Abstract
INTRODUCTION:
Modified proximal radial artery arteriovenous fistula (MPRAVF) can be used to improve the success and patency of basilic vein transposition (BVT) and cephalic vein transposition (CVT). In the present study, surgical experience with patients requiring a two-stage BVT or CVT using MPRAVF as the first stage was reviewed.
METHODS:
All two-stage BVTs and CVTs performed between September 2004 and October 2006 were retrospectively reviewed. The median follow-up for this cohort was 23.7 months. One-year secondary patency of all transpositions was assessed.
RESULTS:
Two hundred nineteen MPRAVFs were constructed. Twelve MPRAVFs failed and underwent a second procedure. Ninety-eight patients required no further procedures and their upper arm cephalic vein was matured and used for dialysis. Of 121 patients whose MPRAVFs were functioning but unusable due to their depth, 87 underwent BVT and 34 underwent CVT. The Kaplan-Meier one-year secondary patencies (± standard error) for BVTs and CVTs were 0.90±0.03 and 0.82±0.06, respectively. At one year, 87% of all transpositions remained patent.
CONCLUSIONS:
Use of MPRAVF as the first stage of a two-stage BVT or CVT can significantly improve the patency rate of autogenous hemodialysis access placement beyond the 66% set forth by the Fistula First guidelines.
Keywords: Basilic, Cephalic, Fistula, Transposition
Fistula construction in the United States has remained steady for many years at approximately 30% to 40% (1,2). Other countries have reported higher success rates with primary autogenous hemodialysis access (3). Primary autogenous hemodialysis access has significantly improved since the new initiatives and goals set forth by Fistula First (www.fistulafirst.org). However, further improvement is required to reach the desired current goal of 66%.
Native access has the best five-year patency rate and requires fewer interventions compared with prosthetic grafts (4). Autogenous radiocephalic direct wrist access provides the best permanent access with the fewest complications (5). Unfortunately, only 30% of patients are candidates for this type of access. The usual approach is first to construct a radiocephalic access followed by a brachiocephalic access, and second, to place a forearm graft. However, the use of a forearm graft has resulted in loss of the basilic vein as an autologous conduit from subsequent graft revisions (6).
To increase the rate of fistula placement, in addition to constructing radiocephalic and brachiocephalic fistulas, other techniques must be used, such as forearm and upper arm basilic and cephalic transpositions. The present retrospective study reviews our experience with patients who underwent selective two-stage basilic vein transposition (BVT) and cephalic vein transposition (CVT) using modified proximal radial artery arteriovenous fistula (MPRAVF) as the first stage.
METHODS
The office medical records of 293 patients were reviewed retrospectively. All patients underwent autogenous access placement by the primary author between September 2004 and October 2006 at the Inova Health System in Fairfax, Virginia, USA. All patients required permanent vascular access for hemodialysis. The majority of patients were being dialyzed using their existing tunnelled catheter or a failing graft or fistula. All patients were evaluated by physical examination, obtaining blood pressures in both arms and by Allen’s test (7).
Subsequently, patients underwent routine vein mapping using duplex ultrasound examination. In some patients who had multiple previous accesses or long-term indwelling catheters, a venogram was performed to assess the patency of the central venous system. All patients underwent duplex ultrasound examination of their primary fistulas before the transposition.
The patients with a patent superficial vein greater than 2.0 mm to 2.5 mm underwent fistula placement. The algorithm followed was to construct a radiocephalic autogenous access. If that was not possible, then an MPRAVF was constructed through a small longitudinal incision in the antecubital space just below the elbow. The median antebrachial vein was dissected out and distally ligated. Heparinized saline was used to dilate the vein.
Both cubital cephalic and basilic veins were visually inspected. If both veins were patent and their sizes were normal, they were not ligated. If a vein was too small, or diseased as a result of previous intravenous cannulation, then it was ligated. The deep communicating vein was routinely ligated to prevent flow into the deep system, and an end-to-side anastomosis was made to the proximal radial artery using an absorbable 7-0 PDS suture (Ethicon Inc, USA). In some patients whose antebrachial vein was diseased or thrombosed, but whose cubital veins were patent, the deep communicating vein was used and anastomosed to the brachial artery. In those patients whose antecubital veins were also occluded, the proximal forearm basilic vein was used as a conduit and was anastomosed to the proximal radial artery.
Patients were evaluated four to six weeks postoperatively with a duplex ultrasound to evaluate the size and patency of both cephalic and basilic veins. If the cephalic vein had matured, was superficial enough to be used, at least 6 mm in diameter and not stenotic, then no further procedure was performed. However, if the cephalic vein was too deep, then either a BVT or CVT was performed.
