Loading…
Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy
There has been a dramatic decline in the prevalence of opportunistic infections, particularly Pneumocystis carinii pneumonia (PCP) since the introduction of highly active antiretroviral therapy (HAART). Recently published short-term observational data now support the view that primary and possibly s...
Saved in:
Published in: | International journal of STD & AIDS 2000-01, Vol.11 (1), p.64-65 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c420t-109a143c5847fda449ad9f8be378dcafada737efc0de3a7eeffbde60306c5e613 |
---|---|
cites | |
container_end_page | 65 |
container_issue | 1 |
container_start_page | 64 |
container_title | International journal of STD & AIDS |
container_volume | 11 |
creator | MAMMEN-TOBIN, A MONTEIRO, E. F |
description | There has been a dramatic decline in the prevalence of opportunistic infections, particularly Pneumocystis carinii pneumonia (PCP) since the introduction of highly active antiretroviral therapy (HAART). Recently published short-term observational data now support the view that primary and possibly secondary PCP prophylaxis should be discontinued following sustained immune restoration afforded by HAART. Weverling and colleagues studied 378 patients with advanced HIV on HAART. Primary and secondary PCP prophylaxis was discontinued when the CD4 count had risen and remained above 200 for over 6 months and viral load was below 10,000 copies/ml. They encountered no episodes of PCP during a total 247 person-years of follow up. Furrer et al. showed the same result amongst 262 patients who stopped primary PCP prophylaxis over a median follow up of 11.3 months. The CD4 count was sustained above 200 for a minimum of 12 weeks in this study. We describe a case of acute PCP following withdrawal of primary prophylaxis despite an apparently excellent immunological and virological response to HAART. |
doi_str_mv | 10.1258/0956462001914805 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70896954</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1258_0956462001914805</sage_id><sourcerecordid>70896954</sourcerecordid><originalsourceid>FETCH-LOGICAL-c420t-109a143c5847fda449ad9f8be378dcafada737efc0de3a7eeffbde60306c5e613</originalsourceid><addsrcrecordid>eNqFkc2LFDEQxYMo7rh69yRBxFtrpTuddI6y-AULetBzU5OuzGTpSdqke9cG_3izzsDKgngqSP3qpV49xp4LeCPqtnsLplVS1QDCCNlB-4BthG67SkBbP2Sb23ZV-vKMPcn5CgBUo81jdiZAKW1Abtivr4GWQ7Rrnn3mFpMP3vPpz2PwyF0cx3jjw44PPtsYZh8WnH0MPDo-JX_AtJYap_064s8iMVCe_Ex873f7ceVoZ39NHMtgojnFa59w5POeEk7rU_bI4Zjp2ames-8f3n-7-FRdfvn4-eLdZWVlDXNxY1DIxrad1G5AKQ0OxnVbanQ3WHQ4oG40OQsDNaiJnNsOpKABZVtSojlnr4-6ZdEfC-W5PxQzNI4YKC6519AZZVr5X1BoqWstmwK-vAdexSWFYqKvQXVKQdcWCI6QTTHnRK4_HawX0N_m19_Pr4y8OOku2wMNfw0cAyvAqxOA2eLoEgbr8x3X1LURqmDVEcu4o7vd_vnvb_zZs4E</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>206866085</pqid></control><display><type>article</type><title>Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy</title><source>SAGE</source><creator>MAMMEN-TOBIN, A ; MONTEIRO, E. F</creator><creatorcontrib>MAMMEN-TOBIN, A ; MONTEIRO, E. F</creatorcontrib><description>There has been a dramatic decline in the prevalence of opportunistic infections, particularly Pneumocystis carinii pneumonia (PCP) since the introduction of highly active antiretroviral therapy (HAART). Recently published short-term observational data now support the view that primary and possibly secondary PCP prophylaxis should be discontinued following sustained immune restoration afforded by HAART. Weverling and colleagues studied 378 patients with advanced HIV on HAART. Primary and secondary PCP prophylaxis was discontinued when the CD4 count had risen and remained above 200 for over 6 months and viral load was below 10,000 copies/ml. They encountered no episodes of PCP during a total 247 person-years of follow up. Furrer et al. showed the same result amongst 262 patients who stopped primary PCP prophylaxis over a median follow up of 11.3 months. The CD4 count was sustained above 200 for a minimum of 12 weeks in this study. We describe a case of acute PCP following withdrawal of primary prophylaxis despite an apparently excellent immunological and virological response to HAART.