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24 Lower Extremity Arterial Reconstruction inPatients withDiabetes Mellitus: Principles ofTreatment
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due to risk of nephrogenic systemic brosis [39, 44]. With these considerations in mind, arteriography need not be withheld due to fear of exacerbating moderate chronic renal insufciency.
Framework forApproach toRevascularization
Crafting a strategy for revascularization depends on a thor­ough evaluation of patient risk, limb severity, and anatomic distribution of disease though history, exam, and imaging, as detailed above.
The ultimate goal of lower extremity revascularization is to restore sufcient perfusion to produce ulcer healing. The general consensus is that short stenoses or occlusions are suitable for endovascular techniques while long segment dis­ease is best treated with surgical bypass. This was previously formalized by the anatomic Trans-Atlantic Inter-Society Consensus (TASC) classication system. [45, 46] This sys­tem categorized aortoiliac and femoropopliteal occlusive disease into classes A-D based on complexity. Endovascular intervention was deemed the treatment of choice for TASC A and the preferred strategy for TASC B and surgery preferred for TASC C and the treatment of choice for TASC D lesions. This classication system is limiting however as it considers the aortoiliac and femoropopliteal segments in isolation, and therefore has limited utility in patients with multilevel dis­ease or diabetic patients with infrapopliteal disease.
More recently, the 2019 Global Vascular Guidelines on Critical Limb-Threatening Ischemia have proposed a new classication system: the Global Anatomic Staging System (GLASS) which replaces the previous TASC classication [47]. GLASS requires the selection of a preferred target artery path (TAP) to achieve in line ow from the groin to the ankle. Assuming that inow disease is addressed, a GLASS stage is determined based on assessment of the femoropopliteal seg­ment and infrapopliteal disease complexity, with an inframal­leolar modier to account for pedal disease. This paradigm of disease staging shifts the focus from primary patency of a spe­cic intervention to limb-based patency (LBP), i.e., mainte­nance of the revascularization through the entire TAP.GLASS stage has been shown to predict rates of technical success and limb-related outcomes in several large studies [48, 49].
Once the anatomic staging is complete, the choice between open and endovascular revascularization will ulti­mately depend on individualized patient and limb factors, as well as the treating surgeon’s experience with both tech­niques. Patency of the TAP is one metric by which to mea­sure the success of a revascularization attempt. However, success can also be dened by time to wound healing, resumption of ambulation, and prevention of ulcer recur­rence. Thus, it is critical to consider the extent of tissue loss
and time required to heal a wound when selecting a revascularization strategy. A small toe ulcer may only require a tibial angioplasty with a 6-month patency to heal, whereas a large wound will require a more durable revascularization such as a bypass. Finally, to ensure successful wound heal­ing, patients must be followed with regular surveillance imaging with constant reevaluation and restaging of the limb.
Endovascular Revascularization
Techniques
If after the diagnostic angiogram, an endovascular approach is chosen, the 4-French sheath is exchanged for a longer (45– 90cm) 5-or 6-French sheath that provides stable access over the bifurcation and into the leg of interest. Some interven­tionalists may prefer using antegrade arterial access for distal lesions. Both approaches are acceptable with some limita­tions for each. Intravenous heparin is infused as a bolus in a dose of 80–100units/kg and an activated clotting time (ACT) is checked periodically. We routinely maintain an ACT greater than 250s for aortoiliac and femoropopliteal inter­ventions, or greater than 300s for tibial interventions. Once fully anticoagulated, various wires and supporting catheters can be utilized in a coaxial fashion to cross stenoses or occlu­sions. Every effort is made to keep the wire within the vessel lumen when crossing a lesion. However, it is sometimes nec­essary to cross an occluded vessel in a subintimal plane and re-enter distally at a site of less diseased artery. Short steno­ses may respond well to balloon angioplasty alone [Figs.
