Literature DB >> 24337214

Comparison of one- and two-stage basilic vein transposition for arterio-venous fistula formation in haemodialysis patients: preliminary results.

Sedat Ozcan1, Ali Kemal Gür, Ali Umit Yener, Dolunay Odabaşi.   

Abstract

OBJECTIVE: This study aimed to compare the results of one-and two-stage basilic vein transposition (BVT) in haemodialysis patients.
METHODS: This was a non-randomised, retrospective study between January 2007 and January 2012 on 96 patients who were diagnosed with end-stage renal failure (ESRF) (54 males, 42 females; mean age 43.6 ± 14 years) and underwent one- or two-stage BVT in our clinic. All patients who were not eligible for a native radio-cephalic or brachio-cephalic arterio-venous fistula (AVF) were scheduled for one- or two-stage BVT after arterial (brachial, radial and ulnar) and venous (basilic and cephalic) Doppler ultrasonography. Patients were retrospectively divided into two groups: group 1, basilic vein diameter > 3 mm and patients who underwent one-stage BVT; and group 2, basilic vein diameter < 3 mm and patients who underwent two-stage BVT. In group 1, the basilic vein with a single incision was anastomosed to the brachial artery, followed by superficialisation. In group 2, the basilic vein was anastomosed to the brachial artery and they underwent the superficialisation procedure one month postoperatively. Fistula maturation and postoperative complications were assessed.
RESULTS: The mean diameter of the basilic vein was statistically significantly higher in group 1 (3.46 ± 0.2 mm) than in group 2 (2.79 ± 0.1 mm) (p < 0.05). In terms of postoperative complications, thrombosis, haemorrhage and haematoma were significantly higher in group 1 (34, 36 and 17%, respectively) than in group 2 (23, 14 and 6%, respectively) (p < 0.05). The rate of fistula maturation was significantly lower in group 1 (66%), compared to group 2 (77%) (p < 0.05).Time to fistula maturation was significantly shorter in group 1 (mean 41 ± 14 days), compared to group 2 (mean 64 ± 28 days) (p < 0.05).
CONCLUSION: Two-stage BVT was superior to one-stage BVT due to its lower rate of postoperative complications and higher fistula maturation, despite its disadvantage of late fistula use. Although the diameter of the basilic vein was larger in patients who underwent one-stage BVT, we observed that one-stage BVT was disadvantageous in terms of postoperative complications and fistula maturation.

Entities:  

Mesh:

Year:  2013        PMID: 24337214      PMCID: PMC3896105          DOI: 10.5830/CVJA-2013-077

Source DB:  PubMed          Journal:  Cardiovasc J Afr        ISSN: 1015-9657            Impact factor:   1.167


Abstract

In recent years, the number of patients requiring haemodialysis (HD) has been rapidly increasing globally, including Turkey. Arterio-venous fistula (AVF) is the most frequently used method in patients with end-stage renal failure (ESRF) for HD.1 The Kidney Disease Outcome Quality Initiative (KDOQI) recommends autologous radio-cephalic or brachio-cephalic AVF as a primary method of choice in HD patients, and basilic vein transposition (BVT) as a secondary option.2,3 In 1976, Dagher et al.4 first described the technique of BVT for HD. In later years, several techniques were used.5-11 This study aimed to compare the patency and complication rates of AVF formed by one-stage and two-stage BVT.

