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364 Chapter 36 Percutaneous laser therapy of telangiectasia and varicose veins
b
c
a
532 nm 1064 nm
b
https://t.me/med1917
When administering the desired amount of laser energy to the target vessel, the time in which it is delivered also is crucial. According to the principle of selective photothermol­ysis (8), the laser pulse duration should not reach the ther­mal relaxation time of the target tissue. Thermal relaxation describes the time course of heat transfer, usually by conduc­tion, from the up-heated target structure to the cooler sur­rounding tissue. The equation describing this phenomenon is an e-function with the thermal relaxation time as its time constant. Practically, this means that if administering laser pulses longer than the thermal relaxation time of the target tissue, the advantage of higher absorption in the target tissue is given away. To have an idea of the magnitude of the ther­mal relaxation time, it can be estimated as follows: its value in seconds is about the square of the target diameter, e.g., the thermal relaxation time is about 250 ms in a 0.5-mm-di­ameter vessel or about 40 ms in a 0.2-mm-diameter vessel. Actually, the thermal relaxation times are a little bit shorter than estimated earlier, but actual pulse durations should stay below this. However, one should not stay below the thermal relaxation time too much. For example, for the 1064 nm
36.4 Semiquantitative display of different volume heating
effects of blood vessels caused by either 532-nm or 1064-nm irradiation. Due to higher absorption of blood at 532 nm, larger vessels get heated only at the most supercial parts, produc­ing kind of a shield for more remote vessel parts, which stay cool. 1064 nm heats the vessel more uniformly due to a lower absorption coefcient; a = epidermis, b = dermal layer, c = sub­cutaneous fat.
ND:YAG laser, it has been shown that longer pulse dura­tions between 20 and 60 ms consistently produce better clin­ical results than 3-ms pulse duration in vessels with a mean diameter of 0.8 mm (16). Histopathology supported these ndings, showing marked shrinkage of perivascular collagen with longer pulses, while short pulses of 3 ms were only able to produce a thrombotic occlusion of the vessel. In conclu­sion, it seems that substantial heat damage around the target vein, at least a solid heat damage of the entire vessel wall, is an absolute condition to get instant and durable vein occlu­sions. However, longer durations of laser pulses are more painful than shorter pulses (14), and therefore patients’ pain sometimes does not allow the administration of longer pulse durations; in particular, pulses above 100 ms duration are not tolerated by many patients.
Additionally, for successful laser ablation of leg telangi­ectasias, the actual penetration depth of laser light should be considered. Interestingly, this depth is not only depen­dent on the wavelength of the laser light and its absorp­tion characteristics but also on its scattering behavior. The actual penetration depth therefore can be increased by increasing the beam diameter (Figure 36.3). Due to
the mentioned scattering effects, the originally cylindric laser beam forms a pencil-like tip before being completely absorbed by surrounding tissue. However, because of the phenomenon of forward scattering itself, the vanishing of the laser beam takes longer and happens in greater tissue depth with greater beam diameters.
After considering the tissue absorption of skin tissue and hemoglobin in general, the absorption characteristics of the target structure, the geometry of the vein vessel itself, needs a closer look with respect to volumetric heating. When using a wavelength that is absorbed too high by hemoglobin, at least in vessels of larger diameter, the remote parts of the vessel do not get heated enough because the energy is pre­dominantly absorbed in the part of the vessel rst hit by the laser beam. In contrast a wavelength that is absorbed more moderately by hemoglobin is able to heat up the vessel in its whole. Figure 36.4 displays this behavior for a 532-nm laser beam in comparison to a 1064-nm beam. For this reason, larger vessels with diameters on the order of 1 mm cannot be successfully treated with short laser wavelengths like 532 nm, 585 nm, or even 595 nm.
To reduce pain and to minimize the risk of numerous side effects elicited by heat damage of the skin, the use of skin cooling is mandatory today. Local use of ice cubes or administration of cooled gel before laser treatment or also laser ring through ice cubes are historical methods, but they cannot guarantee reproducible results. Nowadays sophisti-
a
cated dynamic spray cooling devices, chilled contact tips, or cool air generators are available as discussed later.
c
36.3 Semiquantitative display of penetration depths of 1064
nm into human skin according to different beam diameters. Penetration is deeper for larger beam diameters because of the physical effect of forward scattering (Mie-scattering); a = epi­dermis, b = dermal layer, c = subcutaneous fat.
36.7 LASERS AND IPL FOR
TRANSCUTANEOUS THERAPY OF TELANGIECTASIAS
Meanwhile, treatment of telangiectatic vessels of the legs reached a level that allows transcutaneous treatment in most cases. In general, there was an evolutionary change in laser parameters, particularly an increase of pulse duration
36.7 Lasers and IPL for transcutaneous therapy of telangiectasias
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365
and uence and a move from visible light to near-infrared wavelengths. Today a variety of laser and IPL systems are available for treatment of leg telangiectasia of any diameter between 0.1 and 2.0 mm.
36.7.1 532-nm KTP laser
The frequency-doubled 532-nm Nd:YAG laser system is particularly useful for the treatment of red leg telangiecta­sias with small diameters below 0.7 mm. It is most effec­tive if used on skin types I–III and problematic in tanned or dark-skinned patients because of the high absorption of melanin at this wavelength.
