Epidemiology and clinical characteristics of chronic venous disease in Romania

  • Authors:
    • Toni Feodor
    • Sorin Baila
    • Iuliana-Alma Mitea
    • Daciana-Elena Branisteanu
    • Oana Vittos
  • View Affiliations

  • Published online on: December 5, 2018     https://doi.org/10.3892/etm.2018.7059
  • Pages: 1097-1105
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Chronic venous disorder (CVD) is a complex disease, that affects millions of people worldwide, and due to the fact that in its early stages is often overlooked by healthcare providers and ignored by the patient, the assessment of incidence and prevalence of CVD is difficult to be made. The aim of this project was to assess the CVD prevalence, risk factors and clinical characteristics in the adult population in Romania. A cross-sectional survey was carried out in Romania from June 2015 to July 2015, including 185 general practitioners (GPs). Data regarding patient characteristics, risk factors, family medical history, CVD signs and symptoms, C-classification, and pharmacological management of CVD were collected. The study included 7,210 patients, predominantly female (71.0%), with the mean age of 58.2 years. Within the study population, 2,271 (31.5%) patients had already the CVD diagnosis established prior to the study visit, while for 2,664 (36.9%) patients, CVD was diagnosed during the visit, while for the rest of the patients, 2,275 (31.6%), CVD diagnosis was not established prior or during the study visit. Age, female, sex and previous pregnancies were major risk factors for developing CVD. The newly diagnosed CVD rate was 36.9% and the directly calculated CVD prevalence in June-July 2015 was 68.4%, while the indirectly calculated CVD prevalence was 80.7%. CVD is a very common disease, with a prevalence of CVD within the study population in June-July 2015 of 68.4%. The newly diagnosed CVD cases represent 36.9% of patients included in this study, nevertheless both parameters could be underestimated, as long as a significant percentage of patients presenting symptoms, but no CVD signs, were not considered by GPs as CVD cases.

Introduction

Chronic venous disease (CVD) is a common but complex disease and data regarding its prevalence are still underestimated, as long as CVD early signs and symptoms are overlooked by both health-care professionals and patients, nevertheless the CVD is negatively impacting on the patient's quality of life and has a high impact on health-care budgets. The most common CVD manifestations are telangiectasias, reticular or varicose veins, accompanied or not by pain, swelling sensation, leg edema, skin modifications or ulcerations. The exact prevalence of CVD is difficult to be estimated and available results are widely varying from 2 to 56% in male population and from 1 to 60% in female population. These huge differences appear mainly due to the fact that different studies included variable population in terms of age, race, measuring methods and method used to diagnose disease, relaying only on self-reported symptoms or standardized physical examination (1). At the initiative of the International Union of Phlebology, a large-scale international survey named Vein Consult Program (VCP) was carried out in 20 countries. The Vein Consult Program concluded that the worldwide presence of CVD was 83.6% and the study underlined the importance of adequate screening for CVD and training of both general practitioners (GPs) and specialist physicians (2). The main goal of CVD treatment is reducing the symptoms (heaviness, leg pains, oedema and swelling) as well as preventing complications. Along with advice regarding lifestyle changes (e.g., weight loss, practice a sport, wear appropriate heels), patients need medication. The primary options of treatment are micronized purified flavonoid fraction (MPFF) and pentoxifylline, combined, if necessary, with compression (3).

Materials and methods

The study had a multicentre, cross-sectional, observational design and took place in Romania, based on a transversal method. In this study were included adult patients recruited by 185 GPs as investigators, selected in compliance with national regulations, in a randomly manner from Romania's health care system. The recruitment took place in June-July 2015 and each investigator was allowed to include 40 consecutive patients, with the minimum age at inclusion of 18 years. Patients attending for emergency visits were excluded. The total number of patients included was 7,210. After obtaining the patient signed informed consent regarding study participation, the following information was collected: Demographic data, CVD presence and frequency of disease's signs and symptoms, medical history and associated risk factors, the clinical, aetiological, anatomical and pathophysiological (CEAP) clinical stages, and therapeutic management practice.