Methods

Between January 2007 and January 2012, 96 patients (54 males, mean age 43.6 ± 14 years) who were not eligible for radio-cephalic and brachio-cephalic AVF via native veins and who underwent BVT were included in this retrospective study. Patients were selected according to basilica vein diameter, which was evaluated with vascular Doppler. Group 1 consisted of patients with a basilic vein diameter > 3 mm and who underwent one-stage BVT (47 patients, 28 males; mean age 42.8 ± 14.5 years), and group 2 contained patients with a basilic vein diameter < 3 mm and who underwent two-stage BVT (59 patients, 36 males; mean age 44.5 ± 13.5 years). In group 1, the incision was performed through the basilic vein located in the medial condyle of the humerus and axillary area. The vein was carried over the fascia by tying the lateral branches during release of the basilic vein, while the nervus cutaneus medialis of the forearm was preserved. The basilic vein in the antecubital fossa was anastomosed to the brachial artery end to side, using 6-0 or 7-0 polypropylene continuous sutures. Following evaluation of the presence of thrill, the fascia and other layers were closed, lifting the vein and protecting the nerve. One month was allowed for the anastomosed graft to heal before the possible trauma of HD injection. In group 2 patients, the incision was made through the basilic vein located in the medial and lateral condyle of the humerus and was it anastomosed to the brachial artery laterally using 6-0 or 7-0 polypropylene continuous suture. The incisions were closed in the anatomical layers, after the presence of thrill was evaluated. In the next stage at one month, an incision was made through the basilic vein located in the medial condyle of the humerus and the axillary area. The vein was carried over the fascia by tying the lateral branches during the release of the basilic vein, while the nervus cutaneus medialis of the forearm was preserved. Following the evaluation of the presence of thrill, the fascia and others were closed in anatomical layers, lifting the vein and protecting the nerve. Patients whose wounds had healed after a month underwent HD. Postoperative complications of one- and two-stage BVT, including primary and secondary patency rates, thrombosis, haemorrhage, haematoma, infection and venous aneurysm were retrospectively analysed.

Statistical analysis

Statistical analysis was performed using Windows SPSS 14.0 (SPSS Inc, Chicago, IL, USA). Normally distributed data, which were expressed as mean ± standard deviation, were assessed using the t-test. The Kolmogorov-Smirnov test was used to analyse normal distribution of the numerical data. Categorical data were examined by Fischer’s exact test. The dual logistic regression test was used to assess the effects of clinical parameters such as haematoma or fistula maturation. A p-value of < 0.05 was considered statistically significant.

Results

While 28 (59%) patients were male and 19 (41%) were female in group 1, 36 (61%) were male and 23 (39%) were female in group 2. The mean follow up was 36 months. The means of age, duration of ESRF, number of AVFs, patency duration, co-morbidities and diameter of the basilic vein and brachial artery are shown in Table 1.
Table 1

Demographics Of The Patients

VariablesGroup 1 one-stage BVT (n = 47)Group 2 two-stage BVT (n = 59)p-value
Gender (M/F)M = 28 (59%)M = 36 (61%)NS
F = 19 (41%)F = 23 (39%)NS
Mean age (years)M = 43.1 (± 16)M = 44.9 (± 14)NS
F = 42.5 (± 13)F = 44.1 (± 13)NS
ESRF duration (months)M = 63.1 (± 17)M = 61.7 (± 20)NS
F = 64.5 (± 18)F = 63.3 (± 21)NS
Previously opened AVFM = 5 (± 1.6)M = 5.2 (± 1.7)NS
F = 5.45 (± 1.7)F =5.0 (± 1.6)NS
Hypertension1514NS
Diabetes mellitus911NS
Heart disease43NS
Peripheral vascular disease23NS
Smoking911NS
Mean LDL-C (mmol/l)157 ± 26145 ± 21NS
Mean basilic vein diameter (mm)3.46 ± 0.22.79 ± 0.1< 0.05
Mean brachial artery diameter (mm)3.71 ± 1.43.63 ± 1.5NS

BVT: basilic vein transposition, AVF: arteio-venous fistula, NS: non-significant, LDL-C: low-density lipoprotein cholesterol, ESRF: end-stage renal failure, M = male, F = female.

