PLoS ONE
Home Comparison of long-term outcomes after trans-catheter aortic valve implantation between patients primarily diagnosed by cardiac murmur and those diagnosed by other reasons
Comparison of long-term outcomes after trans-catheter aortic valve implantation between patients primarily diagnosed by cardiac murmur and those diagnosed by other reasons
Comparison of long-term outcomes after trans-catheter aortic valve implantation between patients primarily diagnosed by cardiac murmur and those diagnosed by other reasons

Competing Interests: The authors have declared that no competing interests exist.

Article Type: research-article Article History
Abstract

Careful auscultation is the first step to diagnose aortic stenosis (AS). The aim of this study was to compare clinical outcomes following transcatheter aortic valve implantation (TAVI) between the patients primarily diagnosed by heart murmur and those diagnosed by other reasons. We retrospectively included 258 patients who underwent TAVI in our medical center, and divided those into the murmur group (n = 81) and the other-reason group (n = 177) according to the primary reason for AS diagnosis. The primary endpoint was the major adverse cardiovascular and cerebrovascular events (MACCE), which was defined as the composite of cardiovascular death, hospitalization due to acute decompensated heart failure, and disabling stroke. The murmur group included younger patients than the other-reason group (82.8 year-old vs. 84.0 year-old, P = 0.02). History of AF was more frequently observed in the other-reason group than in the murmur group (21.5% vs. 7.4%, P <0.01). STS score and logistic EuroSCORE were lower in the murmur group than in the other-reason group (STS: 4.7% vs. 7.2%, P <0.01, logistic EuroSCORE: 8.3% vs. 11.2%, P <0.01). The median follow-up period was 562 days. MACCE was more frequently observed in the other-reason group than in the murmur group (27.7% vs. 9.9%, Log Rank P <0.01). The multivariate COX hazard analysis revealed that the AS patients primarily diagnosed by heart murmur was inversely associated with MACCE (HR 0.38, 95%CI 0.17–0.86, P = 0.020). Among AS patients who underwent TAVI, the patients primarily diagnosed by heart murmur were significantly associated with favorable long-term clinical outcomes.

Taniguchi,Sakakura,Nomura,Hatori,Shibata,Tamanaha,Kasahara,Tsukui,Ibe,Yamamoto,Jinnouchi,Wada,Yamaguchi,Fujita,and Lazzeri: Comparison of long-term outcomes after trans-catheter aortic valve implantation between patients primarily diagnosed by cardiac murmur and those diagnosed by other reasons

Introduction

Trans-catheter aortic valve implantation (TAVI) has been a standard therapy for severe aortic valve stenosis (AS), especially in high surgical risk patients [14]. Frailty, lower active daily life (ADL), or malnutrition have been reported as major predictors of poor long-term outcomes after TAVI [59]. Moreover, symptomatic AS was associated with poor clinical outcomes [10], whereas asymptomatic AS was associated with favorable clinical outcomes [11]. Thus, it is important to detect severe AS when patients are asymptomatic.

On the other hand, it is difficult to find asymptomatic patients with severe AS, partly because routine medical checkups do not include echocardiography. Careful auscultation by primary care physician is a key to find asymptomatic patients with severe AS. We hypothesized that severe AS patients primarily diagnosed by heart murmur would have better clinical outcomes as compared to severe AS patients detected by other reasons. The aim of this study was to compare clinical outcomes following TAVI between the patients primarily diagnosed by heart murmur and the patients diagnosed by other reasons.

Materials and methods

Study design

We screened consecutive patients who underwent TAVI in our medical center between July 2014 and December 2019. Indications and procedural strategies of each TAVI were discussed in a weekly heart team conference in our medical center. All patients that underwent TAVI in our center had some symptoms, at least mild symptoms. Inclusion criteria was the patients who underwent TAVI in our medical center during the above study period. Exclusion criteria was the absence of medical records regarding the primary reason for AS diagnosis. We retrospectively investigated each patient’s primary reason for AS diagnosis from their medical records. The final study population was divided into the two groups according to each primary reason for AS diagnosis. The patients whose primary reason for AS diagnosis was “heart murmur” were defined as “the murmur group”, and the other patients were defined as “the other-reason group”.

The primary endpoint of this study was major adverse cardiovascular and cerebrovascular events (MACCE), which was defined as the composite of cardiovascular death, hospitalization due to acute decompensated heart failure (ADHF), and disabling stroke. Cardiovascular death and disabling stroke were defined according to the criteria of Valve Academic Research Consortium 2 (VARC2) [12]. We set the procedure date as the index day, and the final study date as June 30th, 2020. Most patients were followed up by yearly outpatient clinic until five years after TAVI, and when a patient did not come to the outpatient clinic, we followed up by phone. This study was approved by the Institutional Review Board of Saitama Medical Center, Jichi Medical University (S20-138), and written informed consent was waived because of the retrospective study design.

