Clinical Outcomes in Patients With Infection by Resistant Microorganism

Sponsor
Hospital Universitario Virgen Macarena (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05880069
Collaborator
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla (Other)
5,000
1
12
417

Study Details

Study Description

Brief Summary

The goal of this individual patient data meta-analysis is to estimate the attributed and the associated health burden related to bloodstream infections, pneumonia, skin and soft tissue infections, surgical site infections and urinary tract infections, caused by target drug-resistant pathogens, in high income countries.

The main question[s] it aims to answer are:
  • Are common infections caused by drug-resistant pathogens associated with an increased health burden, when compared with individuals with the same infection caused by a susceptible strain (attributed burden)?

  • Are common infections caused by drug-resistant pathogens associated with an increase health burden, when compared with individuals without the infection under study (associated burden)?

Study Design

Study Type:
Observational
Anticipated Enrollment :
5000 participants
Observational Model:
Other
Time Perspective:
Other
Official Title:
Clinical Outcomes in Patients With Infection by Resistant Microorganism
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Drug-resistant pathogen

Individuals of all ages with the target pathogen, resistance phenotype, and infection site combinations as follows: P. aeruginosa, carbapenems resistant: BSI A. baumannii, carbapenems resistant: BSI E. coli, 3rd generation cephalosporins resistant: BSI and UTI K. pneumoniae, 3rd generation cephalosporins resistant: BSI K. pneumoniae, carbapenems resistant: BSI S. aureus, methicillin resistant: BSI, pneumonia, SSI and SSTI E faecium, vancomycin resistant: BSI Enterobacterales, 3rd generation cephalosporins resistant: BSI

Other: Pathogen resistant phenotype
Drug resistant phenotype of the target pathogen under study

Drug-susceptible pathogen

Individuals of all ages with the target pathogen, susceptible phenotype, and infection site combinations as follows: P. aeruginosa, carbapenems susceptible: BSI A. baumannii, carbapenems susceptible: BSI E. coli, 3rd generation cephalosporins susceptible: BSI and UTI K. pneumoniae, 3rd generation cephalosporins susceptible: BSI K. pneumoniae, carbapenems susceptible: BSI S. aureus, methicillin susceptible: BSI, pneumonia, SSI and SSTI E faecium, vancomycin susceptible: BSI Enterobacterales, 3rd generation cephalosporins susceptible: BSI

Other: Pathogen resistant phenotype
Drug resistant phenotype of the target pathogen under study

No infection

Individuals of all ages without the infection under study

Outcome Measures

Primary Outcome Measures

  1. Mortality [Through study completion, an average of 1 year]

    Death any time after infection, during the follow-up time of the original study.

Secondary Outcome Measures

  1. Number of participants with ICU admission [Through study completion, an average of 1 year]

    Need for an admission in ICU setting for more than 24 hours after infection onset.

  2. Number of participants with clinical cure [Through study completion, an average of 1 year]

    Absence of symptoms after completion of an antibiotic treatment course.

  3. Number of participants with microbiological cure [Through study completion, an average of 1 year]

    No isolation of the causal microorganisms after completion of an antibiotic treatment course.

  4. Number of participants with recurrence of infection [Through study completion, an average of 1 year]

    Infection with the same organism after more than two weeks of the initial infection.

  5. Number of participants with superinfection [Through study completion, an average of 1 year]

    Other infections different from the one under assessment.

  6. Number of participants with cognitive impairment / disability [Through study completion, an average of 1 year]

    Impairment is any temporal or permanent loss of function; disability is a restriction or inability to perform a normal activity resulting from an impairment. Assessed using Center for Epidemiologic Studies Depression Scale (CES-D), Mini-Mental State Examination (MMSE) or Trail Making Test (TMT).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Individuals of all ages

  • Individuals with hospital acquired, community acquired, or healthcare associated infections

  • Individuals treated at hospital level, community, or long-term care facilities

  • Individuals with the targeted pathogen, resistance phenotype, and infection site combinations under study

Exclusion Criteria:
  • Individuals with infections in the following systems: central nervous system, genital system, pelvic infections and head and neck infections

  • Individuals with the following specific primary infections: endocarditis, upper respiratory tract infections, lung abscess

  • Individuals with bacterial infections not included in the table of pathogens of interest, polymicrobial infections except for intraabdominal infections, fungal infections, parasitic infections, viral infections, mycobacterial infections, sexually transmitted diseases, and zoonotic infections

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universitario Virgen Macarena Sevilla Spain

Sponsors and Collaborators

  • Hospital Universitario Virgen Macarena
  • Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Investigators

  • Study Director: Jesús Rodríguez-Baño, MD PhD, Unidad Clínica de Enfermedades Infecciosas, Microbiología. Hospital Universitario Virgen Macarena

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospital Universitario Virgen Macarena
ClinicalTrials.gov Identifier:
NCT05880069
Other Study ID Numbers:
  • PRIMAVERA
First Posted:
May 30, 2023
Last Update Posted:
May 30, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 30, 2023