Evidence map›Paper›PMID 33559708›Full record

ArticleEuropean journal of clinical pharmacology2021

Once-daily 1 g ceftriaxone optimizes exposure in patients with septic shock and hypoalbuminemia receiving continuous veno-venous hemodiafiltration.

Marta Ulldemolins, Carla Bastida, Mireia Llauradó-Serra, Chantal Csajka, Alejandro Rodríguez, Joan Ramon Badia, Ignacio Martín-Loeches, Dolors Soy

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European journal of clinical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. 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

8 authors at 5 institutions in 3 countries.

Marta Ulldemolins *Infectious Diseases - Internal Medicine Departments, Bellvitge University Hospital, University of Barcelona, L'Hopspitalet de Llobregat, Spain. marta.ulldemolins@gmail.com.ORCID http://orcid.org/0000-0002-5050-8430
Carla Bastida *Pharmacy Department, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0003-0845-8107
Mireia Llauradó-SerraDepartment of Nursing, School of Medicine and Health Sciences, Universitat Internacional de Catalunya, Barcelona, Spain.ORCID https://orcid.org/0000-0002-5123-0581
Chantal CsajkaService of Clinical Pharmacology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-0660-082X
Alejandro RodríguezCritical Care Department, Joan XXIII University Hospital, Institut d'Investigació Sanitària Pere Virgili (IISPV), Universitat Rovira I Virgili, Tarragona, Spain.
Joan Ramon BadiaCentro de Investigación Biomédica En Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Ignacio Martín-Loeches *Centro de Investigación Biomédica En Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain.ORCID https://orcid.org/0000-0002-5834-4063
Dolors Soy *Pharmacy Department, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0001-8128-345X
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESBellvitge University Hospital · ESHospital Clínic de Barcelona · ESUniversitat Internacional de Catalunya · ESUniversity of Geneva · CH

Funding

Ministerio de Sanidad, Servicios Sociales e Igualdad (ES) EC11-159
6 · The paper itself

Abstract

purposeCeftriaxone total and unbound pharmacokinetics (PK) can be altered in critically ill patients with septic shock and hypoalbuminemia receiving continuous veno-venous hemodiafiltration (CVVHDF). The objective of this study was to determine the dosing strategy of ceftriaxone that maximizes the probability of maintaining the concentration above the MIC of the susceptible bacteria (≤2 mg/L by the EUCAST) for a 100% of the dosing interval (100% ƒ

methodsIn a prospective PK study in the intensive care units of two tertiary Spanish hospitals, six timed blood samples were collected per patient; for each sample, ceftriaxone total and unbound concentrations were measured using a liquid chromatography coupled to tandem mass spectrometry method. Population PK analysis and Monte-Carlo simulations were performed using NONMEMv.7.3®.

resultsWe enrolled 8 critically ill patients that met the inclusion criteria (47 blood samples). Median age (range) was 70 years (47-85), weight 72.5 kg (40-95), albumin concentration 24.2 g/L (22-34), APACHE II score at admission 26 (17-36), and SOFA score on the day of study 12 (9-15). The unbound fraction (ƒ

conclusionOnce-daily 1 g ceftriaxone provides optimal exposure in critically ill patients with septic shock and hypoalbuminemia receiving CVVHDF.

Indexed as

Continuous Renal Replacement TherapyAgedAnti-Bacterial AgentsCeftriaxoneCritical IllnessDose-Response Relationship, DrugDrug Administration ScheduleDrug MonitoringFemaleHumansHypoalbuminemiaMaleMicrobial Sensitivity TestsMiddle AgedMonte Carlo MethodProspective StudiesAnti-Bacterial AgentsCeftriaxoneCeftriaxoneContinuous veno-venous hemodiafiltrationCritically ill patientsHypoalbuminemiaPharmacokineticsSeptic shock

Identifiers

PMID33559708
OpenAlexW3128422335

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.