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252 Chapter 27/Principles of Ambulatory Phlebectomy
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phlebectomy is required, we allow three months to elapse; this allows the infl ammatory response to improve at the original AP sites.
AVOIDING NONTARGET TISSUES
If the treating physician heeds several important sugges­tions, complications will rarely be encountered. The venous surgeon must have a thorough command of neurovascular anatomy to avoid injury to nontarget tissues such as arteries and nerves. Knowledge of the course of the common femoral artery, superfi cial femoral artery, popliteal artery, and ante­rior and posterior tibial arteries will keep the surgeon from injuring these structures while probing to exteriorize a vari­cose vein. It would be very diffi cult, although not impossi­ble, to injure the profunda femoris or peroneal arteries during AP. As stated earlier, the hook rarely needs to plunge deeper than 3 mm to contact the target vein.
The saphenous and sural nerves are particularly prone to injury below the knee because of their proximity to the Great and Small Saphenous veins. If the saphenous or sural nerves are displaced by the hook, the patient usually will complain of shooting pain into the foot. This is a sign for the surgeon to gently release the structure and replace it in situ. The femoral, obturator, sciatic, tibial, and peroneal (common, deep, and superfi cial) nerves are deep and generally not disturbed in the hands of a competent surgeon. However, when placing the post-operative compression bandage, the deep peroneal nerve can be injured if the lateral fi bular head is not properly padded. Occasionally, hair-sized sensory cutaneous nerves are encountered and inadvertently extracted during the course of AP. They are recognized as small threads and the patient will feel acute sharp pain. The pain usually dissipates after two to fi ve minutes without treat­ment. If this occurs in the ankle and foot area, chances are that the patient will develop postoperative paraesthesias or areas of dysesthesia that in most cases will be temporary.
14
techniques with either radiofrequency or laser have proven to be the method of choice for eliminating the GSV from the circulation.
19,20
Varicosities on the anterior thigh usually result from Anterior Accessory Saphenous Vein (AASV) incompetence. These veins usually course over the knee and into the lower leg. Small Saphenous vein (SSV) refl ux produces varicosi­ties on the posterior calf. When also present on the posterior thigh, the surgeon must consider a cranial extension of the SSV, which can be identifi ed with duplex ultrasound imaging. Cranial extensions may enter the GSV (Giacomini vein) or enter the femoral vein directly.
In cases where no “feeding source” is found, phlebec­tomy of the varicosities may be all that is required. Labro­poulos21 has shown that varicose veins may result from a primary vein wall defect and that refl ux may be confi ned to superfi cial tributaries throughout the lower limb. Without great and small saphenous trunk incompetence, perforator and deep-vein incompetence, or proximal obstruction, his data suggest that refl ux can develop in any vein without an apparent feeding source. This is often the case when bulging reticular veins are seen along the course of the lateral leg. This lateral subdermic complex and its vein of Albanese are often dilated and bulging in elderly patients. The underlying source of venous hypertension is usually perigeniculate per­forating veins, not easily identifi able with duplex imaging. AP using an 18-gauge needle stab incision and a small crochet hook for exteriorization of the vein is an excellent procedure for this clinical problem. Perforating veins of the thigh or calf also may become incompetent and be sources of ambulatory venous hypertension. These can be treated by a variety of techniques including ligation, subfascial endo­scopic perforator surgery (SEPS), and ultrasound-guided sclerotherapy (UGS).
AP VERSUS POWERED PHLEBECTOMY
TREATMENT OF VARICOSE VEINS
FROM NONSAPHENOUS ORIGINS
Bulging varicose veins on the surface of the skin can originate from different sources. Identifi cation of these sources is important because this infl uences the treatment plan. Varicosities on the medial aspect of the thigh and calf are usually the result of GSV incompetence. In order to minimize the chance for recurrence, the GSV must be elim­inated from the circulation. This concept has been substanti­ated in several prospective randomized clinical trials involving patients who were treated with or without saphe­nectomy by conventional vein stripping. rates for limbs without saphenctomy were much higher than those with saphenectomy. Of course, now thermal ablation
15–18
The recurrence
In a published prospective comparative randomized trial comparing AP with the new technique of transillumination­powered phlebectomy (TriVex), there was no difference in operating time. Although an incision ratio of 7 : 1 favored TriVex, there was no perceived cosmetic benefi t among the patient groups. There was a higher number of recurrences in the TriVex group (21.2%; 7 of 33) compared with the AP group (6.2%; 2 of 32) at 52 weeks postoperatively. Assessment of pain scores showed no difference between
22
groups. investigators.