TAVI procedure

In our medical center, 80.6% of TAVI were performed by trans-femoral approach (TF). TF-TAVI in our medical center was described in elsewhere [9,13]. In addition, 16.1% of TAVI were performed by trans-apical approach (TA), and other cases were by trans-iliac, direct aorta or trans subclavian approaches (3.3%). During TA-TAVI, valve crossing was achieved by a J-shaped conventional wire (0.035 inch), and then the conventional wire was exchanged to a stiff wire. After wire crossing, we inserted 18- or 21-Fr original sheaths for TA-TAVI, and implanted a balloon expandable bioprosthetic valve. Trans-iliac, direct aorta, or trans subclavian approach TAVI were performed in accordance with TF-TAVI.

In our institution, the protocol of anti-platelet or anti-coagulant therapy after TAVI were generally dual anti-platelet therapy (DAPT) for 3–6 months. After DAPT, permanent single anti-platelet therapy (SAPT) was recommended. However, these protocols were modified according to the patient’s conditions such as presence of AF. For example, if a patient had AF, direct oral anti-coagulant (DOAC) and SAPT might be prescribed.

Definitions

Hypertension was defined as receiving treatment for hypertension before admission [9]. Dyslipidemia was defined as total cholesterol >220 mg/dL, low-density lipoprotein cholesterol >140 mg/dL, or medical treatment for dyslipidemia before admission [14]. Diabetes mellitus (DM) was defined as hemoglobin A1c (HbA1c) >6.5% (national glycol-hemoglobin standardization program (NGSP) value) or medical treatment for DM [15]. Estimated glomerular filtration rate (eGFR) was calculated by modification of diet in renal disease (MDRD) method adjusted for Japanese population [16,17]. Anemia was determined by world health organization (WHO) criteria: hemoglobin value <13 g/dL in males and <12 g/dL in females [18]. Frailty was evaluated according to Clinical Frailty Scale (CFS) by medical professionals who cared the patients directly before TAVI [19]. Each STS score and logistic EuroSCORE were calculated before procedure using with online available calculators [2023]. History of atrial fibrillation (AF) was defined as receiving treatment for AF, or document on electrocardiogram (ECG) or monitoring before procedure. Atrio-ventricular block (AV block) was defined as any degrees of AV block on ECG or monitoring before procedure, and the first degree AV block was defined as that of PR interval >200 ms [24]. Echocardiography recorded that the left ventricular ejection fraction (modified Simpson method), aortic valve peak velocity and mean pressure gradient. Aortic valve area was calculated by equation of continuity from those data. Echocardiography also recorded the severity of aortic valve insufficiency according to the reached distance of regurgitant color jet and that of mitral valve insufficiency according to the percentage of jet area. Pulmonary hypertension (PH) was defined as the pressure gradient of tri-cuspid valve regurgitation ≥30 mmHg. Low-flow low-gradient AS was defined as the combination of peak velocity of aortic valve <4.0 m/s, aortic valve area ≤1.0 cm2, and stroke volume index ≤35 ml/m2 according to the guideline 2017 of European society of cardiology [25]. Screening contrast-enhanced computed tomography (CT) was performed for anatomical characteristics of aortic valve, Valsalva sinus, sino-tubular junction and access information. The complications related to TAVI such as conversion to open surgery, coronary obstruction or ventricular perforation were defined according to the VARC2 criteria [12].

Statistical methods

Categorical data were presented as number and percentage, and continuous data were presented as mean ± standard deviation (SD). Normally distributed continuous variables were compared using an unpaired Student t-test. Other continuous variables were compared using a Mann-Whitney U-test. Categorical data were compared using the chi-square test or Fisher’s exact test. The Kaplan-Meyer survival curves were constructed, and the difference between the two survival curves was compared by a Log Rank test. We also performed multivariate COX hazard analysis with likelihood ratio statistical criteria using backward elimination method to confirm the association between the murmur group and MACCE after controlling confounding factors. In this model, MACCE was used as a dependent variable. We adopted marginally significant variables (P <0.10) in univariate comparisons as independent variables. Variables that had missing values were not included in the multivariate analysis. Hazard ratios (HR) and 95% confidence intervals (95% CI) were calculated. P value <0.05 was considered statistically significant. All analyses were performed using statistical software, SPSS PASW Statistics 25, release 25.0.0 /Windows (IBM corp.).

Results

During the study period, a total of 273 patients underwent TAVI in our medical center. Of 273 patients, 15 patients were excluded because of the absence of records regarding the primary reason for AS diagnosis. Finally, 258 patients were included for the final study population, and were divided into the murmur group (n = 81) and the other-reason group (n = 177) (Fig 1).

Study flowchart.
Fig 1

Study flowchart.

AS, aortic valve stenosis.

