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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3829_Библиотеки_им_академика_М_И_Перельмана

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6. Pascarella L , Schmid-Schönbein GW , Bergan J . An animal model of
https://t.me/med1917
venous hypertension: e role of in ammation in venous valve fail­ure , J Vasc Surg . 2005 . 41 ( 2 ): 303–311 .
7. Labropoulos N , Leon LR Jr. Duplex evaluation of venous insu ­ciency , Semin Vasc Surg . 2005 . 18 ( 1 ): 59 .
8. Lynch TG , Dalsing MC , Ouriel K , Ricotta JJ , Wake eld TW . Developments in diagnosis and classi cation of venous disor­ders:Non-invasive diagnosis , Cardiovasc Surg . 1999 . 7 ( 2 ): 160–178 .
9. Ballard JL , Bergan JJ , DeLange MD . Venous imaging for re ux using duplex ultrasonography. In: AbuRahma AF , Bergan JJ , eds. Noninvasive vascular diagnosis . London : Springer-Verlag . 2000 . 339–334 .
10. Kistner RL , Eklof B , Masuda EM . Diagnosis of chronic venous dis­ease of the lower extremities: e “CEAP” classi cation , Mayo Clin Proc . 1996 . 71 ( 4 ): 338–345 .
11. Eklof B , Rutherford RB , Bergan JJ , etal. Revision of the CEAP clas­si cation for chronic venous disorders:Consensus statement , J Vasc Surg . 2004 . 40 ( 6 ): 1248–1252 .
12. Coleridge-Smith P , Labropoulos N , Partsch H , Myers K , Nicolaides A , Cavezzi A . Duplex ultrasound investigation of the veins in chronic venous disease of the lower limbs—UIP consensus document. Part I.Basic principles , Eur J Vasc Endovasc Surg . 2006 . 31 ( 1 ): 83–92 . Review.
13. Ruckley CV , Allan PL , Evans CJ , Lee AJ , Fowkes FG . Telangiectasia and venous re ux in the Edinburgh Vein Study , Phlebology . 2012 . 27 ( 6 ): 297–302 .
14. Ruckley CV , Evans CJ , Allan PL , Lee AJ , Fowkes FG . Telangiectasia in the Edinburgh Vein Study: epidemiology and association with trunk varices and symptoms , Eur J Vasc Endovasc Surg . 2008 . 36 ( 6 ): 719–724 .
15. Engelhorn CA , Engelhorn ALV , Cassou MF , Salles-Cunha S . Patterns of saphenous venous re ux in women presenting with lower extremity telangiectasias . Dermatol Surg 2007 . 33 : 282–288 .
16. Uhl JF , Cornu- enard A , Carpentier PH , Widmer MT , Partsch H , Antignani PL . Clinical and hemodynamic signi cance of corona phlebectatica in chronic venous disorders . J Vasc Surg . 2005 . 42 ( 6 ): 1163–1168 .
17. Caggiati A , Bergan JJ , Gloviczki P , Jantet G , Wendell-Smith CP , Partsch H . Nomenclature of the veins of the lower limbs:An inter­national interdisciplinary consensus statement , J Vasc Surg . 2002 . 36 ( 2 ): 416–422 .
18. Labropoulos N , Tiongson J , Pryor L , et al. De nition of venous re ux in lower-extremity veins , J Vasc Surg
19. Phillips GW . Review of venous vascular ultrasound , World J Surg . 2000 . 24 ( 2 ): 241–248 .
20. Masuda EM , Kistner RL , Eklof B . Prospective study of duplex scan­ning for venous re ux:Comparison of Valsalva and pneumatic cu techniques in the reverse Trendelenburg and standing positions , JVasc Surg . 1994 . 20 ( 5 ): 711–720 .
21. Labropoulos N , Giannoukas AD , Delis K , etal. Where does venous re ux start? J Vasc Surg . 1997 . 26 ( 5 ): 736–742 .
. 2003 . 38 ( 4 ): 793–798 .
22. Goldman MP , Fronek A . Anatomy and pathophysiology of varicose veins , J Derm Surg Onc . 1989 . 15 ( 2 ): 138–145 .
23. Scultetus AH , Villavicencio JL , Gillespie DL , Kao TC , Rich NM .  e pelvic venous syndromes:Analysis of our experience with 57 patients , J Vasc Surg. 2002 . 36 ( 5 ): 881–888 .
24. Nascimento AB , Mitchell DG , Holland G . Ovarian veins:Magnetic resonance imaging  ndings in an asymptomatic population , J Magn Reson Imaging . 2002 . 15 ( 5 ): 551–556 .
25. Caggiati A , Bergan JJ , Gloviczki P , Eklof B , Allegra C , Partsch  H . Nomenclature of the veins of the lower limb: Extensions, re nements, and clinical application , J Vasc Surg . 2005 . 41 ( 4 ): 719–724 .
26. Pittaluga P , Réa B , Barbe R , Guex JJ . Méthode ASVAL (ablation selective des varices sous anesthésie locale):Principes et résultats pré­liminaires , Phlebologie . 2005 . 58 ( 2 ): 175–181 .
27. Pittaluga P , Réa B , Barbe R , Guex. In: Becquemin JP , Alimi YS , Watelet J ., eds. Updates and controversies in vascular surgery, A.S.V.A.L. method: Principles and preliminary results . Turin, Italy : Minerva Medica . 2005 . 182–189 .
28. Chastanet S , Pittaluga P . Patterns of re ux in the great saphenous vein system , Phlebology . 2013 . 28 Suppl 1 : 39–46 .
29. Pascarella L, Al-Tuwaijri M , Bergan JJ , etal. Lower extremity super­ cial venous aneurysms , Ann Vasc Surg . 2005 . 19 ( 1 ): 6973 .
30. Georgiev M , Myers KA , Belcaro G .  e thigh extension of the lesser saphenous vein:from Giacomini's observations to ultrasound scan imaging , J Vasc Surg . 2003 . 37 : 558–563 .
