Endovenous ablation with a 940 nm laser for the treatment of great saphenous vein insufficiency: short- to mid-term results
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Interventional Radiology - Original Article
P: 106-110
January 2012

Endovenous ablation with a 940 nm laser for the treatment of great saphenous vein insufficiency: short- to mid-term results

Diagn Interv Radiol 2012;18(1):106-110
1. Departments of Cardiovascular Surgery, Gümüşhane State Hospital, Gümüşhane, Turkey
2. Department of Radiology, Bezmialem Vakıf University School of Medicine, Istanbul, Turkey
3. Departments of Cardiovascular Surgery, Akdeniz University School of Medicine, Antalya, Turkey
4. Departments of Biostatistics, Akdeniz University School of Medicine, Antalya, Turkey
No information available.
No information available
Received Date: 22.03.2011
Accepted Date: 29.03.2011
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ABSTRACT

PURPOSE

We aimed to present the short- to mid-term results of endovenous laser ablation (EVLA) procedures that were used to treat great saphenous vein (GSV) insufficiency.

MATERIALS AND METHODS

This prospective study was conducted between December 2009 and January 2011. A total of 112 incompetent GSVs were treated using EVLA with a 940 nm wavelength laser. Ninety patients were treated for varicose veins with saphenous reflux, including 36 females (40%) and 54 males (60%). These patients' ages ranged from 17 to 79 years (median, 48 years). After the EVLA, the patients were monitored using duplex ultrasonography and were assessed clinically at 1 week and 1, 3, 6, and 12 months after the surgery. The patients were scheduled for a three-day examination after the EVLA to assess the level of pain that each patient was experiencing in each limb.

RESULTS

At the end of a one-year follow-up period, the postprocedural duplex scans revealed a total occlusion of the treated GSVs in 88 (97%) patients and a sub-total occlusion in two (2%) patients. The average modified clinical, etiological, anatomical, and pathological score was significantly decreased at 12 months. The following complications were observed in the present study: hypoesthesia (11%), swelling and induration (5%), skin pigmentation (5%), deep vein thrombosis (1%), erythema (1%), and bleeding (1%). The mean visual analog pain score for the entire procedure was 3.14±1.06.

CONCLUSION

Our short- and mid-term results of the EVLA procedure were satisfactory, and the results of this study reaffirmed the safety and effectiveness of an EVLA using a 940 nm wavelength for the treatment of GSV insufficiency.