These fi ndings have been supported by other
23–27
It is important to point out that all Trivex procedures were performed in the hospital under general anesthesia, and the cost of disposable equipment used for the TriVex procedure was to $314 per patient. Because the trend for venous surgery is offi ce-based, with local anesthesia, TriVex will likely fall
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into disfavor in the future if modifi cations for offi ce use are ignored.
AP VERSUS COMPRESSION
SCLEROTHERAPY
The combination of compression therapy with intrave­nous injection of a sclerosing agent for the treatment of varicose veins was introduced in 1953.28 Early studies indi­cated compression sclerotherapy (Sclero) would be an effi ­cient addition to varicose vein surgery practiced at that time. Although ambulatory phlebectomy was “invented” around the same period,2 this technique required considerable time to become well-established worldwide. There is one ran­domized controlled trial on recurrence rates and other com­plications after Sclero and AP. A total of 98 operations were randomized to either AP (n = 49) or Sclero (n = 49) in a total of 82 lateral accessory varicose veins (LAVs). In this study, polidocanol was used in a 3% solution (Aethoxysclerol; Kreussler & Co., Wiesbaden, Germany), which is equivalent to 1.5% sodium tetradecyl sulfate. One year after Sclero, 12 LAVs had recurred (25%), and only one postphlebectomy LAV (2.1%). After two years, the difference in recurrence was even larger because another six recurrences developed, making a total of 18 recurrences in the Sclero group (37.5%) and only one recurrence in the AP group (2.1%). The authors of the study concluded that AP is the treatment of choice for LAV.
29
AP FOR OTHER AREAS OF THE BODY
Foot
agent near the eye or use it in substantially lower concentra­tions and volumes. This is due to fear that the solution may travel to unintended areas of venous circulation such as the central retinal vein, choroidal vortex veins, or even the cav­ernous sinus via valveless anastomoses.33 Blindness has been reported following STS injection into a venous malfor­mation partially located in the orbit.
34
Ambulatory phlebectomy of the periocular vein avoids the concerns regarding thrombotic phenomena within ocular, orbital, or cerebral veins possibly associated with periocular vein sclerotherapy. Weiss35 reported excellent results on 10 patients who underwent removal of periocular reticular blue veins by AP. A single puncture with an 18-gauge needle suffi ced in most cases. It is important to attempt to remove the entire segment, as partial resection may lead to recur­rence. The use of postoperative compression for 10 minutes reduces the incidence of bruising. The puncture sites typi­cally disappear quickly without leaving scars.
Hands
In general, inquiries about hand vein treatment come from elderly women who fi nd them unsightly. Often, they have had prior facelift surgery and worry that their hands need rejuvenation to complement the face. Our initial con­sultation stresses the importance of hand veins for reasons of intravenous access, furthermore, removal of these veins may require central venous access should the patient be hospitalized in the future. If attempts to dissuade the patient fail, we recommend AP as the procedure of choice for hand vein removal. It is performed identical to leg vein treatment, and closely resembles treating the dorsum of foot because of the thin skin overlying the area. Results have been excellent.
In recent years there have been several publications on the use of AP for the treatment of varicose veins of the foot and ankle region.
30–32
There are patients who present with serious phlebologic complaints of varicosities of the foot and ankle region that can be alleviated through simple treat­ment. The venous anatomy of the foot with many parallel veins is complicated; however, safe treatment is possible.