The observational study was approved by the National Agency for Medicines and Medical Devices (NAMMD) and received positive opinion from the National Bioethics Committee for Medicine and Medical Devices (NBCMMD), number 17 SNI/17 June 2015.

Statistical analysis

Statistical analysis was performed with SPSS version 15 (SPSS Inc., Chicago, IL, USA) and included the following: Descriptive analysis, Chi-square test and ANOVA with post hoc Tukey's test.

The scales variables were reported with mean and standard deviation, and summarize categorical variables using frequencies and percentages. P-value <0.05 was considered to indicate a statistically significant difference.

Results

In total, 7,210 patients were included in the survey, mostly female (71.01%), with a mean age of 58.2±14.5 years. The male population was significantly older than female (P<0.001), while mean body mass index (BMI) value for the total group in the overweight category (27.3±5.005 kg/m2) with no significant sex differences. When the distribution of total study population was analyzed regarding CVD diagnosis the following data were obtained: 2,271 (31.5%) patients had already the CVD diagnosis established prior to the study visit, for 2,664 (36.9%) patients, CVD was diagnosed during the study visit, while for the rest of the patients, 2,275 (31.6%), CVD diagnosis was not established prior or during the study visit. Nevertheless, when data were analyzed regarding signs and symptoms reported either spontaneously by the patient, or as a consequence of physician questions and clinical examination, it was noted a that only 1,394 patients (19.3%) did not report any symptoms or signs suggestive for CVD, while 672 patients (9.3%) presented just symptoms, but no CVD sign, fact that is placing them into CEAP C0s category. Data for the total study population were analyzed regarding CEAP class and the following results were obtained: C0s (9.3%), C1 (21.4%), C2 (15.1%), C3 (21%), C4a (10.4%), C4b (1.1%), C5 (1.6%) and C6 (0.8%) (Table I).

Table I.

Patient characteristics and reporting of CVD symptoms.

Table I.

Patient characteristics and reporting of CVD symptoms.

Total group - descriptive dataFemaleMaleTotalP-value
Age (years)
  N5,1082,0887,196a<0.001
  Mean ± SD57.6±14.73559.5±14.07758.2±14.572
BMI
  N5,1202,0907,2100.682
  Mean ± SD27.3±5.10727.4±4.74627.3±5.005

Age (years)No. of patientsaPercent (%)

<451,34418.7
45–541,09515.2
55–642,20930.7
65–741,58122.0
≥7596713.4
Total7,196100.0

CEAP classificationNo. of patientsPercent (%)

No. of CVD1,39419.3
C0s6729.3
C11,54321.4
C21,09115.1
C31,51221.0
C4a75210.4
C4b761.1
C51131.6
C6570.8

a Data for 14 patients not shown. CVD, chronic venous disorder; BMI, body mass index; CEAP, clinical, aetiological, anatomical and pathophysiological.

Data regarding CVD diagnosis and classification were analyzed and it was observed that for 6 patients (representing 0.08% from the study population) the CVD diagnosis was established, despite of the fact that patients did not present any CVD sign or symptoms. C0s stage was not considered by GP as CVD for 569 patients (7.89% of the study population and 84.7% of the C0s population), while for another 318 patients (4.41% of the study population and 6.18% of the C1-C6 population) presenting both CVD signs and symptoms specific for C1-C6 stages, the CVD diagnosis was not established by GPs.

Patient's CVD symptoms reported data proved a significant sex difference in spontaneous reporting in favor of female population, difference which was partially maintained when data regarding CVD symptomatology were obtained after GPs questions. In addition, a difference was observed between patient spontaneous reporting compared to reporting after GPs questions (28.7 vs. 71.3%) (Table II). For the total group of patients included in the survey, the most common spontaneously reported complains were regarding ‘sensation of heavy legs’ (53.44%), followed by ‘sensation of swelling’ (41.62%) and ‘pain’ (38.96%). The percentage of CVD symptoms reported in response to the questions set by the physician increased as follows: ‘sensation of heavy legs’ (61.30%), followed by ‘sensation of swelling’ (43.68%) and ‘pain’ (47.16%) (Table II).

