Key result
Persistent left superior vena cava is a rare congenital anomaly that must be recognized during central venous access device placement to avoid potential complications.
Recognizing persistent left superior vena cava and characterizing its venous return pattern is critical for safe and successful central venous access device placement in cancer patients.
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Incidental PLSVC may complicate central access in surgical patients; leaves open targeted protocols for procedural specialists.
Persistent left superior vena cava (PLSVC) represents the most common congenital venous anomaly of the thoracic systemic venous return, occurring in 0.3% to 0.5% of individuals in the general population, and in up to 12% of individuals with other documented congential heart abnormalities. In this regard, there is very little in the literature that specifically addresses the potential importance of the incidental finding of PLSVC to surgeons, interventional radiologists, and other physicians actively involved in central venous access device placement in cancer patients. In the current review, we have attempted to comprehensively evaluate the available literature regarding PLSVC. Additionally, we have discussed the clinical implications and relevance of such congenital aberrancies, as well as of treatment-induced or disease-induced alterations in the anatomy of the thoracic central venous system, as they pertain to the general principles of successful placement of central venous access devices in cancer patients. Specifically regarding PLSVC, it is critical to recognize its presence during attempted central venous access device placement and to fully characterize the pattern of cardiac venous return (i.e., to the right atrium or to the left atrium) in any patient suspected of PLSVC prior to initiation of use of their central venous access device.
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Povoski et al. (2011) conducted a review in Persistent left superior vena cava (PLSVC) (n=1). Central venous access device placement was evaluated. Persistent left superior vena cava is a rare congenital anomaly that must be recognized during central venous access device placement to avoid potential complications.
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