The 532-nm laser was initially used with uences
between 14 and 20 Joule/cm
2
, with pulse durations of 10–15 milliseconds and with spot sizes of 3–5 mm in 50 patients with leg telangiectasia of varying diameters. Eighty-three percent of patients showed a clearance of 50% or more after two treatments. With the previously men­tioned parameters and a chilled tip for contact cooling, the 532-nm KTP laser proved to be less painful if compared to laser systems with longer wavelengths (17). In another 15-patient study, clinical results were corroborated on telangiectasia below 0.75 mm in diameter. A clearance of more than 75% was achieved after two treatment sessions using a uence of 16 joule/cm
2
with 10-ms pulse duration and three passes over the same treatment area each ses­sion (18). Another study conrmed the favorable pain and side effect prole but found vessel clearance inferior to a long pulse dye laser. The authors recommended the use of the KTP laser system in conjunction with sclerotherapy of larger feeding reticular veins (19). However, when using a multipulse mode with three stacked pulses of 100 ms, 30 ms, and 30 ms duration, each separated by a gap of 250 ms, with a uence of 60 joule/cm
2
and a beam diameter of
0.75 mm, clearance in leg telangiectasia of 0.5–1.0 mm in diameter was 85% after three and 93% after four treat­ment sessions, most likely taking advantage of met-hemo­globin formation during the rst of the three pulses (20).
In another study 79 areas of 20 female subjects, skin types I–III, were treated using a 532-nm KTP laser. A 5-mm-diameter spot, uences from 13 to 15 J/cm², and a pulse duration of 40 ms were used in two treatment session 12 weeks apart. Blinded reviewers rated a more than 50% improvement of telangiectasias in 69%; hyperpigmenta­tion was observed in only 2% (21).
36.7.2 578-nm copper bromide laser
The copper bromide laser is suited for red leg telangiec­tasia. In a study with 46 patients 75%–100% clearance was achieved after an average of 1.7 treatments of vessels with diameters below 1.5 mm. Fluences were in the range of 50–55 joule/cm
2
, and a contact cooling system with a
temperature between 1 and 4°C was used (22).
36.7.3 Flashlamp-pumped pulsed dye
laser
This laser was the rst one to take advantage of the con­cept of selective photothermolysis and the rst one to achieve remarkable results in very small red vessels with
diameters below 0.1 mm, like in telangiectatic matting. At that time—with a wavelength of 577 nm and pulse dura­tions of 360 µs—it proved to be suitable for treatment of infantile hemangioma or port wine stains. It did not show remarkable effects on patients with leg telangiectasia (23).
In the mid-1990s dye lasers with a 595-nm wavelength and a pulse duration of 1.5 ms were introduced. One study with uences of 15 or 18 joule/cm
2
after one single treat­ment showed clearance in up to 65% when treating vessels between 0.6 and 1.1 mm in diameter (24).
In ten patients, more than 75% clearance after three treatments every 6 weeks was achieved with minimal side effects using a 595-nm dye laser with 1.5-msec pulse dura­tion. Fluences between 15 and 20 joule/cm
2
were used on leg telangiectasia with diameters below 1.5 mm (25). In another comparative study on 87 patients and 257 treat­ment sites, 595 nm was compared to 600-nm wavelength using 1.5-msec pulse duration and uences of 16, 18, and 20 joule/cm
2
. A clearance rate above 50% in up to 80% of patients was noted after a single treatment. The authors found the best results with higher uences on vessels below
0.5 mm in diameter. Pigment changes were noticed in 32% of cases (26). The use of a dynamic cooling device in con­junction with 595 nm and 1.5-ms pulse duration treatment reduced patient discomfort without diminishing an average clearance rate of 68% (27). Introduction of dye lasers with pulse durations of 40 ms allowed treatment without or at least with diminished production purpuric lesions after laser treatment. With the use of an extended pulse width of 40 ms and a uence of 16 joule/cm
2
administered up to three passes over the same location during one session, after a total of two treatment sessions, 70% of leg vessels showed a clearance of 75%–100%. A –4°C air cooling sys­tem was used during treatment (28). After only one treat­ment of submillimeter telangiectasia with the 595-nm dye laser at 40-ms pulse duration with a uence of 25 joule/
2
cm
and spray cooling, about half of the patients had clear­ance of 50% or more. In the same study 532-nm KTP laser treatment with 50-ms pulse duration and a uence of 20 joule/cm
2
and contact cooling gave similar results (29).
36.7.4 755-nm long pulsed alexandrite
laser
The long-pulsed alexandrite laser in the near infrared at a wavelength of 755 nm proved to be most effective in a double pulse mode (frequency 1 Hz) at a uence of 20 joule/cm sels with diameters below 0.4 mm did not show signi­cant responses, while larger telangiectasia showed a 63% reduction after three treatments in 4-week intervals. Sub­sequent sclerotherapy improved laser results signicantly. Another study showed that long pulse alexandrite laser treatment at 3 ms pulse duration and uences of 60–70 joule/cm eter frequently caused signicant inammatory skin reac­tion, purpura, and telangiectatic matting. Despite that side effect prole, only 33% of patients had more than 75% clearance after up to three treatment sessions (31). When using the 755-nm alexandrite laser with a uence of 90 joule/cm and 75% of treated telangiectasia with diameters from 0.3
2
with pulse durations of 5–10 ms (30). Small ves-
2
for treatment of veins of 0.3–3.0 mm in diam-
2
, 15 of 20 patients had a clearance between 25%
36
366 Chapter 36 Percutaneous laser therapy of telangiectasia and varicose veins
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to 1.3 mm. Noticeably, in 75% of cases, hyperpigmenta­tion was noted (32).