Table 1 shows the comparison of baseline characteristics. The murmur group included younger patients than the other-reason group (82.8 year-old vs. 84.0 year-old, P = 0.02). History of AF was more frequently observed in the other-reason group than in the murmur group (21.5% vs. 7.4%, P <0.01). Albumin value before procedure were higher in the murmur group than the other-reason group (4.1 g/dL vs. 3.8 g/dL, P <0.01). The eGFR values were also higher in the murmur group (63.2 mL/min/1.73m2 vs. 50.0 mL/min/1.73m2, P <0.01). BNP before TAVI was better in the murmur group than in the other-reason group (297 pg/mL vs. 537 pg/mL, P <0.01). Hemoglobin levels were greater in the murmur group than in the other-reason group (11.9 g/dL vs. 11.0 g/dL, p <0.01). Pulmonary hypertension was more frequently observed in the other-reason group than in the murmur group (15.3% vs. 4.9%. P = 0.02). The prevalence of diuretics users was greater in the other-reason group than in the murmur group (67.8% vs. 39.5%, P <0.01). Both STS score and logistic EuroSCORE were lower in the murmur group than in the other-reason group (STS: 4.7% vs. 7.2%, P <0.01, logistic EuroSCORE: 8.3% vs. 11.2%, P <0.01). Table 2 shows the comparison of TAVI procedures and complications between the two groups. There were no significant differences in TAVI procedures and complications. The incidence of ECMO use during TAVI was only 4.3%.

Table 1
Comparison of baseline characteristics.
Overall (N = 258)Murmur group (n = 81)Other-reason group (n = 177)P value
Age (year-old)83.6 ± 5.282.8 ± 4.284.0 ± 5.60.02
Female gender (no.) (%)168 (65.1)56 (69.1)112 (63.3)0.40
Body surface area (m2)1.46 ± 0.181.48 ± 0.181.45 ± 0.180.12
Smoking (no.) (%)58 (22.7)17 (21.5)41 (23.2)0.87
Hypertension (no.) (%)211 (81.8)69 (85.2)142 (80.2)0.39
Dyslipidemia (no.) (%)138 (53.5)50 (61.7)88 (49.7)0.08
Diabetes mellitus (no.) (%)69 (26.7)23 (28.4)46 (26.0)0.76
History of atrial fibrillation (no.) (%)44 (17.1)6 (7.4)38 (21.5)<0.01
Coronary artery disease (no.) (%)84 (32.6)21 (25.9)63 (35.6)0.15
Old cerebral infarction (no.) (%)18 (7.0)3 (3.7)15 (8.5)0.20
Interstitial Pneumonia (no.) (%)21 (8.1)4 (4.9)17 (9.6)0.23
Malignant diseases (no.) (%)18 (7.0)3 (3.7)15 (8.5)0.20
Electrocardiogram
    Atrio-ventricular block (no.) (%)28 (10.9)4 (4.9)24 (13.6)0.05
    Right bundle branch block (no.) (%)36 (14.0)10 (12.3)26 (14.7)0.70
Laboratory data
    Albumin (g/dL)3.9 ± 0.54.1 ± 0.33.8 ± 0.5<0.01
    eGFR (mL/min/1.73m2)54.2 ± 22.263.2 ± 20.650.0 ± 21.7<0.01
    Hemoglobin (g/dL)11.3 ± 1.611.9 ± 1.611.0 ± 1.6<0.01
    BNP (pg/mL) (n = 243)461 ± 733297 ± 481537 ± 815<0.01
Echocardiogram
    LVEF (Simpson) (n = 139) (%)61 ± 1361 ± 1460 ± 130.44
    Peak velocity of aortic valve (m/s)4.76 ± 0.744.75 ± 0.704.76 ± 0.760.73
    Low-flow low-gradient AS (%)8 (3.1)2 (2.5)6 (3.4)1.00
    Pulmonary hypertension (no.) (%)31 (12.0)4 (4.9)27 (15.3)0.02
Computed tomography
    Annulus area (mm2)404 ± 68397 ± 61407 ± 700.41
    Perimeter (mm) (n = 203)73.4 ± 6.172.4 ± 5.673.8 ± 6.30.20
Medications at admission (no.) (%)
    Aspirin99 (38.4)29 (35.8)70 (39.5)0.58
    P2Y12 inhibitors47 (18.2)11 (13.6)36 (20.3)0.23
    Oral anti-coagulants29 (11.2)5 (6.2)24 (13.6)0.09
    Statins133 (51.6)46 (56.8)87 (49.2)0.28
    ACE inhibitors or ARB135 (52.3)39 (48.1)96 (54.2)0.42
    β blockers89 (34.5)25 (30.9)64 (36.2)0.48
    Diuretics152 (58.9)32 (39.5)120 (67.8)<0.01
    Oral hypoglycemic agents45 (17.4)13 (16.0)32 (18.1)0.73
    Insulin user9 (3.5)3 (3.7)6 (3.4)1.00
    Steroids16 (6.2)7 (8.6)9 (5.1)0.28
    Catecholamine2 (0.8)0 (0)2 (1.1)1.00
Clinical frailty scale before procedure0.22
    1–3132 (51.2)47 (58.0)85 (48.0)
    4–677 (29.8)23 (28.4)54 (30.5)
    7–949 (19.0)11 (13.6)38 (21.5)
STS score (%)6.4 ± 5.54.7 ± 2.37.2 ± 6.4<0.01
logistic EuroSCORE (%) (n = 257)10.3 ± 6.98.3 ± 4.711.2 ± 7.6<0.01
Duration from the date of diagnosis to the date of TAVI (days) (n = 225)666 ± 900962 ± 1045509 ± 772<0.01