BVT: basilic vein transposition, AVF: arteio-venous fistula, NS: non-significant, LDL-C: low-density lipoprotein cholesterol, ESRF: end-stage renal failure, M = male, F = female. The diameter of the operated basilic vein was significantly higher in group 1 (3.46 ± 0.2 mm), than in group 2 (2.79 ± 0.1 mm) (p < 0.05). There was no significant difference in the diameter of the brachial artery between the groups. Bleeding–clotting times of the groups are shown in Table 1 and there was no significant difference.
Table 2

Bleeding–Clotting Times Of The Groups

VariablesGroup 1 one-stage BVT (n = 47)Group 2 two-stage BVT (n = 59)
PT (sec)17 ± 416 ± 4NS
APTT (sec)38 ± 741 ± 7NS
INR1.3 ± 0.51.5 ± 0.7NS
Platelet count (103/ml)385 ± 70367 ± 67NS
Bleeding time (min)6.1 ± 1.35.7 ± 1.2NS
Clotting time (min)7.1 ± 2.37.3 ± 2.1NS
Protein C (%)89 ± 2892 ± 31NS
D-dimer (ng/dl)275 ± 73321 ± 67NS
Fibrinogen (g/l)3.2 ± 0.72.8 ± 0.5NS

PT: prothrombin time, APTT: active partial thromboplastin time, INR: international normalised ratio.

PT: prothrombin time, APTT: active partial thromboplastin time, INR: international normalised ratio. The ratio of fistula maturation, as well as postoperative mortality and morbidity rates are shown in Table 3. There was no significant difference in mortality rate, whereas a significant difference was found in morbidity between the groups (p < 0.05). The rate of fistula maturation was significantly lower in group 1 (66%) compared to group 2 (77%) (p < 0.05). The mean time to fistula maturation was 41 ± 14 days in group 1, while it was 64 ± 28 days in group 2, indicating a significant difference between the groups (p < 0.05).
Table 3

Complications

VariablesGroup 1 one-stage BVT (n = 47)Group 2 two-stage BVT (n = 59)p-value
Mortality3 (6%)2 (4%)NS
Maturation rate31 (66%)45 (77%)< 0.05
Infection6 (12%)5 (10%)NS
Thrombosis16 (34%)11 (23%)< 0.05
Bleeding17 (36%)7 (14%)< 0.05
Haematoma8 (17%)3 (6%)< 0.05
Pseudo-aneurysm2 (4%)3 (6%)NS
Steal syndrome4 (8%)3 (6%)NS
Oedema5 (10%)6 (10%)NS
Mean fistula maturation time (day)41 ± 1464 ± 28< 0.05
Mean fistula flow rate (ml/min)280 ± 23300 ± 31NS

NS: non-significant.

NS: non-significant. With regard to auxiliary interventions, the rate of intervention for early (≤ 10 days) fistula thrombosis was significantly higher in group 1 (21%) compared to group 2 (12%). However, there was no significant difference in rate of intervention for late (≥ 10 days) fistula thrombosis between the groups (20% in group 1; 22% in group 2). The number of auxiliary interventions to manage haemorrhage and haematoma following fistula formation was significantly higher in group 1 (17%, 10%) than in group 2 (6%, 2%) (p < 0.05). Auxiliary surgical interventions are summarised in Table 4.
Table 4

Assisted Interventional Surgery Rates

VariablesGroup 1 one-stage BVT (n = 47)Group 2 two-stage BVT (n = 59)p-value
Early (≤ 10 day) thrombosis10 (21%)6 (12%)< 0.05
Bleeding8 (17%)3 (6%)< 0.05
Haematoma5 (10%)1 (2%)< 0.05
Late (≥ 10 day) thrombosis9 (20%)11 (22%)NS
Pseudo-aneurysm2 (4%)3 (6%)NS
Steal syndrome2 (4%)3 (6%)NS

NS: non-significant.

