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Article

Gender Differences in the Medical Treatment of Peripheral Artery Disease

by
Damien Lanéelle
1,2,†,
Gabriella Sauvet
3,†,
Jérôme Guillaumat
1,
Jean Eudes Trihan
4 and
Guillaume Mahé
5,6,*
1
Vascular Medicine Unit, Centre Hospitalier Universitaire de Caen Normandie, 14000 Caen, France
2
COMETE Laboratory, INSERM 1075, Université de Caen, 14000 Caen, France
3
Medical School, Université de Versailles Saint-Quentin-en-Yvelines, 78180 Montigny-Le-Bretonneux, France
4
Vascular Medicine Unit, Centre Hospitalier Universitaire de Poitiers, 86021 Poitiers, France
5
Vascular Medicine Unit, Centre Hospitalier Universitaire de Rennes, 35033 Rennes, France
6
INSERM CIC 1414, Université de Rennes, 35033 Rennes, France
*
Author to whom correspondence should be addressed.
Both authors contributed equally to this work and share first authorship.
J. Clin. Med. 2021, 10(13), 2855; https://doi.org/10.3390/jcm10132855
Submission received: 17 May 2021 / Revised: 29 May 2021 / Accepted: 22 June 2021 / Published: 28 June 2021
(This article belongs to the Special Issue Peripheral Artery Disease: From Diagnosis to Treatment)

Abstract

:
Background/Objectives: Peripheral arterial disease is a frequent and severe disease with high cardiovascular morbidity and mortality. However, female patients appear to be undertreated. Objectives: The primary goal was to compare the prescription of optimal medical treatment (OMT) of peripheral arterial disease between women and men in primary health care. Material and methods: An observational retrospective study was based on the data collected from general practitioners (GP) office in Brittany. Results: The study included 100 patients, aged 71 ± 10 years old, with 24% of women. Compared to men, women received the OMT less frequently (29.2% vs. 53.9%, p = 0.038), especially after 75 years old. Antiplatelet therapy was largely prescribed (100%), statins less frequently (70.8% women vs. 85.5% men), and prescription of renin-angiotensin-aldosterone system inhibitors was still not optimal in the two genders (41.7% women vs. 61.9% men). Active smoking is important for both women and men (33% and 30% respectively). Conclusion: Optimal medical treatment of peripheral artery disease is insufficiently prescribed, especially in women in this region of France.

1. Introduction

Lower extremity peripheral arterial disease (PAD) is a frequent and increasing pathology, estimated at 235 million people affected worldwide and associated with substantial morbidity and mortality [1]. Lifestyle change and optimal medical treatment are the core of the treatment [2,3,4]. Antiplatelet aggregation inhibitor (AAP), a statin, and an antihypertensive drug (Angiotensin-Converting Enzyme inhibitor, ACE, or an angiotensin Receptor Blocker, ARBs) is the Optimal Medical Treatment (OMT) for PAD [5].
PAD in women is less frequent than in age-matched men; however, women are more likely to have atypical symptoms and greater walking impairment with progressive functional decline [6,7,8,9,10]. Research into gender differences in the prescription of medical and lifestyle therapies for PAD is lacking but women are treated less intensively to achieve cardiovascular risk factor targets [11] and appear to be treated less favorably for PAD than men at discharge from a tertiary-care teaching hospital [12]. Scientific statements have increasingly promoted the need for increased awareness and further research into gender-specific concerns in PAD. Women have been consistently underrepresented in clinical trials [6] and, accordingly, conclusions are hard to draw from case reports.
The present study examined the effect of gender on treatment medical management in patients with PAD in primary health care. The main objective was to compare the proportion of women with the OMT to men.