eGFR, estimated glomerular filtration rate; BNP, brain natriuretic peptide; LVEF, left ventricular ejection fraction; AS, aortic valve stenosis; ACE, Angiotensin converting enzyme; ARB, Angiotensin II receptor blockers; STS, society of thoracic surgeons; TAVI, transcatheter aortic valve implantation.

Table 2
Comparison of procedure and complications.
Overall (N = 258)Murmur group (n = 81)Other-reason group (n = 177)P value
Approach (no.) (%)0.19
    Trans femoral210 (81.4)71 (87.7)139 (78.5)
    Trans apical41 (15.9)8 (9.9)33 (18.6)
    Alternative7 (2.7)2 (2.5)5 (2.8)
Devices (no.) (%) Balloon expandable0.58
    SapienXT61 (23.6)18 (22.2)43 (24.3)
    Sapien3134 (51.9)45 (55.6)89 (50.3)
Self expandable
    Corevalve13 (5.0)2 (2.5)11 (6.2)
    Evolut series50 (19.4)16 (19.8)34 (19.2)
Size (no.) (%)0.66
    20 mm11 (4.3)4 (4.9)7 (4.0)
    23 mm120 (46.5)41 (50.6)79 (44.6)
    26 mm93 (36.0)28 (34.6)65 (36.7)
    29 mm34 (13.2)8 (9.9)26 (14.7)
Balloon aortic valvuloplasty (no.)163 (63.2)50 (61.7)113 (63.8)0.78
Post dilatation (no.)34 (13.2)13 (16.0)21 (11.9)0.43
Operation time (min)144 ± 64140 ± 51146 ± 700.53
Exposure time (min)39 ± 1642 ± 1638 ± 160.07
Contrast volume (mL)144 ± 62147 ± 60143 ± 630.38
Complications (no.) (%)39 (15.1)15 (18.5)24 (13.6)0.35
    Convert to emergent open surgery3 (1.2)2 (2.5)1 (0.6)0.23
    ECMO during procedure11 (4.3)4 (4.9)7 (4.0)0.75
    Acute coronary obstruction6 (2.3)1 (1.2)5 (2.8)0.67
    Disabling acute cerebral infarction3 (1.2)0 (0)3 (1.7)0.55
New pacemaker implantation21 (8.1)5 (6.2)16 (9.0)0.62

ECMO, Extracorporeal membrane oxygenation.

Table 3 shows in-hospital and long-term outcomes after TAVI. Long-term outcomes were better in the murmur group than in the other-reason group with regard to MACCE (9.9% vs. 27.7%, P <0.01), cardiovascular death (1.2% vs. 14.7%, P <0.01), and hospitalization of ADHF (2.5% vs. 11.3%, P = 0.02). Fig 2 shows Kaplan-Meyer curves regarding long-term outcomes. The median follow-up period was 562 days (349–952 days). MACCE was more frequently observed in the other-reason group than in the murmur group (9.9% vs. 27.7%, P <0.01).

Kaplan-Meyer survival curve analyses.
Fig 2

Kaplan-Meyer survival curve analyses.

MACCE, major adverse cardiovascular or cerebrovascular events: Composite of cardiovascular death, history of hospitalization of acute de-compensated heart failure (ADHF), and disabling stroke.

