International Journal of Drug Delivery Technology
Volume 16, Issue 15s, 2026

Dosage Optimization of enoxaparin in the treatment of cardiovascular diseases in Egyptian obese patients

Abdel-Hameed Ibrahim Mohamed Ebid1, Ahmed Gaafar2, Hadeer Mohamed Gamal Mohamed Fahmi Ali Saleh3*, Sara M.M. Abdel-Motalebm4

1Professor of Clinical Pharmacy and Head of Pharmacy Practice Department, Faculty of Pharmacy, Capital University, Egypt

2Associate Professor of Cardiology, Faculty of Medicine, Capital University, Egypt

3*Pharmacist at Badr University Hospital, Capital University, Egypt

4Lecturer of Clinical Pharmacy, Clinical Pharmacy Practice, Faculty of Pharmacy, Capital University, Egypt

* Corresponding author: Hadeer Mohamed Gamal Mohamed Fahmi Ali Saleh

ABSTRACT

Background: Obesity is a growing global health challenge, notably prevalent in Egypt, where it exacerbates cardiovascular risk. Enoxaparin, a low molecular weight heparin, is widely used for anticoagulation, yet standard dosing may not be optimal for obese patients due to altered pharmacokinetics. Limited local data exist on the clinical and economic implications of such dosing discrepancies in critically ill cardiovascular patients.

Objective: To assess the impact of obesity on the efficacy, safety, and ECHO (Economic, Clinical, and Humanistic Outcomes) of therapeutic enoxaparin in obese versus lean patients with cardiovascular diseases.

Methods: A prospective, observational cohort study was conducted at Badr University Hospital from December 2020 to December 2023. Fifty ICU/CCU patients receiving therapeutic enoxaparin (1 mg/kg SC every 12 hours) were grouped by BMI: obese (≥30 kg/m², n=25) and lean (<30 kg/m², n=25). Peak anti-factor Xa levels were measured 3–5 hours after the third dose. Secondary outcomes included oxygen therapy duration, hospital stay, INR, bleeding events, and total direct cost. Correlation and regression analyses explored predictors of anti-Xa activity.

Results: Obese patients had significantly lower anti-Xa levels (0.70 vs. 1.03 IU/mL, p<0.001), more frequent subtherapeutic exposure (32% vs. 0%), longer hospital stay (8.6 vs. 6.8 days), and higher costs (63.8 vs. 50.9 ×10³ LE). BMI was the only independent predictor of anti-Xa levels.

Conclusions: Standard enoxaparin dosing may lead to subtherapeutic anticoagulation in obese patients. Individualized dosing and anti-Xa monitoring are recommended to improve efficacy, reduce adverse outcomes, and optimize resource use.

Keywords: Enoxaparin; Obesity; Anti-factor Xa; Cardiovascular diseases; Intensive care; ECHO model; Pharmacokinetics; Egypt.

How to cite this article: Ebid AHIM, Gaafar A, Saleh HMGMF, Abdel-Motalebm SMM. Dosage Optimization of enoxaparin in the treatment of cardiovascular diseases in Egyptian obese patients. Int J Drug Deliv Technol. 2026;16(15s): 871-879. DOI: 10.25258/ijddt.16.15s.97

Source of support: Nil.

Conflict of interest: None