31. Sandri JL, Barros FS, Pontes S, Jacques C, Salles-Cunha SX . Diameter-re ux relationship in perforating veins of patients with varicose veins , J Vasc Surg. 30 ( 5 ): 119–199.
32. Yamaki T , Nozaki M , Sasaki K . Color duplex ultrasound in the assessment of primary venous leg ulceration , Dermatol Surg . 1998 . 24 ( 10 ): 1124–1128 .
33. Magnusson MB , Nelzen O , Risberg B , Sivertsson R . A colour Doppler ultrasound study of venous re ux in patients with chronic leg ulcers , Eur J Vasc Endovasc Surg . 2001 . 21 ( 4 ): 353–360 .
34. Bergan JJ , Pascarella L . Severe chronic venous insu ciency:Primary treatment with sclerofoam , Semin Vasc Surg . 2005 . 18 ( 1 ): 4956 .
35. Labropoulos N , Landon P , Jay T .  e impact of duplex scanning in phlebology , Dermatol Surg . 2002 . 28 ( 1 ): 15 .
36. Depalma RG , Kowallek DL , Barcia TC , Ca erata HT . Target selection for surgical intervention in severe chronic venous insuf­ ciency:Comparison of duplex scanning and phlebography , J Vasc Surg . 2000 . 32 ( 5 ): 913–920 .
37. Yamaki T , Sasaki K , Nozaki M . Preoperative duplex-derived param­eters and angioscopic evidence of valvular incompetence associ­ated with super cial venous insu ciency , J Endovasc  er . 2002 . 9 ( 2 ): 229–233 .
38. Mekenas L , Bergan J . Venous re ux examination: Technique using miniaturized ultrasound scanning , J Vasc Tech . 2002 . 2 ( 26 ): 139–146 .
148 • PRIMARY SUPERFICIAL VENOUS INSUFFICIENCY
18.
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SCLEROTHERAPY AND ULTRASOUNDGUIDED
SCLEROTHERAPY
P a u l K .  i b a u l t
S C L E R O T H E R A P Y
Varicose veins are a degenerative disease of the venous sys­tem where there is a defect in the strength of the vein wall with associated valvular dysfunction resulting in re ux (reverse)  ow in a ected areas of the super cial venous sys­tem of the legs. Usually re ux from the deep to super cial system through incompetent venous junctions and perfo­rator veins is a major contributor to the super cial venous insu ciency. As venous disease is a chronic disease, treat­ment is usually directed at controlling the disease, rather than curing it. It is therefore important that interventional treatment not aggravate the condition in the longterm.
Sclerotherapy refers to a method of treating varicose veins:a foreign substance, usually a chemical, is introduced into the lumen of a vein to cause endothelial necrosis and subsequent  brosis of the vein. Apart from reducing the size of the vein to a small  brous cord, e ective sclerotherapy also eliminates the physiopathological re ux associated with varicose veins. As such, sclerotherapy is an alternative treatment to surgery and other physical endovenous abla­tion techniques such as endovenous laser ablation (EVLA) in the management of varicose veins. Sclerotherapy di ers from the other ablative techniques in that it can be e ective treatment for all types of pathological venous dilatations from major truncal varicose veins to the  nest telangiectases.
Sclerotherapy for varicose veins associated with great saphenous vein (GSV) and small saphenous vein (SSV) incompetence has been traditionally relegated to treating residual varicose veins following surgical stripping or vari­cose veins associated with isolated perforator vein incom­petence. of the Fegan method of sclerotherapy in the 1960s and early 1970s, surgical methods have generally been accepted as having a signi cantly better long-term recurrence rate com­pared to sclerotherapy.  is has been thought to be due to the fact that traditional sclerotherapy was unable to control the proximal source of re ux—usually the saphenofemoral
1
Apart from a relatively brief period of popularity
(SFJ) and saphenopopliteal (SPJ) junctions—adequately. In addition, preultrasound methods of sclerosing the GSV have been shown to be relatively ine ective. Some meth-
2
ods such as the Cloutier technique
administered a single, “blind” injection of a major sclerosing agent a few centi­meters below the SFJ, repeated every 7 to 21 days until the GSV was occluded. Such methods have been openly discouraged as creditable methods of treating GSV or SSV incompetence as they were thought to have an inherently high risk of damaging the deep venous system or of inadver­tent intra-arterial injection.
Duplex ultrasound has become the gold standard in the investigation of lower limb venous disease. As an indepen­dent investigation, duplex scanning has unrivaled relevance in the clinical decision-making process as well as being used in the serial assessment of disease progress and e ectiveness
3
of treatment.
Ultrasound guidance of sclerosant injec­tions is a logical extension of the pretreatment evaluation and gives sclerotherapy the potential to rival other ablative methods in e ectiveness in the treatment of varicoseveins.
HISTORY OF ULTRASOUNDGUIDED
SCLEROTHERAPYUGS
 e method of ultrasonic guidance of injection into the super cial venous system was  rst published in 1989.  e method was initially used for treatment of incompe­tent saphenous axes, and in 1992 the method of injecting incompetent perforating veins associated with postsurgical
5
recurrences was described.
Medium-term results of SFJ
incompetence treated by UGS were reported by Kanter
6
and  ibault in 1996.
In the late 1990s, several practitio­ners around the world began using sclerosant foam injected using ultrasound guidance, and the  rst medium-term
7
results were reported by Cabrera in 2000.
Since that time
UGS using microfoamed sclerosants (UGFS) has become
8
the accepted method ofUGS.
4
149
PRETREATMENT ULTRASOUND
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MAPPING
Duplex venous scanning is the essential pretreatment inves­tigation prior to either sclerotherapy or ultrasound-guided sclerotherapy of major varicose veins and truncal incompe-
3
 rough duplex scanning, patterns of venous incom-
tence. petence will be found to be extremely variable and o en unexpected. Duplex scanning involves B-mode imaging of the deep and super cial veins combined with directional pulsed Doppler assessment of blood  ow. Color-duplex imaging superimposes blood  ow information onto the B-mode ultrasound image, permitting visual assessment of blood  ow while at the same time creating an anatomical map of the venous anatomy.  e details of venous duplex examination have been described in a previous chapter and will not be dealt withhere.
