Norte n (%) 2862 (41.2) 246 (25.7) 3108 (39.4) <0.001
Centro n (%) 1373 (19.8) 154 (16.1) 1527 (19.3)
LVT n (%) 1835 (26.4) 443 (46.3) 2278 (28.8)
Alentejo n (%) 467 (6.7) 71 (7.4) 538 (6.8)
Algarve n (%) 259 (3.7) 31 (3.2) 290 (3.7)
AR (Azores and Madeira) n (%) 146 (2.1) 11 (1.2) 157 (2.0)
Length of stay Days Mean (SD) 13 (15) 13 (14) 8398 (100.0) 0.602
Type of patient NHS n (%) 7286 (98.0) 954 (98.9) 8240 (98.1) 0.077
No NHS n (%) 147 (2.0) 11 (1.1) 158 (1.9)
Destination after discharge Home n (%) 6605 (88.9) 841 (87.2) 7446 (88.7) 0.058
Death n (%) 284 (3.8) 33 (3.4) 317 (3.8)
Others* n (%) 544 (7.3) 91 (9.4) 635 (7.5)
Severity Minor n (%) 2365 (31.8) 268 (27.8) 2633 (31.3) <0.001
Moderate n (%) 3941 (53.0) 459 (47.6) 4400 (52.4)
Major n (%) 893 (12.0) 213 (22.1) 1106 (13.2)
Extreme n (%) 234 (3.1) 25 (2.6) 259 (3.1)
CCI Index Mean (SD) 1.33 (1.34) 1.80 (1.68) 8398 (100.0) <0.001
CCI 0–2 n (%) 6231 (83.8) 674 (69.8) 6905 (82.2) <0.001
≥ 3 n (%) 1202 (16.2) 291 (30.2) 1493 (17.8)
Myocardial infarction Yes n (%) 466 (6.3) 102 (10.6) 568 (6.8) <0.001
Congestive heart failure Yes n (%) 2568 (34.5) 366 (37.9) 2934 (34.9) 0.041
Peripheral vascular disease Yes n (%) 1507 (20.3) 120 (12.4) 1627 (19.4) <0.001
Cerebrovascular disease Yes n (%) 490 (6.6) 110 (11.4) 600 (7.1) <0.001
Dementia Yes n (%) 21 (0.3) 4 (0.4) 25 (0.3) 0.522†
Chronic pulmonary disease Yes n (%) 764 (10.3) 139 (14.4) 903 (10.7) <0.001
Connective tissue disease Yes n (%) 87 (1.2) 19 (2.0) 106 (1.3) 0.045
Peptic ulcer disease Yes n (%) 15 (0.2) 3 (0.3) 18 (0.2) 0.453†
Mild liver disease Yes n (%) 109 (1.5) 22 (2.3) 131 (1.5) 0.071
Diabetes without chronic complication Yes n (%) 1779 (23.9) 208 (21.6) 1987 (23.7) 0.107
Diabetes with chronic complication Yes n (%) 202 (2.7) 47 (4.9) 249 (3.0) <0.001
Hemiplegia or paraplegia Yes n (%) 78 (1.0) 9 (0.9) 87 (1.0) 0.866
Renal disease Yes n (%) 647 (8.7) 225 (23.3) 872 (10.4) <0.001
Any malignancy, including lymphoma and leukaemia, except malignant neoplasm of skin Yes n (%) 64 (0.9) 28 (2.9) 92 (1.1) <0.001
Moderate or severe liver disease Yes n (%) 8 (0.1) 0 (0.0) 8 (0.1) 0.609†
Metastatic solid tumour Yes n (%) 9 (0.1) 4 (0.4) 13 (0.2) 0.053†
AIDS/HIV Yes n (%) 8 (0.1) 1 (0.1) 9 (0.1) 1.000†

P-values lower than 0.05 were highlighted in bold.

*Another institution with inpatient care, home care, medical counter opinion, specialised care (tertiary), palliative care, posthospital care, long-term medical care.

†Fisher’s exact test.

AR, autonomous regions; CCI, Charlson Comorbidity Index; LVT, Lisbon area; NHS, National Health Service; SAVR, surgical aortic valve replacement; TAVI, transcatheter aortic valve implantation.

