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Nosocomial and Community Acquired Legionella Pneumophila Pneumonia.

Nosocomial and Community Acquired Legionella Pneumophila Pneumonia, a Retrospective Case Series

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04106037
Enrollment
46
Registered
2019-09-26
Start date
2019-08-13
Completion date
2019-09-30
Last updated
2022-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Legionnaires' Disease

Brief summary

Legionnaire's disease (LD) is a major cause of both community acquired and nosocomial pneumonia, with Legionella pneumophila serogroup A (Lp1) being the most virulent and the greatest cause of disease. Sample culture of low respiratory tract is considered the gold standard in the diagnosis of LD, however its sensitivity seems to be poor and its performance is technically demanding. The introduction of urinary antigen detection testing (LUA) brought a major advance in LD diagnosis, with upt to 95% of cases in Europe being diagnosed with this method. Despite the high sensitivity of LUA for Lp1, ranging from 80-90%, its negative predictive value is low in other serogroup than Lp1 and therefore, Legionella may be unrecognized as agent of pneumonia. Although underdiagnosed and underreported, LD represents the second most common cause of pneumonia requiring admission in intensive care unit (ICU). Average fatality rate of LD in Europe reaches 10%, but its mortality is considered to be even higher in nosocomial patients. Despite the higher fatality rate in hospitalized LD patients, poor is the knowledge on the risk factors that could induce disease and that increase mortality in the hospitalized population affected by LD. In order to shed more light on this topic a cohort of patients diagnosed with LD in the last 3 years will be retrospectively examined.

Interventions

Data extraction from medical files

Sponsors

Dr Philippe CLEVENBERGH
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All confirmed human cases of Legionnaires' disease diagnosed within the CHU Brugmann hospital within the last 3 years, from 01/01/2016 till 31/12/2018. A similar approach will be followed for the St Pierre and the UZ Brussel Hospitals.

Exclusion criteria

Pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
All cause mortality3 yearsAll cause mortality
Severity respiratory failure3 yearsArterial pression of oxygen inferior to 600mmHg at diagnosis

Secondary

MeasureTime frameDescription
Charlson comorbidity indexOne dayThis is a health tool that assesses the comorbidity risk associated to a series of conditions in order to offer medical specialists an informed decision making process in terms of specific screenings or medical procedures.The index accounts for the patient age and 16 different conditions, and ranges from 0 till 37.
Smoking statusOne daySmoking (yes/no) at diagnosis
Nosocomial disease (yes/no)One dayNosocomial cases of Legionnaires' disease are defined in this study as having an onset of symptoms more than 10 days after hospitalization.
C reactive proteinOne dayC reactive protein level at diagnosis
White blood cellsOne dayWhite blood cells level at diagnosis
CreatinineOne dayCreatinine level at diagnosis
AgeOne dayAge at diagnosis
Chest X RayOne dayDescriptive analysis of Chest X Ray findings at diagnosis
Method of diagnosisOne dayName of the method of diagnosis (urinary antigen, seroconversion, cultures).
Intensive care unit hospitalizationOne dayIntensive care unit hospitalization (yes/no)
AntibioticsOne dayName of antibiotics given
Antibiotic treatment durationup to 40 daysAntibiotic treatment duration
UreaOne dayUrea level at diagnosis
SexOne daySex

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026