Figures
Abstract
Objective
Aortic stenosis (AS) is a heart valve disease characterized by left ventricular outflow fixed obstruction. It can be managed by surgical aortic valve replacement (SAVR) or transcatheter aortic valve implantation (TAVI). However, real-world evidence for TAVI or SAVR outcomes is lacking in Taiwan. This study aimed to compare the clinical outcomes of TAVI and SAVR for treating of AS in Taiwan.
Materials and methods
The National Health Insurance Research Database is a nationally representative cohort that contains detailed registry and claims data from all 23 million residents of Taiwan. This retrospective cohort study used this database to compare patients who underwent SAVR (bioprosthetic valves) or TAVI from 2017 to 2019. Survival outcomes and length of hospital stay (LOS) and intensive care unit (ICU) stay between TAVI and SAVR in the matched cohort. A Cox proportional hazards model was performed to identify the effect of treatment type on survival rates while controlling variables including age, gender, and comorbidities.
Results
We identified 475 and 1605 patients who underwent TAVI and SAVR with a bioprosthetic valve, respectively. Patients who underwent TAVI were older (82.19 vs. 68.75 y/o) and more likely to be female (55.79% vs. 42.31%) compared with patients who underwent SAVR. Propensity score matching (PSM) on age, gender, and Elixhauser Comorbidity Index (ECI) score revealed that 375 patients who underwent TAVI were matched with patients who underwent SAVR. A significant difference was found in survival rates between TAVI and SAVR. The 1-year mortality rate was 11.44% with TAVI and 17.55% with SAVR. Both the mean total LOS (19.86 vs. 28.24 days) and mean ICU stay (6.47 vs. 11.12 days) for patients who underwent TAVI were shorter than those who underwent SAVR.
Citation: Chung C-H, Wang Y-J, Jiao X, Lee C-Y (2023) Transcatheter aortic valve implantation vs. surgical aortic valve replacement for aortic stenosis in Taiwan: A population-based cohort study. PLoS ONE 18(5): e0285191. https://doi.org/10.1371/journal.pone.0285191
Editor: Kuo-Cherh Huang, Taipei Medical University, TAIWAN
Received: August 10, 2022; Accepted: April 17, 2023; Published: May 3, 2023
Copyright: © 2023 Chung et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The data underlying this study belong to the National Health Insurance Research Database (NHIRD) of Taiwan and cannot be made publicly available due to legal restrictions. However, the data are available through formal application to the Health and Welfare Data Science Centre at Ministry of Health and Welfare, Taiwan (https://dep.mohw.gov.tw/DOS/np-2500-113.html) and require a signed affirmation regarding data confidentiality. The authors have no special privilege of access to the database.
Funding: The current study was supported by Mackay Medical College (Sanzhi, Taiwan; grant nos. 109-CF-G1-01, MMC-RD-110-1B-P014 and MMC-RD-110-CF-G001-01) and Edwards Lifesciences (Taipei, Taiwan) Corporation. The funders had no role in study design, data collection and analysis, publication decision, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
AS is a common valvular pathology among heart valve diseases in the age group of over-75 years, with 2% to 4% of this population suffering from the condition [1]. This disease has poor prognoses, with approximately half of the patients with severe symptomatic AS (ssAS) dying within 2 years of symptom onset if left untreated. Aortic valve replacement (AVR) is the only effective treatment option for ssAS [2]. Surgical AVR (SAVR) was the gold standard for treatment for five decades [3]. However, more than one-third of patients with ssAS referred for SAVR are inappropriate candidates due to comorbidities, advanced age, and/or frailty, and a less-invasive procedure may offer an alternative method for their treatment [4, 5].
Transcatheter aortic valve implantation (TAVI) has been recommended as a therapeutic option to AVR for an increasingly wide spectrum of patients with ssAS over the past two decades [6, 7]. TAVI is performed by inserting a bioprosthetic valve through a catheter, which is then implanted within the diseased aortic valve. Increasing numbers of ssAS patients have been treated using this less-invasive technology worldwide since the first TAVI in 2002 [8–10].
