Research Article - Biomedical Research (2017) Volume 28, Issue 20
Usage rates of treatments for cardiovascular prevention in patients with type 2 diabetes mellitus without diagnosis of coronary artery disease
Dilek Oztas1, Mehmet Kayhan2, Hüseyin Balcıoğlu3, Yasemin Sağlan4, Yunus Emre Sarı3 and Uğur Bilge3*
1Department of Public Health, Faculty of Medicine, Yildirim Beyazıt University, Ankara, Turkey
2Department of Family Medicine, Faculty of Medicine, Abant İzzet Baysal University, Bolu, Turkey
3Department of Family Medicine, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey
4Eskişehir Public Health Directorate, Eskişehir, Turkey
- *Corresponding Author:
- Uğur Bilge
Department of Family Medicine
Faculty of Medicine
Eskisehir Osmangazi University, Turkey
Accepted on October 16, 2017
Abstract
Aim: The aim of this study is to retrospectively investigate the usage rates of antidiabetic treatments, and statin, aspirin and angiotensin (angiotensin converting enzyme inhibitors and angiotensin receptor blockers) based treatments for cardiovascular prevention in patients with type 2 diabetes mellitus.
Material and Methods: Drug exemption reports issued during 2015 and 2016 were evaluated from the hospital's digital database. Among these reports, files of patients with the DM diagnosis code (E11-E14) and without any diagnosis that could be associated with major cardiac events were scanned, and approximately 31685 records were obtained.
Results: A total of 11942 individuals were selected randomly according to simple random sampling method, and the active ingredients of the drugs listed in the drug exemption reports and used by the selected individuals were investigated. When usage in all groups was investigated, it was found that 21.3% of the patients used statin, 26.08% used ACE-I/ARB, and 9.8% used aspirin.
Discussion: In conclusion, the use of multiple treatments such as statins, angiotensinogen-dependent treatments, and aspirin in patients with DM2 is associated with a reduction in all-cause mortality. Secondary prevention, however, depends on the early selection of cases, and the initiation of appropriate preventive treatments; progression of the disease can only be stopped this way.
Keywords
Diabetes mellitus, Cardiovascular prevention.
Introduction
Diabetes Mellitus (DM) is a chronic metabolic disease that occurs due to lack of effect and/or secretion or complete deficiency of insulin [1]. DM is a chronic disease that is very common all over the world, including Turkey. In TURDEP-II study in 2010, DM frequency in adults in Turkey was found to be 13.7% [2]. At present, there are more than 130 million adult DM patients all over the world, and it is estimated that this number will rise to 333 million by 2025 [3]. The main goals of treatment in diabetic patients are blood sugar regulation, control of hypertension, treatment of dyslipidemia and obesity [4]. For blood sugar regulation, proper diet, weight control, diabetes education, physical activity, oral antidiabetic drugs (OAD), and if necessary, insulin therapy are implemented. Hypertension, dyslipidemia and coronary artery diseases are frequently seen as comorbidities in patients with diabetes mellitus. Cardiovascular prevention is particularly important. Statins, ACE inhibitors (ACE-I)/angiotensin receptor blockers (ARB), and aspirin use is predominant in cardiovascular prevention [5-9].
The aim of this study is to retrospectively investigate the usage rates of antidiabetic treatments, and statin, aspirin and angiotensin (angiotensin converting enzyme inhibitors and angiotensin receptor blockers) based treatments for cardiovascular prevention in patients with type 2 diabetes mellitus who are not diagnosed with coronary artery disease, and to determine the distribution of these treatments according to age and gender.
Material and Methods
In Turkey, a report called “drug exemption report” is issued to individuals when a patient with DM diagnosis is thought to have reached the target values, and exemption is made for some payments to be made to the insurance institution, and when the patient report is issued, the doctor can prescribe the medicines again in the light of this report. These reports are prepared for 1 or 2 years. Ankara Atatürk Education and Research Hospital is a medical center located in the capital Ankara, where patients from neighboring cities can also apply. For this reason, it is thought that the data obtained from this center can be generalized for all of Turkey. Drug exemption reports issued during 2015 and 2016 were evaluated from the hospital's digital database. Among these reports, files of patients with the DM diagnosis code (E11-E14) and without any diagnosis that could be associated with major cardiac events were scanned, and approximately 31685 records were obtained.
