Evidence map›Paper›PMID 42410486›Full record

ArticleJournal of intensive care2026

Troponin T clearance via continuous renal replacement therapies in the ICU.

Sean Boyd, Sabina Mason, Sean Griffin, Britto Pereppadan, Stephen Moyles, Krishna Reddy, Colm Keane, Eoin Begley, Evelyn Deasy, Maria Donnelly and 3 more

Abstract read
In one paragraph

Article in Journal of intensive care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sean BoydDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland. seanboyducd@gmail.com.ORCID https://orcid.org/0000-0002-2198-6732
Sabina MasonDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Sean GriffinDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Britto PereppadanDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Stephen MoylesDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Krishna ReddyDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Colm KeaneDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Eoin BegleyDepartment of Clinical Chemistry, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Evelyn DeasyDepartment of Pharmacy, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Maria DonnellyDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Julio ChevarriaDepartment of Nephrology, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.
Deirdre M D'ArcySchool of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Dublin 2, Ireland.
Yvelynne P KellyDepartment of Critical Care, Tallaght University Hospital, Tallaght, Dublin 24, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to compare the removal of cardiac troponin T via continuous venovenous haemofiltration (CVVH), continuous venovenous haemodialysis (CVVHD) and continuous venovenous haemodiafiltration (CVVHDF) as a function of circulating blood troponin T levels in critically ill patients.

methodsThis was a single-centre, prospective observational study conducted at Tallaght University Hospital (Dublin, Ireland). Adult patients admitted to ICU and commenced on continuous renal replacement therapy (CRRT) were included. All patients required a troponin T level > 50 ng/L. All patients were required to have commenced CRRT > 4 h prior to first sample. The aim was to take three serum samples per patient every 24 h, over a total of 72 h, with simultaneous sampling of the waste effluent for troponin T. Our primary outcome measure was estimated troponin T clearance according to CRRT modality.

resultsWe found no significant difference in estimated troponin T clearance according to CRRT modality (overall median troponin T clearance of 2.6 ml/kg/h). As a secondary outcome, it was noted that the percentage of troponin T clearance was statistically significantly higher for CVVH compared to CVVHD and CVVHDF (16% vs. 15% vs. 10%, respectively; p = 0.002).

conclusionsNo significant difference in estimated troponin T clearance was found according to CRRT modality. Our results show that clearance of troponin T on CRRT is generally small across all modalities and that ongoing treatment with CRRT is unlikely to substantially impact interpretation and tracking of troponin T results in patients with concern for acute coronary syndrome.

Indexed as

Acute kidney injuryContinuous renal replacement therapyIntensive careSolute clearanceTroponin

Identifiers

PMID42410486
PMCPMC13501787

What OpenQuestion holds

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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.