The skin of the foot is thin and fi brotic. Further, there is minimal subcutaneous fat, less protection against trauma of the skin, and important underlying tissues such as tendons, tendon sheaths, and joints. There are more small nerve branches that can be damaged by the hook. As in the pop­liteal space, there is greater risk of injuring an artery. More­over, it is possible to grasp and avulse a tendon.
Eyelid
Many ophthalmic plastic surgeons and dermatologic sur­geons experienced in sclerotherapy avoid the use of this
OFFICE-BASED AP WITH
TUMESCENT ANESTHESIA
Although there are reports of death and serious complica­tions with tumescent anesthesia, these have largely been found in the plastic surgery literature.36 Complications are described when tumescent anesthesia is used in conjunction with intravenous sedation, and/or general anesthesia.37 Coldiron et al. recently studied State of Florida data over a four-year period to help clarify actual adverse events occur­ring in the offi ce setting. There were 77 events reported to the Florida Agency for Health Care Administration (ACHA) from March 1, 2000, to March 1, 2004. Liposuction per­formed under general anesthesia was the most frequent procedure reported. Five reported deaths and 14 transfer incidents occurred as a complication of liposuction (with or without another associated procedure) under general anes­thesia or deep sedation. According to the Florida data, there
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Before
After
A
FIGURE 27.4 Before and after photos.
were no problems associated with liposuction using dilute or tumescent anesthesia.38 Similarly, a malpractice claims study by Coleman and colleagues study supported the safety of offi ce-based liposuction performed by dermatologists using tumescent anesthesia for small-volume fat removal.39 In addition, Housman and colleagues surveyed 261 derma­tologic surgeons performing a total of 66,570 liposuction procedures and found a low rate of serious adverse events (0.68 per 1000) and no reports of associated deaths.40 All three studies support the safety of tumescent liposuction performed by dermatologists in an offi ce setting.
Because the tumescent anesthetic technique for venous procedures has been adopted from the liposuction commu­nity, we feel these data are relevant to subcutaneous venous surgery using dilute tumescent anesthesia. There have been no adverse events reported to the Florida ACHA as a result of varicose vein surgery using tumescent anesthesia.
Advantages of offi ce-based surgery are ease of schedul­ing for doctor and patient, less paper work (unnecessary duplication of information and record keeping), no waiting for other surgeons to fi nish their operations, elimination of travel time, and cost containment for the health care system. Furthermore, a staff that performs the same procedures daily is more streamlined and safe.
B
CONCLUSION
Ambulatory phlebectomy is elegant by its mere simplic­ity. It is effective and safe with acceptable cosmetic results (see Figure 27.4). AP is a perfect complement to endove­nous thermal ablation of the saphenous veins. With this combination, patients can expect all varicose veins to vanish following a one-hour procedure that employed only local anesthesia, in the comfort of a physician’s offi ce.
References
1. Celsus AC. Medicinae Libri Octo, Patavii. Typis Seminarii Apud
Joannem Manfre, Liber Septimus. 1749. 473–474.
2. Muller R. Traitement des varices par la phlebectomie ambulatoire,
Phlebologie. 1966. 19: 277–279.
3. Goren G, Yellin AE. Surgery for varicose veins: The ambulatory stab
avulsion phlebectomy, Am J Surg. 1991. 162: 166–174.
4. Weiss RA, Goldman MP. Transillumination mapping prior to ambula-
tory phlebectomy, Dermatol Surg. 1998. 24: 447–450.
5. Proebstle TM, Paepcke U, Weisel G, Gass S, Weber L. High ligation
and stripping of the long saphenous vein using the tumescent technique for local anaesthesia, Dermatol Surg. 1998. 24: 149–153.
6. Klein JA. The tumescent technique for liposuction surgery, Am J
Cosmet Surg. 1987. 4: 263–267.
References 255
https://t.me/med1917
7. Cohn MS, Seiger E, Goldman S. Ambulatory phlebectomy using the tumescent technique for local anaesthesia, Dermatol Surg. 1995. 21: 315–318.
8. Klein JA. Tumescent technique for local anaesthesia improves safety in large-volume liposuction, Plast Reconstr Surg. 1993. 92: 1085–
1098.
