Abstract
Background
The annual incidence of sudden death has been reported to be low (<1%/year) in asymptomatic patients with severe aortic stenosis (AS), and there is a paucity of data on the risk factors of sudden death in patients with severe AS.
Methods and Results
We evaluated the incidence and risk factors of sudden death during the median follow‐up period of 1334 days in the Contemporary Outcomes After Surgery and Medical Treatment in Patients With Severe Aortic Stenosis (CURRENT AS) registry enrolling 3815 consecutive patients with severe AS between 2003 and 2011. The mean age was 78 years, and the prevalences of male sex and prior myocardial infarction were 38% and 8%, respectively. Sudden death occurred in 175 patients without aortic valve replacement. The cumulative 5‐year incidences of sudden death, censored at aortic valve replacement, which accounted for the competing risk, were 9.2% in symptomatic patients and 7.2% (1.4%/year) in asymptomatic patients (P<0.001). Among 82 asymptomatic patients experiencing sudden death, 54 patients (66%) died abruptly without any preceding symptoms, and 35 (65%) of these sudden deaths occurred within 3 months of the last clinical follow‐up visit. Independent risk factors for sudden death were hemodialysis (hazard ratio [HR] 3.63; 95% confidence interval [CI] 2.42‐5.43), prior myocardial infarction (HR 2.11; 95% CI 1.28‐3.50), body mass index <22 (HR 1.51; 95% CI 1.03‐2.21), peak aortic jet velocity ≥5 m/s (HR 1.76; 95% CI 1.12‐2.78), and left ventricular ejection fraction <60% (HR 1.52; 95% CI 1.08‐2.14).
Conclusions
The incidence of sudden death in asymptomatic patients with severe AS might be higher than that reported in previous reports. Several baseline clinical and echocardiographic characteristics were associated with increased risk of sudden death.
Clinical Trial Registration
URL: http://www.umin.ac.jp/ctr/index.htm. Unique identifier: UMIN000012140.
Keywords: aortic stenosis, aortic valve replacement, sudden death
Subject Categories: Valvular Heart Disease, Aortic Valve Replacement/Transcather Aortic Valve Implantation, Mortality/Survival
Clinical Perspective
What Is New?
This is the first large‐scale report examining the incidence of sudden death and the risk factors associated with sudden death in a contemporary multicenter registry of consecutive patients with severe aortic stenosis.
The incidence of sudden death in asymptomatic patients with severe aortic stenosis might be higher than that reported in previous studies. The cumulative 5‐year incidence of sudden death censored at aortic valve replacement, accounting for the competing risk, was 7.2% (1.4%/year) in asymptomatic patients.
Several clinical and echocardiographic characteristics were found to be significantly associated with the risk of sudden death, particularly hemodialysis, prior myocardial infarction, body mass index <22, peak aortic jet velocity ≥5 m/s, and left ventricular ejection fraction <60%.
What Are the Clinical Implications?
Identification of characteristics associated with an increased risk for sudden death might improve the understanding of potential mechanisms.
Baseline clinical factors can help inform sudden death risk stratification. We should take these risk factors for sudden death into account when we decide the appropriate timing for surgical or transcatheter intervention.
Aortic stenosis (AS) is a progressive disease, and survival during the asymptomatic phase has been reported to be similar to that of age‐matched controls with a low risk of sudden death when patients were followed prospectively and promptly report symptom onset.1, 2, 3 The current guidelines generally recommend a strategy of watchful waiting until symptoms emerge for aortic valve replacement (AVR) in asymptomatic patients with severe AS, based on the low annual incidence of sudden death (<1%/year) in asymptomatic patients with severe AS.1, 3, 4, 5, 6, 7 However, the low annual incidence of sudden death was reported mostly from small single‐center studies conducted in the 1990s and 2000s. Inclusion of relatively younger patients in these studies might not allow us to extrapolate these findings to contemporary patients with more advanced age. There is a paucity of data regarding the predictive factors for an increased risk of sudden death in patients with severe AS, although nearly 70% of sudden death episodes were not preceded by any of the classical AS symptoms.3, 4, 5 Therefore, we sought to investigate the incidence of sudden death and the risk factors associated with sudden death in a large contemporary multicenter registry of consecutive patients with severe AS.
Methods
The data, analytic methods, and study materials will not be made available to other researchers for purposes of reproducing the results or replicating the procedure.
Study Population
The Contemporary Outcomes After Surgery and Medical Treatment in Patients With Severe Aortic Stenosis (CURRENT AS) registry is a multicenter, retrospective registry enrolling consecutive patients with severe AS among 27 centers (on‐site surgical facility in 20 centers) in Japan between 2003 and 2011 (Data S1). The design and patient enrollment of the CURRENT AS registry have been described previously.6 The institutional review boards in all participating centers approved the protocol. This study included 3815 patients who met the definition of severe AS (peak aortic valve velocity >4.0 m/s, mean aortic pressure gradient >40 mm Hg, or aortic valve area <1.0 cm2) for the first time during the study period.7, 8 Written informed consent from each patient was waived because clinical information was obtained from the routine practice, and no patient refused to participate in the study when contacted for follow‐up. Among the 3815 study patients, 2618 were managed with the conservative strategy in which AVR was not planned based on the findings of the index echocardiography, and 1197 patients were managed with the initial AVR strategy in which AVR was planned based on the findings of the index echocardiography. Collection of baseline clinical information including symptomatic status was conducted through hospital chart or database review. Symptoms related to AS at baseline were classified into angina, syncope, and heart failure including both acute heart failure requiring hospitalization and chronic exertional dyspnea. Patients were deemed to be asymptomatic at baseline if they were described as asymptomatic or there were no records regarding the symptoms related to AS defined above. Among 3815 patients enrolled in the registry, there were 2005 patients with and 1808 patients without AS‐related symptoms at the time of index echocardiography, excluding 2 patients whose symptomatic status was not available. Follow‐up was commenced on the day of the index echocardiography.