Overall, 7 of the 17 health conditions that comprise the CCI were not statistically significant associated with TAVI procedure. Most individuals were diagnosed with congestive heart failure (37.9% in TAVI, compared with 34.5% in SAVR, p=0.041). Additionally, the four conditions with the highest occurrence among individuals undergoing SAVR, were diabetes without chronic complications, peripheral vascular disease, and chronic pulmonary disease. As for individuals that underwent TAVI, the most prevalent conditions were kidney disease, diabetes without chronic complications and chronic pulmonary disease.

Factors associated with undergoing TAVI

The year of hospitalisation was associated with the likelihood of undergoing TAVI. The more recent hospitalisations had a higher likelihood of being TAVI, TAVI, considering 2015 as a reference (OR=2.87 (2.34–3.52) for 2017, and OR=1.68 (1.37–2.07) for 2016) (table 2). Older patients also had an increase in likelihood of undergoing TAVI: each additional year of age represented a 21% increase in the odds of undergoing TAVI (OR=1.21 (1.20–1.23)). The geographical location was associated with the procedure. In most of the regions was observed an increased likelihood of undergoing TAVI, when compared with the Northern Region of the country (OR=1.64 (1.29–2.08) for Centro and OR=1.84 (1.34–2.53) for Alentejo). In the Lisbon region, the odds of having TAVI were even higher, and patients living in this region had more than two times the likelihood of undergoing TAVI OR=2.62 (2.16–3.18). Additionally, individuals with higher CCI also showed an increased chance of undergoing TAVI, when compared with lower CCI (OR=2.55 (2.10–3.10)).

Table 2.

Results for the logistic regression models for the likelihood of TAVI use, in the Portuguese NHS, from 2015 to 2017.

Characteristics Unadjusted Adjusted
OR (95% CI) P value OR (95% CI) P value
Sex Male Reference Reference
Female 1.64 (1.43 to 1.88) <0.001 1.17 (0.10 to 1.37) 0.053
Age (per 1 unit increase) Years 1.22 (1.21 to 1.24) <0.001 1.21 (1.20 to 1.23) <0.001
Year of hospitalisation 2015 Reference Reference
2016 1.73 (1.44 to 2.09) <0.001 1.68 (1.37 to 2.07) <0.001
2017 2.44 (2.04 to 2.91) <0.001 2.87 (2.34 to 3.52) <0.001
Type of admission Elective Reference Reference
Non-elective 1.59 (1.30 to 1.94) <0.001 1.18 (0.92 to 1.50) 0.191
Country region Norte Reference Reference
Centro 1.31 (1.06 to 1.61) 0.014 1.64 (1.29 to 2.08) <0.001
Lisbon 2.81 (2.38 to 3.32) <0.001 2.62 (2.16 to 3.18) <0.001
Alentejo 1.77 (1.34 to 2.34) <0.001 1.84 (1.34 to 2.53) <0.001
Algarve 1.39 (0.94 to 2.07) 0.100 1.44 (0.93 to 2.24) 0.101
Azores and Madeira* 0.88 (0.47 to 1.64) 0.680 1.21 (0.61 to 2.41) 0.582
Type of patient NHS Reference
No NHS 1.75 (0.95 to 3.24) 0.075
Severity Minor Reference
Moderate 1.03 (0.88 to 1.21) 0.736
Major 2.11 (1.73 to 2.56) <0.001
Extreme 0.94 (0.61 to 1.45) 0.789
Charlson Comorbidity Index Index 1.24 (1.18 to 1.29) <0.001
Charlson Comorbidity Index 0–2 Reference Reference
≥ 3 2.24 (1.93 to 2.60) <0.001 2.55 (2.10 to 3.10) <0.001

P-values lower than 0.05 were highlighted in bold.

*Autonomous Regions of Azores and Madeira.

NHS, National Health Service.

Discussion

This study aimed to identify the factors associated with TAVI use in inpatients with AS in Portugal and its geographical distribution. The results showed an increasing trend in patients undergoing TAVI over the years (p<0.001). Being older, living in the Lisbon region and having a higher CCI were individual characteristics associated with an increased likelihood of undergoing TAVI procedure (p<0.001). There was a geographic concentration in the SAVR utilisation in the Northern region and of TAVI in the Lisbon region.

