NDT Plus Advance Access originally published online on December 19, 2007
NDT Plus 2008 1(2):100-102; doi:10.1093/ndtplus/sfm031
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Haemodialysis catheterization via type II persistent left superior vena cava
Department of Nephrology and Haemodialysis, Rouen University Hospital, Rouen, F-76031, France
Correspondence: Melanie Hanoy, Department of Nephrology and Haemodialysis, Rouen University Hospital, Rouen, F-76031, France. Tel: +33-2-32-88-90-15; Fax: +33-2-32-88-91-15; E-mail: melanie.hanoy{at}chu-rouen.fr
Key Words: catheter coronary sinus haemodialysis persistent left superior vena cava
Received for publication September 21, 2007. Accepted for publication November 23, 2007.
| Introduction |
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Persistent left superior vena cava (PLSVC) is an anatomic variant of central veins, characterised by the persistence of a left-sided superior vena cava. Owing to the frequency of this anomaly, it is important for nephrologists to be aware of the potential per- and post-procedure complications that can be experienced during catheterization in PLSVC patients. We report the case of a 45-year-old patient presenting a rare type II PLSVC, detected after right internal jugular catheterization for haemodialysis. This article reviews the most frequent and clinically relevant abnormalities related to PLSVC and discusses their implications in haemodialysis practice.
| Case report |
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A 45-year-old woman with end-stage renal disease due to diabetic nephropathy was admitted for the pose of a central venous haemodialysis catheter. At that time, the patient was awaiting double kidney–pancreas transplantation and had failed on an attempt at peritoneal dialysis.
The catheter pose was initiated by a successful punction of the right internal jugular vein. Progression of the metallic leader guide was followed by simultaneous radioscopic imagery. An unusual curve towards the left was noticed as the leader over-reached the right internal jugular vein. The procedure was stopped. A CO2-phlebocavography was performed, which diagnosed a type II PLSVC.
Subsequently, it was decided to insert two single-lumen haemodialysis catheters through the left internal jugular vein, the straightest route to the superior vena cava in our patient. Postoperative radiography is presented in Figure 1.
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Four weeks later, the catheters were replaced because of a systemic infection. A temporary double-lumen central venous haemodialysis catheter was posed through the right internal jugular vein. The control radiography showed the atypical route of the catheter, through the innominated vein and the PLSVC towards the coronary sinus. Our patient experienced no immediate or secondary cardiovascular effect attributable to the placement of catheters in the type II PLSVC.
PLSVC is a thoracic venous anomaly described in 0.3% to 0.5% of the general population [1–3]. Eighty-five percent of PLSVC have persistence of both the left and right superior venae cavae (type IIIa and IIIb PLSVC) and originate from an abnormal development of the innominated vein during embryogenesis [2,3]. Our patient had a rare type II PLSVC with persistence of a unique left superior vena cava, responsible for the atypical route during both right- and left-sided procedures. Variants of the superior vena cava are presented in Figure 2.
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Fortuitous discovery of PLSVC after central venous catheterisation can cause dangerous misinterpretation of post-operative radiography. Per-procedure x-ray assistance used by informed physicians may prevent short-term complications due to repeated catheterization attempts, delayed dialysis or use of contrast media. PLSVC usually remains asymptomatic and has no significant haemodynamic adverse consequence. Its role in the pathogenesis of atrial fibrillation and organized arrhythmias related to abnormal distribution of cardiac conduction tissue has been described [4–6]. Cases of coronary sinus thrombosis, supraventricular arrhythmia and cardiac arrest are reported in PLSVC patients after central venous catheterization [7,8]. It has been hypothesized that these dramatic arrhythmias were attributable to the drugs administrated via the catheter, rather than to the catheter itself.
According to some authors, central venous catheters should not be systematically contra-indicated in adults with PLSVC [9,10]. To date, the safety of haemodialysis via central catheters in type II or type III PLSVC has not been accurately evaluated. Owing to the potential complications, we believe that haemodialysis through PLSVC should remain an exceptional and short-term therapeutic alternative in dialysis patients.
In our case, the decision was taken to further explore upper arm veins. A left humero-basilic fistula was created, the dialysis catheter removed and our patient finally received a double kidney–pancreas graft.
This case illustrates the importance for nephrologists, anaesthesiologists and critical care intensivists to be aware of the existence and complications of PLSVC variants, for a safer practice of central venous catheterization.
Conflict of interest statement: None declared.
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