All patients underwent a comprehensive 2‐dimensional and Doppler echocardiographic evaluation in each participating center according to the guidelines.9 Peak and mean aortic pressure gradient were obtained with the use of the simplified Bernoulli equation, and aortic valve area was calculated using the standard continuity equation and indexed to body surface area.
Outcome Measures
The primary outcome measure in the current analysis was sudden death. Sudden death was defined as death that occurred suddenly and unexpectedly in previously stable patients, in whom specific causes of sudden death were not identified other than severe AS. Death was not judged as sudden death if the death was confirmed to be due to other causes such as myocardial infarction or acute aortic dissection. The causes of death were classified according to the Valve Academic Research Consortium definitions and were adjudicated by a clinical event committee (Data S1).10, 11 A 3‐member adjudication committee composed of 3 cardiologists reviewed the details of deaths. When the members disagreed on the causes of death, a final decision was made by consensus.
Statistical Analysis
Categorical variables were expressed as numbers and percentages, and continuous variables were reported as the mean and SD or median and interquartile range. Cumulative incidence of sudden death in asymptomatic and symptomatic patients as well as the entire population was estimated by the Gray method, which accounted for the competing risk of death other than sudden death.12 We estimated the cumulative incidence of sudden death both with and without censoring at surgical or transcatheter AVR. A multivariable Cox regression model described by Fine and Gray was developed to identify clinical and echocardiographic characteristics associated with an increased risk for sudden death with censoring at surgical or transcatheter AVR in the entire cohort, accounting for the competing risk of death other than sudden death.13 Consistent with our previous report,6 we used 20 clinically relevant potential factors listed in Table 1 in the multivariable Cox proportional hazard models, and the centers were incorporated as the stratification variable. We also explored the clinical characteristics associated with sudden death in asymptomatic and symptomatic patients. We constructed parsimonious models with a limited number of potential risk factors for sudden death in asymptomatic and symptomatic patients with severe AS because the number of patients with this event was too small in this subgroup. We thus selected 10 clinically relevant factors as the potential risk factors with strong evidence as listed in Table 1 for parsimonious models. This was consistent with our previous report14 except for the addition of prior myocardial infarction, male sex, body mass index <22, and left ventricular ejection fraction (LVEF). We included LVEF <60% instead of the traditional LVEF <50% as a potential risk predictor because we previously reported that the negative prognostic impact of LVEF 50% to 59% was comparable to that of LVEF <50% in patients with severe AS who were managed conservatively.15 As the subgroup analyses, we assessed the cumulative incidence of sudden death in patients with hemodialysis (HD) (N=405) and non‐HD patients (N=3410) because we previously reported an extremely high rate of sudden death in HD patients.14 We also explored the clinical characteristics associated with sudden death in non‐HD patients. Statistical analyses were conducted by a physician (T. Taniguchi) and a statistician (T. Morimoto) with the use of JMP 10.0.2 (SAS Institute Inc, Cary, NC) or SAS 9.4 (SAS Institute Inc, Cary, NC). All reported P values were 2 tailed, and P<0.05 was considered statistically significant.
Table 1.