The obtained data were randomly selected in the IBM SPSS Statistics v21.0 package based on simple random sampling method. After the selection process, drug exemption reports of 11942 individuals were received. The sample used in this study comprises all drug exemption reports issued during this period and recorded in the electronic system.
Statistical analysis
The descriptive data are given in percentages (%). Pearson Chi Square, Yate's Exact Chi Square and Fisher's Exact Chi Square analyses were used in the analysis of the generated cross tables. The analysis was performed using IBM SPSS Statistics 21.0 software (IBM Corp. Released 2012. IBM SPSS Statistics for Windows, Version 21.0, Armonk, NY: IBM Corp.). For statistical significance, p<0.05 was considered.
Results
Approximately 32 thousand individuals, who were diagnosed with DM2 with the determined criteria, applied to Ankara Atatürk Education Research Hospital between 2015-2016. A total of 11942 individuals were selected randomly according to simple random sampling method, and the active ingredients of the drugs listed in the drug exemption reports and used by the selected individuals were investigated. In the treatment of DM, since the use of single medication as well as the simultaneous use of different medications is often the case, the analysis was done accordingly. When gender distributions were analyzed, it was found that 6153 (51.5%) individuals were female and 5789 (48.5%) were male. The average age of the study group was 60.48 ± 11.35, with a minimum age of 18 and a maximum age of 107. The average age of women was 61.43 ± 11.43, and the average age of men was found to be 59.47 ± 11.18. It was found that the age of women participating in the study was significantly higher than that of men (p<0.001). When the accompanying diseases of 11942 individuals diagnosed with DM were examined, it was found that 3591 (30.1%) individuals had HT, 46 (0.4%) individuals had COPD and 54 (0.5%) individuals had Asthma.
In Table 1, in which the frequency distributions of active ingredients are defined, two different percentages are given as percentage among the number of individuals and percentage among the active ingredient. The table is presented in three sections; including diabetes medicines, hypertension medicines, and other medicines (Statins, Acetylsalicylic Acid and Alpha Lipoic Acid). While percentage among the number of individuals indicates percent usage in all units participating in the study, percentage of the active ingredient indicates the percentage of which the active substance is used or not. Metformin was the most commonly used active ingredient in DM medicines, used by 8332 people and in 69.77% of individuals. Insulin Glargine used by 2168 people (18.16%), and Insulin Aspart and Insulin Aspart Protamine combination, used by 1396 people (11.69%) were found to be the 2nd and 3rd most commonly used active ingredients in diabetes medication. The least used active ingredient was a combination of Metformin and Gliclazide with only 3 people. Among HT medicines, Metoprolol was the most commonly used active ingredient and was used by 682 people (5.71%). The least used active ingredient was a combination of Amlodipine and Valsartan and Hydrochlorothiazide with 2 people. Among other medicines, 1096 (9.15%) individuals were found to use Acetylsalicylic Acid. The most commonly used active ingredient in Statins was Atorvastatin Calcium with 2182 people (18.27%).
