Figures
Abstract
Objective
To investigate the cost-effectiveness of screening and subsequent intervention for age-related macular degeneration (AMD) in Japan.
Methods
The clinical effectiveness and cost-effectiveness of screening and subsequent intervention for AMD were assessed using a Markov model. The Markov model simulation began at the age of 40 years and concluded at the age of 90 years. The first-eye and second-eye combined model assumed an annual state-transition probability, development of prodromal symptoms, choroidal neovascularization (CNV), and reduction in visual acuity. Anti–vascular-endothelial-growth-factor (anti-VEGF) intravitreal injection therapy and photodynamic therapy (PDT) were performed to treat CNV. Intake of supplements was recommended to patients who had prodromal symptoms and unilateral AMD. Data on prevalence, morbidity, transition probability, utility value of each AMD patient, and treatment costs were obtained from published clinical reports.
Results
In the base-case analysis, screening for AMD every 5 years, beginning at the age of 50 years, showed a decrease of 41% in the total number of blind patients. The screening program reduced the incidence of blindness more than did the additional intake of supplements. However, the incremental cost-effectiveness ratio (ICER) of screening versus no screening was 27,486,352 Japanese yen (JPY), or 259,942 US dollars (USD) per quality-adjusted life year (QALY). In the sensitivity analysis, prodromal symptom-related factors for AMD had great impacts on the cost-effectiveness of screening. The lowest ICER obtained from the best scenario was 4,913,717 JPY (46,470 USD) per QALY, which was approximately equal to the willingness to pay in Japan.
Citation: Tamura H, Goto R, Akune Y, Hiratsuka Y, Hiragi S, Yamada M (2015) The Clinical Effectiveness and Cost-Effectiveness of Screening for Age-Related Macular Degeneration in Japan: A Markov Modeling Study. PLoS ONE 10(7): e0133628. https://doi.org/10.1371/journal.pone.0133628
Editor: Chung-Jung Chiu, Tufts University, UNITED STATES
Received: February 3, 2015; Accepted: June 30, 2015; Published: July 27, 2015
Copyright: © 2015 Tamura 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: All relevant data are available through the Harvard Dataverse: https://thedata.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/193GKB.
Funding: This study was supported in part by grants-in-aid for scientific research (Nos. 24592626) from the Japan Society for the Promotion of Science, Tokyo, Japan, http://www.jsps.go.jp/j-grantsinaid/index.html; the Japan Ophthalmologists Association, Tokyo, Japan, http://www.gankaikai.or.jp/; and the Japan National Society for the Prevention of Blindness, Tokyo, Japan, http://www.business1.jp/jnspb/pc/index.html. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Age-related macular degeneration (AMD) is the leading cause of blindness in developed countries.[1–6] In Japan, AMD ranks fourth among the causes of visual impairment, and about 700,000 patients suffer from the disease.[7, 8] Although no treatment for AMD has been available until recently, AMD is now commonly treated with anti–vascular-endothelial-growth-factor (anti-VEGF) intravitreal injection therapy and photodynamic therapy (PDT).[9] AMD frequently develops in only one eye of an elderly person; binocular involvement of AMD is minor[10, 11] because of slow involvement of the other eye.[12–14] Patients may be unaware of their vision changes in daily life when only one of the two eyes is affected, because the impairment of quality of life (QOL) may be limited. Consequently, it may be difficult to detect early-stage AMD, particularly monocular AMD, and subsequent adequate treatment of AMD may be delayed. In addition, treatment for AMD has economic costs to the patients and to society, and the injections require frequent visits to medical institutions over a long period. Thus, conclusions on the reported cost-effectiveness of therapies for AMD are not consistent.[15–17]
Early detection of AMD, however, increases the likelihood of better visual acuity results with the improvement of treatment[18] and of detecting imaging technology[19]. Intake of supplements is also reported to delay the onset of AMD.[20–22] For these reasons, early detection of AMD is considered important. This article addresses the cost-effectiveness of screening for AMD in adults for the critical early detection.
Previous studies on the cost-effectiveness of AMD treatment have identified three important factors influencing their results:[15]
- the model selected for verification (a second-eye model, a first-eye model, or a combination first-eye and second-eye model);[23]
- the time horizon;[24]
- the scope of costs (e.g., whether long-term nursing care costs or indirect costs are included).[17]
Many studies assessing the cost-effectiveness of AMD therapies have used the second-eye model proposed by Brown.[25] Accordingly, their assumption is that therapy is not initiated until the disease develops in the second eye (the previously unaffected eye). This model does not always represent the actual treatment procedure. However, a smaller number of studies have employed the first-eye and second-eye combined model,[15] which more accurately reflects actual treatment procedure. Since screening aims at early disease detection and early intervention based on such early detection, consideration must be given to the first eye.
The Markov model describes repetitive events that occur over a long period. It has been widely used in studies on cost-effectiveness.[26, 27] In fact, the Markov model has been widely used to evaluate the cost-effectiveness of strategies to treat or prevent various ophthalmologic diseases and is therefore the gold standard method for such economic evaluation.[28, 29] The aim of this study was to investigate the clinical effectiveness (reduction in the number of patients with blindness) and the cost-effectiveness (from a value-for-money perspective) of screening and subsequent treatment of AMD in Japan. Specifically, our aim was to use a Markov model to evaluate the reduction in the incidence of blindness and the incremental cost-effectiveness of screening for AMD and subsequent treatment of AMD.
