Can endoscopists differentiate cytomegalovirus esophagitis from herpes simplex virus esophagitis based on gross endoscopic findings?
Differential diagnosis between herpes simplex virus (HSV) esophagitis and cytomegalovirus (CMV) esophagitis is challenging because there are many similarities and overlaps between their endoscopic features. The aims of this study were to investigate the implications of the endoscopic findings for th...
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Veröffentlicht in: | Medicine (Baltimore) 2019-06, Vol.98 (23), p.e15845-e15845 |
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creator | Jung, Kyung Hwa Choi, Jonggi Gong, Eun Jeong Lee, Jeong Hoon Choi, Kee Don Song, Ho June Lee, Gin Hyug Jung, Hwoon-Yong Chong, Yong Pil Lee, Sang-Oh Choi, Sang-Ho Kim, Yang Soo Woo, Jun Hee Kim, Do Hoon Kim, Sung-Han |
description | Differential diagnosis between herpes simplex virus (HSV) esophagitis and cytomegalovirus (CMV) esophagitis is challenging because there are many similarities and overlaps between their endoscopic features. The aims of this study were to investigate the implications of the endoscopic findings for the diagnosis of HSV and CMV esophagitis, and to develop a predictive model for differentiating CMV esophagitis from HSV esophagitis.Patients who underwent endoscopic examination and had pathologically-confirmed HSV or CMV esophagitis were eligible. Clinical characteristics and endoscopic features were retrospectively reviewed and categorized. A predictive model was developed based on parameters identified by logistic regression analysis.During the 8-year study period, HSV and CMV esophagitis were diagnosed in 85 and 63 patients, respectively. The endoscopic features of esophagitis were categorized and scored as follows: category 1 (-3 points): discrete ulcers or ulcers with vesicles, bullae, or pseudomembranes, category 2 (-2 points): coalescent or geographic ulcers, category 3 (1 points): ulcers with an uneven base, friability, or with a circumferential distribution, category 4 (2 points): punched-out, serpiginous, or healing ulcers with yellowish exudates. And previous history of transplantation (2 point) was included in the model as a discriminating clinical feature. The optimal cutoff point of the prediction model was 0 (area under receiver operating characteristic curve: 0.967), with positive scores favoring CMV esophagitis. Sensitivity, specificity, accuracy, positive predictive value, and negative predictive value were 96.8%, 89.4%, 92.6%, 87.3%, and 97.5%, respectively.The predictive model based on endoscopic and clinical findings appears to be accurate and useful in differentiating CMV esophagitis from HSV esophagitis. |
doi_str_mv | 10.1097/MD.0000000000015845 |
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The aims of this study were to investigate the implications of the endoscopic findings for the diagnosis of HSV and CMV esophagitis, and to develop a predictive model for differentiating CMV esophagitis from HSV esophagitis.Patients who underwent endoscopic examination and had pathologically-confirmed HSV or CMV esophagitis were eligible. Clinical characteristics and endoscopic features were retrospectively reviewed and categorized. A predictive model was developed based on parameters identified by logistic regression analysis.During the 8-year study period, HSV and CMV esophagitis were diagnosed in 85 and 63 patients, respectively. The endoscopic features of esophagitis were categorized and scored as follows: category 1 (-3 points): discrete ulcers or ulcers with vesicles, bullae, or pseudomembranes, category 2 (-2 points): coalescent or geographic ulcers, category 3 (1 points): ulcers with an uneven base, friability, or with a circumferential distribution, category 4 (2 points): punched-out, serpiginous, or healing ulcers with yellowish exudates. And previous history of transplantation (2 point) was included in the model as a discriminating clinical feature. The optimal cutoff point of the prediction model was 0 (area under receiver operating characteristic curve: 0.967), with positive scores favoring CMV esophagitis. Sensitivity, specificity, accuracy, positive predictive value, and negative predictive value were 96.8%, 89.4%, 92.6%, 87.3%, and 97.5%, respectively.The predictive model based on endoscopic and clinical findings appears to be accurate and useful in differentiating CMV esophagitis from HSV esophagitis.