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Diagnostic yield of the cytomegalovirus (CMV) antigenemia assay and clinical features in solid organ transplant recipients and hematopoietic stem cell transplant recipients with CMV pneumonia
: Data are limited on the value of non‐invasive diagnostic methods, such as the cytomegalovirus (CMV) antigenemia assay, and the clinical features of CMV pneumonia in patients who have undergone solid organ transplant (SOT) compared with those who have had hematopoietic stem cell transplant (HSCT)....
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Published in: | Transplant infectious disease 2012-04, Vol.14 (2), p.192-197 |
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Data are limited on the value of non‐invasive diagnostic methods, such as the cytomegalovirus (CMV) antigenemia assay, and the clinical features of CMV pneumonia in patients who have undergone solid organ transplant (SOT) compared with those who have had hematopoietic stem cell transplant (HSCT). All adult patients with suspected CMV pneumonia, who had received SOT or HSCT in a tertiary hospital during a 5‐year period, were retrospectively enrolled. CMV pneumonia was defined as clinical and radiographic evidence of pneumonia in association with the isolation of CMV in viral cultures of bronchoalveolar lavage or lung tissue specimens, or with the identification of CMV in lung tissue. In total, 36 patients with CMV pneumonia were identified. Of these, 29 (80%) had received SOT and 7 (20%) had received HSCT. The incidence of CMV pneumonia in the patients with SOT (3.0 per 1000 person‐years [95% confidence interval {CI} 0.6–8.7]) was lower than in those with HSCT (17.0 per 1000 person‐years [95% CI 9.9–27.2], P = 0.003) and CMV‐related mortality showed a tendency to have lower mortality in patients with SOT (10% [3/29]) than with HSCT (43% [3/7], P = 0.07). The overall sensitivity of the CMV assay (≥ 1/200,000 leukocytes) in patients with CMV pneumonia was 69% (95% CI 52–84%). The CMV antigenemia test is of limited value in diagnosing CMV pneumonia, given the high cost of false‐negative diagnoses of CMV pneumonia. |
doi_str_mv | 10.1111/j.1399-3062.2011.00703.x |
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Data are limited on the value of non‐invasive diagnostic methods, such as the cytomegalovirus (CMV) antigenemia assay, and the clinical features of CMV pneumonia in patients who have undergone solid organ transplant (SOT) compared with those who have had hematopoietic stem cell transplant (HSCT). All adult patients with suspected CMV pneumonia, who had received SOT or HSCT in a tertiary hospital during a 5‐year period, were retrospectively enrolled. CMV pneumonia was defined as clinical and radiographic evidence of pneumonia in association with the isolation of CMV in viral cultures of bronchoalveolar lavage or lung tissue specimens, or with the identification of CMV in lung tissue. In total, 36 patients with CMV pneumonia were identified. Of these, 29 (80%) had received SOT and 7 (20%) had received HSCT. The incidence of CMV pneumonia in the patients with SOT (3.0 per 1000 person‐years [95% confidence interval {CI} 0.6–8.7]) was lower than in those with HSCT (17.0 per 1000 person‐years [95% CI 9.9–27.2], P = 0.003) and CMV‐related mortality showed a tendency to have lower mortality in patients with SOT (10% [3/29]) than with HSCT (43% [3/7], P = 0.07). The overall sensitivity of the CMV assay (≥ 1/200,000 leukocytes) in patients with CMV pneumonia was 69% (95% CI 52–84%). The CMV antigenemia test is of limited value in diagnosing CMV pneumonia, given the high cost of false‐negative diagnoses of CMV pneumonia.</description><identifier>ISSN: 1398-2273</identifier><identifier>EISSN: 1399-3062</identifier><identifier>DOI: 10.1111/j.1399-3062.2011.00703.x</identifier><identifier>PMID: 22260384</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Adult ; Alveoli ; Antigenemia ; antigenemia assay ; Antigens, Viral - isolation & purification ; Bronchus ; Cell culture ; Confidence intervals ; Cytomegalovirus ; Cytomegalovirus Infections - blood ; Cytomegalovirus Infections - immunology ; Data processing ; diagnostic yield ; Female ; hematopoietic stem cell transplant ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hospitals ; Humans ; Leukocytes ; Lung ; Male ; Middle Aged ; Mortality ; Organ Transplantation - adverse effects ; Pneumonia ; Pneumonia, Viral - etiology ; Pneumonia, Viral - virology ; Retrospective Studies ; solid organ transplant ; stem cell transplantation ; Stem cells</subject><ispartof>Transplant infectious disease, 2012-04, Vol.14 (2), p.192-197</ispartof><rights>2012 John Wiley & Sons A/S</rights><rights>2012 John Wiley & Sons A/S.