24.6 and 24.7]. In the aortoiliac and femoropopliteal seg-
ments, long, calcied stenoses or occlusions are likely to have residual luminal compromise even after balloon angio­plasty and may require stent placement. In the femoral pop­liteal segment, drug coated stents and balloons are available that likely confer a slight patency advantage compared to untreated devices [5053]. Unfortunately, there are currently no such drug-coated balloons or stents that are sized for treatment of the tibial vessels. Stenosis or occlusions of tibial vessels are most commonly treated with balloon angioplasty alone [Fig. 24.8] with balloon diameters ranging from
1.5mm to 3mm and lengths from 20mm to 200mm. Despite a wide variety of atherectomy devices that can facilitate angioplasty, their use does not confer any patency advantage over conventional balloon angioplasty alone. Typically, a single tibial target is treated if it provides pulsatile ow to the ankle and transitions into the pedal circulation. Occasionally peroneal artery revascularization will sufce if there are ade­quate forefoot or hindfoot collateral branches that perfuse the foot. Some proceduralists advocate treating more than one tibial vessel or the plantar arch but there is no data to support this on a routine basis. Angiography is repeated fol-
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Fig. 24.6 (a) Percutaneous angiogram showing occlusion of right tib- ioperoneal trunk (TPT) and three tibial vessels. (b) Balloon angioplasty of TPT stenosis. (c) Balloon angioplasty of posterior tibial artery origin
lowing angioplasty or stenting to evaluate the success of the intervention and to assess for complications including dis­section and distal embolization. There are no available self­expanding stents currently available for the treatment of residual stenosis or dissection. In this situation, a balloon expandable coronary stent can be considered.
In some cases, in may be impossible to cross an infrap­opliteal stenosis or occlusion from an antegrade approach (either from ipsilateral or contralateral femoral access) but there may be a patent distal tibial or pedal vessel that recon­stitutes via collateral ow on angiography. Though this anatomic pattern of disease has typically been best served with bypass surgery, CLTI patients who are at high surgical risk or those who lack appropriate conduit can be consid­ered for retrograde pedal access to facilitate endovascular treatment of previously un-crossable tibial artery occlu­sions [54]. In our experience, this technique has been required with increasing frequency in patients with com­plex tibial disease, after standard endovascular approaches have been attempted [Fig. 24.9].
Deep vein arterialization for limb salvage patients without other conventional endovascular or surgical bypass options has recently re-emerged. The initial description of this technique is attributed to Halstead in 1912 and involves arterial pressuriza­tion of the venous capillary bed in order to improve tissue per­fusion. Initial techniques of AV stula creation or an arterial
stenosis. (d) Completion angiogram showing restoration of in-line ow to the posterior tibial artery
bypass into a venous target have long been abandoned but there has been renewed interest in a purely percutaneous option. Percutaneous deep vein arterialization (DVA) is a technique that creates an arteriovenous connection, usually between the posterior tibial artery and vein. From this connection, stent­grafts are used to reline the posterior tibial vein down to the level of the ankle. This reversal of ow within the venous sys­tem is allowed to perfuse the foot once the nal venous valves in the plantar arch are disrupted. This has been used in patients with “desert foot” where there are no patent pedal arteries for conventional revascularization [Fig. 24.10]. The foot must be stable enough to for several weeks while the foot improves so proper patient selection is critical. Initial results in single arm trials using the commercially available devices (Limow, Inc. San Jose, CA) as well as off-the-shelf devices are sparse [55,
56] but appear to suggest some benet in very well selected
patients and randomized controlled trials are ongoing [57].
Outcomes
The Bypass versus Angioplasty for Severe Ischaemia of the Leg (BASIL) trial was the rst randomized, multicenter, pro­spective trial comparing angioplasty to bypass for critical limb ischemia due to infrainguinal arterial occlusive disease [58
60]. Though the endovascular techniques utilized in the percu-
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24 Lower Extremity Arterial Reconstruction inPatients withDiabetes Mellitus: Principles ofTreatment
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Fig. 24.7 (a) Pretreatment angiogram showing long­segment left posterior tibial artery occlusion. (b) Completion angiogram showing patent posterior tibial artery following angioplasty. Wide collateral network lls less robustly now that in-line ow has been re-established in the PT
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taneous transluminal angioplasty (PTA) arm are now fairly outdated, at 2 years follow up, mortality, limb salvage, and survival were identical for the two groups. The cost of bypass was found to be higher but the PTA group required reinterven­tion more frequently. Surprisingly, functional outcomes and quality of life measures were identical for both groups. In a post hoc analysis of patients surviving beyond 2years, limb salvage and survival were higher for patients undergoing bypass. In spite of its shortcomings, this study validated the use of tibial angioplasty for critical limb ischemia especially for those patients with strong contraindications to surgery or anesthesia and with an anticipated life expectancy of less than 2years. The recently published BEST-CLI trial, discussed in more detail later, has demonstrated that endovascular inter­vention has equivalent outcomes to bypass in patients with no suitable single-segment vein conduit for bypass but otherwise re-afrms the role of bypass.