Several studies have demonstrated that TAVI was non-inferior or even superior to SAVR across countries in the real-world setting [11–14]. TAVI was introduced in Taiwan in 2012 [15]. However, the comparative study between TAVI and SAVR based on Taiwan’s real-world practice is limited. The present article aimed to compare the survival outcomes of patients who underwent TAVR and those who underwent SAVR in Taiwan using whole-population data. Moreover, the hospital utilization between these two treatments was evaluated.
Materials and methods
Data source and patient definition
This retrospective population-based study accessed claim records from the National Health Insurance Research Database (NHIRD) from 2017 to 2019. NHIRD contains details of all the beneficiaries in Taiwan (23,603,121 in 2019). Taiwan’s NHIRD is a public database available through a formal application and approved by the Health and Welfare Data Science Centre of the Ministry of Health and Welfare, Taiwan. This study is based on data from the Health and Welfare Data Science Center in the Ministry of Health and Welfare (H108111). The cause of aortic valve diseases and the inclusion criteria were identified using the International Classification of Diseases (ICD)-10 diagnosis and procedure codes. Patients with two or more outpatient coding or one inpatient coding of ICD-10 I35.0 or I35.2 were identified as AS patients. Patients receiving SAVR were identified by bioprosthetic valve code, porcine valve (FHV02), or durable valve (FHVD1) [16]. Patients who underwent TAVI were identified by procedure code (68040B). We identified 475 patients who underwent TAVI and 1,605 patients who underwent SAVR and received bioprosthetic heart valves.
Assessment
Baseline characteristics were compared between the TAVI and SAVR groups in the unmatched cohort. Then, a PSM design with one-to-one matching was used. The characteristics used in matching including gender, age(+-2), and ECI score [17]. The matching yielded 376 pairs of well-matched patients.
A Kaplan-Meier survival curve was used for time-to-event analysis in the matched sample, using a stratified log-rank to test the equality of the estimated survival curves for all-cause mortality. The time-to-event stars from the first day of the procedure until death. Additionally, a Cox proportional hazards model, which adjusted for age, gender, and comorbidities, was performed. The difference in comorbidities among treatments was tested by the chi-square test. LOS was measured as the total number of days of hospitalization during SAVR or TAVI.
Research ethics approval
The study protocol was approved by the MacKay Memorial Hospital Institutional Review Board Taiwan, R.O.C. (Protocol Number: 19MMHIS083e). Informed consent was waived by the ethics committee.
Data analyzes
Data analyses were performed with SAS 9.4 (SAS Institute Inc., Cary, NC). Variable measures were identified based on the above-described criteria. The categorical variables were described using frequencies or percentages. The mean (Std) was used to describe the continuous variables. The Cox proportional hazards model included the following variables: TAVI, age, gender, congestive heart failure, cardiac arrhythmias, valvular disease, pulmonary circulation disorders, peripheral vascular disorders, hypertension (uncomplicated), hypertension (complicated), paralysis, other neurological disorders, chronic pulmonary disease, diabetes (uncomplicated), diabetes (complicate), hypothyroidism, renal failure, liver disease, peptic ulcer disease (excluding bleeding), metastatic cancer, solid tumor (without metastasis), rheumatoid arthritis/collagen vascular diseases, coagulopathy, weight loss, fluid and electrolyte disorders, blood loss anemia, deficiency anemia, alcohol abuse and depression.
Results
Sample description
The cohort was established using the entire population in NHIRD from 2017 to 2019 (Fig 1). Patients receiving TAVI or those with aortic valve disease who had undergone SAVR with a bioprosthetic heart valve replacement were included: 475 TAVI and 1,605 SAVR. Table 1 presents the baseline characteristics. A porcine valve and a durable valve were used in 573 and 1,032 patients among those with AS who received SAVR. Patients who underwent TAVI were older (82.19 vs. 68.75 y/o) and more likely to be female (55.79% vs. 42.31%) compared with those who underwent SAVR. The imbalanced characteristics imbalance was much improved after PSM, with the mean age being 78.64 ± 6.53 and 80.69 ± 7.36 years in the SAVR and TAVI groups, respectively, with the same gender distribution.
We examined each patient’s medical claims before the heart valve procedure and the result indicated that patients who underwent TAVI had higher rates of these nine underlying diseases before PSM compared to those who underwent SAVR: congestive heart failure, cardiac arrhythmias, hypertension (uncomplicated and complicated), chronic pulmonary disease, diabetes (complicated), liver disease, rheumatoid arthritis, and obesity. The patients in the TAVI group were more likely to be in worse condition than those in the SAVR group (Table 1). The underlying diseases in patients receiving TAVI or SAVR were similar after PSM.
