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Chapter
https://t.me/med1917
9
Clinical Methods for Sclerotherapy of Varicose Veins
A
Figure 9.42 Case Study 15. A, At presentation, multiple bilateral ulcers.
B, 4 months after treatment with sclerosant microfoam, the varicose veins
are reduced and the ulcers closed.
B
nights, then for 7 days only during daytime. The patient was
evaluated with duplex ultrasound at days 1 and 7 and at
months 1, 3, 6, and 12. No complications occurred. Minor
ecchymosis at the access site for 1 week resolved
spontaneously. Complete sclerosis of the desired segment
occurred. Vein size was 1.2 mm (almost not visible) at 12
months (Fig. 9.41D).
The ultrasound images are from 12 months post treatment:
you may see the epigastric vein patent (Fig. 9.41E) and the GSV
with firm sclerosis and echogenicity similar to surrounding
tissue (a little more dense) (Fig. 9.41F). The femoral vein is
patent.
Case Study 15
Varicose veins and venous ulcers treated with
sclerosant microfoam
DDI Wright, JC Cabrera
Elderly patients with leg ulcers frequently remain uninvestigated
and untreated, as the prospect of surgery in the presence of
open ulcers is discounted and often not acceptable to the
patient. Microfoam sclerotherapy offers an effective and
acceptable alternative in appropriate cases.
A 64-year-old woman presented with bilateral leg ulcers open
for 1 and 2 years (right and left, respectively). She had bilateral
varicose veins which had been severe for in excess of 20 years
(Fig. 9.42A). Previous treatment was confined to compression
and local antiseptics.
Duplex scanning revealed bilateral GSV incompetence from
groin to ankle and incompetent perforating veins near the left
ulcer. The SPJs were competent, but distally both small
saphenous veins were incompetent. The deep venous systems
were normal.
Initial treatment consisted of 19 mL of 1% POL microfoam (1%
POL mf) injected under ultrasound guidance through a
20-gauge cannula into the right GSV and an additional 4 mL
injected directly into varicose veins. Two weeks later, the left
GSV was injected with 15 mL of 1% POL mf in the same
manner, and further injections of 15 mL to the varicose veins
and IPVs were administered. At review 1 month later,
recanalization of the proximal segment of the right GSV was
observed and reinjected with an additional 6 mL of 1% POL mf.
By this visit, all ulcers had healed and the varicose veins were
occluded.
Photographs taken 3 months later show the healed ulcers and
greatly reduced varicose veins (Fig. 9.42B). Two years later,
recanalization of both GSV with narrow lumens was detected,
but the ulcers remained healed. A further 12 mL of 1% POL
mf was injected into recanalized segments. There were no
complications following any of the treatments. At last review 43
months after the first treatment, the ulcers remained healed, no
varicosities were visible, and there was no reflux.
This case illustrates that microfoam sclerotherapy can be a
simple, effective, and durable treatment for patients with
venous hypertension and ulceration caused by superficial vein
and perforator incompetence. Minor recanalization can be
retreated and normal venous function restored.
Case Study 16
Microfoam sclerotherapy in Klippel-Trenaunay Syndrome
(KTS) and a patent foramen ovale (PFO)
P Redondo, G Bastarrika, A Sierra, A Martinez-Cuesta, J Cabrera
A 25-year-old women presented with KTS manifested as
widespread venous varicosities and a segmental port wine stain
affecting the left leg with associated intralesional pain.
Multidectector-row computed tomography (MDCT) revealed
that the aberrant vessels originated from the superficial
venous system with a normal deep venous system. Duplex
ultrasound demonstrated incompetence in the superficial
system. She was then treated with polidocanol microfoam
(POL mf) injected into the marginal, great saphenous, and
peripheral small veins via 20, 23, and 25-guage needles,
respectively, under ultrasound guidance with limb elevation for
15–20 minutes followed by graduated compression with a
Struva 23-mmHg stocking for 7 to 15 days (Medi-Bayreuth,
Bayreuth, Germany). Eight separate treatment sessions over 12
months with injection of 20 to 80 mL of POL mf at 0.25 to 2%
concentration was required. A migraine headache after the
second session resulted in a work-up which demonstrated
bubbles in the middle cerebral artery. Magnetic resonance
imaging at 24 hours showed no evidence of cerebral damage
and all subsequent treatments were without incident.
Examinations 6 months after the final sclerotherapy session with
MDCT revealed significant clinical improvement and reduction
in the number and size of the percutaneously treated aberrant
veins (Fig. 9.43).
274

References
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A
D
Figure 9.43 Case Study 16. Clinical and multidetector-row computed tomography venography images from a 25-year-old women with Klippel-Trénauny
Syndrome. Upper row, initial images; lower row, follow-up images. A and D, Anterior views (left); B and E, lateral views; and C and F, posterior views.
(Extracted and used with permission from Arch Dermatol 145:1147, 2009).
B
E
C
F
References
1. Faxon HH. End results in the injection
treatment of varicose veins. N Engl J
Med 1934;208:357.
2. Goldman MP, Fronek A. Anatomy and
pathophysiology of varicose veins. J
Dermatol Surg Oncol 1989;15:138.
3. Goldman MP, Bennett RG. Treatment
of telangiectasia: a review. J Am Acad
Dermatol 1987;17:167.
4. De Groot WP. Treatment of varicose
veins: modern concepts and methods.
J Dermatol Surg Oncol 1989;15:191.
5. Pittaluga P, Rea B, Barbe R. Méthode
ASVAL (ablation selective des varices
sous anesthesia locale): principes et
resultants preliminaires. Phlebologie
2005;58:175.
6. Tournay R, et al. La sclerose des
varices. 4th ed. Paris: Expansion
Scientifique Francaise; 1985.
7. Heyerdale WW, Stalker LK.
Management of varicose veins of the
lower extremities. Ann Surg
1941;114:1042.
8. Moszkowicz L. Behandlung der
Krampfadern mit Zuckerinjektionen
kombinurt mit Venenligatur. Zentralbl
Chir 1927;54:1732.
9. De Takats G, Quint H. The injection
treatment of varicose veins. Surg
Gynecol Obstet 1930;50:545.
10. Sigg K. Neure Gesichtspunkte zur
Technik der Varizenbehandlung. Ther
Umsch 1949;6:127.
11. Dodd H, Cockett FB. The pathology
and surgery of the veins of the lower
limbs. London: ES Livingstone; 1956.
12. Reid RG, Rothnie NG. Treatment of
varicose veins by compression
sclerotherapy. Br J Surg 1968;55:889.