In our initial published series of infrapopliteal angio­plasty in 176 limbs with CLTI, technical success was achieved in 93% of patients overall and was noted to be
related to lesion length: it was 100% for short, focal steno­ses (1–4cm) or occlusions (< 2cm) but decreased to 75% for longer occlusions or diffusely diseased arteries. Patency of the treated vessel at 1year was only 39% but limb sal­vage was 84% [61].
Following this report, we updated our institutional experi­ence performing infrapopliteal angioplasty for patients with CLTI [62]. Over an 8year period, infrapopliteal PTA was per­formed in 459 limbs (average age 71 years). Of the 413 patients treated, comorbid diabetes was present in 75%. Technical success (residual stenosis <30%) was achieved in 93% of limbs. The 30-day mortality rate was found to be 6% and when only surgical candidates were considered, the 30-day mortality was slightly lower at 4%. In long-term fol­low- up, survival at 1, 3, and 5years was 83%, 64%, and 49% respectively [Fig. 24.11]. Diabetes was not found to be an independent predictor of perioperative or long-term mortality. At 1-year follow-up, primary patency was 57% and limb sal­vage was 84% and at 5-years follow-up, primary patency was 34% and limb salvage was 81%. Restenosis rate at 5years
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Fig. 24.8 (a, b) Subtracted pre-treatment angiogram showing long segment occlusion of right anterior tibial artery with reconstitution of dorsalis pedis. (c, d) Subtracted angigoram showing patent AT following balloon angioplasty
Fig. 24.9 (a) Subtracted pre-treatment angiogram showing long segment occlusion of right popliteal artery which was not amenable to antegrade crossing via contralateral femoral access. (b) Retrograde access to the anterior tibial artery facilitates (c) retrograde crossing of the lesion. Note that anterograde access is maintained with wire in the above knee popliteal
was found to be 74%. Perhaps not surprisingly, worse out­comes were associated with more advanced occlusive dis­ease, as indicated by TASC I classication [63], a nding which has been shown in other small series as well [64, 65]. The incongruity between excellent limb salvage rates and high restenosis rates is partially explained by the frequency
ab c
and presumed efcacy of reintervention. Of all patients treated, 50% required repeat PTA and/or bypass at 5 years follow-up. These ndings reinforce the need for continued surveillance and likelihood of repeat interventions in patients undergoing infrapopliteal angioplasty. The mortality rate of 4% in patients who are also surgical candidates challenges the
ef
100%
433 342 253 186115 88 50 32 1
Number at r
ve
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Fig. 24.10 (a) Pretreatment angiogram demonstrating “desert foot” with no DP or PT in the foot. (b) Percutaneous deep vein arterialization performed through venous access in the posterior tibial and arterial access to the common femoral artery. (c) Gooseneck snares in the pos­terior tibial artery and posterior tibial vein are aligned on uoroscopy. A micropuncture needle is advanced transcutaneously through both snares to create the arteriovenous stula. (d) Contrast angiogram conrms cre-
83%
75%
50%
Overall Survival
25%
0%
02
isk
Fig. 24.11 Long-term survival following infrapopliteal angioplasty. Adapted from Lo, et al. J Vasc Surg. 2013;57(6):1455–63
72%
64%
54%
49%
42%
SE does not exceed 10% for any cur
345
Years
6781
notion that endovascular tibial interventions are safer than surgical bypass. For context, in our institutional report on 1000 cases of dorsalis pedis bypass (average age 66.8years), a 30-day mortality rate of 0.9% was reported [66].
Others have reported their experience with infrapopliteal angioplasty as well. In a meta-analysis of infrapopliteal angioplasty for critical limb ischemia, more than 2500 patients were included, of which 61% had diabetes [67]. Technical success rate was estimated to be 89% and primary patency rates were 77% and 49% at 1 and 3years, respec­tively. Similar to our reported experience, limb salvage rates were 93% at 1year and 82% at 3years indicating acceptable limb salvage rates in the setting of frequent restenosis.
ation of an arteriovenous stula with placement of a balloon expandable stent across the stula. (e) After stenting of the posterior tibial vein with a Viabahn from stula to the PT vein at the ankle, wire access through stula into posterior tibial vein and veins of the foot allows for valvu­lotomy performed with cutting balloons through to the anterior tibial vein. (f) Completion angiogram following percutaneous deep vein arte­rialization demonstrating signicantly improved ow in the foot
For comparison, the authors also performed a meta­analysis of popliteal-dorsalis pedis bypass and found that the limb salvage rate was comparable at 3years (82.3% bypass vs. 82.4% PTA) [68]. Based on the results of the BASIL trial, 3years of follow-up should be adequate to show differences between treatment modalities. These non-randomized results are encouraging, and suggest that endovascular interventions for infrapopliteal occlusive disease may be comparable to bypass in well selected patients.