Anti-diabetic drugs | (n) | Percentages in study population (n) (%) | Percentages in the ingredients (%) |
---|---|---|---|
Metformin | 8332 | 69.77 | 42.10 |
Insulin glargine | 2168 | 18.16 | 10.96 |
Insulin aspart and insulin protamine | 1396 | 11.69 | 7.05 |
Sitagliptin | 1211 | 10.14 | 6.12 |
Insulin aspart | 1130 | 9.46 | 5.71 |
Repaglinide | 766 | 6.41 | 3.87 |
Sitagliptin and metformin | 727 | 6.09 | 3.67 |
Insulin lispro and insulin protamin | 635 | 5.32 | 3.21 |
Vildagliptin ve metformin | 477 | 3.99 | 2.41 |
Insulin detemir | 450 | 3.77 | 2.27 |
Linagliptin | 377 | 3.16 | 1.91 |
Insulin lispro | 371 | 3.11 | 1.87 |
Nateglinide | 322 | 2.70 | 1.63 |
Vildagliptin | 303 | 2.54 | 1.53 |
Acarbose | 289 | 2.42 | 1.46 |
Pioglitazone | 253 | 2.12 | 1.28 |
Insulin glulisin | 144 | 1.21 | 0.73 |
Saxagliptin | 118 | 0.99 | 0.60 |
Insulin nph human | 101 | 0.85 | 0.51 |
Insulin human regular | 87 | 0.73 | 0.44 |
Insulin human regular ve insulin Nph human | 67 | 0.56 | 0.34 |
Pioglitazone and Metformin | 57 | 0.48 | 0.29 |
Metformin and Repaglinide | 5 | 0.04 | 0.03 |
Metformin and Gliclazide | 3 | 0.03 | 0.02 |
Anti-hypertensive drugs | |||
Metoprolol | 682 | 5.71 | 12.22 |
Amlodipine | 620 | 5.19 | 11.11 |
Valsartan and hydrochlorothiazide | 435 | 3.64 | 7.80 |
Ramipril | 430 | 3.60 | 7.71 |
Candesartan and hydrochlorothiazide | 266 | 2.23 | 4.77 |
Losartan and hydrochlorothiazide | 211 | 1.77 | 3.78 |
Irbesartan and hydrochlorothiazide | 200 | 1.67 | 3.58 |
Carvedilol | 161 | 1.35 | 2.89 |
Perindopril and indapamid | 155 | 1.30 | 2.78 |
Lercanidipine | 134 | 1.12 | 2.40 |
Telmisartan and hydrochlorothiazide | 134 | 1.12 | 2.40 |
Ramipril and hydrochlorothiazide | 133 | 1.11 | 2.38 |
Nifedipine | 132 | 1.11 | 2.37 |
Doxazosin | 131 | 1.10 | 2.35 |
Perindopril | 131 | 1.10 | 2.35 |
Olmesartan and hydrochlorothiazide | 129 | 1.08 | 2.31 |
Valsartan | 126 | 1.06 | 2.26 |
Amlodipin and Valsartan | 118 | 0.99 | 2.12 |
Losartan | 104 | 0.87 | 1.86 |
Indapamid | 84 | 0.70 | 1.51 |
Olmesartan | 83 | 0.70 | 1.49 |
Candesartan | 81 | 0.68 | 1.45 |
Perindopril and Amlodipin | 78 | 0.65 | 1.40 |
Furosemide | 61 | 0.51 | 1.09 |
Lacidipin | 58 | 0.49 | 1.04 |
Cilazapril and hydrochlorothiazide | 56 | 0.47 | 1.00 |
Diltiazem | 53 | 0.44 | 0.95 |
Irbesartan | 49 | 0.41 | 0.88 |
Lisinopril and hydrochlorothiazide | 48 | 0.40 | 0.86 |
Verapamil and trandolapril | 48 | 0.40 | 0.86 |
Bisoprolol fumarat | 45 | 0.38 | 0.81 |
Telmisartan | 42 | 0.35 | 0.75 |
Cilazapril | 39 | 0.33 | 0.70 |
Benidipin | 38 | 0.32 | 0.68 |
Atenolol | 36 | 0.30 | 0.65 |
Lisinopril | 27 | 0.23 | 0.48 |
Atenolol and chlorthalidone | 24 | 0.20 | 0.43 |
Spironolactone | 24 | 0.20 | 0.43 |
Fosinopril and hydrochlorothiazide | 22 | 0.18 | 0.39 |
Quinapril and hydrochlorothiazide | 18 | 0.15 | 0.32 |
Verapamil | 18 | 0.15 | 0.32 |
Zofenopril Kalsiyum ve hydrochlorothiazide | 18 | 0.15 | 0.32 |
Enalapril maleat | 14 | 0.12 | 0.25 |
Zofenopril kalsiyum | 13 | 0.11 | 0.23 |
Spironolakton and Hydrochlorothiazide | 12 | 0.10 | 0.22 |
Enalapril and nitrendipin | 10 | 0.08 | 0.18 |
Captopril | 10 | 0.08 | 0.18 |
Quinapril | 9 | 0.08 | 0.16 |
Trandolapril | 9 | 0.08 | 0.16 |
Amlodipin and atorvastatin | 5 | 0.04 | 0.09 |
Benazepril and hydrochlorothiazide | 5 | 0.04 | 0.09 |
Enalapril and lercanidipin | 5 | 0.04 | 0.09 |
Fosinopril | 3 | 0.03 | 0.05 |
Amlodipin and Valsartan and hidroklorotiazit | 2 | 0.02 | 0.04 |
Other drugs | |||
Atorvastatin | 2182 | 18.27 | 54.04 |
Rosuvastatin | 455 | 3.81 | 11.27 |
Pravastatin | 15 | 0.13 | 0.37 |
Fluvastatin | 4 | 0.03 | 0.10 |
Pitavastatin | 3 | 0.03 | 0.07 |
Acetylsalicylic acid | 1096 | 9.18 | 27.14 |
Alpha lipoic acid | 283 | 2.37 | 7.01 |
Table 1. Ingredients of the drugs used (anti-hypertensive, anti-diabetic drugs and others).
