Evidence map›Paper›PMID 28986703›Full record

Trial reportClinical research in cardiology : official journal of the German Cardiac Society2018

Relationship between baseline systolic blood pressure and long-term outcomes in acute heart failure patients treated with TRV027: an exploratory subgroup analysis of BLAST-AHF.

Gad Cotter, Beth A Davison, Javed Butler, Sean P Collins, Justin A Ezekowitz, G Michael Felker, Gerasimos Filippatos, Phillip D Levy, Marco Metra, Piotr Ponikowski and 7 more

Abstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical research in cardiology : official journal of the German Cardiac Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Noninvasive pulse contour analysis for determination of cardiac output in patients with chronic heart failure.Clinical research in cardiology : official journal of the German Cardiac Society · 2018
    Trial
  4. β-Arrestin-2 Regulates Sodium Taste Processing.Hypertension (Dallas, Tex. : 1979) · 2026
    Article
  5. Article
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  12. Insights Into the Role of Angiotensin-II ATHypertension (Dallas, Tex. : 1979) · 2024
    Review
  13. Article
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  15. Review
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  17. Review
  18. β-Arrestin-Biased Agonist Targeting the Brain ATHypertension (Dallas, Tex. : 1979) · 2021
    Article
  19. Mechanisms of troponin release into serum in cardiac injury associated with COVID-19 patients.International journal of cardiology and cardiovascular diseases · 2021
    Article
  20. Biased agonists at the human YCellular and molecular life sciences : CMLS · 2020
    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 13 institutions in 6 countries.

Gad CotterMomentum Research Inc., Suite 801, 3100 Tower Blvd, Durham, NC, 27707, USA. gadcotter@momentum-research.com.
Beth A DavisonMomentum Research Inc., Suite 801, 3100 Tower Blvd, Durham, NC, 27707, USA.
Javed ButlerSUNY Stony Brook School of Medicine, New York, NY, USA.
Sean P CollinsVanderbilt University, Nashville, TN, USA.
Justin A EzekowitzUniversity of Alberta, Edmonton, AB, Canada.
G Michael FelkerDuke University School of Medicine and the Duke Clinical Research Institute, Durham, NC, USA.
Gerasimos FilippatosDepartment of Cardiology, School of Medicine, Heart Failure Unit, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.
Phillip D LevyWayne State University School of Medicine and Cardiovascular Research Institute, Detroit, MI, USA.
Marco MetraCardiology, University of Brescia, Brescia, Italy.
Piotr PonikowskiMedical University, Clinical Military Hospital, Wroclaw, Poland.
John R TeerlinkSection of Cardiology, San Francisco Veterans Affairs Medical Center and School of Medicine, University of California San Francisco, San Francisco, CA, USA.
Adriaan A VoorsUniversity of Groningen, Groningen, The Netherlands.
Stefanie SengerMomentum Research Inc., Suite 801, 3100 Tower Blvd, Durham, NC, 27707, USA.
David BharuchaAllergan plc (Forest Labs), Jersey City, NJ, USA.
Kathleen GoinTrevena Inc, King of Prussia, PA, USA.
David G SoergelTrevena Inc, King of Prussia, PA, USA.
Peter S PangIndiana University School of Medicine and Regenstrief Institute, Indianapolis, IN, USA.
Momentum Research · USAllergan (United States) · USDuke University · USNational and Kapodistrian University of Athens · GRRegenstrief Institute · USSan Francisco VA Medical Center · USStony Brook School · USUniversity of Alberta · CAUniversity of Brescia · ITUniversity of Groningen · NLVanderbilt University · USWayne State University · USWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTRV027, a 'biased' ligand of the angiotensin II type 1 receptor (AT1R), did not affect a composite clinical outcome at 30 days in a phase 2b acute heart failure (AHF) trial (BLAST-AHF).

methodsPost-hoc analyses from BLAST-AHF (n = 618) examined the effects of TRV027 by baseline systolic blood pressure (SBP) on changes in renal function and 180-day outcomes. Interactions between baseline SBP and select endpoints were identified utilizing a subpopulation treatment effect pattern plots (STEPP) analysis, then grouping of patients by SBP tertile: < 127, ≥ 127 to < 140, and ≥ 140 mmHg.

resultsA trend towards increased creatinine in the first 3 days was noted in the lower SBP tertile, while in those in the higher two tertiles, TRV027, especially the 1 mg/h dose, reduced creatinine at days 5 and 30. Beneficial effects on 180-day all-cause mortality and cardiovascular (CV) death or readmission were observed in the two higher SBP tertiles (SBP ≥ 127 mmHg) in the TRV027 1 mg/h dose group (all-cause mortality HR 0.39, 95% CI 0.14-1.06, p = 0.056; CV death or HF/RF rehospitalization HR 0.53, 95% CI 0.28-1.01, p = 0.049), while more adverse outcomes were observed in patients in the lower SBP tertile.

conclusionsThis post-hoc analysis of the BLAST-AHF study suggests contrasting effects of TRV027 by baseline SBP, with trends towards lower 180-day event rates in patients enrolled with higher baseline SBP, especially when given lower doses of TRV027.

Indexed as

Acute DiseaseAgedBlood PressureCardiovascular AgentsFemaleHeart FailureHumansKidneyMaleMiddle AgedOligopeptidesPatient ReadmissionReceptor, Angiotensin, Type 1Signal TransductionSystoleTime FactorsAGTR1 protein, humanCardiovascular AgentsOligopeptidesReceptor, Angiotensin, Type 1Sar-Arg-Val-Tyr-Ile-His-Pro-Ala-OHBLAST-AHFBlood pressureOutcomes

Identifiers

PMID28986703
OpenAlexW2762516087

What OpenQuestion holds

Textmetadata
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.