In short, duplex examination is able to provide an accu­rate anatomical and physiological map of super cial and deep venous incompetence and localize points of re ux from the deep to super cial venous system. With duplex examination a detailed map of re ux paths in the super cial system, from the proximal origin of the re ux (usually from the deep system), to a distal reentry point, can be created.  is map will allow optimal decisions regarding sclerother­apy intervention and will ensure that all signi cant areas of re ux are addressed by treatment and, conversely, that all normal veins are preserved. Diameters of major veins and junctions are also recorded during the duplex examination.  ese measurements may in uence various parameters of the treatment process including selection of sclerosing agent and form, and postsclerotherapy compression.
Following the duplex examination, the treatment pro­cess is then directed toward eliminating all the incom­petent super cial pathways mapped out with duplex ultrasound and then, in the posttreatment phase, reex­amining with duplex to ensure that the re ux pathways have not recanalized prior to complete  brosis of the vein, which usually occurs between 6 to 12months following initial treatment.
TECHNIQUESOFUGS
SCLEROSINGAGENTS
Generally, only relatively strong sclerosants are used in
9
UGS. In an international survey
of forty-four phlebologists who were known to use UGS extensively, 95% used sodium tetradecyl sulfate (STS; Fibrovein; STD Pharmaceuticals, Hereford, England), and 5% used 3% polidocanol (POL; Aethoxysclerol; Kreusler Pharma, Wiesbaden, Germany). Asmall minority of phlebolog ists used polyiodinated iodine as an alternative solution in particular circumstances, such
Table18.1 APPROXIMATE EQUIVALENT CONCENTRATIONS OF STS AND POL REQUIRED FOR EFFECTIVE SCLEROSIS OF INCREASING CALIBER OF LOWER LIMBVEINS.
VEIN
CALIBER
MM
0.1–0.5 0.1 0.25
0.5–1.0 0.15 0.5
1.0–2.0 0.3 1.0
2.0–3.0 0.5 1.5
3.0–5.0 0.75 2.0
5.0–8.0 1.0–3.0 3.0–5.0
STS
CONCENTRATION
%
POL
CONCENTRATION
%
as in the presence of allergy to STS or at deep-to-super cial junctions. With sclerosant concentration, generally 3% STS was used, although some phlebologists use STS in various strengths from 0.75to2%.
In the above survey, 34% of phlebologists used foamed sclerosants, with STS again being the most common agent used as foam. It is likely that the ratio of phlebologists using foam sclerosants compared with solution has increased signi cantly since that survey, as the bene ts of foam have become more widely known.  e use of foam is described in more detail in another chapter.
STS and POL, in both solution and foam formula­tions have been shown to have similar e cacy, toler-
10
ability, and patient satisfaction.
 ere is good evidence
however, that POL is a weaker detergent type of scle-
11
rosant than STS
and higher concentrations are neces­sary to produce complete vascular sclerosis for any given diameter of vein (Table18.1).  is is the most likely rea­son why many phlebologists prefer STS when performing UGS, as in general, larger truncal veins are being treated
8
with this technique.
PATIENT POSITIONING
For treatment of veins on the medial aspect of the leg, patients are placed in the supine position with the treated leg level and externally rotated at the hip.  e knee is usually slightly  exed in order to relax all muscle groups. Ifsmall incompetent veins are being treated, the patient can be placed in the semireclining position in order to dilate the veins, thereby slightly assisting ultrasound visu­alization and subsequent injection. For treatment of veins on the posterior thigh or calf, the patient is positioned in the prone position with the foot supported by a pil-
4
low so that the knee is  exed slightly.
 is positioning is important when injecting the SSV near the popliteal fossa, where the vein will be compressed if the knee is totally extended.
150 • PRIMARY SUPERFICIAL VENOUS INSUFFICIENCY
CLOSED NEEDLE TECHNIQUE
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M a t e r i a l s
 e needle size used can vary from 21 to 25 g.  e most common size used are 25 g 1 1/2inch (0.50mm × 38mm), as these are the smallest diameter needles that are readily visualized by B-mode ultrasound and are long enough to reach most super cial veins from the point of skin penetra­tion. Usually the sclerosant is drawn up into a 2- or 3-ml luer lock syringe. When microfoam is used, the Tessari method
12
will also require the use of 5-ml luer lock syringe to draw up air or other gas to form the microfoam.  e ratio of sclerosant to air may vary from 1:3 (wet foam) to 1:6 (dry
13
foam).
Wet foam tends to have longer duration, but dry foam is a better displacer of blood. Individual practitioners will inevitably vary this ratio depending on their prefer­ences, although Tessari and Cavezzi basing their opinion of
13
physicochemical properties recommend the ratio of1:4.
M e t h o d
 e closed needle technique is the most commonly used method. the syringe containing the sclerosant at all times. Asmall proportion of phlebologists use an open needle technique (needle is removed to determine color/ ow of blood).  e procedure may be performed with the assistance of a vascu­lar sonographer, or with the phlebologist performing both the ultrasound and the injections alone (“solo” technique).
proximal origin of the venous re ux. of practitioners inject more distally then manually “milk” the sclerosant proximally toward the proximal source of re ux using real-time ultrasound monitoring. the  nal objective is to have the total segment of incompe­tent vein, from the proximal re ux point to the distal reen­try point, uniformly  lled with sclerosant foam.  is can be observed with real-time B-mode ultrasound and will be accompanied by vasospasm of the treatedvein.