However, more recently, a long pulse 755-nm alexan­drite laser proved similar efcacy compared to a long pulse 1064-nm Nd:YAG laser for treatment of leg telangiectasia in Asian skin type IV (33).
36.7.5 Diode lasers between 810 nm
and 1064 nm
One study used an 810-nm diode laser with a 5-mm spot size and a pulse protocol of four consecutive stacked pulses (frequency 2 Hz), each of a uence of 3 to 4.5 Joule/cm
2
No side effects were observed, but neither was clearance of leg telangiectasia (34). Inconsistent results with only 29% of sites clearing more than 75% were also reported from another group using an 810-nm long pulse diode laser on vessels with diameters between 0.3 and 3.0 mm (31). Using a 940-nm diode laser with a 1-mm spot size, a pulse duration of 40–70 msec, and uences between 300–350 joule/cm
2
in a single treatment resulted in a clearance of more than 75% of treated telangiectasia in 12 of 26 patients (46%) (35). The same group reported an additional 1-year follow-up with further improvement of clearing rates in 35% of patients (36). Another group from France using spot diameters between 0.5 and 1.5 mm, a pulse duration between 10 and 70 ms, and uences slightly above 300 joule cm
2
found clear­ance rates superior to 75% after up to 3 treatment sessions in only 13% of cases if vessel diameters were below 0.4 mm and in 88% of cases if vessel diameters were between 0.8 and 1.4 mm (37). An 810-nm laser used with a 12-mm spot size, a pulse duration of 60 ms, and uences in the range of 80–100 joule/cm
2
managed to clear 43% of spider veins completely after one session with two treatment passes (38). A combination of a 915-nm diode laser with 1 MHz radiof­requency energy with up to three treatment sessions showed more than 75% clearance in 77 % of treatment sites when using 80–140 joule/cm
2
laser uence and 80–100 joule/cm3 of RF energy with pulses of 100–300 ms duration (39). A 980-nm diode laser that was used with a contact cooling device, with uences between 300 and 500 Joule/cm
2
and pulse durations of 150 ms achieved up to 50% clearance in 60% of patients; however, with such long pulse durations pain was pronounced in the majority of patients (40). More recently, a 1064-nm diode laser showed its feasibility to improve vascular lesion appearance in a small series of 15 patients (41).
36.7.6 1064-nm long pulsed Nd:YAG laser
The wavelength of 1064 nm shows less absorption in mel­anin compared to shorter laser wavelengths and is less absorbed in hemoglobin. Because of the relatively low hemoglobin absorption, laser energy can also heat up the larger vessels in their entirety. In 1999 Weiss reported a study on 30 patients using a Nd:YAG laser at 1064-nm wavelength with a pulse duration of 16 mc. They observed a 75% improvement after a single treatment in 0.5- to 3.0­mm diameter vessels (42). Another study reported 64% clearance after a maximum of three treatment sessions
using a 1064-nm Nd:YAG laser with a contact cooling device. The author used a 6-mm spot size, pulse durations up to 14 msec, and a uence of 130 joule/cm vessel diameters between 0.2 and 4.0 mm (43). The same author achieved 75%–100% clearance when using the Nd:YAG system only for telangiectasia of 1.0–4.0 mm in diameter but treating 0.1- to 1.0-mm vessels with a 550­nm IPL device (44). Interestingly, in comparison to Sotra­decol sclerotherapy in leg telangiectasia of 0.25–3.0 mm in diameter, the long pulse Nd:YAG laser achieved equal results (45). Utilizing a spray cooling device, long pulse Nd:YAG treatment of leg veins of 0.3–3.0 mm in diameter showed clearance of more than 75% in 85% of treated
.
sites after a maximum of three sessions (46). This nding was corroborated in vein diameters between 1.0 and 3.0 mm. With a single treatment using a uence of 100 joule/
2
and pulse duration of 50 ms, a clearance of more than
cm 75% was achieved in 66% of cases (47). In a highly inter­esting approach to take advantage of met-hemoglobin for­mation using a nonuniform pulse sequence, a French group achieved a clearance rate of 98% after three sessions. They used a 2-mm spot, uences between 300 and 340 joule/
2
, and a contact cooling device to treat blue leg telangi-
cm ectasia of diameters between 1 and 2 mm (48).
36.7.7 Combination of 1064 nm Nd:YAG laser with sclerosants
More recently, lasers have been used for combination treat­ment modalities after either a systemic intravenous injec­tion of a green dye (49) or injecting the target vessel with a polidocanol-based foam sclerosant (50). Energy from a 810-nm diode or a 1064-nm Nd:YAG laser was delivered.
In a prospective randomized trial, telangiectasias of 29 subjects were treated either in the rst arm with a 1064-nm Nd:YAG laser with uencies between 160 and 240 J/cm–², a pulse duration of 65 ms, and a 5-mm spot size or in the second arm, after intravenous injection of 4 mg per kilo­gram body mass of an indocyanine green dye, using an 810­nm diode laser with uence from 60 to 110 J/cm–², 48- to 87-ms pulse duration, and a 6-mm spot size. Blinded investi­gators and the participants assessed clearance rate, cosmetic appearance, and adverse events up to 3 months after one single treatment session. Both investigators and participants ranked clearance rates of the dye-augmented diode laser treatment over those after 1064-nm Nd:YAG treatment, but also rated the dye-augmented treatment more painful.