13. Fegan WC, Fitzgerald DE, Milliken JC.
The results of simultaneous pressure
recordings from the superficial and
deep veins of the leg. Ir J Med Sci
1964;6:363.
14. Quill RD, Fegan WG. Reversibility of
femorosaphenous reflux. Br J Surg
1971;55:389.
15. Schalin L. Arteriovenous communication
localized by thermography and
identified by operative microscopy.
Acta Chir Scand 1981;147:109.
16. Kakkar VV, Howe CT, Flanc C.
Compression sclerotherapy for
varicose veins – a phlebographic
study. Br J Surg 1969;56:620.
17. Zukowski AJ, Nicolaides AN, Szendro
G, et al. Haemodynamic significance
of incompetent calf perforating veins.
Br J Surg 1991;78:625.
18. Tolins SH. Treatment of varicose veins:
an update. Am J Surg 1983;145:248.
19. Doran FSA, White M. A clinical trial
designed to discover if the primary
treatment of varicose veins should be
by Fegan’s method or by operation.
Br J Surg 1975;62:72.
20. Hobbs JT. Surgery and sclerotherapy
in the treatment of varicose veins: a
random trial. Arch Surg 1974;
109:793.
21. Tretbar LL, Pattisson PH. Injection-
275

Chapter
https://t.me/med1917
9
Clinical Methods for Sclerotherapy of Varicose Veins
compression treatment of varicose
veins. Am J Surg 1970;120:539.
22. Sladen JG. Compression sclerotherapy:
preparation, technique, complications,
and results. Am J Surg 1983;146:228.
23. Hobbs JT. A random trial of the
treatment of varicose veins by surgery
and sclerotherapy. In: Hobbs JT,
editor. The treatment of venous
thrombosis. Philadelphia: JB
Lippincott; 1977.
24. Kerner J, Schultz-Ehrenburg U.
Funktionele auswirkungen
unterschiedlicher angriffspunkte bei
der Sklerosierungstherapie. Phlebol
Proktol 1988;17:101.
25. Kerner J, Schultz-Ehrenburg U.
Functional meaning of different
injection levels in the course of
sclerotherapy. Phlebology 1989;4:123.
26. Goldman MP. Rational treatment of
varicose and spider leg veins. In:
Robins P, editor. Surgical gems in
dermatology, vol 2. New York:
Igaku-Shoin Medical; 1991.
27. Hobbs JT. Surgery or sclerotherapy for
varicose veins. In: Superficial and deep
venous diseases of the lower limbs.
Turin: Minerva Medica; 1984.
28. Neglen P. Treatment of varicosities of
saphenous origin: comparison of
ligation, selective excision, and
sclerotherapy. In: Goldman MP, Weiss
RA, Bergan JJ, editors. Varicose veins
and telangiectasias: diagnosis and
treatment. 2nd ed. St Louis: Quality
Medical Publishing; 1999.
29. Bishop CCR, Fronek HS, Froneck A,
et al. Real-time color duplex scanning
after sclerotherapy of the greater
saphenous vein. J Vasc Surg
1991;14:505.
30. Butie A. Experience with injections at
the saphenofemoral junction in the
United States. In: Davy A, Stemmer R,
editors. Phlébologie ’89. Montrouge,
France: John Libbey Eurotext; 1989.
31. Biegeleisen K, Nielsen RD. Failure of
angioscopically guided sclerotherapy
to permanently obliterate greater
saphenous varicosity. Phlebology
1994;9:21.
32. Cooper WM. The treatment of
varicose veins. Ann Surg 1934;99:799.
33. Boyd AM, Robertson DJ. Treatment of
varicose veins: possible danger of
injection of sclerosing fluids. Br Med J
1947;2:452.
34. Raymond-Martimbeau P. Two different
techniques for sclerosing the
incompetent saphenofemoral
junction: a comparative study. J
Dermatol Surg Oncol 1990;16:626.
35. Bassi G. Indikationen und Resultate
der Sklerotherapie bzw Chirurgie in
der Behandlung der Insuffizienzen.
Zbl Phlebol 1965;4:143.
36. Hordegen K, Sigg K. Krosseverodung
der Vena saphena magna:
kasuistischer beitrag zur Technik der
Verodungsinjektion. Phlebol Proktol
1985;14:231.
37. Cloutier G, Zummo M. La sclerose des
crosses avec compression: resultats a
long terme. Phlebologie 1986;39:145.
38. Leu HJ. Zur Therapie der Saphenamagna-Varikosis: Chirurgie oder
Sklerosierung? Praxis 1968;14:491.
39. Avramovic A, Avramovic M. Statistical
evaluation of sclerotherapy of the
long saphenous vein and the
sapheno-femoral junction. In:
Raymond-Martimbeau P, Prescott R,
Zummo M, editors. Phlébologie ’92.
Paris: John Libbey Eurotext; 1992.
40. Schultz-Ehrenburg U, Weindorf N,
Tourbier H. Moderne,
hämodynamisch orientierte
Richtlinien fur die Sklerosierung der
Stamm- und Seitenastvaricosis der V
saphena magna und parva. Phlebol
Proktol 1988;17:83.
41. Raymond-Martimbeau P. Role of
sclerotherapy in greater saphenous
vein incompetence. In: Goldman MP,
Weiss RA, Bergan JJ, editors. Varicose
veins and telangiectasias: diagnosis
and treatment. 2nd ed. St Louis:
Quality Medical Publishing; 1999.
42. Bjordal RI. Circulation patterns in
incompetent perforating veins in the
calf and in the saphenous system in
primary varicose veins. Acta Chir
Scand 1972;138:251.
43. Trempe J. Long-term results of
sclerotherapy and surgical treatment
of the varicose short saphenous vein.
J Dermatol Surg Oncol 1991;17:
597.
44. McAdam WAF, Horrocks JC, de
Dombal FT. Assessment of the results
of surgery for varicose veins. Br J Surg
1976;63:137.
45. Sigg K. Varizen-ulcus cruris und
thrombose. Berlin: Springer-Verlag;
1976.
46. McCaffrey JJ. An approach to the
treatment of varicose veins. Med J
Aust 1969;1:1379.
47. Sigg K. The treatment of varicosities
and accompanying complications.
Angiology 1952;3:355.
48. Kimmonth JB. Discussion on primary
treatment of varicose veins. Proc R Soc
London 1948;41:631.