NS: non-significant. Primary and secondary patency rates in both groups are shown in Tables 5, 6, 7, 8. Statistical comparisons of primary/secondary patency rates between the groups are shown in Figs 1 and 2.
Table 5

Secondary Patency Rates Of Group 1

Monthn = 47Function lossFunction loss ratePatency rateCumulative patency rate
64040.150.8585.00
123640.100.9076.00
183510.020.9874.00
243410.020.9872.00
303310.020.9870.00
363120.060.9466.00
Table 6

Primary Patency Rates Of Group 1

Monthn = 47Function lossFunction loss ratePatency rateCumulative patency rate
63980.170.8383.00
123360.150.8570.00
183210.030.9768.00
243020.060.9464.00
302820.070.9360.00
362710.030.9757.00
Table 7

Secondary Patency Rates Of Group 2

Monthn = 59Function lossFunction loss ratePatency rateCumulative patency rate
64630.060.9494.00
124420.040.9690.00
184130.070.9384.00
244010.020.9882.00
303910.020.9880.00
363810.020.9877.00
Table 8

Primary Patency Rates Of Group 2

Monthn = 59Function lossFunction loss ratePatency rateCumulative patency rate
64360.120.8888.00
124120.040.9684.00
183920.050.9580.00
243630.070.9373.00
303510.030.9771.00
363410.020.9869.00
Fig. 1.

Secondary patency rates of the two groups.

Fig. 2.

Primary patency rates of the two groups.

Secondary patency rates of the two groups. Primary patency rates of the two groups.

Discussion

Patients with ESRF must receive HD to survive, until they undergo renal transplantation. AVF surgery to supply extracorporeal blood flow has been performed for many years during HD.12 The optimal flow rate is ≥ 200 ml/min with an easy-to-use device, providing sufficient supply in a durable and safe procedure.13,14 For this purpose, arteries and veins of the upper limbs are mostly used. Alternative methods can be applied for patients without suitable veins.15,16 In compliance with the KDOQI recommendations, BVT is the most preferred method for fistula formation in our clinic when autologous veins are not suitable to construct radio-cephalic and brachio-cephalic AVF.2,3 In our study, fistulae formed by one- and two-stage BVT were examined in terms of patency and complication rates. No significant difference was found between the groups in terms of age, gender, ESRF and the number of fistulae previously formed. In addition, there was no significant difference in co-morbidity or the mean diameter of the brachial artery. The diameter of the basilic vein was significantly larger in group 1 (3.46 ± 0.2 mm) compared to group 2 (2.79 ± 0.1 mm) (p < 0.05). There was no significant difference in mortality rate between the groups (6% in group 1; 4% in group 2) or mean flow rate of BVT. Time to fistula maturation was significantly shorter in group 1 (mean 41 ± 14 days) compared to group 2 (mean 64 ± 28 days) (p < 0.05). The rates of postoperative complications, including infection (12% in group 1; 10% in group 2), pseudoaneurysm (4% in group 1; 6% in group 2), steal syndrome (8% in group 1; 6% in group 2), and oedema (10% in group 1; 10% in group 2) were similar, indicating no significant difference between the groups. However, there was a significant difference between the groups in respect of thrombosis (34% in group 1; 23% in group 2), haemorrhage (36% in group 1; 14% in group 2) and haematoma (17% in group 1; 6% in group 2) (p < 0.05). A review of the literature revealed that infection rate was 7% in a study conducted by Dilege et al.17 and 14% in a study carried out by Veeramanive et al.18 In our study, the infection rate was 12 and 13% in groups 1 and 2, respectively. Rivers et al.19 found the rate of pseudoaneurysm to be 3%. In our study, the rate of pseudoaneurysm was 4 and 5% in group 1 and group 2, respectively. The rate of steal syndrome was 3.2–6.5% in published studies.21-23 We found that 8% of the patients in group 1 and 11% of those in group 2 had steal syndrome, indicating a higher rate compared to the literature. A