Table 3
In Hospital and long-term outcomes after TAVI.
Overall (N = 258)Murmur group (n = 81)Other-reason group (n = 177)P value
Echocardiogram after TAVI
    LVEF (Simpson) (n = 134) (%)59 ± 1359 ± 1459 ± 120.04
Aortic valve
    Peak velocity (m/s) (n = 257)2.43 ± 1.572.80 ± 2.682.27 ± 0.500.02
    Para-valvular leakage (no.) (%)0.27
    None or trivial110 (42.8)36 (44.5)74 (42.0)
    Mild144 (56.0)43 (53.1)101 (57.4)
    Moderate/Severe3 (1.2)2 (2.5)1 (0.6)
Laboratory data before discharge
    Hemoglobin (lowest) (g/dL)9.6 ± 1.510.1 ± 1.49.3 ± 1.4<0.01
    Platelet (lowest) (x105/μL)10.0 ± 4.410.2 ± 4.99.9 ± 4.20.92
    BNP (n = 213) (pg/mL)183 ± 183120 ± 120216 ±201<0.01
Medications at discharge (no.) (%)0.04
    SAPT or DOAC alone37 (14.3)6 (7.4)31 (17.5)
    DAPT183 (70.9)67 (82.7)116 (65.5)
    SAPT + DOAC34 (13.2)7 (8.6)27 (15.3)
    Others4 (1.6)1 (1.2)3 (1.7)
Long-term outcomes (no.) (%)
    All cause death41 (15.9)3 (3.7)38 (21.5)<0.01
    Any coronary revascularization2 (0.8)1 (1.2)1 (0.6)0.53
    MACCE57 (22.1)8 (9.9)49 (27.7)<0.01
    Cardiovascular death27 (10.5)1 (1.2)26 (14.7)<0.01
    Hospitalization of ADHF22 (8.5)2 (2.5)20 (11.3)0.02
    Disabling stroke15 (5.8)5 (6.2)10 (5.6)1.00

TAVI, trans-catheter aortic valve implantation; LVEF, left ventricular ejection fraction; BNP, brain natriuretic peptide; SAPT, single anti-platelet therapy; DAPT, dual anti-platelet therapy; DOAC, direct oral anti-coagulant; MACCE, major adverse cardiovascular or cerebrovascular events: Composite of cardiovascular death, history of hospitalization due to acute de-compensated heart failure (ADHF), and disabling stroke.

Table 4 shows the results of multivariate COX hazard analysis. The initial model included elderly, history of AF, history of AV blocks, value of albumin, eGFR, anemia determined by WHO criteria, moderate or severe PH, diuretics users, STS score and AS detected by heart murmur as independent variables. The AS patients primarily diagnosed by heart murmur was inversely associated with MACCE (HR 0.38, 95%CI 0.17–0.86, P = 0.020). Elderly (age ≥90 year-old) (HR 1.83, 95%CI 1.00–3.35, P = 0.049), history of AF (HR 2.67, 95%CI 1.53–4.66, P = 0.001), and lower albumin (<3.5 g/dL) (HR 1.92, 95%CI 1.04–3.55, P = 0.036) were significantly associated with MACCE.

Table 4
Multivariate COX hazard analysis.
Dependent variables: “MACCE”HR95%CIP value
AS detected by heart murmur0.380.17–0.860.020
Elderly (≥90 year-old)1.831.00–3.350.049
History of AF2.671.53–4.660.001
Albumin (<3.5 g/dL)1.921.04–3.550.036

MACCE, major adverse cardiovascular or cerebrovascular events: Composite of cardiovascular death, history of hospitalization due to acute de-compensated heart failure, and disabling stroke; AS, aortic valve stenosis, AF, atrial fibrillation.

Furthermore, since the other-reason group included two different types of patients, the other-reason group was further divided into the following two groups: one was the screening group, defined as patients underwent screening echocardiography because of any cardiac symptom or non-cardiac surgery, and the other was the cardiac events group, defined as patients underwent echocardiography after having cardiovascular events. Kaplan-Meier survival curves were constructed among the murmur group, screening group, and cardiac events group (Fig 3). MACCE was less frequently observed in the murmur group than in other two groups (P <0.01).

Kaplan-Meyer survival curve analysis among three groups.
Fig 3

Kaplan-Meyer survival curve analysis among three groups.

Each group defined according to the primary reasons like below; Murmur group: Equal the murmur group. Screening group: Composite of screening for cardiac symptom and non-cardiac pre-operations. Cardiac events group: hospitalization for some cardiovascular events.

Discussion

We included 258 AS patients who underwent TAVI, and divided those into the murmur group (n = 81) and the other-reason group (n = 177). Kaplan-Meier curves showed that the incidence of MACCE was significantly less in the murmur group than in the other-reason group. Multivariate COX hazard analysis also showed that the murmur group was inversely associated with MACCE after controlling confounding factors.