9. Keel D, Goldman MP. Tumescent anaesthesia in ambulatory phlebec­tomy: Addition of epinephrine, Dermatol Surg. 1999. 25: 371–372.
10. Schmid RM, Rosenkranz HS. Antimicrobial activity of local anaesthet­ics: Lidocaine and procaine, J Infect Dis. 1970. 121: 597.
11. Ricci S. Ambulatory phlebectomy: Principles and evolution of the method, Dermatol Surg. 1998. 24: 459–464.
12. Olivencia JA. Complications of ambulatory phlebectomy: Review of 1,000 consecutive cases, Dermatol Surg. 1997. 23: 51–54.
13. Gauthier Y. Incidents and complications. In: Dortu J, Raymond­Martimbeau P, eds. Ambulatory Phlebectomy/Phlebectomie Ambul­atoire. Houston: PRM Editions. 1993. 109–112.
14. Ramelet AA. Complications of ambulatory phlebectomy, Dermatol Surg. 1997. 23: 947–954.
15. Jones L, Braithwaite BD, Selwyn D, Cooke S, Earnshaw JJ. Neovas­cularisation is the principal cause of varicose vein recurrence: Results of a randomized trial of stripping the long saphenous vein, Eur J Vasc Endovasc Surg. 1996. 12(4): 442–445.
16. Winterborn RJ, Foy C, Earnshaw JJ. Causes of varicose vein recur­rence: Late results of a randomized controlled trial of stripping the long saphenous vein, J Vasc Surg. 2004. 40(4): 634–639.
17. Dwerryhouse S, Davies B, Harradine K, Earnshaw JJ. Stripping the long saphenous vein reduces the rate of reoperation for recurrent vari­cose veins: Five-year results of a randomized trial, J Vasc Surg. 1999. 29(4): 589–592.
18. Sarin S, Scurr JH, Coleridge Smith PD. Stripping of the long saphenous vein in the treatment of primary varicose veins, Br J Surg. 1994. 81(10): 1455–1458.
19. Min RJ, Khilnani N, Zimmet SE. Endovenous laser treatment of saphe­nous vein refl ux: Long-term results, J Vasc Interv Radiol. 2003. 14(8): 991–996.
20. Merchant RF, Pichot O, Myers KA. Four-year follow-up on endovas­cular radiofrequency obliteration of great saphenous refl ux, Dermatol Surg. 2005. 31(2): 129–134.
21. Labropoulos N, Kang SS, Mansour MA, Giannoukas AD, Buckman J, Baker WH. Primary superfi cial vein refl ux with competent saphenous trunk, Eur J Vasc Endovasc Surg. 1999. 18(3): 201–206.
22. Aremu MA, Mahendran B, Butcher W, Khan Z, Colgan MP, Moore DJ et al. Prospective randomized controlled trial: Conventional versus powered phlebectomy, J Vasc Surg. 2004. 39(1): 88–94.
23. Spitz GA, Braxton JM, Bergan JJ. Outpatient varicose vein surgery with transilluminated powered phlebectomy, Vasc Surg 2000. 34: 547–555.
24. Arumugasamy M, McGreal G, O’Connor A, Kelly C, Bouchier-Hayes D, Leahy A. The technique of transilluminated powered phlebectomy: A novel minimally invasive system for varicose vein surgery, Eur J Vasc Endovasc Surg. 2002. 23: 180–182.
25. Scavée V, Theys S, Schoevaerdts J-C. Transilluminated powered mini­phlebectomy: Early clinical experience, Acta Chir Belg. 2001. 101: 247–249.
26. Cheshire N, Elias SM, Keagy B et al. Powered phlebectomy (TriVex) in treatment of varicose veins, Ann Vasc Surg. 2002. 16: 488–494.
27. Scavée V, Lesceu O, Theys S, Jamart J, Louagie Y, Schoevaerdts JC. Hook phlebectomy versus transilluminated powered phlebectomy for varicose vein surgery: Early results, Eur J Vasc Endovasc Surg. 2003. 25: 473–475.