49. Steinacher J, Kammerhuber F. Weg
und verweildauer eines kontrastmittels
im oberflachlichen Venesystem unter
bedingungender Varicenverodung:
eine studie zur Technik der
Varicenverodung. Zschr Haut-GeschlKrkh 1968;43:369.
50. Heyn G, Waigand J, Tamaschke C.
Flow behaviour of sclerosants in the
treatment of primary varicose veins.
In: Davy A, Stemmer R, editors.
Phlébologie ’89. Montrouge, France:
John Libbey Eurotext; 1989.
51. Meisen V. A lecture on injectiontreatment of varicose veins and their
sequelae (eczema and ulcus cruris),
clinically and experimentally. Acta
Chir Scand 1926;60:435.
52. Foote RR. Varicose veins. St Louis: CV
Mosby; 1949.
53. Thornhill R. Varicose veins and their
treatment by ‘empty vein’ injection.
London: Balliere, Tindall & Cox;
1929.
54. Lufkin H, McPheeters HO.
Pathological studies on injected
varicose veins. Surg Gynecol Obstet
1932;54:511.
55. Orbach EJ. A new approach to the
sclerotherapy of varicose veins.
Angiology 1950;1:302.
56. Fegan WG. Continuous compression
technique of injecting varicose veins.
Lancet 1963;282:109.
57. Foley DP, Forrestal MD. A comparative
evaluation of the empty vein utilizing
duplex ultrasonography. In: RaymondMartimbeau P, Prescott R, Zummo M,
editors. Phlébologie ’92. Paris: John
Libbey Eurotext; 1992.
58. Perchuk E. Injection therapy of
varicose veins: a method of
obliterating huge varicosities with
small doses of sclerosing agent.
Angiology 1974;25:393.
59. Fegan WG. Personal communication,
1990.
60. Orbach EJ. Sclerotherapy of varicose
veins: utilization of an intravenous air
block. Am J Surg 1944;66:362.
61. Wollmann JC. The history of
sclerosing foams. Dermatol Surg
2004;30:694.
62. Guex JJ. Foam sclerotherapy: an
overview of use for primary venous
insufficiency. Semin Vasc Surg
2005;18:25.
63. Guex J-J. Sclerotherapy in venous
disease. In: Davies AH, editor.
Vascular surgery highlights 2003–4.
London: Health Press; 2004. p.
38–44.
64. Monfreux A. Traitement sclérosant des
troncs saphéniens et leurs collaterals
de gros caliber par la méthode MUS.
Phlebologie 1997;50:351.
65. Cabrera J, Garrido JR, Garcia-Olmedo
A. Nuevo metodo de esclerosis enlas
varices tronculares. Pathologica
Vasculares 1995;4:55.
66. Tessari L, Cavezzi A, Frullini A.
Preliminary experience with a new
sclerosing foam in the treatment of
varicose veins. Dermatol Surg
2001;27:58.
67. Hamel-Desnos C, Desnos P,
Wollmann JC, et al. Evaluation of the
efficacy of polidocanol in the form of
foam compared with liquid form in
sclerotherapy of the greater saphenous
vein: initial results. Dermatol Surg
2003;29:1170.
68. Jia X, Mowatt G, Burr JM, et al.
Systematic review of foam
sclerotherapy for varicose veins. Br J
Surg 2007;94:925.
69. Sadoun S. Testing the viscosity and
adherence of the ‘on-site’ made foam
for sclerosing varicose veins. Int
Angiol 2005;24(S1–3):75.
70. Yamaki T, Nozaki M, Iwasaka S.
Comparative study of duplex guided
foam sclerotherapy and duplex guided
liquid sclerotherapy for the treatment
276

of superficial venous insufficiency.
https://t.me/med1917
Dermatol Surg 2004;30:718.
71. Hamel-Desnos C, Allaert FA. Liquid
versus foam sclerotherapy. Phlebology
2009;24:240.
72. Ouvry P, Allaert FA, Desnos P,
Hamel-Desnos C. Efficacy of
polidocanol foam versus liquid in
sclerotherapy of the great saphenous
vein: a multicentre randomised
controlled trial with a 2-year
follow-up. Eur J Vasc Endovasc Surg
2008;36:366.
73. Van Den Bos R, Arends L, Kockaert M,
et al. Endovenous therapies of lower
extremity varicosities: a meta-analysis.
J Vasc Surg 2009;49:230.
74. Kendler M, Wetzig T, Simon JC. Foam
sclerotherapy –a possible option in
therapy of varicose veins. J Dtsch
Dermatol Ges 2007;5:648.
75. Hill D, Hamilton R, Fung T.
Assessment of techniques to reduce
sclerosant foam migration during
ultrasound-guided sclerotherapy of
the great saphenous vein. J Vasc Surg
2008;48:934.
76. Hu, WS. Oxygen transfer in cell
culture bioreactors. Cellular
Bioprocess Technology 2004;1–14.
77. Trigilia TCS. Foam preparation for
sclerotherapy by means of heat
application. Int Angiol 2005;
24(S1–3):70.
78. Frullini A, Cavezzi A. Sclerosing foam
in the treatment of varicose veins and
telangiectases: history and analysis of
safety and complications. Dermatol
Surg 2002;28:11.
79. Redondo P, Cabrera J. Microfoam
treatment of Klippel-Trénaunay
syndrome and vascular malformations.
J Am Acad Dermatol 2008;59:355.
80. Breu FX, Guggenbichler S, Wollmann
JC: 2nd European Consensus Meeting
on Foam Sclerotherapy 2006,
Tegernsee, Germany. Vasa
2008;37(Suppl 71):1.
81. Cavezzi A, Tessari L. Foam
sclerotherapy techniques: different
gases and methods of preparation,
catheter versus direct injection.
Phlebology 2009;24:247.
82. Rao J, Goldman MP. Stability of foam
in sclerotherapy: differences between
sodium tetradecyl sulfate and
polidocanol and the type of connector
used in the double-syringe system
technique. Dermatol Surg 2005;31:19.
83. Peterson JD, Goldman MP. An
investigation on the influence of
various gases and concentrations of
sclerosants in foam stability.
Phlebology 2011 [In Press].
84. Lai SW, Goldman MP. Does the
relative silicone content of different
syringes affect the stability of foam in
sclerotherapy? J Drugs Dermatol
2008;7:399.
85. Hill D. Effect of a 5 micron filter on
CO2 sclerosant foam stability. Int
Angiol 2009;29(S1–3):8.
86. Rush JE, Wright DD. More on
microembolism and foam
sclerotherapy. N Engl J Med 2008,
author reply 657; 359:656.
