A prospective audit evaluating use of urokinase in oncology patients with occluded central venous access devices

Br J Nurs. 2019 Oct 24;28(19):S30-S36. doi: 10.12968/bjon.2019.28.19.S30.

Abstract

This article reports the results of a single-site prospective audit evaluating the safety and effectiveness of urokinase (Syner-Kinase®) to restore patency in central venous access devices (CVADs) for cancer patients. CVADs are routinely inserted to allow the safe and timely administration of systemic anti-cancer therapies; therefore, catheter dysfunction can interrupt the treatment schedule and adversely affect patient outcome. The aim was to contribute to the development of evidence-based, standardised, best practice guidelines. Prospective data were collected from all patients (n=22) identified with an occluded CVAD, requiring use of Syner-Kinase to manage a persistent withdrawal occlusion or total occlusion, over a 6-month period. Findings revealed a single administration of Syner-Kinase for catheter occlusion clearance to be effective in 92% of cases. Results suggest that use of the thrombolytic agent is well-tolerated and an effective means of restoring patency for long-term CVADs in cancer patients.

Keywords: Catheter occlusion; Central venous access device; Oncology; Systemic anti-cancer therapy; Thrombolytic; Urokinase.

MeSH terms

  • Catheterization, Central Venous / adverse effects*
  • Clinical Audit
  • Equipment Failure
  • Female
  • Humans
  • Male
  • Neoplasms / therapy*
  • Prospective Studies
  • State Medicine
  • Treatment Outcome
  • United Kingdom
  • Urokinase-Type Plasminogen Activator / therapeutic use*

Substances

  • Urokinase-Type Plasminogen Activator