Factors affecting cardiac function in dialysis patients include arterial blood pressure, anemia, intra-vascular volume and the arteriovenous fistula (AVF). We investigated the acute and chronic effects of basilic vein transposition (mean upper arm brachial artery-basilic vein anastomosis) on both the cardiovascular system and the oxygen status.
Sixteen patients with end stage renal failure were enrolled in this study. Patients with heart failure, pericardial effusion or valvular heart disease were not included in the study. Echocardiography (preoperatively and six months after, stages 1 and 2 respectively) and a Swan-Ganz catheter (perio-peratively) were used to assess the hemodynamic status during the phases of AVF construction. Flow measurements were made in the parts of the AVF system before, during and after the construction of the AVF.Moreover, at the same time phases blood sampling from the arterial line and the pulmonary artery catheter was performed, in order to assess oxygen and acid-base status.
Cardiac output, cardiac index, stroke volume, stroke volume index, left ventricular stroke work increased statistically significant 20 and 30min after the AVF construction and they returned to base-line at 40min after the procedure. On the contrary, systemic vascular resistance decreased statistically significant 20 and 30min after the operation and they remained decreased for the whole study period. No other differences were recorded regarding the hemodynamic, oxygen and acid-base status. As far as the echocardiographical findings are concerned, ejection fraction showed a tendency to increase but not significantly in contrast to the inter-ventricular septum which increased statistically significant in both systole and diastole (p<0.01). Posterior wall thickness decreased minimally in both systole and diastole. Regarding the AVF system diameters, there were no changes recorded during the study.
Basilic vein transposition in selected patients provides a well functioning AV fistula and is not an appreciable cause of circulatory or pulmonary congestion for at least a period of six months.
Brescia and colleagues were the first surgeons to describe radiocaephalic fistula in the nondominant arm for hemodialysis1. This still remains the first choice procedure for vascular access in patients who require long term hemodialysis. Lack of suitable cephalic veins, led the surgeons to investigate alternative procedures, such as basilic vein transposition and prosthetic vascular access grafts (polytetrafluoroethylene [PTFEE])2.
Use of a brachiobasilic arteriovenous (AVF) fistula with transposed basilic vein was first described in 1976 by Dagher3. Due to the subfascial localization of the vein, protecting it from venipuncture, basilic vein is usually available in the upper arm region. The primary patency of this fistula is about 60% to 70% and the long-term patency is similar to that of a graft4,5.
This special type of AVF is used, when other AVFs have failed or when the patient’s vessels are not suitable for the construction of a distal AVF6,7,8. It is well known that many patients undergoing haemodialysis, usually show an increase in cardiac output, which may be due either to the presence of AVF or to anaemia9-15.
Cardiac output and other hemodynamic parameters can be studied by both non-invasive techniques, i.e. echocardiography, as well as by invasive techniques e.g. by using a Swan-Ganz catheter.
Most literature studies have investigated the hemodynamic parameters during surgical occlusion or manual compression of AV fistula. Futhermore, there are not many reports on the acute and late effects after basilic vein transposition.
The purpose of this study was to evaluate immediate and long term (after six months) cardiac effects of basilic vein transposition, by using echocardiography (preoperatively and six months after the creation of AVF) and a Swan Ganz catheter perioperatively.