Table II.

CVD symptoms and signs.

Table II.

CVD symptoms and signs.

Symptoms/signs reporting methodTotal group (n=7,210)% of patientsFemale (%)Male (%)
Direct reporting2,06628.774.125.9
After physicians questions5,14471.369.830.2

Patient spontaneous reporting of health issuesTotal group (n=7,210)Percent (%)

Pain2,80938.96
Sensation of heavy legs3,85353.44
Sensation of swelling3,00141.62
Cramps2,28031.62
Sensation of burning1,44320.01
Telangiectasias2,11229.29
Reticular veins1,14815.92
Varicose veins1,92026.63
Swollen legs96613.40
Skin alterations5667.85
Leg ulcer1051.46
None1,58121.93

Symptoms detected during medical consultation after GPs specific questionsTotal group (n=7,210)Percent (%)

Pain3,40047.16
Sensation of heavy legs4,42061.30
Sensation of swelling3,14943.68
Cramps2,27931.61
Sensation of burning1,74024.13
None1,39419.33

Patient spontaneous reporting of health issuesFemale (n=5,120) (%)Male (n=2,090) (%)P-value

Pain40.335.6<0.001
Sensation of heavy legs58.142.0<0.001
Sensation of swelling46.330.2<0.001
Cramps32.728.9<0.001
Sensation of burning21.017.7<0.001
Telangiectasias34.117.6<0.001
Reticular veins18.010.7<0.001
Varicose veins28.222.7<0.001
Swollen legs14.510.7<0.001
Skin alterations7.68.60.150
Leg ulcer1.22.10.003
No problem18.131.2<0.001

Patient reporting symptoms after physician addressing specific questionsFemale (n=5120) (%)Male (n=2090) (%)P-value

Pain47.845.60.090
Sensation of heavy legs64.952.4<0.001
Sensation of swelling47.534.2<0.001
Cramps31.931.00.481
Sensation of burning24.323.60.529

Patients (50.85%) addressing GPs due to consultation regarding another disease. GPs methodology regarding CVD diagnostic was analyzed and it was noted that only 55.7% of GPs are asking directly questions regarding CVD complains, while only 62.7% are examining all patients. The CVD prevalence directly calculated by GP answers was 68.4%, while the rate of new cases diagnosed with CVD during GPs office visit was 36.9% (Table III).

Table III.

Reason attending GPs office and GPs methodology in establishing CVD diagnosis.

Table III.

Reason attending GPs office and GPs methodology in establishing CVD diagnosis.

Reason of doctor visitNo. of patientsPercent (%)
Medical consult for CVD5898.17
Medical consult for other disease3,66650.85
Periodic check-up2,16029.96
Administrative reason3434.76
Other reason4526.27
Total7,210100.00

GPs methodology to establish CVD diagnosisNo. of patientsPercent (%)

Ask directly all patients about CVD4,01655.7
Ask directly all patients during summer time about CVD3404.7
Ask directly some of the patients about CVD1,68223.3
Ask directly about CVD when I have enough time6489.0
Ask all patients about predisposing jobs2,39133.2
Ask all patients about predisposing jobs during summer time1031.4
Ask some of the patients about predisposing jobs83311.6
Ask about predisposing jobs only when I have time2423.4
Examine all patients4,52362.7
Examine all patients only during summer time2223.1
Examine some of the patients1,28817.9
Examine only when I have time3895.4
Ask directly and examine only when the patient complains6819.4

GPs establishing CVD diagnosis for the patients included in the studyNo. of patientsPercent (%)

No2,27531.6
Yes4,93568.4
Total7,210100.0

GPs establishing CVD diagnosis for the patients included in the studyNo. of patientsPercent (%)

CVD diagnosed prior study visit2,27131.5
CVD diagnosed during study visit (new cases)2,66436.9
CVD diagnosis was not established2,27531.6
Total7,210100.0

[i] CVD, chronic venous disorder; GPs, general practitioners.