In Table 2, differences between the distributions of active ingredients according to gender were examined. Acetylsalicylic Acid, an active ingredient listed under other medicines, was found to be used by 551 male individuals (9.57%), and 545 female individuals (8.86%). Acetylsalicylic Acid was not found to be significantly different between men and women (p=0.211). It was found that Atorvastatin Calcium, the most commonly used active ingredient in Statins, was used by 944 male individuals (16.39%), and 1139 female individuals (18.51%). Use of Atorvastatin Calcium was found to be significantly different between men and women (p=0.002). When the distributions of medication groups according to gender in Table 2 were examined, it was found that female individuals with 1406 people (%22.9) were significantly higher than male individuals with 1133 people (%19.6) among people who used medication with Statin as an active ingredient (p<0.001). Similarly, active ingredients ARB, CCB, Beta Blocker (BB) and OAD were found to be significantly higher in women (p<0.001 for each). However, it was found that the use of insulin by men with 2364 people (40.8%) was significantly higher compared to women with 2200 people (35.8%) (p<0.001). Unlike these groups, no significant difference was found between genders in the use of ACE-I (p=0.727).
Sex | p* | ||
---|---|---|---|
Male | Female | ||
Statin | 1133 (19.6%) | 1406 (22.9%) | 19.157 <0.001 |
ACE-Inhibitor | 589 (10.2%) | 638 (10.4%) | 0.122 0.727 |
Angiotensin Receptor Blocker | 686 (11.9%) | 1202 (19.5%) | 132.351 <0.001 |
Calcium Chanel Blocker | 475 (8.2%) | 809 (13.1%) | 75.942 <0.001 |
Beta Blocker | 409 (7.1%) | 531 (8.6%) | 10.071 0.002 |
Insulin | 2364 (40.8%) | 2200 (35.8%) | 32.614 <0.001 |
Oral Anti-Diabetic Agents | 4829 (83.4%) | 5363 (87.2%) | 33.429 <0.001 |
*Pearson Chi-Square test
Table 2. Distributions of the drugs among sexes.
Acetylsalicylic Acid was found to be used by 498 (6.00%) patients under 65 years of age, and by 598 patients (14.00%) at 65 years of age and above. Acetylsalicylic Acid was found to be significantly different for patients at 65 years of age and above (p<0.001). Atorvastatin Calcium, the most commonly used active ingredient in Statins, was found to be used by 1261 patients (16.00%) under 65 years of age, and by 822 patients (19.00%) at 65 years of age and above. Atorvastatin Calcium was found to be significantly different for patients under 65 years of age (p<0.001). When the distributions of medication groups with respect to the age of 65 were examined in Table 3, it was found that statin, ACE-I, insulin and OAD groups within active ingredients were significantly over-used in patients under 65 years of age compared to patients at the age of 65 and above (p<0.001 for each). However, ARB, CCB, and BB groups were found to be significantly over-used in patients at the age of 65 and above compared to patients under years of age (p<0.001 for each).
Age | p* | ||
---|---|---|---|
<65 | ≥ 65 | ||
Statin | 1509 (59.43%) | 1030 (40.56%) | 38.213 <0.001 |
ACE-Inhibitor | 705 (57.45%) | 522 (42.54%) | 30.844 <0.001 |
Angiotensin Receptor Blocker | 921 (48.78%) | 967 (51.21%) | 246.649 <0.001 |
Calcium Chanel Blocker | 605 (47.11%) | 679 (52.88%) | 193.178 <0.001 |
Beta Blocker | 377 (40.10%) | 563 (59.89%) | 268.619 <0.001 |
Insulin | 2853 (62.51%) | 1711 (37.48%) | 14.614 <0.001 |
Oral Anti-Diabetic Agents | 6765 (66.37%) | 3427 (33.62%) | 91.930 <0.001 |
*Pearson chi-square test
Table 3. Distributions of the drugs according to adult and elderly population (65 older and other population).