87. Rabe E, Pannier-Fisher F, Gerlach H, et
al. German Society of Phlebology:
Guidelines for sclerotherapy of
varicose veins (ICD 10: I83.0, I83.1,
I83.2, and I83.9). Dermatol Surg
2004;30:687.
88. Hamel-Desnos C, Ouvry P, Benigni JP,
et al. Comparison of 1% and 3%
polidocanol foam in ultrasound
guided sclerotherapy of the great
saphenous vein: a randomised,
double-blind trial with 2 yearfollow-up: ‘The 3/1 Study’. Eur J Vasc
Endovasc Surg. 2007;34:723.
89. Thibault P. Internal compression
(peri-venous compression) following
ultrasound guided sclerotherapy to the
great and small saphenous veins. Aust
N Z J Phlebol 2005;9:29.
90. 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 10 mm or
greater compared with a subgroup of
less than 10 mm. Dermatol Surg
2004;30:1386.
91. Barrett JM, Allen B, Ockelford A,
Goldman MP. Microfoam ultrasound
guided sclerotherapy of varicose veins
in 100 legs. Dermatol Surg 2004;30:6.
92. Martimbeau PR. A randomized
clinical trial comparing the sclerosing
and side effects of foam vs. liquid
formula for sclerotherapy of primary
varicose veins. Presented at the UIP
World Congress Chapter Meeting. San
Diego, Calif, 2003.
93. Cabrera J, Cabrera J Jr, Garcia-Olmedo
A. Treatment of varicose long
saphenous veins with sclerosant in
microfoam form: long-term outcomes.
Phlebology 2000;15:19.
94. Tessari L. Compression following
trans-catheter foam sclerotherapy.
Presented at the UIP World Congress
Chapter Meeting. San Diego, Calif,
2003.
95. Wright D, et al. Varisolve(r)
polidocanol microfoam compared
with surgery or sclerotherapy in the
management of moderate to severe
varicose veins: European randomized
controlled trial. J Vasc Surg
2006;21:180.
96. Myers KA, Jolley D, Clough A, Kirwan
J. Outcome of ultrasound-guided
sclerotherapy for varicose veins:
medium-term results assessed by
ultrasound surveillance. Eur J Vasc
Endovasc Surg 2007;33:116.
97. Chapman-Smith P, Browne A.
Prospective five-year study of
ultrasound-guided foam sclerotherapy
in the treatment of great saphenous
vein reflux. Phlebology 2009;24:183.
98. Darke SG, Baker SJ. Ultrasoundguided foam sclerotherapy for the
treatment of varicose veins. Br J Surg
2006;93:969.
99. O’Hare JL, Parkin D, Vandenbroeck
CP, Earnshaw JJ. Mid term results of
ultrasound guided foam sclerotherapy
for complicated and uncomplicated
varicose veins. Eur J Vasc Endovasc
Surg 2008;36:109.
100. Ceulen RP, Bullens-Goessens YI,
Pi-van de Venne SJ, et al. Outcomes
and side effects of duplex-guided
sclerotherapy in the treatment of great
saphenous veins with 1% versus 3%
polidocanol foam: results of a
randomized controlled trial with
1-year follow-up. Dermatol Surg
2007;33:276.
101. Ceulen RP, Shadid N, Essers SM, et al.
Outcomes and side effects of
duplex-guided sclerotherapy in the
treatment of great saphenous veins
with 1% versus 3% polidocanol foam:
results of a randomized controlled
trial with 2.5-years follow-up.
Dermatol Surg 2007;33:276.
102. Yamaki T, Nozaki M, Sakurai H, et al.
Multiple small-dose injections can
reduce the passage of sclerosant foam
into deep veins during foam
sclerotherapy for varicose veins. Eur J
Vasc Endovasc Surg 2009;37:343.
103. Gillet JL, Guedes JM, Guex JJ, et al.
Side-effects and complications of
foam sclerotherapy of the great and
small saphenous veins: a controlled
multicentre prospective study
including 1,025 patients. Phlebology
2009;24:131.
104. Morrison N, Neuhardt DL, Rogers CR,
et al. Comparisons of side effects
using air and carbon dioxide foam for
endovenous chemical ablation. J Vasc
Surg 2008;47:830.
105. Neuhardt D, Morrison N, SallesCunha S. Cerebral emboli comparison
detected by transcranial Doppler
during ultrasound-guided
sclerotherapy using CO
foam or air-based foam. Int Angiol
2009;29(S1–3):108.
106. Cabrera J, Redondo P, Becerra A, et al.
Ultrasound-guided injection of
polidocanol microfoam in the
management of venous ulcers. Arch
Dermatol 2004;140:667.
107. Guex JJ, Allaert FA, Gillet JL, Chleir F.
Immediate and midterm
complications of sclerotherapy: report
of a prospective multicenter registry of
12,173 sclerotherapy sessions.
Dermatol Surg 2005;31:123.
108. Besnard S, Capri A, Philippot M, et al.
Vascular distribution of an ultrasound
contrast agent used to simulate
decompression bubbles. Aviat Space
Environ Med 2006;77:846.
109. Ceulen RP, Sommer A, Vernooy K.
Microembolism during foam
sclerotherapy of varicose veins. N Engl
J Med 2008;358:1525.
110. Morrison N, Neuhardt D, Knopf K.
Simultaneous echocardiography with
ultrasound guided foam sclerotherapy.
Int Angiol 2005;24(S1–3):81.
111. Morrison N, Neuhardt DL. Foam
sclerotherapy: cardiac and cerebral
monitoring. Phlebology 2009;24:
2-O2
-based
References
277

Chapter
https://t.me/med1917
9
Clinical Methods for Sclerotherapy of Varicose Veins
278
252.
112. Forlee MV, Grouden M, Moore DJ,
Shanik G. Stroke after varicose vein
foam injection sclerotherapy. J Vasc
Surg 2006;43:162.
113. Bush RG, Derrick M, Manjoney D.
Major neurological events following
foam sclerotherapy. Phlebology
2008;23:189.
114. Raymond-Martimbeau P. Pre-foam
scleotherapy patent foramen ovale
screening. Int Angiol
2007;26(S1–S2):SS12–03.
115. Eckmann D, Kobayashi S, Li M.
Microvascular embolization following
polidocanol microfoam sclerosant
administration. Dermatol Surg
2005;31:636.
116. Guex JJ. Complications and sideeffects of foam sclerotherapy.
Phlebology 2009;24:270.
