Evidence map›Paper›PMID 38103056›Full record

ArticleAnnals of intensive care2023

Angiotensin II treatment is associated with improved oxygenation in ARDS patients with refractory vasodilatory shock.

Daniel E Leisman, Damian R Handisides, Lakhmir S Chawla, Timothy E Albertson, Laurence W Busse, David W Boldt, Adam M Deane, Michelle N Gong, Kealy R Ham, Ashish K Khanna and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Annals of intensive care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02338843 (A Phase 3, Placebo-Controlled, Randomized, Double-Blind, Multi-Center Study of LJPC-501 in Patients With Catecholamine-Resistant Hypotension), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.1field-weighted citation impact, top 5% 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.

NCT02338843 phase3completednot on this map

A Phase 3, Placebo-Controlled, Randomized, Double-Blind, Multi-Center Study of LJPC-501 in Patients With Catecholamine-Resistant Hypotension (CRH)

TypeinterventionalSponsorLa Jolla Pharmaceutical CompanyRan2015 to 2017Enrolled344ConditionsCatecholamine-resistant Hypotension (CRH), Distributive Shock, High Output Shock, SepsisArmsLJPC-501, Placebo
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Vasoactive Agents in Burn Patients: Perspectives on Angiotensin-II.Journal of burn care & research : official publication of the American Burn Association · 2025
    Review
  6. Article
  7. Vasopressor Therapy.Journal of clinical medicine · 2024
    Review
  8. Review
  9. Review
  10. 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

17 authors at 14 institutions in 3 countries.

Daniel E LeismanDepartment of Medicine, Massachusetts General Hospital, 55 Fruit St., GRB 7-730, Boston, MA, 02114, USA. dleisman@mgh.harvard.edu.ORCID http://orcid.org/0000-0001-9670-9425
Damian R HandisidesInnoviva Specialty Therapeutics, Waltham, MA, USA.
Lakhmir S ChawlaDepartment of Medicine, Veterans Affairs Medical Center, San Diego, CA, USA.
Timothy E AlbertsonDepartments of Medicine, Emergency Medicine and Anesthesiology, School of Medicine, UC Davis, Sacramento, CA, USA.
Laurence W BusseDepartment of Medicine, Emory University, Atlanta, GA, USA.
David W BoldtDivision of Critical Care, Department of Anesthesiology and Perioperative Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Adam M DeaneDepartment of Medicine and Radiology, Royal Melbourne Hospital, The University of Melbourne, Melbourne Medical School, Parkville, Australia.
Michelle N GongDivision of Critical Care Medicine, Division of Pulmonary Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Kealy R HamDepartment of Critical Care, Mayo Clinic, Phoenix, AZ, USA.
Ashish K KhannaDepartment of Anesthesiology, Section On Critical Care Medicine, Wake Forest University School of Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, NC, USA.
Marlies OstermannDepartment of Critical Care, King's College London, Guy's & St Thomas' Hospital, London, UK.
Michael T McCurdyDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
B Taylor ThompsonDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
James S TumlinRenal Division, Department of Medicine, Emory University Medical Center, Emory University, Atlanta, GA, USA.
Christopher D AdamsInnoviva Specialty Therapeutics, Waltham, MA, USA.
Tony N HodgesInnoviva Specialty Therapeutics, Waltham, MA, USA.
Rinaldo BellomoAustralian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
Innoviva (United States) · USThe Royal Melbourne Hospital · AUAlbert Einstein College of Medicine · USAtrium Health Wake Forest Baptist · USEmory Healthcare · USEmory University · USHarvard University · USMassachusetts General Hospital · USMayo Clinic Hospital · USSan Francisco VA Medical Center · USSt Thomas' Hospital · GBUniversity of California, Davis · USUniversity of California, Los Angeles · USUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe physiological effects of renin-angiotensin system modulation in acute respiratory distress syndrome (ARDS) remain controversial and have not been investigated in randomized trials. We sought to determine whether angiotensin-II treatment is associated with improved oxygenation in shock-associated ARDS.

methodsPost-hoc subgroup analysis of the Angiotensin Therapy for High Output Shock (ATHOS-3) trial. We studied patients who met modified Berlin ARDS criteria at enrollment. The primary outcome was PaO

resultsOf 81 ARDS patients, 34 (42%) and 47 (58%) were randomized to angiotensin-II or placebo, respectively. In angiotensin-II patients, mean P:F increased from 155 mmHg (SD: 69) at baseline to 265 mmHg (SD: 160) at hour-48 compared with no change with placebo (148 mmHg (SD: 63) at baseline versus 164 mmHg (SD: 74) at hour-48)(baseline-adjusted difference: + 98.4 mmHg [95%CI 35.2-161.5], p = 0.0028). Similarly, oxygenation index decreased by - 6.0 cmH

conclusionsIn post-hoc analysis of the ATHOS-3 trial, angiotensin-II was associated with improved oxygenation versus placebo among patients with ARDS and catecholamine-refractory vasodilatory shock. These findings provide a physiologic rationale for trials of angiotensin-II as treatment for ARDS with vasodilatory shock.

trial registrationClinicalTrials.Gov Identifier: NCT02338843 (Registered January 14th 2015).

Indexed as

Angiotensin IIARDSNorepinephrineRenin–angiotensin systemSepticShock

Identifiers

PMID38103056
PMCPMC10725390
OpenAlexW4389833391

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.