When data were cross-checked regarding CVD symptoms reported after GP questions and associated CVD signs, we indirectly calculated the ‘real’ CVD prevalence as 80.7%. Most of the difference between the direct and indirect prevalence calculation comes from the C0s class CVD patients, which were not considered as CVD patients in most of the cases. We identified through indirect calculation a C0s prevalence of 9.3%.

We performed analysis comparing C0s and C1-C6 patients, which proved that patients included in the C1-C6 group were significantly older, with higher BMI, compared to C0s patients (P<0.001). Significant differences were found when patient's answers were analyzed in regards to spontaneous CVD complains or CVD symptoms reported in response to the questions set by the physician. There was a clear predominance of CVD complains within the C1-C6 group (P<0.001), nevertheless even in C0s stage the following patients' spontaneously reported symptoms were registered at high rates: ‘Pain’ (38.7%), ‘sensation of heavy legs’ (41.5%) (Table IV).

Table IV.

Comparison of clinical characteristics of C0s vs. the C1-C6 CVD patients.

Table IV.

Comparison of clinical characteristics of C0s vs. the C1-C6 CVD patients.

CharacteristicsC0s (n=672)C1-C6 (n=5,144)P-value
Age56.7±15.060.2±13.4<0.001
BMI26.4±4.127.9±5.2<0.001
Female (% of patients)6276<0.001

Patient spontaneous reporting of health issuesC0s (n=672) (%)C1-C6 (n=5,144) (%)P-value

Pain38.749.6<0.001
Sensation of heavy legs41.569.5<0.001
Sensation of swelling25.055.1<0.001
Cramps28.740.6<0.001
Sensation of burning18.225.7<0.001
Telangiectasias0.741.0<0.001
Reticular veins0.322.3<0.001
Varicose veins0.337.3<0.001
Swollen legs0.618.7<0.001
Skin modifications0.610.9<0.001
Leg ulcer0.02.0<0.001
No problem0.03.6<0.001

CVD symptoms reported when questioned by physicianC0s (n=672) (%)C1-C6 (n=5,144) (%)P-value

Pain39.055.3<0.001
Sensation of heavy legs36.973.7<0.001
Sensation of swelling19.056.6<0.001
Cramps22.535.3<0.001
Sensation of burning16.725.7<0.001

Average number of reported CVD symptomsC0s (n=672) (%)C1-C6 (n=5,144) (%)P-value

Spontaneously reported by patient1,52±0,832,40±1,36<0.001
Reported by patient when questioned by physician1,34±0,722,47±1,25<0.001

Time when CVD symptoms are most intenseC0s (n=103) (%)C1-C6 (n=4,826) (%)P-value

In the morning1.94.10.271
After standing a long time54.469.7<0.001
In the evening64.165.60.747
During the night14.624.20.024

Frequency of CVD symptomsC0s (n=103) (%)C1-C6 (n=4,826) (%)P-value

Rarely11.78.20.209
Occasionally54.434.1<0.001
Regularly30.144.40.004
All the time2.912.40.004

Risk factorsC0s (n=672) (%)C1-C6 (n=5,144) (%)P-value

Positive CVD family history6.046.3<0.001
Positive CVD family history - relative 1st degree (1 parent)a85.074.50.130
Positive CVD family history - relative 2nd degreea15.017.20.710
Positive CVD family history - relative 3rd degreea2.52.90.871
Smoker4.819.0<0.001
Standing <5 h/day35.044.10.064
Standing 5–10 h/day50.545.60.327
Standing >10 h/day14.610.30.158
Sitting <5 h/day39.850.20.037
Sitting 5–10 h/day46.640.40.208
Sitting >10 h/day13.69.30.144

For women onlyC0s (%)C1-C6 (%)P-value

Previous pregnancy52.867.8<0.001

a Answers available only for 2,424 patients. CVD, chronic venous disorder; BMI, body mass index.