In a randomized controlled trial in 320 female patients skin type II–IV, polidocanol foam sclerotherapy of leg telangiectasia followed by 1064-nm Nd:YAG laser was compared to polidocanol foam sclerotherapy alone (50). Each patient received two single treatment sessions at a 3-week intervals, with treatment of both legs in full in each session. Up to 20 cc foam prepared from an 0.3% polidocanol solution were injected per session. In the laser group, depending on the vessel diameter, 2-mm spot size was used with a uence of about 300 joule/cm² of 5-mm spot size with a uence of around 60 joule/cm². Depend­ing on the diameter of the vessel, the pulse duration was chosen between 20 and 50 ms. Evaluation was performed
2
to treat
36.9 Side effects and complications 367
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by a blinded analysis of photographs taken up to 3-years follow-up and patients’ self-assessment in 79 control legs and 517 legs treated with the foam–laser combination. Depending on the vessel diameter, clearance rates of the combination laser treatment were 89%–95%, while in the control group after foam sclerotherapy alone, correspond­ing clearance rates were only 15%–18%.
A promising combination concept using laser on the same vessels before sclerotherapy under continuous air cooling has been described as the Cryo-Laser-Cryo-Sclero (CLaCS) therapy (51, 52). Under continuous –20°C air­ow, initial laser treatment reduces the vessel diameter before either 75% glucose or 0.3% polidocanol is injected in the same area. The cooled air contributes to pain reduc­tion and furthermore minimizes intravascular thrombus formation like laser-induced diameter reduction does as well, while elimination of 86% of vessels was achieved (51). Different sclerosants used in this method more or less seem to act with equal efcacy (52).
36.7.8 Intense pulsed light
Intense pulsed light (IPL) sources make use of neither monochromatic nor coherent light emission. A polychro­matic spectrum is emitted, which is dened by lters placed between the IPL source and the patient. In its initial phase without concomitant use of special cooling devices, side effects like skin burns or hyperpigmentation could happen more easily than with today’s devices.
However, even in its early days, IPL was able to achieve clearance of leg telangiectasia. In a multicenter trial treat­ing 349 lesions in 159 patients, a clearance of more than 75% was achieved in 79% vessels between 0.1 and 3 mm of diameter. The rate of adverse effects was low (53).
In a more recent comparative study between Nd:YAG and IPL, the IPL treatment was judged to be more effective in vessels with diameters below 1.0 mm, while leg veins of more than 1.0 mm in diameter were more effectively treated by the Nd:YAG laser (54). Logically, treatment approaches combining IPL treatment for smaller vessels with diameters below 1.0 mm and Nd:YAG laser treatment for vessels with diameters above 1.0 mm were reported to be very successful (55, 56).
36.8 COOLING SYSTEMS
Skin cooling is crucial to minimize thermal side effects on skin structures apart from telangiectasia. Today, icing of the skin cannot be judged reproducible enough but is more reliable than the use of cooled gels. Gels provide only a temperature decrease of about 5° and can even dis­turb the spot geometry of the laser beam and account for energy loss of about 35% (26). Reliable and more effective techniques are contact cooling devices (22, 29, 43), e.g., sapphire handpieces, dynamic spray cooling (27, 29, 46), and using tetrauoroethene or low-temperature air cool­ing devices (28, 51). Also, for IPL a collar contact cooling device improved clinical results, allowing the delivery of higher uences with less pain (57).
36.9 SIDE EFFECTS AND COMPLICATIONS
To identify patients prone to idiopathic hypersensitiv­ity reactions after laser treatment, a test treatment of a small area is necessary before a full treatment session is administered. Furthermore, informed consent about the following treatment-related risks should be signed by the patient. The most frequent side effects of laser treatment are:
Transient or, rarely, permanent hyperpigmentation
Telangiectatic matting
Incomplete elimination of telangiectasia
Treatment-related pain
Restricted to special laser types, particularly to the old­type ashlamp pumped dye lasers, is the side effect of purpura. As mentioned earlier, the long pulse alexandrite laser therapy of leg telangiectasia under certain condi­tions is associated with pronounced inammatory skin reactions. Hyperpigmentation can happen with the use of any laser or IPL light source but is more likely to happen after treatment of telangiectasia with shorter wavelength lasers like 532-nm KTP devices. In general, according to a Cochrane database systematic review, lasers seem to cause less hyperpigmentation (RR 0.57, 95% CI 0.40–0.80; 4 studies, 262 participants/procedures) if compared to sclerotherapy (58).
Patients with activation of their pigment system after sunny vacations or use of sunbeds should strictly avoid laser or IPL treatments. In addition, sun exposure and use of sunbeds should be strictly avoided after laser therapy as long as any skin response is visible, usually for 3–4 weeks. Dark-skinned patients should be treated with special cau­tion, if treated at all.
A less frequent side effect of laser treatment is throm­bosis of telangiectasia mostly associated with diameters above 1 mm. To accelerate the clearing of this phenom­enon, thrombosis should be removed by needle puncture within the rst week after treatment.
Rare complications of laser treatment include blistering of the skin with or without subsequent scarring. These side effects most frequently happen with overdosing of laser energy. Overdosing of laser or IPL can happen in conjunc­tion with:
Administration of too high uences
Inadvertent pulse stacking or inadvertent overlapping of
pulses
Intended pulse stacking with too small cooling intervals
in between
Inappropriate cooling of the skin surface during treat-
ment
Also laser treatment of skin that is covered with lotions or ointments can result in skin burns and hyperpigmentation. Removal of all of these externals before laser treatment is therefore mandatory.
