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Comparison of intensive versus standard hemodialysis central venous catheter dysfunction protocol using rt-PA: a quality assurance initiative

Comparison of intensive versus standard hemodialysis central venous catheter dysfunction protocol using rt-PA: a quality assurance initiative

forthcoming

Article Type: ORIGINAL ARTICLE

Article Subject: Dialysis

DOI:10.5301/jva.5000501

Authors

Wilson, Jo-Anne S. Mossop, Paula Soroka, Steven D. Dipchand, Christine Drost, Sarah Sheehy, Niall Tennankore, Karthik

Abstract

Catheter locking solutions such as recombinant tissue plasminogen activator (rt-PA) are used to treat and prevent clotting of hemodialysis (HD) catheters during HD treatments and the interdialytic period. However, evidence to guide the use of rt-PA for catheter dysfunction is limited.

We evaluated outcomes using two catheter dysfunction protocols in a cohort of consecutive prevalent dialysis patients (Jan 2013 to Sep 2014) undergoing HD with a tunneled catheter. In the intensive protocol, rt-PA was administered to all catheters based on blood flow and/or line reversal. In the standard protocol, rt-PA administration was based only on blood flow. The primary outcome was the rate of rt-PA use for catheter malfunction (rt-PA treatment days/1000 total line days; [TLD]). Secondary outcomes included the cost of rt-PA/TLD and the rate of catheter-related bacteremia.

There were 26 and 35 patients managed by the intensive and standard protocols, respectively. The rate of rt-PA use was 52/1000 TLD (intensive) versus 39/1000 TLD (standard) (rate ratio 1.30, 95% CI 1.12-1.52 CI, p<0.001). The rate of bacteremia was 0.43 and 0.22/1000 TLD for the intensive and standard protocols, respectively (p = 0.491). The cost of rt-PA was CDN $5.58 and CDN $6.15 per TLD for the intensive protocol and standard protocol groups (p<0.001).

Managing catheter dysfunction based on line reversal and blood flow as opposed to only blood flow was associated with a higher rate of rt-PA use, but at a reduced overall cost.

Article History

Disclosures

Financial support: This study was supported by research grants from the Division of Nephrology, Department of Medicine, Nova Scotia Health Authority, Halifax, Nova Scotia, Canada and Hoffman-La Roche Limited, Misissauga, Ontario, Canada.
Conflict of interest: Drs. Wilson, Soroka and Ms. Mossop were advisory board members for Hoffman-La Roche Limited in the past two years. Ms. Mossop also received an honorarium for speaking engagements for Hoffman-La Roche Limited. There are no other potential conflicts of interest relevant to this article.

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Authors

  • Wilson, Jo-Anne S. [PubMed] [Google Scholar] 1, 2, * Corresponding Author (Jo-Anne.Wilson@Dal.ca)
  • Mossop, Paula [PubMed] [Google Scholar] 3
  • Soroka, Steven D. [PubMed] [Google Scholar] 1, 4
  • Dipchand, Christine [PubMed] [Google Scholar] 1, 4
  • Drost, Sarah [PubMed] [Google Scholar] 3
  • Sheehy, Niall [PubMed] [Google Scholar] 3
  • Tennankore, Karthik [PubMed] [Google Scholar] 1, 4

Affiliations

  • Division of Nephrology, Department of Medicine, Nova Scotia Health Authority Central Zone, Halifax, Nova Scotia - Canada
  • College of Pharmacy, Faculty of Health Professions, Dalhousie University, Halifax, Nova Scotia - Canada
  • Nova Scotia Health Authority Central Zone Renal Program, Halifax, Nova Scotia - Canada
  • Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia - Canada

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