There were significant differences between groups regarding the time when CVD symptoms were most intense: after standing a long time (p<0.001) and during the night (p=0.024), as well as in regards to the frequency of CVD symptoms appearance, occasionally (p<0.001), regularly, respectively all the time (p=0.004) (Table IV). The average number of symptoms is significantly higher in C1-C6 group (P<0.001) (Table IV). Interestingly, within the C0s group, after physician questions, the average number of symptoms decreased compared to the spontaneous reporting (1.34±0.72 vs. 1.52±0.83). The significant differences regarding risk factors were observed for family CVD history, smoker status, previous pregnancy (P<0.001), and sitting <5 h/day as well (Table IV).

We compared the therapeutic management practice between C0s and C1-C6 patients and a significant difference was noted between the groups in regards to addressing GPs office for CVD reason as well as receiving recommendation towards a specialist physician (Table V). All patients diagnosed with CVD (prior or during the visit) received lifestyle advice and the most common prescription of venoactive drug was MPFF (74.6% of treated patients) with a treatment duration of ≥12 weeks (93.5% of treated patients). It is important to mention that only 103 out of 672 C0s patients were in fact diagnosed with CVD and as a consequence only those received treatment. We analyzed the entire CVD group regarding GPs recommendations for a specialist consultation and 42% of CVD patients received such recommendation, most of them being referred to a vascular surgeon (41.7%).

Table V.

Comparison of the therapeutic management in C0s vs. the C1-C6 CVD patients.

Table V.

Comparison of the therapeutic management in C0s vs. the C1-C6 CVD patients.

Medical consultationsC0s (n=672) (%)C1-C6 (n=5,144) (%)P-value
Addressing for CVD consultation0.48.72<0.001
Recommendation for a specialist consultation0.539.8<0.001

CVD diagnosis for this patient

CVD classificationaNoYesTotal

C0s569   103   672
C1-C63184,8265,144

Patient diagnosed with CVD referred to a specialist.N(%)

Yes2,07542.0
No2,86058.0

Preferences for specialist recommendationN(%)

Internal medicine24912.0
Vascular surgery86541.7
Dermatology41319.9
Cardiology27013.0
General surgery371.8
Imagistics21210.2
Other291.4

a Based on registered CVD symptoms and clinical examination. CVD, chronic venous disorder.

Discussion

The study took place in 2015 and the newly diagnosed CVD rate was 36.9% and the reported CVD prevalence in June-July 2015 was 68.4%. These figures do not include all possible CVD patients and, therefore, when we indirectly calculated the CVD prevalence by including patients with concomitant symptoms, and no signs (C0s) and the once not diagnosed with CVD, instead presenting both signs and symptoms we reached a prevalence rate of 80.7%. Indeed, this value of the prevalence rate might be overestimated, due to the fact that some of the symptoms such as night cramps, sensation of heavy legs or restless legs could be caused also by other diseases than CVD and often, it is not possible to make a differential diagnosis, between CVD C0s stage and other diseases, especially in a GP office, were it is usually not possible to perform additional examinations such as duplex-ultrasound, nevertheless it is important to mention that apart of those patients, there were relatively high percentage of patients reporting specific CVD symptoms and some presenting even CVD signs, but GPs considered that CVD suspicion could not be formulated for those patients. Those data are suggestive for the fact that patients are ignoring CVD-related symptoms, while physicians are overlooking them, making early CVD diagnosis and implementation of adequate therapeutic management not to be applied in early disease stages. A similar conclusion regarding adequate screening and additional training for physicians was reached by the Vein Consult Program (2). The percentage of C1-C6 CVD patients was 71.4%, which is higher than in most of the results from other countries, and this might be explained due to the fact that the mean age of patients included in this survey was higher than the one registered for other countries (2,47). In Romania, according to Sponsor's internal unpublished data, in the studies SEPIA (2004), VEIN CONSULT (2009) and Vein PREVENT (2010), the CVD diagnosis rates increased in recent years: +32% (2004), +45% (2009) and 66% (2010). This increase is probably due to trainings and the raised awareness. On the other hand, the number of patients who addressed the physicians in order to ask questions about the CVD is very low and almost unchanged: 9% (2004); 10% (2009) and 9% (2010) and 8.7% in this survey. It is important to continue to support the GPs to evaluate constantly the presence of CVD symptoms and to educate the adult population to address their physician.