Importantly, adjunctive technologies including drug­coated balloon angioplasty and drug-eluting stents have developed considerably in recent years [69]. Initial enthusi­asm for drug-coated balloon (DCB) angioplasty in infrapop­liteal arteries has diminished as the results of the INPACT-DEEP trial have become available [70]. This is the largest randomized trial of DCB vs. PTA and showed no additional benet to paclitaxel DCB at 12 months and at 5years [50]. In fact, in the INPACT-DEEP study, DCB was associated with a trend towards higher rates of major ampu­tation compared to PTA. There is currently no compelling evidence that DCB has any additional benet compared to PTA in this setting [69, 71]. However, recent data from the PRESTIGE study of the sirolimus-eluting balloon used below the knee for CLTI patients with TASC C and D lesions has demonstrated promising short-term patency, renewing the interest in DCB technology for tibial disease.
Results regarding the use of drug-eluting stents (DES) have been more uniform. Four RCTs using drug eluting stents in the supercial femoral and proximal popliteal arteries have shown excellent primary patency for DES at 1-year follow-up [72
76]. Similarly, the Dutch PADI trial has demonstrated
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improved patency and limb salvage rates with DES (pacli­taxel, balloon expandable coronary stents) versus angioplasty with or without bare metal stenting in the below knee segment [77]. Taken together, these studies have shown that DES appears to demonstrate clinically relevant improvements in patency, reduced reintervention rates, and reduced amputation rates over PTA and bare metal stenting [7882]. However, lon­ger and more complex stenoses and occlusions may not be amenable to extensive stenting and, as our own experience has shown, these are the lesion types that are prone to failure with endovascular therapy. As DES becomes more widely available for use, the anatomic situations in which DES deployment is most useful should be carefully considered.
Endovascular procedure
Major amputation (1 year follow-up) Atherectomy Drug eluting Stent Drug eluting balloon Plain old balloon angioplasty Plain old balloon angioplasty Stent bare metal
Major amputation (3 year follow-up) Drug eluting Stent Plain old balloon angioplasty Plain old balloon angioplasty Stent bare metal
± Stent bare metal
± Stent bare metal
Number of studies
2 6 2 7 1 5
3 1 1 1
number of patients
95 468 310 554 66 307
254 48 66 41
Although there are is a large armamentarium available for the endovascular treatment of CLTI, there is a relative scarcity of comparative trials. It can be difcult to decide between competing strategies. Almasri etal. recently pub­lished an excellent meta-analysis of 44 trials comparing outcomes in CLTI patients [83]. In the infrapopliteal seg­ment, bare metal stenting (BMS) and DES were associ­ated with the lowest 3-year amputation rates. Three-year primary patency was signicantly higher for DES com­pared to BMS.Overall three-year mortality rates for DES, angioplasty, angioplasty with BMS, and BMS were simi­lar [Fig. 24.12].