vein to be injected in transverse view.  e depth of the vein below the skin surface will be noted, as this will determine the angle of approach of the needle.  e injection can then be performed either with the vein viewed in transverse sec­tion or in sagittal or longitudinal section. Approximately 50% of practitioners utilize the transverse approach solely, 33% the longitudinal approach solely, and the remainder use both approaches depending on various technical variables associated with each individual injection. approach is favored by some, especially when performing the procedure “solo” because it appears to be technically easier to cannulate the vein with this method. It is therefore par­ticularly useful when injecting smaller veins less than 3mm in diameter.  e advantages of the longitudinal approach
9
With this technique, the needle is attached to
 e initial injection is usually performed near to the
5
Asmall proportion
14
Either way,
 e sonographer initially will localize the site of the
9
 e transverse
9
are: rst, that the direction of  ow of the sclerosant can be observed and, second, the linear array probes can be used to compress the segment of vein for a length of about 50mm during the injection, thereby allowing better contact of the sclerosant with the vein wall at the injectionsite.
 e imaging frequency of the transducer used may vary from 7.5 to 15 MHz, the lower frequencies are used for deeper-placed subcutaneous veins (>3 cm below the skin) and higher frequencies for more super cial veins. Commonly a 10-MHz transducer is used for its ability to imagine most subcutaneous veins adequately. Most trans­ducers will have an indicator line or light-emitting diode (LED) that will indicate the alignment of the sagittal plane of the transducer. For either approach, the needle is inserted close to the transducer tip and along the sagittal plane of the
5
transducer (Figure18.1).
When the needle pierces the skin, the tip should be visualized by the ultrasound. Adequate amounts of ultrasound gel need to be applied to the skin to obtain optimum visualization.
As the needle is slowly inserted it appears as a re ective straight line angling toward the target vein. It is important to verify early in the procedure that the needle is being intro­duced in the correct sagittal plane of the transducer. When injecting in the transverse section of the vein, the transducer can be moved in small increments to align with the needle. When injecting in the longitudinal section of the vein, the direction of needle may need to be altered in small incre­ments, to align with the sagittal plane of the transducer. For either method, the needle and vein should be imaged simul­taneously at alltimes.
As the needle tip makes contact with the target vein, an indentation will be seen on the vein wall (Figure18.2). At
Figure18.1  e needle is aligned directly along the longitudinal axis of the ultrasound probe prior to piercing theskin.
SCLEROTHERAPY AND ULTRASOUNDGUIDED SCLEROTHERAPY • 151
Skin
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Skin
Needle tip
Vein lumen
Figure18.2 B-mode ultrasound image of needle tip indenting vein wall immediately prior to vein puncture.
this stage a little extra pressure is required to pierce the vein wall and a er this occurs, the needle can be seen within the lumen (Figure18.3) and a small amount of blood is drawn into the needle hub to con rm correct intraluminal posi­tioning of the needle tip. Asmall volume (approx. 0.2 ml) of sclerosant is then injected and should be seen on the ultrasound image to be  owing into the vein (Figure18.4). Extravasation is readily visible on the B-mode image and is manifested as a separation between the vein wall and the perivenous tissues. Should this occur, injection is stopped immediately, and the needle tip is repositioned correctly, or alternatively, the needle withdrawn and reinserted at an appropriate nearby site. When the initial small volume is seen to  ow intraluminally, the remainder of the injection is then completed under continuous ultrasound imaging (Figure18.5).
Sclerosant foam
Needle
Figure18.4 B-mode ultrasound image demonstrating initial bolus of sclerosant foam entering the vein lumen and  owing upstream initially.
When using the longitudinal approach, during injec­tion the direction of  ow of sclerosant can be determined and with a combination probe pressure and digital pressure applied distal or proximal to the injection site, the direction of sclerosant  ow can be modi ed to optimize the localiza­tion of the sclerosant.
 e volume of sclerosant injected at any one site var­ies between practitioners, but usually ranges from 0.25 to
2.0 ml depending on the site and size of the vein. It is the author’s preference to inject smaller quantities at multiple sites rather than larger volumes at one site, as the former technique, while equalizing the sclerosant concentration
15
along the segment of vein,
minimizes the risk of over ow of sclerosant into the deep system through nearby perforat­ing veins that can cause deep and muscular vein sclerosis and possible subsequent deep venous thrombosis(DVT).
Figure18.3 B-mode ultrasound image of needle tip clearly centered in the vein lumen. It is important to verify correct placement of the needle tip by withdrawing a small amount of blood into the hub of the needle prior to injection.
Skin
Vein lumen
Needle tip
Figure18.5 B-mode ultrasound image demonstrating uniform distribution of the sclerosant foam throughout the visualized lumen of the vein in both directions from the injectionpoint.
152 • PRIMARY SUPERFICIAL VENOUS INSUFFICIENCY
Skin
Sclerosant foam within vein lumen
Injection point
When injecting the incompetent GSV or SSV, it is usual
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to place the  rst injection 5 to 10cm distal to the incompe­tent SFJ or SPJ.  e author uses STS 3% or POL 3% micro­foam at a sclerosant:air ratio of 1:3. As the recommended maximum dose of Fibrovein is 4 ml, the maximum micro­foam volume is 16 ml. If a ratio of 1:4 is used, the maximum volume becomes 20 ml.  e maximum volume of POL will vary according to concentration used and patient weight (2mg/kg/d). When using foam the author prefers to draw up 1.5 ml of foam in each syringe (so this becomes the maxi­mum injectate volume), although many practitioners inject
8
2 ml at most sites.
16
Kanter
compared the e ect of 1 ml and 2 ml sclerosant (3% STS) injectate volumes on immediate vasospasm and later clinical outcomes a er UGS. He found that 2-ml injectate volumes were less e ective than 1 ml and did not reduce the number of injections given.  e 2-ml injectate group received twice the volume of sclerosant and therefore some reported transient  u-like symptoms 4 to 6 hours a er treatment. Hence, when injecting solution (rather than foam), it is advisable not to inject more than 1 ml at any one site. When injecting with several centimeters of visible calf perforating veins, it is advisable to inject less than 0.5 ml.