This survey measured the prevalence of CVD in a population visiting a GPs office in Romania. Despite randomly choosing sites all over Romania and including consecutive patients addressing the GPs office, the population included in the survey does not exactly represent the average population of Romania. The mean age (58.2 years) of the study population is higher than the median age registered for Romania population (41.1 years) (8). The female predominance (71.0%) is also higher. These differences have influenced the reported prevalence of CVD for Romanian population. In addition, we need to keep in mind that for this observational study the CVD was classified by using only the C (clinical) part of CEAP and classification was done by GPs, which are not routinely using the CEAP classification. This fact could link to a moderate reproducibility of data, as already described in the literature (9). Another important aspect regarding prevalence is the involvement of correct diagnosis of the C0s stage of CVD. Despite the fact that the C0s profile is a globally recognized, data regarding its prevalence are limited. C0s patients are defined as those presenting with one or more CVD-related symptoms, without presenting any clinical signs of the disease during a physical examination. Some indirect calculations of C0s prevalence was made for certain studies as follows: VEINES study (3.8%), Brazilian survey (3.9%), Polish study (13–23%), the San Diego Vein Study (15%) and was directly detected through the Vein Consult Program to be ~20% of the population (10), while a meta-analysis estimated the prevalence as ~20% (11). In the present study we identified through indirect calculation a C0s prevalence of 9.3%. There were significant differences between C0s and C1-C6 CVD patients. As expected, C0s patients were younger, with lower BMI, with less CVD-related symptoms, and overall less treated compared to C1-C6 CVD stages.

An important aspect that needs further investigation, will be the relative low percentage of patients referred to venous specialist (42.0%). Among referrals most of those were towards vascular surgeons (41.7%), regardless of the fact that corresponding CEAP class for those patients would not be indicative for surgery. Only 19.9% of referred patients were directed towards dermatologists. One explanation for this type of referral behavior might be the availability of different venous specialists in certain geographic areas, or GPs intrinsic psychological variables, where GPs who consider disease as serious or are less tolerant regarding unknown details about the proper disease management have a higher referral rate. A similar pattern regarding variations in GPs referral was noted also by other studies, nevertheless a large proportion of it cannot be explained easily (12). All patients diagnosed with CVD (prior or during the visit) received lifestyle advice and within this group of patients the most common prescription of venoactive drug was MPFF (74.6% of treated patients) with a treatment duration of ≥12 weeks (93.5% of treated patients). It is important to mention that only 103 out of 672 C0s patients were in fact diagnosed with CVD and as a consequence only those received treatment.

Whether pharmacological therapy can heal CVD remains unclear, nevertheless there is evidence suggesting a possible effect on leg-ulcer healing (13). Prophylactic use of venoactive drugs might be possible given the anti-inflammatory mechanisms of venoactive drugs, which could suggest that retardation of CVD progression is possible, nevertheless more research is needed in this direction. Available literature data prove that the use of venoactive drugs is safe and economic (14,15). In other literature it is suggested that the use of textile biomaterials in patients with high risks in developing CVD, might be an efficient method of preventing the occurrence of CVD (16). Also, for CVD patients with co-morbidites, mainly diabetes, it is crucial to implement promptly all possible therapeutic methods, if possible by preventing the occurrence of the CVD ulcers, which could become extremely difficult to treat (17). For those patients, the diabetic neuropathy, additional to CVD is negatively impacting the patient's quality of life and those conditions are associated with important health care costs (18).