MATERIAL AND METHODS
This study was carried out in 16 patients with end-stage renal disease (ESRD) in the Nephrology Department (Hemodialysis Unit) of AHE-PA University Hospital, Thessaloniki, Greece. Informed written consent was taken from each patient. The institutional ethical committee on human research and the University thesis approval committee approved the study. Patients were already on a hemodialysis program using a hemodialysis catheter. A two lumen (12Fr. X 6’’-16cm) hemodialysis catheter (Arrow International) was already inserted in the jugular or subclavian vein, as their AVFs for hemodialysis were not functioning properly. The previous AVFs had been constructed in various sites in the upper limb e.g. between the radial artery and cephalic vein or brachial artery to cubital vein, but basilic vein transposition has never been performed in these patients. All such patients were scheduled for an AVF construction using the basilic vein (basilic vein transposition); 6-12hrs preoperatively they underwent hemodialysis. Patients with heart failure, pericardial effusion or valvular heart disease were not included in the study. Pre-operative duplex ultrasound investigation (SSD-2000, Aloka Co. Ltd, Tokyo, Japan) was performed according to a standard protocol by experienced vascular technicians, measuring the diameters of brachial arteries and basilic veins in the upper arm. An echocardiographic evaluation of cardiac function was performed within 6hrs after hemodialysis in order to achieve a water balance close to the “dry’” weight. Shortly thereafter patients were transferred to the operating theater for the scheduled procedure (stage 1). Left ventricular ejection fraction (EF%), posterior wall of left ventricular during diastole (PLV-Wd), posterior wall of left ventricular during systole (PLVWs), left ventricular dimension during systole (LVDs), left ventricular dimension during diastole (LVDd), interventricular septum during systole (IVSs) and interventricular septum during systole (IVSs) were measured and recorded. On the day of the study, standard monitoring included electrocardiography (ECG),pulse oxymetry (SpO2) and invasive measurement of arterial pressure (IABP). In addition, a special thermodilution Swan-Ganz catheter (OptiQ SvO2/CCO Abbott Laboratories North Chicago, IL, USA) was inserted for monitoring of central filling pressures, continuous monitorring of cardiac output and SVO2. The catheter was inserted by using the pre-existing vascular access for hemodialysis through an introducer sheath (Seldinger method). Measurements were made at the individual phases of AVF construction (0-5): before (phase=0), during (phase=1) and 10 min (phase=2), 20 min (phase=3), 30 min (phases=4), 40 min (phase=5) min after construction of the AVF. Results were calculated by using the following equation: Blood flow =π*V*d*d (Abbreviations: π= 3,14, V= Velocity in cm/min, d= vessel’s diameter in cm). Detailed measurements were made in the basilic vein and brachial artery before and after the AVF construction and in the transposed basilic vein with the feeding artery closed (in this case the flow is called retrograde). Blood samples were drawn at phases 0, 1 and 2 from the peripheral arterial line and from the pulmonary artery in order to assess the oxygen and acid-base status during AVF construction. All the procedures for the AVF formation were performed under local anesthesia and sedation (small doses of propofol) by using the “one stage procedure technique. The incision was started at the antecubital crease in a vertical fashion just medial to the brachial artery pulse. The incision was extended through the subcutaneous tissue; the fascia was incised and the brachial artery exposed. The medial nerve was always identified and preserved. Proceeding slightly more medially and still deep to the fascia, the basilic vein was visualized and traced proximally, all the way to its junction with the axillary vein. Occasionally, usually in the proximal third of the arm, the medial cutaneous nerve was encountered and preserved. Once the basilic vein was mobilized and all its branches were ligated, it was divided as far distal to the arm as possible and brought superficial to the medial cutaneous nerve. Then, the vein was tunneled in a more lateral, subcutaneous location. Proximal and distal control of the brachial artery was obtained and the patient was given heparin. A 6- to 7-mm arteriotomy was then made and an end-to-side anastomosis between the basilic vein and the brachial artery was constructed using fine, nonabsorbable monofilament suture. Clamps were then released and flow established in the arterialized basilic vein. The deep fascia was then closed with interrupted, absorbable sutures, keeping the basilic vein superficial to the fascia. The basilic vein was positioned in the subcutaneous pocket, thereby relocating it in a more lateral and more superficial position (Figure 1). There was also a continuous supply of oxygen via a face mask (6-8l/min).
