000 04601nam a22004937a 4500
008 240807s20242024 xxu||||| |||| 00| 0 eng d
022 _a2415-1289
024 _aPMC11074486 [pmc]
024 _atgh-09-23-44 [pii]
040 _aOvid MEDLINE(R)
099 _a38716211
245 _aViral esophagitis in non-human immunodeficiency virus patients: a case-control study.
251 _aTranslational Gastroenterology & Hepatology. 9:19, 2024.
252 _aTransl. gastroenterol. hepatol.. 9:19, 2024.
253 _aTranslational gastroenterology and hepatology
260 _c2024
260 _fFY2024
260 _p2024
265 _sepublish
265 _tPubMed-not-MEDLINE
266 _d2024-08-07
266 _z2024/05/08 03:46
520 _aBackground: Esophagitis, inflammation of the esophagus, can result from various causes, including reflux, infections, food allergies, medications, and trauma. Infectious esophagitis is the third most common cause after gastroesophageal reflux disease (GERD) and eosinophilic esophagitis worldwide. The primary causes of infectious esophagitis are candida esophagitis and viral esophagitis (VE) caused by herpes simplex virus (HSV) or cytomegalovirus (CMV). VE is typically associated with immunosuppression, with risk factors such as malignancy, chemotherapy, organ transplant, and human immunodeficiency virus (HIV). Infectious esophagitis is prevalent in about one-third of untreated acquired immunodeficiency syndrome (AIDS) patients, but recent reports indicate an increase in VE cases among immunocompetent individuals. This study aims to explore risk factors and patient demographics in non-HIV individuals.
520 _aConclusions: The study's findings contribute to a better understanding of the clinical characteristics and risk factors associated with VE in non-HIV patients. The identification of immunosuppression and specific risk factors can aid in early detection, appropriate management, and targeted interventions for VE. Further research is warranted to explore the rising incidence of VE in immunocompetent individuals and to optimize preventive strategies and treatment approaches for this condition. Copyright 2024 Translational Gastroenterology and Hepatology. All rights reserved.
520 _aMethods: A case-control study that included patients 18 years and older diagnosed with HSV or CMV esophagitis who were identified through histopathologic examination or immunohistochemical staining. Cases were obtained by searching pathology reports between 2009-2022 from five MedStar Health Hospitals in the District of Columbia and Maryland. Controls were selected based on International Classification of Diseases (ICD) codes for esophagogastroduodenoscopy (EGD) with negative VE results within the same period. Patient demographics, comorbidities, laboratory parameters, endoscopic findings, and potential risk factors were collected through chart review.
520 _aResults: Out of 40,224 cases between 2009-2022, 50 cases of VE were identified, with 30 cases attributed to HSV, 19 cases to CMV, and one case of HSV/CMV coinfection. Hematemesis was the predominant symptom in patients with HSV (33%), while dysphagia was more prevalent in CMV patients (42%). The most common finding during EGD was ulceration in HSV patients (67%) and esophagitis in CMV patients (37%). Patients with VE had a higher likelihood of a history of immunosuppressive therapy, organ transplant, active malignancy, and systemic steroid use. However, a significant portion (34%) had no identifiable risk factors.
546 _aEnglish
650 _zAutomated
651 _aMedStar Washington Hospital Center
656 _aGastroenterology Fellowship
656 _aInternal Medicine Residency
656 _aMedStar Georgetown University Hospital/MedStar Washington Hospital Center
656 _aPathology Residency
657 _aJournal Article
700 _aAl-Dwairy, Ahmad
_bMWHC
_cInternal Medicine Residency
_dMBBS
700 _aAzar, Loai
_bMWHC
_cInternal Medicine Residency
_dMD
700 _aBakain, Tarek
_bMWHC
_cInternal Medicine Residency
_dMBBS
700 _aNithagon, Pichayut
_bMGUH
_cPathology Residency
_dMD
700 _aWoo, Stephanie
_bMGUH
_cGastroenterology Fellowship
_dMD
790 _aAl-Dwairy A, Azar L, Bakain T, Ahmad A, Woo S, Nithagon P, Chalhoub W
856 _uhttps://dx.doi.org/10.21037/tgh-23-44
_zhttps://dx.doi.org/10.21037/tgh-23-44
858 _yAl-Dwairy, Ahmad
_uhttps://orcid.org/0009-0004-3185-5826
_zhttps://orcid.org/0009-0004-3185-5826
942 _cART
_dArticle
999 _c14512
_d14512