4,15
Injections proceed distally, as previously injected seg­ments are observed to spasm or  ll with foam. Treatment end-point is when all segments of incompetent vein have undergone spasm and become incompressible to probe maneuvers.  e ultrasound transducer can also be used to compress the treated vein in a rhythmical up and down motion as the vein is followed post injection to observe for uniform vasospasm.  e maneuver also has the e ect of uniformly distributing the sclerosant longitudinally and circumferentially along the venous endothelium, thereby accelerating the process of vasospasm.
CATHETER TECHNIQUES
Open Catheter Technique
In the early days of UGS, especially when the procedure was being developed and techniques re ned, there were a num­ber of reports of inadvertent intra-arterial injections that concerned many phlebologists. UGS were  rst introduced to minimize the risk of inadver­tent intra-arterial injection and the resultant extensive tis­sue loss that could occur.  e  rst “open catheter” technique was described by Grondin in 1992. ommended a 20-gauge 44-mm cannula for cannulation of the GSV or SSV 6 to 8cm distal to the SFJ and SPJ, which were thought to be the sites of maximum risk of inadvertent intra-arterial injection. Correct placement of the cannula could be con rmed by aspiration of nonpulsatile venous blood, ultrasound visualization of the cannula tip and  nally, injection of normal saline into the vein prior to sclerosant injection. A er con rmation that the cannula was correctly
5,17
Catheter techniques of
18
 is technique rec-
inserted into the vein, the sclerosant was injected at that site as a bolus in a similar manner to that described above in the “closed” technique.  e technique could be used to treat the remaining distal trunk by recannulating distal to the initial cannulationpoint.
19
Coleridge Smith
has described a modi ed version of the open cannula technique whereby he inserts multiple cannulas or 23-gauge butter y needles into previously ultrasound-mapped varicose veins and incompetent trunks while the patient lies in the supine position.  e limb being treated is then elevated to an angle of 30 degrees to empty the veins prior to injection. A er the sclerosant foam is injected at each site, the progress of foam is monitored by ultrasound as described previously.
Extended Long Line Echosclerotherapy(ELLE)
 e ELLE technique was  rst described by Parsi in 1997 20 and later by Min and Navarro. oped not only to reduce the risk of intra-arterial injection, but also to improve the e ectiveness of UGS especially in the treatment of larger diameter incompetent trunks by improv­ing the delivery of the sclerosant to the venous endothelium.  e method is described in detail by Parsi andLim.
Cannulation
 e entry point for cannulation is selected a er com­pletion of pretreatment mapping of the super cial truncal incompetence.  e ideal entry point will be at the most dis­tal incompetent point of the axial trunk that is to be treated (GSV or SSV). For example, if the SSV is incompetent to the mid calf, the SSV would be cannulated in the mid calf; if the GSV was incompetent to the proximal calf, the GSV would be cannulated just below the knee. In the presence of signi cant perforator incompetence, the cannulation is done distal to the incompetent perforators.  e segment of vein chosen should ideally be straight, and cannulation is easier if super cial segments of vein are chosen.
Cannulation can be performed with or without local anesthesia. If local aesthesia is used, the injection should be performed intradermally and not contain adrenaline so as to avoid causing vasoconstriction of the vein to be cannulated.
Cannula selection and penetration
 e depth and lumen diameter of the selected vein is measured to assist in appropriate cannula selection. Usually 16- to 18-gauge cannulas are used with cannula lengths varying from 4 to7cm.
 e procedure is carried out using aseptic techniques.  e vein is visualized with B-mode ultrasound in the longitu­dinal axis, and the selected entry point is marked on the skin. Atourniquet can be applied proximal to the selected point of entry to facilitate the cannulation. Once local anesthesia is achieved, the vein is cannulated under ultrasound guidance. Successful entry of the cannula into the vein is signaled by
21
 is technique was devel-
22
SCLEROTHERAPY AND ULTRASOUNDGUIDED SCLEROTHERAPY • 153
spontaneous venous return.  e tourniquet is then released
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and the cannula is  ushed with normal saline, which is also visualized with ultrasound, ensuring correct placement.  e cannula is then taped to the skin. Technically, cannulation is usually the most challenging part of this procedure.
Catheterization
 e length of the selected vein is measured to assist in selection of the appropriate catheter.  e selected cath­eter is fed through the cannula (catheter through cannula technique) and introduced into the lumen of the vein and advanced toward the junction under ultrasound guidance. Once the catheter is about 5cm distal to the junction, the guide wire is removed.  e leg is then raised to about 45 degrees to empty the vein as much as possible. It is this maneu­ver that is readily performed with the ELLE technique, but more di cult with the close needle technique, that theoreti­cally will result in better contact of the sclerosant with the venous endothelium with larger truncal veins.  e proximal
22
SFJ/SPJ is then compressed (Cloutier technique)
and the leg is brought back to about 30 degrees while maintaining the compression on the junction.  e sclerosant is then introduced as the catheter is being withdrawn. Parsi and Lim believe that a number of “pulse” injections of approximately
0.8 ml of STS 3% solution is more e ective than continuous and gradual infusion of sclerosant.  is is consistent with the
15
principles of sclerosant distribution described by Guex.
Special attention is given to T junctions with tributar­ies and perforators as the catheter is gradually withdrawn. Extra volume of sclerosant may be required at these escape points to ensure full sclerosis of these openings. Failure to sclerose the escape points may lead to partial recanalization
6
of the vein.
As with the closed needle technique, the end point of the treatment include vasospasm, noncompressibil­ity along the entire length of the treated vein, and absence of any blood  ow in the vein, all con rmed with ultrasound.
 ere are several limitations of the ELLE technique. First, it is not useful in treating complex patterns and tor­tuous postsurgical recurrences. Second, it is technically dif­ cult to treat smaller incompetent veins less than 5mm in diameter owing to di culty in cannulating these veins with the relatively large diameter cannula that is required for the procedure.
