Evidence map›Paper›PMID 31801287›Full record

ReviewInternational journal of molecular sciences2019

Re-Evaluating Biologic Pharmacotherapies that Target the Host Response during Sepsis.

Kristopher Tuttle, Matthew McDonald, Ethan Anderson

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. 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

3 authors at 1 institution in 1 country.

Kristopher TuttleDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
Matthew McDonaldDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
Ethan AndersonDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
University of Iowa · US

Funding

Myocardial redox status, catecholamine metabolism and post-operative arrhythmiaR01HL122863 · NHLBI · UNIVERSITY OF IOWA · PI ANDERSON, ETHAN JOHN · 2014 to 2018
$2.1M
Toxic neurotransmitter metabolites in aged and diabetic human myocardiumR21AG057006 · NIA · UNIVERSITY OF IOWA · PI ANDERSON, ETHAN JOHN, DOORN, JONATHAN A · 2017 to 2018
$419k
NHLBI NIH HHS R01HL122863NIH HHS R21AG057006U.S. Department of Defense PR181276
6 · The paper itself

Abstract

Multiple organ dysfunction syndrome (MODS) caused by the systemic inflammatory response during sepsis is responsible for millions of deaths worldwide each year, and despite broad consensus concerning its pathophysiology, no specific or effective therapies exist. Recent efforts to treat and/or prevent MODS have included a variety of biologics, recombinant proteins targeting various components of the host response to the infection (e.g., inflammation, coagulation, etc.) Improvements in molecular biology and pharmaceutical engineering have enabled a wide range of utility for biologics to target various aspects of the systemic inflammatory response. The majority of clinical trials to date have failed to show clinical benefit, but some have demonstrated promising results in certain patient populations. In this review we summarize the underlying rationale and outcome of major clinical trials where biologics have been tested as a pharmacotherapy for MODS in sepsis. A brief description of the study design and overall outcome for each of the major trials are presented. Emphasis is placed on discussing targets and/or trials where promising results were observed. Post hoc analyses of trials where therapy demonstrated harm or additional risk to certain patient subgroups are highlighted, and details are provided about specific trials where more stringent inclusion/exclusion criteria are warranted.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseAlkaline PhosphataseAnti-Inflammatory AgentsBiological ProductsBlood CoagulationClinical Trials as TopicCytokinesGene ExpressionGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunity, InnateImmunoglobulins, IntravenousInflammationMultiple Organ FailureSepsis1-Alkyl-2-acetylglycerophosphocholine EsteraseAlkaline PhosphataseAnti-Inflammatory AgentsBiological ProductsCytokinesGranulocyte-Macrophage Colony-Stimulating FactorImmunoglobulins, IntravenousPLA2G7 protein, humanbiologicscoagulationinflammationmultiple organ dysfunction syndromepharmacologysepsis

Identifiers

PMID31801287
PMCPMC6929091
OpenAlexW2989802453

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.