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4673-718a40fdde0a5968052f57e4919a4dbf755adc11527e1d354eafb44a06c28f923</citedby><cites>FETCH-LOGICAL-c4673-718a40fdde0a5968052f57e4919a4dbf755adc11527e1d354eafb44a06c28f923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22260384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moon, S.M.</creatorcontrib><creatorcontrib>Sung, H.</creatorcontrib><creatorcontrib>Kim, M.-N.</creatorcontrib><creatorcontrib>Lee, S.-O.</creatorcontrib><creatorcontrib>Choi, S.-H.</creatorcontrib><creatorcontrib>Kim, Y.S.</creatorcontrib><creatorcontrib>Woo, J.H.</creatorcontrib><creatorcontrib>Kim, S.-H.</creatorcontrib><title>Diagnostic yield of the cytomegalovirus (CMV) antigenemia assay and clinical features in solid organ transplant recipients and hematopoietic stem cell transplant recipients with CMV pneumonia</title><title>Transplant infectious disease</title><addtitle>Transpl Infect Dis</addtitle><description>:
Data are limited on the value of non‐invasive diagnostic methods, such as the cytomegalovirus (CMV) antigenemia assay, and the clinical features of CMV pneumonia in patients who have undergone solid organ transplant (SOT) compared with those who have had hematopoietic stem cell transplant (HSCT). All adult patients with suspected CMV pneumonia, who had received SOT or HSCT in a tertiary hospital during a 5‐year period, were retrospectively enrolled. CMV pneumonia was defined as clinical and radiographic evidence of pneumonia in association with the isolation of CMV in viral cultures of bronchoalveolar lavage or lung tissue specimens, or with the identification of CMV in lung tissue. In total, 36 patients with CMV pneumonia were identified. Of these, 29 (80%) had received SOT and 7 (20%) had received HSCT. The incidence of CMV pneumonia in the patients with SOT (3.0 per 1000 person‐years [95% confidence interval {CI} 0.6–8.7]) was lower than in those with HSCT (17.0 per 1000 person‐years [95% CI 9.9–27.2], P = 0.003) and CMV‐related mortality showed a tendency to have lower mortality in patients with SOT (10% [3/29]) than with HSCT (43% [3/7], P = 0.07). The overall sensitivity of the CMV assay (≥ 1/200,000 leukocytes) in patients with CMV pneumonia was 69% (95% CI 52–84%). The CMV antigenemia test is of limited value in diagnosing CMV pneumonia, given the high cost of false‐negative diagnoses of CMV pneumonia.</description><subject>Adult</subject><subject>Alveoli</subject><subject>Antigenemia</subject><subject>antigenemia assay</subject><subject>Antigens, Viral - isolation & purification</subject><subject>Bronchus</subject><subject>Cell culture</subject><subject>Confidence intervals</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus Infections - blood</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Data processing</subject><subject>diagnostic yield</subject><subject>Female</subject><subject>hematopoietic stem cell transplant</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Leukocytes</subject><subject>Lung</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Organ Transplantation - adverse effects</subject><subject>Pneumonia</subject><subject>Pneumonia, Viral - etiology</subject><subject>Pneumonia, Viral - virology</subject><subject>Retrospective Studies</subject><subject>solid organ transplant</subject><subject>stem cell transplantation</subject><subject>Stem cells</subject><issn>1398-2273</issn><issn>1399-3062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNktFu0zAUhiMEYmPwCsgSN-MixXacOJG4QS2UoQ24GHBpnSYnnUtiZ7bD2qfj1XDa0QskpPnGlv1_v4_9nyQhjM5YHG82M5ZVVZrRgs84ZWxGqaTZbPsoOT0ePN6vy5RzmZ0kz7zfUMpkJaqnyQnnvKBZKU6T3wsNa2N90DXZaewaYlsSbpDUu2B7XENnf2k3enI-v_r-moAJeo0Gew0EvIdd3GlI3Wmja-hIixBGh55oQ7ztdHRzazAkODB-6CJNHNZ60GiC36M32EOwg9U4VeAD9qTGrvsPcafDDYmFkMHg2Fuj4XnypIXO44v7-Sz59uH99fxjevlleTF_d5nWopBZKlkJgrZNgxTyqihpzttcoqhYBaJZtTLPoakZy7lE1mS5QGhXQgAtal62Fc_OkvOD7-Ds7Yg-qF77qVIwaEevGOW0zKQo2QOklAqaSy6i9NU_0o0dnYkPUTEqxrOiyCfD8qCqnfXeYasGp3twu2ilpn5QGzXFrqbY1dQPat8PahvRl_cXjKsemyP4twGi4O1BcKc73D3YWF1fLOIi4ukB1zG67REH91PFb5e5-vF5qZZsIT8JeaW-Zn8AVXPVtA</recordid><startdate>201204</startdate><enddate>201204</enddate><creator>Moon, S.M.</creator><creator>Sung, H.</creator><creator>Kim, M.-N.</creator><creator>Lee, S.-O.</creator><creator>Choi, S.-H.</creator><creator>Kim, Y.S.</creator><creator>Woo, J.H.</creator><creator>Kim, S.-H.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201204</creationdate><title>Diagnostic yield of the cytomegalovirus (CMV) antigenemia assay and clinical features in solid organ transplant recipients and hematopoietic stem cell transplant recipients with CMV pneumonia</title><author>Moon, S.M. ; Sung, H. ; Kim, M.