UGS FOR RESISTANT TELANGIECTASES
AND TELANGIECTATIC MATTING
Using a high frequency ultrasound imaging transducer,
23
Somjen etal.
have shown that 89% of areas of thigh tel­angiectases have associated incompetent reticular veins identi able. Alarge proportion of these were found to be associated with deeper subcutaneous vein re ux or with per­forating vein re ux. Some of the incompetent reticular veins were invisible from the surface, and these invisible reticular veins can be a cause of treatment failure when using standard
techniques of sclerotherapy. Using high-frequency duplex
24
ultrasound, Forrestal
has also observed incompetent retic­ular veins associated with resistant telangiectases and telangi­ectatic matting. Using ultrasound guidance, these “invisible” veins can be injected with STS 0.5–1% or POL1%.
P O S T S C L E R O T H E R A P Y
COMPRESSION TECHNIQUES
External Compression
Various forms of external compression have been recom­mended following sclerotherapy to varicose veins. Although
25
Fegan
advised 6 weeks of continuous external compres­sion with bandages, this is not generally required with UGS owing to the fact that the principal of the technique is that all proximal sources of re ux are controlled in the initial treatment.
 e reasons for using external compression with UGS relate to increased patient comfort, reduction of symp­tomatic chemical phlebitis, and maintenance of optimal deep venous  ow during the postinjection period. For this reason, the most commonly used compression following treatment is the application of ClassII (25- to 35-mmHg) graduated compression stockings. Generally the stockings are worn during the day for 2 to 3 weeks. Some practitio­ners also advise their patients to wear the stockings at night for the  rst 3 to 4days in order to maintain optimum deep venous  ow in the early postinjection period, thereby mini­mizing the risk of DVT.  e stocking may be removed each day for showering, without any undue adverse e ects.
Internal Compression (Perivenous Compression)
 is novel method has been introduced recently to improve sclerosant contact with the vein wall during the immediate postsclerotherapy period and therefore reduce the incidence of recanalization. perivenous local anesthetic technique for EVLA. With this method, following each injection of the main stem (GSV or SSV ) with sclerosant foam, normal saline or preferably Klein’s tumescent solution ment between the deep and super cial fascia (Figure18.6) at 3 to 5 locations equally spaced along the axial vein in the thigh (GSV ) or calf (SSV). Usually between 20 and 30 ml of tumescent solution is required, or about 5 to 10 ml at each cross-sectional segment.  e injection is performed using ultrasound guidance with a cross-sectional approach using a 25g 1 1/2inch needle.  e e ect is to give greater immedi­ate compression to the vein, thereby decreasing the diameter of the already spasmed vessel by approximately another 50%, resulting in better apposition of the veins walls and more complete contact of the veins wall with the sclerosant.
 e author now uses this method routinely when treat­ing larger axial vessels (GSV and SSV) greater than 3mm in
26
 e technique was developed from the
27
is injected perivenously in the compart-
154 • PRIMARY SUPERFICIAL VENOUS INSUFFICIENCY
Needle
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Fascial envelope
foam in vein
Saline
with standard sclerotherapy methods.  e patient is then reviewed 4–6weeks a er the initial treatment, when repeat ultrasound examination is performed and any intravascular coagula are removed through a small incision using either a 18- to 21-gauge needle or number 11 blade. Generally this procedure can be performed without any anesthesia or with local anesthetic when using the number 11blade.
Further follow-up visits may be scheduled at 3, 6, and 12months to ensure that there has not been recanalization of the treatedvein.
Figure18.6 Post-UGS perivenous compression of GSV with normal saline.
diameter and early experience indicates a reduction in early recurrence and recanalization resulting in less early retreat­ments. In addition further bene ts including reduced inci­dence of transient neurological episodes including migraine and chest tightness are obtained by using this method.
Many sclerotherapists now also use the tumescent com­pression techniques prior to injection of the sclerosant when using the cannula or catheter techniques resulting in improved sclerosis and reduced concentration and volumes of scle­rosant, again resulting in reduced incidence of local adverse e ects. (personal communications Parsi K, CavezziA).
P O S T T R E A T M E N T M E T H O D S A N D
FOLLOWUP.
Immediately a er treatment, patients are advised to walk continuously for 15 to 20 minutes and are then instructed to walk for at least 45 minutes daily.  is signi cantly improves any discomfort, which is generally minimal. Pain requiring treatment following the procedure is unusual and indicates that the patient needs to be reviewed by the phlebologist to ascertain the cause. Walking reduces super cial ambulatory pressures and ensures high  ow in the deep venous system of the leg for a prolonged period at least once perday.
Patients are usually reviewed 1 to 2 weeks following treatment, at which time the venous system is reexam­ined with duplex ultrasound to determine (1) whether the treated veins are incompressible and have no  ow and (2)the patency and  ow in the deepveins.
If a treated segment of vein is found to be partially or completely patent and have persistent re ux, the segment is reinjected using ultrasound guidance.  e phlebologist should be aware that lower concentrations of sclerosant may be necessary, as the vein endothelium will be partially destroyed making the vein more prone to chemical throm­bophlebitis if too strong a concentration isused.
At the  rst post-UGS visit, once proximal closure of the treated veins has been con rmed, residual distal branch varicose veins and telangiectases may be treated
ADVERSE EFFECTSOFUGS
Varcoe 9 performed a survey of forty-four experienced UGS phlebologists from seven countries and reported on their experience with adverse e ects from UGS. In this survey, side e ects were grouped into “minor” or “major” reactions. Minor reactions were phlebitis, pigmentation, edema, pain, minor (asymptomatic) DVT, and minor allergic reaction. Major reactions were major DVT, pulmonary embolus, and severe allergic reaction. In this survey, the incidence of major adverse e ects were all less than 0.1%. Only one phle­bologist reported pulmonary embolus occurring, indicating the low risk of this event. In 20years of performing UGS, the author has not observed any pulmonary emboli follow­ing UGS and only one DVT (a ecting the popliteal vein extending from a sclerosed gastrocnemius perforatingvein).
