Central Venous Catheter Colonisation Among Critically Ill Patients in Intensive Care Units

Makerere University

Status: Completed

Conditions: Acute Liver Failure; Head Injury; Post-cardiac Surgery; Diabetic Ketoacidotic Hyperglycaemic Coma; Post-Cardiorespiratory Arrest Coma; Septic Shock; Hypoxic Brain Damage; Sepsis

Study type: Observational

Funder types: Other

Identifiers

NCT03270774

CVC Study

Details and patient eligibility

About

Background: Central Venous catheter insertion technique and indwelling time are major risk factors for CVC colonisation. Colonisation occurs through microbial migration and biofilm formation along the catheter insertion tract. This study set out to determine the prevalence and associated factors for central venous catheter colonisation among critically ill patient. No data exists in this clinical setting addressing this topic.

Methods: The study population included 100 participants with central venous catheters in situ for at least 24 hours. Catheter tip (distal 5-cm segment) and blood cultures (10mls peripheral blood) were obtained at the time of catheter removal.

Full description

Introduction : Central venous catheter (CVC) insertion technique and time spent in situ (dwell period) are major risk factors for CVC colonisation among patients admitted to intensive care units (ICU) worldwide. Normal skin flora colonizes CVCs early in their dwell period (< 7-10 days) causing variable occurrence of infections in all categories of patients. Uganda has no data on CVC colonisation and with increasing use there is concern of CVC colonisation and its consequences. This study was done to determine the prevalence and associated factors of CVC colonization among patients in general ICUs.

Methodology: This was prospective cohort study. Critically ill patients with CVCs in situ from four general ICUs were consecutively enrolled into the study. Data on socio-demographic, clinical characteristics (diagnosis, comorbidities) and CVC insertion (site, technique, experience) was collected using a standardised questionnaire until a sample size of 100 was achieved. At the time of CVC removal, the CVC tip (distal 5cm segment) was aseptically obtained and cultured for microorganisms using the semi-quantitative method. A blood culture sample (10mls) was also collected from a peripheral site at the same time. Data was double entered into EPIDATA version 3.1.5 and exported to STATA version 12.0 for analysis.

Enrollment: 100 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients of all age groups were included in this study
• All critically ill patients admitted to the ICU with Central Venous Catheters in situ
• Written informed consent/assent
• Waiver of consent for unconscious patients with no attendant/valid surrogate respondent to provide the required information

Exclusion criteria

•Patients who were already on treatment for CVC-related infectious complications.