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000015845</identifier><identifier>PMID: 31169688</identifier><language>eng</language><publisher>United States: the Author(s). Published by Wolters Kluwer Health, Inc</publisher><subject>Adult ; Aged ; Antiviral Agents - therapeutic use ; Comorbidity ; Cytomegalovirus Infections - diagnosis ; Cytomegalovirus Infections - drug therapy ; Diagnosis, Differential ; Esophagitis - diagnosis ; Esophagitis - virology ; Esophagoscopy - standards ; Female ; Herpes Simplex - diagnosis ; Herpes Simplex - drug therapy ; Humans ; Immunocompromised Host ; Male ; Middle Aged ; Observational Study ; Retrospective Studies ; Sensitivity and Specificity ; Severity of Illness Index ; Tertiary Care Centers ; Transplants - immunology</subject><ispartof>Medicine (Baltimore), 2019-06, Vol.98 (23), p.e15845-e15845</ispartof><rights>the Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5162-88f7018a846e4666b40e2ff5ce8d881eb71b614dfd4cc1183538839b189e3a113</citedby><cites>FETCH-LOGICAL-c5162-88f7018a846e4666b40e2ff5ce8d881eb71b614dfd4cc1183538839b189e3a113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571398/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571398/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31169688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Kyung Hwa</creatorcontrib><creatorcontrib>Choi, Jonggi</creatorcontrib><creatorcontrib>Gong, Eun Jeong</creatorcontrib><creatorcontrib>Lee, Jeong Hoon</creatorcontrib><creatorcontrib>Choi, Kee Don</creatorcontrib><creatorcontrib>Song, Ho June</creatorcontrib><creatorcontrib>Lee, Gin Hyug</creatorcontrib><creatorcontrib>Jung, Hwoon-Yong</creatorcontrib><creatorcontrib>Chong, Yong Pil</creatorcontrib><creatorcontrib>Lee, Sang-Oh</creatorcontrib><creatorcontrib>Choi, Sang-Ho</creatorcontrib><creatorcontrib>Kim, Yang Soo</creatorcontrib><creatorcontrib>Woo, Jun Hee</creatorcontrib><creatorcontrib>Kim, Do Hoon</creatorcontrib><creatorcontrib>Kim, Sung-Han</creatorcontrib><title>Can endoscopists differentiate cytomegalovirus esophagitis from herpes simplex virus esophagitis based on gross endoscopic findings?</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Differential diagnosis between herpes simplex virus (HSV) esophagitis and cytomegalovirus (CMV) esophagitis is challenging because there are many similarities and overlaps between their endoscopic features. The aims of this study were to investigate the implications of the endoscopic findings for the diagnosis of HSV and CMV esophagitis, and to develop a predictive model for differentiating CMV esophagitis from HSV esophagitis.Patients who underwent endoscopic examination and had pathologically-confirmed HSV or CMV esophagitis were eligible. Clinical characteristics and endoscopic features were retrospectively reviewed and categorized. A predictive model was developed based on parameters identified by logistic regression analysis.During the 8-year study period, HSV and CMV esophagitis were diagnosed in 85 and 63 patients, respectively. The endoscopic features of esophagitis were categorized and scored as follows: category 1 (-3 points): discrete ulcers or ulcers with vesicles, bullae, or pseudomembranes, category 2 (-2 points): coalescent or geographic ulcers, category 3 (1 points): ulcers with an uneven base, friability, or with a circumferential distribution, category 4 (2 points): punched-out, serpiginous, or healing ulcers with yellowish exudates. And previous history of transplantation (2 point) was included in the model as a discriminating clinical feature. The optimal cutoff point of the prediction model was 0 (area under receiver operating characteristic curve: 0.967), with positive scores favoring CMV esophagitis. Sensitivity, specificity, accuracy, positive predictive value, and negative predictive value were 96.8%, 89.4%, 92.6%, 87.3%, and 97.5%, respectively.The predictive model based on endoscopic and clinical findings appears to be accurate and useful in differentiating CMV esophagitis from HSV esophagitis.