NCT01143155

Brief Summary

Although failure and mortality are the most relevant outcomes in patients with Community-acquired Pneumonia (CAP), there is little discussion in the literature on their incidence and etiology. A pathophysiological approach has been recently developed and used to evaluate clinical failure in CAP patients. Clinical failure has been analyzed as related versus unrelated to CAP, considering the role that the pulmonary infection and the inflammatory response played in the development of this outcome. Cardiac events were identified as triggers of clinical failures in a significant percentage of CAP patients. The development of cardiovascular events have been also identified in CAP patients both on admission to the hospital and during hospitalization. However, data on this topic belong to studies evaluating only selected populations of veteran patients with CAP. Understanding clinical failure, as well as cardiovascular events in hospitalized patients with CAP would be useful in order to prevent complications during the hospitalization, to develop new treatment modalities and, thus, to improve outcomes. The objectives of this international, multicenter, observational, prospective cohort study will be: 1) To define incidence, timing, etiology and risk factors of clinical failure, related vs. unrelated to CAP, in hospitalized patients with CAP; 2) To define incidence, timing, and risk factors for cardiovascular events either on hospital admission or during hospitalization in hospitalized patients with CAP.Consecutive adult patients hospitalized for CAP in acute care hospitals in Europe and US will be enrolled. Daily clinical evaluations. Demographics, history, clinical, radiological, and antibiotic therapy data will be recorded, as well as serum, urinary and respiratory samples will be collected both on admission and during hospitalization from consenting individuals. Patients will be classified as having a CAP-related versus CAP-unrelated failure, according to a pathophysiological classification. Patients will be also classified as having or not a cardiovascular event either on admission or during hospitalization.The following outcomes will be measured: 1\) Incidence, timing, etiology and risk factors of clinical failure related vs. unrelated to CAP; 2) Incidence, timing and risk factors of cardiovascular events; 3)time to clinical stability, length of hospital stay, mortality at hospital discharge, and mortality at 30 and 180 days.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2009

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2009

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 10, 2010

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 14, 2010

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2012

Completed
Last Updated

January 3, 2014

Status Verified

December 1, 2013

Enrollment Period

3 years

First QC Date

June 10, 2010

Last Update Submit

December 31, 2013

Conditions

Keywords

PneumoniaCommunity-acquired pneumoniaHealthcare-associated pneumoniaFailureCardiovascular eventsOutcome

Outcome Measures

Primary Outcomes (1)

  • Clinical failure

    Incidence rates for clinical failure will be standardized and reported. Statistically significant differences between clinical failure related vs. unrelated to CAP will be investigated. Timing of clinical failure rates for those with clinical failure related vs. unrelated to pneumonia will be standardized and reported. Etiology and risk factors of clinical failure will be investigated through linear models, in order to identify associations of factors with the outcome and possible independent groups of factors in the explanation of the outcome.

    30 days

Secondary Outcomes (5)

  • Cardiovascular event

    30 days

  • Time to clinical stability

    7 days

  • Length of hospital stay

    30 days

  • In-hospital mortality

    30 days

  • Adverse events after hospital discharge

    up to 180 days after hospital discharge

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All consecutive patients admitted to any of the study centers will be screened for study entry. Patients with a diagnosis of community-acquired pneumonia (including those with health-care associated pneumonia) will be evaluated to define study entry criteria

You may qualify if:

  • \) Signed inform consent to participate in the study
  • \) Criteria for community-acquired pneumonia:
  • New pulmonary infiltrate seen on chest radiograph or CT Scan of the chest within 48 hours after hospitalization.
  • plus at least one of the following:
  • New or increased cough with/without sputum production
  • Fever (documented temperature -rectal or oral- \> 38.3 or hypothermia (documented temperature -rectal or oral- \< 36 C)
  • Evidence of systemic inflammation (such as abnormal white blood cell count -either leukocytosis (\> 10,000/cm3) or leukopenia (\< 4,000/cm3) - or C-reactive protein (CRP) or procalcitonin (PCT) values above the local upper limit.
  • \) Patients with a diagnosis of healthcare-associated pneumonia (HCAP) will be included in the study and a secondary analysis will performed on this subgroup of patients.

You may not qualify if:

  • Patients who meet at least one of the following definitions will be excluded from the analysis:
  • Patient has hospital-acquired pneumonia, defined as pneumonia that develops after 48 hours of the current hospitalization, or pneumonia that develops in a patient who had been discharged from the hospital within the prior 14 days of the current hospitalization.
  • Patient is re-admitted with a new episode of pneumonia during the 14-day follow up period from the previous hospitalization.
  • Unstable psychiatric or psychological condition rendering the subject unlikely to be cooperative or to complete the study requirements.
  • Subject history that in the investigator's opinion would preclude subject compliance with the protocol.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dipartimento toraco-polmonare e cardio-circolatorio, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Milan, 20122, Italy

Location

Related Publications (7)

  • Niederman MS, Mandell LA, Anzueto A, Bass JB, Broughton WA, Campbell GD, Dean N, File T, Fine MJ, Gross PA, Martinez F, Marrie TJ, Plouffe JF, Ramirez J, Sarosi GA, Torres A, Wilson R, Yu VL; American Thoracic Society. Guidelines for the management of adults with community-acquired pneumonia. Diagnosis, assessment of severity, antimicrobial therapy, and prevention. Am J Respir Crit Care Med. 2001 Jun;163(7):1730-54. doi: 10.1164/ajrccm.163.7.at1010. No abstract available.