The decision concerning which vein to transpose was made on the basis of the ultrasound. Regardless of size, the larger of the two veins was used as long as it measured more than 5 mm to 6 mm. All the CVTs were performed under intravenous sedation using a few small-bridged incisions. The cephalic vein was completely dissected out and the cubital cephalic vein was transected in a bevelled fashion. A superficial tunnel was created using a Vectra tunneller (Bard Peripheral Vascular Inc, USA) to minimize damage to the vein. This device also allowed the operator to flush the vein and check for any twist in the vein before removing the sheath. The cephalic vein was reanastomosed to the cubital cephalic vein in an end-to-end fashion using two 7-0 PDS sutures to prevent a purse-string effect.
Seventy BVTs were performed under general anesthesia and 17 were performed with intravenous sedation and a mixture of lidocaine and bupivacaine administered locally. An incision was made from the cubital basilic vein to the junction of the basilic and axillary veins. All the tributaries were ligated and a subcutaneous tunnel was made in the same fashion as in CVT. If the cubital cephalic vein was patent, the cubital basilic vein was divided and reanastomosed in an end-to-end fashion after the vein was passed through the tunnel. If the cubital cephalic vein was not patent, the cubital basilic vein was divided and passed through the tunnel, and either reanastomosed to the same site in an end-to-end fashion or anastomosed to the brachial artery in an end-to-side fashion. All wounds were closed with two-layer subcutaneous closures. No patient received prophylactic antibiotics unless a revision with prosthetic material was required. All procedures were performed on an outpatient basis unless the patient was admitted to the hospital for other medical reasons.
All patients were evaluated two to three weeks postoperatively. If the fistula was patent, a routine ultrasound was performed four weeks later. Ultrasound was performed regardless of the physical examination findings. If the ultrasound revealed any stenosis in the fistula, then a fistulogram was performed. If indicated, an intervention was conducted with either open-patch angioplasty or percutaneous angioplasty.
If the patient underwent revision of the fistula, then another ultrasound was obtained to document satisfactory elimination of stenosis. At this time, the patient was allowed to proceed with the use of their fistula. Thereafter, the patient was seen as needed, with no other routine follow-up ultrasound performed. However, all the patients were instructed to return to the office if any problems were encountered, such as excessive bleeding after dialysis, swelling, aneurysm formation or development of high pressures within the arteriovenous fistula. All follow-up information on the status of patients and their accesses was obtained by contacting the dialysis centres.
Primary patency was defined as the interval between fistula placement and the first intervention. Assisted primary patency was defined as the interval from the time of fistula placement until thrombosis or the time of measurement of patency, including intervening manipulations (surgical or endovascular intervention) designed to maintain the functionality of the access. Secondary patency was defined as the interval between access placement and failure, or time of follow-up to one year (7). A χ2 analysis, using exact methods for all cells with less than five counts, was used to examine the frequency of complications and fistula success among the three groups. Kaplan-Meier estimates were calculated to examine the one-year secondary patency rates among groups. All statistical analyses were performed using SAS software (version 9.12, SAS Institute, USA).
RESULTS
During the 24-month study period, 293 patients underwent 473 procedures to construct native hemodialysis accesses. These procedures included 293 primary autogenous accesses, 121 transpositions and 21 second procedures performed on failed autogenous accesses. Thirty-eight interventions performed in all four groups after primary fistulas or transpositions were constructed. During the same period, 28 patients underwent brachial-axillary prosthetic graft placement. These patients did not have suitable veins for autogenous access placement. Patients who underwent revision of their existing graft were excluded. The mean follow-up period was 23.7 months. Patient demographics and complications are shown in Tables 1 and 2, respectively.
TABLE 1.
Patient demographics (n=293)
| Mean age (range), years | 57 (16–91) | |
| Primary fistulas | ||
| Male | 167 (57) | |
| Female | 126 (43) | |
| Hypertension | 278 (95) | |
| Diabetes mellitus | 185 (63) | |
Data provided as n (%) unless otherwise indicated
TABLE 2.
Frequency of complications (n=340)
| Complications | MPRAVF (n=219) | BVT (n=87) | CVT (n=34) |
|---|---|---|---|
| Infection | 2 | 3 | 0 |
| Hematoma | 6 | 3 | 0 |
| Steal syndrome | 2 | 3 | 1 |
| Swelling* | 3 | 7 | 4 |
| Myocardial infarction† | 0 | 2 | 0 |
| Death | 0 | 1 | 0 |
Data presented as n.