Baseline Clinical and Echocardiographic Characteristics in the Entire Cohort
| Variables | Whole Cohort | Symptomatic | Asymptomatic | P Value |
|---|---|---|---|---|
| N=3815 | N=2005 | N=1808 | ||
| Clinical characteristics | ||||
| Age, y | 77.8±9.8 | 78.6±9.8 | 76.8±9.6 | <0.001 |
| Age ≥80 ya | 1729 (45%) | 978 (49%) | 749 (41%) | <0.001 |
| Malea | 1443 (38%) | 713 (36%) | 730 (40%) | 0.002 |
| BMI, kg/m2 | 21.8±3.8 | 21.6±3.8 | 22.0±3.8 | 0.01 |
| BMI <22 kg/m2 a | 2326 (61%) | 1268 (63%) | 1057 (58%) | 0.003 |
| BSA, m2 | 1.46±0.18 | 1.44±0.19 | 1.47±0.18 | <0.001 |
| Hypertensiona | 2667 (70%) | 1418 (71%) | 1248 (69%) | 0.25 |
| Current smokinga | 196 (5%) | 101 (5%) | 95 (5%) | 0.76 |
| History of smoking | 830 (22%) | 428 (21%) | 402 (22%) | 0.51 |
| Dyslipidemia | 1327 (35%) | 679 (34%) | 648 (36%) | 0.20 |
| On statin therapy | 970 (25%) | 506 (25%) | 464 (26%) | 0.76 |
| Diabetes mellitus | 897 (24%) | 463 (23%) | 434 (24%) | 0.51 |
| On insulin therapya | 188 (5%) | 97 (5%) | 91 (5%) | 0.78 |
| Prior myocardial infarctiona | 323 (8%) | 172 (9%) | 151 (8%) | 0.80 |
| Coronary artery diseasea | 1144 (30%) | 656 (33%) | 488 (27%) | <0.001 |
| Prior PCI | 502 (13%) | 216 (11%) | 286 (16%) | <0.001 |
| Prior CABG | 199 (5%) | 101 (5%) | 98 (5%) | 0.60 |
| Prior open‐heart surgery | 316 (8%) | 151 (8%) | 165 (9%) | 0.07 |
| Prior symptomatic strokea | 503 (13%) | 249 (12%) | 253 (14%) | 0.15 |
| Atrial fibrillation or fluttera | 828 (22%) | 490 (24%) | 338 (19%) | <0.001 |
| Aortic/peripheral vascular diseasea | 282 (7%) | 111 (6%) | 171 (9%) | <0.001 |
| Serum creatinine, mg/dL | 0.9 (0.7‐1.3) | 0.9 (0.7‐1.3) | 0.8 (0.7‐1.2) | <0.001 |
| Creatinine level >2 mg/dL | 558 (15%) | 309 (15%) | 249 (14%) | 0.15 |
| Hemodialysisa | 405 (11%) | 198 (10%) | 207 (11%) | 0.12 |
| Anemiaa, b | 2117 (55%) | 1254 (63%) | 862 (48%) | <0.001 |
| Liver cirrhosis (Child‐Pugh B/C) | 38 (1%) | 27 (1%) | 11 (1%) | 0.02 |
| Malignancy | 517 (14%) | 240 (12%) | 276 (15%) | 0.003 |
| Malignancy currently under treatmenta | 149 (4%) | 55 (3%) | 94 (5%) | <0.001 |
| Chest wall irradiation | 25 (1%) | 13(1%) | 12 (1%) | 0.95 |
| Immunosuppressive therapy | 131 (3%) | 71 (4%) | 60 (3%) | 0.71 |
| Chronic lung disease | 400 (10%) | 239 (12%) | 161 (9%) | 0.002 |
| Chronic lung disease (moderate or severe)a | 112 (3%) | 69 (3%) | 43 (2%) | 0.052 |
| Logistic EuroSCORE, % | 9.7 (5.8‐16.7) | 11.4 (6.6‐20.0) | 8.4 (5.1‐13.9) | <0.001 |
| EuroSCORE II, % | 2.9 (1.6‐4.8) | 3.6 (2.0‐6.3) | 2.4 (1.4‐3.6) | <0.001 |
| STS score (PROM), % | 3.8 (2.2‐6.6) | 4.5 (2.5‐8.0) | 3.3 (2.0‐5.2) | <0.001 |
| Symptom related to ASa | 2005 (53%) | |||
| Chest pain | 498 | 498 | 0 | ··· |
| Syncope | 198 | 198 | 0 | ··· |
| Heart failure | 1603 | 1603 | 0 | ··· |
| HF hospitalization at the index echocardiography | 790 (21%) | 790 | 0 | ··· |
| Echocardiographic variables | ||||
| Vmax, m/s | 4.1±0.9 | 4.3±0.9 | 3.9±0.8 | <0.001 |
| Vmax ≥5 m/sa | 698 (18%) | 490 (24%) | 207 (11%) | <0.001 |
| Vmax ≥4 m/s | 2185 (57%) | 1320 (66%) | 864 (48%) | <0.001 |
| Peak aortic PG, mm Hg | 72±32 | 78±33 | 65±28 | <0.001 |
| Mean aortic PG, mm Hg | 41±20 | 45±21 | 36±17 | <0.001 |
| AVA (equation of continuity), cm2 | 0.72±0.18 | 0.67±0.19 | 0.77±0.17 | <0.001 |
| Indexed AVA, cm2/m2 | 0.50±0.13 | 0.47±0.13 | 0.53±0.12 | <0.001 |
| LV end‐diastolic diameter, mm | 45.9±7.0 | 47.0±7.6 | 44.8±6.0 | <0.001 |
| LV end‐systolic diameter, mm | 30.2±7.9 | 31.9±8.8 | 28.4±6.2 | <0.001 |
| LVEF, % | 62.8±13.5 | 59.9±14.9 | 65.9±10.9 | <0.001 |
| LVEF <50% | 593 (16%) | 451 (22%) | 142 (8%) | <0.001 |
| LVEF <60%a | 1153 (30%) | 798 (40%) | 355 (20%) | <0.001 |
| IVST in diastole, mm | 11.3±2.3 | 11.6±2.4 | 11.1±2.2 | <0.001 |
| PWT in diastole, mm | 11.0±2.0 | 11.2±2.1 | 10.7±2.0 | <0.001 |
| Any combined valvular disease (moderate or severe)a | 1558 (41%) | 997 (50%) | 560 (31%) | <0.001 |
| Moderate or severe AR | 791 (21%) | 497 (25%) | 293 (16%) | <0.001 |
| Moderate or severe MS | 133 (3%) | 84 (4%) | 49 (3%) | 0.01 |
| Moderate or severe MR | 763 (20%) | 550 (27%) | 213 (12%) | <0.001 |
| Moderate or severe TR | 628 (16%) | 412 (21%) | 216 (12%) | <0.001 |
| TR pressure gradient ≥40 mm Hga | 606 (16%) | 433 (22%) | 173 (10%) | <0.001 |
| Treatment strategy | ||||
| Initial AVR strategy | 1197 (31%) | 905 (45%) | 291 (16%) | <0.001 |
| Conservative strategy | 2618 (69%) | 1100 (55%) | 1517 (84%) | |
Comparison between symptomatic and asymptomatic patients was performed after excluding 2 patients whose symptomatic status was not available. Abbreviations: AR, aortic regurgitation; AS, aortic stenosis; AVA, aortic valve area; AVR, aortic valve replacement; BMI, body mass index; BSA, body surface area; CABG, coronary artery bypass grafting; HF, heart failure; IVST, interventricular septum thickness; LV, left ventricular; LVEF, left ventricular ejection fraction; MR, mitral regurgitation; MS, mitral stenosis; PCI, percutaneous coronary intervention; PG, pressure gradient; PROM, predicted risk of mortality; PWT, posterior wall thickness; STS, Society of Thoracic Surgeons; TR, tricuspid regurgitation; Vmax, peak aortic jet velocity.