We should discuss why the murmur group showed the better prognosis than the other-reasons group did. First, the murmur group included relatively younger patients, and had better values of albumin, eGFR, hemoglobin, and BNP as compared with the other-reason group. Furthermore, STS score and logistic EuroSCORE were also better in the murmur group than in the other-reason group. Thus, the murmur group was consisted of the patients who had less background diseases. Second, the other-reason group might include many AS patients with severe symptoms, whereas the murmur group might include many AS patients with mild or slight symptoms. In fact, the other-reason group included 79 patients with some cardiovascular symptoms and 71 patients who were hospitalized for cardiovascular events, which accounted for 85% of the other-reason group. As compared to asymptomatic AS patients, symptomatic AS patients would have worse clinical outcomes [10,11]. Third, the other-reason group might include more patients who were suffering from malignant diseases. Fig 1 shows that there were at least 11 patients who had active malignancy in the other-reason group. On the other hand, no patients in the murmur group had active malignant diseases at the time of TAVI. Thus, the greater prevalence of active malignant disease might have influenced the long-term outcomes in the other-reason group. Although the deaths directly related to malignancy were counted as non-cardiovascular death [12], patients with active malignancy disease would have the greater risk of cardiovascular events such as pulmonary embolism. Forth, the other-reason group included more preoperative patients for orthopedic diseases, such as hip fractures. Several groups reported that the long-term mortality was greater in patients after lower limb fracture than in the general population [2628]. Of note, Sathiyakumar et al. reported that the mortality was emphasized by aging and cardiovascular diseases in patients after hip fraction [29].

Elderly has been well known predictors for long-term outcomes related to TAVI because of their limited lifetime or more backgrounds diseases such as malignancy [9,30]. AF has been reported as one of major predictors for MACCE after TAVI [31,32]. Several mechanisms such as structural remodeling, myocardial fibrosis or loss of atrioventricular synchronicity reduced were reported [33,34]. Some articles have also reported the relationship between malnutrition or hypoalbuminemia and MACCE after TAVI [8,9]. Our results were consistent with those literatures.

The present study might shed light on the auscultation to find AS patients. Since the clinical outcomes of the patients primarily diagnosed by heart murmur were better, the importance of regular auscultation by the primary care physicians should be emphasized, especially in asymptomatic elderly patients who had not been diagnosed with AS. It is also important to order echocardiography if the primary care physicians notice heart murmur. Furthermore, even asymptomatic AS patients sometimes have a poor prognosis, especially in the cases of rapid progression, low left ventricular (LV) function, or very severe AS (the max velocity >5 m/s) [11,3537]. Auscultation would be also important to find those high-risk asymptomatic AS patients.

Study limitations

The present study has several study limitations. As this study was a retrospective, single-center study, there is a potential selection bias. Since most patients were referred to our medical center from other clinics or hospitals, the initial medical history largely depended on the description of the referral letter, which might not contain sufficient information. Moreover, although the heart murmur of AS is typically systolic ejection murmur, pan-systolic murmur cases were also included in the murmur group, because some medical records did not describe the detailed characteristics of each murmur. Because sample size was limited, the statistical analysis has an inherent risk of beta error [38].

Conclusions

Among AS patients who underwent TAVI, the patients whose primary reason for AS diagnosis was heart murmur was significantly associated with favorable long-term clinical outcomes.

Acknowledgements

The authors acknowledge entire staff in the operating room and catheter laboratory in Saitama Medical Center, Jichi Medical University for their technical support in this study.

References

CRSmith, MBLeon, MJMack, DCMiller, JWMoses, LGSvensson, et al Transcatheter versus surgical aortic-valve replacement in high-risk patients. N Engl J Med. 2011;364(23):218798. Epub 2011/06/07. 10.1056/NEJMoa1103510 .

MBLeon, CRSmith, MJMack, RRMakkar, LGSvensson, SKKodali, et al Transcatheter or Surgical Aortic-Valve Replacement in Intermediate-Risk Patients. N Engl J Med. 2016;374(17):160920. Epub 2016/04/05. 10.1056/NEJMoa1514616 .

EGrube, NMVan Mieghem, SBleiziffer, TModine, JBosmans, GManoharan, et al Clinical Outcomes With a Repositionable Self-Expanding Transcatheter Aortic Valve Prosthesis: The International FORWARD Study. J Am Coll Cardiol. 2017;70(7):84553. Epub 2017/08/12. 10.1016/j.jacc.2017.06.045 .

JKForrest, AAMangi, JJPopma, KKhabbaz, MJReardon, NSKleiman, et al Early Outcomes With the Evolut PRO Repositionable Self-Expanding Transcatheter Aortic Valve With Pericardial Wrap. JACC Cardiovasc Interv. 2018;11(2):1608. Epub 2018/01/20. 10.1016/j.jcin.2017.10.014 .

ESkaar, LSPEide, TMNorekval, AHRanhoff, JENordrehaug, DEForman, et al A novel geriatric assessment frailty score predicts 2-year mortality after transcatheter aortic valve implantation. Eur Heart J Qual Care Clin Outcomes. 2019;5(2):15360. Epub 2018/09/27. 10.1093/ehjqcco/qcy044 .

MSaitoh, MSaji, AKozono-Ikeya, TArimitsu, ASakuyama, HUeki, et al Hospital-Acquired Functional Decline and Clinical Outcomes in Older Patients Undergoing Transcatheter Aortic Valve Implantation. Circ J. 2020;84(7):10839. Epub 2020/05/29. 10.1253/circj.CJ-19-1037 .