2. Materials and Methods

A retrospective observational study was conducted using data collected anonymously from general practitioners (GP) office in Brittany after a declaration of conformity and registration at the National Institute of Health Data (MR 0711090620). Thirty-two GPs were randomly selected out of 5288 (0.6%) in Brittany to search for the last five consecutive patients with PAD, based on medical record, who have consulted in the last 12 months and with a collection of medical elements on the whole medical record. Each patient was notified by a written information sheet and, in the absence of opposition, data were collected from the medical record. The study was conducted in Brittany (Brittany contains 4 departments) in France from June to August 2020 and involved 7 to 9 GP per department. The general collected data were age; sex; weight and height; history of vascular diseases (coronary heart disease (CHD), cerebrovascular disease (CVD), define by transient ischemic attack, stroke and/or carotid endarterectomy); smoking (current, at least 1-year cessation or never); diabetes; hypertension (HT), dyslipidemia, low-density lipoprotein cholesterol (LDL-c) and creatinemia. The PAD data collected were Leriche and Fontaine classification: stage 1 (asymptomatic), stage 2 (claudication), stage 3–4 (chronic permanent ischemia without and with trophic disorder, respectively); history of revascularization procedures; ankle–brachial index (ABI); date to the last vascular or cardiologist follow-up and all current medical and surgical treatments. OMT was defined as the association of Antiplatelet agent (or anticoagulation) + Statin + Angiotensin ACE/ARBs.
Statistical analyses: Quantitative results are expressed as mean ± standard deviation and analyzed by the Student’s test after verification of the conditions of application, including the normal distribution of observations. Qualitative results are expressed in frequency and percentage, which have been compared by the χ2 test or the Fisher exact test if necessary. The analyses, tables and figures were performed on RStudio (version 1.3.959) and edited on Microsoft Excel 2016. A value of p < 0.05 was chosen as statistically significant in the two-tailed analysis.

3. Results

3.1. Characteristics of the Patients with Lower Extremity Peripheral Artery Disease

A total of 100 patients with PAD were included (Table 1). The study population was composed by 72% of patients over 65 years of age (75% female and 71% male) and 28% were over 75 years of age. With respect to the Leriche and Fontaine classification, 54% were stage 2 (21% without revascularization, 34% with revascularization), 27% were stage 1 (8% without revascularization, 19% with revascularization), and 17% had a stage 3–4 PAD (3% without revascularization, 14% with revascularization). The mean LDL level was 1.03 ± 0.35 g/L with 50% LDL < 1 g/L, 16% with LDL < 0.7 g/L and 5% with LDL < 0.55 g/L.
Forty-eight percent of patients received OMT, regardless of the severity of the disease or risk factors and 42% for patients with only a PAD (patients with a history of CHD and CVD excluded).

3.2. Gender Differences

There were no significant gender differences with respect to risk factors or according to the severity of the disease but the proportion of women with the OMT (AAP or anticoagulant + statin + ACE or ARBs) was significantly lower than that of men (29% vs. 54%, p = 0.038, Table 2), particularly in the oldest patients ≥75 years old (p = 0.016).
There was no difference in the medical treatment according to the gender of the GP. On statins, the LDL target is mostly not reached with 80% of patients with LDL > 0.7 g/L. In hypertensive patients (n = 65), 61% had OMT compared to only 23% in non-hypertensive patients (p < 0.001). Adverse side effects were mainly myalgia (8%) for statins and cough (4%) for ACE or ARBs, there was no gender difference in side effects.
A follow-up visit to a vascular physician occurred in 90% of patients within 2 years (87% for women and 91% for men), 9% within 2–5 years and 1% beyond. ABI was not performed at the last vascular consultation in 25 patients (in 18 revascularized and 7 non-revascularized patients). A check-up with a cardiologist was performed within 2 years in 75% of patients (70.8% women and 76.3% men), 13% within 2–5 years and 12% beyond.