Participants and Methods
In this study, a model was created and analyzed by using TreeAge Pro 2009 Suite (Release 1.0) to estimate screening outcomes. The model consisted of a decision tree and a Markov model. The decision tree was used to group adults into those receiving ophthalmologic screening (the screened group) and those not receiving screening (the non-screened group). The strategy of the non-screened group was considered representative of the current actual practice for AMD, which involves visits and treatments. The Markov model of disease progression compared two strategies: a screening strategy and non-screening strategy. The first-eye and second-eye combined model was employed. The steps of disease progression were categorized by the following six Markov states (Fig 1): normal, prodromal, moderate AMD, severe AMD, blindness, and death. The severity of AMD was classified into one of the following three stages based on best corrected visual acuity (VA): moderate (VA: 0.5–0.9), severe (VA: 0.1–0.4), and blindness (VA: < 0.1). The model simulated a hypothetical Japanese cohort of 50,000 persons aged 40 years without any eye disease, and the simulation ran until they reached 90 years of age or died according to age-specific background mortality based on the 2009 Japan abridged life tables. Cumulative costs of screenings and treatments and quality-adjusted life years (QALYs) were calculated per person for the entire simulation period, using an annual discount rate of 3%.
In the current study, AMD is assumed to develop from a normal eye via prodromal state. AMD is categorized in three stages: moderate AMD, severe AMD, and blindness. VA: best corrected visual acuity.
Based on published data of incidence rates, it was assumed that the cohort would develop prodromal symptoms and then moderate AMD. In each cycle, each patient’s disease condition was rated as aggravated, maintained, or improved using transition probabilities. For members of the non-screened group, the disease was detected during a coincidental consultation or consultation due to subjective symptoms. For members of the screened group, the disease was detected during a coincidental consultation, consultation due to subjective symptoms, or screening visit. Coincidental consultations refer to visits to ophthalmologic clinics for treatment of eye diseases unrelated to AMD. Consultations due to subjective symptoms refer to visits to ophthalmologic clinics because of subjective symptoms. In the model, increased severity referred to loss of vision in one or both eyes. Visits for screening began at age 50 years, occurred once every 5 years, and ended at age 90 years (base case).
It was assumed that once AMD was detected it was under medical control, with patients receiving the appropriate treatments; the eyes with prodromal symptoms or AMD were examined periodically, the patients were advised to take supplements, and the patients received treatment with intravitreal injection (of anti-VEGF drug) and/or PDT, depending on the stage of AMD.
Model parameters
Table 1 shows the parameters used in our model. For these parameters, clinical research data on the Japanese population was obtained to the extent possible; if no applicable Japanese data were available, overseas data were used. For the sensitivity analysis, the range of values for each parameter was set for the 95% confidence interval (CI) or ±50% from the reported baseline value.
Model validation
To validate our model, we compared the reported numerical values (for prevalence of AMD, incidence of unilateral AMD, and rate of blindness) with simulated values, which are described later, for the non-screened group. To simulate the future number of AMD patients and to validate the model, the number of AMD patients after controlling ages was calculated by using as a starting point the current population, by age, in each Markov status.
Ophthalmologic screening program
It was assumed that ophthalmologists used fundus photographs in making their diagnoses.
Morbidity rate
AMD was assumed to develop in eyes with prodromal symptoms. Probabilities of the onset of prodromal symptoms and AMD (one eye) in the Japanese population were obtained from published reports.[30, 31, 40] When AMD developed in only one eye, the probability of AMD occurring in the unaffected eye was quite high. The probability of AMD occurring in the second eye was obtained from the literature and used in cases of prodromal stage disease being detected in the second eye.[12–14]
Participation rate for screening
Because there is currently no concrete and consistent ophthalmologic screening program for adults, data on the participation rates for screening and detailed examination are limited. Arbitrary numbers for these parameters were set in the base-case analysis and sensitivity analysis was performed to evaluate the effect of these parameters on the model.
Although the coincidental consultation may take place in a variety of clinical settings, our model assumed that patients visited ophthalmologic clinics with presbyopia or AMD at specific rate. The prevalence of presbyopia in Japan is reported to be 43.8% for those aged 40 years or older,[35] and our estimate of the annual rate of increase in presbyopia was 3%. We assumed that 20% of those with presbyopia would visit ophthalmologic clinics and be diagnosed with AMD. However, the probability of these assumptions was applicable only for a 1-year period after the onset of presbyopia.
Dropout from treatment
In the early stages of AMD, patients rarely notice their symptoms, thus their motivation to continue treatment is weak, leading to some drop out of treatment. Our model assumed that patients with prodromal symptoms (therefore at high risk for AMD) would undergo periodic monitoring of symptoms and receive supplement therapy. Dropouts in this group were expected to be particularly high: the rate of withdrawal was set at 50% for the first year of therapy and at 10% for subsequent years. For patients with later stages of the disease, the rate of withdrawal was set at 5%. For patients with unilateral or bilateral blindness, no withdrawal was considered because of their high adherence to medical services.
Prognosis and therapy
The progression of a patient through the stages of AMD was characterized by transition probabilities obtained from published reports.[33, 37, 41–48] For prodromal symptoms, supplement intake, which reduces the incidence of AMD,[21, 49, 50] was assumed in addition to follow-up observations.