</description><identifier>ISSN: 0956-4624</identifier><identifier>EISSN: 1758-1052</identifier><identifier>DOI: 10.1258/0956462001914805</identifier><identifier>PMID: 10667904</identifier><identifier>CODEN: INSAE3</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>AIDS-Related Opportunistic Infections - drug therapy ; AIDS-Related Opportunistic Infections - immunology ; AIDS-Related Opportunistic Infections - prevention & control ; AIDS/HIV ; Anti-HIV Agents - therapeutic use ; Anti-Infective Agents - therapeutic use ; Biological and medical sciences ; CD4 Lymphocyte Count ; Human immunodeficiency virus ; Human mycoses ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Middle Aged ; Mycoses ; Mycoses of the respiratory system ; Pneumocystis carinii ; Pneumonia, Pneumocystis - drug therapy ; Pneumonia, Pneumocystis - prevention & control ; Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>International journal of STD & AIDS, 2000-01, Vol.11 (1), p.64-65</ispartof><rights>Royal Society of Medicine Press Limited</rights><rights>2000 INIST-CNRS</rights><rights>Copyright Royal Society of Medicine Press Ltd. Jan 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-109a143c5847fda449ad9f8be378dcafada737efc0de3a7eeffbde60306c5e613</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904,79111</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1322916$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10667904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MAMMEN-TOBIN, A</creatorcontrib><creatorcontrib>MONTEIRO, E. F</creatorcontrib><title>Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy</title><title>International journal of STD & AIDS</title><addtitle>Int J STD AIDS</addtitle><description>There has been a dramatic decline in the prevalence of opportunistic infections, particularly Pneumocystis carinii pneumonia (PCP) since the introduction of highly active antiretroviral therapy (HAART). Recently published short-term observational data now support the view that primary and possibly secondary PCP prophylaxis should be discontinued following sustained immune restoration afforded by HAART. Weverling and colleagues studied 378 patients with advanced HIV on HAART. Primary and secondary PCP prophylaxis was discontinued when the CD4 count had risen and remained above 200 for over 6 months and viral load was below 10,000 copies/ml. They encountered no episodes of PCP during a total 247 person-years of follow up. Furrer et al. showed the same result amongst 262 patients who stopped primary PCP prophylaxis over a median follow up of 11.3 months. The CD4 count was sustained above 200 for a minimum of 12 weeks in this study. We describe a case of acute PCP following withdrawal of primary prophylaxis despite an apparently excellent immunological and virological response to HAART.</description><subject>AIDS-Related Opportunistic Infections - drug therapy</subject><subject>AIDS-Related Opportunistic Infections - immunology</subject><subject>AIDS-Related Opportunistic Infections - prevention & control</subject><subject>AIDS/HIV</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Anti-Infective Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>CD4 Lymphocyte Count</subject><subject>Human immunodeficiency virus</subject><subject>Human mycoses</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mycoses</subject><subject>Mycoses of the respiratory system</subject><subject>Pneumocystis carinii</subject><subject>Pneumonia, Pneumocystis - drug therapy</subject><subject>Pneumonia, Pneumocystis - prevention & control</subject><subject>Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>0956-4624</issn><issn>1758-1052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkc2LFDEQxYMo7rh69yRBxFtrpTuddI6y-AULetBzU5OuzGTpSdqke9cG_3izzsDKgngqSP3qpV49xp4LeCPqtnsLplVS1QDCCNlB-4BthG67SkBbP2Sb23ZV-vKMPcn5CgBUo81jdiZAKW1Abtivr4GWQ7Rrnn3mFpMP3vPpz2PwyF0cx3jjw44PPtsYZh8WnH0MPDo-JX_AtJYap_064s8iMVCe_Ex873f7ceVoZ39NHMtgojnFa59w5POeEk7rU_bI4Zjp2ames-8f3n-7-FRdfvn4-eLdZWVlDXNxY1DIxrad1G5AKQ0OxnVbanQ3WHQ4oG40OQsDNaiJnNsOpKABZVtSojlnr4-6ZdEfC-W5PxQzNI4YKC6519AZZVr5X1BoqWstmwK-vAdexSWFYqKvQXVKQdcWCI6QTTHnRK4_HawX0N_m19_Pr4y8OOku2wMNfw0cAyvAqxOA2eLoEgbr8x3X1LURqmDVEcu4o7vd_vnvb_zZs4E</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>MAMMEN-TOBIN, A</creator><creator>MONTEIRO, E. F</creator><general>SAGE Publications</general><general>Royal Society of Medicine Press</general><general>Sage Publications Ltd</general><scope>IQODW</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20000101</creationdate><title>Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy</title><author>MAMMEN-TOBIN, A ; MONTEIRO, E. F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-109a143c5847fda449ad9f8be378dcafada737efc0de3a7eeffbde60306c5e613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>AIDS-Related