Proportion (95% CI)
0.05 (0.02, 0.15)
0.04 (0.01, 0.14)
0.08 (0.05, 0.13)
0.08 (0.03, 0.25)
0.20 (0.11, 0.31)
0.07 (0.02, 0.25)
0.12 (0.06, 0.24)
0.23 (0.12, 0.37)
0.23 (0.13, 0.35)
0.17 (0.07, 0.32)
Mortality (1 year follow-up) Atherectomy Drug eluting Stent Drug eluting balloon Plain old balloon angioplasty Plain old balloon angioplasty Stent bare metal
Mortality (3 year follow-up) Drug eluting Stent Plain old balloon angioplasty Plain old balloon angioplasty Stent bare metal
Primary patency (1 year follow-up) Atherectomy Drug eluting Stent Plain old balloon angioplasty Plain old balloon angioplasty Stent bare metal
Primary patency (3 year follow-up) Drug eluting Stent Plain old balloon angioplasty Stent bare metal
Secondary patency (1 year follow-up) Drug eluting Stent Plain old balloon angioplasty
± Stent bare metal
± Stent bare metal
± Stent bare metal
± Stent bare metal
2 6 2 7 1 5
3 2 1 1
2 6 3 1 5
2 1 1
1 1
95 452 304 662 66 297
242 263 66 41
166 408 205 71 262
115 39 41
66 72
0.07 (0.03, 0.17)
0.17 (0.11, 0.27)
0.10 (0.07, 0.14)
0.15 (0.11, 0.22)
0.24 (0.15, 0.36)
0.15 (0.11, 0.20)
0.33 (0.26, 0.42)
0.31 (0.15, 0.65)
0.47 (0.35, 0.60)
0.32 (0.18, 0.48)
0.78 (0.72, 0.85)
0.73 (0.65, 0.81)
0.66 (0.51, 0.85)
0.42 (0.31, 0.55)
0.50 (0.42, 0.60)
0.49 (0.31, 0.79)
0.21 (0.09, 0.37)
0.10 (0.03, 0.23)
0.65 (0.52, 0.77)
0.56 (0.43, 0.67)
Fig. 24.12 Forest plot demonstrating outcomes following endovascular intervention for infrapopliteal lesions. (Adapted from Almasri, etal. J Vasc Surg. 2019;69(6):126S–136S)
.1 .2 .3 .4 .5 .6 .7 .8 .9 1
0
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Surgical Revascularization
Technique
A patient deemed to be a good candidate for surgical bypass must have an adequate inow source and outow target artery, both of which are typically determined using diagnos­tic DSA.The outow target artery at the location of the distal anastomosis should be relatively free of occlusive disease and demonstrate unimpeded arterial ow into the arteries of the foot. In general, the most proximal artery distal to an occlusion meeting these two criteria is chosen as a bypass target vessel. Distal arterial reconstructions present special technical challenges for the vascular surgeon and require meticulous attention to detail [Fig. 24.13]. The target arteries are usually small, approximately 2.0 millimeters in diameter, and are often affected by medial calcication.
Vein bypass grafts for chronic limb-threating ischemia have well established safety and efcacy. Perioperative mortality in most contemporary series ranges from 1% to 5% and limb salvage may approach 90% at 5years for many patients [84, 85]. Although these results are excellent, they do not reect the high cost of recovery for many patients to achieve this outcome. Wound morbidity is common ranging from 10 to 50% [86, 87]. Limb swelling, delayed healing of ischemic wounds, and the need for additional procedures may delay full recovery for many months. In our study eval­uating quality of life measures in patients undergoing arte­rial bypass for limb salvage, less than 50% reported feeling they were back to normal 6months after surgery [88]. In a
similar study, only 15% of patients achieved the ideal out­come of a patent graft with no need for revision, no wound complications, and a healed foot following bypass. These observations are especially sobering when considering the fact that 50% of patients survive less than 5years after their limb salvage procedure [89].
One of the most important developments in vascular sur­gery has been the demonstration that autogenous saphenous vein, as opposed to prosthetic graft material, gives the best short–and long-term results for distal bypass. In a large multi-center prospective randomized clinical trial, 6-year patency of saphenous vein grafts was more than four times higher than that of prosthetic grafts [90]. For over six decades, the standard graft orientation performed for lower extremity arterial revascularization has been the reversed saphenous vein bypass. The vein is completely harvested and its distal end is translocated to the proximal anastomotic site in order to prevent the impediment of ow from intact venous valves. For tibial bypass especially, this often creates a size discrepancy between the venous conduit and the inow and target arterial anastomoses. To avoid this problem and mini­mize vein harvest trauma, valvulotomy was developed to render the valves incompetent. This allows the vein to be used as a non-reversed conguration. A non-reversed graft can be similarly excised, translocated, tunnelled, or left within its native position as an “in-situ” conguration. In the late 1970s, Leather and associates popularized this technique using a modied Mills valvulotome that atraumatically cuts the valves to render them incompetent [91]. Vascular sur­geons enthusiastically embraced the Leather technique and
Fig. 24.13 Intraoperative photograph of a femoral to posterior tibial bypass using non-reversed greater saphenous vein. (Courtesy of Mark Wyers, MD)
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Fig. 24.14 Intraoperative photograph of vein angioscopy for evaluation of vein quality and valvulotomy. (Courtesy of Mark Wyers, MD)
began reporting improved results with the non-reversed, in situ bypass compared with the conventional reversed vein approach [9294]. This led some to conclude that the in situ bypass possesses inherent biologic superiority to the reversed saphenous vein graft [95]. However, further evidence to sup­port this concept has not been presented [96]. Moreover, when in situ bypasses are compared to more contemporary series of reversed saphenous vein bypasses, no superiority is evident [97]. In our own experience, we have frequently used both procedures and have observed similar results with either vein conguration [98]. We also routinely perform angios­copy to evaluate the overall vein quality and to perform val­vutotomy under direct vision, favoring this over blind valvulotomy techniques [Fig. 24.14]. Flexible valvulotomes are used for in situ grafts and a traditional Mills valvulotome is used for completely harvested grafts.
