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Comparison of Solid Organ Transplant

Comparison of Solid Organ Transplant Specific and Hospital-wide Gram-Negative Antibiograms

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04055922
Enrollment
150
Registered
2019-08-14
Start date
2018-05-03
Completion date
2021-05-31
Last updated
2020-01-02

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

Conditions

Gram-negative Bacteremia, Gram-Negative Bacterial Infections, Healthcare-associated Pneumonia, Hospital-acquired Pneumonia, Multidrug-Resistant Organism

Brief summary

Solid organ transplant (SOT) recipients have increased incidence of infections with MDRO pathogens. This difference leads to a disparity in antibiograms between SOT recipients and other hospitalized patients.

Detailed description

There is limited guidance for empiric antimicrobial therapy in this population. Local epidemiology plays a voluble role in managing infections empirically within the hospital setting. Antibiograms can serve as a critical tool in optimizing empiric antimicrobial decisions. Refining antibiogram data to specific populations such as SOT patients may allow for timelier and appropriate empiric use of antimicrobials, and improve clinical outcomes. Time to appropriate therapy (antimicrobial testing susceptible in vitro to the pathogen identified) is of vital importance in management of serious infections. SOT may have different resistance rates at Methodist Dallas Medical Center making the applicability of the yearly hospital-wide antibiogram unknown for use in this specialized patient population. A SOT-Specific antibiogram may highlight common resistance patterns identified in pathogens seen in this patient population. Additionally, this investigation may further emphasize the importance of antimicrobial stewardship activities such as: appropriate empiric antibacterial decisions, de-escalation, and effective durations of therapy.

Interventions

None listed

Sponsors

Methodist Health System
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

* 18 years or older

Exclusion criteria

* Missing data necessary to determine study outcomes

Design outcomes

Primary

MeasureTime frameDescription
Creation of a liver transplant specific antibiogramJan 1, 2012 - December 31, 2016Creation of a liver transplant specific antibiogram (cumulative susceptibility rates per bacterial organism for select antibiotics)
Creation of a kidney transplant specific antibiogramJan 1, 2012 - December 31, 2016Creation of a kidney transplant specific antibiogram (cumulative susceptibility rates per bacterial organism for select antibiotics)
Comparison of SOTJan 1, 2012 - December 31, 2016Comparison of SOT (liver and kidney) antibiograms with the hospital-wide antibiogram

Secondary

MeasureTime frameDescription
Creation of transplant antibiogram for subgroupsJan 1, 2012 - December 31, 2016Creation of transplant antibiogram for subgroups of patients including the following: ICU patients, Kidney transplant urinary tract infections (UTI), SOT bloodstream infections (BSI)
Identification of risk factors among liver transplant recipientsJan 1, 2012 - December 31, 2016Identification of risk factors among liver transplant recipients for vancomycin-resistant enterococci infections

Countries

United States

Outcome results

None listed

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