In Table 4, distribution frequencies according to the number of active ingredients from different medications simultaneously used by patients are given. It was found that the highest number of active ingredients simultaneously used by individuals participating in the study was 13. 3679 patients (30.807%) used a single active ingredient, 3693 patients (30.924%) used 2 active ingredients, 2140 patients (17.919%) used 3 active ingredients, 1210 patients (10.132%) used 4 active ingredients, 652 patients (5.459%) used 5 active ingredients, 326 patients (2.729%) used 6 active ingredients, 146 patients (1.222%) used 7 active ingredients, 52 patients (0.435%) used 8 active ingredients, 29 patients (0.242%) used 9 active ingredients, and 15 patients (0.131%) used 10 or more active ingredients.
Patients’ total drug numbers used (n) | Percentages of the Patients’ total drug numbers used (%) | |
---|---|---|
1 | 3679 | 30.807 |
2 | 3693 | 30.924 |
3 | 2140 | 17.919 |
4 | 1210 | 10.132 |
5 | 652 | 5.459 |
6 | 326 | 2.729 |
7 | 146 | 1.222 |
8 | 52 | 0.435 |
9 | 29 | 0.242 |
10 | 5 | 0.041 |
11 | 6 | 0.050 |
12 | 2 | 0.016 |
13 | 2 | 0.016 |
Table 4. Total number of the drugs and their percentages.
It was determined that 420 of the patients included in the study (3.5%) used ACE-I/ARB, ASA, and Statin treatment together as preventive treatment. Of these patients, 216 (51.4%) were male and 204 (48.6%) were female. No significant difference was found in use of preventive treatment between genders (p=0.218). When the use of preventive treatment with respect to age was investigated, it was found that 237 of the patients (56.4%) aged 65 and above were using preventive treatment, whereas 183 of the patients (43.6%) under 65 years of age were using preventive treatment. Prevalence of preventive treatment over 65 years of age was found to be significantly higher than under 65 years of age (p<0.001). When usage in all groups was investigated, it was found that 21.3% of the patients used the statin, 26.08% used ACE-I/ARB, and 9.8% used aspirin.
Discussion
Cardiovascular Disease (CVD) is the most important cause of morbidity and mortality in diabetic patients. In type 2 diabetes patients, the risk of coronary artery disease (CAD) in particular is 2-4 times higher than in non-diabetics. 60-75% of these patients are lost due to macrovascular events. In diabetic patients, atherosclerosis occurs at an earlier age and is more common. Prevalence of acute diabetic complications has decreased considerably with increasing awareness and improvement of treatment efficacy and possibilities, and mortality frequency has decreased. Development of late complications is mostly related to duration of diabetes (10). 26.08% of patients were using ACE-I/ARB. ACE inhibitors (ACE-I), angiotensin receptor blockers (ARB), low dose thiazide group diuretics, and calcium channel blockers (CCB) are agents with positive effects that are indicated in clinically controlled studies in the pharmacological treatment of diabetic hypertension (HT) cases. In all guidelines, modification of life style is recommended as initial therapy, followed by selection of one of the ACE-I or ARB group of drugs that block the renin-angiotensin system (RAS) in patients with albuminuria. In type 2 diabetes however, in the presence of HT, it is known that the progression of microalbuminuria may be delayed with ACE-I or ARB [6]. Diabetic nephropathy displays increased albuminuria and decreased glomerular filtration rate. Both of these are independent risk factors for CVD. Especially in patients with type 2 diabetes, renal function should be assessed at the time of diagnosis. Angiotensin converting enzyme inhibitor therapy should be initiated if albumin excretion is over 300 mg per day or if the glomerular filtration rate is <60 mL/min/1.73 m2. This treatment has a role in renal function as well as prevention of CVD development [10].