Treatment of AMD depended on its stage and type. AMD is classified into one of three types: typical neovascular AMD (tAMD), polypoidal choroidal vascularization (PCV), and retinal angiomatous proliferation (RAP). In our model, the probability of a patient having each type of AMD was based on previously published rates of AMD onset.[34] It was assumed that the type of AMD affecting the second eye would be the same as that affecting the first eye. The treatment strategies assumed in our model were in accordance with a Japanese clinical guideline.[51] Specifically, intravitreal injection (of ranibizumab) was administered to those with moderately severe conditions irrespective of AMD type. For those who did not drop out of a series of treatments, the number of injections per year was set at 6 for the first year of treatment, 4 for the second year, and 2 for the third year and each subsequent year, based on actual world data.[52] It was assumed that the treatment would maintain the visual acuity in 95% of patients but that disease severity would increase in the remaining 5%. Beginning in the second year of treatment, the annual transition probability—the probability of developing a more severe stage of the disease—was assumed to be 22%.[38]
When a patient’s disease condition was severe, a patient with tAMD was assumed to receive only intravitreal injection, and a patient with PCV or RAP was assumed to undergo both intravitreal injection and PDT. The number of injections administered to a patient with severe condition was assumed the same as that administered to a patient with moderate condition. PDT was performed only once, in the first year of treatment, and then never again. Since PDT does not substantially contribute to improvement of visual acuity but rather aims primarily at maintaining current visual acuity, the therapeutic prognosis of intravitreal injection (of ranibizumab) was evaluated using outcomes obtained from published reports.[37] The probability of a patient transitioning from severe AMD to moderate AMD in the first year of treatment was set at 40.3%, and from severe AMD to blindness at 5%. During and after the second year of treatment, it was assumed that the disease was severe in 95% of patients. When blind, patients were assumed to receive no treatment but to be under observation. Figs 2 and 3 show the transition in patient health status in the first-eye and second-eye combined model used in the study.
Transition probabilities were derived from previous reports, including the Hisayama Study,[30] MARINA,[33] FOCUS[47] and PIER[48].
Transition probabilities were derived from previous reports, mainly ANCHOR.[37]
Clinical Effectiveness Analysis
We calculated the reduction in the rate of blindness and the future number of AMD patients by comparing the base-case analysis values shown in Table 1 to the simulated numbers for each screening strategy.
Costs
Our model considered only direct medical costs. Specialists estimated the costs of screening, detailed examination required to make a definite diagnosis of AMD, tests and examinations, and various types of treatments, based on reimbursement rates defined in fees schedules for Japanese social health insurance. All costs were in Japanese yen (JPY) and were converted into US dollars (USD) (2014) using Federal Reserve historical foreign exchange rates (1 US$ = ¥ 105.74), accessed on the following web site: https://www.federalreserve.gov/releases/g5a/current/.
Utility value
The utility value for each AMD patient, or the patient’s preference-based QOL, was set at 1 for a healthy member of the population and at 0.97 for a patient having prodromal symptoms in both eyes. Utility data were obtained using a time trade-off (TTO) method for measuring visual-acuity–specific utility in patients with AMD. However, since the utility value may be somewhat reduced when visual acuity differs between the better-seeing and worse-seeing eye, as mentioned in previous reports,[53, 54] utility value was reduced for the worse-seeing eye to allow the worse-seeing eye to affect utility value, based on those previous reports.[54] The reasonability of the utility value assumptions was also assessed by incorporating ranges in the sensitivity analysis. Table 1 shows the utility value assumed for each stage of AMD.
Cost-utility analysis
We calculated an incremental cost-effectiveness ratio (ICER) using the base-case analysis values shown in Table 1, to enable comparisons of cost versus utility value for each screening strategy. ICER was calculated using the following formula:
Screening program
To determine the optimal screening program, the age at which to start screening, the age at which to end screening, and the interval between screenings were each varied within their respective ranges shown in Table 1, and the resulting ICER was calculated.
Results
Model validation
We tested the model’s external validity by comparing the model’s simulated values for the non-screened group (prevalence of AMD in persons 40 years or older, incidence of unilateral AMD, and incidence of blindness due to AMD in persons 40 years or older) to reported values. The prevalence of AMD in the simulated cohort was 1.31%, which was comparable to the 1.30% reported in the Hisayama study.[30, 31] The model’s unilateral AMD incidence of 84.1% was comparable to the 79.3% reported in the Nagahama study.[11] The cumulative incidence of blindness due to AMD was 0.026% in the simulated cohort, which was comparable to the 0.019% estimate reported by the Japan Ophthalmologists Association in 2007.[55] The model was validated, shown to represent adequately, but not perfectly or exactly, the current epidemiologic status.
Clinical effectiveness analysis
Table 2 shows the results of clinical effectiveness in the base case. Screening interventions reduced the rate of blindness by 41% after controlling for age (the crude reduction rate calculated by the Markov model was 37%). AMD incident rate was reduced 5% by supplement intake subsequent to prodromal detection from screening. Fig 4 shows the reduction in rate of blindness and AMD by age. Reduction effect of blindness was more apparent and occurred earlier than did a reduction in the number of AMD patients, and the screening program reduced blindness rate by more than did the additional intake of supplements. The rate of blindness decreased more between no supplements without screening and no supplements with screening than it did between no supplements with screening and supplements with screening (Fig 4, top).
Cost-effectiveness analysis
Table 2 also shows the results of cost-effectiveness in the base case. Comparison of the screened group with the non-screened group revealed an incremental cost of ¥81,148, incremental utility of 0.00295, and ICER of 27,486,352 JPY, or 259,943 USD per QALY. The willingness to pay (WTP) in Japan, representing the threshold value of ICER for cost-effectiveness, is considered to be 5,000,000 JPY/QALY, or 47,286 USD/QALY.[56] These results indicate that ophthalmologic screening for AMD is not cost-effective.
Efficient screening program
The age at which to start screening, age at which to end screening, and interval between screenings were each varied within their respective ranges (Table 1), and an ICER was calculated for the screening group and for the non-screening group. For the screening group, the minimum ICER was 15,003,591 JPY/QALY, in the model for which screening starts at age 50, occurs at 6-year intervals, and ends at age 60 (actually ends at age 56 so that no screening would occur at age 62), and the maximum ICER was 58,593,956 JPY/QALY, in the model for which screening starts at age 60, occurs at 7-year intervals, and ends at age 90 (actually ends at age 88 so that no screening would occur at age 95). In USD, the ICER range is between 141,891 USD/QALY and 554,132 USD/QALY. For all screening programs, both the incremental costs and the incremental utility values of screening versus no screening were positive numbers. However, none of the screening programs had an ICER less than 5,000,000 JPY, Japan’s threshold for cost-effectiveness.