MSvan Mourik, JFVelu, VRLanting, JLimpens, BJBouma, JJPiek, et al Preoperative frailty parameters as predictors for outcomes after transcatheter aortic valve implantation: a systematic review and meta-analysis. Neth Heart J. 2020;28(5):28092. Epub 2020/03/20. 10.1007/s12471-020-01379-0 .

MMinamisawa, TMiura, HMotoki, YUeki, HNishimura, KShimizu, et al Geriatric Nutritional Risk Index Predicts Cardiovascular Events in Patients at Risk for Heart Failure. Circ J. 2018;82(6):161422. Epub 2017/12/08. 10.1253/circj.CJ-17-0255 .

YTaniguchi, KSakakura, KYuri, YNomura, YTamanaha, NAkashi, et al Appetite Predicts Clinical Outcomes in High Risk Patients Undergoing Trans-Femoral TAVI. Int Heart J. 2019;60(6):13507. Epub 2019/11/19. 10.1536/ihj.19-258 .

10 

JRossJr., EBraunwald. Aortic stenosis. Circulation. 1968;38(1 Suppl):617. Epub 1968/07/01. 10.1161/01.cir.38.1s5.v-61 .

11 

PAPellikka, MESarano, RANishimura, JFMalouf, KRBailey, CGScott, et al Outcome of 622 adults with asymptomatic, hemodynamically significant aortic stenosis during prolonged follow-up. Circulation. 2005;111(24):32905. Epub 2005/06/16. 10.1161/CIRCULATIONAHA.104.495903 .

12 

APKappetein, SJHead, PGenereux, NPiazza, NMvan Mieghem, EHBlackstone, et al Updated standardized endpoint definitions for transcatheter aortic valve implantation: the Valve Academic Research Consortium-2 consensus document. J Am Coll Cardiol. 2012;60(15):143854. Epub 2012/10/06. 10.1016/j.jacc.2012.09.001 .

13 

YTaniguchi, KSakakura, KYuri, YImamura, TTsukui, KYamamoto, et al Determinants of prolonged hospitalization in patients who underwent trans-femoral transcatheter aortic valve implantation. Postepy Kardiol Interwencyjnej. 2019;15(4):4318. Epub 2020/01/15. 10.5114/aic.2019.90217 .

14 

KYamamoto, KSakakura, NAkashi, YWatanabe, MNoguchi, MSeguchi, et al Novel Acute Myocardial Infarction Risk Stratification (nARS) System Reduces the Length of Hospitalization for Acute Myocardial Infarction. Circ J. 2019;83(5):103946. Epub 2019/03/21. 10.1253/circj.CJ-18-1221 .

15 

YTaniguchi, KSakakura, YAdachi, NAkashi, YWatanabe, MNoguchi, et al In-hospital outcomes of acute myocardial infarction with cardiogenic shock caused by right coronary artery occlusion vs. left coronary artery occlusion. Cardiovasc Interv Ther. 2018;33(4):33844. Epub 2017/09/18. 10.1007/s12928-017-0490-9 .

16 

SMatsuo, EImai, MHorio, YYasuda, KTomita, KNitta, et al Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis. 2009;53(6):98292. Epub 2009/04/03. 10.1053/j.ajkd.2008.12.034 .

17 

ASLevey, LAStevens, CHSchmid, YLZhang, AFCastro, 3rd, Feldman HI, et al A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):60412. Epub 2009/05/06. 10.7326/0003-4819-150-9-200905050-00006 .

18 

Nutritional anaemias. Report of a WHO scientific group. World Health Organ Tech Rep Ser. 1968;405:537. Epub 1968/01/01. .

19 

KRockwood, XSong, CMacKnight, HBergman, DBHogan, IMcDowell, et al A global clinical measure of fitness and frailty in elderly people. CMAJ. 2005;173(5):48995. Epub 2005/09/01. 10.1503/cmaj.050051 .

20 

SMO’Brien, DMShahian, GFilardo, VAFerraris, CKHaan, JBRich, et al The Society of Thoracic Surgeons 2008 cardiac surgery risk models: part 2—isolated valve surgery. Ann Thorac Surg. 2009;88(1 Suppl):S2342. Epub 2009/07/09. 10.1016/j.athoracsur.2009.05.056 .

21 

DMShahian, SMO’Brien, GFilardo, VAFerraris, CKHaan, JBRich, et al The Society of Thoracic Surgeons 2008 cardiac surgery risk models: part 1—coronary artery bypass grafting surgery. Ann Thorac Surg. 2009;88(1 Suppl):S222. Epub 2009/07/09. 10.1016/j.athoracsur.2009.05.053 .

22 

SANashef, FRoques, PMichel, EGauducheau, SLemeshow, RSalamon. European system for cardiac operative risk evaluation (EuroSCORE). Eur J Cardiothorac Surg. 1999;16(1):913. Epub 1999/08/24. 10.1016/s1010-7940(99)00134-7 .

