Evidence map›Paper›PMID 32920531›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2022

Haemorrhagic complications in patients with renal insufficiency during treatment or prophylaxis with dalteparin.

Estrella Díaz Gómez, David Suárez Del Olmo, Laura Corregidor Luna, Irene Iglesias-Peinado, Benito García Díaz

Open access · greenAbstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2022. 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
0.3field-weighted citation impact, top 38% of its field
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, 5 citations in OpenAlex.

  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

5 authors at 2 institutions in 1 country.

Estrella Díaz GómezPharmacy Department, Hospital Universitario Severo Ochoa, Leganes, Madrid, Spain estrelladg15@hotmail.com.ORCID 0000-0001-7924-3029
David Suárez Del OlmoPharmacy Department, Hospital Universitario Severo Ochoa, Leganes, Madrid, Spain.
Laura Corregidor LunaPharmacy Department, Hospital Universitario Severo Ochoa, Leganes, Madrid, Spain.
Irene Iglesias-PeinadoDepartment of pharmacology, Universidad Complutense de Madrid Facultad de Farmacia, Madrid, Comunidad de Madrid, Spain.
Benito García DíazPharmacy Department, Hospital Universitario Severo Ochoa, Leganes, Madrid, Spain.
Hospital Universitario Severo Ochoa · ESUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLow-molecular-weight heparins are widely used in clinical practice for the treatment or prophylaxis of venous thromboembolism (VTE). As these drugs are eliminated mainly by renal means, any renal function impairment may lead to higher plasma concentrations and increase the risk of bleeding. This study aims to evaluate whether in clinical practice there is an increase in the occurrence of bleeding in patients with renal insufficiency (RI) during treatment or prophylaxis with dalteparin, and to analyse the risk factors potentially influencing the appearance of such bleeding events.

methodsPatients were sampled from the Universitary Severo Ochoa Hospital, Leganés, Spain. This was a retrospective cohort study with a 1 year inclusion period, conducted at a Spanish university hospital with 400 beds, on patients undergoing treatment or prophylaxis for VTE with dalteparin for a minimum of 3 days. The main outcome measure was the number of patients who had bleeding events, independently of their severity, during dalteparin administration in patients with RI.

results367 patients were included in the study. Bleeding occurred in 17.9% of patients in the group with RI and in 7.3% of patients with normal renal function (NRF). Most haemorrhages in both cohorts were grade 2 on the WHO scale (64.7% in the RI group and 69.2% in the NRF group). Logistic regression analysis allowed the presence of RI (MDRD-4 (Modification of Diet in Renal Disease) <50 mL/min) to be identified as a risk factor.

conclusionPatients with RI treated with dalteparin face a higher risk of bleeding than those with NRF, which seems to make it necessary to monitor and seek new dosage adjustments for these patients.Impact on practice statements: This study yields new data on dalteparin in RI, which has not been widely studied before.

Indexed as

Renal InsufficiencyVenous ThromboembolismAnticoagulantsDalteparinHumansRetrospective StudiesAnticoagulantsDalteparinacute renal failurechronic renal failureclinical pharmacyhealth & safetynephrology

Identifiers

PMID32920531
PMCPMC9251166
OpenAlexW3085181771

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.