</description><subject>Adult</subject><subject>Aged</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Comorbidity</subject><subject>Cytomegalovirus Infections - diagnosis</subject><subject>Cytomegalovirus Infections - drug therapy</subject><subject>Diagnosis, Differential</subject><subject>Esophagitis - diagnosis</subject><subject>Esophagitis - virology</subject><subject>Esophagoscopy - standards</subject><subject>Female</subject><subject>Herpes Simplex - diagnosis</subject><subject>Herpes Simplex - drug therapy</subject><subject>Humans</subject><subject>Immunocompromised Host</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Observational Study</subject><subject>Retrospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><subject>Tertiary Care Centers</subject><subject>Transplants - immunology</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplUctu1TAQtRCIXgpfgIT8A2k98XsDQre0ILViA-vIScaJIYkjO7ePPR_elAt9wGxGmjkPHR1C3gI7Amb18cXJEXsYkEbIZ2QDkqtCWiWekw1jpSy01eKAvMr5xwriuhQvyQEHUFYZsyG_tm6iOLUxN3EOecm0Dd5jwmkJbkHa3CxxxM4N8TKkXaaY49y7LiwhU5_iSHtMM2aawzgPeE3_R9UuY0vjRLsUc37waqgPUxumLn94TV54N2R882cfku-nn75tPxfnX8--bD-eF40EVRbGeM3AOCMUCqVULRiW3ssGTWsMYK2hViBa34qmATBccmO4rcFY5A6AH5L3e915V4_YNmvI5IZqTmF06aaKLlRPP1Poqy5eVkpq4NasAnwv0NxlSejvucCqu1Kqi5Pq31JW1rvHtvecvy2sALEHXMVhwZR_DrsrTFWPblj633pS27IoGVimmGbFeilLfgtNaJxZ</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Jung, Kyung Hwa</creator><creator>Choi, Jonggi</creator><creator>Gong, Eun Jeong</creator><creator>Lee, Jeong Hoon</creator><creator>Choi, Kee Don</creator><creator>Song, Ho June</creator><creator>Lee, Gin Hyug</creator><creator>Jung, Hwoon-Yong</creator><creator>Chong, Yong Pil</creator><creator>Lee, Sang-Oh</creator><creator>Choi, Sang-Ho</creator><creator>Kim, Yang Soo</creator><creator>Woo, Jun Hee</creator><creator>Kim, Do Hoon</creator><creator>Kim, Sung-Han</creator><general>the Author(s). Published by Wolters Kluwer Health, Inc</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20190601</creationdate><title>Can endoscopists differentiate cytomegalovirus esophagitis from herpes simplex virus esophagitis based on gross endoscopic findings?</title><author>Jung, Kyung Hwa ; Choi, Jonggi ; Gong, Eun Jeong ; Lee, Jeong Hoon ; Choi, Kee Don ; Song, Ho June ; Lee, Gin Hyug ; Jung, Hwoon-Yong ; Chong, Yong Pil ; Lee, Sang-Oh ; Choi, Sang-Ho ; Kim, Yang Soo ; Woo, Jun Hee ; Kim, Do Hoon ; Kim, Sung-Han</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5162-88f7018a846e4666b40e2ff5ce8d881eb71b614dfd4cc1183538839b189e3a113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Comorbidity</topic><topic>Cytomegalovirus Infections - diagnosis</topic><topic>Cytomegalovirus Infections - drug therapy</topic><topic>Diagnosis, Differential</topic><topic>Esophagitis - diagnosis</topic><topic>Esophagitis - virology</topic><topic>Esophagoscopy - standards</topic><topic>Female</topic><topic>Herpes Simplex - diagnosis</topic><topic>Herpes Simplex - drug therapy</topic><topic>Humans</topic><topic>Immunocompromised Host</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Observational Study</topic><topic>Retrospective Studies</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><topic>Tertiary Care Centers</topic><topic>Transplants - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Kyung Hwa</creatorcontrib><creatorcontrib>Choi, Jonggi</creatorcontrib><creatorcontrib>Gong, Eun Jeong</creatorcontrib><creatorcontrib>Lee, Jeong