36
368 Chapter 36 Percutaneous laser therapy of telangiectasia and varicose veins
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36.10 ALTERNATIVE TREATMENT OPTIONS FOR LEG TELANGIECTASIA
A serious alternative option to light-based systems or some of the described combination treatments of leg telangiecta­sia is sclerotherapy with various liquid or foam sclerosants. The technique of sclerotherapy is presented in detail in a different chapter of this book.
36.11 FUTURE DIRECTIONS
The laser and IPL treatment of leg telangiectasia still offers a big evolution potential. Bimodal wavelength approaches, longer pulse durations, and improved skin cooling contrib­uted much to more effective laser and IPL treatment of leg telangiectasia (59).
Despite a solid theoretical basis, concepts like the exploitation of laser-induced met-hemoglobin formation are still not fully developed (48, 60). Similarly, feedback loops for measurement of vessel and skin temperature during laser treatment and subsequent online adjustment of laser uence and skin cooling are technically possible but not yet intro­duced in daily clinical practice. The same is true for auto­matic scanner systems which would direct the laser beam to the previously traced course of the target vessel.
Combination treatments consisting of laser treatment of telangiectatic vessels after systemic injection of a dye or after injection of a sclerosing foam at the treatment site look promising as well (49, 50). However, the scientic exploration of these concepts has just begun.
36.12 CONCLUSION
Small leg telangiectasias: For diameters below 0.5
mm and telangiectatic matting, the dye laser at 595 nm is effective (24[1C], 26[1B], 28[1C]). The KTP laser at 532 nm is suitable on diameters below 0.7 mm (18[1C], 21[1C]). Multipass treatment (18[2C], 28[2C]) or pulse stacking (20 [2C]) may improve clin­ical results.
Larger telangiectasias and reticular veins up to 3 mm
diameter: These can be effectively treated by long pulse Nd:YAG lasers with 1064-nm wavelength (42[1C], 46[1C], 47[1C], 48[1C]).
Combination of laser treatment of leg telangiectasias
with prior injection of a polidocanol foam seems to increase clearance rates dramatically [50, 1B]; systemic injection of an indocyanine green dye prior to laser therapy may increase treatment success as well [49, 2C].
Effective skin cooling is mandatory to avoid thermal
skin damage. Appropriate cooling devices are dynamic spray cooling (27[1C], 29[1C], 46[1C]), contact cool­ing (22 [1C], 29[1C], 43[1C]), or cooled air (28[1C]). Cooled gels do not provide sufcient or homogenous skin cooling (26[1C]).
In human skin, melanin is the main competing light
absorber to hemoglobin (13[1A]); therefore, laser treatment of telangiectasias can cause long-lasting hyperpigmentation as a side effect. An increased epi­dermal melanin content after sun exposure—so-called tanned skim—therefore should be regarded a contrain­dication to cosmetic laser treatment of leg telangiecta­sias.
Guidelines 36.0 of the American Venous Forum on laser treatment of reticular veins and telangiectasias
No. Guideline Grade of recommendation Quality of evidence
36.1 For patients with symptomatic telangiectasias or reticular veins, we suggest transcutaneous laser treatment if the patient has a sclerosant allergy, needle phobia, sclerotherapy failure, or small veins (<1 mm) with telangiectatic matting.
2 (weak)
B (moderate)
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20. Fournier N, Brisot D, Mordon S. Treat­ment of leg telangiectases with a 532 nm KTP laser in multipulse mode. Dermatol Surg 2002;28:564–71.
21. Bernstein EF, Noyaner-Turley A, Renton B. Treatment of spider veins of the lower extremity with a novel 532 nm KTP laser. Lasers Surg Med 2014;46:81–8.
22. Sadick NS, Weiss R. The ulilization of a new yellow light laser (578 nm) for the treatment of class I red telangiectasia of the lower extremities. Dermatol Surg 2002;28:21–5.
23. Polla LL, Tan OT, Garden JM, Parrish JA. Tunable pulsed dye laser for the treatment of benign cutaneous vascular lesions. Dermatologica 1987;174:11–7.
24. Hsia J, Lowery JA, Zelickson B. Treatment of leg telangiectasia using a long-pulse dye laser at 595 nm. Lasers Surg Med 1997;20:1–5.
25. Bernstein EF, Lee J, Lowery J, Brown DB, Geronemus R, Lask G, Hsia J. Treatment of spider veins with the 595 nm pulsed-dye laser. J Am Acad Dermatol 1998;39: 746–50.
26. Hohenleutner U, Walther T, Wenig M, Baumler W, Landthaler M. Leg telangiec­tasia treatment with a 1.5 ms pulsed dye laser, ice cube cooling of the skin and 595 vs 600 nm: Preliminary results. Lasers Surg Med 1998;23:72–8.
27. Buscher BA, McMeekin TO, Goodwin D. Treatment of leg telangiectasia by using a long-pulse dye laser at 595 nm with and without dynamic cooling. Laser Surg Med 2000;27:171–5.
28. Tanghetti E, Sherr E. Treatment of telangiectasia using the multi-pass technique with the extended pulse width, pulsed dye laser. J Cosmet Laser Ther 2003;5:71–5.