All healthcare providers should focus on increasing patient treatment adherence, where GPs, venous specialists as well as pharmacists have to deliver correct and complete information that will enable patients to follow correctly the prescribed treatment (19).

In conclusion, CVD is a very common disease, with a prevalence of CVD in Romania within the study population in June-July 2015 of 68.4%. The newly diagnosed CVD cases represent 36.9% of patients included in this study, nevertheless both parameters could be underestimated, as long as a significant percentage of patients presenting symptoms, but no CVD signs were not considered by GPs as CVD cases. Additional training for GPs regarding recognition of CVD in early stages is critical, together with initiation of CVD therapeutic management and referral to venous specialist, mainly in advance disease stages.

Acknowledgements

Not applicable.

Funding

The observational study was funded by Servier (Bucharest, Romania).

Availability of data and materials

The datasets generated and/or analyzed during the present study are not publicly available due to the fact that they belong to Servier, as Sponsor of the study, but are available from the corresponding author on reasonable request, and with prior permission of Servier.

Authors' contributions

TF and SB, DEB contributed to the design of study, acquisition of data and review of the manuscript. IAM contributed to the conception, writing and reviewing of the manuscript. OV contributed to the design, analysis and interpretation of the patient data, writing and reviewing the manuscript. All authors read and approved the final version of manuscript.

Ethics approval and consent to participate

The observational study was approved by the National Bioethics Committee for Medicines and Medical Devices (NBCMMD) with approval no. 17 SNI dated 17 June 2015, and signed written informed consent was obtained from all the patients.

Patient consent for publication

Not applicable.

Competing interests

IAM is an employee of Servier. OV received honoraria for the interpretation of data. The other authors declare that they have no competing interests.

References

1 

Robertson L, Evans C and Fowkes FG: Epidemiology of chronic venous disease. Phlebology. 23:103–111. 2008. View Article : Google Scholar : PubMed/NCBI

2 

Rabe E, Guex JJ, Puskas A, Scuderi A, Fernandez Quesada F and Coordinators VC: VCP Coordinators: Epidemiology of chronic venous disorders in geographically diverse populations: Results from the Vein Consult Program. Int Angiol. 31:105–115. 2012.PubMed/NCBI

3 

Jull A, Waters J and Arroll B: Pentoxifylline for treatment of venous leg ulcers: A systematic review. Lancet. 359:1550–1554. 2002. View Article : Google Scholar : PubMed/NCBI

4 

Jawien A, Grzela T and Ochwat A: Prevalence of chronic venous insufficiency (CVI) in men and women in Poland: Multicenter cross-sectional study in 40095 patients. Phlebology. 18:110–122. 2003. View Article : Google Scholar

5 

Zahariev T, Anastassov V, Girov K, Goranova E, Grozdinski L, Kniajev V and Stankev M: Prevalence of primary chronic venous disease: The Bulgarian experience. Int Angiol. 28:303–310. 2009.PubMed/NCBI

6 

Vlajinac HD, Radak DJ, Marinkovic JM and Maksimovic MZ: Risk factors for chronic venous disease. Phlebology. 27:416–422. 2012. View Article : Google Scholar : PubMed/NCBI

7 

Zolotukhin IA, Seliverstov EI, Shevtsov YN, Avakiants IP, Nikishkov AS, Tatarintsev AM and Kirienko AI: Prevalence and risk factors for chronic venous disease in the general Russian population. Eur J Vasc Endovasc Surg. 54:752–758. 2017. View Article : Google Scholar : PubMed/NCBI

8 

National Institute of Statistics. https://www.indexmundi.com/romania/median_age.htmlMay 29–2018

9 

Sinabulya H, Holmberg A and Blomgren L: Interobserver variability in the assessment of the clinical severity of superficial venous insufficiency. Phlebology. 30:61–65. 2015. View Article : Google Scholar : PubMed/NCBI

10 

Geux JJ, Rabe E, Escotto SI, Escudero JR, Scuderi A and Yowono HS; Vein Consult Program coordinators, : The ‘C0s’ patient: Worldwide results from the Vein Consult Program. Phlebolymphology. 19:182–192. 2012.