117. Shadid N, Frank J, Sommer A.
Superficial thrombophlebitis of the
venous dorsal arch of the foot and
deep venous thrombosis after foam
sclerotherapy. Int J Dermatol
2008;47(Suppl 1):29.
118. Kölbel T, Hinchliffe RJ, Lindblad B.
Catheter-directed foam sclerotherapy
of axial saphenous reflux: early results.
Phlebology 2007;22:219.
119. Wilson G. Two cases of infection
complicating foam ultrasound guided
sclerotherapy (UGS). Aust N Z J
Phlebol 2005;9:39.
120. Goldman MP. Sclerotherapy treatment
of varicose and telangiectatic leg veins:
my way and my practice. Int Angiol
2005;24(S1–3):48.
121. Goldman MP. My sclerotherapy
technique for telangiectasias and
reticular veins. Dermatol Surg
2010;36(Suppl 2):967.
122. Yamaki T, Nozaki M, Sakurai H, et al.
Prospective randomized efficacy of
ultrasound-guided foam sclerotherapy
compared with ultrasound-guided
liquid sclerotherapy in the treatment
of symptomatic venous
malformations. J Vasc Surg
2008;47:578.
123. Kalodiki E, Azzam M, Kakkos SK,
et al. Ultrasound-guided foam
sclerotherapy combined with
saphenofemoral ligation versus
surgical treatment of varicose veins:
intermediate results of a randomized
control trial. Phlebology 2008;23:242.
124. King T. Preliminary experience with
concomitant ultrasound-guided foam
sclerotherapy and endovenous laser
ablation: a series of 1000 cases.
Phlebology 2008;23:241.
125. Tejedor C, Guex JJ. Foramen ovale
perméable et sclérothérapie.
Phlébologie 2008;61:319.
126. Wright DD, Gibson KD, Barclay J,
et al. High prevalence of right-to-left
shunt in patients with symptomatic
great saphenous incompetence and
varicose veins. J Vasc Surg
2010;51:104.
127. Handke M, Harloff A, Olschewski M,
et al. Patent foramen ovale and
cryptogenic stroke in older patients.
N Engl J Med 2007;357:2262.
128. Diener HC, Weimar C, Katsarava Z.
Patent foramen ovale: paradoxical
connection to migraine and stroke.
Curr Opin Neurol 2005;18:299.
129. Post MC, Thijs V, Herroelen L, Budts
WI. Closure of a patent foramen ovale
is associated with a decrease in
prevalence of migraine. Neurology
2004;62:1439.
130. Schwerzmann M, Wiher S, Nedeltchev
K, et al. Percutaneous closure of
patent foramen ovale reduces the
frequency of migraine attacks.
Neurology 2004;62:1399.
131. Raymond-Martimbeau P. Transient
adverse events positively associated
with patent foramen ovale after
ultrasound-guided foam sclerotherapy.
Phlebology 2009;24:114.
132. Orbach EJ. Clinical evaluation of a
new technique in the sclerotherapy of
varicose veins. J Int Coll Surg
1948;11:396.
133. Knight RM. Treatment of superficial
venous disease with accurate
sclerotherapy. Proceedings of the
Canadian Society of Phlebology, 1991,
Whistler, British Columbia, Canada.
134. Raymond-Martimbeau P. Advanced
sclerotherapy treatment of varicose
veins with duplex ultrasonographic
guidance. Semin Dermatol
1993;12:123.
135. Knight RM, Vin F, Zygmunt JA.
Ultrasonic guidance of injections into
the superficial system. In: Davy A,
Stemmer R, editors. Phlébologie ‘89.
Montrouge, France: John Libbey
Eurotext; 1989.
136. Misery G, Reinharez D, Ecalard P.
Sclerose sous echographie dans
certaines zones a risques. Phlebologie
1991;44:84.
137. Cornu-Thenard A, Boivin P.
Treatment of varicose veins by
sclerotherapy: an overview. In:
Goldman MP, Weiss RA, Bergan JJ,
editors. Varicose veins and
telangiectasias: diagnosis and
treatment. ed 2. St Louis: Quality
Medical Publishing; 1999.
138. Thibault PK, Lewis WA. Recurrent
varicose veins: Part 2: Injection of
incompetent perforating veins using
ultrasound guidance. J Dermatol Surg
Oncol 1992;18:895.
139. Grondin L, Soriano J.
Echosclerotherapy, a Canadian study.
In: Raymond-Martimbeau P, Prescott
R, Zummo M, editors. Phlébologie
’92. Paris: John Libbey Eurotext;
1992.
140. Parsi K, Lim AC. Extended long line
echosclerotherapy (ELLE). Aust N Z J
Phlebol 2000;4:6.
141. Kanter A, Thibault P. Saphenofemoral
incompetence treated by ultrasoundguided sclerotherapy. Dermatol Surg
1996;22:648.
142. Thibault PK: ‘5 year’ follow-up of
greater saphenous vein incompetence
treated by ultrasound guided
sclerotherapy. Aust N Z J Phlebol
2003;7:5.
143. Oishi AJ, Zietlow SP, Sarr MG.
Erroneous arterial placement of a
central venous catheter. Mayo Clin
Proc 1994;69:287.
144. Grondin L, Raymond-Martimbeau P.
Superficial venous disease disorders.
In: Leclerc JR, editor. Venous
thrombo-embolic disorders.
Philadelphia: Lea & Febiger; 1991.
145. Thibault PK, Lewis WA. Recurrent
varicose veins. Part 1: Evaluation
utilizing duplex venous imaging. J
Dermatol Surg Oncol 1992;18:618.
146. Royle JP. Recurrent varicose veins.
World J Surg 1986;10:944.
147. Doran FSA, Barkat S. The management
of recurrent varicose veins. Ann R Coll
Surg Engl 1981;63:432.
148. de Waard MM, der Kinderen DJ.
Duplex ultrasonography-guided foam
sclerotherapy of incompetent
perforator veins in a patient with
bilateral venous leg ulcers. Dermatol
Surg 2005;31:580.
149. Van Neer PAFA. Perforans varicosis:
treatment of the incompetent
perforating vein is important.
Dermatol Surg 2004;30:754.
150. Schadeck M. Duplex-guided
sclerotherapy of the lesser saphenous
vein. Scope Phlebol Lymphol
2002;1:330.
151. Bullens-Goessens YIJM, Mentink LF,
Nelemans PJ, van Geest AJ, Veraart
JCJM. Ultrasound-guided sclerotherapy
of the insufficient short saphenous
vein. Phlebologie 2004;33:89.