28. Fegan WG. Continuous compression technique for injecting varicose veins, Lancet 1963. 20(2): 109–109.
29. De Roos KP, Nieman FH, Neumann HA. Ambulatory phlebectomy versus compression sclerotherapy: Results of a randomized controlled trial, Dermatol Surg. 2003. 29(3): 221–226.
30. Olivencia JA. Ambulatory phlebectomy of the foot; review of 75 patients, Dermatol Surg. 1997. 23: 279–280.
31. Muller R. Traitement des varices du pied par la phlebectomie ambu- latoire, Phlebologie. 1990. 43: 317–318.
32. Constancias-Dortu I. Indications therapeutiques de la phlebectomie ambulatoire, Phlebologie. 1987. 40: 853–858.
33. Fante RG, Goldman MP. Removal of periocular veins by scler­otherapy, Ophthalmology. 2001. 108: 433–434.
34. Siniluoto TM, Svendsen PA, Wikholm GM, Fogdestam I, Edstrom S. Percutaneous sclerotherapy of venous malformations of the head and neck using sodium tetradecyl sulphate (sotradecol), Scand J Plast Reconstr Surg Hand Surg. 1997. 31: 145–150.
35. Weiss RA, Ramelet AA. Removal of blue periocular lower eyelid veins by ambulatory phlebectomy, Dermatol Surg. 2002. 28(1): 43–45.
36. Rao RB, Ely SF, Hoffman RS. Deaths related to liposuction, N Engl J Med. 1999. 340: 1471–1475.
37. Hanke CW, Bernstein G, Bullock S. Safety of tumescent liposuction in 15,336 patients, Dermatol Surg. 1995. 21: 459–462.
38. Coldiron B, Fisher AH, Adelman E, Yelverton CB, Balkrishnan R, Feldman MA, Feldman SR. Adverse event reporting: lessons learned from 4 years of Florida offi ce data, Dermatol Surg. 2005. 31(9): 1079–
1093.
39. Coleman W, Hanke C, Lillis P et al. Does the location of the surgery or the specialty of the physician affect malpractice claims in liposuc­tion? Dermatol Surg. 1999. 25: 343–347.
40. Housman TS, Lawrence N, Mellen BG et al. The safety of liposuction: Results of a national survey, Dermatol Surg. 2002. 28: 971–978.
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CHAPTER
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28
Powered Phlebectomy in Surgery of
Varicose Veins
STEVE ELIAS
PREMISE
The generic name of the TriVex technique is transillumi­nated powered phlebectomy (TIPP). TriVex is a mechanical method used to remove tributary varicose veins that nor­mally would be excised with the traditional techniques of stab avulsion and hook phlebectomy. The indications for TriVex are the same as for the use of traditional procedures.
INSTRUMENTATION
The TriVex system consists of a transilluminator/irriga­tor (see Figure 28.1) and a powered resector (see Figure
28.2). The transilluminator/irrigator is placed subcutane­ously to provide for visualization of the varicose veins and instillation of the tumescent fl uid (see Figure 28.3). Utilizing the powered resector with its rotating blade on suction mode, the varicosities are removed (see Figure 28.4). TriVex has been described as “liposuction of the veins.” The resector is a modifi cation of an arthroscopic shaver. The complete up­to-date step-by-step technique will be described later, in a subsequent section of this chapter.
The advantages of the TriVex technique compared to traditional open surgery are speed, effi ciency, decreased number of incisions, and more complete removal due to direct visualization of the target veins. Fewer residual and recurrent varicosities are also a theoretical possibility, again, due to a more complete removal of the primary targets. These are presumptive advantages and, in fact, most have been realized.
THE BEGINNING
The TriVex system was developed in 1996 by Greg Spitz, MD, a surgeon from Aurora, Illinois. He was looking for a faster, more effi cient way to remove varicose veins. It was a Friday afternoon and Greg was on his third or fourth extensive bilateral vein case. He asked the scrub nurse if there was anything available to more quickly excise the varicose veins. Together they decided to try a small arthroscopic shaver used to treat carpal tunnel syndrome. This seemed to work. Later on, specifi c instrumentation to allow visualization and transillumination with a modifi ed cystoscope was developed.
