Evidence map›Paper›PMID 39853909›Full record

ArticlePharmacology research & perspectives2025

A Clinical Practice-Based Comparison of Conventional and Individualized Dosing Strategies for Therapeutic Enoxaparin.

Anthony Damiani, Viviane De Menezes Caceres, Greg Roberts, Jessica Coddo, Nicholas Scarfo, Desmond B Willliams, Vinosshini Tharmathurai, Rami Tadros, Stephen Fitzgerald, Alice O'Connell and 18 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in Pharmacology research & perspectives, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Anthony DamianiSA Pharmacy, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Viviane De Menezes CaceresSchool of Allied Health Science and Practice, The University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-6052-0273
Greg RobertsSA Pharmacy, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Jessica CoddoSA Pharmacy, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Nicholas ScarfoSA Pharmacy, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Desmond B WillliamsPharmacy and Biomedical Sciences, University of South Australia, Adelaide, South Australia, Australia.
Vinosshini TharmathuraiDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Rami TadrosDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Stephen FitzgeraldDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Alice O'ConnellDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Amrit Kaur SandhuDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Andrew VanlintMedical Services Division, Northern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Arduino A MangoniDepartment of Clinical Pharmacology, Flinders University and Flinders Medical Centre, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-8699-1412
Dirk HofmannDepartment of General Internal Medicine, Noarlunga Hospital, Southern Adelaide Local Health Network Adelaide, South Australia, Australia.
Hosam BonySA Pharmacy, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Jeff FauntDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Jir Ping BoeyDepartment of Internal Medicine Flinders Medical Centre, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Nicholas FarinolaDepartment of Clinical Pharmacology, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Rachel WellsDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Stephen HedgerDepartment of Internal Medicine Flinders Medical Centre, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Udul HewageDepartment of Internal Medicine Flinders Medical Centre, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Yogesh SharmaDepartment of Internal Medicine Flinders Medical Centre, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Zuhair JabbarDepartment of Internal Medicine Flinders Medical Centre, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Josephine ThomasDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Katerina FlabourisDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.
Toby GilbertDiscipline of Medicine, The University of Adelaide, Adelaide, South Australia, Australia.
Campbell ThompsonDiscipline of Medicine, The University of Adelaide, Adelaide, South Australia, Australia.
Patrick RussellDepartment of Internal Medicine, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-2534-3371

Funding

South Australian Association of Internal Medicine
6 · The paper itself

Abstract

To understand differences in anti-factor-Xa levels produced by two different dosing strategies (conventional and individualized) for therapeutic enoxaparin in a cohort of hospital inpatients. A multicenter, retrospective cohort study over a two- and a half-year period for inpatients with stable renal function and on therapeutic enoxaparin. Anti-factor-Xa levels were taken 3-5 h after enoxaparin administration and a minimum of 48 h of dosing. The final analysis included 278 patients from five hospitals: conventional dosing was used for 141, while 137 were given an unconventional dose, that is, individualized for their renal function and weight. Out-of-range levels were frequent (35% to 40% of all inpatients). After adjustment for age, renal function, and body mass index (BMI), the conventional group was more likely to experience above-range levels (> 1.0 IU/mL; OR 2.50 [95% CI 1.38-4.56], p < 0.003) than the individualized group. Individualized dosing was independently associated with higher odds of a below-range anti-Xa level (< 0.5 IU/mL) compared to conventional dosing (OR 2.27 [95% CI 1.07-4.76], p = 0.03). Within the conventional group, above-range levels were significantly and independently associated with decreasing renal function (OR 0.97, 95% CI 0.96-0.99, p = 0.004) and with increasing BMI (OR 1.06, 95% CI 1.01-1.10, p = 0.02). No such associations were seen with an individualized approach. Clinical event rates were low and not different between groups (p > 0.24). Conventional therapeutic dosing of enoxaparin exposed people with obesity or renal impairment to more frequent above-range anti-factor-Xa levels; individualizing the dose could improve this but might expose people to subtherapeutic levels. More research is needed.

Indexed as

AnticoagulantsEnoxaparinFactor Xa InhibitorsAdultAgedAged, 80 and overBody Mass IndexDose-Response Relationship, DrugFactor XaFemaleHumansMaleMiddle AgedPrecision MedicineRetrospective StudiesAnticoagulantsEnoxaparinFactor XaFactor Xa Inhibitorsenoxaparinfactor Xalow‐molecular‐weight heparin

Identifiers

PMID39853909
PMCPMC11760983

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.