Opportunistic Infections - drug therapy</topic><topic>AIDS-Related Opportunistic Infections - immunology</topic><topic>AIDS-Related Opportunistic Infections - prevention & control</topic><topic>AIDS/HIV</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Anti-Infective Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>CD4 Lymphocyte Count</topic><topic>Human immunodeficiency virus</topic><topic>Human mycoses</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mycoses</topic><topic>Mycoses of the respiratory system</topic><topic>Pneumocystis carinii</topic><topic>Pneumonia, Pneumocystis - drug therapy</topic><topic>Pneumonia, Pneumocystis - prevention & control</topic><topic>Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MAMMEN-TOBIN, A</creatorcontrib><creatorcontrib>MONTEIRO, E. F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Journals (ProQuest)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of STD & AIDS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MAMMEN-TOBIN, A</au><au>MONTEIRO, E. F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy</atitle><jtitle>International journal of STD & AIDS</jtitle><addtitle>Int J STD AIDS</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>11</volume><issue>1</issue><spage>64</spage><epage>65</epage><pages>64-65</pages><issn>0956-4624</issn><eissn>1758-1052</eissn><coden>INSAE3</coden><abstract>There has been a dramatic decline in the prevalence of opportunistic infections, particularly Pneumocystis carinii pneumonia (PCP) since the introduction of highly active antiretroviral therapy (HAART). Recently published short-term observational data now support the view that primary and possibly secondary PCP prophylaxis should be discontinued following sustained immune restoration afforded by HAART. Weverling and colleagues studied 378 patients with advanced HIV on HAART. Primary and secondary PCP prophylaxis was discontinued when the CD4 count had risen and remained above 200 for over 6 months and viral load was below 10,000 copies/ml. They encountered no episodes of PCP during a total 247 person-years of follow up. Furrer et al. showed the same result amongst 262 patients who stopped primary PCP prophylaxis over a median follow up of 11.3 months. The CD4 count was sustained above 200 for a minimum of 12 weeks in this study. We describe a case of acute PCP following withdrawal of primary prophylaxis despite an apparently excellent immunological and virological response to HAART.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>10667904</pmid><doi>10.1258/0956462001914805</doi><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0956-4624 |
ispartof | International journal of STD & AIDS, 2000-01, Vol.11 (1), p.64-65 |
issn | 0956-4624 1758-1052 |
language | eng |
recordid | cdi_proquest_miscellaneous_70896954 |
source | SAGE |
subjects | AIDS-Related Opportunistic Infections - drug therapy AIDS-Related Opportunistic Infections - immunology AIDS-Related Opportunistic Infections - prevention & control AIDS/HIV Anti-HIV Agents - therapeutic use Anti-Infective Agents - therapeutic use Biological and medical sciences CD4 Lymphocyte Count Human immunodeficiency virus Human mycoses Human viral diseases Humans Infectious diseases Male Medical sciences Middle Aged Mycoses Mycoses of the respiratory system Pneumocystis carinii Pneumonia, Pneumocystis - drug therapy Pneumonia, Pneumocystis - prevention & control Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | Pneumocystis carinii pneumonia following discontinuation of primary prophylaxis despite highly active antiretroviral therapy |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T00%3A22%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pneumocystis%20carinii%20pneumonia%20following%20discontinuation%20of%20primary%20prophylaxis%20despite%20highly%20active%20antiretroviral%20therapy&rft.jtitle=International%20journal%20of%20STD%20&%20AIDS&rft.au=MAMMEN-TOBIN,%20A&rft.date=2000-01-01&rft.volume=11&rft.issue=1&rft.spage=64&rft.epage=65&rft.pages=64-65&rft.issn=0956-4624&rft.eissn=1758-1052&rft.coden=INSAE3&rft_id=info:doi/10.1258/0956462001914805&rft_dat=%3Cproquest_cross%3E70896954%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c420t-109a143c5847fda449ad9f8be378dcafada737efc0de3a7eeffbde60306c5e613%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=206866085&rft_id=info:pmid/10667904&rft_sage_id=10.1258_0956462001914805&rfr_iscdi=true |