dc.contributor.author
Ahnert, Peter
dc.contributor.author
Creutz, Petra
dc.contributor.author
Scholz, Markus
dc.contributor.author
Schuette, Hartwig
dc.contributor.author
Engel, Christoph
dc.contributor.author
Hossain, Hamid
dc.contributor.author
Chakraborty, Trinad
dc.contributor.author
Bauer, Michael
dc.contributor.author
Kiehntopf, Michael
dc.contributor.author
Voelker, Uwe
dc.contributor.author
Hammerschmidt, Sven
dc.contributor.author
Loeffler, Markus
dc.contributor.author
Suttorp, Norbert
dc.date.accessioned
2018-06-08T03:01:44Z
dc.date.available
2016-10-18T10:31:42.798Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/14359
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-18553
dc.description.abstract
Background Community acquired pneumonia (CAP) is a high incidence disease
resulting in about 260,000 hospital admissions per year in Germany, more than
myocardial infarction or stroke. Worldwide, CAP is the most frequent
infectious disease with high lethality ranging from 1.2 % in those 20–29 years
old to over 10 % in patients older than 70 years, even in industrial nations.
CAP poses numerous medical challenges, which the PROGRESS (Pneumonia Research
Network on Genetic Resistance and Susceptibility for the Evolution of Severe
Sepsis) network aims to tackle: Operationalization of disease severity
throughout the course of disease, outcome prediction for hospitalized patients
and prediction of transitions from uncomplicated CAP to severe CAP, and
finally, to CAP with sepsis and organ failure as a life-threatening condition.
It is a major aim of PROGRESS to understand and predict patient heterogeneity
regarding outcome in the hospital and to develop novel treatment concepts.
Methods PROGRESS was designed as a clinical, observational, multi-center study
of patients with CAP requiring hospitalization. More than 1600 patients
selected for low burden of co-morbidities have been enrolled, aiming at a
total of 3000. Course of disease, along with therapy, was closely monitored by
daily assessments and long-term follow-up. Daily blood samples allow in depth
molecular-genetic characterization of patients. We established a well-
organized workflow for sample logistics and a comprehensive data management
system to collect and manage data from more than 50 study centers in Germany
and Austria. Samples are stored in a central biobank and clinical data are
stored in a central data base which also integrates all data from molecular
assessments. Discussion With the PROGRESS study, we established a
comprehensive data base of high quality clinical and molecular data allowing
investigation of pressing research questions regarding CAP. In-depth molecular
characterization will contribute to the discovery of disease mechanisms and
establishment of diagnostic and predictive biomarkers. A strength of PROGRESS
is the focus on younger patients with low burden of co-morbidities, allowing a
more direct look at host biology with less confounding. As a resulting
limitation, insights from PROGRESS will require validation in representative
patient cohorts to assess clinical utility. Trial registration The PROGRESS
study was retrospectively registered on May 24th, 2016 with
ClinicalTrials.gov: NCT02782013
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Prospective observational study
dc.subject
Disease progression
dc.subject
Innate immunity
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
PROGRESS – prospective observational study on hospitalized community acquired
pneumonia
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
BMC Pulmonary Medicine. - 16 (2016), Artikel Nr. 108
dcterms.bibliographicCitation.doi
10.1186/s12890-016-0255-8
dcterms.bibliographicCitation.url
http://bmcpulmmed.biomedcentral.com/articles/10.1186/s12890-016-0255-8
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000025563
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000007226
dcterms.accessRights.openaire
open access