Potential independent variables selected for the Cox proportional hazard model.
Anemia was defined by the World Health Organization criteria (hemoglobin <12.0 g/dL in women and <13.0 g/dL in men).
Results
Baseline Clinical and Echocardiographic Characteristics
Among the 3815 patients with severe AS enrolled in this registry, the mean age was 77.8 years, and 1443 patients (38%) were male. Clinical and echocardiographic characteristics of the entire cohort are shown in Table 1. The prevalence of prior myocardial infarction was 8%. The peak aortic jet velocity was 4.1±0.9 m/s, and aortic valve area was 0.72±0.18 cm2 (Table 1). There were 405 patients (11%) with HD, and 1808 patients (47%) were asymptomatic at baseline. Symptomatic patients at baseline were much older and more often had coronary artery disease, atrial fibrillation or flutter, or anemia than asymptomatic patients. Surgical risk scores such as Logistic EuroSCORE, EuroSCORE II, and Society of Thoracic Surgeons score were significantly higher in symptomatic patients than in asymptomatic patients. Regarding the echocardiographic parameters, symptomatic patients compared with asymptomatic patients had lower LVEF, larger left ventricular dimensions, and higher incidence of pulmonary hypertension. Symptomatic patients more often had greater AS severity and combined valvular disease such as mitral regurgitation, tricuspid regurgitation, and aortic regurgitation.
Incidences of Sudden Death
The median follow‐up period of the surviving patients in the entire cohort was 1334 (interquartile range 1019‐1701) days with 93% follow‐up rate at 2‐years. Sudden death occurred in 175 patients and in 196 patients with and without censoring at surgical AVR or TAVI, respectively. The cumulative 5‐year incidences of sudden death in the entire cohort were 8.0% and 5.7% (1.6%/year and 1.1%/year) with and without censoring at surgical AVR or transcatheter aortic valve implantation (TAVI), respectively (Figure 1).
Figure 1.

Kaplan‐Meier curves for sudden death in the entire cohort with and without censoring at AVR/TAVI. Cumulative incidence of sudden death was estimated by the Gray method, taking the competing risk of death other than sudden death. AVR indicates aortic valve replacement; TAVI, transcatheter aortic valve implantation.
Among 175 patients with sudden death with censoring at surgical AVR or TAVI, 139 (79%) sudden deaths occurred out of hospital. Eleven patients died suddenly while waiting for surgical AVR or TAVI, and 10 patients with HD had sudden death during dialysis. Among 82 patients with sudden death who did not have any symptoms at baseline, 54 patients (66%) died abruptly without preceding symptoms, and 35 (65%) of these sudden deaths with no preceding symptoms occurred within 3 months of the last clinical follow‐up visit.
The cumulative 5‐year incidence of sudden death was significantly higher in symptomatic patients than in asymptomatic patients (9.2% [N=93/2005] versus 7.2% [N=82/1808], P=0.008; 1.8%/year and 1.4%/year) (Figure 2). The cumulative 5‐year incidence of sudden death in asymptomatic patients with severe AS was 5.8% without censoring at surgical AVR or TAVI. The cumulative 5‐year incidence of sudden death was markedly higher in the HD group than in the non‐HD group (23.3% versus 6.5%, P<0.001; 4.7%/year and 1.3%/year) (Figure S1).
Figure 2.

Kaplan‐Meier curves for sudden death: symptomatic and asymptomatic patients with severe AS after excluding 2 patients whose symptomatic status was not available. Cumulative incidence of sudden death was estimated by the Gray method, taking the competing risk of death other than sudden death. AS indicates aortic stenosis; AVR, aortic valve replacement; TAVI, transcatheter aortic valve implantation.
Clinical Characteristics Associated With Sudden Death
Independent predictors associated with a higher risk for sudden death included HD (hazard ratio [HR] 3.63; 95% confidence interval [CI] 2.42‐5.43), prior myocardial infarction (HR 2.11; 95% CI 1.28‐3.50), body mass index <22 (HR 1.51; 95% CI 1.03‐2.21), peak aortic jet velocity ≥5 m/s (HR 1.76; 95% CI 1.12‐2.78), and LVEF<60% (HR 1.52; 95% CI 1.08‐2.14) (Table 2). The results after exclusion of HD patients were consistent with those from the main analysis set (Table S1). Independent predictors for sudden death in asymptomatic and symptomatic patients were consistent with those identified in the entire cohort (Table 3).