Modified proximal radial artery arteriovenous fistula (MPRAVF) versus basilic vein transposition (BVT) (P=0.007), MPRAVF versus cephalic vein transposition (CVT) (P=0.007);
MPRAVF versus BVT (P=0.08)
Twenty-eight per cent (83 of 293) of these patients were good candidates for radiocephalic access placement on the basis of physical examination and preoperative ultrasound or selective venogram. Eighty-nine per cent (74 of 83) of the fistulas in these patients remained patent and were used successfully for dialysis. Three failing fistulas required surgical intervention. Two patients were lost to follow-up, and in one of these patients the fistula thrombosed.
Two hundred ten patients who were not candidates for radiocephalic access formation, and nine patients whose radiocephalic access failed, underwent a MPRAVF procedure. Ninety-five per cent (207 of 219) of the MPRAVF procedures remained patent. Twelve patients whose original MPRAVF procedure failed underwent the same procedure in the contralateral extremity and all 12 remained patent. Forty-five per cent (98 of 219) of the MPRAVF patients required no additional procedures and their cephalic veins were used for dialysis. Seven interventions were performed in the MPRAVF group. In this cohort, two fistulas thrombosed, two patients died and two patients were lost to follow-up.
Six weeks after the first stage was performed in 121 patients whose MPRAVFs were functioning but unusable due to their depth, 72% (87 of 121) underwent BVT and 28% (34 of 121) underwent CVT. On the basis of venous duplex ultrasound, the average diameter of the cephalic and basilic veins was 3.6 mm (range 2.4 mm to 4.9 mm) before their first-stage access placement. This increased to an average of 6.2 mm (range 4.1 mm to 8.2 mm), a 72% increase in the size of the veins four to six weeks later. Of the 87 BVTs, 95% (83 of 87) remained patent and were used successfully for dialysis. Of these BVTs, 28% (23 of 83) required intervention either before or after the use of the fistula. In this cohort, three fistulas thrombosed, one patient died and two patients were lost to follow-up.
One patient required ligation of his access secondary to massive swelling as a result of chronic central venous occlusion. Another patient required emergency ligation in the office secondary to massive bleeding which occurred as a result of a percutaneous stent angioplasty of the basilic vein performed by her nephrologist one week postoperatively. Of the 23 BVT interventions, 18 were open procedures and five were performed percutaneously.
Of the 34 CVTs, 91% (31 of 34) remained patent and were used for dialysis. Five fistulas underwent surgical revision, either before or after being used for dialysis. Two patients developed significant swelling secondary to their occluded central venous system and had to undergo ligation of their functioning transposition. One patient was lost to follow-up.
No statistically significant differences in complications among the three groups were found except for swelling (Table 2). There was significantly more swelling in the BVT and CVT groups, as would be expected in the presence of a central venous stenosis or occlusion. Under these circumstances, a high-flow proximal fistula (BVT and CVT) would have a greater probability of creating swelling than distal fistulas (radiocephalic and MPRAVF). The one-year secondary Kaplan-Meier patency rates were uniformly high, as shown in Table 3, and a log-rank test for equality showed no statistically significant differences in patency among the three groups (P=0.61). A historical comparison of the present results with the recent literature from 2000 to 2007 is shown (Table 4).
TABLE 3.
One-year secondary patency rates*
| Group |
Fistula |
Kaplan-Meier survival estimates ± SE |
|||
|---|---|---|---|---|---|
| Success/Failure, n | 3 months | 6 months | 9 months | 12 months | |
| MPRAVF (n=98) | 87/11 | 0.90±0.03 | 0.90±0.03 | 0.90±0.03 | 0.90±0.03 |
| BVT (n=87) | 77/10 | 0.99±0.01 | 0.95±0.02 | 0.92±0.03 | 0.90±0.03 |
| CVT (n=34) | 28/6 | 0.91±0.05 | 0.88±0.06 | 0.85±0.06 | 0.82±0.06 |
*Log-rank test for differences in patency among groups, P=0.61. BVT Basilic vein transposition; CVT Cephalic vein transposition; MPRAVF Modified proximal radial artery arteriovenous fistula; SE Standard error
TABLE 4.