Hospital resource utilization
The LOS and ICU stay for patients who underwent TAVI or SAVR were measured in this study. The patients who underwent SAVR in unmatched groups exhibited a remarkably longer LOS than those who underwent TAVI (24.46 days vs. 19.96 days, p < 0.001). Similarly, the unmatched ICU stay for patients undergoing SAVR was longer than those who underwent TAVI (8.13 days vs. 6.40 days, p < 0.001). Patients who underwent SAVR also exhibited a remarkably longer LOS than those who underwent TAVI after PSM matching (28.24 days vs. 19.86 days, p < 0.001). The ICU stay for patients undergoingSAVR had a longer ICU stay than those who underwent TAVI (11.12 days vs. 6.47 days, p < 0.001).
Clinical outcomes of patients who underwent SAVR
The all-cause mortality was used as the clinical outcome. The mortality rate in patients who underwent TAVI and SAVR after PSM were compared. Patients who received TAVI exhibited lower all-cause mortality rates than those who received SAVR, as shown in Fig 2 (hazard ratio (HR) = 0.66 and p = 0.0172). The 1-year mortality rate was 11.44% with TAVI and 17.55% with SAVR.
Cox proportional hazards model for patients with TAVI and SAVR
Cox proportional hazards model was used to investigate the clinical manifestations of all patients who had undergone TAVI or SAVR with a bioprosthetic valve. The results revealed that patients with poor outcomes were generally older (1.06, 1.03–1.09) and more likely to have underlying hypothyroidism (1.88, 1.20–2.93), liver disease (2.83, 1.95–4.12), fluid and electrolyte disorders (2.80, 1.48–5.32), and depression (17.07, 6.06–48.08) (Table 2).
Complications after surgery
We monitored the complications for 30-day and 90-day spans to understand the postoperative health status among patients who underwent SAVR and TAVI. The 30 day postoperative diagnosis for underlying diseases for both groups was very close to the baseline (Table 3). The 90 day postoperative diagnosis among each treatment group was slightly increased as compared with 30 days.
Discussion
This NHIRD based study mainly revealed a significantly lower risk of all-cause mortality in patients who underwent TAVI than those who underwent SAVR in real-world practice in Taiwan. To our best knowledge, this is the largest real-world outcome study for TAVI in Taiwan in recent years.
This study revealed that most of the patients in the TAVI group were >70 years (N = 442, 93.05%), which indicates that TAVI procedures in Taiwan followed the appropriate guidelines [18]. In contrast, a high number of patients aged ≤70 years received bioprosthetic valve replacement (57.39%). Only 42.31% (N = 679) of patients who underwent SAVR were >70 years old. The percentage of older patients who underwent TAVI was significantly higher than those who underwent SAVR. Age, gender, and comorbidities were most comparable between these groups after matching. The all-cause mortality of SAVR was significantly higher than that of TAVI (p = 0.0172). This may be due to long recovery time needed for open-heart surgeries and complications. Our findings were consistent with several published articles. Two studies reported faster and better left ventricular function recovery and less frequent pulmonary complications after TAVI than after SAVR [19, 20]. These events might potentially increase all-cause mortality associated with SAVR. Another meta-analysis revealed significantly lower 30-day and 1-year all-cause mortality after TAVI than after SAVR [21]. Our results indicate TAVI as a good alternative option for the elderly or for patients who are not suitable for surgery due to some specific condition.
Atrial fibrillation (AF) is one of the most frequent cardiac arrhythmias in the general population associated with high mortality [22, 23]. AF has been associated with several adverse events following SAVR and has been proven as a factor in poor prognoses [24, 25]. Previous studies revealed that TAVI-treated patients have a higher prevalence of preexisting AF compared to patients who underwent SAVR (32.1% vs. 12.8%) and a lower post-procedure rate of AF in TAVI compared to SAVR (6% vs. 33.7%) [26, 27]. However, this study not reveal this result, where the preexisting rates (22.34% vs. 22.87%) and post-procedure rates (30 days after the procedure, 22.61% vs. 23.14% at 30 days; 25.80% vs. 26.30% at 90 days) of cardiac arrhythmias were slightly lower in SAVR. However, cardiac arrhythmias are prevalent comorbidity in patients receiving TAVI, affecting approximately one-quarter of patients in Taiwan, which supports findings in other cohort studies/randomized control trials, although we did not find any significant difference between TAVI and SAVR [28–30]. Hence, cardiac arrhythmias following TAVI can still impact long-term prognoses and treatment outcomes for patients with severe AS.