Table 2.
Clinical Factors Associated With Sudden Death in the Entire Cohort in the Univariate and Multivariable Analyses
| Variables | Unadjusted HRa (95% CI) | P Value | Adjusted HR (95% CI) | P Value |
|---|---|---|---|---|
| Hemodialysis | 5.35 (3.78‐7.46) | <0.001 | 3.63 (2.42‐5.43) | <0.001 |
| Prior myocardial infarction | 2.68 (1.84‐3.81) | <0.001 | 2.11 (1.28‐3.50) | 0.004 |
| BMI <22 | 1.85 (1.32‐2.65) | <0.001 | 1.51 (1.03‐2.21) | 0.03 |
| LVEF <60% | 2.84 (2.10‐3.82) | <0.001 | 1.52 (1.08‐2.14) | 0.02 |
| Vmax ≥5 m/s | 1.58 (1.02‐2.36) | 0.04 | 1.76 (1.12‐2.78) | 0.01 |
| Symptoms related to AS | 1.90 (1.41‐2.57) | <0.001 | 1.28 (0.90‐1.82) | 0.17 |
| Age ≥80 y | 1.38 (1.02‐1.87) | 0.03 | 1.09 (0.77‐1.53) | 0.64 |
| Male | 1.75 (1.30‐2.36) | <0.001 | 1.34 (0.95‐1.89) | 0.09 |
| TRPG ≥40 mm Hg | 1.55 (1.05‐2.22) | 0.03 | 1.17 (0.75‐1.81) | 0.49 |
| Any valvular disease (moderate‐severe) | 1.25 (0.92‐1.68) | 0.15 | 1.07 (0.75‐1.51) | 0.72 |
| Prior symptomatic stroke | 1.07 (0.69‐1.60) | 0.74 | 0.78 (0.50‐1.22) | 0.28 |
| Atrial fibrillation or flutter | 1.02 (0.71‐1.44) | 0.91 | 0.91 (0.63‐1.33) | 0.64 |
| Chronic lung disease (moderate‐severe) | 1.07 (0.42‐2.20) | 0.88 | 0.93 (0.41‐2.09) | 0.85 |
| Malignancy currently under treatment | 1.21 (0.51‐2.39) | 0.63 | 0.85 (0.38‐1.88) | 0.68 |
| Aortic/peripheral disease | 2.11 (1.33‐3.22) | 0.002 | 1.05 (0.64‐1.70) | 0.85 |
| Current smoking | 0.71 (0.30‐1.41) | 0.36 | 0.83 (0.38‐1.80) | 0.64 |
| Diabetes mellitus on insulin | 1.79 (0.97‐3.03) | 0.06 | 1.16 (0.61‐2.19) | 0.65 |
| Coronary artery disease | 1.81 (1.33‐2.45) | <0.001 | 0.91 (0.60‐1.37) | 0.64 |
| Anemia | 2.03 (1.49‐2.80) | <0.001 | 0.92 (0.65‐1.32) | 0.66 |
| Hypertension | 1.36 (0.96‐1.95) | 0.08 | 1.30 (0.90‐1.88) | 0.16 |
Abbreviations: AS, aortic stenosis; AVR, aortic valve replacement; BMI, body mass index; CI, confidence interval; HR, hazard ratio; LVEF, left ventricular ejection fraction; TAVI, transcatheter aortic valve implantation; TRPG, tricuspid regurgitation pressure gradient; Vmax, peak aortic jet velocity.
Competing risk of death other than sudden death was not taken into account in the univariate analysis, but it was taken into account in the multivariable analysis. Patients who had AVR or TAVI were censored at AVR/TAVI.
Table 3.