152. Cornu-Thenard A. Sclerotherapy:
Doppler-guided injection. Presented at
the Annual Meeting of the North
American Society of Phlebology,
Maui, Hawaii, February 23, 1994.
153. Cornu-Thenard A, De Cottreau H,
Weiss RA. Sclerotherapy: continuous
wave Doppler-guided injections.
Dermatol Surg 1995;21:867.
154. Van Cleef JF, Desvaux P, Griton P,
Cloarec M. Sclerose de la saphene
externe sous controle endoscopique.
Phlebologie 1991;44:131.
155. Van Cleef JF. Sclerotherapy of the
external saphenous vein under
endoscopic control. Presented at the
World Congress of Phlebology,
Strasbourg, France, 1989.
156. Cavaye DM, White RA, Kopchok GE,
et al. Intravascular ultrasound
imaging: the new standard for
guidance and assessment of
endovascular interventions? J Clin
Laser Med Surg 1992;10:349.
157. Gussenhoven WJ, Essed CE, Lancee
CT. Arterial wall characteristics
determined by intravascular
ultrasound imaging: an in vitro study.
J Am Coll Cardiol 1989;14:947.
158. Mallery JAS, Tobis JM, Griffith J, et al.
Assessment of normal and
atherosclerotic arterial wall thickness

within intravascular ultrasound
https://t.me/med1917
imaging catheter. Am Heart J
1990;119:1392.
159. Nissen SE, Grines CL, Gurley JC, et al.
Application of a new phased-array
ultrasound imaging catheter in the
assessment of vascular dimensions.
Circulation 1990;81:660.
160. Raymond-Martimbeau P. Intravenous
ultrasound in the management of
varicose veins. Phlebology
1995;1(Suppl):326.
161. Raymond-Martimbeau P. Role of
sclerotherapy in greater saphenous
vein incompetence. In: Goldman MP,
Weiss RA, Bergan JJ, editors. Varicose
veins and telangiectasias: diagnosis
and treatment. 2nd ed. St Louis:
Quality Medical Publishing; 1999.
162. Min RJ, Navarro L. Transcatheter
duplex ultrasound-guided
sclerotherapy for treatment of greater
saphenous vein reflux: preliminary
report. Dermatol Surg 2000;26:410.
163. Goldman MP, Weiss RA, Bergan JJ.
Varicose veins and telangiectasias:
diagnosis and treatment. 2nd ed. St
Louis: Quality Medical Publishing;
1999.
164. Sadoun S, Benigni JP, Chahim M,
et al. Multicenter international
prospective study on the side effects
of the sclerosing treatment of the
greater saphenous vein: SESIS study of
the secondary effects of sclerosis of
the internal saphenous vein.
Phlebologie 2000;53:345.
165. Ferrara F, Berbach HR. Sclerotherapy
of the sapheno-femoral junction: a
duplex examination. Acta Phlebol
2002;3:35.
166. Valsamis M. Diameter of the greater
saphenous vein near the
saphenofemoral junction and
response to injection sclerotherapy
treatment. Presented at the UIP World
Congress Chapter Meeting. San Diego.
Calif., 2003.
167. Ninia JG, Goldberg TL. Treatment of
vulvar varicosities by injectioncompression sclerotherapy and a
pelvic supporter. Obst Gynecol
1996;87:786.
168. Ninia JG. Treatment of vulvar
varicosities by injection-compression
sclerotherapy. Dermatol Surg
1997;23:573.
169. Yamaki T, Nozaki M, Sasaki K. Color
duplex-guided sclerotherapy for the
treatment of venous malformations.
Dermatol Surg 2000;26:323.
170. Lee BK, Kim DI, Huh S, et al. New
experiences with absolute ethanol
sclerotherapy in the management of a
complex form of congenital venous
malformation. J Vasc Surg 2001;
33:764.
171. Lee BB, Do YS, Byun HS, Choo IW,
Kim DI, Huh SH. Advanced
management of venous malformations
with ethanol sclerotherapy: mid-term
results. J Vasc Surg 2003;37:533.
172. Cabrera J, Cabrera J Jr, Garcia-Olmedo
A, Redondo P. Treatment of venous
malformations with sclerosant in
microfoam form. Arch Dermatol
2003;139:1409.
173. Ku H-W, Yang C-H. Venous lake of the
lip treated with a sclerosing agent:
report of two cases. Dermatol Surg
2003;29:425.
174. Matsumoto K, Nakanishi H, Koizumi
Y, Seike T, Kanda I, Kubo Y.
Sclerotherapy of hemangioma with
late involution. Dermatol Surg
2003;29:668.
175. Parsi K, Kossard S. Multiple hereditary
glomangiomas: successful treatment
with sclerotherapy. Australas J
Dermatol 2002;43:43.
176. Matsumoto K, Nakanishi H, Seike T,
Koizumi Y, Mihara K, Kubo Y.
Treatment of pyogenic granuloma
with a sclerosing agent. Dermatol Surg
2001;27:521.
177. Moon S, Hwang E, Cho KH.
Treatment of pyogenic granuloma by
sodium tetradecyl sulfate
sclerotherapy. Arch Dermatol
2005;141:644.
178. Perrin MR, Guex J-J, Ruckley CV, et al,
and the REVAS group: Recurrent
varices after surgery, a consensus
document. Cardiovasc Surg
2000;8:233.
179. Keates JS, Fitzgerald DE. Limb volume
and blood flow changes during the
menstrual cycle. Angiology
1969;20:618.
180. Vin F. Principles, technique, and
results of treatment of the greater
saphenous vein by sclerotherapy.
Presented at the second Annual
International Congress of the North
American Society of Phlebology, New
Orleans, February 25, 1989.
181. Merlen JF, Curri SB, Saout J, et al.
Histologic study of a sclerosed vein.
Phlebologie 1978;31:17.
182. Sackmann LA. Etude physique de
l’injection sclerosante. Soc Fr Phlebol
1969;22:149.
183. Green D. Mechanism of action of
sclerotherapy. Semin Dermatol
1993;12:88.
184. Guex J-J. Indications for the sclerosing
agent polidocanol. J Dermatol Surg
Oncol 1993;19:959.
185. Cornu-Thenard A. Sclerotherapy of
varicose veins: value of measurement
of vessel diameter before the first
injection. Presented at the second
Annual International Congress of the
North American Society of
Phlebology, New Orleans, February
25, 1989.