    PMID: 11401897BACKGROUND
  • Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, Dowell SF, File TM Jr, Musher DM, Niederman MS, Torres A, Whitney CG; Infectious Diseases Society of America; American Thoracic Society. Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007 Mar 1;44 Suppl 2(Suppl 2):S27-72. doi: 10.1086/511159. No abstract available.

    PMID: 17278083BACKGROUND
  • Aliberti S, Amir A, Peyrani P, Mirsaeidi M, Allen M, Moffett BK, Myers J, Shaib F, Cirino M, Bordon J, Blasi F, Ramirez JA. Incidence, etiology, timing, and risk factors for clinical failure in hospitalized patients with community-acquired pneumonia. Chest. 2008 Nov;134(5):955-962. doi: 10.1378/chest.08-0334. Epub 2008 Jun 26.

    PMID: 18583514BACKGROUND
  • Ramirez J, Aliberti S, Mirsaeidi M, Peyrani P, Filardo G, Amir A, Moffett B, Gordon J, Blasi F, Bordon J. Acute myocardial infarction in hospitalized patients with community-acquired pneumonia. Clin Infect Dis. 2008 Jul 15;47(2):182-7. doi: 10.1086/589246.

    PMID: 18533841BACKGROUND
  • Musher DM, Rueda AM, Kaka AS, Mapara SM. The association between pneumococcal pneumonia and acute cardiac events. Clin Infect Dis. 2007 Jul 15;45(2):158-65. doi: 10.1086/518849. Epub 2007 Jun 6.

    PMID: 17578773BACKGROUND
  • Jasti H, Mortensen EM, Obrosky DS, Kapoor WN, Fine MJ. Causes and risk factors for rehospitalization of patients hospitalized with community-acquired pneumonia. Clin Infect Dis. 2008 Feb 15;46(4):550-6. doi: 10.1086/526526.

    PMID: 18194099BACKGROUND
  • Mortensen EM, Coley CM, Singer DE, Marrie TJ, Obrosky DS, Kapoor WN, Fine MJ. Causes of death for patients with community-acquired pneumonia: results from the Pneumonia Patient Outcomes Research Team cohort study. Arch Intern Med. 2002 May 13;162(9):1059-64. doi: 10.1001/archinte.162.9.1059.

    PMID: 11996618BACKGROUND

Biospecimen

Retention: SAMPLES WITHOUT DNA

Urine Sputum Blood Exhaled Breath Condensate Tracheal Aspirate Pleural effusion Bronchoalveolar lavage Nasopharyngeal swabs

MeSH Terms

Conditions

Community-Acquired PneumoniaPneumoniaHealthcare-Associated Pneumonia

Condition Hierarchy (Ancestors)

Community-Acquired InfectionsInfectionsRespiratory Tract InfectionsRespiratory Tract DiseasesLung DiseasesCross InfectionIatrogenic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Francesco Blasi, M.D., PhD

    Dipartimento toraco-polmonare e cardio-circolatorio, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy

    STUDY DIRECTOR
  • Stefano Aliberti, M.D.

    Respiratory Department, AO San Gerardo, University of Milan-Bicocca, Monza, Italy

    PRINCIPAL INVESTIGATOR
  • Julio Ramirez, M.D.

    Division of Infectious Diseases, Department of Medicine, University of Louisville, Louisville, Kentucky, USA

    STUDY DIRECTOR
  • Roberto Cosentini, M.D.

    Emergency Medicine Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy

    PRINCIPAL INVESTIGATOR
  • Vincenzo Valenti, M.D.

    UO Pneumologia, IRCCS Policlinico San Donato, University of Milan, Milan, Italy

    PRINCIPAL INVESTIGATOR
  • Antonio Voza, M.D.

    UO Medicina d'Urgenza, Istituto Clinico Humanitas; Milan, Italy

    PRINCIPAL INVESTIGATOR
  • Delfino Legnani, M.D.

    UO Pneumologia, Ospedale "Luigi Sacco", University of Milan, Milan, Italy

    PRINCIPAL INVESTIGATOR
  • Alberto Pesci, M.D.

    Clinica Pneumologia, Azienda Ospedaliera S. Gerardo di Monza, University of Milano-Bicocca, Monza, Italy

    PRINCIPAL INVESTIGATOR
  • Luca Richeldi, M.D.

    Department of Respiratory Disease, University of Modena and Reggio Emilia, Modena, Italy

    PRINCIPAL INVESTIGATOR
  • Daiana Stolz, M.D., MPH

    Clinic of Pneumology, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland

    PRINCIPAL INVESTIGATOR
  • Paula Peyrani, M.D.

    Division of Infectious Diseases, University of Louisville, KY; USA

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 10, 2010

First Posted

June 14, 2010

Study Start

October 1, 2009

Primary Completion

October 1, 2012

Study Completion

October 1, 2012

Last Updated

January 3, 2014

Record last verified: 2013-12

Locations