29. Woo WK, Jasmin ZF, Handley JM. 532 nm Nd:YAG and 595 nm pulsed dye laser treatment of leg telangiectasia using
ultralong pulse duration. Dermatol Surg 3002;29:1176–80.
30. McDaniel DH, Ash K, Lord J, Newman J, Adrian RM, Zukowski M. Laser therapy of spider leg veins: Clinical evaluation of a new long pulsed alexandrite laser. Derma­tol Surg 1999;25:52–8.
31. Eremia S, Li C, Umar SH. A side-by-side comparative study of 1064 nm Nd:YAG, 810 nm diode and 755 nm alexandrite lasers for treatment of 0.3–3.0 mm leg veins. Dermatol Surg 2002;28:224–30.
32. Brunnberg S, Lorenz S, Landthaler M, Hohenleutner U. Evaluation of the long pulsed high uence alexandrite laser the­rapy of leg telangiectasia. Laser Surg Med 2002;31:359–62.
33. Nguyen HTN, Firas AN, Van TT. Long­pulsed 1064-nm and 755-nm lasers for C1 leg veins on skin type IV patients: A side-by-side comparison. Lasers Med Sci 2021;34:829–35.
34. Varma S, Lanigan SW. Laser therapy of telangiectatic leg veins: Clinical evalua­tion of the 810 nm diode laser. Clin Exp Dermatol 2000;25:419–22.
35. Kaudewitz P, Klovekorn W, Rother W. Effective treatment of leg vein telangiec­tasia with a new 940 nm diode laser. Dermatol Surg 2001;27:101–6.
36. Kaudewitz P, Klovekorn W, Rother W. Treatment of leg vein telangiectases: 1-year results with a new 940 nm diode laser. Dermatol Surg 2002;28:1031–4.
37. Passeron T, Olivier V, Duteil L, Desruelles F, Fontas E, Ortonne JP. The new 940 nm diode laser: An effective treatment for leg venulectasia. J Am Acad Dermatol 2003;48:768–74.
38. Wollina U, Konrrad H, Schmidt WD, Haroske G, Astafeva LG, Fassler D Res­ponse of spider leg veins to pulsed diode laser (810 nm)> a clinical, histological and remission spectroscopy study. J Cosmet Laser Ther 2003;5:154–62.
39. Chess C. Prospective study on combination diode laser and radiofrequency energies (ELOS) for the treatment of leg veins. J Cosmet Laser Ther 2004;6:86–90.
40. Levy JL, Berwald C. Treatment of vascular abnormalities with a long-pulse diode at 980 nm. J Cosmet Laser Ther 2004;6:217–21.
41. Gold MH, Biron J, Sensing W. Evaluation of a new diode laser for the treatment of lower extremity leg veins. J Cosmet Der­matol 2019;18:773–77.
42. Weiss RA, Weiss MA. Early clinical results with a multiple synchronized pulse 1064 nm laser for leg telangiectasias and reticu­lar veins. Dermatol Surg 1999;25:399–402.
43. Sadick NS. Long-term results with a multi­ple synchronized-pulse 1064 nm Nd:YAG laser for the treatment of leg venulecta­sias and reticular veins. Dermatol Surg 2001;27:345–9.
44. Sadick NS. A dual wavelength approach for laser/intense pulsed light source treat­ment of lower extremity veins. J Am Acad Dermatol 2002;46:66–72.
45. Coles CM, Werner RS, Zelickson BD. Comparative pilot study evaluating the treatment of leg veins with a long pulse Nd:YAG laser and sclerotherapy. Laser Surg Med 2002;30:154–9.
46. Eremia S, Li Cy. Treatment of leg and face veins with a cryogen spray variable pulse
width 1064- nm Nd:YAG laser— prospec­tive study of 47 patients. J Cosmet Laser Ther 2001;3:147–53.
47. Omura NE, Dover JS, Arndt KA, Kauvar AN. Treatment of reticular leg veins with a 1064 nm long-pulsed Nd:YAG laser. J Am Acad Dermatol 2003;48:76–81.
*48. Mordon S, Brisot D, Fournier N. Using a
“non uniform pulse sequence” can improve selective coagulation with a Nd:YAG laser (1.06 microm) thanks to met-hemoglobin absorption: A clinical study on blue leg veins. Lasers Surg Med 2003;32:160–70.
49. Klein A, Buschmann M, Babilas P, Landthaler M, Bäumler W. Indocyanine green-augmented diode laser therapy vs. long-pulsed Nd:YAG (1064 nm) laser treatment of telangiectatic leg veins: A randomized controlled trial. Br J Dermatol 2013;169:345–73.
50. Moraga JM, Smarandache A, Pascu ML, Royo J, Trelles MA. 1064 nm Nd:YAG long pulse laser after polidocanol microfoam injection dramatically improves the result of leg vein treatment: A randomized controlled trial on 517 legs with a three-year fol­low-up. Phlebology 2014;29:658–66.
51. Miyake RK, Chi YW, Franklin IJ, Gianesini S. State of the art on cryo-laser cryo-scle­rotherapy in lower limb venous aesthetic treatment. J Vasc Surg Venous Lymphat Disord 2020;8:893–95.
52. Fonseca MM, Mocelin FJ, Grill MH, et al. Nd:Yag laser combined with injection sclerotherapy in the treatment of reticular veins and telangiectasias (CLaCS method): A triple-blind randomized clinical trial comparing two sclerosing agents asso­ciated with same laser patterns. Phlebology 2023;38:165–71.