11 

Serra R, Andreucci M, De Caridi G, Massara M, Mastroroberto P and de Franciscis S: Functional chronic venous disease: A systematic review. Phlebology. 32:588–592. 2017. View Article : Google Scholar : PubMed/NCBI

12 

O'Donnell CA: Variation in GP referral rates: What can we learn from the literature? Fam Pract. 17:462–471. 2000. View Article : Google Scholar : PubMed/NCBI

13 

Bozkurt B, Rabe E and Sharkawy M: Chronic venous disease and Haemorrhoidal disease: Their management and treatment MASTERCLASS (Lisbon, Portugal, 23rd-24th September 2016). EMJ Dermatol. 5 Suppl 2:2–13. 2017.

14 

Ramelet AA, Boisseau MR, Allegra C, Nicolaides A, Jaeger K, Carpentier P, Cappelli R and Forconi S: Veno-active drugs in the management of chronic venous disease. An international consensus statement: Current medical position, prospective views and final resolution. Clin Hemorheol Microcirc. 33:309–319. 2005.PubMed/NCBI

15 

Nicolaides AN, Allegra C, Bergan J, Bradbury A, Cairols M, Carpentier P, Comerota A, Delis C, Eklof B, Fassiadis N, et al: Management of chronic venous disorders of the lower limbs: Guidelines according to scientific evidence. Int Angiol. 27:1–59. 2008.PubMed/NCBI

16 

Brănișteanu DE, Nichifor M, Dorobăț CM, Brănișteanu DC, Petrariu FD, Molodoi AD, Radu DC and Boda D: Use of textile biomaterials for the topic treatment of chronic venous disease. Rom Biotechnol Lett. 20:10618–10625. 2015.

17 

Nwabudike LC and Tatu AL: Magistral prescription with silver nitrate and Peru Balsam in difficult to heal diabetic foot ulcers. Am J Ther. Jun 13–2017.(Epub ahead of print). View Article : Google Scholar

18 

Căruntu C, Negrei C, Boda D, Constantin C, Căruntu A and Neagu M: Biotechnological advances for diagnosis of peripheral diabetic neuropathy. Rom Biotechnol Lett. 19:9846–9858. 2014.

19 

Ratiu MP, Purcarea I, Popa F, Purcarea VL, Purcarea TV, Lupuleasa D and Boda D: Escaping the economic turn down through performing employees, creative leaders and growth driver capabilities in the Romanian pharmaceutical industry. Farmacia. 59:119–130. 2011.

Related Articles

Journal Cover

February-2019
Volume 17 Issue 2

Print ISSN: 1792-0981
Online ISSN:1792-1015

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Feodor T, Baila S, Mitea I, Branisteanu D and Vittos O: Epidemiology and clinical characteristics of chronic venous disease in Romania. Exp Ther Med 17: 1097-1105, 2019
APA
Feodor, T., Baila, S., Mitea, I., Branisteanu, D., & Vittos, O. (2019). Epidemiology and clinical characteristics of chronic venous disease in Romania. Experimental and Therapeutic Medicine, 17, 1097-1105. https://doi.org/10.3892/etm.2018.7059
MLA
Feodor, T., Baila, S., Mitea, I., Branisteanu, D., Vittos, O."Epidemiology and clinical characteristics of chronic venous disease in Romania". Experimental and Therapeutic Medicine 17.2 (2019): 1097-1105.
Chicago
Feodor, T., Baila, S., Mitea, I., Branisteanu, D., Vittos, O."Epidemiology and clinical characteristics of chronic venous disease in Romania". Experimental and Therapeutic Medicine 17, no. 2 (2019): 1097-1105. https://doi.org/10.3892/etm.2018.7059