Sensitivity analysis
Fig 5 is a tornado diagram showing the blindness reduction rate ranges for the 15 most effective parameters among the 52 total parameters. The reduction rates of blindness were calculated for the screened group as compared to the non-screened group. The dropout rate from the recursive treatment for AMD, denoted by “sensor (moderate/severe),” had the greatest effect in our model, resulting in blindness reduction ranging from 12.5% (+50%) to 42.6% (0%) in the sensitivity analysis. Several factors that lacked sufficient evidence included “detailed examination,” “rate of continuation of supplement intake every year,” “rate of supplement intake.” Furthermore, screening participation rate might weaken other factors’ effects on reduction of blindness rate.
The 15 most effective parameters of the 52 total parameters are shown.
Fig 6 is a tornado diagram showing the ICER ranges for the 15 most effective parameters among the 52 total parameters. ICERs were calculated for the screened group as compared to the non-screened group. The probability of transition from the prodromal stage to moderate AMD had the greatest effect in our model, resulting in ICER ranging from 23,552,326 JPY/QALY (222,738 USD/QALY) (+50%) to 57,321,478 JPY/QALY (542,098 USD/QALY) (-50%) in the sensitivity analysis. Other prodromal symptom-related factors for AMD, including “risk reduction by supplements,” “probability of transition from the prodromal stage to moderate disease in the second eye,” and “cost of supplements” also had major effects on cost-effectiveness. When it was assumed that the drug was switched from ranibizumab to bevacizumab (but with the same therapeutic effect), the ICER decreased to 19,906,587 JPY/QALY (188,260 USD/QALY). In a best-case scenario for cost-effectiveness, assuming that a patient in the prodromal stage of AMD was followed up once annually, supplements cost 0 JPY, and bevacizumab was used, the ICER decreased to 4,913,717 JPY/QALY (46,470 USD/QALY), approximately equal to the WTP in Japan, while the prophylactic effect against future blindness was maintained at the same level.
The 15 most effective parameters of the total 52 parameters are shown.
Probabilistic sensitivity analysis
In Fig 7, the results of PSA are presented graphically. The 10.4% of simulation results located in quadrant 1 are below the WTP threshold of 5,000,000 JPY. The screening program was more effective than the no-screening option in 82.8% of the results, although screening was dominated by no-screening in the remaining 17.2% of the results.
Discussion
The screening program reduced both the rate of blindness caused by AMD and the cumulative incidence rate of AMD. However, the decrease in the rate of AMD-caused blindness was more apparent and occurred earlier than did the decrease in the incidence of AMD. This comparative success might derive from current medical intervention’s ability to only ameliorate the symptoms or delay the progression of the disease rather than eliminate the disease itself. The screening program evaluated in this study reduced by 41% the cumulative number of patients to suffer blindness from AMD. The reduction is as compared to the non-screening population and assumes current medical intervention with intravitreal injection of inhibitors of vascular endothelial growth factor (VEGF). Without anti-VEGF drug therapy, the reduction would be much greater, because, since the introduction of intravitreally injected anti-VEGF in 2006, the incidence of legal blindness from AMD has already fallen to half the previous baseline incidence rate.[57] The screening program reduced the blindness rate by more than did additional intake of supplements. This comparative findings is confirmed by the rate of blindness decreasing more between no supplement without screening and no supplement with screening than it did between no supplement without screening and supplement without screening (Fig 4, bottom). The screening program’s greater effectiveness than supplement intake has not been well discussed until now. This finding should be confirmed in future discussion of early detection approaches.
Previous studies on the cost-effectiveness of ophthalmologic treatments have frequently used the second-eye model.[17, 23, 43, 58–60]. However, the following assumptions of the second-eye model are not necessarily adequate to the study of cost-effectiveness of the AMD screening program:
- unilateral AMD assumed not to be treated, whereas in reality, many patients with unilateral AMD (about 80% of patients with AMD suffer from unilateral disease[11]) are treated;
- the worse eye in bilateral AMD assumed not to be treated, whereas in actual clinical settings, both of the affected eyes are frequently treated; and
- treatment of the worse eye assumed to be effective but not improving patients’ QOL, whereas in reality, many patients are at least somewhat satisfied with improvement in their worse eyes. Recent studies have reported the worse-seeing eye to have a stronger influence on vision-related QOL than is generally assumed.[54, 61]
Therefore, a first-eye and second-eye combined model, which has been used infrequently,[23, 24] was used in this study.
Some published studies included non-medical costs (such as the cost of long-term care) in the direct costs to be evaluated,[23, 37, 58, 62] while Hurley, et al. indicated that cost-effectiveness is greater when indirect long-term care costs are included.[17] Whether or not indirect long-term care costs should be included in our present analysis was an important issue. We decided not to include these costs in our study, because the costs depend on how the screening program is conducted and where the targeted population is located. If we were to include these costs, the results would be even more cost-ineffective—costs would be higher. Furthermore, the sensitivity analysis showed that the cost of screening had little effect on cost-effectiveness.