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36
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CHAPTER
37
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Physician-compounded foam
sclerotherapy for ablation of superficial
truncal veins and varicose tributaries
Claudine Hamel-Desnos and Peter Gloviczki
37.1 INTRODUCTION
Endovenous methods of treating varicose veins have been used with increasing frequency in recent years, but foam sclerotherapy (FS), thanks to its unrivaled versatil­ity, remains an important part of the phlebologist’s arma­mentarium. It is quick, inexpensive, and can be used in the ofce setting. This chapter will address the treatment of supercial axial veins and tributary veins with physi­cian-compounded foam (PCF).
37.2 HISTORY
Sclerotherapy has been used to treat varicose veins since the 1850s. However, early sclerosants were associated with an unacceptably high incidence of serious, even life-threat­ening complications, such as tissue necrosis, sepsis, and pulmonary embolism. It was not until the 1960s, with the introduction of modern, safe sclerosants, such as sodium tetradecyl sulfate (STS) and polidocanol (POL) that sclero­therapy gained widespread popularity. The history of FS has been described by Wollmann please see also Chapter 1 in this book. In 1957, Mayer and Brücke introduced a double-piston syringe to produce what they termed “microfoam,” likely the rst production of foam compared to froth. In 1969, Gillesberger, a Bavar­ian, invented a technique by creating negative pressure in a glass syringe so that air could enter through a gap between the syringe piston and plunger to mix with the sclerosant, but the ratio between air and sclerosant could not be stan­dardized. In 1986, the Australian Grigg used two syringes connected by a tube, and air and uid were pumped back and forth, a prelude to the most widely used techniques today. In 2000, Tessari published his technique for produc­ing foam using two plastic syringes and a three-way stop-
3,4
In 1993, Garrido patented a microfoam that uses
cock.
as a carrier gas and mixed it with POL using a high-
CO
2
speed rotating brush sclerotherapy was rst introduced by Knight in 1989,
5
1
and by Myers.2 For details,
. The concept of ultrasound-guided
6
then
became ultrasound-guided foam sclerotherapy (UGFS) with the use of foam. Adding ultrasound guidance to FS in the 1990s resulted in a veritable revolution.
37.3 SCLEROSANTS AND MECHANISM OF ACTION
In Europe, most phlebologists use PCF with STS or POL microfoam. In the United States, polidocanol endovenous microfoam (PEM) is a commercially prepared 1% POL microfoam, approved by the Food and Drug Administration (FDA) (see Chapter 38). Sclerosing agents cause endothelial damage, which exposes collagen and leads to inammation of the vein wall and activation of platelets and the intrinsic coagulation pathway, ideally leading to obliteration of the venous lumen and ultimately to brosis of the vein. Only sclerosing agents in the detergent class, such as STS and POL, can be transformed into foam. Detergents cause endothelial damage by altering cell wall surface tension, leading to rapid overhydration (maceration). STS is a long-chain fatty acid salt; it is painless to inject and available at concentrations of 0.2%, 0.5%, 1%, and 3%. POL is a urethane anesthetic agent; it is also painless to inject in the form of foam and thought to be less likely to produce extravasation necrosis than STS; it is available at concentrations of 0.25%, 0.5%, 1%, 2%, and 3%. The foam form is authorized for STS and POL in many countries other than the United States, par­ticularly for high concentrations of 1%–3%. Practitioners should refer to authorizations in their country. Injection of STS or POL as a foam as opposed to a liquid result in the displacement of blood, thus minimizing deactivation (bind­ing) by protein and maximizing contact with the endothe­lium (“foam block effect”). Foam advantages over liquid also include better adherence to the vein wall, better venous spasm, and excellent echogenicity. All these factors contrib­ute to the greater efcacy of this form of sclerosant, as well as safer injection procedures when coupled with ultrasound guidance. Both STS and POL are well tolerated, with almost similar side effect proles.
DOI: 10.1201/9781003328971-42
371371
372 Chapter 37 PCF sclerotherapy for ablation of superficial truncal veins and varicose tributaries
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37.4 FOAM PREPARATION TECHNIQUES
The Tessari (Tourbillon) technique is probably the most used method for reproducibly making stable microfoam, for about 1 minute (Figure 37.1). are connected via a three-way stopcock. Room air is drawn into one syringe and liquid sclerosant into the other. In a variant of this method, the three-way stopcock is replaced with a dedicated biconnector use of sterile air, oxygen, carbon dioxide, a mix of CO
, etc., has been advocated. However, they add cost and
O
2
complexity, and there is no evidence these adjuncts con­fer any benet in terms of safety or clinical effectiveness. The air and sclerosant are mixed back and forth (usually around 20 times) through the three-way stopcock (or biconnector) to produce the microfoam. The three-way stopcock can be angulated to narrow the aperture to pro­duce smaller bubbles, and so more stable, and arguably
3
Typically, two syringes
7
(Figures 37.2 and 37.3). The
+
2
8
37.3 Foam production: 10 to 20 back-and-forth movements.
37.1 Tessari technique with three-way stopcock with two
low-silicone syringes of 2.5 mL (1 volume of sclerosant + 4 vol­umes of air).
37.2 Dedicated biconnector with two low-silicone syringes of
2.5 mL (1 + 4 mix).
37.4 An automated foam production system.
more effective microfoam can be prepared. The most effec­tive and commonly used sclerosant-to-gas mix appears to be 1 + 4, but high level of evidence is lacking. Low-silicone syringes and connectors are preferred, as silicone destroys the surfactant arrangement of the foam lamellae, thus making it less stable.