After a series of modifi cations and the addition of tumes­cent anesthesia for hydrodissection, the essential compo­nents of the system were in place. Eventually, these included a transilluminator/irrigator, which is similar to the present device, and a resector, which was still a modifi ed arthroscopic shaver with a 4.5 mm blade.
Spitz’s original experience was reported fi ve years ago.1 His original description of the technique is very similar to the present-day method with some modifi cations. “The TriVex System” combination tumescent anesthesia delivery system and illuminator were used to select sites for the local anesthesia. Transillumination was obtained with light from a 45-degree illuminator specifi cally designed for this purpose. Varicose clusters were extracted by use of a mod­ifi cation of Smith and Nephew EP-1 endoscopic powered tissue dissector. Then, as now, this device is a rotating, tubular inner blade encased in a protective stationary outer sheath. The working opening is placed adjacent to the vari­cosities, which are then aspirated, morcellated, and removed
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FIGURE 28.1 Original transilluminator/irrigator.
FIGURE 28.3 Instillation tumescent fl uid.
FIGURE 28.4 Resection varicosities.
FIGURE 28.2 Original powered resector.
by irrigation suction. Control of vein removal is through a handpiece that directs the vein fragments into a container connected to hospital wall suction.
1
As reported, the initial results were encouraging. The operation appeared faster (41 vs. 75 minutes) and required fewer incisions (5.6 vs. 17). Cellulitis, hematoma, signifi ­cant bruising, and swelling were recorded as complications. However, cosmetic scores appeared acceptable.
The discussion following the initial presentation com­mented, “Despite knowing that change is constant, who would have thought that change would occur in routine varicose vein surgery. Yet change has occurred. This pre­sentation by Spitz demonstrates ingenuity and imagination in pursuing development of a dedicated tool for better removal of venous varicosities.” TriVex was now ready for a larger clinical trial.
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FIGURE 28.6 Transillumination intra op.
Trendelenburg position. An initial 3 mm incision was made
FIGURE 28.5 Pre-op marking.
INITIAL CLINICAL TRIAL
AND TECHNIQUE
The initial clinical trial consisted of centers in the United States (4) and Europe (4), in which we participated.2 Prior to instituting the trial, Spitz visited each site or the partici­pants visited him to gain hands-on proctored experience. This, of course, insured relative consistency of methodol­ogy. There were variations developed on the original theme especially regarding irrigation pressure devices.
The technique ultimately used in the trial was very similar to that described in Spitz’s original presentation. For pur­poses of understanding, the original technique and technol­ogy are described next, because these have implications regarding the subsequent modifi cations. The technique being described is the original method and not the present modifi cation.
Initial patient evaluation is exactly as is traditional in varicose vein surgery. Full duplex imaging is obtained and all abnormal vein segments are identifi ed and marked. The markings are placed around the veins and not directly on the varices themselves (see Figure 28.5). The reason for not placing markings directly over the veins is that these may be misinterpreted under transillumination as residual unre­sected veins. Saphenous incompetence is managed by sur­geon’s choice, laser (EVLT), radiofrequency (VNUS), or by traditional stripping.
The operation was done using general, spinal, or laryn­geal mask airway anesthesia with the patient positioned in
just outside the marked area of varicosities. The transillumi­nator/irrigator was placed subcutaneously and distal to the level of the veins The room lights were dimmed for better transillumination (see Figure 28.6).
The fi rst stage of tumescence was infused using a mix­ture of 40 cc of 2% xylocaine and 1 cc epinephrine in a liter of saline. This is infused using a pressure bag, high pressure blood transfuser, or a peristaltic pump as that used for liposuction.
As will be discussed later, infusion techniques became a signifi cant variable.
The tumescent fl uid hydrodissects the veins, partially exsanguinates the veins, and allows better diffusion of light in the subcutaneous tissue.