Clinical Factors Associated With Sudden Death in Asymptomatic and Symptomatic Patients With Severe AS in the Univariate and Multivariable Analyses
| Variables | Unadjusted HRa (95% CI) | P Value | Adjusted HR (95% CI) | P Value |
|---|---|---|---|---|
| Asymptomatic patients (N=1808) | ||||
| Hemodialysis | 7.79 (4.85‐12.3) | <0.001 | 4.23 (2.48‐7.22) | <0.001 |
| Prior myocardial infarction | 2.76 (1.56‐4.60) | <0.001 | 1.75 (0.97‐3.16) | 0.07 |
| BMI <22 | 1.79 (1.12‐2.95) | 0.01 | 1.47 (0.87‐2.48) | 0.15 |
| LVEF <60% | 3.33 (2.11‐5.18) | <0.001 | 1.76 (1.08‐2.87) | 0.02 |
| Vmax ≥5 m/s | 1.62 (0.72‐3.19) | 0.22 | 2.36 (1.09‐5.14) | 0.03 |
| Age ≥80 y | 1.10 (0.71‐1.71) | 0.66 | 0.97 (0.61‐1.53) | 0.89 |
| Male | 1.77 (1.15‐2.74) | 0.01 | 1.20 (0.72‐1.99) | 0.48 |
| Any valvular disease (moderate‐severe) | 0.97 (0.60‐1.54) | 0.90 | 1.06 (0.65‐1.73) | 0.80 |
| Atrial fibrillation or flutter | 1.07 (0.60‐1.80) | 0.81 | 0.78 (0.43‐1.40) | 0.40 |
| Malignancy currently under treatment | 1.66 (0.58‐3.73) | 0.31 | 1.01 (0.36‐2.82) | 0.99 |
| Symptomatic patients (N=2005) | ||||
| Hemodialysis | 3.87 (2.25‐6.32) | <0.001 | 3.11 (1.73‐5.59) | <0.001 |
| Prior myocardial infarction | 2.54 (1.51‐4.09) | <0.001 | 2.30 (1.31‐4.07) | 0.004 |
| BMI <22 | 1.65 (1.02‐2.82) | 0.04 | 1.62 (0.94‐2.80) | 0.08 |
| LVEF <60% | 2.04 (1.35‐3.08) | <0.001 | 1.32 (0.84‐2.07) | 0.23 |
| Vmax ≥5 m/s | 1.24 (0.72‐2.04) | 0.42 | 1.51 (0.87‐2.60) | 0.14 |
| Age ≥80 y | 1.46 (0.96‐2.28) | 0.08 | 1.28 (0.76‐2.17) | 0.35 |
| Male | 2.02 (1.33‐3.06) | 0.001 | 1.48 (0.94‐2.34) | 0.09 |
| Any valvular disease (moderate‐severe) | 1.20 (0.80‐1.82) | 0.39 | 1.21 (0.78‐1.87) | 0.40 |
| Atrial fibrillation or flutter | 0.85 (0.52‐1.34) | 0.50 | 0.99 (0.60‐1.61) | 0.95 |
| Malignancy currently under treatment | 0.90 (0.15‐2.86) | 0.88 | 0.52 (0.12‐2.20) | 0.37 |
Abbreviations: AS, aortic stenosis; AVR, aortic valve replacement; BMI, body mass index; CI, confidence interval; HR, hazard ratio; LVEF, left ventricular ejection fraction; TAVI, transcatheter aortic valve implantation; Vmax, peak aortic jet velocity.
Competing risk of death other than sudden death was not taken into account in the univariate analysis, whereas it was taken into account in the multivariable analysis. Patients who had AVR or TAVI were censored at AVR/TAVI.
Discussion
The main findings of the present study were the following: (1) the incidence of sudden death in asymptomatic patients with severe AS might be higher than that reported in previous studies; (2) we identified several baseline clinical characteristics as well as echocardiographic parameters that were associated with increased risk of sudden death in patients with severe AS, including potent predictors such as HD, prior myocardial infarction, and modest predictors such as body mass index <22, baseline peak aortic valve velocity ≥5 m/s, and LVEF <60%.
Sudden death in patients with severe AS is a clinically important issue. Previous studies have reported relatively low annual risk of sudden death (<1%/year) in asymptomatic patients with severe AS (Rosenhek et al, 1 out of 106 patients [0.42%/year], mean age of 57 years1; Pellikka et al, 11 out of 270 patients [0.75%/year], mean age of 72 years3; Kang et al, 9 out of 95 patients [1.9%/year], mean age of 63 years16; and Rosenhek et al, 1 out of 116 patients [0.3%/year], mean age of 67 years2). In the present contemporary multicenter study, however, the annual risk of sudden death censored at surgical or transcatheter AVR (1.4%/year) was numerically higher than those reported in previous studies in asymptomatic patients with severe AS. One of the possible reasons for the seemingly higher rate of sudden death might be related to the more advanced age in the present study population, who often have multiple comorbidities such as HD and prior myocardial infarction predisposing to sudden death. Another possible reason might be the difference in the modes of clinical follow‐up between the single‐center and multicenter studies. In smaller single‐center studies, patients might have been followed more closely than in larger multicenter studies. Closer follow‐up would make it possible to detect emergence of symptoms earlier. Pellikka et al reported that no patient had sudden death unpreceded by symptoms in their earlier small study (N=113).17 However, in their later study with a larger cohort, 11 out of 270 patients who did not undergo surgical AVR experienced sudden death without any preceding symptoms.3 In the present study as well as in the aggregates of the previous studies, sudden death often occurs without any preceding symptoms in asymptomatic patients with severe AS. Absence of the preceding symptoms might be related to the difficulties in interpreting mild symptoms as aortic valve–related symptoms in elderly patients with a sedentary lifestyle. Therefore, the strategy of watchful waiting for the emergence of symptoms might not be very effective in preventing sudden death.