Hoon</creatorcontrib><creatorcontrib>Choi, Kee Don</creatorcontrib><creatorcontrib>Song, Ho June</creatorcontrib><creatorcontrib>Lee, Gin Hyug</creatorcontrib><creatorcontrib>Jung, Hwoon-Yong</creatorcontrib><creatorcontrib>Chong, Yong Pil</creatorcontrib><creatorcontrib>Lee, Sang-Oh</creatorcontrib><creatorcontrib>Choi, Sang-Ho</creatorcontrib><creatorcontrib>Kim, Yang Soo</creatorcontrib><creatorcontrib>Woo, Jun Hee</creatorcontrib><creatorcontrib>Kim, Do Hoon</creatorcontrib><creatorcontrib>Kim, Sung-Han</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Kyung Hwa</au><au>Choi, Jonggi</au><au>Gong, Eun Jeong</au><au>Lee, Jeong Hoon</au><au>Choi, Kee Don</au><au>Song, Ho June</au><au>Lee, Gin Hyug</au><au>Jung, Hwoon-Yong</au><au>Chong, Yong Pil</au><au>Lee, Sang-Oh</au><au>Choi, Sang-Ho</au><au>Kim, Yang Soo</au><au>Woo, Jun Hee</au><au>Kim, Do Hoon</au><au>Kim, Sung-Han</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Can endoscopists differentiate cytomegalovirus esophagitis from herpes simplex virus esophagitis based on gross endoscopic findings?</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>98</volume><issue>23</issue><spage>e15845</spage><epage>e15845</epage><pages>e15845-e15845</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Differential diagnosis between herpes simplex virus (HSV) esophagitis and cytomegalovirus (CMV) esophagitis is challenging because there are many similarities and overlaps between their endoscopic features. The aims of this study were to investigate the implications of the endoscopic findings for the diagnosis of HSV and CMV esophagitis, and to develop a predictive model for differentiating CMV esophagitis from HSV esophagitis.Patients who underwent endoscopic examination and had pathologically-confirmed HSV or CMV esophagitis were eligible. Clinical characteristics and endoscopic features were retrospectively reviewed and categorized. A predictive model was developed based on parameters identified by logistic regression analysis.During the 8-year study period, HSV and CMV esophagitis were diagnosed in 85 and 63 patients, respectively. The endoscopic features of esophagitis were categorized and scored as follows: category 1 (-3 points): discrete ulcers or ulcers with vesicles, bullae, or pseudomembranes, category 2 (-2 points): coalescent or geographic ulcers, category 3 (1 points): ulcers with an uneven base, friability, or with a circumferential distribution, category 4 (2 points): punched-out, serpiginous, or healing ulcers with yellowish exudates. And previous history of transplantation (2 point) was included in the model as a discriminating clinical feature. The optimal cutoff point of the prediction model was 0 (area under receiver operating characteristic curve: 0.967), with positive scores favoring CMV esophagitis. Sensitivity, specificity, accuracy, positive predictive value, and negative predictive value were 96.8%, 89.4%, 92.6%, 87.3%, and 97.5%, respectively.The predictive model based on endoscopic and clinical findings appears to be accurate and useful in differentiating CMV esophagitis from HSV esophagitis.</abstract><cop>United States</cop><pub>the Author(s). Published by Wolters Kluwer Health, Inc</pub><pmid>31169688</pmid><doi>10.1097/MD.0000000000015845</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antiviral Agents - therapeutic use Comorbidity Cytomegalovirus Infections - diagnosis Cytomegalovirus Infections - drug therapy Diagnosis, Differential Esophagitis - diagnosis Esophagitis - virology Esophagoscopy - standards Female Herpes Simplex - diagnosis Herpes Simplex - drug therapy Humans Immunocompromised Host Male Middle Aged Observational Study Retrospective Studies Sensitivity and Specificity Severity of Illness Index Tertiary Care Centers Transplants - immunology |
title | Can endoscopists differentiate cytomegalovirus esophagitis from herpes simplex virus esophagitis based on gross endoscopic findings? |
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