Evidence map›Paper›PMID 42262352›Full record

ArticleASAIO journal (American Society for Artificial Internal Organs : 1992)2026

Nitric Oxide-Releasing Surfaces Reduce Thrombosis in Venovenous Extracorporeal Life Support: A 5 day Long Ovine Study.

Jensyn J VanZalen, Megan V Stein, Ryan T Kauffman, Jamie Ho, Josef E Hill, Daniela P Peláez-Palacio, Gergely Lautner, Mark E Meyerhoff, Robert H Bartlett, Orsolya Lautner-Csorba and 1 more

Abstract read
In one paragraph

Article in ASAIO journal (American Society for Artificial Internal Organs : 1992), 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

11 authors.

Jensyn J VanZalenFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Megan V SteinFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Ryan T KauffmanFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Jamie HoFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Josef E HillFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Daniela P Peláez-PalacioFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Gergely LautnerDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan Medical School, Ann Arbor, Michigan.
Mark E MeyerhoffDepartment of Chemistry, College of Literature, Sciences and the Arts, University of Michigan Medical School, Ann Arbor, Michigan.
Robert H BartlettFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Orsolya Lautner-CsorbaFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Alvaro Rojas-PeñaFrom the Robert H. Bartlett Extracorporeal Life Support (ECLS) Laboratory, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-6197-8892

Funding

Research Supplement to Promote Diversity Supplement for the ECMO without AnticoagulationR01HL155100 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROJAS-PENA, ALVARO · 2021 to 2024
$3.2M
NHLBI NIH HHS R01 HL155100
6 · The paper itself

Abstract

Extracorporeal life support (ECLS) components designed to reduce clot formation have been developed, but thrombosis remains a significant challenge, requiring systemic anticoagulation. To address this, we evaluated a nitric oxide (NO) releasing extracorporeal circuit (ECC) in a 5 day ovine venovenous ECLS model without systemic anticoagulation. Fifteen sheep, weighing 40-52 kg, were instrumented and assigned to three groups (n = 5 each): 1) Control- "naïve" ECC without anticoagulation; 2) Sham-CarboSil-coated ECC; and 3) NOSA-NO-releasing ECC+100 ppm NO in the sweep gas. Animals were monitored until meeting two of the three end-point criteria defined by device resistance five times baseline, greater than 50% decrease in blood flow after RPM adjustments, or post-oxygenator SO2 less than 95%. Extracorporeal Life Support flow was adjusted from 1 L/min (0-24 h), 0.75 L/min (25-48 h) to 0.5 L/min (49 h to study end). Data collected included hemodynamics, ECC performance, coagulation markers, cellular activity, and NO toxicity. The NO-releasing ECC prolonged survival to ~120 h with lower resistance and plasma-free hemoglobin, stable coagulation, and final MetHb levels less than 5%. Activated clotting times (ACTs) were less than 200 s in all groups. These findings suggest that NO-releasing ECCs in a highly translational preclinical ovine model may improve ECLS safety while reducing reliance on systemic anticoagulation.

Indexed as

ECLSECMOextracorporeal supportlocal anticoagulationnitric oxideovine modelsystemic anticoagulationtranslationalvenovenous ECLS

Identifiers

PMID42262352
PMCPMC13654273

What OpenQuestion holds

Textmetadata
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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.