After the fi rst stage of tumescence, the veins are ready for resection. A second 3 mm incision is made, preferably 180º from the fi rst incision. The resector is passed subcuta­neously immediately beneath the veins in a more superfi cial plane than the illuminator (see Figure 28.7). The resector targets the veins and these are suctioned into the rotating blade, morcellated, and removed (see Figure 28.4).
Most of the veins are removed with the fi rst pass. The operator should not go back and forth over a resected area, as more bruising will occur. The skin lying over the area of resection is kept taut to minimize skin trauma and stabilize the veins that are being resected (see Figure 28.8). To treat other areas, the resector is removed and redirected. Shearing through tissue is therefore minimized. To reach more distant areas the resector and irrigator/illuminator ports may be reversed or inserted through other incisions.
After resection, a second stage tumescence is infused. This has a two-fold goal: irrigation and removal of any residual blood and creation of subcutaneous pressure to
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incisions required were three. Most patients were happy with the results. Complications did occur: hematoma, sub­cutaneous scarring, bruising, and hyperpigmentation were the most notable.
CLINICAL TRIAL AND
TECHNIQUE DISCUSSION
Every procedure has a learning curve. Changes were made to address the technique and technology issues that were identifi ed in the initial experience. These led to a better procedure, thus giving the present excellent results.
We entered the maximum number of cases (20) that could be entered into the trial and patients operated upon later in
FIGURE 28.7 Level of resector.
FIGURE 28.8 Resection with skin tension.
the series did better than those treated earlier. Overresecting and shearing through tissue caused some of the subcutane­ous scarring and bruising. In the beginning it was not appre­ciated by most of us that veins were removed with the fi rst pass of the resector. This lead to overresecting. After a vein segment is resected blood fi lls that resected channel from either end of the resected vein. This can appear as an unresected vein and the operator may re-resect the area leading to excessive subcutaneous trauma. The resection vein site does appear different from an unresected vein. It appears as if a vein has been smudged and has a less defi ned outline.
Hematoma and hyperpigmentation are caused by residual trapped blood. The initial technique called for closing inci­sions with steri-strips or suture to keep the second stage tumescence in the subcutaneous tissue to help tamponade bleeding from the ends of the resected veins. This of course, did not enhance drainage of any residual blood.
tamponade the ends of resected veins. Enough fl uid is infused to create a peau d’orange effect on the skin. The incisions are closed with steri-strips and overwrapped with an absorbent compression dressing.
Postoperatively, the leg is redressed on the second or third day, and compression stockings are prescribed for two to three weeks.
Initial visual results are usually good. Bag Balm, an oint­ment with hydroquinilone, is used with massage to help minimize scarring and hasten subcutaneous healing.
This was the technique and technology for the initial trial. This was also the technique that was taught and used during the initial three years of TriVex use. Results of the clinical trial were good. The procedure was relatively quick: 14 minutes for phlebectomy and 45 minutes for phle­bectomy and saphenous excision. The median number of
CLINICAL TRIAL TECHNOLOGY ISSUES
As mentioned previously, the irrigator/illuminator was used with various pressure infusion devices. This did not allow standard instillation of fl uid for tumescence or for evacuation of blood post resection. Various trial centers were able to be highly effective, whereas others could not attain signifi cant fl ow rates. This lead to residual hematomas.
Blade speeds of 800–1000 rpms were used. In general
4.5 mm (smaller) blades were used. Both of these factors did not allow suction to be applied adequately to the veins to be resected due to the small blade aperture. Some residual seg­ments were left and areas needed multiple passes to resect veins. This enhanced subcutaneous scarring.
The counterintuitive notion of slow blade speeds and larger blades being less traumatic did not surface until later in the experience.
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SUMMARY OF INITIAL TRIAL
Despite some of the shortcomings identifi ed earlier, most patients and surgeons participating in the trial were quite happy. The procedure was faster, required less incisions, and was more enjoyable and less tedious than traditional proce­dures. Cosmetic scores and patient satisfaction scores were acceptable.
EARLY RESULTS AND EXPERIENCE
After the initial clinical trial, training of other physicians began. This consisted of a variety of methods. Didactic presentations were held throughout the country. Training also involved observing cases, hands-on experience, as well as proctoring of initial cases. Many surgeons began to utilize the technique; the appeal being a faster, more complete vein removal with fewer incisions.