The base-case analysis, shown in Table 2, demonstrated that the screening program evaluated in this study reduced the cumulative number of patients with blindness by 41%. Screening for AMD, however, was not cost-effective, because the ICER was above the threshold WTP estimated for Japan. A major factor contributing to this cost-ineffectiveness finding may be the unilaterality of the disease. In our model, patients with unilateral AMD at age 90 accounted for 84.8% of all AMD patients in the screened group and 82.7% of all AMD patients in the non-screened group. The utility value, or QALY, of these patients would not be improved even by expensive treatments such as anti-VEGF drugs for worse eyes, because QALY is defined by the condition of the better eye (the unaffected eye).[25] In this study, we incorporated the real-life situation, allowing the worse eye to affect utility value, by reducing utility values when visual acuity differed between the better and the worse eye. In the future, cost-utility analysis using utility values based on actual TTO methods should be incorporated when the eyes of an AMD patient differ in visual acuity. Further study is needed to strengthen the opinion we have derived from this study’s results.
In this study, we relied on data regarding treatment mainly from reports of ideal randomized controlled trials with two-year follow-up periods, because they were the only ones available. Recently, outcomes from actual clinics with relatively long follow-up periods have been reported.[63] Using the newly available data may worsen the cost-effectiveness result, because visual acuity was reported to decrease after the first two years and to be even worse than baseline after four years.
One-way sensitivity analysis revealed that the probability of a patient’s transition to AMD, the prodromal symptom-related factors (including the preventive effect of supplement intake and the cost of supplements), and utility values had the greatest effects on the model, but those effects were not sufficiently large to make screening intervention cost-effective. In addition, discount rates also affected the cost-effectiveness of screening, because there is a long interval of time between screening and the confirmation of its effectiveness.[24] Accordingly, it is desirable to use a common discount rate across studies that compare similar types of medical procedures; as a result, we employed 3% in this study. With regard to utility values, when the fellow eyes of normal or prodromal eyes is affected by AMD (when better-seeing eye is normal or prodromal, while worse-seeing eye is blind, sever AMD or moderate AMD), they impacted the results. Although previous reports have paid little attention to the phenomenon, our results showed that such difference in utility values when the two eyes are in different stages should be considered. Further research on such differing utility values when the two eyes are in different stages should be incorporated in studies of the cost-effectiveness of treatment for one-eye–dominant disease.
This study suggests that factors regarding treatment and progression in early stages of AMD are important, influencing the analysis of cost-effectiveness. This may be because, as shown in the Table 2, screening remarkably increases detection of the prodromal stage of AMD. The cost of intravitreal injection of ranibizumab also had an impact. When bevacizumab was substituted for ranibizumab and both drugs were assumed to have the same therapeutic effects, the ICER decreased only to 19,906,587 JPY/QALY (188,260 USD/QALY). Thus, screening only for AMD is not cost-effective.
When screening for AMD, however, other vision-threatening ocular diseases, including glaucoma and diabetic retinopathy, can be detected. A comprehensive approach to ocular disease screening, in which AMD is one of several diseases that could be detected, may yield better cost-effectiveness, because single screenings for other ocular diseases are reported to be cost-effective.[64] On the other hand, sensitivity analysis revealed that screening cost had only a limited effect on ICER. In other words, even though the incremental cost of medical examination in the screening is low, particularly when no additional screening procedure is conducted to detect AMD, the cost-effectiveness of screening will not be much improved. The cost-effectiveness of both AMD screening included in a comprehensive ocular disease screening and an entirely separate AMD screening is not high.
Conclusion
We evaluated the clinical effectiveness and cost-effectiveness of ophthalmologic screening for AMD in adults using a Markov model based on clinical data from Japan. In evaluating the AMD screening program from the viewpoint of clinical effectiveness (reduction in the number of patients with blindness) and cost-effectiveness (from a value-for-money perspective), our results indicate that the screening program is highly effective in reducing the number of patients with blindness but not cost-effective. The PSA results confirm that the screening program is beneficial in terms of health gain in most cases but that its cost-effectiveness is low given the present ICER threshold (WTP). Although parameter uncertainty has a great effect on analysis of the results, further epidemiological and prognostic knowledge about AMD would lead to more robust cost-effectiveness research.
Author Contributions
Conceived and designed the experiments: HT, YH, and MY Performed the experiments: HT, RG, and YA Analyzed the data: HT and YA Contributed reagents/materials/analysis tools: RG, and YA Wrote the paper: HT, RG, and SH No.
References
- 1. Sommer A, Tielsch JM, Katz J, Quigley HA, Gottsch JD, Javitt JC, et al. Racial differences in the cause-specific prevalence of blindness in east Baltimore. N Engl J Med. 1991;325(20):1412–7. pmid:1922252.
- 2. Wang JJ, Foran S, Mitchell P. Age-specific prevalence and causes of bilateral and unilateral visual impairment in older Australians: the Blue Mountains Eye Study. Clin Experiment Ophthalmol. 2000;28(4):268–73. Epub 2000/10/06. pmid:11021555.
- 3. Weih LM, VanNewkirk MR, McCarty CA, Taylor HR. Age-specific causes of bilateral visual impairment. Arch Ophthalmol. 2000;118(2):264–9. Epub 2000/02/17. pmid:10676793.
- 4. Munoz B, West SK, Rubin GS, Schein OD, Quigley HA, Bressler SB, et al. Causes of blindness and visual impairment in a population of older Americans: The Salisbury Eye Evaluation Study. Arch Ophthalmol. 2000;118(6):819–25. Epub 2000/06/24. pmid:10865321.
- 5. Klaver CC, Wolfs RC, Vingerling JR, Hofman A, de Jong PT. Age-specific prevalence and causes of blindness and visual impairment in an older population: the Rotterdam Study. Arch Ophthalmol. 1998;116(5):653–8. Epub 1998/05/22. pmid:9596502.
