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30 Varicose Veins <strong>KCE</strong> Reports 164<br />

5.3.2.1 Liquid sclero<strong>the</strong>rapy versus foam sclero<strong>the</strong>rapy (2 RCTs)<br />

Efficacy<br />

No RCTs measured clinical outcomes (CEAP classification): both RCTs evaluated <strong>the</strong><br />

efficacy of <strong>the</strong> interventions based on <strong>the</strong> results of Doppler-ultrasound.<br />

In <strong>the</strong> first trial from Rabe et al. (2008) elimination of reflux was more successful in <strong>the</strong><br />

foam group (69%) compared with <strong>the</strong> liquid group (27%) (p < 0.0001) 92 at three months.<br />

In <strong>the</strong> second trial from Ouvry et al. (2008), at three weeks post-intervention, similar<br />

efficacy results were seen (85% foam versus 35% liquid; p < 0.001) 90 . At two year<br />

follow-up, <strong>the</strong>se rates had dropped to 12% in <strong>the</strong> liquid group (4 patients) and 53% in<br />

<strong>the</strong> foam group (25 patients) but <strong>the</strong>se results are based on low patient numbers due to<br />

high drop-out rates 90 .<br />

Quality of life and patient satisfaction<br />

Quality of life data was lacking in <strong>the</strong>se trials. Rabe et al. (2008) found that patient<br />

satisfaction was significantly higher in <strong>the</strong> foam group compared with <strong>the</strong> liquid group 92 .<br />

Complications<br />

There was no difference in <strong>the</strong> adverse event data between <strong>the</strong> groups 92 . Adverse<br />

events most commonly <strong>report</strong>ed for sclero<strong>the</strong>rapy included pain, haematoma,<br />

phlebitis/thrombophlebitis and pigmentation or hyperpigmentation.<br />

5.3.2.2 Foam sclero<strong>the</strong>rapy versus surgery (1 RCT)<br />

Efficacy<br />

At 180 day follow-up in <strong>the</strong> foam sclero<strong>the</strong>rapy compared with surgery trial, 90% of<br />

foam sclero<strong>the</strong>rapy patients had saphenous vein obliteration compared with 78% in <strong>the</strong><br />

surgery group with a non-significant difference between <strong>the</strong> two methods 85 .<br />

Complications<br />

There was no difference in <strong>the</strong> adverse event data between <strong>the</strong> groups. The most<br />

frequent complications were suture dehiscence in <strong>the</strong> surgery group and thrombus not<br />

requiring drainage in <strong>the</strong> sclero<strong>the</strong>rapy group 85 .<br />

5.3.3 Summary: Sclero<strong>the</strong>rapy<br />

• The advantage of sclero<strong>the</strong>rapy is that no anaes<strong>the</strong>sia is required;<br />

• The studies provided a follow-up to two years for foam sclero<strong>the</strong>rapy and to<br />

10 years for liquid sclero<strong>the</strong>rapy;<br />

• There is evidence of moderate quality to support a similar efficacy<br />

(occlusion rates) of foam sclero<strong>the</strong>rapy, liquid sclero<strong>the</strong>rapy and surgery<br />

with follow-ups to 2 years but <strong>the</strong>re are few data on clinical efficacy;<br />

• Evidence of low quality suggests that surgery performs better than liquid<br />

sclero<strong>the</strong>rapy at 10 years;<br />

• Adverse events <strong>report</strong>ed for sclero<strong>the</strong>rapy included pain, haematoma,<br />

phlebitis/thrombophlebitis, thrombosis, transient neurological symptoms<br />

and pigmentation.

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