The present study showed an increase in the number of hospitalisations with procedures for AS from 2015 to 2017. This uprising was more expressive for TAVI, contrasting with a decreased in SAVR. The upward trend in TAVI, found in this study, is in accordance with a worldwide trend.10 12 This result may characterise a substitution effect in the use of technologies.10

Although TAVI showed an increasing trend, its spatial distribution was not uniform across the Portuguese territory, as there was a concentration of TAVI among patients living in the Lisbon region. At the same time, the SAVR procedure was concentrated among patients living in the northern region of Portugal. It is crucial to understand whether this spatial variability would result in disparities on access to health technology.14 This could be an important public health issue since inequalities on access to technologies can exacerbate health inequities.

Adequate access to healthcare can promote better levels of health.27 28 This requires a comprehensive, timely and high-quality health system coverage (adequate healthcare services, screening, diagnosis and treatment) to improve the population’s health status.27 This study revealed significant differences in the geographical distribution of AS procedures according to the patients’ residence, even when adjusted for its individual characteristics. This could suggest the existence of health disparities, which may worsen health inequalities.

This geographical variability may be associated with a concentration of medical expertise regarding the type of procedures. According to the available evidence, regional differences in service provision may be associated with heterogeneous professional training and technical specialisation. Furthermore, financial incentives, as well as population preferences to be treated in a particular region, might also contribute to regional differences in healthcare utilisation.27 28 The variability in the geographic distribution may be a result of technological incorporation. Technology can be incorporated progressively across the country, at a various regional place. Delays in providing specific procedures or treatments can deteriorate patients health status, decrease their quality of life and/or worsen disease severity.29 This might contribute to escalation of consumption of health resources in the future, and potentially increasing health system expenditures.14 30

This study showed that TAVI was more frequent in older patients, that is, 80 years old. Other studies have also demonstrated a positive association with age.31 In the review conducted by Osnabrugge et al,1 patients over 75 years of age were more likely to be at more severe stages of the AS disease due to late diagnosis. Thus, TAVI was commonly the only possible approach due to their clinical frailty.

Additionally, higher CCI values were associated with an increased chance of TAVI, suggesting that it is used for more frail individuals. In contrast, many patients with lower CCI classification have undergone in SAVR. These results are consistent with the literature,19 20 22 32 33 which suggests that TAVI is usually performed more often in patients with grater frailty.

In summary, the results showed that older age and higher CCI were relevant explanatory factors of TAVI utilisation, which is consistent with international guidelines34 and the Portuguese consensus,5 which state that TAVI is indicated for the treatment of patients at increased surgical risk.11 20 TAVI is a less invasive procedure, recommended for inoperable patients not eligible for SAVR.11 34 This could explain why TAVI patients had a higher percentage of admission from non-elective services, comparing with SAVR, as TAVI does not require an open-heart surgery.12 34

All studies have limitations, and this study is no exception. This is a secondary database, so the data was not intended for academic research. We cannot infer causality with the present study design and data. Therefore, the results should be interpreted as associations between the variables. Finally, the CCI is represented by a specific group of comorbidities commonly used in observational studies.19 20 22 32 Other important comorbidities might influence AS severity and medical decision on therapeutic choice might not be considered.

Implications for practice and future research

The findings of this study have important implications. It was identified that increasing age and a higher CCI were associated with TAVI. Additionally, asymmetries in the spatial distribution of AS treatment might impact the access to healthcare services and technologies.

Future studies should update the existing evidence by extending the time horizon and using a longitudinal design. Also, research can focus on other AS-specific indicators, such as the Society of Thoracic Surgeons risk index, the New York Heart Association functional classification or the European System for Cardiac Operative risk assessment. Future studies could also focus on other therapeutic alternatives, such as therapeutic management without surgical intervention.

The place of residence should not be the most relevant determinant of treatment pattern. A more in-depth analysis is needed to understand if AS treatment is being performed according to appropriate referral criteria and if freedom of choice of treatment location is being guaranteed to the patients.

Health policies should aim to reduce barriers to healthcare access while promoting access to technologies at all levels of care. This goal can be achieved by training and updating health professionals’ knowledge and skills, and if needed, providing incentives for innovative health technologies adoption.