- 6. Klein R, Wang Q, Klein BE, Moss SE, Meuer SM. The relationship of age-related maculopathy, cataract, and glaucoma to visual acuity. Invest Ophthalmol Vis Sci. 1995;36(1):182–91. Epub 1995/01/01. pmid:7822146.
- 7. Nakae K MK, Senoo T, Sawa M, Kanai A, Ishibashi T. Aging society and eye disease: a recent epidemiological study on underlying diseases responsible for visual impairment [in Japanese]. Geriatr Med. 2006;44:1221–4.
- 8. Wako R, Yasukawa T, Kato A, Omori T, Ishida S, Ishibashi T, et al. Causes and prevalence of visual impairment in Japan [in Japanese] Nippon Ganka Gakkai Zasshi. 2014;118(6):495–501. pmid:25016791
- 9. Jager RD, Mieler WF, Miller JW. Age-Related Macular Degeneration. New England Journal of Medicine. 2008;358(24):2606–17. pmid:18550876.
- 10. Mori K, Horie-Inoue K, Gehlbach PL, Takita H, Kabasawa S, Kawasaki I, et al. Phenotype and genotype characteristics of age-related macular degeneration in a Japanese population. Ophthalmology. 2010;117(5):928–38. Epub 2010/02/06. pmid:20132989.
- 11. Nakata I, Yamashiro K, Nakanishi H, Akagi-Kurashige Y, Miyake M, Tsujikawa A, et al. Prevalence and characteristics of age-related macular degeneration in the Japanese population: the Nagahama study. Am J Ophthalmol. 2013;156(5):1002–9 e2. pmid:23938127.
- 12. Tamura H, Tsujikawa A, Yamashiro K, Akagi-Kurashige Y, Nakata I, Nakanishi H, et al. Association of ARMS2 genotype with bilateral involvement of exudative age-related macular degeneration. Am J Ophthalmol. 2012;154(3):542–8 e1. pmid:22809783.
- 13. Uyama M, Takahashi K, Ida N, Miyashiro M, Ando A, Takahashi A, et al. The second eye of Japanese patients with unilateral exudative age related macular degeneration. Br J Ophthalmol. 2000;84(9):1018–23. Epub 2000/09/01. pmid:10966957; PubMed Central PMCID: PMC1723651.
- 14. Ueta T, Iriyama A, Francis J, Takahashi H, Adachi T, Obata R, et al. Development of typical age-related macular degeneration and polypoidal choroidal vasculopathy in fellow eyes of Japanese patients with exudative age-related macular degeneration. Am J Ophthalmol. 2008;146(1):96–101. Epub 2008/04/29. pmid:18439567.
- 15. Mitchell P, Annemans L, White R, Gallagher M, Thomas S. Cost effectiveness of treatments for wet age-related macular degeneration. PharmacoEconomics. 2011;29(2):107–31. Epub 2011/01/20. pmid:21244102.
- 16. Cohen SY, Bremond-Gignac D, Quentel G, Mimoun G, Citterio T, Bisot-Locard S, et al. Cost-effectiveness sequential modeling of ranibizumab versus usual care in age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol. 2008;246(11):1527–34. pmid:18642019.
- 17. Hurley SF, Matthews JP, Guymer RH. Cost-effectiveness of ranibizumab for neovascular age-related macular degeneration. Cost effectiveness and resource allocation: C/E. 2008;6(1):12. pmid:18573218; PubMed Central PMCID: PMC2443361.
- 18. Group AHSR, Chew EY, Clemons TE, Bressler SB, Elman MJ, Danis RP, et al. Randomized trial of a home monitoring system for early detection of choroidal neovascularization home monitoring of the Eye (HOME) study. Ophthalmology. 2014;121(2):535–44. Epub 2013/11/12. pmid:24211172; PubMed Central PMCID: PMC3918479.
- 19. Kanagasingam Y, Bhuiyan A, Abramoff MD, Smith RT, Goldschmidt L, Wong TY. Progress on retinal image analysis for age related macular degeneration. Progress in retinal and eye research. 2014;38:20–42. Epub 2013/11/12. pmid:24211245.
- 20. Seddon JM, Ajani UA, Sperduto RD, Hiller R, Blair N, Burton TC, et al. Dietary carotenoids, vitamins A, C, and E, and advanced age-related macular degeneration. Eye Disease Case-Control Study Group. Jama. 1994;272(18):1413–20. Epub 1994/11/09. pmid:7933422.
- 21. The Age-Related Eye Disease Study 2 (AREDS2) Research Group. Lutein + zeaxanthin and omega-3 fatty acids for age-related macular degeneration: the Age-Related Eye Disease Study 2 (AREDS2) randomized clinical trial. Jama. 2013;309(19):2005–15. Epub 2013/05/07. pmid:23644932.
- 22. Krishnadev N, Meleth AD, Chew EY. Nutritional supplements for age-related macular degeneration. Curr Opin Ophthalmol. 2010;21(3):184–9. Epub 2010/03/11. pmid:20216418; PubMed Central PMCID: PMCPMC2909501.
- 23. Brown MM, Brown GC, Brown HC, Peet J. A value-based medicine analysis of ranibizumab for the treatment of subfoveal neovascular macular degeneration. Ophthalmology. 2008;115(6):1039–45 e5. pmid:17976724.
- 24. Fletcher EC, Lade RJ, Adewoyin T, Chong NV. Computerized model of cost-utility analysis for treatment of age-related macular degeneration. Ophthalmology. 2008;115(12):2192–8. pmid:18930556
- 25. Brown GC. Vision and quality-of-life. Trans Am Ophthalmol Soc. 1999;97:473–511. pmid:10703139; PubMed Central PMCID: PMC1298275.
