Evidence map›Paper›PMID 18695372›Full record

ReviewCurrent opinion in hematology2008

Activated protein C in sepsis: the promise of nonanticoagulant activated protein C.

Hartmut Weiler, Wolfram Ruf

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Pterostilbene attenuates acute kidney injury in septic mice.Experimental and therapeutic medicine · 2018
    Article
  4. Article
  5. Pathophysiology, staging and therapy of severe sepsis in baboon models.Journal of cellular and molecular medicine · 2012
    Review
  6. Safety threshold of intravitreal activated protein-C.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2011
    Article
  7. Blood coagulation disorders in septic patients.Wiener medizinische Wochenschrift (1946) · 2010
    Review
  8. 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

2 authors.

Hartmut WeileraBlood Research Institute, BloodCenter of Wisconsin, Milwaukee, Wisconsin, USA. Hartmut.weiler@bcw.edu
Wolfram Ruf

Funding

VASCULAR MOLECULAR AND CELLS BIOLOGYP01HL016411 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 1985 to 2008
$21.5M
TF Signaling in Systemic InflammationR01HL077753 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 2004 to 2011
$3.6M
THROMBOMODULIN FUNCTION IN CELLULAR PHYSIOLOGYR01HL060655 · NHLBI · VERSITI WISCONSIN, INC. · PI WEILER, HARTMUT KARL-HEINZ · 1999 to 2007
$2.6M
Mechanism of Activated Protein C Action in Sepsis TherapyR01HL093388 · NHLBI · VERSITI WISCONSIN, INC. · PI WEILER, HARTMUT KARL-HEINZ · 2008 to 2011
$1.6M
NHLBI NIH HHS HL-16411NHLBI NIH HHS HL-60655NHLBI NIH HHS HL-77753NHLBI NIH HHS P01 HL016411NHLBI NIH HHS R01 HL060655NHLBI NIH HHS R01 HL077753NHLBI NIH HHS R01 HL093388
6 · The paper itself

Abstract

purpose of reviewTo discuss the potential use of recombinant activated protein C (aPC) variants with altered bioactivity in sepsis therapy. RECENT

findingsSince the initial Protein C Worldwide Evaluation in Severe Sepsis trial demonstrating efficacy of aPC therapy to reduce mortality of severe sepsis, follow-up studies have failed to resolve concerns about the low overall risk-to-benefit ratio of this therapy and suggest that it might only be effective in severely ill patients with the most aggravated forms of coagulopathy. New studies begin to shed light on the potential mechanisms of how aPC therapy may alter sepsis outcome, and how recombinant aPC variants with altered bioactivities may improve the efficacy and safety of this therapy. SUMMARY: aPC variants with selectively diminished antithrombotic activity, but normal cytoprotective potential, may allow more efficient dosing without increasing adverse bleeding effects and therefore provide a safer and possibly more efficient alternative to normal aPC. Critical questions about the precise mechanisms by which aPC therapy reduces mortality remain to be resolved in order to identify patients most likely to benefit from it and to reevaluate potential efficacy of aPC therapy in children and patients with less than severe sepsis.

Indexed as

Fibrinolytic AgentsHumansProtein CRecombinant ProteinsSepsisTreatment OutcomeFibrinolytic AgentsProtein CRecombinant Proteins

Identifiers

PMID18695372
PMCPMC2742321

What OpenQuestion holds

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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.