Conclusions

The TAVI procedure changed the management of AS worldwide. Two decades ago, it emerged as a solution for individuals not eligible for SAVR, since it was a less invasive procedure. According to this study, older age and higher CCI were significant explanatory factors of TAVI utilisation in the Portuguese NHS hospitals, from 2015 to 2017. This is consistent with the literature, and with national and international guidelines. Additionally, it was observed geographic differences in the use of TAVI that did not seem to be explained by patients’ individual characteristics. This should be further investigated since this access variability might contribute to worsening health inequalities.

Supplementary Material

Reviewer comments

Acknowledgments

We acknowledge the institutional support of the National School of Public Health—ENSP/UNL and the Central Administration of the Health System for providing the hospital morbidity database.

Footnotes

Contributors: FGA: Conception and design, analysis and interpretation of data; drafting of the manuscript, revising critically the manuscript; final approval of the manuscript submitted; and responsible for the overall content as guarantor. JRA: Acquisition of data, analysis and interpretation of data; revising critically the manuscript; and final approval of the manuscript submitted. IE: Analysis and interpretation of data; revising critically the manuscript; and final approval of the manuscript submitted. All authors have read the manuscript and approved the submission to BMJ Open.

Funding: The present publication was funded by Fundação Ciência e Tecnologia, IP national support through CHRC (UIDP/04923/2020).

Map disclaimer: The inclusion of any map (including the depiction of any boundaries therein), or of any geographic or locational reference, does not imply the expression of any opinion whatsoever on the part of BMJ concerning the legal status of any country, territory, jurisdiction or area or of its authorities. Any such expression remains solely that of the relevant source and is not endorsed by BMJ. Maps are provided without any warranty of any kind, either express or implied.

Competing interests: None declared.

Patient and public involvement: Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

Provenance and peer review: Not commissioned; peer reviewed for ethical and funding approval prior to submission.

Supplemental material: This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

Data availability statement

The data of hospitalisations are the property of Central Administration of Health Services (ACSS, I.P.) and transferred to the NOVA National School of Public Health (ENSP). However, the data are available from the authors upon request and with permission of the ACSS and ENSP. The data of hospitalisations are not publicly available, however the authors confirm that interested researchers can ask for access to these data by contacting ACSS directly at the following: Parque da Saúde de Lisboa, Edifício 16, Avenida do Brasil, 53 1700-063 Lisboa, Portugal (e-mail: geral@acss.min-saude. pt).

Ethics statements

Patient consent for publication

Not applicable.

Ethics approval

Not applicable.