The echocardiographic evaluation of cardiac function was performed six months later by the same operator (precisely) within 6hrs after the hemodialysis session (stage 2). The exact timing of the second echocardiography evaluation was important in order to preserve a water balance close to the “dry’” weight, as in the first study (stage 1). Equations were used to calculate the following cardiovascular parameters: cardiac index (CI), stroke volume index (SVI), systemic vascular resistance (SVR), systemic vascular resistance index (SVRI) pulmonary vascular resistance (PVR), pulmonary vascular resistance index (PVRI), left ventricular cardiac work (LVSW), left ventricular cardiac work index (LVSWI), right ventricular cardiac work(RVSW)and right ventricular cardiac work index (RVSWI). Equations were also used to calculate the following oxygen transport indicators: arterial oxygen content (CaO2), MixedVenousBloodContent (CvO2), Pulmonary Capillary O2 Content (Cc’O2), Alveolar Oxygen Tension (PA-O2), Arterial-Venous Content Difference (C (a-v) O2), Venous Admixture (Qs/Qt, Shunt %), Oxygen Delivery (DO2) and Oxygen Consumption (VO2). The t-test, paired t-test and repeated measures ANOVA were used for statistical analysis. Their nonparametric analogues; the Wilcoxon-Mann-Whitney, Wilcoxon signed rank, and Friedman tests were used for the validation of the results due to the small sample used in the study. Statistical analysis was performed with SPSS 14.0″.
A total of 16 patients with ESRD (8 males and 8 females; mean age 48 years with range of 25 – 75 years) were studied. Demographic data are shown in Table 1. Vessel’s diameters in the AVF system are depicted in Table 2 and flow measurements in the parts of the AVF system in Table 3. As expected, blood flow in the basilic vein increased statistically significant after the AFV construction. Likewise, blood flow in the proximal artery increased but not in a statistically significant manner. As far as the hemodynamic parameters are concerned, CO, CI, SV and SVI increased in a statistically significant manner after the AVF construction, namely at phases 3 and 4, and they returned back to their preoperative values at phase 5. On the contrary, SVR decreased statistically significant at phases 3 and 4 and they remained decreased throughout the study period. LVSW showed similar alterations to CO and increased at phases 3 and 4 and returned back to baseline at phase 5.
Table 1. Patient’s demographic data
|Mean ± SD||Median|
|BMI||25,3 ± 4,79||26,39|
|Patients on hemodialysis (yrs)||3,84±4,51||1,5|
|Blood glucose (mg/dL)||124,73±24,9||119|
Table 2. Vessels diameters in AVF system
|Mean ± SD||Median|
|Transposed Basilic Vein||0,61±0,18||0,61±0,18|
|Feeding Artery after AVF Construction||0,4±0,04||0,4±0,04|
Table 3. Blood flow in the AVF system
|Blood flow (ml/ min)|
|Mean ± SD||Median|
|Basilic vein blood flow before AVF|
|Arterial blood flow before AVF|
|Blood flow in the transposed basilic vein |
with the feeding artery “open”
|Blood flow in the transposed basilic vein|
with the feeding artery “closed”
|Blood flow in the feeding artery|
Table 4. CO, CI, SV, SVI, SVR and LVSW alterations during the study
The PLVW decreased minimally in both systole and diastole. The individual elements of the echocardiographic evaluation at stages 1 and 2 are summarized in Table 5.
Table 5. Echocardiographic Parameters
AVFs are the preferred vascular access in dialysis patients due to their higher blood flow rates, superior patency and low incidence of infections compared with either arteriovenous grafts or catheters16,17,18. Basilic vein transposition, a kind of AVF above the elbow, allows the patient to have a native fistula, while preserving deep brachial venous systems for future placement of forearm or upper arm PTFE arteriovenous grafts. It is also well documented, that transposition of a basilic vein and creation of brachio-basilic arteriovenous fistula, result in a satisfactory patency rate and provide good blood flows19,20,21. This type of AVF is usually considered as the last option for autologous vascular access for hemodialysis (HD) on the upper extremity. Depending on the diameter of the AV communication and the size of the artery feeding it, an AVF increases venous return to the heart and at the same time it decreasesperipheral vascular resistance22,23. This, in accordance with Starling’s law, increases CO and work of the heart. The impact on CO correlates tightly with the blood flow through the AVF. In patients with compromised cardiac function, the aforementioned hemodynamic changes could result in cardiomegaly and congestive heart failure24,25,26. However, elevated CO alone does not cause symptoms of congestive heart failure or high output cardiac failure. Six months after basilic vein transposition, all the fistulas were functioning well, there were no clinical signs of pulmonary oedema or other cardiac disease (e.g. heart failure) and echocardiographic evaluation revealed:
- The cardiac EF showed a tendency to increase, which has been recorded by other authors31,32.
