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Vascular and Interventional Radiology |
1 From the Departments of Radiology (H.L.L., H.B.P., M.T.W., P.H.L., C.K.H.C., C.F.Y.), Internal Medicine (Nephrology) (H.M.C., H.C.F.), Education and Research (L.P.G.), and Surgery (Cardiovascular) (T.H.W.), Kaohsiung Veterans General Hospital, National Yang-Ming University, 386 Ta-Chung 1st Rd, Kaohsiung, Taiwan 813, Republic of China. Received April 20, 2001; revision requested May 31; revision received August 24; accepted September 28. Address correspondence to C.F.Y. (e-mail: cfyang@isca.vghks.gov.tw).
| ABSTRACT |
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MATERIALS AND METHODS: Forty patients with 42 thrombosed arteriovenous fistulas were percutaneously treated. Thrombosis occurred within 24 hours of attempted angioplasty in five fistulas, between 24 and 72 hours in 27, and longer than 72 hours in 10. Thrombosed fistulas were approached in a retrograde fashion followed by direct balloon dilation with 58-mm balloon catheters. If retrograde catheterization failed to cross the arterial anastomosis, an antegrade puncture directly into the thrombosed drainage vein close to the anastomosis was performed with ultrasonographic guidance, as an aid to catheterize the arterial inflow. Thrombolytic therapy with infusion of urokinase directly into the thrombus was performed in selected patients with visible thrombus that had compromised blood flow in the partially restored vascular access. Postintervention primary and secondary patency was calculated by using Kaplan-Meier analysis. Patency rates between patients without and with urokinase infusion were examined by using the log-rank test.
RESULTS: Anatomic success was achieved in 39 (93%) of 42 fistulas; and clinical patency, in 38 (90%) of 42 fistulas. Postintervention primary and secondary patencies (including initial technical failure) at 6, 12, and 18 months were 81% and 84%, 70% and 80%, and 63% and 80%, respectively. No significance of patency rate between patients without and with urokinase infusion was found (P = .912). Three patients died of unrelated causes at 1, 2, and 5 months after the procedures. No major complications were encountered.
CONCLUSION: High anatomic success and excellent clinical patency can be achieved in the salvage of thrombosed arteriovenous fistulas. Percutaneous restoration of arteriovenous fistulas should be attempted before surgical recreation to optimize outcome in patients undergoing hemodialysis.
© RSNA, 2002
Index terms: Dialysis, shunt, 91.457 Fistula, arteriovenous, 91.494 Thrombolysis, 91.1265 Veins, transluminal angioplasty, 916.454
| INTRODUCTION |
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| MATERIALS AND METHODS |
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6 months old), eight fistulas were 6 months old or less, and 11 fistulas were 3 months old or less. Thirty-seven fistulas were created with radial-cephalic arteriovenous anastomosis, while five fistulas were created with brachio-basilic (cephalic) anastomosis.
Salvage Technique
Thrombosed vascular access was first examined (H.L.L., H.B.P.) by using high-frequency (7.0-MHz) color ultrasonography (US) (128XP; Acuson, Mountain View, Calif) from its arteriovenous anastomosis. The outflow drainage vein was traced for at least 20 cm in the cephalad direction. The puncture site was chosen as far away as possible from the anastomosis. In most patients, the entry sites were at the elbow region. In patients with brachio-basilic (cephalic) anastomoses, the access was approached either at the shoulder region or by puncturing of the ipsilateral internal jugular vein. Puncture sites were anesthetized with lidocaine hydrochloride (Xylocain; Abbott Laboratories, North Chicago, Ill). Intramuscular meperidine (50 mg) (Demerol; Abbott Laboratories) injection was used for analgesic purposes in each patient.
