Published online Sep 18, 2023. doi: 10.5500/wjt.v13.i5.264
Peer-review started: June 28, 2023
First decision: August 4, 2023
Revised: August 17, 2023
Accepted: September 4, 2023
Article in press: September 4, 2023
Published online: September 18, 2023
Processing time: 78 Days and 8.9 Hours
During the past two decades, the incidence rate and onset time of invasive fungal infections (IFIs), such as aspergillosis, have changed in liver transplant recipients.
Determining the new risk factors and treatment outcomes of early and late-onset invasive aspergillosis (IA) in high-volume centers for liver transplants is essential. It may have a key role in improving the prognosis of these patients.
This study sought to determine the prevalence, risk factors, treatment outcomes, and prognosis of IA infection among liver transplant recipients at our institution. We also investigated the study patients' major clinical, laboratory, and radiologic manifestations of IA.
To determine the prevalence of IA, we analyzed the data of 850 patients who received a liver transplant at the Imam Khomeini Hospital Complex in Tehran, Iran, between 2014 and 2019, and recorded the study variables for patients with an IA diagnosis. In addition, we devised a case-control study to identify the risk factors for IA and compare the prognoses of patients with and without IA.
Our center's IA rate was 2.7%. Pulmonary aspergillosis was the most common presentation of the patients with IA. In most of our patients, imaging findings indicative of aspergillosis, including nodule and halo signs, were detected. The high level of creatinine before and after the transplant, renal replacement therapy after transplantation, induction therapy with antithymocyte globulin, longer duration of intensive care unit admission after the transplant, pneumonia 2 wk before the IA diagnosis, cytomegalovirus viremia within 1 mo before the IA diagnosis, receiving systemic antibiotics for more than three days within the 2 wk before the IA diagnosis, treatment-required transplant rejection within three months before the IA diagnosis, receiving systemic antibiotics for longer than three months before the IA diagnosis, repeated surgery within 30 d after the transplant, biliary leakage after the transplant and hepatic artery thrombosis were the risk factors associated with increased risk of IA.
In this study, the prevalence of IA among liver transplant recipients was relatively low. However, it was one of the leading causes of mortality following liver transplantation. Identifying and addressing risk factors for IA, early diagnosis and prompt treatment of this fatal disease may improve the prognosis and decrease the mortality rate of liver transplant recipients.
The primary risk factors of IA in liver transplant recipients should be determined through a large, multicenter study. Moreover, we must investigate the role of noninvasive and rapid diagnostic tests in diagnosing patients suspected of IFI early.