4. Discussion

Fifty percent of patients in the study received OMT, regardless of the severity of the disease but solely 42% for patients with only PAD (excluding patients with a history of CHD and CVD). This is an improvement over the 2003 situation observed in the French ATTEST study using a similar population in primary care (31% of the patients received OMT and 13% of patients with only a PAD, excluding CHD and CVD, out of 3811 patients, recruited from 3020 GPs). This improvement can be explained by the increase in the quality of follow-up, especially for patients with PAD alone, possibly related to the professionalization of vascular medicine in a primary care setting [13]. This improvement mainly concerns male patients. Indeed, this study shows that the proportion of women with PAD (29.2%) who received the optimal medical treatment (antiplatelet or anticoagulant therapy, statin and ACE or ARBs) is lower than that of men (53.9%), especially after age 75. This gender difference has already been found in a larger scale Canadian observational study of PAD in 2010 from a tertiary-care teaching hospital (n = 5962 patients; 18.2% women vs. 22.4% men; p < 0.001).
The study was not designed to determine whether gender difference in OMT had an impact on morbidity. The clinical impact of the gender difference in OMT remains to be studied.
PAD prevalence among women may differ within elderly age groups. As such, a study of demographic data from PAD patients evaluated at a vascular laboratory revealed that women were 3.3 years older than men and made up a larger percentage of the patients aged >65 years (n = 410, 69% women vs. 57% men) [14]. The same trend is observed in the sample presented here, without reaching the significance level, probably because of the smaller sample size (women were 5 years older than men; p = 0.059). A trend already reported in an Italian study in 2008 (n = 231; 2.7 years; p = 0.058) [15].
Antiplatelet therapy was widely prescribed (100%, counting those on anticoagulants), statin prescription (82%) appears to be improving over previous studies (62.2% from the REACH study, n = 5861) in both men (85.5%) and women (70.8%) but the prescription of ACE/ARBs was still suboptimal in both genders (61.9% and 41.7%, men and women respectively).
Non-prescription of statin (28%) appears to be only partially related to the adverse effect (7.8%) and non-prescription of ACE/ARBs (43%) is clearly not secondary to the onset of cough or hyperkalemia (3.7%). The fact could be partially explained by the discrepancies in the latest recommendations, some recommending the prescription of ACE/ARBs for all patients with PAD and others only in case of hypertension [2,3,4,5].
Statins have proven to be effective for patient with PAD in reducing major vascular events (strokes, revascularizations, major coronary events) both in registry studies such as REACH [1] and in randomized studies such as the HPS study [2], regardless of the initial LDL level. AAP also been shown to be effective in reducing major vascular events, notably clopidogrel [3] in patients with PAD. ACE and ARBs also allow a reduction of major vascular events in patients with PAD, regardless of hypertension. In this PAD population, the HOPE study compared the efficacy of ramipril 10 mg vs. placebo in 3577 diabetics and found a significant reduction in major vascular events of 25% in symptomatic patients with PAD [4]. Similarly, the ONTARGET study compared telmisartan 80 mg, ramipril 10 or both, with 1150 patients with PAD in each group and found an identical decrease in major vascular events, with no benefit to the combination [5].
Standardization of international recommendations regarding drug management could probably lead to improved prescribing, particularly with regard to renin-angiotensin-aldosterone system inhibitors.
Smoking is still significant in patients with PAD (31% actives smokers) and smoking cessation remains stable (51%) in comparison with 2003 data from the REACH study (50.9%, n = 5861 patients with PAD).
Another interesting observation is the rate of non-achievement of ABI measurement (25%) at the last consultation with the vascular physician, as part of the annual follow-up for severe disease (72% with a history of revascularization among those who did not have an ABI measurement). This can be explained by the duration of this measure for the vascular physician, its price set by the French health agency (€21), and the imprecision of the measure in some patients. However, performing ABI at each PAD appointment is recommended by international guidelines [2,5].
It is also interesting to note that the percentage of revascularization is particularly high (68%). This is not surprising given the rates of endovascular and surgical revascularization of patients with PAD, which exceed 10% per year in France [16], whereas the data presented here concerns the history of revascularization without time limit.
Among the remaining questions to be clarified was the clinical impact of differential treatment by gender. Anecdotally, non-statin cholesterol-lowering drug was not screen. The most important limitation of this study is its sample size of 100 patients with PAD, which seems low in relation to the incidence of this disease. This is related to the lack of external funding for this study and the need for on-site data collection from each randomized GP. Other limitations are those inherent to retrospective analyses such as selection bias and the presence of unmeasured confounders even if the randomization of GPs tends to limit it. Moreover, this was a Breton population and extrapolation of these results is not possible.

5. Conclusions

Optimal medical treatment of peripheral artery disease is insufficiently prescribed, especially in women in this region of France.

