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. 2017 Jul;15(4):369-377.
doi: 10.2450/2016.0031-16. Epub 2016 Jul 21.

Anticoagulants for the prevention and treatment of catheter-related thrombosis in adults and children on parenteral nutrition: a systematic review and critical appraisal

Affiliations

Anticoagulants for the prevention and treatment of catheter-related thrombosis in adults and children on parenteral nutrition: a systematic review and critical appraisal

Stefano Barco et al. Blood Transfus. 2017 Jul.

Abstract

Background: Patients on parenteral nutrition require a central venous access and are at risk of catheter-related thrombosis, pulmonary embolism, and vena cava syndrome. Parenteral nutrition guidelines suggest anticoagulation for the primary prevention of catheter-related thrombosis during long-term parenteral nutrition. We conducted a systematic review of the efficacy, safety and feasibility of anticoagulant use for preventing and treating catheter-related thrombosis during parenteral nutrition.

Materials and methods: We searched for interventional and observational studies on adults and children receiving systemic anticoagulants during either short- or long-term parenteral nutrition delivered via central venous access. Primary outcomes were: objectively-confirmed catheter-related thrombosis, pulmonary embolism and bleeding. Secondary outcomes were: heparin-induced thrombocytopenia, prevalence of anticoagulation, and quality of International Normalised Ratio management in vitamin K antagonist-treated patients.

Results: We identified 1,199 studies, of which 23 were included. Seven interventional studies of short-term parenteral nutrition (adult population, n=5) were classified as low-quality: in those, intravenous unfractionated heparin did not prevent catheter-related thrombosis if compared to saline. No interventional studies were conducted in patients on long-term parenteral nutrition. Observational data were sparse, rarely focusing on anticoagulation, and overall of low quality. The reported use of anticoagulants was between 22 and 66% in recent multicentre cohorts.

Discussion: The amount and quality of data in this area are very suboptimal: most studies are outdated and involved heterogeneous populations. Currently, there is insufficient evidence to allow conclusions to be reached regarding the efficacy and safety of anticoagulants in this setting.

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Conflict of interest statement

Disclosure of conflicts of interest

SB received an educational travel grant from Daiichi Sankyo; his work has been supported by the German Federal Ministry of Education and Research (BMBF 01EO1003 and 01EO1503) since August 01, 2015, and by the University of Pavia (Italy) before May 15, 2015. JJA has no relevant conflicts to disclose. MC received consulting and lecturing fees from Boehringer Ingelheim, Daiichi Sankyo, the alliance of Bristol-Myers Squibb and Pfizer and Sanquin Blood Supply, and research support from Boehringer Ingelheim and Sanquin Blood Supply. MJS received consulting fees from Fresenius Kabi and research support from Baxter and TEFA Mediq. SM received consulting fees from Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Pfizer, Daiichi-Sankyo, and research support from Glaxo SmithKline, Aspen, Bristol-Meyers Squibb/Pfizer and Sanquin Blood Supply. The present work was not funded.

Figures

Figure 1
Figure 1
Summary of risk of bias in interventional studies. The “Risk of bias” figure was drawn on the basis of the indications provided by the Cochrane Collaborations using the model available in RevMan software. The evaluation of each study is summarised adopting the following symbols: “Low risk” of bias (+), “High risk” of bias (−), or “Unclear risk” of bias (?).

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