Evidence map›Paper›PMID 35193645›Full record

ArticleCritical care (London, England)2022

The role of cell-free hemoglobin and haptoglobin in acute kidney injury in critically ill adults with ARDS and therapy with VV ECMO.

Jan A Graw, Philip Hildebrandt, Alexander Krannich, Felix Balzer, Claudia Spies, Roland C Francis, Wolfgang M Kuebler, Steffen Weber-Carstens, Mario Menk, Oliver Hunsicker

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Haemolytic injury and cardiovascular disease.Nature reviews. Cardiology · 2026
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Observational
  18. Review
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Jan A GrawDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany. jan-adriaan.graw@charite.de.ORCID 0000-0002-6920-8868
Philip HildebrandtDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0001-7511-8634
Alexander KrannichClinical Trial Office, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-4025-6495
Felix BalzerInstitute of Medical Informatics, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-1575-2056
Claudia SpiesDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0002-1062-0495
Roland C FrancisDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0003-1958-9364
Wolfgang M KueblerInstitute of Physiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4100-2961
Steffen Weber-CarstensDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0001-7405-0172
Mario MenkDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0003-1340-9211
Oliver HunsickerDepartment of Anesthesiology and Operative Intensive Care Medicine CCM / CVK, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, 13353, Berlin, Germany.ORCID 0000-0002-3998-409X
Humboldt-Universität zu Berlin · DECharité - Universitätsmedizin Berlin · DE

Funding

Deutsche Forschungsgemeinschaft GR 4446/3-1
6 · The paper itself

Abstract

backgroundIncreased plasma concentrations of circulating cell-free hemoglobin (CFH) are supposed to contribute to the multifactorial etiology of acute kidney injury (AKI) in critically ill patients while the CFH-scavenger haptoglobin might play a protective role. We evaluated the association of CFH and haptoglobin with AKI in patients with an acute respiratory distress syndrome (ARDS) requiring therapy with VV ECMO.

methodsPatients with CFH and haptoglobin measurements before initiation of ECMO therapy were identified from a cohort of 1044 ARDS patients and grouped into three CFH concentration groups using a risk stratification. The primary objective was to assess the association of CFH and haptoglobin with KDIGO stage 3 AKI. Further objectives included the identification of a target haptoglobin concentration to protect from CFH-associated AKI. MEASUREMENTS AND MAIN

resultsTwo hundred seventy-three patients fulfilled the inclusion criteria. Of those, 154 patients (56.4%) had AKI at ECMO initiation. The incidence of AKI increased stepwise with increasing concentrations of CFH reaching a plateau at 15 mg/dl. Compared to patients with low [< 5 mg/dl] CFH concentrations, patients with moderate [5-14 mg/dl] and high [≥ 15 mg/dl] CFH concentrations had a three- and five-fold increased risk for AKI (adjusted odds ratio [OR] moderate vs. low, 2.69 [95% CI, 1.25-5.95], P = 0.012; and OR high vs. low, 5.47 [2.00-15.9], P = 0.001). Among patients with increased CFH concentrations, haptoglobin plasma levels were lower in patients with AKI compared to patients without AKI. A haptoglobin concentration greater than 2.7 g/l in the moderate and 2.4 g/l in the high CFH group was identified as clinical cutoff value to protect from CFH-associated AKI (sensitivity 89.5% [95% CI, 83-96] and 90.2% [80-97], respectively).

conclusionsIn critically ill patients with ARDS requiring therapy with VV ECMO, an increased plasma concentration of CFH was identified as independent risk factor for AKI. Among patients with increased CFH concentrations, higher plasma haptoglobin concentrations might protect from CFH-associated AKI and should be subject of future research.

Indexed as

Acute Kidney InjuryExtracorporeal Membrane OxygenationRespiratory Distress SyndromeAdultCritical IllnessHaptoglobinsHemoglobinsHumansRetrospective StudiesHaptoglobinsHemoglobinsAcute kidney injuryARDSCell-free hemoglobinHaptoglobin

Identifiers

PMID35193645
PMCPMC8864920
OpenAlexW4213090010

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.