Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia
Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appe...
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Veröffentlicht in: | Southern medical journal (Birmingham, Ala.) Ala.), 1978-07, Vol.71 (7), p.858-859 |
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creator | McDonald, C R Eichner, E R |
description | Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appear ill upon initial presentation but rapidly developed disseminated intravascular coagulation and died. |
doi_str_mv | 10.1097/00007611-197807000-00032 |
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A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appear ill upon initial presentation but rapidly developed disseminated intravascular coagulation and died.</description><identifier>ISSN: 0038-4348</identifier><identifier>DOI: 10.1097/00007611-197807000-00032</identifier><identifier>PMID: 663736</identifier><language>eng</language><publisher>United States</publisher><subject>Adolescent ; Anemia, Sickle Cell - complications ; Anemia, Sickle Cell - immunology ; Disseminated Intravascular Coagulation - complications ; Humans ; Male ; Pneumococcal Infections - complications ; Sepsis - complications ; Sepsis - etiology</subject><ispartof>Southern medical journal (Birmingham, Ala.), 1978-07, Vol.71 (7), p.858-859</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c224t-db49b587763e1249fa6f036fd0335a689752441afadbb1c8d9b9c5f51dfbd67d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/663736$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McDonald, C R</creatorcontrib><creatorcontrib>Eichner, E R</creatorcontrib><title>Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia</title><title>Southern medical journal (Birmingham, Ala.)</title><addtitle>South Med J</addtitle><description>Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appear ill upon initial presentation but rapidly developed disseminated intravascular coagulation and died.</description><subject>Adolescent</subject><subject>Anemia, Sickle Cell - complications</subject><subject>Anemia, Sickle Cell - immunology</subject><subject>Disseminated Intravascular Coagulation - complications</subject><subject>Humans</subject><subject>Male</subject><subject>Pneumococcal Infections - complications</subject><subject>Sepsis - complications</subject><subject>Sepsis - etiology</subject><issn>0038-4348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMlOwzAQhn1gK4U34OATpwbs2PFyRBWbVIkLnC3HCzIkcbETJN4eh5aONJoZ6f_H4w8AiNENRpLfohKcYVxhyQXiZapKkvoILEoRFSVUnIHznD9mYSPYKThhjHDCFkCv42CmlNwwwm0KvU4_cDu4qY8mGuP6oFfQhpxLN-jRWRiGMelvnc3U6QRN1O-lGUMcVlAPFuZgPjsHjeu6Ms_-C3DsdZfd5b4uwdvD_ev6qdq8PD6v7zaVqWs6Vralsm0E54w4XFPpNfOIMG8RIY1mQvKmphRrr23bYiOsbKVpfIOtby3jlizB9W7vNsWvyeVR9SHPd5Qz4pQVp6iWlKEiFDuhSTHn5Lzaf1xhpGag6h-oOgBVf0CL9Wr_xtT2zh6MO5rkF_S8dPw</recordid><startdate>197807</startdate><enddate>197807</enddate><creator>McDonald, C R</creator><creator>Eichner, E R</creator><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>7X8</scope></search><sort><creationdate>197807</creationdate><title>Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia</title><author>McDonald, C R ; Eichner, E R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c224t-db49b587763e1249fa6f036fd0335a689752441afadbb1c8d9b9c5f51dfbd67d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><topic>Adolescent</topic><topic>Anemia, Sickle Cell - complications</topic><topic>Anemia, Sickle Cell - immunology</topic><topic>Disseminated Intravascular Coagulation - complications</topic><topic>Humans</topic><topic>Male</topic><topic>Pneumococcal Infections - complications</topic><topic>Sepsis - complications</topic><topic>Sepsis - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McDonald, C R</creatorcontrib><creatorcontrib>Eichner, E R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Southern medical journal (Birmingham, Ala.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McDonald, C R</au><au>Eichner, E R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia</atitle><jtitle>Southern medical journal (Birmingham, Ala.)</jtitle><addtitle>South Med J</addtitle><date>1978-07</date><risdate>1978</risdate><volume>71</volume><issue>7</issue><spage>858</spage><epage>859</epage><pages>858-859</pages><issn>0038-4348</issn><abstract>Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appear ill upon initial presentation but rapidly developed disseminated intravascular coagulation and died.</abstract><cop>United States</cop><pmid>663736</pmid><doi>10.1097/00007611-197807000-00032</doi><tpages>2</tpages></addata></record> |
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subjects | Adolescent Anemia, Sickle Cell - complications Anemia, Sickle Cell - immunology Disseminated Intravascular Coagulation - complications Humans Male Pneumococcal Infections - complications Sepsis - complications Sepsis - etiology |
title | Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia |
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