Evidence map›Paper›PMID 32462049›Full record

ArticleOpen forum infectious diseases2020

Post Hoc Assessment of Time to Clinical Response Among Adults Hospitalized with Community-Acquired Bacterial Pneumonia Who Received Either Lefamulin or Moxifloxacin in 2 Phase III Randomized, Double-Blind, Double-Dummy Clinical Trials.

Thomas Lodise, Sam Colman, Daniel S Stein, David Fitts, Lisa Goldberg, Elizabeth Alexander, Patrick J Scoble, Jennifer Schranz

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. 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

8 authors at 2 institutions in 1 country.

Thomas LodiseAlbany College of Pharmacy and Health Sciences, Albany, New York, USA.
Sam ColmanCovance Market Access Services Inc., Gaithersburg, Maryland, USA.
Daniel S SteinNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
David FittsNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
Lisa GoldbergNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
Elizabeth AlexanderNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
Patrick J ScobleNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
Jennifer SchranzNabriva Therapeutics US, Inc., King of Prussia, Pennsylvania, USA.
Albany College of Pharmacy and Health Sciences · USCovance (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Time to clinical response, a proxy for hospital "discharge readiness," was compared between CABP inpatients who received lefamulin or moxifloxacin in the Lefamulin Evaluation Against Pneumonia (LEAP) trials. The analysis included 926 inpatients. A short and comparable median time to clinical response (4 days) was observed in both treatment groups.

Indexed as

community-acquired bacterial pneumoniafluoroquinoloneslefamulinpatient dischargetime to clinical response

Identifiers

PMID32462049
PMCPMC7240345
OpenAlexW3019613325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.