-N. ; Lee, S.-O. ; Choi, S.-H. ; Kim, Y.S. ; Woo, J.H. ; Kim, S.-H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4673-718a40fdde0a5968052f57e4919a4dbf755adc11527e1d354eafb44a06c28f923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Alveoli</topic><topic>Antigenemia</topic><topic>antigenemia assay</topic><topic>Antigens, Viral - isolation & purification</topic><topic>Bronchus</topic><topic>Cell culture</topic><topic>Confidence intervals</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus Infections - blood</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Data processing</topic><topic>diagnostic yield</topic><topic>Female</topic><topic>hematopoietic stem cell transplant</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Leukocytes</topic><topic>Lung</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Organ Transplantation - adverse effects</topic><topic>Pneumonia</topic><topic>Pneumonia, Viral - etiology</topic><topic>Pneumonia, Viral - virology</topic><topic>Retrospective Studies</topic><topic>solid organ transplant</topic><topic>stem cell transplantation</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moon, S.M.</creatorcontrib><creatorcontrib>Sung, H.</creatorcontrib><creatorcontrib>Kim, M.-N.</creatorcontrib><creatorcontrib>Lee, S.-O.</creatorcontrib><creatorcontrib>Choi, S.-H.</creatorcontrib><creatorcontrib>Kim, Y.S.</creatorcontrib><creatorcontrib>Woo, J.H.</creatorcontrib><creatorcontrib>Kim, S.-H.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplant infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moon, S.M.</au><au>Sung, H.</au><au>Kim, M.-N.</au><au>Lee, S.-O.</au><au>Choi, S.-H.</au><au>Kim, Y.S.</au><au>Woo, J.H.</au><au>Kim, S.-H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic yield of the cytomegalovirus (CMV) antigenemia assay and clinical features in solid organ transplant recipients and hematopoietic stem cell transplant recipients with CMV pneumonia</atitle><jtitle>Transplant infectious disease</jtitle><addtitle>Transpl Infect Dis</addtitle><date>2012-04</date><risdate>2012</risdate><volume>14</volume><issue>2</issue><spage>192</spage><epage>197</epage><pages>192-197</pages><issn>1398-2273</issn><eissn>1399-3062</eissn><abstract>:
Data are limited on the value of non‐invasive diagnostic methods, such as the cytomegalovirus (CMV) antigenemia assay, and the clinical features of CMV pneumonia in patients who have undergone solid organ transplant (SOT) compared with those who have had hematopoietic stem cell transplant (HSCT). All adult patients with suspected CMV pneumonia, who had received SOT or HSCT in a tertiary hospital during a 5‐year period, were retrospectively enrolled. CMV pneumonia was defined as clinical and radiographic evidence of pneumonia in association with the isolation of CMV in viral cultures of bronchoalveolar lavage or lung tissue specimens, or with the identification of CMV in lung tissue. In total, 36 patients with CMV pneumonia were identified. Of these, 29 (80%) had received SOT and 7 (20%) had received HSCT. The incidence of CMV pneumonia in the patients with SOT (3.0 per 1000 person‐years [95% confidence interval {CI} 0.6–8.7]) was lower than in those with HSCT (17.0 per 1000 person‐years [95% CI 9.9–27.2], P = 0.003) and CMV‐related mortality showed a tendency to have lower mortality in patients with SOT (10% [3/29]) than with HSCT (43% [3/7], P = 0.07). The overall sensitivity of the CMV assay (≥ 1/200,000 leukocytes) in patients with CMV pneumonia was 69% (95% CI 52–84%). The CMV antigenemia test is of limited value in diagnosing CMV pneumonia, given the high cost of false‐negative diagnoses of CMV pneumonia.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>22260384</pmid><doi>10.1111/j.1399-3062.2011.00703.x</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Alveoli Antigenemia antigenemia assay Antigens, Viral - isolation & purification Bronchus Cell culture Confidence intervals Cytomegalovirus Cytomegalovirus Infections - blood Cytomegalovirus Infections - immunology Data processing diagnostic yield Female hematopoietic stem cell transplant Hematopoietic Stem Cell Transplantation - adverse effects Hospitals Humans Leukocytes Lung Male Middle Aged Mortality Organ Transplantation - adverse effects Pneumonia Pneumonia, Viral - etiology Pneumonia, Viral - virology Retrospective Studies solid organ transplant stem cell transplantation Stem cells |
title | Diagnostic yield of the cytomegalovirus (CMV) antigenemia assay and clinical features in solid organ transplant recipients and hematopoietic stem cell transplant recipients with CMV pneumonia |
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