Several intra-arterial injections were reported early on
4,17
in the history of UGS,
and the incidence reported in the Varcoe survey was 0.01%.  e risk of this event appears to be directly related to the experience and training of the phlebologist in UGS and rarely occurs in skilledhands.
 e most common serious adverse e ect experienced by
the author has been anaphylactoid reactions to the sclerosant
28
 e incidence of anaphylactoid reaction in 2,686
STS. treatment sessions was 0.15%.  is reaction appears to be concentration- and volume-dependent. Interestingly, since the advent of foam this incidence has been greatly reduced.  e author has not observed any anaphylactoid reactions to STS 3% foam in the circa 2000, and Chapman-Smith
29
similarly reports zero incidence of this complication when using STSfoam.
SHORT AND LONGTERM RESULTS
 ere are now are number of studies documenting the e ec­tiveness of UGS. Most of these studies have examined the results of treating GSV incompetence, although there are several now published on SSV incompetence.
G S V I N C O M P E T E N C E
 e  rst reported objective ultrasound results of SFJ and GSV incompetence treated with UGS were those of Kanter
SCLEROTHERAPY AND ULTRASOUNDGUIDED SCLEROTHERAPY • 155
and  ibault. 6 Using STS 3% solution, they reported a 76%
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7
success rate at 24months. Cabrera etal.
followed-up 500 lower limbs with SFJ and GSV incompetence treated with UGS using Lauromacrogol 400 (POL) microfoam. A er 3years, 81% of treated GSVs were obliterated, and 96.5% of super cial branches disappeared.  e obliteration of saphe­nous veins required one treatment in 86%, two in 10.5%, and three in3.5%.
30
Cavezzi and Frullini
in a study of 106 saphenous axes or recurrent postsurgical varices achieved 95% sclerosis at 21 weeks using STS 1% or 3% sclerosant foam.  ere were three completely unsuccessful cases despite three treatment sessions and ten cases of early recanalization (with re ux or retrograde  ow), subsequently successfully retreated withUGS.
31
Myers et al.
reported objective ultrasound results on 100 limbs (seventy-eight GSV and twenty-two SSV) a er 12months using STS or aethoxysclerol according to pref­erence and partly determined by the diameter of the veins. All but one vein treated were less than 10mm in diameter. UGS was successful in the  rst treatment in eighty-six limbs (primary success), but it was necessary to repeat treatment once in eleven and twice in three limbs to give the “second­ary success.” At 1year, the cumulative primary success was 77% and the secondary success rate was 88%. During the same period, thirty-one limbs (twenty-four GSV and seven SSV) were treated surgically (primary treatment) and then with UGS for early recurrence to give a secondary success rate. In this group at 12months cumulative primary success was 71% and the secondary success rate was87%.
29
Chapman-Smith,
by using a regular posttreatment review with weekly ultrasound examinations initially until closure was achieved and therea er periodical reviews and retreatment when recanalizations were detected, was able to achieve a 4% clinical recurrence at 5years with an average of 2.53 treatments in the  rst year. 16.5% of patients then required an average of 2.0 treatments in the second year, and 8% of patients required average of 2.0 treatments in the thirdyear.
Several studies have examined the e ect that various
clinical determinants had on UGS outcomes. Kanter
32
looked at the e ects of age, gender, and vein size. He found that larger doses of STS were required to induce vaso­spasm in older patients, males, and those with larger veins. Regardless of gender and age, larger veins were more likely to recanalize, but were not necessarily associated with clini­cal recurrence. Although older patients and males tended to have larger veins, their recanalization rates were similar to younger patients and females when su ciently higher STS
7
doses were used to induce vasospasm. Barrett etal.
in a study of 115 saphenous veins treated with STS microfoam UGS con rmed a small increase in failure to close the SFJ and SPJ with increasing size of junction diameter (>10mm), but this did not signi cantly alter the results with respect to clearance of visible varicosities and patient satisfaction with results.
33
In a separate study, Barrett et al.
followed 100 ran­domly chosen legs with varicose veins treated by UGS using STS 3% microfoam a er an average of 22.5months (range 20to 26months). An average number of 2.1 treatments were required to close incompetent varicose veins.  irty-one percent of legs required a second treatment at the 3-month follow-up. Such treatments were generally for a small channel in the saphenous trunk, a small feeding vessel or perforator creating the channel, or minor residual varicosities. Success was analyzed from two perspectives:patient satisfaction and clinical and ultrasound assessment.  ere was an extremely high patient satisfaction, with 100% of patients stating that foam UGS had been successful in treating their varicose veins and related symptoms. Clinically, 92% had complete removal of their varicosities, with 5% developing new vari­cosities related generally to perforator incompetence unre­lated to the treated saphenous veins. Duplex examination revealed four saphenous veins with persistent re ux.
34
 ibault
reported the 5-year recurrence rate in thirty- ve limbs with GSV incompetence treated with UGS. Nine limbs (25.7%) had recurrent varicose veins clinically. Ten had persistent re ux at the SFJ, and fourteen limbs (40%) had persistent re ux at the SFJ. Comparing these results with the shorter term studies indicates that there is a slow but steady increase in cumulative recurrence with time, indicating the need for period review and retreat­ment when clinically indicated in this group of patients.
When comparing the results of foam UGS and solu-
tion or liquid sclerotherapy, it appears that foam is mark-
35
edly superior. random control trials.
 is has been demonstrated by at least two
36,37
For this reason, virtually all phle­bologists currently use foam when treating incompetent saphenous trunks.
S S V I N C O M P E T E N C E
Padbury and Benveniste 38 reported patient satisfaction and clinical and sonographic success in a prospective study on   een limbs with SSV incompetence. Primary success was achieved in all patients (SSV injected and obliterated). At 6months,  ve (33%) had minor residual varices. Duplex examination at 6months revealed one limb with a residual patent incompetent SSV.  is patient had a 9-mm vein pre­treatment. Patient satisfaction as gauged by the Aberdeen QoL questionnaire demonstrated an excellent response, with all patients recording a positive improvement.