TAVI procedures have been reimbursed since March 2017, while TAVI medical device reimbursement did not begin until February 2021. The reimbursement guidelines for TAVI are relatively more restrictive than those for other treatments to avoid their overuse and any ensuing financial burden [31]. Patients must meet all of the four essential criteria and at least one of the optional criteria listed below. Essential criteria are: 1) classified as New York Heart Association Function Class II–IV; 2) aortic valve area of <0.8 cm2 and <0.6 cm2/m2, transaortic valve pressure difference≧40 mmHg, or aortic valve blood flow velocity≧4.0 m/sec; 3) at least two cardiac surgery specialists must judge that SAVR cannot be used for AVR or the risk posed by surgery is too high; and 4) the patient life expectancy after TAVI is more than 1 year. Concurrently, at least one of the following three optional criteria must be met: 1) STS Score >10% or Logistic EuroSCORE I > 20%; 2) >80 years old; or 3) previous heart surgery (coronary artery bypass and heart valve surgery) or mediastinal radiation therapy, severe aortic calcification (porcelain aorta), ineligible for open-heart surgery due to thoracic cauterization sequelae, severe connective tissue disease leading to inoperability, liver cirrhosis (Child class A or B) with pulmonary insufficiency (FEV < 1 liter). TAVI medical devices were not eligible for reimbursement in this study period (2017–2019), and patients needed to cover the costs by themselves or be privately insured for TAVI medical devices.
The analyzes of the NHIRD data have provided several benefits, but such data still have limitations due to the nature of the NHIRD design. First, lacking information on self-payment for medications, laboratory data, and patient information (height, weight, etc.) due to NHIRD was designed as a claim database. Second, the severity of the disease cannot be measured. Third, this study design was strictly based on the ICD-10-CM, ICD-10-OP systems, thus coding errors, misclassifications, or differences between hospitals and physicians can affect these results, making the proportions of our subjects incorrect. Finally, TAVI was not reimbursed in Taiwan until March 2017. The National Health Insurance Administration needs almost a year to systematically list annual data and release them. Hence, our study cannot include more patients who underwent TAVI for long-term observation until more data are updated.
Conclusion
This study revealed that patients in the TAVI group were older and more likely to be in worse condition than patients receiving SAVR. The all-cause mortality of patients who underwent TAVI was lower than those who underwent SAVR after PSM by age, gender, and ECI score. Patients who underwent TAVI had significantly shorter LOS and ICU stays than those who underwent SAVR. These findings indicate statistically significant differences in survival rates in TAVI compared to SAVR in these older patients with severe AS. Further studies over a long-term are required to understand the clinical and economic outcomes of TAVI.
References
- 1. Van Hemelrijck M, Taramasso M, De Carlo C, Kuwata S, Regar E, Nietlispach F, et al. Recent advances in understanding and managing aortic stenosis. F1000Res. 2018;7:58. Epub 2018/01/30. pmid:29375823; PubMed Central PMCID: PMC5770996.
- 2. Ross J Jr., Braunwald E. Aortic stenosis. Circulation. 1968;38(1 Suppl):61–7. pmid:4894151.
- 3. Kang G, Kim JB. Expanding transcatheter aortic valve replacement into uncharted indications. Korean J Intern Med. 2018;33(3):474–82. Epub 20180320. pmid:29551053; PubMed Central PMCID: PMC5943666.
- 4. Iung B, Cachier A, Baron G, Messika-Zeitoun D, Delahaye F, Tornos P, et al. Decision-making in elderly patients with severe aortic stenosis: why are so many denied surgery? Eur Heart J. 2005;26(24):2714–20. Epub 2005/09/06. pmid:16141261.