Literature review of basilic vein transposition (BVT)
| Author (reference) | Year published | Transpositions, n | Secondary patency (1-year), % |
|---|---|---|---|
| Murphy et al (19) | 2000 | 74 | 73 |
| Oliver et al (12) | 2001 | 59 | 64 |
| Ascher et al (32) | 2001 | 63 | Not reported |
| Tsai et al (33) | 2002 | 54 | 96 |
| Taghizadeh et al (23) | 2003 | 75 | 66 |
| Segal et al (20) | 2003 | 99 | Not reported |
| Hossny (15) | 2003 | 70 | 84–90 |
| Lee et al (24) | 2004 | 20 | Not reported |
| Rao et al (18) | 2004 | 56 | 47 |
| Hill et al (34) | 2005 | 32 | Not reported |
| Keuter et al (13) | 2005 | 31 | 90 |
| Wolford et al (22) | 2005 | 100 | 47 |
| Weale et al (35) | 2007 | 71 | 54 |
| Hashemi et al (present study) | 2009 | BVT 87 | 90 |
| CVT 34 | 82 |
CVT Cephalic vein transposition
Ninety-one per cent (268 of 293) of the patients who underwent construction of a fistula (primary or transposition) had a functioning fistula after one year (Table 5). Eighty-seven per cent (105 of 121) of the combined transpositions remained patent after one year. These results are in line with the reported results from Europe and Japan (8). However, 21 patients were required to undergo additional fistula construction (excluding two-stage transpositions) and 34 patients underwent 38 interventions (percutaneous and open) to achieve these results.
TABLE 5.
One-year follow-up with primary, assisted primary and secondary patency
| MPRAVF (n=219)* | BVT (n=87) | CVT (n=34) | |
|---|---|---|---|
| Primary patency† | 98/98 (100)‡ | 83/87 (95) | 31/34 (91) |
| Assisted primary patency§ | 91/98 (93) | 60/87 (69) | 26/34 (76) |
| Secondary patency | 92/98 (94) | 77/87 (89) | 28/34 (82) |
| Interventions¶ | 7/98 (7) | 23/83 (28) | 5/31 (16) |
Data presented as n/n (%).
In this group, 12 arteriovenous fistulas thrombosed, but were redone and remained patent;
Modified proximal radial artery arteriovenous fistula (MPRAVF) versus basilic vein transposition (BVT) (P=0.047), MPRAVF versus cephalic vein transposition (CVT) (P=0.02);
98 patients in the MPRAVF group did not require transpositions;
MPRAVF versus BVT (P<0.001), MPRAVF versus CVT (P=0.02);
MPRAVF versus BVT (P=0.0002)
In the present patient series, the incidence of intervention was five times higher in the BVT/CVT group than in the radiocephalic/MPRAVF group (RR=5.3, 95% CI 2.3 to 13, P<0.0001). Compared with CVT, those in the BVT group were twice as likely to require intervention, but this finding was not statistically significant (RR=2.0, 95% CI 0.64 to 7.4, P=0.30).
DISCUSSION
Radiocephalic autogenous access was first reported by Brescia et al (9) and remains the gold standard for formation of autogenous hemodialysis access. However, usually less than 30% of patients are candidates for this type of access placement. In the present study, 28% of the patients were candidates for radiocephalic access placement. Dagher et al (10) reported the first series of BVT in 1976. Since that time, multiple studies have reported a wide range of long-term patency results for BVT (4,6,11–24). Gormus et al (25) have shown no significant differences between forearm and upper arm BVT. Literature regarding CVT is sparse (17). Other techniques using the brachial vein (26) or translocated femoral vein (27) have been reported, with acceptable results. However, due to extensive dissection and morbidity, these procedures have not become popular.
One weakness of the single-stage procedure is that a small basilic vein can easily twist during tunnelling and cause immediate thrombosis or stenosis in the vein near the axillary and basilic junction (swing point). By performing a two-stage transposition, the vein is allowed to mature in situ, resulting in improved success of the BVT. The veins usually increased in size by 72% in four to six weeks after performing the first stage. This was documented with follow-up duplex ultrasound.
Bruns and Jennings (28) described a novel approach of using the median antebrachial vein and proximal radial artery in a side-to-side fashion to create a fistula. Retrograde flow was established in the forearm by disrupting the first valve in the antebrachial vein. In most cases, the cubital basilic vein was ligated. Bruns and Jennings have reported 80% cumulative patency in 71 patients after 42 months.
In our experience with Bruns and Jennings’ technique, the fistulas remained patent, but there was significant swelling of the forearm. In addition, the dialysis nurses had difficulty accessing the fistula due to unconventional direction of flow in the forearm veins (cephalad to caudad). Therefore, the primary author decided to modify this technique by performing an end-to-side anastomosis without ligating the cubital basilic vein. This technique allows both basilic and cephalic veins to mature. As a result, 45% (98 of 219) required no further procedures because their cephalic veins were superficial and could be used without any transposition. The remaining patients underwent either a CVT or BVT.