PERFORATOR VEIN INCOMPETENCE
 e e ectiveness of UGS for incompetent perforator
4
veins (IPVs) was reported by  ibault.
 irty-six patients (thirty-eight limbs) with incompetent perforating veins were treated with UGS using STS 3% solution.  e IPVs were classi ed according to anatomical location as thigh ( n =12), gastrocnemius ( n =13) or posterior tibial
156 • PRIMARY SUPERFICIAL VENOUS INSUFFICIENCY
( n =18). Two thigh IPVs, three posterior tibial IPVs, and
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one gastrocnemius IPV required repeat injection at the 6- to 8-week follow-up examination.  e IPVs were then reexam­ined with duplex ultrasound 6months a er treatment. All (100%) the gastrocnemius IPVs remained sclerosed with no  ow at 6months, 83% of the thigh IPVs were sclerosed, and 72% of the posterior tibial IPVs remained occluded with no re ux at 6months.  e di culty of obtaining good long-term results with posterior tibial IPVs probably relates to the high hydrostatic forces present in the distalleg.
MANAGEMENT OF POSTSURGICAL
RECURRENT VARICOSEVEINS
UGS has become the preferred management of postsurgi­cal recurrent varicose veins.  ere are four common sources of re ux associated with recurrence of varicose veins a er surgical ligation and stripping:(1)recurrence of re ux at the SFJ or SPJ because of neovascularization or inadequate ligation; (2) incompetent thigh or calf perforating veins; (3) incompetent gastrocnemius veins; (4) persistent vari­cose tributaries or duplication of the GSV in the thigh, with these medial thigh veins receiving re ux from pelvic tribu-
39
taries.
For obvious technical reasons and to avoid the risks of redo surgery (nerve and lymphatic damage) these sources of recurrent re ux are best treated withUGS.
As with primary varicose veins, there needs to be a thor­ough mapping of the super cial venous re ux and assess­ment of the deep venous system in the leg.  e segments and points of re ux are then methodically treated using real-time ultrasound guidance. Standard sclerotherapy is then used to treat any residual super cial varicosities 1 to 4 weekslater.
MANAGEMENT OF VENOUSULCERS
Foam UGS has been reported to be an e ective method for accelerating healing of venous ulcers associated with super-
40
 cial venous incompetence.
 irteen patients with lower leg ulceration clinically suggestive of venous ulceration were con rmed to have super cial venous incompetence with or without deep venous insu ciency.  e average ulcer dura­tion was 27months (range 3 to 96months).  e thirteen limbs were then treated with foam echosclerotherapy to all areas of super cial venous incompetence detected on duplex scanning. Nine patients had complete healing of their ulcers within 5months of commencing treatment (Figure18.7), two ulcers healed by 12months, and another healed a er 20 months.  e remaining patient’s ulceration was still improving but not fully healed at 14months. Another case study of nine patients with 13 venous ulcers, showed rapid
41
healing of the ulcers just 7days a er treatment.
 e advantage of this approach is that the underlying cause of the ulceration is being addressed, thereby reducing prolonged morbidity and cost of long-term management of
A B
Figure18.7 (A) Chronic venous ulcer a ecting the right leg in a 90-year-old male who had had high ligation and stripping of the GSV 15years previously. Duplex scanning revealed incompetence in the femoral, popliteal, and posterior tibial veins and associated incompetence of a medial thigh perforating vein and recurrent super cial medial thigh and calf veins. (B)Healed venous ulcer 14weeks a er two UGS treatment sessions with STS 3% sclerosant foam to the incompetent thigh perforating vein and recurrent medial thigh and calf veins. Also note the signi cant improvement in general skin condition following treatment.
chronic venous ulceration. UGFS is now used routinely by many phlebologists as a simple, e ective means of healing venous ulcers, but randomized clinical controlled trials are needed to con rm these clinical bene t s .
R E F E R E N C E S
1. Hobbs JT . Surgery and sclerotherapy in the treatment of varicose veins , Arch Surg. 1974. 190 : 793–796.
2. Cloutier G . Sclerose des crosses des saphenes internes et externes avec compression:Nouvelle approche , Phlebologie. 1976. 3 : 227–232 .
3 .  ibault PK . Duplex examination , Dermatol Surg. 1995. 21 : 77–82.
4. Knight RM , Vin F , Zygmunt JA . Ultrasonic guidance of injections into the super cial venous system. In: Davy A , Stemmer R , eds. Phlebologie ’89 . Montrouge, France: John Libbey Eurotext . 1989.
5 .  ibault PK , Lewis WA . Recurrent varicose veins:Part2:Injection
of incompetent perforating veins using ultrasound guidance , J Derm Surg Onc. 1992. 18 : 895–900.
6 . K a n t e r A ,  ibault P . Saphenofemoral junction incompetence
treated by ultrasound-guided sclerotherapy , Dermatol Surg. 1996. 22 : 648–652.
7. Cabrera J , Cabrera J Jr, Garcia-Olmedo MA . Treatment of varicose long saphenous veins with sclerosant in microfoam form:Long-term outcomes , Phlebology. 2000. 15 : 19–23.
8. Barrett JM , Allen B , Ockelford A , Goldman MP . Microfoam ultrasound-guided sclerotherapy treatment for varicose veins in a subgroup with diameters at the junction of 10mm or greater com­pared with a subgroup of less than 10mm , Dermatol Surg. 2004. 30 : 1386–1390.
9. Varcoe PF . Ultrasound guided sclerotherapy:E cacy, adverse events, and dosing:An international survey , ANZ J Phleb. 2003. 7 : 17–24.
10. Rao J , Wildemore JK , Goldman MP . Double-blind prospective comparative trial between foamed and liquid POL and sodium tet­radecyl sulphate in the treatment of varicose and telangiectatic leg veins , Dermatol Surg. 2005. 31 : 631–635.
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