Abstract

Background and Aims Tissue-invasive gastrointestinal cytomegalovirus (TI-GI CMV) disease is common in immunocompromised patients, but the increasing prevalence in immunocompetent patients has been reported. This study compared the clinical manifestations, endoscopic features, treatment outcomes, and predictors for inhospital mortality of TI-GI CMV between immunocompromised and immunocompetent patients. Methods Patients with HIV infection, malignancy, or receiving immunosuppressive agents (chemotherapy, high dose, or long-term corticosteroids) were defined as the immunocompromised group. Demographic and inhospital mortality data were obtained and retrospectively analyzed. Results A total of 213 patients (89 immunocompetent) with histologically confirmed TI-GI CMV were enrolled. Immunocompetent patients were older (70 vs. 52 years; p < 0.001), had more GI bleeding as a presenting symptom (47.2% vs. 29.0%; p = 0.010), and shorter symptom onset (2 vs. 14 days, p = 0.018). Concomitant extra-GI involvement was only seen in the immunocompromised group (6.5% vs. 0%; p = 0.02). Diffuse GI tract (14.5% vs. 4.5%; p = 0.032) and esophageal involvement (14.5% vs. 5.6%; p = 0.046) were more frequent in the immunocompromised, while small bowel involvement was more frequent in the immunocompetent group (19.1% vs. 8.1%; p = 0.029). An overall inhospital mortality was 27.7%. There was no significant difference in inhospital survival probability between the two groups (Peto-Peto test, p = 0.65). ICU admission (hazard ratio [HR] 7.21; 95% CI 2.55-20.36), sepsis or shock (HR 1.98; 95% CI 1.08-3.66), malnutrition (HR 2.62; 95% CI 1.05-7.01), and receiving chemotherapy (HR 5.2; 95% CI 1.89-14.29) were independent factors for inhospital mortality. Antiviral treatment for more than 14 days was the only protective factor to improve survival (Peto-Peto test, p < 0.001). Conclusions Immunocompetent and immunocompromised patients with TI-GI CMV disease had distinct clinical and endoscopic characteristics. There was no significant difference in the inhospital mortality between the two groups. The factors for mortality were ICU admission, sepsis/shock, malnutrition, and receiving chemotherapy. Early diagnosis and initiation of antiviral treatment might improve the survival probability.

Highlights

  • The gastrointestinal (GI) tract is the most common site of tissue-invasive cytomegalovirus (TI-CMV) disease [1], defined as the presence of CMV antigens in the immunohistochemistry (IHC) or CMV cytopathic change on the tissue specimen together with symptoms localized to the GI organs [2,3,4,5,6]

  • The use of systemic corticosteroid, chemotherapy, and other immunosuppressive agents was accounted for 26.6%, 5.6%, and 16.9%, respectively

  • Among patients with human immunodeficiency virus (HIV), the median CD4 count was 52 cell/mm3, and 88.4% had a history of opportunistic infections of acquired immune deficiency syndrome (AIDS)

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Summary

Introduction

The gastrointestinal (GI) tract is the most common site of tissue-invasive cytomegalovirus (TI-CMV) disease [1], defined as the presence of CMV antigens in the immunohistochemistry (IHC) or CMV cytopathic change on the tissue specimen together with symptoms localized to the GI organs [2,3,4,5,6]. TI-GI CMV disease in immunocompetent patients has become more prevalent in recent reports due to increased recognition and improved diagnostic methods [11,12,13,14,15,16,17,18]. Recent studies described the clinical manifestations and associated factors of GI CMV infection in the immunocompetent host [12, 15,16,17,18]. Understanding the manifestation and clinical course of TI-GI CMV disease may emphasize an early recognition and improve outcome in the immunocompetent patients. Tissue-invasive gastrointestinal cytomegalovirus (TI-GI CMV) disease is common in immunocompromised patients, but the increasing prevalence in immunocompetent patients has been reported. This study compared the clinical manifestations, endoscopic features, treatment outcomes, and predictors for inhospital mortality of TI-GI CMV between immunocompromised and immunocompetent patients. Diagnosis and initiation of antiviral treatment might improve the survival probability

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