- 5. Varadarajan P, Kapoor N, Bansal RC, Pai RG. Survival in elderly patients with severe aortic stenosis is dramatically improved by aortic valve replacement: Results from a cohort of 277 patients aged > or = 80 years. Eur J Cardiothorac Surg. 2006;30(5):722–7. Epub 2006/09/05. pmid:16950629.
- 6. Praz F, Siontis GC, Verma S, Windecker S, Juni P. Latest evidence on transcatheter aortic valve implantation vs. surgical aortic valve replacement for the treatment of aortic stenosis in high and intermediate-risk patients. Curr Opin Cardiol. 2017;32(2):117–22. Epub 2017/01/13. pmid:28079554.
- 7. Cahill TJ, Chen M, Hayashida K, Latib A, Modine T, Piazza N, et al. Transcatheter aortic valve implantation: current status and future perspectives. Eur Heart J. 2018;39(28):2625–34. Epub 2018/05/03. pmid:29718148.
- 8. Cribier A, Eltchaninoff H, Bash A, Borenstein N, Tron C, Bauer F, et al. Percutaneous transcatheter implantation of an aortic valve prosthesis for calcific aortic stenosis: first human case description. Circulation. 2002;106(24):3006–8. Epub 2002/12/11. pmid:12473543.
- 9. Cribier A, Eltchaninoff H, Tron C, Bauer F, Agatiello C, Sebagh L, et al. Early experience with percutaneous transcatheter implantation of heart valve prosthesis for the treatment of end-stage inoperable patients with calcific aortic stenosis. J Am Coll Cardiol. 2004;43(4):698–703. Epub 2004/02/21. pmid:14975485.
- 10. Cribier A, Eltchaninoff H, Tron C, Bauer F, Agatiello C, Nercolini D, et al. Treatment of calcific aortic stenosis with the percutaneous heart valve: mid-term follow-up from the initial feasibility studies: the French experience. J Am Coll Cardiol. 2006;47(6):1214–23. Epub 2006/03/21. pmid:16545654.
- 11. Deharo P, Bisson A, Herbert J, Lacour T, Saint Etienne C, Theron A, et al. Outcomes in nonagenarians undergoing transcatheter aortic valve implantation: a nationwide analysis. EuroIntervention. 2020;15(17):1489–96. pmid:31763981.
- 12. Gaede L, Blumenstein J, Liebetrau C, Dorr O, Kim WK, Nef H, et al. Transvascular transcatheter aortic valve implantation in 2017. Clin Res Cardiol. 2020;109(3):303–14. Epub 20190624. pmid:31236692.
- 13. Takeji Y, Taniguchi T, Morimoto T, Saito N, Ando K, Shirai S, et al. Transcatheter Aortic Valve Implantation vs. Surgical Aortic Valve Replacement for Severe Aortic Stenosis in Real-World Clinical Practice. Circ J. 2020;84(5):806–14. Epub 20200201. pmid:32009065.
- 14. Virtanen MPO, Airaksinen J, Niemela M, Laakso T, Husso A, Jalava MP, et al. Comparison of Survival of Transfemoral Transcatheter Aortic Valve Implantation Versus Surgical Aortic Valve Replacement for Aortic Stenosis in Low-Risk Patients Without Coronary Artery Disease. Am J Cardiol. 2020;125(4):589–96. Epub 20191119. pmid:31831151.
- 15. Chen YH, Chang HH, Chen PL, Weng ZC, Chen IM, Leu HB, et al. Procedural Characteristics and Outcomes of Transcatheter Aortic Valve Implantation: A Single-Center Experience of the First 100 Inoperable or High Surgical Risk Patients with Severe Aortic Stenosis. Acta Cardiol Sin. 2017;33(4):339–49. pmid:29033504; PubMed Central PMCID: PMC5534413.
- 16. Chung CH, Wang YJ, Lee CY. Epidemiology of Heart Valve Disease in Taiwan. Int Heart J. 2021;62(5):1026–34. Epub 20210917. pmid:34544973.
- 17. Quan H, Sundararajan V, Halfon P, Fong A, Burnand B, Luthi JC, et al. Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Med Care. 2005;43(11):1130–9. Epub 2005/10/15. pmid:16224307.