References

  • 1.Osnabrugge RLJ, Mylotte D, Head SJ, et al. Aortic stenosis in the elderly. Journal of the American College of Cardiology 2013;62:1002–12. 10.1016/j.jacc.2013.05.015 [DOI] [PubMed] [Google Scholar]
  • 2.Tarride JE, Luong T, Goodall G, et al. A Canadian cost-effectiveness analysis of SAPIEN 3 transcatheter aortic valve implantation compared with surgery, in intermediate and high-risk severe aortic stenosis patients. Clinicoecon Outcomes Res 2019;11:477–86. 10.2147/CEOR.S208107 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Gavina C. Epidemiology of valvular heart disease in Portugal: the time has come for the heart valve unit. Rev Port Cardiol (Engl Ed) 2018;37:999–1000.:S0870-2551(18)30790-X. 10.1016/j.repc.2018.11.002 [DOI] [PubMed] [Google Scholar]
  • 4.Gialama F, Prezerakos P, Apostolopoulos V, et al. Systematic review of the cost-effectiveness of transcatheter interventions for valvular heart disease. Eur Heart J Qual Care Clin Outcomes 2018;4:81–90. 10.1093/ehjqcco/qcx049 [DOI] [PubMed] [Google Scholar]
  • 5.Campante Teles R, Gama Ribeiro V, Patrício L, et al. Posição de consenso sobre válvulas aórticas percutâneas transcatéter em Portugal. Revista Portuguesa de Cardiologia 2013;32:801–5. 10.1016/j.repc.2013.02.009 [DOI] [PubMed] [Google Scholar]
  • 6.Généreux P, Stone GW, O’Gara PT, et al. Natural history, diagnostic approaches, and therapeutic strategies for patients with asymptomatic severe aortic stenosis. J Am Coll Cardiol 2016;67:2263–88.:S0735-1097(16)01028-7. 10.1016/j.jacc.2016.02.057 [DOI] [PubMed] [Google Scholar]
  • 7.Kang D-H, Park S-J, Lee S-A, et al. Early surgery or conservative care for asymptomatic aortic stenosis. N Engl J Med 2020;382:111–9. 10.1056/NEJMoa1912846 [DOI] [PubMed] [Google Scholar]
  • 8.Bakaeen FG, Rosengart TK, Carabello BA. Aortic stenosis. Ann Intern Med 2017;166:ITC1–16. 10.7326/AITC201701030 [DOI] [PubMed] [Google Scholar]
  • 9.Lester SJ, Heilbron B, Gin K, et al. The natural history and rate of progression of aortic stenosis. Chest 1998;113:1109–14. 10.1378/chest.113.4.1109 [DOI] [PubMed] [Google Scholar]
  • 10.Pilgrim T, Windecker S. Expansion of transcatheter aortic valve implantation: new indications and socio-economic considerations. Eur Heart J 2018;39:2643–5. 10.1093/eurheartj/ehy228 [DOI] [PubMed] [Google Scholar]
  • 11.Leon MB, Smith CR, Mack M, et al. Transcatheter aortic-valve implantation for aortic stenosis in patients who can not undergo surgery. N Engl J Med 2010;363:1597–607. 10.1056/NEJMoa1008232 [DOI] [PubMed] [Google Scholar]
  • 12.Guerreiro C, Ferreira PC, Teles RC, et al. Short and long-term clinical impact of transcatheter aortic valve implantation in Portugal according to different access routes: data from the Portuguese national Registry of TAVI. Rev Port Cardiol (Engl Ed) 2020;39:705–17.:S0870-2551(20)30436-4. 10.1016/j.repc.2020.02.014 [DOI] [PubMed] [Google Scholar]
  • 13.Durko AP, Osnabrugge RL, Kappetein AP. Long-Term outlook for transcatheter aortic valve replacement. Trends Cardiovasc Med 2018;28:174–83.:S1050-1738(17)30121-4. 10.1016/j.tcm.2017.08.004 [DOI] [PubMed] [Google Scholar]
  • 14.Timmermans S, Kaufman R. Technologies and health inequities. Annu Rev Sociol 2020;46:583–602. 10.1146/annurev-soc-121919-054802 Available: https://www.annualreviews.org/toc/soc/46/1 [DOI] [Google Scholar]
  • 15.Carnero-Alcázar M, Maroto-Castellanos LC, Hernández-Vaquero D, et al. Isolated aortic valve replacement in Spain: national trends in risks, valve types, and mortality from 1998 to 2017. Rev Esp Cardiol (Engl Ed) 2021;74:700–7.:S1885-5857(20)30262-0. 10.1016/j.rec.2020.06.008 [DOI] [PubMed] [Google Scholar]
  • 16.Quan H, Sundararajan V, Halfon P, et al. Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Med Care 2005;43:1130–9. 10.1097/01.mlr.0000182534.19832.83 [DOI] [PubMed] [Google Scholar]
  • 17.Charlson ME, Pompei P, Ales KL, et al. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 1987;40:373–83. 10.1016/0021-9681(87)90171-8 [DOI] [PubMed] [Google Scholar]
  • 18.Charlson ME, Carrozzino D, Guidi J, et al. Charlson comorbidity index: a critical review of Clinimetric properties. Psychother Psychosom 2022;91:8–35. 10.1159/000521288 [DOI] [PubMed] [Google Scholar]
  • 19.Bagur R, Martin GP, Nombela-Franco L, et al. Association of comorbid burden with clinical outcomes after transcatheter aortic valve implantation. Heart 2018;104:2058–66. 10.1136/heartjnl-2018-313356 [DOI] [PubMed] [Google Scholar]
  • 20.Bouleti C, Himbert D, Iung B, et al. Long-Term outcome after transcatheter aortic valve implantation. Heart 2015;101:936–42. 10.1136/heartjnl-2014-306694 [DOI] [PubMed] [Google Scholar]
