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Risk Factors for Invasive Surgical Site Infections Among Adult Single Liver Transplant Recipients at Duke University
Manuela Carugati1, Sana Arif1, Michael E Yarrington1
1Department of Medicine, Division of Infectious Diseases, Duke University, Durham, NC.
Invasive primary surgical site infections (IP-SSI) after liver transplants are linked to surgical factors, not just infection prevention. These infections increase hospital stays and mortality, necessitating close monitoring and tailored antimicrobial strategies.
Area of Science:
- Transplant Surgery
- Infectious Diseases
- Surgical Outcomes
Background:
- Invasive primary surgical site infections (IP-SSI) are a serious complication following liver transplant surgery.
- Identifying risk factors is crucial for developing effective IP-SSI prevention strategies.
Purpose of the Study:
- To identify risk factors associated with invasive primary surgical site infections (IP-SSI) in adult liver transplant recipients.
- To analyze the impact of IP-SSI on patient outcomes, including hospitalization duration and mortality.
Main Methods:
- Retrospective review of adult single liver transplants performed between 2015-2020.
- Utilized least absolute shrinkage and selection operator (LASSO) for variable selection to identify risk factors.
- Statistical significance was determined with a 2-sided P value <0.05.
Main Results:
- IP-SSI occurred in 7.2% of transplants (34/470).
- Risk factors included repeat transplantation, split liver, Roux-en-Y biliary anastomosis, anastomotic leak, and post-transplant renal replacement therapy.
- IP-SSI significantly increased hospitalization length (24.5 vs 10.0 days) and 1-year mortality (14.7% vs 4.1%). Gram-positive bacteria were the most common pathogens, with a notable increase in multidrug-resistant bacteria over time.
Conclusions:
- Surgical factors, rather than antimicrobial prophylaxis, were the primary drivers of IP-SSI in this cohort.
- IP-SSI negatively impacts hospitalization duration and 1-year mortality.
- While modifiable surgical factors are limited, close clinical monitoring and tailored antimicrobial therapy are key to managing IP-SSI risk.
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