total of 4% of the patients in group 1 and 6% of those in group 2 underwent secondary corrective surgery due to steal syndrome, which is a limb-threatening disease. The incidence of corrective surgery due to steal syndrome was up to 6.5% in the literature.22,24,25 Our results for surgery due to steal syndrome were consistent with that in the literature. In our study, the rate of fistula maturation was 66% in group 1 and 77% in group 2, indicating a higher rate in group 2, whereas the rate of thrombosis was 34% in group 1 and 23% in group 2, indicating a higher rate in group 1 (p < 0.05). Review of the literature revealed that the rate of fistula maturation following BVT was 62–97%.24,26-29 In our study, the mean diameter of the operated basilic vein was significantly higher in group 1 (3.46 ± 0.2 mm) than in group 2 (2.79 ± 0.1 mm) (p < 0.05). However, the rate of fistula maturation was higher in group 2, suggesting that the basilic vein that was arterialised using two-stage BVT may have adopted the changes seen in the venous configuration, although this is a controversial issue in the literature. The rate of patency at 36 months reported by Cantelmo et al.30 was 57%, while it was 52% at 30 months as reported by Rivers et al.19 In the literature, the rate of thrombosis was 3–38% with a wide range.23,24,26-29 There are few studies in the literature comparing different techniques for BVT.5,8,31 Kakkos et al.31 compared one-stage and modified two-stage BVT and found that fistula maturation was 85.5% in group 1 and 81.6% in group 2. The authors concluded that there was no significant difference between the groups. In our study, the rate of fistula maturation was higher in group 2 than in group 1, although the mean diameter of the basilic vein was larger in group 1. This is the most important aspect of our study. The mean diameter of the basilic vein that underwent BVT was not predetermined and it is well known that many factors influence fistula maturation.1,24,26,28,29,32,33 In addition, the most important limitation of our study compared to that of Kakkos et al.31 was the non-randomised design. With the study limitations, we discuss the possible effects of two complications, haemorrhage and haematoma, on thrombosis and fistula maturation. In our study, a significant difference was observed in terms of haemorrhage (36% in group 1; 17% in group 2) and haematoma (14% in group 1; 6% in group 2) between the groups (p < 0.05). Considering an equivalent heparin dose was administered to both groups, the higher rate of haemorrhage and haematoma may have resulted from wider surgical incisions in group 1. However, randomised clinical studies are required to draw a firm conclusion. Review of the literature revealed that the rate of haematoma was 3.6–11% in other studies.10,11,34 In our study, we found the rate of haematoma to be higher in group 1(17%) than in group 2 (8%). The rate of haematoma in group 2 was therefore consistent with the literature. With regard to possible factors affecting fistula maturation following BVT, postoperative haematoma and venous hypertension may be more important than the diameter of the basilic vein. This finding is also consistent with data published in the literature.21-23,24,25,31 With regard to auxiliary interventions, the rate of intervention for early (≤ 10 days) fistula thrombosis was significantly higher in group 1 (21%) than in group 2 (12%). The number of surgeries due to haemorrhage and haematoma was 17 and 10%, respectively in group 1, and 6 and 2%, respectively in group 2 (p < 0.05). These findings support the assumption that haemorrhage and haematoma are the most important factors in fistula maturation and thrombosis. There was no statistically significant difference in auxiliary interventions due to late (≥ 10 days) fistula thrombosis (20, 22%), pseudo-aneurysm (4, 6%) and steal syndrome (4, 6%) between the groups.

