Enoxaparin for VTE thromboprophylaxis during inpatient rehabilitation care: assessment of the standard fixed dosing regimen.

Enoxaparin Rehabilitation Venous pulmonary embolism Venous thromboembolism

Journal

BMC pharmacology & toxicology
ISSN: 2050-6511
Titre abrégé: BMC Pharmacol Toxicol
Pays: England
ID NLM: 101590449

Informations de publication

Date de publication:
10 Jan 2024
Historique:
received: 19 02 2023
accepted: 22 12 2023
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 10 1 2024
Statut: epublish

Résumé

We aimed to examine the efficiency of fixed daily dose enoxaparin (40 mg) thromboprophylaxis strategy for patients undergoing inpatient rehabilitation. This was an observational, prospective, cohort study that included 63 hospitalized patients undergoing rehabilitative treatment following sub-acute ischemic stroke (SAIS) or spinal cord injury (SCI), with an indication for thromboprophylaxis. Anti-Xa level measured three hours post-drug administration (following three consecutive days of enoxaparin treatment or more) was utilised to assess in vivo enoxaparin activity. An anti-Xa level between 0.2-0.5 U/ml was considered evidence of effective antithrombotic activity. We found sub-prophylactic levels of anti-Xa (<0.2 U/ml) in 19% (12/63). Results were within the recommended prophylactic range (0.2-0.5 U/ml) in 73% (46/63) and were supra-prophylactic (>0.5 U/ml) in 7.9% (5/63) of patients. Anti-Xa levels were found to inversely correlate with patients' weight and renal function as defined by creatinine clearance (CrCl) (p<0.05). Our study confirmed that a one-size-fits-all approach for venous thromboembolism (VTE) prophylaxis may be inadequate for rehabilitation patient populations. The efficacy of fixed-dose enoxaparin prophylaxis is limited and may be influenced by renal function and weight. This study suggests that anti-Xa studies and prophylactic enoxaparin dose adjustments should be considered in certain patients, such as those who are underweight, overweight and or have suboptimal renal function. No. NCT103593291, registered August 2018.

Sections du résumé

BACKGROUND BACKGROUND
We aimed to examine the efficiency of fixed daily dose enoxaparin (40 mg) thromboprophylaxis strategy for patients undergoing inpatient rehabilitation.
METHODS METHODS
This was an observational, prospective, cohort study that included 63 hospitalized patients undergoing rehabilitative treatment following sub-acute ischemic stroke (SAIS) or spinal cord injury (SCI), with an indication for thromboprophylaxis. Anti-Xa level measured three hours post-drug administration (following three consecutive days of enoxaparin treatment or more) was utilised to assess in vivo enoxaparin activity. An anti-Xa level between 0.2-0.5 U/ml was considered evidence of effective antithrombotic activity.
RESULTS RESULTS
We found sub-prophylactic levels of anti-Xa (<0.2 U/ml) in 19% (12/63). Results were within the recommended prophylactic range (0.2-0.5 U/ml) in 73% (46/63) and were supra-prophylactic (>0.5 U/ml) in 7.9% (5/63) of patients. Anti-Xa levels were found to inversely correlate with patients' weight and renal function as defined by creatinine clearance (CrCl) (p<0.05).
CONCLUSIONS CONCLUSIONS
Our study confirmed that a one-size-fits-all approach for venous thromboembolism (VTE) prophylaxis may be inadequate for rehabilitation patient populations. The efficacy of fixed-dose enoxaparin prophylaxis is limited and may be influenced by renal function and weight. This study suggests that anti-Xa studies and prophylactic enoxaparin dose adjustments should be considered in certain patients, such as those who are underweight, overweight and or have suboptimal renal function.
TRIAL REGISTRATION BACKGROUND
No. NCT103593291, registered August 2018.

Identifiants

pubmed: 38200581
doi: 10.1186/s40360-023-00728-0
pii: 10.1186/s40360-023-00728-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8

Informations de copyright

© 2024. The Author(s).

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Auteurs

Amir Haim (A)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel. amirhaim@gmail.com.
School of Medicine, Tel Aviv University, Tel Aviv, Israel. amirhaim@gmail.com.

Orli Avnery (O)

School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Hematology Institute, Meir Medical Center, Kfar Saba, Israel.

Deborah Rubin-Asher (D)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel.
School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Hagay Amir (H)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel.
School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Kaifa Hashem (K)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel.

Harel Ben Zvi (HB)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel.

Motti Ratmansky (M)

Loewenstein Rehabilitation Medical Center, 278 Achuza St, Raanana, POB 3, 43100, Israel.
School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Classifications MeSH