Dosing of Enoxaparin in Renal Impairment.

نویسندگان

  • Suhail A Shaikh
  • Randolph E Regal
چکیده

OBJECTIVE To review enoxaparin treatment dosing, pharmacokinetics, and clinical outcomes data in patients with renal impairment and to examine the current two-tiered dosing regimen approved by the Food and Drug Administration (FDA). DATA SOURCES A literature search of PubMed (1990-2016) was performed using the search terms low-molecular-weight heparin, unfractionated heparin, bleeding, enoxaparin, renal impairment, pharmacokinetics, and hemodialysis. STUDY SELECTION AND DATA EXTRACTION All studies assessing the pharmacokinetic properties of enoxaparin in patients with renal impairment were evaluated. In addition, all retrospective and prospective studies assessing the safety and efficacy of enoxaparin treatment in this population were evaluated. DATA SYNTHESIS Five pharmacokinetic studies evaluated changes in the pharmacokinetics of enoxaparin in patients with renal impairment. In these studies, enoxaparin clearance was reduced by 17% to 44% in patients with mild and moderate renal impairment. Six retrospective studies evaluated the safety of enoxaparin in patients with renal impairment. In one study, patients with moderate renal impairment were at increased risk of bleeding when using the current FDA-approved two-tiered scheme (odds ratio, 4.7; 95% confidence interval, 1.7-13.0; P = 0.002). Another study demonstrated that individualized enoxaparin dosing, when compared to FDA-approved dosing, resulted in a decreased risk of bleeding. Two retrospective studies evaluated efficacy. One of these studies compared reduced-dose enoxaparin with unfractionated heparin; there was a trend toward lower incidences of thromboembolism and 30-day mortality with reduced-dose enoxaparin. Hospital length of stay also decreased with reduced-dosed enoxaparin. CONCLUSIONS This paper highlights the differences in the pharmacokinetic properties and safety and efficacy outcomes in multiple degrees of renal impairment when using treatment-dose enoxaparin. Given the literature highlighted in this review, a more multitiered enoxaparin renal dosing strategy-perhaps shifting from the current two-tier approach to at least three or four tiers-should be considered.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Individualized dosing of enoxaparin for subjects with renal impairment is superior to conventional dosing at achieving therapeutic concentrations.

INTRODUCTION Enoxaparin is an anticoagulant used in the treatment of thromboembolic diseases. It is a hydrophilic molecule that is, predominantly, eliminated renally with few data to support dosing for subjects with renal impairment and/or obesity. A recently conducted randomized controlled clinical trial compared individualized enoxaparin doses based on lean body weight and renal function to c...

متن کامل

Enoxaparin outcomes in patients with moderate renal impairment.

BACKGROUND Enoxaparin sodium has predictable pharmacokinetics that allow for simplified dosing without laboratory monitoring. Reliance on renal function for excretion may lead to accumulation of enoxaparin in patients with moderate renal impairment. However, there is no dose adjustment recommended for these patients. We conducted a review to compare bleeding events in patients with moderate ren...

متن کامل

Dosing practices and risk factors for bleeding in patients receiving enoxaparin for the treatment of an acute coronary syndrome.

OBJECTIVES To describe dosing practices and to identify risk factors for bleeding in patients with an acute coronary syndrome (ACS) who received treatment with enoxaparin. DESIGN Retrospective chart review. SETTING Coronary care unit of a tertiary-care teaching hospital. PATIENTS Patients with a discharge diagnosis of an ACS who received at least one dose of enoxaparin, 1 mg/kg, were elig...

متن کامل

Enoxaparin utilization evaluation in inpatients with or at risk of thromboembolic disorders: A one-year, single-centered, retrospective Study

The aim of this study was evaluation of enoxaparin utilization in hospitalized patients who had received enoxaparin either for prophylaxis or for treatment of thromboembolic disorders. A total of  356 patients were included in this retrospective study and were analyzed for enoxaparin utilization in terms of prescription patterns, treatment strategy, dosing regimen, indications/contraindica...

متن کامل

Risk Factors for Bleeding Events with Enoxaparin, Dabigatran and Fondaparinux in Hospitalized Patients with Varying Levels of Renal Impairment

Background: Anticoagulants with renal elimination may accumulate in patients with renal impairment and potentially increase the risk of bleeding. Limited data are available to elucidate the potential bleeding risk present in patients with moderate renal impairment defined as creatinine clearance of 30-50 mL/min. Objective: To evaluate potential risk factors for bleeding over various renal funct...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • P & T : a peer-reviewed journal for formulary management

دوره 42 4  شماره 

صفحات  -

تاریخ انتشار 2017