As more surgeons became involved, a number of tech­nical and technological issues began to surface. From a technology perspective there was not standardization of irrigation and tumescent infusion. A variety of devices were used, including pressure bags, gravity, blood infusers, laparoscopic irrigators, and peristaltic pumps. These all delivered varying rates and pressures of infusion. The dictum was to use the highest pressure available, but that varied from institution to institution. This led to signifi cant residual subcutaneous blood and, at times, hematomas requiring drainage.
Another technological issue was blade size. Most sur­geons utilized the smaller original blade at 1000 rpm. This led to excessive mechanical trauma and less effi ciency in suctioning veins into the blade. From a technique viewpoint, some surgeons did not appreciate the damage that a patient could incur if one was rough and swept through the subcu­taneous tissue when one was resecting. The concept of “tar­geted gentle” resection was not always adhered to. Many surgeons continued the pulling and tugging required during traditional techniques.
The instillation of second stage tumescence after vein resection and the closure of incision sites led to trapped blood and fl uid, not allowing adequate drainage. The origi­nal thinking was that the pressure of tumescence would tamponade the ends of resected veins, and minimize bleed­ing. What did occur in some cases was prolonged subcutane­ous edema from the tumescence. Most edema did resolve over a period of time.
Despite some of these issues, many surgeons gained signifi cant experience and results continued to improve. Groups then began reporting results with very consistent fi ndings.
RESULTS
The original reported results of Spitz et al. continued to be obtained by other investigators. At the core were consis­tent fi ndings: shorter procedure, decreased number of inci­sions, similar patient satisfaction, and similar complication rates, when compared to traditional methods. results with experience was expected and was echoed by a number of investigators.
5,6
The resection of extensive vari­cosities was an area in which TriVex was found to be sig­nifi cantly faster than traditional procedures. time varied between investigators but most were within the range of 12 to 30 minutes for the TriVex part of the proce-
2,3,7
dure.
This difference became more important and achieved greater statistical signifi cance as the extent of resected varicosities increased.
The initial multicenter safety and effi cacy trial had an
average phlebectomy time of 14 minutes and the median
2
number of incisions as 3.
All other reports showed a sig­nifi cant decrease in incisions ranging from 3.6 reported by Arumugasamy to 4.0 (compared to 18.9) attained by Ray­Chaudhuri et al. in a prospective trial. In the only prospec­tive randomized trial Aremu et al. found a signifi cant difference between traditional (29) and TriVex (5) incisions (p < .0001). What is also clear and consistent is the conclu­sion that post-op pain scores, patient satisfaction, patient cosmetic scores, and complication rates are essentially the same as traditional methods. Ray-Chaudhuri et al. compared post-operative pain scores with the results after 14 days being 2.6 (traditional) and 1.9 (TriVex) (NS). Mean cos­metic scores were also similar 6.9 (traditional) and 5.9 (TriVex) (NS).3 Scavee, after gaining experience, reported midterm clinical experience.8 The mean pain score at six weeks was 0 (no pain) for TriVex. Patient satisfaction and patient cosmetic scores showed no signifi cant differences in the two randomized trials.
3,4
This was fi rst pointed out in Spitz’s original report. Complications do occur and have been reported. The rates appear to be similar to conventional procedures. Arumugasamy et al. reported that, “bruising was seen in nearly all patients at 1 week and this settled between 6–12 weeks later.”
7
Mackay9 reported a 66% incidence of perceived com­plications, including bruising, within the fi rst two weeks following conventional surgery. Aremu et al. in a prospec­tive randomized trial found no difference with regard to bruising, cellulitis, or numbness between techniques. Nerve injury was 3% at one year.
4
The learning curve has been discussed by a number of investigators. It is no surprise that earlier cases resulted in poorer results and experience improved results. Scavee in his midterm trial results states “our initial clinical experience was associated with a high rate of hematoma formation, especially in the calf region, resulting from our learning
3–5
Improved
3,4
Operative