186. Kinmonth JB, Robertson DJ. Injection
treatment of varicose veins:
radiological and histological
investigations of methods. Br J Surg
1949;36:294.
187. Green D. Sclerotherapy for the
permanent eradication of varicose
veins: theoretical and practical
considerations. J Am Acad Dermatol
1998;38:461.
188. Corcos L, et al. Peripheral venous
biopsy: significance, limitations,
indications and clinical applications.
Phlebology 1989;4:271.
189. Stegall HF. Muscle pumping in the
dependent leg. Circ Res 1966;19:
180.
190. Orbach EJ. The importance of removal
of postinjection coagula during the
course of sclerotherapy of varicose
veins. Vasa 1974;3:475.
191. Guex J-J. Les contre indications de la
sclérothérapie en 2005. J Mal Vasc
2005;30:144.
192. Barwin BN, Roddie IC. Venous
distensibility during pregnancy
determined by graded venous
congestion. Am J Obstet Gynecol
1976;125:921.
193. Skudder PA Jr, Farrington DT, Weld E,
Putnam C. Venous dysfunction of late
pregnancy persists after delivery. J
Cardiovasc Surg 1990;31:748.
194. McPheeters HO. Prophylactic injection
treatment of varicose veins during
pregnancy. Lancet 1931;51:589.
195. Kilbourne NJ. Varicose veins of
pregnancy. Am J Obstet Gynecol
1933;25:104.
196. Mullane DJ. Varicose veins of
pregnancy. Am J Obstet Gynecol
1952;63:620.
197. McCausland AM. Varicose veins in
pregnancy. West J Surg 1939;47:81.
198. Fegan G. Varicose veins: compression
therapy. London: Heinemann Medical;
1967.
199. Mantse L. The treatment of varicose
veins with compression sclerotherapy:
technique, containdications,
complications. Am J Cosmetic Surg
1986;3:47.
200. Dodd H, Payling Wright H. Vulval
varicose veins in pregnancy. Br Med J
1959;1:831.
201. Tibbs DJ. Varicose veins and related
disorders. Oxford: ButterworthHeinemann; 1992.
202. Rabe E, et al. Die pudendale varicosis.
Phlebologie 1991;20:222.
203. De Takats G. Ambulatory ligation of
the saphenous vein. JAMA
1930;94:1194.
204. Faxon HH. Treatment of varicosities.
Arch Surg 1934;29:794.
205. Conrad P. Sclerostripping – a ‘new’
procedure for the treatment of
varicose veins. Med J Aust 1975;
2:42.
206. Hubner K. The outpatient therapy of
trunk varicosis of the greater
saphenous vein by means of ligation
and sclerotherapy. J Dermatol Surg
Oncol 1991;17:818.
207. De Groot WP. Practical phlebology:
sclerotherapy of large veins. J
Dermatol Surg Oncol 1991;17:589.
208. Bihari I. Can varicetomy be performed
if deep veins are occluded? J Dermatol
Surg Oncol 1990;16:806.
209. Passas H. One case of tetradecyl-
References
279

Chapter
Distal sclerotherapy and/or Muller’s phlebectomy
Ultrasound-guided foam sclerotherapy
‘Classical’ surgery
https://t.me/med1917
9
sodium sulfate allergy with general
symptoms. Soc Fr Phlebol 1972;25:19.
210. Stroncek DF, Hutton SW, Silvis SE,
et al. Sodium morrhuate stimulates
granulocytes and damages erythrocytes
and endothelial cells: probable
mechanism of an adverse reaction
during sclerotherapy. J Lab Clin Med
1985;106:498.
211. Duffy DM, Garcia C, Clark RE. The
role of sclerotherapy in abnormal
varicose hand veins. Plast Reconstr
212. Duffy DM. Complications of
Chapter 9: Appendix
Schematic principal types of varicose networks, schematic treatments
Surg 1999;104:1474.
sclerotherapy for vessels involving the
hands and face. Aesth Dermatol
Cosmet Surg 1999;1:91.
Clinical Methods for Sclerotherapy of Varicose Veins
Varicose
reservoir
Appendix 9.1
• 1 + 2 = ‘Classical’
• Fill up network through
2 only = ‘new trend’
Source of reflux
Long/high reflux
Source
High reflux
Short reflux
Varicose
reservoir
1
No long/truncal reflux
Appendix 9.2
Crossectomy
Stripping
2
Appendix 9.3
280
Muller
phlebectomy
Appendix 9.4

With preservation
Laser and radio-frequency
ASVAL and peripheral foam therapy
https://t.me/med1917
of junction and
last/upper tributaries
Additional
treatment
of reservoir
required
Secondary
reduction of
short reflux
Varicose reservoir
Ablation/sclero
Source
High reflux
Chapter 9: Appendix
Appendix 9.5
Appendix 9.6
281

10
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C H A P T E R
Role of Surgery in the Treatment of Varicose Veins
Michael Perrin
Background
Surgery for treating varicose veins (VVs) has been advocated
for centuries. The first description is attributed to A.C. Celsus
from the Roman era and consisted of hook extraction of varicose veins, double ligation and phlebectomy. Modern surgery
based on supposed hemodynamic treatment started at the
beginning of the 19th century when T. Rima performed a
high ligation (HL) of the upper great saphenous vein (GSV),
although F. Trendelenburg is usually credited as having been
the first to do it in 1890. Complementary saphenous trunk
stripping came some years later with W.L. Keller in 1905
(internal stripping), C. Mayo in 1906 (external stripping) and
W.W. Babcock in 1907 (flexible stripper). Various alternative
techniques to conventional HL plus trunk stripping were
proposed in the second half of the twentieth century (Van
der Stricht, Muller, Large, Milleret, Franceschi, Lane, Yamaki,
Pittaluga, etc.).
The first to suggest interruption of perforators to treat VVs
was probably Remy in 1901.
Duplex ultrasound (DUS) investigation was the cornerstone to our changing knowledge and attitude in the management of VVs; nevertheless it must be emphasized that there is
presently no consensus regarding the best procedure for the
operative treatment of VVs when taking into account their
various patterns of clinical and hemodynamic presentation.
Basis and Aim of Surgery
In theory, surgery, as with other operative methods (e.g.
thermal and chemical ablation), aims to suppress or reduce
reflux in the standing position (orthostatism) in the incompetent, enlarged and tortuous superficial veins.
