Evidence map›Paper›PMID 19917756›Full record

ArticleAntimicrobial agents and chemotherapy2010

Efficacy profiles of daptomycin for treatment of invasive and noninvasive pulmonary infections with Streptococcus pneumoniae.

Stefanie Henken, Jennifer Bohling, Jens Martens-Lobenhoffer, James C Paton, A David Ogunniyi, David E Briles, Vyvyan C Salisbury, Dirk Wedekind, Stefanie M Bode-Böger, Thomas Welsh and 3 more

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Role of Proteomics in Bacterial Response to Antibiotics.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  5. Animal Models ofInternational journal of molecular sciences · 2019
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Local delivery of GM-CSF protects mice from lethal pneumococcal pneumonia.Journal of immunology (Baltimore, Md. : 1950) · 2011
    Article
  18. Article
  19. Review
  20. 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

13 authors at 7 institutions in 5 countries.

Stefanie HenkenClinic for Pulmonary Medicine, Department of Experimental Lung Research, Hannover School of Medicine, Hannover 30625, Germany.
Jennifer Bohling
Jens Martens-Lobenhoffer
James C Paton
A David Ogunniyi
David E Briles
Vyvyan C Salisbury
Dirk Wedekind
Stefanie M Bode-Böger
Thomas Welsh
Franz C Bange
Tobias Welte
Ulrich A Maus
Otto-von-Guericke University Magdeburg · DEUniversity of Adelaide · AUInstitute of Laboratory Animal Science · CNMedizinische Hochschule Hannover · DENovartis (Germany) · DEUniversity of Alabama at Birmingham · USUniversity of the West of England · GB

Funding

Department of Health II-3A-0409-10019
6 · The paper itself

Abstract

Daptomycin is a novel lipopeptide antibiotic with excellent activity against Gram-positive bacterial pathogens, but its therapeutic value for the treatment of invasive pneumococcal disease compared to that for the treatment of pneumococcal pneumonia is incompletely defined. We investigated the efficacy of daptomycin in two models of Streptococcus pneumoniae-induced lung infection, i.e., pneumococcal pneumonia and septic pneumococcal disease. Mice were infected with a bioluminescent, invasive serotype 2 S. pneumoniae strain or a less virulent serotype 19 S. pneumoniae strain and were then given semitherapeutic or therapeutic daptomycin or ceftriaxone. Readouts included survival; bacterial loads; and septic disease progression, as determined by biophotonic imaging. Semitherapeutic daptomycin treatment fully protected the mice against the progression of septic disease induced by serotype 2 S. pneumoniae, while therapeutic treatment of the mice with daptomycin or ceftriaxone led to approximately 70% or approximately 60% survival, respectively. In contrast, mice infected with serotype 19 S. pneumoniae developed severe pneumonia and lung leakage even in the presence of increased intra-alveolar daptomycin levels, resulting in only 40% survival, whereas the ceftriaxone-treated mice had 100% survival. Together, although daptomycin demonstrates little efficacy in the treatment of pneumococcal pneumonia, daptomycin is highly effective in preventing S. pneumoniae-induced septic death, thus possibly offering a therapeutic option for patients with life-threatening septic pneumococcal disease.

Indexed as

AnimalsAnti-Bacterial AgentsCeftriaxoneDaptomycinDisease Models, AnimalMiceMice, Inbred C57BLPneumococcal InfectionsPneumonia, PneumococcalSepsisStreptococcus pneumoniaeAnti-Bacterial AgentsCeftriaxoneDaptomycin

Identifiers

PMID19917756
PMCPMC2812129
OpenAlexW2145851941

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.