  • 21.Pylväläinen J, Talala K, Murtola T, et al. Charlson comorbidity index based on hospital episode statistics performs adequately in predicting mortality, but its discriminative ability diminishes over time. Clin Epidemiol 2019;11:923–32. 10.2147/CLEP.S218697 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Dautzenberg L, Pals JEM, Lefeber GJ, et al. Predictors of clinical outcome following transcatheter aortic valve implantation: a prospective cohort study. Open Heart 2021;8:e001766. 10.1136/openhrt-2021-001766 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Naing NN. Easy way to learn standardization: direct and indirect methods. Malays J Med Sci 2000;7:10–5. [PMC free article] [PubMed] [Google Scholar]
  • 24.QGIS. Development Team . QGIS geographic information system. open source geospatial foundation project. 2022. Available: https://www.qgis.org/en/site/ [Accessed 26 Jul 2022].
  • 25.AMA - Agência para a Modernização Administrativa, I. P. Distritos de Portugal . 2021. Available: https://dados.gov.pt/en/datasets/distritos-de-portugal/
  • 26.INE . Instituto nacional de estatística [Internet]. 2022. Available: https://www.ine.pt/xportal/xmain?xpid=INE&xpgid=ine_indicadores&indOcorrCod=0004163&xlang=pt&contexto=bd&selTab=tab2
  • 27.Andersen RM, Davidson PL, Baumeister SE. IMPROVING ACCESS TO CARE. In: Changing the US Health Care System: Key Issues in Health Services Policy and Management. 4th Edition. Jossey-Bass, 2014: 33–69. [Google Scholar]
  • 28.Babitsch B, Gohl D, von Lengerke T. Re-revisiting Andersen’s behavioral model of health services use: a systematic review of studies from 1998-2011. Psychosoc Med 2012;9:Doc11. 10.3205/psm000089 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Lakdawalla DN, Phelps CE. Health technology assessment with risk aversion in health. J Health Econ 2020;72:102346.:S0167-6296(19)30920-8. 10.1016/j.jhealeco.2020.102346 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Skedgel C, Henderson N, Towse A, et al. Considering severity in health technology assessment: can we do better? Value Health 2022;25:1399–403.:S1098-3015(22)00105-X. 10.1016/j.jval.2022.02.004 Available: https://www.sciencedirect.com/science/article/pii/S109830152200105X [DOI] [PubMed] [Google Scholar]
  • 31.Wenaweser P, Pilgrim T, Kadner A, et al. Clinical outcomes of patients with severe aortic stenosis at increased surgical risk according to treatment modality. J Am Coll Cardiol 2011;58:2151–62. 10.1016/j.jacc.2011.05.063 [DOI] [PubMed] [Google Scholar]
  • 32.George S, Kwok CS, Martin GP, et al. The influence of the Charlson comorbidity index on procedural characteristics, VARC-2 endpoints and 30-day mortality among patients who undergo transcatheter aortic valve implantation. Heart Lung Circ 2019;28:1827–34.:S1443-9506(18)31989-9. 10.1016/j.hlc.2018.11.006 [DOI] [PubMed] [Google Scholar]
  • 33.Mendez-Bailon M, Lorenzo-Villalba N, Muñoz-Rivas N, et al. Transcatheter aortic valve implantation and surgical aortic valve replacement among hospitalized patients with and without type 2 diabetes mellitus in Spain (2014-2015). Cardiovasc Diabetol 2017;16:144. 10.1186/s12933-017-0631-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Vahanian A, Beyersdorf F, Praz F, et al. 2021 ESC/EACTS guidelines for the management of valvular heart disease: developed by the task force for the management of valvular heart disease of the European Society of cardiology (ESC) and the European association for cardio-thoracic surgery (EACTS). Rev Esp Cardiol (Engl Ed) 2022;75:524.:S1885-5857(22)00112-8. 10.1016/j.rec.2022.05.006 [DOI] [PubMed] [Google Scholar]

Associated Data

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Supplementary Materials

Supplementary data

bmjopen-2022-070715supp001.pdf (281.8KB, pdf)

Reviewer comments

Data Availability Statement

The data of hospitalisations are the property of Central Administration of Health Services (ACSS, I.P.) and transferred to the NOVA National School of Public Health (ENSP). However, the data are available from the authors upon request and with permission of the ACSS and ENSP. The data of hospitalisations are not publicly available, however the authors confirm that interested researchers can ask for access to these data by contacting ACSS directly at the following: Parque da Saúde de Lisboa, Edifício 16, Avenida do Brasil, 53 1700-063 Lisboa, Portugal (e-mail: geral@acss.min-saude. pt).


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