It would be important to identify those asymptomatic severe AS patients who are at high risk for sudden death. The strengths of the present study include (1) assessment of the incidence of sudden death in consecutive patients both with or without AS‐related symptoms, (2) inclusion of large numbers of patients enough to explore the baseline characteristics independently associated with sudden death, and (3) a contemporary multicenter cohort of patients with severe AS including hemodialysis patients. Several baseline clinical characteristics as well as echocardiographic parameters such as HD, and prior myocardial infarction as well as greater peak aortic valve velocity, lower LVEF, and smaller body mass index were significantly associated with increased risk of sudden death in patients with severe AS. This is the first large‐scale contemporary multicenter study reporting the incidence of sudden death and the clinical factors independently associated with sudden death in consecutive patients with severe AS. We should take these risk factors for sudden death into account when we decide the appropriate timing for the surgical or transcatheter intervention. In this regard, it is essential to balance the natural risk of severe AS with the risk of surgical or transcatheter AVR. Improved surgical techniques have led to lower operative mortality, and TAVI outcomes have also improved with experience and device development. Therefore, the risk of sudden death in some high‐risk patients with asymptomatic severe AS might outweigh the procedural mortality risk in the contemporary clinical practice. Early surgical or transcatheter intervention might be able to prevent sudden death, which is under investigation in the ongoing EARLY TAVR (Evaluation of Transcatheter Aortic Valve Replacement Compared to Surveillance for Patients With Asymptomatic Severe Aortic Stenosis) trial (NCT03042104).
Study Limitations
This study had several limitations. First, patient follow‐up in this multicenter study might have been less close than the follow‐up in previous single‐center studies. However, it would be important to note that 65% of sudden death occurred within 3 months of the last clinical follow‐up visit among 54 patients experiencing sudden death without any symptoms. Second, not all sudden death could be attributed to severe AS, although clinical events were adjudicated according to the Valve Academic Research Consortium definitions by a clinical events committee. Third, we did not collect information on exercise testing, thereby leaving the possibility of unrecognized symptoms in some patients due to sedentary lifestyle. Although the current guidelines recommend an exercise test to confirm symptomatic status in asymptomatic patients with severe AS, exercise testing cannot be commonly performed in a satisfactory manner in many patients with severe AS because of their advanced age, limited exercise capacities, frailties, and comorbidities. Fourth, we could not deny residual confounding and selection bias for AVR, although we performed the extensive multivariable analysis for the risk factors of sudden death. Actually, the cumulative incidence of sudden death in symptomatic patients was relatively low, because symptomatic patients, as compared with asymptomatic patients, were more often referred to surgical or transcatheter AVR after diagnosis of severe AS with the index echocardiography. Finally, we did not collect data on ECG features such as QRS duration and QRS morphology, which were reported to be associated with sudden death in asymptomatic patients with mild to moderate AS.18
Conclusions
The incidence of sudden death in asymptomatic patients with severe AS might be higher than that reported in previous reports. Several baseline clinical characteristics as well as echocardiographic parameters were associated with increased risk of sudden death in patients with severe AS.
Sources of Funding
This work was supported by an educational grant from the Research Institute for Production Development (Kyoto, Japan).
Disclosures
None.
Supporting information
Appendix S1. CURRENT AS Registry Investigators
Data S1. Definitions of the Clinical Events
Table S1. Clinical Factors Associated With Sudden Death in the Non‐HD Cohort in the Univariate and Multivariable Analyses
Figure S1. Cumulative incidence of sudden cardiac death in HD and non‐HD patients with severe AS.
(J Am Heart Assoc. 2018;7:e008397 DOI: 10.1161/JAHA.117.008397.)29776957
References
- 1. Rosenhek R, Binder T, Porenta G, Lang I, Christ G, Schemper M, Maurer G, Baumgartner H. Predictors of outcome in severe, asymptomatic aortic stenosis. N Engl J Med. 2000;343:611–617. [DOI] [PubMed] [Google Scholar]
- 2. Rosenhek R, Zilberszac R, Schemper M, Czerny M, Mundigler G, Graf S, Bergler‐Klein J, Grimm M, Gabriel H, Maurer G. Natural history of very severe aortic stenosis. Circulation. 2010;121:151–156. [DOI] [PubMed] [Google Scholar]
- 3. Pellikka PA, Sarano ME, Nishimura RA, Malouf JF, Bailey KR, Scott CG, Barnes ME, Tajik AJ. Outcome of 622 adults with asymptomatic, hemodynamically significant aortic stenosis during prolonged follow‐up. Circulation. 2005;111:3290–3295. [DOI] [PubMed] [Google Scholar]