9
To better standardize foam making, an automated foam production system has recently been introduced (Figure 37.4). Moreover, the U.S. market has PEM (see Chapter 38), a 1% POL foam, industrialized and
37.5 Treatment tactics and technique 373
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composed of a mixture of “physiological” gases and distrib­uted from a pressurized container. PEM bubbles are appre­ciably smaller than those found in “home-made” foam, and this, together with the low nitrogen rate, may reduce the risks of air embolism. clinical benet in terms of safety and clinical effectiveness compared to PCF is not available.
To date, none of the foam manufacturing methods have proved their superiority over the others, and barring national regulations, cost and convenience are still the overriding considerations.
10
However, thus far, clear evidence of
37.5 TREATMENT TACTICS AND
TECHNIQUE
37.5.1 Tactics
In the 1930s–1960s, three schools of thought emerged on the most appropriate tactics: Sigg’s Swiss school, Fegan’s Irish school, and the French school led by R. Tournay. In the Swiss “bottom-up” technique, varicose veins were rst sclerosed distally, and the treatment was completed by obliterating the feeder trunks. Meticulous compression was essential after each treatment, and this slow, cautious method required many sessions. The Irish technique was based on a different concept, giving a primordial role to the perfo­rators, which were sclerosed as a priority, usually ignoring the trunk and junction. Postprocedural compression was also imperative here. The French technique, also called the “top-bottom” technique (“proximal to distal”), consisted of rst treating the highest or most important leakage points, the saphenofemoral (SFJ) or saphenopopliteal junctions (SPJ), saphenous trunks, perforators, etc. Tributary varicose veins were initially ignored and only injected if they per­sisted after treatment of the trunks. Unlike the two previous schemes, compression was not an integral part of the proce­dure here since inammation post-sclerotherapy was much less frequent. This could historically explain the differences between the positions of French practitioners and those in other countries regarding post-sclerotherapy compression.
The top-down technique is now the reference and most widely used in many countries. tioners still apply strong compression, contrary to the orig­inal description, which does not include any compression. This could also historically explain why some practitioners rst inject incompetent trunks and only treat tributary veins later, if still necessary. This concept applies to thermal ablation as well.
14,15
However, many practi-
37.5.2 Techniques
Injections can be made using needles, buttery needles, cannulas, long catheters, etc., but two main principles exist for sclerotherapy: UGFS and visual sclerotherapy.
There is a simple but essential safety rule in sclerother­apy: a “nonvisible” varicose vein should never be treated without ultrasound guidance. Consequently, the saphenous trunks must always be treated under ultrasound guidance, while certain tributary veins can sometimes be injected under visual control. Purely cosmetic treatments are not discussed in this chapter.
2,11,13
Prior to any treatment of varicose veins, the patient’s expectations, the history-taking, the pathological venous network, and its implications must be carefully identied during clinical and ultrasound examinations.
Successful sclerotherapy requires thorough planning. The decision to treat varicose veins with sclerotherapy must be shared with the patient. Clear information and a wait­ing period are therefore necessary. An initial treatment ses­sion is then planned. During each session, the clinical and duplex ultrasound scanning (DUS) of the varicose veins to be treated is rst carried out in the standing position, then the patient is asked to lie down. The practitioner should be aware of the anatomical and ultrasonic congurations. The ultrasound ndings help to choose the most appropri­ate puncture sites in terms of safety and efcacy. DUS is performed with a high-frequency probe (10–15 MHz). The diameters of the target trunks or varicose veins are mea­sured at the beginning of the session while the patient is standing. The concentrations of the sclerosant will be cho­sen according to these diameters (Figure
37.1 for suggested concentrations.)
37.5). (See Table
37.5.2.1 Direct puncture
In the direct puncture technique, a needle is attached directly to a syringe containing foam to perform the injec­tion. A 2.5- or 3-mL low-silicone syringe is used. For UGFS, the needle is 22 or 23 gauge (30- or 40-mm length); for visual sclerotherapy, we use a 26-gauge (12-mm length) needle. Sclerotherapy is generally performed in the order of proximal to distal leakage points, proceeding from the larger to the smaller varicose veins. sion, the injections are therefore staggered from top to bot­tom, repeated progressively or not, depending on whether the foam lls the target veins.
37.5.2.1.1 Direct puncture UGFS
Direct puncture UGFS is by far the most widely used technique in France and has been accurately described by one of the authors (CHD) and by other French experts.
and makes the injection, while the second hand holds the ultrasound probe throughout the procedure, the two hands acting independently but in a coordinated manner.
injection site may differ depending on the extent of GSV incompetence. In axial reux, the rst injection should be made in the proximal part of the thigh, approximately 10 cm from the groin; the second injection is made farther down the thigh, depending on how well the foam lls the vein. With this technique, the GSV in the calf is not treated during the rst session
rst injection is made in the interfascial segment of the vein, and the small saphenous vein (SSV) is punctured in the proximal third of the calf or mid-calf
stages:
1. Ultrasound identication of the venous segment to be
7,15–20
In this technique, the dominant hand punctures the vein
For a great saphenous vein (GSV), the choice of the rst
15
(Figure 37.6).
For the anterior accessory saphenous vein (AASV), the
A direct puncture UGFS procedure has seven essential
15–20
injected and of the neighboring arterioles to choose the
14,16,17
During the ses-
7
(Figure 37.7).
37