23 

FRoques, PMichel, ARGoldstone, SANashef. The logistic EuroSCORE. Eur Heart J. 2003;24(9):8812. Epub 2003/05/03. 10.1016/s0195-668x(02)00799-6 .

24 

RSBexton, AJCamm. First degree atrioventricular block. Eur Heart J. 1984;5 Suppl A:1079. Epub 1984/03/01. 10.1093/eurheartj/5.suppl_a.107 .

25 

HBaumgartner, VFalk, JJBax, MDe Bonis, CHamm, PJHolm, et al 2017 ESC/EACTS Guidelines for the management of valvular heart disease. Eur Heart J. 2017;38(36):273991. Epub 2017/09/10. 10.1093/eurheartj/ehx391 .

26 

JAKanis. The incidence of hip fracture in Europe. Osteoporos Int. 1993;3 Suppl 1:105. Epub 1993/01/01. 10.1007/BF01621853 .

27 

ELHannan, JMagaziner, JJWang, EAEastwood, SBSilberzweig, MGilbert, et al Mortality and locomotion 6 months after hospitalization for hip fracture: risk factors and risk-adjusted hospital outcomes. JAMA. 2001;285(21):273642. Epub 2001/06/21. 10.1001/jama.285.21.2736 .

28 

MJGoldacre, SERoberts, DYeates. Mortality after admission to hospital with fractured neck of femur: database study. BMJ. 2002;325(7369):8689. Epub 2002/10/19. 10.1136/bmj.325.7369.868 .

29 

VSathiyakumar, FRAvilucea, PSWhiting, AAJahangir, HRMir, WTObremskey, et al Risk factors for adverse cardiac events in hip fracture patients: an analysis of NSQIP data. Int Orthop. 2016;40(3):43945. Epub 2015/07/22. 10.1007/s00264-015-2832-5 .

30 

HYokoyama, TTobaru, YMuto, KHagiya, RHiguchi, MSaji, et al Long-term outcomes in Japanese nonagenarians undergoing transcatheter aortic valve implantation: A multi-center analysis. Clin Cardiol. 2019 Epub 2019/04/17. 10.1002/clc.23183 .

31 

RChopard, ETeiger, NMeneveau, SChocron, MGilard, MLaskar, et al Baseline Characteristics and Prognostic Implications of Pre-Existing and New-Onset Atrial Fibrillation After Transcatheter Aortic Valve Implantation: Results From the FRANCE-2 Registry. JACC Cardiovasc Interv. 2015;8(10):134655. Epub 2015/09/01. 10.1016/j.jcin.2015.06.010 .

32 

ASannino, GGargiulo, GGSchiattarella, CPerrino, EStabile, MALosi, et al A meta-analysis of the impact of pre-existing and new-onset atrial fibrillation on clinical outcomes in patients undergoing transcatheter aortic valve implantation. EuroIntervention. 2016;12(8):e1047e56. Epub 2015/11/28. 10.4244/EIJY15M11_12 .

33 

BBurstein, SNattel. Atrial fibrosis: mechanisms and clinical relevance in atrial fibrillation. J Am Coll Cardiol. 2008;51(8):8029. Epub 2008/02/26. 10.1016/j.jacc.2007.09.064 .

34 

TJWang, MGLarson, DLevy, RSVasan, EPLeip, PAWolf, et al Temporal relations of atrial fibrillation and congestive heart failure and their joint influence on mortality: the Framingham Heart Study. Circulation. 2003;107(23):29205. Epub 2003/05/29. 10.1161/01.CIR.0000072767.89944.6E .

35 

RRosenhek, RZilberszac, MSchemper, MCzerny, GMundigler, SGraf, et al Natural history of very severe aortic stenosis. Circulation. 2010;121(1):1516. Epub 2009/12/23. 10.1161/CIRCULATIONAHA.109.894170 .

36 

TKitai, SHonda, YOkada, TTani, KKim, SKaji, et al Clinical outcomes in non-surgically managed patients with very severe versus severe aortic stenosis. Heart. 2011;97(24):202932. Epub 2011/09/29. 10.1136/heartjnl-2011-300137 .

37 

YBohbot, Cde Meester de Ravenstein, GChadha, DRusinaru, KBelkhir, CTrouillet, et al Relationship Between Left Ventricular Ejection Fraction and Mortality in Asymptomatic and Minimally Symptomatic Patients With Severe Aortic Stenosis. JACC Cardiovasc Imaging. 2019;12(1):3848. Epub 2018/11/19. 10.1016/j.jcmg.2018.07.029 .

38 

CGBrown, GDKelen, JJAshton, HAWerman. The beta error and sample size determination in clinical trials in emergency medicine. Ann Emerg Med. 1987;16(2):1837. Epub 1987/02/01. 10.1016/s0196-0644(87)80013-6 .