- IVSs and IVSd increased statistically significant.
- PLVWs, PLVWd, LVDs and LVDd did not show any significant change, which is in agreement with other literature studies33,34.
The recorded increase of the thickness of the IVS does not constitute a specific feature of LV hypertrophy, since both the ventricular wall thickness and the left ventricular dimensions did not change. Therefore, establishing an AVF by transposition of the basilica vein, does not hamper the cardiac function in terms of cardiomegaly or congestive heart failure.
- Brescia M, Cimino J, Appel K, et al. Chronic hemodialysis using venipuncture and surgically created arterio-venous fistula. N Engl J Med 1966;275:1089-92.
- Matsuura J, Rosenthal D, Clark M, et al. Transposed basilic vein versus polytratefluorethylene for brachial axillary arteriovenous fistulas. Am J Surg 1998;176:219-21.
- Dagher F, Gelber R, Ramos E. et al. The use of basilic vein and brachial artery as an AV fistula for long-term haemodialysis. J Surg Res 1976; ;20:373-6.
- Keuter X, van der Sande F, Kessels A, et al. Excellent performance of one-stage brachial-basilic arteriovenous fistula. Nephrol Dial Transplant 2005; ;20:2168-71.
- Lazarides M, Georgiadis G, Papasideris C,et al.Transposed brachial-basilic arteriovenous fistulas versus prosthetic upper limb grafts: A meta-analysis. Eur J Vasc Endovasc Surg 2008 ; 36 : 597 -601.
- Torina P, Westheimer E, Schanzer H. Brachial vein transposition arterio-venous fistula is it acceptable option for chronic dialysis vascular access. J Vasc Access 2008;9:39 -44.
- Lee C, Ko PJ, Liu Y, et al. Brachiobasilic fistula as a secondary access procedure: an alternative to a dialysis prosthetic graft. Chang Gung Med J 2004;27:816 -23.
- Rao RMD, Azin D G, Hood D, et al. Basilic vein transposition fistula: A good option for maintaining hemo-dialysis access site options. J Vasc Surg 2004;39: 1043-7.
- Mac Rae J, Levin A, Belenkie N. The cardiovascular effects of arteriovenous fistulas in chronic kidney disease: a cause for concern. Seminars In Dialysis 2006 ; 19 : 349-52.
- Dikow R, Schwenger V, Zeler M, et al. Do AV fistulas contribute to cardiac mortality in hemodialysis patients. Semin Dial 2002;15:14-7.
- Anderson C, Codd J, Graff R, et al. Cardiac failure and upper extremity arteriovenous dialysis fistulas. Arch Intern Med 1976;136:292-7.
- Nakhoul F, Yiglia M, Gilman R, et al. The pathogensis of pulmonary hypertension in haemodialysis patients via arterio-venous access. Nephrol Dial Transplant 2005;20:1686-92.
- Young P, Rohr M, Marterre W. High-output cardiac failure secondary to a brachiocephalic arteriovenous hemodialysis fistula: two cases. Am Surg 1996;64:239-42.
- Ponsin J, Levy B, Martineaud J. Cardiac effects of the flow in the arteriovenous fistula. Study in 66 chronic hemodialysis patients. Presse Med 1983;29:217-21.
- Schreiber B. Congestive heart allure in patients with chronic kidney disease and on dialysis. Am J Med Sci. 2003;325:179-93.