- 26. Weinstein MC, Toy EL, Sandberg EA, Neumann PJ, Evans JS, Kuntz KM, et al. Modeling for health care and other policy decisions: uses, roles, and validity. Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research. 2001;4(5):348–61. pmid:11705125.
- 27. Johannesson M, Jonsson B, Kjekshus J, Olsson AG, Pedersen TR, Wedel H. Cost effectiveness of simvastatin treatment to lower cholesterol levels in patients with coronary heart disease. Scandinavian Simvastatin Survival Study Group. N Engl J Med. 1997;336(5):332–6. pmid:9011785.
- 28. Eye Care Comparative Effectiveness Research Team (ECCERT), Hiratsuka Y, Yamada M, Akune Y, Murakami A, Okada AA, et al. Cost-utility analysis of cataract surgery in Japan: a probabilistic Markov modeling study. Jpn J Ophthalmol. 2013;57(4):391–401. pmid:23588297.
- 29. Sharma S, Brown GC, Brown MM, Hollands H, Shah GK. The cost-effectiveness of photodynamic therapy for fellow eyes with subfoveal choroidal neovascularization secondary to age-related macular degeneration. Ophthalmology. 2001;108(11):2051–9. pmid:11713079
- 30. Oshima Y, Ishibashi T, Murata T, Tahara Y, Kiyohara Y, Kubota T. Prevalence of age related maculopathy in a representative Japanese population: the Hisayama study. Br J Ophthalmol. 2001;85(10):1153–7. PMC1723746. pmid:11567955
- 31. Yasuda M, Kiyohara Y, Hata Y, Arakawa S, Yonemoto K, Doi Y, et al. Nine-year incidence and risk factors for age-related macular degeneration in a defined Japanese population the Hisayama study. Ophthalmology. 2009;116(11):2135–40. Epub 2009/09/12. pmid:19744734.
- 32. Uyama M, Takahashi K, Ida N, Miyashiro M, Ando A, Takahashi A, et al. The second eye of Japanese patients with unilateral exudative age related macular degeneration. Br J Ophthalmol. 2000;84(9):1018–23. Epub 2000/09/01. pmid:10966957; PubMed Central PMCID: PMC1723651.
- 33. Rosenfeld PJ, Brown DM, Heier JS, Boyer DS, Kaiser PK, Chung CY, et al. Ranibizumab for neovascular age-related macular degeneration. N Engl J Med. 2006;355(14):1419–31. pmid:17021318
- 34. Maruko I, Iida T, Saito M, Nagayama D, Saito K. Clinical characteristics of exudative age-related macular degeneration in Japanese patients. Am J Ophthalmol. 2007;144(1):15–22. pmid:17509509.
- 35. Holden BA, Fricke TR, Ho SM, Wong R, Schlenther G, Cronje S, et al. Global vision impairment due to uncorrected presbyopia. Arch Ophthalmol. 2008;126(12):1731–9. pmid:19064856.
- 36. Brown GC, Sharma S, Brown MM, Kistler J. Utility values and age-related macular degeneration. Arch Ophthalmol. 2000;118(1):47–51. pmid:10636413.
- 37. Brown DM, Kaiser PK, Michels M, Soubrane G, Heier JS, Kim RY, et al. Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med. 2006;355(14):1432–44. pmid:17021319.
- 38. Pushpoth S, Sykakis E, Merchant K, Browning AC, Gupta R, Talks SJ. Measuring the benefit of 4 years of intravitreal ranibizumab treatment for neovascular age-related macular degeneration. British Journal of Ophthalmology. 2012;96(12):1469–73. pmid:23001255.
- 39. Cheung CS, Wong AW, Lui A, Kertes PJ, Devenyi RG, Lam W-C. Incidence of endophthalmitis and use of antibiotic prophylaxis after intravitreal injections. Ophthalmology. 2012;119(8):1609–14. pmid:22480743
- 40. Miyazaki M, Nakamura H, Kubo M, Kiyohara Y, Oshima Y, Ishibashi T, et al. Risk factors for age related maculopathy in a Japanese population: the Hisayama study. Br J Ophthalmol. 2003;87(4):469–72. pmid:12642312; PubMed Central PMCID: PMC1771615.
- 41. Treatment of Age-related Macular Degeneration With Photodynamic Therapy (TAP) Study Group. Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin: one-year results of 2 randomized clinical trials—TAP report. Treatment of age-related macular degeneration with photodynamic therapy (TAP) Study Group. Arch Ophthalmol. 1999;117(10):1329–45. Epub 1999/10/26. pmid:10532441.
- 42. Bressler NM, Treatment of Age-Related Macular Degeneration with Photodynamic Therapy Study G. Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin: two-year results of 2 randomized clinical trials-TAP report 2. Arch Ophthalmol. 2001;119(2):198–207. Epub 2001/02/15. pmid:11176980.
- 43. Neubauer AS, Holz FG, Sauer S, Wasmuth T, Hirneiss C, Kampik A, et al. Cost-effectiveness of ranibizumab for the treatment of neovascular age-related macular degeneration in Germany: Model analysis from the perspective of Germany's statutory health insurance system. Clin Ther. 2010;32(7):1343–56. pmid:20678682.
- 44. Brown DM, Kaiser PK, Michels M, Soubrane G, Heier JS, Kim RY, et al. Ranibizumab versus verteporfin for neovascular age-related macular degeneration. New England Journal of Medicine. 2006;355(14):1432–44. pmid:17021319
- 45. Group CR, Martin DF, Maguire MG, Ying GS, Grunwald JE, Fine SL, et al. Ranibizumab and bevacizumab for neovascular age-related macular degeneration. N Engl J Med. 2011;364(20):1897–908. pmid:21526923; PubMed Central PMCID: PMC3157322.
