T81.4
Conditions
Interventions
Group 1: Retrospective analysis of clinical routine data from approximately 150 patients who underwent interventional percutaneous placement of an irrigation drainage (episodic irrigation with isotoni
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who underwent interventional percutaneous placement of an irrigation drainage.
Exclusion criteria
Exclusion criteria: Pregnancy, history of organ transplantation, inability to administer antibiotics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints are the drainage dwell time and the duration of antibiotic therapy. The decision to remove the drainage or discontinue antibiotic therapy remains with the treating physicians. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include the length of hospital and intensive care unit stay after drainage placement, hospital readmissions, type of antibiotic therapy, re-operations or re-drainages, mortality and morbidity during the hospital stay (Comprehensive Complication Index), infection parameters during the peri- and post-intervention period, intra- and peri-interventional microbial samples, incidence of multi-resistant pathogens at drainage placement and during drainage therapy, hollow organ perforations, post-interventional bleeding, total days of possible catecholamine therapy, total days of possible mechanical ventilation therapy, nosocomial infections (urinary tract infections, pneumonias, bacteremias), myocardial infarctions, pulmonary embolisms, strokes, Clostridium difficile-associated diarrhea, as well as analysis of bacteria detected in samples. | — |
Countries
Germany
Contacts
Public ContactJulian-Camill Harnoss
Universitätsklinikum Universitätsklinikum Heidelberg Klinik für Allgemein-, Viszeral- und Transplantationschirurgie Heidelberg
Outcome results
None listed