Evidence map›Paper›PMID 39728803›Full record

ArticleToxins2024

The Choice of Anti-Inflammatory Influences the Elimination of Protein-Bound Uremic Toxins.

Víctor Joaquín Escudero-Saiz, Elena Cuadrado-Payán, María Rodriguez-Garcia, Gregori Casals, Lida María Rodas, Néstor Fontseré, María Del Carmen Salgado, Carla Bastida, Nayra Rico, José Jesús Broseta and 1 more

Abstract read
In one paragraph

Article in Toxins, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Víctor Joaquín Escudero-SaizNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0003-0411-207X
Elena Cuadrado-PayánNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0003-2412-6911
María Rodriguez-GarciaBiochemistry and Molecular Genetics Department-CDB, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Gregori CasalsBiochemistry and Molecular Genetics Department-CDB, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-3271-1371
Lida María RodasNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Néstor FontseréNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
María Del Carmen SalgadoBiochemistry and Molecular Genetics Department-CDB, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Carla BastidaPharmacy Department, University of Barcelona, 08036 Barcelona, Spain.ORCID 0000-0003-0845-8107
Nayra RicoBiochemistry and Molecular Genetics Department-CDB, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0001-5667-0650
José Jesús BrosetaNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-4559-9083
Francisco MaduellNephrology and Renal Transplantation, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-1673-0353

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pain is a frequent and disturbing symptom among hemodialysis patients. Protein-bound uremic toxins (PBUTs) are related to cardiovascular and overall mortality, and they are difficult to remove with current hemodialysis treatments. The PBUT displacers, such as furosemide, tryptophan, or ibuprofen, may be promising new strategies for improving their clearance. This study aims to compare ibuprofen versus other analgesic drugs in PBUT removal. A prospective study was carried out in 23 patients. Patients underwent four dialysis sessions with routine dialysis parameters, except for analgesic drugs administered (lysine acetylsalicylic acid, acetaminophen, dexketoprofen, and ibuprofen). The reduction ratios (RRs) of a wide range of molecular weight molecules were assessed, including total p-cresyl sulfate and total indoxyl-sulfate. There were no complications related to the administered drug, and pain was controlled independently of the drug. There were no differences in the RR of small-size and medium-sized molecules between all four study treatments. However, indoxyl sulfate and p-cresyl sulfate RRs when ibuprofen was administered were significantly higher than lysine acetylsalicylic acid, acetaminophen, and dexketoprofen treatments. In conclusion, patients with pain may benefit from treatment with ibuprofen instead of lysine acetylsalicylic acid, paracetamol, or dexketoprofen, since in addition to improving pain, it increases the removal of PBUTs.

Indexed as

IbuprofenRenal DialysisUremic ToxinsAgedAnalgesicsAnti-Inflammatory AgentsFemaleHumansMaleMiddle AgedPainProspective StudiesProtein BindingUremiaAnalgesicsAnti-Inflammatory AgentsIbuprofenUremic Toxinsdialysis efficiencyhemodiafiltrationindoxyl sulfatepainp-cresyl sulfateprotein-bound toxinsuremic toxins

Identifiers

PMID39728803
PMCPMC11679929

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Registered trials

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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.