To access the collapsed fistula, a sterile latex tourniquet was placed tightly on the upper arm or shoulder region. The fistula was punctured with an 18-gauge cannula sheath either directly or mostly with US guidance (H.L.L.). A 0.035-inch hydrophilic guide wire and a 7-F vascular sheath (Terumo; Radiofocus, Tokyo, Japan) were introduced in a retrograde fashion. With the aid of the road-map technique, the occluded segment of the vascular access was carefully obtained with catheterization. However, in some instances, because of preexisting venous stenosis in the occluded segment and coexisting accessory vein(s) close to the arteriovenous anastomosis, retrograde catheterization into arterial inflow was not feasible. For these patients, a second antegrade puncture (18-gauge cannula sheath) directly into the thrombosed vein was performed (Fig 1). This puncture was usually performed with US guidance due to the small caliber of the thrombosed vein (Fig 2). Subsequently, a small amount of contrast medium was slowly injected to try to opacify the lumen of the thrombosed drainage vein for guiding of retrograde catheterization. If high resistance was felt during contrast medium injection or retrograde catheterization was still not feasible, a guide wire was introduced into the lower cannula sheath. Most of the stenotic segment in the thrombosed AVF was threaded without much difficulty by using this antegrade approach. This guide wire was then moved into the lumen of the 7-F vascular sheath, and both were pulled out from the upper puncture site (Fig 1). With the guide wire held tightly on both sides, an angiocatheter (RC1-65 cm, Cordis; Johnson and Johnson, Roden, the Netherlands) was advanced in a retrograde fashion, with the catheter tip placed close to the lower puncture site. (The cannula sheath was pulled back a little but was still kept in the thrombosed lumen.) The guide wire was withdrawn and reintroduced into the catheter with its soft tip in a retrograde fashion to enter the arterial inflow (Fig 3).
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Definitions
According to recently published reporting standards from the Society of Cardiovascular and Interventional Radiology (16), anatomic success was defined as restoration of flow combined with a less than 30% maximal residual diameter stenosis at the conclusion of the interventional procedure, which was performed by one of the authors (H.L.L.). Clinical success was determined by one of three authors (H.M.C., H.C.F., or T.H.W.) and defined as resumption of normal dialysis for at least one session. Postintervention primary patency is the interval following intervention until the next access thrombosis or repeated intervention. Postintervention secondary patency is the interval after intervention until the access is surgically declotted, revised, or abandoned. Follow-up of this study ended on April 1, 2001.
Kaplan-Meier analysis was used to calculate all patency data. The patency rates of anatomic success between patients without and those with urokinase infusion were examined by using the log-rank test. A P value of less than .05 was considered to indicate a statistically significant difference.
| RESULTS |
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The overall anatomic success rate was 93%. One fistula failed to achieve clinical success. Twenty-two thrombosed fistulas (52%) were successfully restored with the one-puncture technique in our study, whereas 20 fistulas required a second puncture. Urokinase was infused in 13 (31%) of 42 thrombosed fistulas, with the doses ranging from 240,000 to 480,000 IU (average dose, 320,000 IU).
The overall postintervention primary and secondary patencies of the restored vascular access (including the initial technical failure) at 6, 12, and 18 months were 81% and 84%, 70% and 80%, and 63% and 80%, respectively (Fig 5). The primary patencies at 18 months between patients without and those with urokinase infusion of the 39 anatomic successful fistulas were 69% and 62%, respectively. There was no statistical significance (P = .912) between these two groups. Three patients died of unrelated causes at 1, 2, and 5 months after the procedures.
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| DISCUSSION |
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The effectiveness of percutaneous angioplasty in maintaining access patency in patients undergoing hemodialysis has been well documented. The success rate was approximately 88%95% for polytetrafluoroethylene graft (1719,2225) and 80%91% for stenotic AVFs (912). The primary patencies at 6 and 12 months were 20%34% and 4%26%, respectively, for polytetrafluoroethylene grafts (1719,2225) and 77% and 64%, respectively, for stenotic AVFs (9). For thrombosed AVFs, poor patency rate was initially reported; Vorwerk et al (17) reported a primary patency of 50% at 6 months. Overbosch et al (18) reported the median primary patency being 14 weeks. Later, Turmel-Rodrigues et al (19) reported better results, with primary and secondary patency rates (including initial technical failure) at 6 and 12 months of 74% and 81% and 60% and 81%, respectively. In the study of Zaleski et al (14), the primary and secondary patency rates (excluding initial treatment failure) at 6 and 12 months were 71% and 100% and 64% and 100%, respectively (14). In our study, the primary and secondary patency rates (including initial technical failure) at 6 and 12 months were 81% and 84% and 70% and 80%, respectively, which were comparable to those of Zaleski and colleagues (14).
Percutaneous restoration of failed vascular access as early as possible is usually recommended to increase the technical success rate and to avoid unnecessary central venous catheter placement. On the basis of data from surgical thrombectomies, immediate surgical revision has been advocated to restore function of recently thrombosed fistulas (7). In thrombosed AVFs, angioplastic attempt within 24 hours of occlusion has been considered essential for successful restorations. However, some successful restoration of thrombosed AVFs in patients with occlusions of 2472 hours has been reported (14,20). However, the authors of these studies still recommended performing angioplasty within 24 hours of occlusion. In a review (26) of 263 patients receiving catheter-directed thrombolysis for deep venous thrombosis of the iliofemoral vein, 88% of acute or subacute clots (<4 weeks old) and 60% of old clots (>4 weeks old) were successfully treated. Therefore, it is not the thrombus per se that has prevented the intervention from being performed within 24 or 72 hours of occlusion, but the technical consideration that the thrombosed vascular lumen will obliterate as time passes and consequently increase the difficulty of interventional cannulation and catheterization. Since technical cannulation and catheterization can be accomplished with the use of our technique, we had successfully restored thrombosed AVFs with occlusion of 49 days. Therefore, we recommend performing percutaneous restoration first for any failed vascular access, even in the case of occlusion of more than 72 hours.