- 4. Genereux P, Stone GW, O'Gara PT, Marquis‐Gravel G, Redfors B, Giustino G, Pibarot P, Bax JJ, Bonow RO, Leon MB. Natural history, diagnostic approaches, and therapeutic strategies for patients with asymptomatic severe aortic stenosis. J Am Coll Cardiol. 2016;67:2263–2288. [DOI] [PubMed] [Google Scholar]
- 5. Bhattacharyya S, Hayward C, Pepper J, Senior R. Risk stratification in asymptomatic severe aortic stenosis: a critical appraisal. Eur Heart J. 2012;33:2377–2387. [DOI] [PubMed] [Google Scholar]
- 6. Taniguchi T, Morimoto T, Shiomi H, Ando K, Kanamori N, Murata K, Kitai T, Kawase Y, Izumi C, Miyake M, Mitsuoka H, Kato M, Hirano Y, Matsuda S, Nagao K, Inada T, Murakami T, Takeuchi Y, Yamane K, Toyofuku M, Ishii M, Minamino‐Muta E, Kato T, Inoko M, Ikeda T, Komasa A, Ishii K, Hotta K, Higashitani N, Kato Y, Inuzuka Y, Maeda C, Jinnai T, Morikami Y, Sakata R, Kimura T. Initial surgical versus conservative strategies in patients with asymptomatic severe aortic stenosis. J Am Coll Cardiol. 2015;66:2827–2838. [DOI] [PubMed] [Google Scholar]
- 7. Nishimura RA, Otto CM, Bonow RO, Carabello BA, Erwin JP III, Guyton RA, O'Gara PT, Ruiz CE, Skubas NJ, Sorajja P, Sundt TM III, Thomas JD. 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;129:e521–e643. [DOI] [PubMed] [Google Scholar]
- 8. Vahanian A, Alfieri O, Andreotti F, Antunes MJ, Baron‐Esquivias G, Baumgartner H, Borger MA, Carrel TP, De Bonis M, Evangelista A, Falk V, Iung B, Lancellotti P, Pierard L, Price S, Schafers HJ, Schuler G, Stepinska J, Swedberg K, Takkenberg J, Von Oppell UO, Windecker S, Zamorano JL, Zembala M. Guidelines on the management of valvular heart disease (version 2012). Eur Heart J. 2012;33:2451–2496. [DOI] [PubMed] [Google Scholar]
- 9. Lang RM, Bierig M, Devereux RB, Flachskampf FA, Foster E, Pellikka PA, Picard MH, Roman MJ, Seward J, Shanewise JS, Solomon SD, Spencer KT, Sutton MS, Stewart WJ. Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005;18:1440–1463. [DOI] [PubMed] [Google Scholar]
- 10. Leon MB, Piazza N, Nikolsky E, Blackstone EH, Cutlip DE, Kappetein AP, Krucoff MW, Mack M, Mehran R, Miller C, Morel MA, Petersen J, Popma JJ, Takkenberg JJ, Vahanian A, van Es GA, Vranckx P, Webb JG, Windecker S, Serruys PW. Standardized endpoint definitions for transcatheter aortic valve implantation clinical trials: a consensus report from the Valve Academic Research Consortium. J Am Coll Cardiol. 2011;57:253–269. [DOI] [PubMed] [Google Scholar]
- 11. Kappetein AP, Head SJ, Genereux P, Piazza N, van Mieghem NM, Blackstone EH, Brott TG, Cohen DJ, Cutlip DE, van Es GA, Hahn RT, Kirtane AJ, Krucoff MW, Kodali S, Mack MJ, Mehran R, Rodes‐Cabau J, Vranckx P, Webb JG, Windecker S, Serruys PW, Leon MB. Updated standardized endpoint definitions for transcatheter aortic valve implantation: the Valve Academic Research Consortium‐2 consensus document. J Am Coll Cardiol. 2012;60:1438–1454. [DOI] [PubMed] [Google Scholar]
- 12. Gray RJ. A class of K‐sample tests for comparing the cumulative incidence of a competing risk. Ann Stat. 1988;16:1141–1154. [Google Scholar]
- 13. Fine JP, Gray RJ. A proportional hazards model for the subdistribution of a competing risk. J Am Stat Assoc. 1999;94:496–509. [Google Scholar]
- 14. Kawase Y, Taniguchi T, Morimoto T, Kadota K, Iwasaki K, Kuwayama A, Ohya M, Shimada T, Amano H, Maruo T, Fuku Y, Izumi C, Kitai T, Saito N, Minamino‐Muta E, Kato T, Inada T, Inoko M, Ishii K, Komiya T, Hanyu M, Minatoya K, Kimura T. Severe aortic stenosis in dialysis patients. J Am Heart Assoc. 2017;6:e004961 DOI: 10.1161/jaha.116.004961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Taniguchi T, Morimoto T, Shiomi H, Ando K, Kanamori N, Murata K, Kitai T, Kadota K, Izumi C, Nakatsuma K, Sasa T, Watanabe H, Kuwabara Y, Makiyama T, Ono K, Shizuta S, Kato T, Saito N, Minatoya K, Kimura T. Prognostic impact of left ventricular ejection fraction in patients with severe aortic stenosis. JACC Cardiovasc Interv. 2018;11:145–157. [DOI] [PubMed] [Google Scholar]
- 16. Kang DH, Park SJ, Rim JH, Yun SC, Kim DH, Song JM, Choo SJ, Park SW, Song JK, Lee JW, Park PW. Early surgery versus conventional treatment in asymptomatic very severe aortic stenosis. Circulation. 2010;121:1502–1509. [DOI] [PubMed] [Google Scholar]
- 17. Pellikka PA, Nishimura RA, Bailey KR, Tajik AJ. The natural history of adults with asymptomatic, hemodynamically significant aortic stenosis. J Am Coll Cardiol. 1990;15:1012–1017. [DOI] [PubMed] [Google Scholar]
- 18. Greve AM, Gerdts E, Boman K, Gohlke‐Baerwolf C, Rossebo AB, Devereux RB, Kober L, Ray S, Willenheimer R, Wachtell K. Impact of QRS duration and morphology on the risk of sudden cardiac death in asymptomatic patients with aortic stenosis: the SEAS (Simvastatin and Ezetimibe in Aortic Stenosis) Study. J Am Coll Cardiol. 2012;59:1142–1149. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Appendix S1. CURRENT AS Registry Investigators
Data S1. Definitions of the Clinical Events
Table S1. Clinical Factors Associated With Sudden Death in the Non‐HD Cohort in the Univariate and Multivariable Analyses
Figure S1. Cumulative incidence of sudden cardiac death in HD and non‐HD patients with severe AS.