In the 1980s Ascher and associates reported the rst series of bypass grafts with inow taken from the popliteal artery [99]. Because atherosclerotic occlusive disease often spares the supercial femoral artery in diabetes, the popliteal artery can be readily used as a source of inow for the bypass graft. Doing so shortens the operative procedure time, shortens the length of the bypass, and avoids potentially troublesome groin wound complications, which often accompany thigh and groin dissections. Short vein grafts are also advanta­geous in patients who have a limited quantity of adequate
saphenous vein. Frequently, thigh saphenous vein is har­vested and translocated to the lower leg to avoid parallel incisions between the distal vein harvest site and target artery exposure. They showed results that were equivalent to those of the traditional approach that preferentially used the com­mon femoral artery. Such results have been conrmed by other groups and this technique has proven to be another important advancement in arterial reconstruction for patients with diabetes [100, 101]. Our experience with extreme distal arterial reconstructions has shown that popliteal artery inow is possible in about 60% of diabetic patients undergoing vas­cular reconstruction in the lower extremity [98].
Ipsilateral, single-segment greater saphenous vein is the conduit of choice for infrainguinal leg bypass. When the ipsilateral saphenous vein is unavailable due to varicosities, previous harvesting, or stripping, alternative sources of con­duit must be used. Although some surgeons use prosthetic grafts in these circumstances, alternative vein grafts includ­ing contralateral greater saphenous vein, arm vein, or lesser saphenous vein can be used. In patients with an absent ipsi­lateral greater saphenous vein, the likelihood of requiring another arterial reconstruction in the opposite extremity approaches 40% at 3 years following the rst operation [102]. Because of this, some surgeons hesitate to harvest the contralateral saphenous vein even though it remains the bet­ter option [103].
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When saphenous vein is unavailable bilaterally, our vein conduit of choice is cephalic or basilic vein. Our results with arm vein grafts have been improved by examining the vein with intraoperative angioscopy to exclude segments with strictures or scarring from trauma commonly induced by pre­vious venipuncture or thrombosis [104] [Fig. 24.14]. Using the angioscope to evaluate the quality of arm vein conduit has signicantly improved our results and further reduces the number of patients requiring prosthetic conduit [105]. Although arm vein is a reasonable conduit in most patients, we hesitate to harvest arm vein for leg bypass in patients with end-stage renal disease given the need potential arterio­venous access surgery. One potential disadvantage of arm vein conduits is their limited length. The use of popliteal artery inow makes the use of shorter arm vein grafts possi­ble in many patients. Moreover, in carefully selected patients, the use of composite grafts made by combining vein seg­ments can provide enough conduit length to reach from the groin to the distal tibial and even foot vessels in many patients [31]. Our results with arm vein grafts in over 500 procedures have been reported [106]. Patency was 57.5% and limb salvage was 71.5% at 5years. These results were inferior to those with reconstructions done with saphenous vein, however signicantly better than those reported with prosthetic conduits.
A recent report on the outcomes of tibial bypass with prosthetic graft, heparin bonded polyuorotetraethylene (ePTFE), versus saphenous vein conduit noted a signicant improvement in patency rates associated with saphenous vein use. Patency of the graft was 75% with ePTFE versus 86% with saphenous vein graft during the follow-up period that ranged from 1 to 12months [107]. Large metanalyses also demonstrate that saphenous vein is superior to pros­thetic grafts with lower amputation rates and higher primary and secondary patency out to 3 years after infrapopliteal bypass [Fig. 24.15]. This demonstrates the patency advan­tage of using saphenous vein when available despite the advances in prosthetic graft construction.