The safety of direct balloon dilation prior to clearing the whole thrombus has been of concern (15). Zaleski et al (14) routinely injected 500,000 IU of urokinase for 1 minute immediately after the arterial anastomosis was dilated and used a 827-mm-diameter compliant occlusion balloon catheter to displace the residual adherent thrombus in their patients (14). Schon and Mishler (20) infused low-dose thrombolytic agents (0250,000 IU of urokinase or 2.511.0 mg of tissue plasminogen activator) in their patients before balloon angioplasty. Turmel-Rodrigues and colleagues (15) questioned the effectiveness of bolus injection of thrombolytic agent in dissolving thrombus. They recommended manual thromboaspiration to clear all of the thrombus before balloon dilation (19). We agree that bolus injection of thrombolytic agent cannot dissolve the whole thrombus, but we disagree that the whole thrombus has to be removed before balloon dilation to prevent the complication of pulmonary emboli and to achieve better patency. Vorwerk and colleagues (17) used a hydrodynamic thrombectomy catheter to remove thrombus in the failed vascular accesses. They estimated the average residual thrombus left in the native fistula to be 21% (10%50%). They stated that despite residual thrombus found in many cases, arterialized flow was completely established in 84% of their native fistulas. In the patients, 69% of thrombosed AVFs were successfully restored by using direct angioplasty. Comparison of the patency rates of anatomic success between 35 patients without and with urokinase revealed no significant difference. Winkler et al (27) reported that the volume of thrombus obtained from hemodialysis access grafts at surgical thrombectomy ranges from 1.5 to 4.7 mL. Although the real clot burden in thrombosed AVF is uncertain, our color sonographic study before balloon angioplasty revealed that the thrombi in most patients were usually confined in the distal drainage vein below the lower two-thirds of forearm. The length of thrombosed vascular lumen was much shorter than that of a thrombosed U-loop graft. Thus, we considered the real clot burden in these patients to be less than that in patients with polytetrafluoroethylene grafts. Although small pulmonary emboli may inevitably ensue, they were probably small and were lysed by using physiologic and/or therapeutic fibrinolysis. In our method, we only dilated the occluded vascular access without intending to remove or declot all of the adherent thrombus. None of the patients in this study complained of respiratory distress during or immediately after the procedure. Thrombolytic therapy was performed only in patients requiring it (31% of the patients). The infusion dose of urokinase ranging from 240,000 to 480,000 IU was considered safe. No complications related to drug infusion occurred in the patients.
To prevent the complication of distal arterial emboli, Zaleski et al (14) attempted to establish patency of the outflow veins before crossing the arterial anastomosis. However, it still occurred in four patients. This complication could be easily managed by using direct administration of thrombolytic agent, such as in two of the patients in this study. The incidence of venous rupture resulting from hemodialysis-related angioplasty was reported to be around 1.7%20.0% (2830). To restore the flow and stop extravasation, prolonged inflation of a balloon catheter or placement of a metallic stent is the treatment of choice (2830). We placed a metallic stent in one patient because ensuing thrombolysis was considered mandatory for its residual thrombus. The benefit of placement of a metallic stent in the venous segment intended for cannulation is debated. An experimental study (31) has confirmed the feasibility of direct puncture into the stent for hemodialysis. In conclusion, although percutaneous restoration of a thrombosed arteriovenous fistula is technically more complicated, our study offers a standardized percutaneous technique with a high technical success rate and excellent vascular patency.
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Author contributions: Guarantor of integrity of entire study, C.F.Y.; study concepts and design, H.L.L.; literature research, H.B.P., C.K.H.C.; clinical studies, H.M.C., H.C.F., T.H.W.; data acquisition and analysis/interpretation, M.T.W., P.H.L.; statistical analysis, L.P.G., H.L.L.; manuscript preparation, definition of intellectual content, and editing, H.L.L.; manuscript revision/review, C.F.Y., H.B.P.; manuscript final version approval, C.F.Y., H.L.L.
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