The first step in the treatment of dyslipidemia in diabetic patients is lifestyle changes. These changes are regulating the diet, weight loss if necessary, and increasing physical activity. However, if LDL cholesterol level>100 mg/dL despite the change in life style for those with proven cardiovascular disease (CVD), those with microvascular and macrovascular complications of diabetes, those over 40 and with one or more other cardiovascular risk factors (CVD family history, hypertension, smoking, dyslipidemia or albuminuria), those under 40 and with no CVD, statin should be added to the treatment regardless of baseline lipid levels [7]. In dyslipidemia, the primary goal should be lowering LDL-cholesterol. Target level of LDL-cholesterol should be <100 mg/dL in patients without proven cardiovascular disease and <70 mg/dl in patients with cardiovascular disease. If the desired values are not reached despite maximal statin therapy, a 50% reduction of baseline LDL cholesterol levels should be aimed [8].
21.3% of the patients were using statin, and this percentage was significantly higher (59.43%) for patients under 65 years of age as compared with patients over 65 years of age (40.56%). Morbidity and mortality in type 2 diabetes patients is due to major cardiovascular events. For this reason, the main goal of treatment in these patients is to reduce vascular risks. Dyslipidemia is the most important risk factor for atherosclerotic events and deaths, and must definitely be investigated and treated. As with other diseases, it is essential to lower LDL-cholesterol primarily to prevent vascular complications related to diabetes. Effective treatment of diabetic dyslipidemia is important in reducing cardiovascular risk. Lowering LDL-cholesterol with statins is the most effective treatment option. However, it should be kept in mind that LDL cholesterol levels are a significant residual risk in diabetic patients, even if they are maintained within safe limits. ADA suggests lifestyle changes to diabetic patients over 40 years of age, independent of lipid levels. American Heart Association and American College of Cardiology guidelines recommend statin therapy independent of cardiovascular risk for diabetic patients aged 40-75 years with LDL-C ≥ 70 mg/dL.
In another guideline, statin therapy is recommended for diabetic patients aged 40-75 years, even if there is no additional cardiovascular risk. Our results indicate that the use of statin remains relatively low and is an indication that these patients do not fully benefit from primary prevention [11]. Following American Heart Association's 2013 guideline, there has been an increase in the use of statins, but there is insufficient evidence of the effects of statin use in primary prevention in patients who are older than 75 years of age. It should not be forgotten that there might be an increase in muscle symptoms and risks of side effects due to drug interactions due to the use of statin in the elderly [12-15].
Aspirin was used by 9.8% of our patients. The risk of coronary artery disease (CAD) is increased in DM patients, even more so in type 2 DM patients. Low-dose aspirin (75-150 mg/day) may be administered to diabetic patients with stable cardiovascular disease (CVD). Aspirin (75-150 mg) may be administered with the purpose of primary prevention to diabetic patients with a 10-year CV event risk>10% [9]. It should be noted that the use of aspirin in older patients, even with low doses, increases the risk of gastrointestinal bleeding, therefore cardiovascular risks and possible side effects should be carefully questioned when using aspirin in elderly diabetic patients [16,17].
Routine cardiac control is necessary for asymptomatic diabetic patients. Exercise stress test is recommended for both symptomatic and asymptomatic diabetics with certain criteria (those with typical or atypical cardiac symptoms, those with findings of ischemia or infections in resting ECG, those with peripheral artery and/or carotid obstruction). In addition, exercise stress test may be recommended in type 1 diabetic patients with more than 15 years of diabetes, type 2 diabetics with more than 10 years of diabetes, and type 2 diabetic patients older than 35 years [18]. Clinicians should be on the alert for diabetic patients who describe atypical symptoms (resting tachycardia, postural hypotension, erectile dysfunction, peripheral arterial disease, etc.).
In conclusion, the use of multiple treatments such as statins, angiotensinogen-dependent treatments, and aspirin in patients with DM2 is associated with a reduction in all-cause mortality. Secondary prevention, however, depends on the early selection of cases, and the initiation of appropriate preventive treatments; progression of the disease can only be stopped this way. Nephropathy and other complications should be investigated in patients with known diabetes mellitus with CAD, and the goal of glycemic control that is most appropriate to the patient should be ensured without increasing the risk of hypoglycemia. In addition to mild glycemic control to reduce the risk of CAD in type 2 diabetes, a multifactorial approach (change in lifestyle, lipid and BP control and antiaggregant use, as well as avoidance of harmful agents such as smoking) should be adopted.
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