Why the study?
Does nadroparin cause bleeding complications in patients with end-stage renal disease and deep vein thrombosis?
Does nadroparin cause bleeding complications in patients with end-stage renal disease and deep vein thrombosis?
Low-molecular-weight heparins like nadroparin can cause severe bleeding complications in patients with severe renal disease and should be used with caution.
May signal bleeding risk with LMWH in ESRD; leaves open need for prospective trials on dosing in renal impairment.
Low-molecular-weight heparin (LMWH), a mixture of polysaccharide molecules, is derived from unfractionated heparin (UFH) by physical and/or chemical processes. Using subcutaneous injections of LMWH to treat patients with deep vein thrombosis has several major advantages over the use of conventional intravenous or subcutaneous UFH therapy. For instance, there is no requirement for laboratory monitoring of activated partial thromboplastin time with LMWH. However, in the report we observed a 65-year-old female with end-stage renal disease and found that she, after receiving anti-coagulant treatment with Nadroparin (LMWH), developed bleeding complications. It indicates that the potential bleeding adverse effect of LMWHs should be taken into account when applied to patients with severe renal disease.
No takes yet. Share an insight, caveat, or question.
Kao et al. (2007) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: