Analýza operacních výkonů na vena saphena magna v Ceské republice a efekt Detralexu pri jejím strippingu
[Analysis of surgical procedures on the vena saphena magna in the Czech Republic and an effect of Detralex during its stripping]
Jazyk čeština Země Česko Médium print
Typ dokumentu klinické zkoušky, anglický abstrakt, časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
16218350
- MeSH
- chronická nemoc MeSH
- diosmin terapeutické užití MeSH
- dospělí MeSH
- fixní kombinace léků MeSH
- hesperidin terapeutické užití MeSH
- kvalita života MeSH
- lidé středního věku MeSH
- lidé MeSH
- měření bolesti MeSH
- mladiství MeSH
- pooperační bolest prevence a kontrola MeSH
- pooperační komplikace MeSH
- vena saphena chirurgie MeSH
- výkony cévní chirurgie MeSH
- žilní insuficience chirurgie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
- klinické zkoušky MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- diosmin MeSH
- fixní kombinace léků MeSH
- hesperidin MeSH
- S 5682 MeSH Prohlížeč
The aim of this clinical study was to compare the degree of postoperative pain (VAS--10 cm, quality of life questionnaire CIVIQ and patient diary) between two groups of patients: patients treated with Detralex 14 days before and 14 days after the stripping of greater saphenous vein (GSV) and patients not treated with Detralex. In addition, the two groups were also compared for the incidence of symptoms associated with chronic venous insufficiency (CVI) (using the VAS scale: edema, tired and heavy legs, cramps, itching sensation), size of hematoma, use of analgesics and overall efficacy of the treatment. Clinical study included 181 patients from 15 medical centers throughout the Czech Republic. High ligation and partial stripping of greater saphenous vein on one lower extremity was performed in all patients (short stripping from groin to knee). Patients were randomly assigned in two groups: patients treated with Detralex (92) and patients not treated with Detralex (89). Patients in the first group were treated with Detralex for the period of 1 month. Degree of pain and patient's health condition were evaluated by the physician during D-14 (14 days prior to the surgery), D7 and D14 (7 and 14 days after the surgery) visits using the 10-cm visual analog scale VAS. The results indicate that Detralex reduced the intensity of postoperative pain, which resulted in decreased consumption of analgesics. Hematoma was smaller in patients already using Detralex 14 days prior to the scheduled stripping procedure. These patients also showed significant improvement of CVI symptoms and the quality of life of patients with CVI. High quality venoactive drugs administered 14 days prior to the surgery improve postoperative course in patients indicated for surgical treatment of varices.