Author Contributions

Conceptualization, D.L., G.S. and G.M.; methodology, D.L. and G.S.; software, D.L. and G.S.; validation, D.L., G.S., G.M. and J.E.T.; formal analysis, D.L. and G.S.; investigation, D.L. and G.S.; resources, D.L. and G.S.; data curation, D.L. and G.S.; writing—original draft preparation, D.L. and G.S.; writing—review and editing, D.L., G.S., J.G. and J.E.T.; visualization, D.L. and G.S.; supervision, D.L. and G.S.; project administration, D.L. and G.S.; funding acquisition, G.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The questionnaire and methodology for this study was declared and registered at the National Institute of Health Data (MR 0711090620).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Acknowledgments

We thank all the general practitioners who made this work possible.

Conflicts of Interest

Guillaume Mahé declares that he has no conflict of interest. Damien Lanéelle declares that he has no conflict of interest. Jean-Eudes Trihan declares that he has no conflict of interest. Gabriella Sauvet declares that he has no conflict of interest. Jérôme Guillaumat declares that he has no conflict of interest.

References

  1. Song, P.; Rudan, D.; Zhu, Y.; Fowkes, F.J.; Rahimi, K.; Fowkes, F.; Rudan, I. Global, regional, and national prevalence and risk factors for peripheral artery disease in 2015: An updated systematic review and analysis. Lancet Glob. Health 2019, 7, e1020–e1030. [Google Scholar] [CrossRef] [Green Version]
  2. Aboyans, V.; Ricco, J.B.; Bartelink, M.L.; Björck, M.; Brodmann, M.; Cohner, T.; Collet, J.P.; Czerny, M.; De Carlo, M.; Debus, S.; et al. 2017 ESC Guidelines on the Diagnosis and Treatment of Peripheral Arterial Diseases. Eur Heart J. 2018, 39, 763–816. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Gerhard-Herman, M.D.; Gornik, H.L.; Barrett, C.; Barshes, N.R.; Corriere, M.A.; Drachman, D.E.; Fleisher, L.A.; Fowkes, F.G.R.; Hamburg, N.M.; Kinlay, S.; et al. 2016 AHA/ACC Guideline on the Management of Patients With Lower Extremity Peripheral Artery Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J. Am. Coll. Cardiol. 2017, 69, 1465–1508. [Google Scholar] [CrossRef] [PubMed]
  4. Frank, U.; Nikol, S.; Belch, J.; Boc, V.; Brodmann, M.; Carpentier, P.H.; Chraim, A.; Canning, C.; Dimakakos, E.; Gottsäter, A.; et al. ESVM Guideline on peripheral arterial disease. Vasa 2019, 48 (Suppl. S102), 1–79. [Google Scholar] [CrossRef] [Green Version]
  5. Mahé, G.; Boge, G.; Bura-Rivière, A.; Chakfé, N.; Constans, J.; Goueffic, Y.; Lacroix, P.; Le Hello, C.; Pernod, G.; Perez-Martin, A.; et al. Disparities Between International Guidelines (AHA/ESC/ESVS/ESVM/SVS) Concerning Lower Extremity Arterial Disease: Consensus of the French Society of Vascular Medicine (SFMV) and the French Society for Vascular and Endovascular Surgery (SCVE). Ann. Vasc. Surg. 2021, 72, 1–56. [Google Scholar] [CrossRef]
  6. Hirsch, A.T.; Allison, M.A.; Gomes, A.S.; Corriere, M.A.; Duval, S.; Ershow, A.G.; Hiatt, W.R.; Karas, R.H.; Lovell, M.B.; McDermott, M.M.; et al. A call to action: Women and peripheral artery disease: A scientific statement from the American Heart Association. Circulation 2012, 125, 1449–1472. [Google Scholar] [CrossRef] [Green Version]