- 46. Tano Y, Ohji M, Group E-IS. EXTEND-I: safety and efficacy of ranibizumab in Japanese patients with subfoveal choroidal neovascularization secondary to age-related macular degeneration. Acta Ophthalmol. 2010;88(3):309–16. pmid:20163368.
- 47. Antoszyk AN, Tuomi L, Chung CY, Singh A, Group FS. Ranibizumab combined with verteporfin photodynamic therapy in neovascular age-related macular degeneration (FOCUS): year 2 results. Am J Ophthalmol. 2008;145(5):862–74. Epub 2008/03/07. pmid:18321465.
- 48. Regillo CD, Brown DM, Abraham P, Yue H, Ianchulev T, Schneider S, et al. Randomized, double-masked, sham-controlled trial of ranibizumab for neovascular age-related macular degeneration: PIER Study year 1. Am J Ophthalmol. 2008;145(2):239–48. pmid:18222192.
- 49. Bressler NM, Bressler SB, Congdon NG, Ferris FL 3rd, Friedman DS, Klein R, et al. Potential public health impact of Age-Related Eye Disease Study results: AREDS report no. 11. Arch Ophthalmol. 2003;121(11):1621–4. Epub 2003/11/12. pmid:14609922; PubMed Central PMCID: PMCPMC1473209.
- 50. Bonds DE, Harrington M, Worrall BB, Bertoni AG, Eaton CB, Hsia J, et al. Effect of long-chain omega-3 fatty acids and lutein + zeaxanthin supplements on cardiovascular outcomes: results of the Age-Related Eye Disease Study 2 (AREDS2) randomized clinical trial. JAMA internal medicine. 2014;174(5):763–71. Epub 2014/03/19. pmid:24638908.
- 51. Takahashi K, Ogura Y, Ishibashi T, Shiraga F, Yuzawa M. Treatment guidelines for age-related macular degeneration [in Japanese]. Nihon Ganka Gakkai Zasshi. 2012;116(12):1150–5. Epub 2013/02/06. pmid:23379205.
- 52. Holz FG, Tadayoni R, Beatty S, Berger A, Cereda MG, Cortez R, et al. Multi-country real-life experience of anti-vascular endothelial growth factor therapy for wet age-related macular degeneration. Br J Ophthalmol. 2015;99(2):220–6. pmid:25193672; PubMed Central PMCID: PMC4316940.
- 53. Pineles SL, Birch EE, Talman LS, Sackel DJ, Frohman EM, Calabresi PA, et al. One eye or two: a comparison of binocular and monocular low-contrast acuity testing in multiple sclerosis. Am J Ophthalmol. 2011;152(1):133–40. pmid:21570055; PubMed Central PMCID: PMC3637955.
- 54. Hirneiss C. The impact of a better-seeing eye and a worse-seeing eye on vision-related quality of life. Clinical ophthalmology. 2014;8:1703–9. pmid:25214763; PubMed Central PMCID: PMC4159393.
- 55.
Japan Ophthalmologists Association. Social burden of visual disturbance in Japan [in Japanese]. 2009.
- 56. Shiroiwa T, Sung YK, Fukuda T, Lang HC, Bae SC, Tsutani K. International survey on willingness-to-pay (WTP) for one additional QALY gained: what is the threshold of cost effectiveness? Health economics. 2010;19(4):422–37. Epub 2009/04/22. pmid:19382128.
- 57. Bloch SB, Larsen M, Munch IC. Incidence of legal blindness from age-related macular degeneration in denmark: year 2000 to 2010. Am J Ophthalmol. 2012;153(2):209–13 e2. pmid:22264944.
- 58. Brown GC, Brown MM, Brown HC, Kindermann S, Sharma S. A value-based medicine comparison of interventions for subfoveal neovascular macular degeneration. Ophthalmology. 2007;114(6):1170–8. pmid:17320964.
- 59. Hernandez-Pastor LJ, Ortega A, Garcia-Layana A, Giraldez J. Cost-effectiveness of ranibizumab compared with photodynamic treatment of neovascular age-related macular degeneration. Clin Ther. 2008;30(12):2436–51. pmid:19167602.
- 60. Hernandez-Pastor LJ, Ortega A, Garcia-Layana A, Giraldez J. Cost-effectiveness of ranibizumab compared with pegaptanib in neovascular age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol. 2010;248(4):467–76. pmid:19669678.
- 61. Hiratsuka Y, Yamada M, Akune Y, Murakami A, Okada AA, Yamashita H, et al. Assessment of vision-related quality of life among patients with cataracts and the outcomes of cataract surgery using a newly developed visual function questionnaire: the VFQ-J11. Jpn J Ophthalmol. 2014;58(5):415–22. pmid:25037865.
- 62. Yanagi Y, Aihara Y, Fukuda T, Hashimoto H. Cost-effectiveness of ranibizumab, photodynamic therapy and pegaptanib sodium in the treatment of neovascular age-related macular degeneration [in Japanese]. Nihon Ganka Gakkai Zasshi. 2011;115(9):825–31. pmid:22073599.
- 63. Rofagha S, Bhisitkul RB, Boyer DS, Sadda SR, Zhang K. Seven-year outcomes in ranibizumab-treated patients in ANCHOR, MARINA, and HORIZON: a multicenter cohort study (SEVEN-UP). Ophthalmology. 2013;120(11):2292–9. Epub 2013/05/07. pmid:23642856.
- 64. Kawasaki R, Akune Y, Hiratsuka Y, Fukuhara S, Yamada M. Cost-utility analysis of screening for diabetic retinopathy in Japan: a probabilistic Markov modeling study. Ophthalmic epidemiology. 2015;22(1):4–12. Epub 2014/12/18. pmid:25517603.