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The pharmacokinetics of ketoconazole in severely immunocompromised patients
Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics,...
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Published in: | Journal of antimicrobial chemotherapy 1982-12, Vol.10 (6), p.489-496 |
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container_end_page | 496 |
container_issue | 6 |
container_start_page | 489 |
container_title | Journal of antimicrobial chemotherapy |
container_volume | 10 |
creator | Hann, I. M. Prentice, H. G. Keaney, M. Corringham, R. Blacklock, H. A. Fox, J. Gascoigne, E. Van Custem, J. |
description | Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics, skin antisepsis, sterile food and oral co-trimoxazole. Mean (±S.D.) peak serum ketoconazole levels of 5·14±1·4 mg/l occurred 3 h after drug intake. In patients not receiving an allogeneic bone marrow transplant (BMT), the mean serum level at 2 h post-dose remained in the range of 3 to 5 mg/l during prolonged therapy. In contrast, serum ketoconazole levels in allogeneic BMT patients declined during continued treatment. In addition, the incidence of fungal infections was significantly higher in allogeneic-BMT patients than in the other group (P |
doi_str_mv | 10.1093/jac/10.6.489 |
format | article |
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In contrast, serum ketoconazole levels in allogeneic BMT patients declined during continued treatment. In addition, the incidence of fungal infections was significantly higher in allogeneic-BMT patients than in the other group (P<0·005).</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/10.6.489</identifier><identifier>PMID: 6298171</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; Antifungal Agents - metabolism ; Bone Marrow Transplantation ; Female ; Humans ; Imidazoles - metabolism ; Immune Tolerance ; Ketoconazole ; Kinetics ; Leukemia - immunology ; Leukemia - metabolism ; Male ; Piperazines - metabolism</subject><ispartof>Journal of antimicrobial chemotherapy, 1982-12, Vol.10 (6), p.489-496</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c324t-37234e0fe312d08efeea5d02d9fe6a2b6ca6a9e0a534e5973a5c24d4ab890f623</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6298171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hann, I. M.</creatorcontrib><creatorcontrib>Prentice, H. G.</creatorcontrib><creatorcontrib>Keaney, M.</creatorcontrib><creatorcontrib>Corringham, R.</creatorcontrib><creatorcontrib>Blacklock, H. A.</creatorcontrib><creatorcontrib>Fox, J.</creatorcontrib><creatorcontrib>Gascoigne, E.</creatorcontrib><creatorcontrib>Van Custem, J.</creatorcontrib><title>The pharmacokinetics of ketoconazole in severely immunocompromised patients</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics, skin antisepsis, sterile food and oral co-trimoxazole. Mean (±S.D.) peak serum ketoconazole levels of 5·14±1·4 mg/l occurred 3 h after drug intake. In patients not receiving an allogeneic bone marrow transplant (BMT), the mean serum level at 2 h post-dose remained in the range of 3 to 5 mg/l during prolonged therapy. In contrast, serum ketoconazole levels in allogeneic BMT patients declined during continued treatment. In addition, the incidence of fungal infections was significantly higher in allogeneic-BMT patients than in the other group (P<0·005).</description><subject>Adult</subject><subject>Antifungal Agents - metabolism</subject><subject>Bone Marrow Transplantation</subject><subject>Female</subject><subject>Humans</subject><subject>Imidazoles - metabolism</subject><subject>Immune Tolerance</subject><subject>Ketoconazole</subject><subject>Kinetics</subject><subject>Leukemia - immunology</subject><subject>Leukemia - metabolism</subject><subject>Male</subject><subject>Piperazines - metabolism</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNo9kE1Lw0AURQdRaq3u3ApZuTLtfCezlKJWWhGhQnEzTCcvNG2SqZlErL_eKS1dvQvncHlchG4JHhKs2Ght7ChkOeSpOkN9wiWOKVbkHPUxwyJOuGCX6Mr7NcZYCpn2UE9SlZKE9NF0voJouzJNZazbFDW0hfWRy6MNtM662vy5EqKijjz8QAPlLiqqqqsDqraNqwoPWbQ1bQF166_RRW5KDzfHO0Cfz0_z8SSevb-8jh9nsWWUtzFLKOOAc2CEZjiFHMCIDNNM5SANXUprpFGAjQiaUAkzwlKecbNMFc4lZQN0f-gNH3x34Fsd_rBQlqYG13mdYqoE4WkQHw6ibZz3DeR62xSVaXaaYL3fToft9lnqsF3Q74693bKC7CQfxwo8PvDCt_B7wqbZaJmwROjJ4ktLtvh4mzIRwj-I-nsH</recordid><startdate>198212</startdate><enddate>198212</enddate><creator>Hann, I. 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G.</creatorcontrib><creatorcontrib>Keaney, M.</creatorcontrib><creatorcontrib>Corringham, R.</creatorcontrib><creatorcontrib>Blacklock, H. A.</creatorcontrib><creatorcontrib>Fox, J.</creatorcontrib><creatorcontrib>Gascoigne, E.</creatorcontrib><creatorcontrib>Van Custem, J.</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>MEDLINE - Academic</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hann, I. M.</au><au>Prentice, H. G.</au><au>Keaney, M.</au><au>Corringham, R.</au><au>Blacklock, H. A.</au><au>Fox, J.</au><au>Gascoigne, E.</au><au>Van Custem, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The pharmacokinetics of ketoconazole in severely immunocompromised patients</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>1982-12</date><risdate>1982</risdate><volume>10</volume><issue>6</issue><spage>489</spage><epage>496</epage><pages>489-496</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics, skin antisepsis, sterile food and oral co-trimoxazole. Mean (±S.D.) peak serum ketoconazole levels of 5·14±1·4 mg/l occurred 3 h after drug intake. In patients not receiving an allogeneic bone marrow transplant (BMT), the mean serum level at 2 h post-dose remained in the range of 3 to 5 mg/l during prolonged therapy. In contrast, serum ketoconazole levels in allogeneic BMT patients declined during continued treatment. In addition, the incidence of fungal infections was significantly higher in allogeneic-BMT patients than in the other group (P<0·005).</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>6298171</pmid><doi>10.1093/jac/10.6.489</doi><tpages>8</tpages></addata></record> |
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issn | 0305-7453 1460-2091 |
language | eng |
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source | Oxford University Press Archive |
subjects | Adult Antifungal Agents - metabolism Bone Marrow Transplantation Female Humans Imidazoles - metabolism Immune Tolerance Ketoconazole Kinetics Leukemia - immunology Leukemia - metabolism Male Piperazines - metabolism |
title | The pharmacokinetics of ketoconazole in severely immunocompromised patients |
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