In practice the aim is twofold:
• To eliminate reflux originating from the deep venous
system (DVS) into the superficial venous system (SVS) by
suppressing abnormal leak points, which result from calf
pump muscular systolic pressures being higher in the
DVS than in the SVS. In healthy subjects, terminal valves
of the saphenous trunks and perforator valves prevent
reflux from deep into superficial systems. Reflux occurs
when these valves are incompetent.
• To suppress the reflux in the incompetent superficial
veins which are visualized as varices.
The Different Surgical Procedures
Procedures depend on the different concepts of VV disease
progression and evolution as well as on the principles of
hemodynamic anomalies correction, which are currently con-
troversial and are reviewed below. The procedures discussed
can be performed alone or in combination:
• Resection of all the refluxing veins
• Resection of the incompetent ‘reservoir’
• Ligation of the leak points between the DVS and SVS at
the saphenofemoral junction (SFJ), saphenopopliteal
junction (SPJ) and perforator
• Redirecting reflux from the SVS into the DVS.
As this book is not an atlas of venous surgery, the different
procedures will not be described in detail. However, the
advantages and inconveniences of the different surgical
methods will be underlined.
Surgery without saphenous
trunk preservation
Conventional surgery includes GSV and/or small saphenous
vein (SSV) termination ligation flush to the corresponding
deep vein, plus saphenous trunk stripping with or without
incompetent tributaries phlebectomy and/or incompetent
perforator interruption.
Principle and Controversies
This method is based on the VV descending progression
hemodynamic concept that was established at the beginning
of the 20th century. It was believed that reflux always started
at the SFJ and/or the SPJ, due to incompetence of the terminal
valve, and extended progressively in a distal direction within
the saphenous trunk and into the suprafascial accessory or
tributary veins in which the varices developed. Consequently,
SFJ and/or SPJ ligation completed by trunk stripping and/or
phlebectomy of tributary varices was the ‘cure all’ method. But
the systematic use of DUS for investigating VVs has shown that
this concept was wrong in many cases:
• Reflux and dilatation are frequently segmental in any
location of the saphenous and nonsaphenous systems.
• Onset of the VV can occur in any segment of the
superficial veins without incompetence of the SFJ, SPJ
and saphenous trunk itself.
• The VV reservoir volume favors magnitude and extension
of reflux. Compression of an incompetent tributary
vein termination can reduce or suppress reflux in the
saphenous trunk when they are not dilated beyond 6 to
8 mm in diameter (Fig. 10.1)
• Furthermore we have learned that leak points between
the DVS and the SVS can disappear after ablation of the
VVs even though they have not been treated. After VV
ablation 80% of previously incompetent perforator veins
became competent.
• More surprisingly, incompetent terminal valves can
recover their normal function after ablation of the
refluxing varices.
9,10
1–8

1
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2
A
Figure 10.1 Reservoir reduction capacity allows reduction or suppression
reflux in the main trunk. A, Reflux of the main trunk drains in an
incompetent tributary. This siphon effect increases reflux volume in the
main trunk. B, Compression at the termination of the incompetent tributary
suppresses reflux in the main trunk.
superficielle: notions fondamentales. EMC (Elsevier Masson SAS, Paris), Techniques
chirurgicales
– Chirurgie vasculaire, 43-161-A, 2007.)
B
(Adapted from Perrin M. Insuffisance veineuse
All of these findings have enhanced development of new
surgical procedures that will be described later.
Technical Information
• Ligation of the SFJ and SPJ can be performed by using a
4 to 6-cm transverse incision without cosmetic prejudice,
particularly when the incision is made within the groin
crease.
• Saphenous trunk stripping is most frequently performed
using the endoluminal technique, with invagination or
pin stripping, and is credited with causing fewer
neurologic complications (Figs 10.2 and 10.3).
• Extension of trunk resection depends more on operator
conviction than on the extent of reflux.
• Incompetent tributary phlebectomy is performed
through a very small skin incision, usually 2 to 3 mm in
length.
• Surgical perforator ablation can be performed directly
by skin incision overlying the perforator in the absence
of overlying skin pathology. In the presence of
lipodermatosclerosis, subfascial endoscopic perforator
surgery is strongly recommended, at least for medial leg
perforator veins.
Conventional surgery variants
Saphenous Trunk Stripping with Preservation of
Saphenofemoral Confluence, with or without
Incompetent Tributary Phlebectomy and/or
Incompetent Perforator Interruption
Non-flush ligation at the SFJ and/or SPJ was, until recently,
described as a technical mistake responsible for in situ recurrence in all cases as reflux through the incompetent terminal
valve persisted. But preoperative ultrasound investigations
have proved that in GSV varices the terminal valve is competent in approximately half the patients.
In this situation it looks obvious that high flush tie is not
recommended as tributaries of the saphenofemoral confluence
can drain in a physiologic way into the common femoral vein.
Besides neovascularization, elimination of normal physiologic
reflux is the main cause of recurrence after flush ligation,
rarely identified after confluence conservation.
11,12
13
14
but
3
4
5
Figure 10.2 Invagination stripping. 1. Vein is catheterized from the ankle to
the groin. 2. A thread is fixed on the stripper. 3. The rigid stripper is pulled
up from the ankle to the groin. 4. The thread is fixed on the vein at the
groin. 5. Pull on the thread allows the removal of the vein by the
invagination technique.
veineuse superficielle. Principes. Techniques. R
Techniques chirurgicales
(Adapted from Perrin M. Chirurgie à ciel ouvert de l’insuffisance
ésultats. EMC (Elsevier Masson SAS, Paris),
– Chirurgie vasculaire, 43-161-B, 2007).
When the terminal valve is incompetent, non-flush ligation
was thought to promote recurrence, as previously stated (Fig.
10.4). However, one prospective study has demonstrated that
this concept is wrong. In this large series neither postoperative
outcome nor clinical and diagnostic evaluation found a difference in terms of recurrence if the terminal valve was competent or not.
14
The explanation for this may be that suppression of the
reservoir represented by an incompetent saphenous trunk
and tributaries allows the terminal valve to recover its
competence.
Cryostripping
The only difference with cryostripping in comparison to classical surgery is the ablation modality of the saphenous trunk.
After HL, the saphenous trunk is catheterized downward with
the cryoprobe until reaching the lower limit of the vein to be
stripped. The generator is activated and when the vein is
attached to the cryoprobe (by freezing to it) the vein is broken
off easily. No distal ligation is needed and the vein attached
to the probe is progressively pulled up and extracted through
the groin incision (Fig. 10.5).
Cryostripping is said to cause less postoperative bruising
and hematoma along the path of the saphenous trunk than
The Different Surgical Procedures
283
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