Conclusion

AVF formation using BVT is a compelling procedure for the surgeon in order to avoid possible complications, including loss of function, infection, distal ischaemia and venous oedema. Two-stage BVT is superior to one-stage BVT due to its lower rate of postoperative complications, despite the disadvantage of late fistula use. Although the diameter of the basilic vein was higher in our patients who underwent one-stage BVT, we found one-stage BVT was disadvantageous in terms of postoperative complications and fistula maturation. However, we believe the method to be applied should be individually designed until further studies can be performed to establish the superiority of either of these techniques.
  27 in total

1.  Provision of long-term vascular access for haemodialysis in a patient with exhausted superficial arm veins.

Authors:  S Sunil; S Sinha; A K Sharma
Journal:  Br J Surg       Date:  2002-01       Impact factor: 6.939

2.  Cannulation of blood vessels for prolonged hemodialysis.

Authors:  W QUINTON; D DILLARD; B H SCRIBNER
Journal:  Trans Am Soc Artif Intern Organs       Date:  1960 Apr 10-11

3.  Outcome after autogenous brachial-basilic upper arm transpositions in the post-National Kidney Foundation Dialysis Outcomes Quality Initiative era.

Authors:  Heather Y Wolford; Jeffrey Hsu; Jeffrey M Rhodes; Cynthia K Shortell; Mark G Davies; Arvind Bakhru; Karl A Illig
Journal:  J Vasc Surg       Date:  2005-11       Impact factor: 4.268

4.  Brachiobasilic and brachiocephalic fistulas as secondary angioaccess routes.

Authors:  N L Cantelmo; F W LoGerfo; J O Menzoian
Journal:  Surg Gynecol Obstet       Date:  1982-10

5.  Delayed superficialization of brachiobasilic fistula: technique and initial experience.

Authors:  C M Zielinski; S K Mittal; P Anderson; J Cummings; S Fenton; J Reiland-Smith; J T Frock; R W Dunlay
Journal:  Arch Surg       Date:  2001-08

6.  Long-term results of arteriovenous fistulas using transposed autologous basilic vein.

Authors:  G J Murphy; S A White; A J Knight; T Doughman; M L Nicholson
Journal:  Br J Surg       Date:  2000-06       Impact factor: 6.939

7.  Durability and cumulative functional patency of transposed and nontransposed arteriovenous fistulas.

Authors:  Hung Michael Choi; Brajesh K Lal; Joaquim J Cerveira; Frank T Padberg; Michael B Silva; Robert W Hobson; Peter J Pappas
Journal:  J Vasc Surg       Date:  2003-12       Impact factor: 4.268

8.  Basilic vein transposition fistula: a good option for maintaining hemodialysis access site options?

Authors:  Rajeev K Rao; G Darius Azin; Douglas B Hood; Vincent L Rowe; Roy D Kohl; Steven G Katz; Fred A Weaver
Journal:  J Vasc Surg       Date:  2004-05       Impact factor: 4.268

9.  Failure of arteriovenous fistula maturation: an unintended consequence of exceeding dialysis outcome quality Initiative guidelines for hemodialysis access.

Authors:  Sheela T Patel; John Hughes; Joseph L Mills
Journal:  J Vasc Surg       Date:  2003-09       Impact factor: 4.268

10.  Arteriovenous fistula formation using transposed basilic vein: extensive single centre experience.

Authors:  S J F Harper; I Goncalves; T Doughman; M L Nicholson
Journal:  Eur J Vasc Endovasc Surg       Date:  2008-04-18       Impact factor: 7.069

View more
  4 in total

Review 1.  One-stage vs. two-stage brachio-basilic arteriovenous fistula for dialysis access: a systematic review and a meta-analysis.

Authors:  Khalid Bashar; Donagh A Healy; Sawsan Elsheikh; Leonard D Browne; Michael T Walsh; Mary Clarke-Moloney; Paul E Burke; Eamon G Kavanagh; Stewart R Walsh
Journal:  PLoS One       Date:  2015-03-09       Impact factor: 3.240

2.  Review of Patency Rates between One-Stage and Two-Stage Brachial-Basilic Transposition Arteriovenous Fistulae Creation in an Asian Population.

Authors:  Hongyan Yu; Baoxian Huang; Joachim Wen Kien Yau; Sadhana Chandrasekar; Glenn Wei Leong Tan; Zhiwen Joseph Lo
Journal:  Ann Vasc Dis       Date:  2018-09-25

Review 3.  A Systematic Review and Meta-Analysis of Randomized Trials Comparing Two-Stage with One-Stage Brachio-Basilic Vein Fistulas.

Authors:  Stavros K Kakkos; George C Lampropoulos; Konstantinos M Nikolakopoulos; Ioannis A Tsolakis; Spyros I Papadoulas; Evangelos C Papachristou; Dimitrios Goumenos; Miltos K Lazarides
Journal:  Vasc Specialist Int       Date:  2018-09-30

4.  Transposed Brachial-Basilic Arteriovenous Fistula for Vascular Access in Japan.

Authors:  Juno Deguchi; Osamu Sato
Journal:  Ann Vasc Dis       Date:  2018-06-25
  4 in total

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