- 18. Baumgartner H, Falk V, Bax JJ, De Bonis M, Hamm C, Holm PJ, et al. 2017 ESC/EACTS Guidelines for the Management of Valvular Heart Disease. Rev Esp Cardiol (Engl Ed). 2018;71(2):110. Epub 2018/02/10. pmid:29425605.
- 19. Bauer F, Coutant V, Bernard M, Stepowski D, Tron C, Cribier A, et al. Patients with severe aortic stenosis and reduced ejection fraction: earlier recovery of left ventricular systolic function after transcatheter aortic valve implantation compared with surgical valve replacement. Echocardiography. 2013;30(8):865–70. Epub 20130312. pmid:23489257.
- 20. Pettet JK, McGhee MN, McIlrath ST, Collins GL. Comparison of pulmonary complications in patients undergoing transcatheter aortic valve implantation versus open aortic valve replacement. J Cardiothorac Vasc Anesth. 2014;28(3):497–501. Epub 20130828. pmid:23992656.
- 21. Takagi H, Hari Y, Nakashima K, Kuno T, Ando T, Group A. Mortality after transcatheter versus surgical aortic valve replacement: an updated meta-analysis of randomised trials. Neth Heart J. 2020;28(6):320–33. pmid:32166571; PubMed Central PMCID: PMC7270388.
- 22. Miyasaka Y, Barnes ME, Bailey KR, Cha SS, Gersh BJ, Seward JB, et al. Mortality trends in patients diagnosed with first atrial fibrillation: a 21-year community-based study. J Am Coll Cardiol. 2007;49(9):986–92. Epub 2007/03/06. pmid:17336723.
- 23. Chugh SS, Havmoeller R, Narayanan K, Singh D, Rienstra M, Benjamin EJ, et al. Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study. Circulation. 2014;129(8):837–47. Epub 2013/12/19. pmid:24345399; PubMed Central PMCID: PMC4151302.
- 24. Levy F, Garayalde E, Quere JP, Ianetta-Peltier M, Peltier M, Tribouilloy C. Prognostic value of preoperative atrial fibrillation in patients with aortic stenosis and low ejection fraction having aortic valve replacement. Am J Cardiol. 2006;98(6):809–11. Epub 2006/09/05. pmid:16950191.
- 25. Ngaage DL, Schaff HV, Barnes SA, Sundt TM 3rd, Mullany CJ, Dearani JA, et al. Prognostic implications of preoperative atrial fibrillation in patients undergoing aortic valve replacement: is there an argument for concomitant arrhythmia surgery? Ann Thorac Surg. 2006;82(4):1392–9. Epub 2006/09/26. pmid:16996940.
- 26. Motloch LJ, Reda S, Rottlaender D, Khatib R, Muller-Ehmsen J, Seck C, et al. Postprocedural atrial fibrillation after transcatheter aortic valve implantation versus surgical aortic valve replacement. Ann Thorac Surg. 2012;93(1):124–31. Epub 2011/11/26. pmid:22115334.
- 27. Tarantini G, Mojoli M, Urena M, Vahanian A. Atrial fibrillation in patients undergoing transcatheter aortic valve implantation: epidemiology, timing, predictors, and outcome. Eur Heart J. 2017;38(17):1285–93. Epub 2016/10/17. pmid:27744287.
- 28. Smith CR, Leon MB, Mack MJ, Miller DC, Moses JW, Svensson LG, et al. Transcatheter versus surgical aortic-valve replacement in high-risk patients. N Engl J Med. 2011;364(23):2187–98. Epub 2011/06/07. pmid:21639811.
- 29. Adams DH, Popma JJ, Reardon MJ. Transcatheter aortic-valve replacement with a self-expanding prosthesis. N Engl J Med. 2014;371(10):967–8. Epub 2014/09/04. pmid:25184874.
- 30. Leon MB, Smith CR, Mack MJ, Makkar RR, Svensson LG, Kodali SK, et al. Transcatheter or Surgical Aortic-Valve Replacement in Intermediate-Risk Patients. N Engl J Med. 2016;374(17):1609–20. Epub 2016/04/05. pmid:27040324.
- 31.
NHIA. TAVI reimbursement guideline in Taiwan. https://wwwnhigovtw/query/Query2_Detailaspx?Ser_id=9210. 2017.