  7. Higgins, J.P.; Higgins, J.A. Epidemiology of peripheral arterial disease in women. J. Epidemiol. 2003, 13, 1–14. [Google Scholar] [CrossRef] [PubMed]
  8. Parvar, S.L.; Thiyagarajah, A.; Nerlekar, N.; King, P.; Nicholls, S.J. A systematic review and meta-analysis of gender differences in long-term mortality and cardiovascular events in peripheral artery disease. J. Vasc. Surg. 2020, 3, 1456–1465. [Google Scholar] [CrossRef] [PubMed]
  9. Paul, N.; Vuddanda, V.; Mujib, M.; Aronow, W.S. Advances in our understanding of the influence of gender on patient outcomes with peripheral arterial disease co-occurring with diabetes. Expert Rev. Endocrinol. Metab. 2016, 11, 271–279. [Google Scholar] [CrossRef] [PubMed]
  10. McDermott, M.M.; Greenland, P.; Liu, K.; Criqui, M.H.; Guralnik, J.M.; Celic, L.; Chan, C. Sex differences in peripheral arterial disease: Leg symptoms and physical functioning. J. Am. Geriatr. Soc. 2003, 51, 222–228. [Google Scholar] [CrossRef] [PubMed]
  11. Garcia, M.; Mulvagh, S.L.; Bairey Merz, C.N.; Buring, J.E.; Manson, J.E. Cardiovascular Disease in Women: Clinical Perspectives. Circ. Res. 2016, 118, 1273–1293. [Google Scholar] [CrossRef] [PubMed]
  12. Pâquet, M.; Pilon, D.; Tétrault, J.-P.; Carrier, N. Protective vascular treatment of patients with peripheral arterial disease: Guideline adherence according to year, age and gender. Can. J. Public Health 2010, 101, 96–100. [Google Scholar] [CrossRef] [PubMed]
  13. Heiss, C.; Madaric, J.; Belch, J.; Brodmann, M.; Mazzolai, L. The compelling arguments for the need of medical vascular physicians in Europe. Vasa 2019, 48, 487–491. [Google Scholar] [CrossRef] [PubMed]
  14. Feinglass, J.; McDermott, M.M.; Foroohar, M.; Pearce, W.H. Gender differences in interventional management of peripheral vascular disease: Evidence from a blood flow laboratory population. Ann. Vasc. Surg. 1994, 8, 343–349. [Google Scholar] [CrossRef] [PubMed]
  15. Brevetti, G.; Bucur, R.; Balbarini, A.; Melillo, E.; Novo, S.; Muratori, I.; Chiariello, M. Women and peripheral arterial disease: Same disease, different issues. J. Cardiovasc. Med. 2008, 9, 382–388. [Google Scholar] [CrossRef] [PubMed]
  16. Riviere, A.B.; Bouée, S.; Laurendeau, C.; Torreton, E.; Gourmelen, J.; Thomas-Delecourt, F. Outcomes and management costs of peripheral arterial disease in France. J. Vasc. Surg. 2018, 67, 1834–1843. [Google Scholar] [CrossRef] [PubMed]
Table 1. Baseline characteristics of the 100 patients with lower extremity peripheral artery disease.
Table 1. Baseline characteristics of the 100 patients with lower extremity peripheral artery disease.
VariablesValue (n = 100)
Female sex24%
Age, years (mean ± SD)71 ± 10
Body-mass index
≥30 kg/m221%
25 to 30 kg/m238%
Body-mass index, kg/m2 (mean ± SD)27 ± 5
Risk factors
Diabetes26%
Hypertension65%
Low-density lipoprotein cholesterol, g/L (mean ± SD)1.03 ± 0.35
Active smoking31%
Past smoking 51%
History of vascular disease
Coronary Heart Disease32%
Cerebrovascular Disease14%
Chronic kidney Disease Stage
Stage 4 (GFR < 30 mL/min/1.73 m²)1%
Stage 3 (GFR 30 to 59 mL/min/1.73 m²)18%
Stage 2 (GFR 60 to 89 mL/min/1.73 m²)44%
Stage 1 (GFR > 89 mL/min/1.73 m²)37%
GFR, mL/min/1.73 m² (mean ± SD)80.8 ± 21.8
ABI
≤0.9051%
0.91 to 0.995%
1.00 to 1.4019%
No data available25%
ABI, no unit (mean ± SD)0.79 ± 0.22
PAD Leriche and Fontaine Classification
Stage 3–417%