One advantage of MPRAVF is its ability to allow simultaneous maturation of both cephalic and basilic veins. In many cases, if the first transposition fails, then a second vein will be available for transposition. Another advantage of MPRAVF is reduction in frequency of steal syndrome because the flow through the ulnar artery is not disturbed (28). Occasionally, there are disadvantages. In the present series, three female diabetic BVT patients needed to have their cubital cephalic veins ligated because the radial artery could not support adequate flow through both cephalic and basilic veins.
Overall, we believe the advantages outweigh the disadvantages. Even if ligation of the cubital cephalic vein is required, the cephalic vein has already matured and will remain patent. The ligation procedure is very simple and can be well tolerated under light sedation. Finally, all anastomoses were performed using monofilament absorbable sutures. This has been shown to significantly reduce the inflammatory and foreign body reaction at the site of anastomosis, possibly improving patency of the fistula (29).
The majority of interventions for BVTs were due to stenosis at the ‘swing point’, where the basilic vein joins the axillary vein. Almost all were treated with open-patch angioplasty. We attributed this stenosis to tension on the vein, partial twisting of the vein during tunnelling, or whether the angle between the basilic and axillary veins is too acute, resulting in a significant change in the flow dynamics. Therefore, during the procedure the axillary area was thoroughly dissected out to avoid any tension or encroachment on the vein.
In patients in whom both cephalic and basilic veins had similar diameters, the basilic veins were preferentially transposed because were more BVT procedures described in the literature. Our data demonstrated no significant differences in one-year secondary patency between the two transposition groups, although there was a trend toward fewer interventions for CVT. Therefore, we currently perform more CVTs, especially in obese patients. The procedure is shorter, less involved, less morbid and eliminates the ‘swing point’. With CVT, the vein can also be positioned more anteriorly in the arm, making access easier for the dialysis nurses.
Use of prophylactic antibiotics has not been strongly recommended for cutaneous or superficial tissue procedures (30). No patient undergoing primary fistula construction or transposition received prophylactic antibiotics, and there were no cases of infection in radiocephalic and CVT patients. Three BVT patients and two MPRAVF patients developed wound breakdown. All were female, obese and diabetic, but none had gross infection. All wounds healed with debridement and local care. All the patients who underwent revision with a prosthetic patch received prophylactic antibiotics and none developed any infection.
One radiocephalic patient and two MPRAVF patients developed steal syndrome, requiring ligation of the fistulas. Three BVT patients developed steal syndrome and all three underwent distal revascularization and interval ligation procedures with complete resolution of their symptoms. These patients had anastomoses to the brachial artery instead of the proximal radial artery. All six patients with steal syndrome were diabetic and five were women.
Preoperative vein mapping with ultrasound was mandatory in all patients, as has been recommended by others (31). Selective venograms were performed in patients who had multiple previous grafts or central venous catheters because the evaluation of the central veins could not be accurately performed with ultrasound. This allowed appropriate selection of the extremity and procedure, resulting in the best outcome. In a subset of the patients, the routine venogram had been performed by interventional nephrologists before the patients visited our service.
Four to six weeks post-transposition, all patients underwent duplex ultrasound examination. If any abnormality was detected, a fistulogram was performed and if any stenosis was present, patients were treated either with balloon or open angioplasty. Open-patch angioplasty was the preferred intervention for anatomical abnormalities, such as a partial twist in the vein that usually occurs near the ‘swing point’. Focal stenosis in the body of the vein, if present, often indicates a sclerotic valve or a stenosis at the site of a previous intravenous cannulation. In these cases, balloon angioplasty was performed. If the result was not satisfactory, then open angioplasty was performed.
A patient’s access could be used once the final physical examination and ultrasound were normal. No other routine follow-up ultrasound or physical examination was performed. Recently, we have instituted routine yearly follow-up examination of all the patients who have undergone an access procedure. If clinically indicated, an ultrasound is performed to identify a potential failing access.
CONCLUSION
On the basis of these results, we recommend first creating a radiocephalic fistula. If not possible, then a MPRAVF should be constructed. Finally, if the cephalic vein is not superficial enough for use, either CVT or BVT should be performed. By following this algorithm, we have been able to improve markedly on the patency rate goals recommended by the Fistula First and Kidney Disease Outcomes Quality Initiative guidelines (www.kidney.org/professionals/KDOQI).
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