- Sidawy A, Gray R, Besarab A, et al. Recommended standards for reports dealing with arteriovenous hemodialysis access. J Vasc Surg 2002;35:603-10.
- Murphy G, White S, Knight A, et al. Vascular access for hemodialysis. Br J Surg 2000;87:1300-15.
- Mac Rae J, Pandeya S, Hummmen, et al. Arteriovenous fistula-associated high-output cardiac failure: a review of mechanisms. Am J Kidney Dis 2004 ; ;5:17-22.
- Rao R, Azin G, Hood D, et al. Basilic vein transposition fistula: a good option for maintaining hemodialysis access site options.J Vasc Surg. 2004 ; ;39:1043-47.
- Chin A, Chang W, Fitzerland J, et al. Intra-access blood flow in patients with newly created upper-arm arteriovenous native fistulae for hemodialysis access. Am J Kidney Dis. 2004;44:850-58.
- BazanH, Schanzer H. Transposition of the brachial vein: a new source for autologous arteriovenous fistulas. J Vasc Surg 2004;40:184-86.
- Van Duijnhoven E, Cheriex E, Tordoir J, et al. Effect of closure of the arteriovenous fistula on left ventricular dimensions in renal transplant patients. Nephrol Dial Transplant 2001;16:368-72.
- De Lima J, Vieira M, Molnar L et al. Cardiac effects of persistent hemodialysis arteriovenous access in recipients of renal allograft. Cardiology 1999;92:236- 9.
- Ori Y, Korzets A, Katz M, et al. Hemodialysis arteriovenous access-A prospective hemodynamic evaluation. Nephrol Dial Transplant 1996;11:94-7.
- Dikow R, Schwenger V, Zeier M, et al. Do AV fistulas contribute to cardiac mortality in hemodialysis patients. Sem Dial 2002;15:14-7.
- Engelberts I, Tordoir J, Boon E, at al. High output cardiac failure due to excessive shunting in hemodialysis access fistula: An easily overlooked diagnosis. Am J Nephrol 1995;15:323-6.
- Mahmud M, Gao S, et al. Hyperdynamic circulation of arterio-venous fistula preconditions the heart and limits infarct size. Ann Thorac Surg 1999;68:22-8.
- Sandhu J, Wander D, Gupta M, et al. Hemodynamic effects of arteriovenous fistula in end stage renal failure. Renal Failure, 2004;26:695-701.
- Bos W, Zietse R, Wesseling K, et al. Effects of arteriovenous fistulas on cardiac oxygen supply and demand. Kidney Int 1999;55:2049-53.
- Wijnen E, Keuter X, Planken N, et al. The Relation Between Vascular Access Flow and Different Types of Vascular Access With Systemic Hemodynamics in Hemodialysis Patients. Artificial Organs 2005;29:960-4.
- Krajewska M, Weyde W, Kosmala W, et al. Influence of the arteriovenous fistula on cardiovascular system in patients with particular cardiovascular risk. Pol Merkur Lekarski 2006; ;21:145-6.
- Ma K, Raij L, et al. Cardiovascular risk factors in chronic renal failure and hemodialysis populations. Am J Kidney Dis 1992;19:505-13.
- Von Vibra H, Castro L, Autenriech G, et al. The effects of arteriovenous shunts on cardiac function in renal dialysis patients: an echocardiographic evaluation. Clin Nephrol 1978;9:205-9.
- Unger P, Wissing K.M, Pauw DL, et al. Reduction of left ventricular diameter and mass after surgical arteriovenous fistula closure in renal transplant recipients. Transplantation 2002;74:73-9.
Author Disclosures: Authors Theodosiadis P, GrosomanidisV, Hatzibaloglou A, Fyntanidou B, Kotso E, OloktsidouE, Skourtis Ch, have no conflicts of interest or financial ties to disclose. Corresponding author: Dr. Panagiotis Theodosiadis Consultant Anesthetist 8 Larisas str., 54249, Harilaou, Thessaloniki, Greece Tel. (Mob) +306944763219 Email: email@example.com