Human cytomegalovirus: a survey of end-organ diseases and diagnostic challenges in solid organ transplant recipients

被引:1
|
作者
Contreras, Gustavo [1 ,2 ]
Ho, Dora [1 ]
机构
[1] Stanford Univ, Dept Infect Dis & Geog Med, Stanford, CA USA
[2] Stanford Univ, Dept Infect Dis & Geog Med, 300 Pasteur Dr Lane L134, Stanford, CA 94305 USA
关键词
cytomegalovirus; DNAemia; end-organ disease; solid organ transplant; viremia; POLYMERASE-CHAIN-REACTION; BILE-DUCT SYNDROME; VIRAL-LOAD; LIVER-TRANSPLANTATION; BRONCHOALVEOLAR LAVAGE; CLINICAL UTILITY; GASTROINTESTINAL-DISEASE; PREEMPTIVE THERAPY; ANTIGENEMIA ASSAY; RISK-FACTORS;
D O I
10.1097/MOT.0000000000000992
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of reviewHuman cytomegalovirus (CMV) infection is one of the most important infectious complications in solid organ transplant (SOT) recipients, leading to significant morbidity and mortality. Therefore, early detection and prompt treatment are imperative to improve transplant outcomes. This article highlights the clinical characteristics of the most common CMV end-organ diseases in SOT recipients and their diagnostic modalities and challenges.Recent findingsCMV can cause a variety of end-organ diseases in SOT recipients. Although CMV nucleic acid amplification by polymerase chain reaction (PCR) is frequently employed to detect CMV reactivation or infection, its predictive value for various CMV end-organ diseases remains uncertain. Given the limitation of PCR or other noninvasive tests, confirmation of CMV end-organ disease may require tissue biopsy, which may not be feasible or available, or may cause untoward complications.The utility of PCR to diagnose CMV end-organ disease is limited. As CMV can infect any organ system(s), clinicians caring for SOT recipients need to maintain vigilance for any signs and symptoms of end-organ disease to allow early recognition and prompt treatment. Invasive procedures might be needed to confirm the diagnosis and minimize the empirical use of antiviral therapy that may have substantial drug toxicities.
引用
收藏
页码:243 / 249
页数:7
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