Although the current guidelines recommend single anti­platelet therapy following lower extremity bypass [47, 108], there is signicant heterogeneity in the prescribed antithrom­botic regimen following lower extremity bypass. Escalating regimens are typically used to improve patency of prosthetic or disadvantaged vein bypasses. Dual antiplatelet therapy has been demonstrated to improve patency of prosthetic grafts, [109] and the recent VOYAGER trial has demon­strated a reduction in major cardiac and limb events follow­ing revascularization in patients randomized to low dose rivaroxaban plus aspirin, compared to aspirin alone [110,
111]. Our recent observational study on antithrombotic ther-
apy following infrapopliteal bypass for CLTI demonstrated no signicant reduction in major adverse limb events with antithrombotic regimens beyond an antiplatelet alone [112].
In general, the goal of treatment is to restore maximal arterial ow to the foot since this provides the best chance for healing. The preoperative diagnostic arteriogram is the key piece of information necessary in planning the appropri­ate surgical procedure for each patient. If a bypass to the popliteal or tibial artery will restore maximal arterial ow and restoration of palpable foot pulses, bypasses need not extend to the level of the foot. Since the quality of venous conduit is the most important determinant in long-term suc­cess, using the shortest length of high-quality venous conduit necessary to achieve this goal is the basic rule. Each opera­tion must be individualized based on the patient’s available venous conduit and arterial anatomy.
Outcomes
The BEST-CLI (Best Endovascular versus Best Surgical Therapy for Critical Limb Ischemia) is the largest, most con­temporary randomized clinical trial designed to compare outcomes after open and endovascular revascularization in the CLTI population [113]. In the recently published results, 1830 patients were randomized in two cohorts to bypass or endovascular revascularization based on availability of vein. The primary outcome was a composite of major adverse limb events and all-cause mortality. For patients who had single-segment great saphenous vein available for conduit, those who received surgery had signicantly lower risk of a major adverse limb event or death (43% vs. 57%, HR 0.68) over a median follow-up of 2.7years. However, in the cohort of patients who did not have single-segment GSV available, both groups had similar rates of adverse outcomes.
Based on these trial results, it is clear that in CLTI patients with acceptable surgical risk and adequate GSV, surgical bypass should be the initial revascularization strategy. Bypass has superior outcomes over 3 years compared to endovascular interventions in this subgroup. However, the initial strategy in patients without adequate vein is not so clear—consideration of the individual patient’s risk, anat­omy, and limb severity is required to select the optimal approach.
The independent effect of diabetes on outcomes in patients undergoing surgical bypass is controversial and con­tinues to be debated. Although the majority of patients in BEST-CLI (>70%) were diabetic, an analysis of outcomes by diabetic status has not yet been published. In the PREVENT III trial, 1404 patients underwent bypass for CLI, of which 64% had diabetes [114]. The authors found that diabetes status did not affect graft patency. Congruent with these results was the nding that when optimal vein conduit was used, there were no signicant differences in patency between femoropopliteal bypasses and distal bypasses (tibial or pedal target vessels) [114, 115]. Our institutional experi-
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S. X. Wang and M. C. Wyers
Fig. 24.15 Forest plot demonstrating outcomes following bypass surgery for infrapopliteal lesions. (Adapted from Almasri, etal. J Vasc Surg. 2019;69(6):126S–136S)
ence with greater than 800 lower extremity bypass proce­dures has also shown no independent effect of comorbid diabetes on outcomes [116] [Fig. 24.16]. Our updated analy­sis of institutional experience with 650 rst-time lower extremity bypass for CLTI has also demonstrated no impact of diabetes (regardless of insulin dependence) on graft patency or reintervention rate. Although insulin-dependent diabetes (IDDM) was associated with incomplete wound healing and higher amputation rate following initial endo­vascular intervention, IDDM was only associated with poor wound healing but equivalent limb salvage outcomes after
bypass, suggesting that a bypass rst strategy may be more suitable in IDDM patients [117].
Findings from PREVENT III, CIRCULASE, and BASIL trials were combined by the Society for Vascular Surgery to formulate objective performance goals for bypass surgery [15]. This analysis included only the highest quality random­ized, controlled data of patients undergoing bypass with autogenous vein. The investigators found that older patients (age>80) and patients with tissue loss should be considered “clinical high risk” due to demonstrably worse outcomes at 1 year follow-up. Diabetes was not determined to signi-