Stage 254%
Stage 127%
Surgical treatment
Revascularization68%
Amputation9%
Medical treatment
Antiplatelet agent or anticoagulation100%
Statin82%
ACE/ARBs57%
OMT 48%
SD: Standard Deviation; GFR: Glomerular Filtration Rate; PAD: Peripheral Artery Disease; ABI: Ankle-Brachial Index; ACE: Angiotensin-Converting Enzyme Inhibitor; ARBs: Angiotensin Receptor Blockers. Patients were considered to be past smokers if they achieved at least a 1-year cessation. OMT: Optimal Medical Treatment means antiplatelet agent or anticoagulation + Statin + ACE/ARBs.
Table 2. Gender differences in risk factors, presentation and management of peripheral vascular disease.
Table 2. Gender differences in risk factors, presentation and management of peripheral vascular disease.
VariableWomen (n = 24)Men (n = 76)
Age, years (mean ± SD)74 ± 1069 ± 10
Body-mass index
≥30 kg/m217%22%
25 to 30 kg/m233%40%
Body-mass index, kg/m2 (mean ± SD)25 ± 427 ± 5
Risk factors
Diabetes33%24%
Hypertension75%62%
LDLc, g/L (mean ± SD)1.09 ± 0.361.01 ± 0.34
Active smoking33%30%
Past smoking 37%55%
History of vascular disease
Coronary Heart Disease29%32%
Cerebrovascular Disease4%17%
Chronic kidney Disease Stage
Stage 4 (GFR < 30 mL/min/1.73 m²)0%1%
Stage 3 (GFR 30 to 59 mL/min/1.73 m²)21%17%
Stage 2 (GFR 60 to 89 mL/min/1.73 m²)46%43%
Stage 1 (GFR > 89 mL/min/1.73 m²)33%39%
GFR, mL/min/1.73 m² (mean ± SD)78.04 ± 18.881.68 ± 22.7
ABI
≤0.9065%69%
0.91 to 0.996%7%
1.00 to 1.4029%24%
Not measured24%29%
ABI, no unit (mean ± SD)0.83 ± 0.190.78 ± 0.22
PAD Leriche and Fontaine Classification
Stage 3–417%17%
Stage 252%56%
Stage 130%37%
Surgical treatment
Revascularization67%68%
Amputation4%10%
Medical treatment
Antiplatelet agent or anticoagulation100%100%
Statin71%85%
ACE/ARBs42%62%
OMT 29% *54% *
SD: Standard Deviation; LDLc: Low-density lipoprotein cholesterol; GFR: Glomerular Filtration Rate; PAD: lower extremity peripheral arterial disease; ABI: Ankle-Brachial Index; ACE: Angiotensin-Converting Enzyme Inhibitor; ARBs: Angiotensin Receptor Blockers. Patients were considered to be past smokers if they achieved at least a 1-year cessation. OMT: Optimal Medical Treatment means antiplatelet agent or anticoagulation + Statin + ACE/ARBs. *: p < 0.05.
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MDPI and ACS Style

Lanéelle, D.; Sauvet, G.; Guillaumat, J.; Trihan, J.E.; Mahé, G. Gender Differences in the Medical Treatment of Peripheral Artery Disease. J. Clin. Med. 2021, 10, 2855. https://doi.org/10.3390/jcm10132855

AMA Style

Lanéelle D, Sauvet G, Guillaumat J, Trihan JE, Mahé G. Gender Differences in the Medical Treatment of Peripheral Artery Disease. Journal of Clinical Medicine. 2021; 10(13):2855. https://doi.org/10.3390/jcm10132855

Chicago/Turabian Style

Lanéelle, Damien, Gabriella Sauvet, Jérôme Guillaumat, Jean Eudes Trihan, and Guillaume Mahé. 2021. "Gender Differences in the Medical Treatment of Peripheral Artery Disease" Journal of Clinical Medicine 10, no. 13: 2855. https://doi.org/10.3390/jcm10132855

APA Style

Lanéelle, D., Sauvet, G., Guillaumat, J., Trihan, J. E., & Mahé, G. (2021). Gender Differences in the Medical Treatment of Peripheral Artery Disease. Journal of Clinical Medicine, 10(13), 2855. https://doi.org/10.3390/jcm10132855

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