Iatrogenic hypercortisolism complicating triamcinolone acetonide injections in patients with HIV on ritonavir-boosted protease inhibitors
Epidural corticosteroid injection is a commonly used approach for managing back pain of several etiologies. The risk of clinical complications from systemic absorption is felt to be rare. Ritonavir is a protease inhibitor whose potent cytochrome P450 3A4 inhibition is exploited for pharmacologic boo...
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Veröffentlicht in: | Pain physician 2012-11, Vol.15 (6), p.489-493 |
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description | Epidural corticosteroid injection is a commonly used approach for managing back pain of several etiologies. The risk of clinical complications from systemic absorption is felt to be rare. Ritonavir is a protease inhibitor whose potent cytochrome P450 3A4 inhibition is exploited for pharmacologic boosting in human immunodeficiency virus (HIV) infection. It has been associated with systemic hypercortisolism when used in combination with nasal and inhaled corticosteroids. This is a case series describing 2 patients with HIV on ritonavir-containing regimens who developed iatrogenic hypercortisolism following epidural injection of triamcinolone acetonide. The 2 patients developed cushingoid symptoms, with detectable serum triamcinolone acetonide levels weeks after their epidural injections. Their symptoms took several weeks to resolve, in one case necessitating a change to an HIV regimen that did not contain ritonavir. Iatrogenic hypercortisolism is a rarely reported, but potentially devastating complication of injectable corticosteroids. Individuals receiving ritonavir-based therapy appear to be at increased risk for this process due to pharmacologic boosting of the corticosteroid. The preponderance of reported cases of iatrogenic hypercortisolism following injectable corticosteroids has involved triamcinolone acetonide, which may be due to the relatively rapid absorption characteristics and high serum levels of this compound compared with other preparations. For individuals on ritonavir-containing HIV therapy, we recommend close coordination with the involved HIV clinicians prior to use of injectable corticosteroids, and avoidance of injections with triamcinolone acetonide whenever possible. Choosing an alternative corticosteroid preparation to triamcinolone acetonide may reduce the risk of systemic absorption, though more research is needed to confirm this hypothesis. |
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The risk of clinical complications from systemic absorption is felt to be rare. Ritonavir is a protease inhibitor whose potent cytochrome P450 3A4 inhibition is exploited for pharmacologic boosting in human immunodeficiency virus (HIV) infection. It has been associated with systemic hypercortisolism when used in combination with nasal and inhaled corticosteroids. This is a case series describing 2 patients with HIV on ritonavir-containing regimens who developed iatrogenic hypercortisolism following epidural injection of triamcinolone acetonide. The 2 patients developed cushingoid symptoms, with detectable serum triamcinolone acetonide levels weeks after their epidural injections. Their symptoms took several weeks to resolve, in one case necessitating a change to an HIV regimen that did not contain ritonavir. Iatrogenic hypercortisolism is a rarely reported, but potentially devastating complication of injectable corticosteroids. Individuals receiving ritonavir-based therapy appear to be at increased risk for this process due to pharmacologic boosting of the corticosteroid. The preponderance of reported cases of iatrogenic hypercortisolism following injectable corticosteroids has involved triamcinolone acetonide, which may be due to the relatively rapid absorption characteristics and high serum levels of this compound compared with other preparations. For individuals on ritonavir-containing HIV therapy, we recommend close coordination with the involved HIV clinicians prior to use of injectable corticosteroids, and avoidance of injections with triamcinolone acetonide whenever possible. Choosing an alternative corticosteroid preparation to triamcinolone acetonide may reduce the risk of systemic absorption, though more research is needed to confirm this hypothesis.</description><identifier>ISSN: 1533-3159</identifier><identifier>EISSN: 2150-1149</identifier><identifier>DOI: 10.36076/ppj.2012/15/489</identifier><identifier>PMID: 23159966</identifier><language>eng</language><publisher>United States: American Society of Interventional Pain Physician</publisher><subject>Adult ; Back Pain - drug therapy ; Case reports ; Cushing Syndrome - chemically induced ; Drug Interactions ; Epidural ; Female ; Glucocorticoids - administration & dosage ; Glucocorticoids - adverse effects ; HIV ; HIV Infections - drug therapy ; HIV Protease Inhibitors - therapeutic use ; Human immunodeficiency virus ; Humans ; Iatrogenesis ; Iatrogenic Disease ; Injections, Epidural ; Male ; Middle Aged ; Ritonavir - therapeutic use ; Steroids ; Triamcinolone Acetonide - administration & dosage ; Triamcinolone Acetonide - adverse effects</subject><ispartof>Pain physician, 2012-11, Vol.15 (6), p.489-493</ispartof><rights>2012. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-7d0191fa8b895171f679ace0b86fe1fa9902f286304f34b692f2ebc0a9762e4c3</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/23159966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fessler, David</creatorcontrib><creatorcontrib>Beach, Jennifer</creatorcontrib><creatorcontrib>Keel, John</creatorcontrib><creatorcontrib>Stead, Wendy</creatorcontrib><title>Iatrogenic hypercortisolism complicating triamcinolone acetonide injections in patients with HIV on ritonavir-boosted protease inhibitors</title><title>Pain physician</title><addtitle>Pain Physician</addtitle><description>Epidural corticosteroid injection is a commonly used approach for managing back pain of several etiologies. The risk of clinical complications from systemic absorption is felt to be rare. Ritonavir is a protease inhibitor whose potent cytochrome P450 3A4 inhibition is exploited for pharmacologic boosting in human immunodeficiency virus (HIV) infection. It has been associated with systemic hypercortisolism when used in combination with nasal and inhaled corticosteroids. This is a case series describing 2 patients with HIV on ritonavir-containing regimens who developed iatrogenic hypercortisolism following epidural injection of triamcinolone acetonide. The 2 patients developed cushingoid symptoms, with detectable serum triamcinolone acetonide levels weeks after their epidural injections. Their symptoms took several weeks to resolve, in one case necessitating a change to an HIV regimen that did not contain ritonavir. Iatrogenic hypercortisolism is a rarely reported, but potentially devastating complication of injectable corticosteroids. Individuals receiving ritonavir-based therapy appear to be at increased risk for this process due to pharmacologic boosting of the corticosteroid. The preponderance of reported cases of iatrogenic hypercortisolism following injectable corticosteroids has involved triamcinolone acetonide, which may be due to the relatively rapid absorption characteristics and high serum levels of this compound compared with other preparations. For individuals on ritonavir-containing HIV therapy, we recommend close coordination with the involved HIV clinicians prior to use of injectable corticosteroids, and avoidance of injections with triamcinolone acetonide whenever possible. Choosing an alternative corticosteroid preparation to triamcinolone acetonide may reduce the risk of systemic absorption, though more research is needed to confirm this hypothesis.</description><subject>Adult</subject><subject>Back Pain - drug therapy</subject><subject>Case reports</subject><subject>Cushing Syndrome - chemically induced</subject><subject>Drug Interactions</subject><subject>Epidural</subject><subject>Female</subject><subject>Glucocorticoids - administration & dosage</subject><subject>Glucocorticoids - adverse effects</subject><subject>HIV</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Protease Inhibitors - therapeutic use</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Iatrogenesis</subject><subject>Iatrogenic Disease</subject><subject>Injections, Epidural</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Ritonavir - therapeutic use</subject><subject>Steroids</subject><subject>Triamcinolone Acetonide - administration & dosage</subject><subject>Triamcinolone Acetonide - adverse effects</subject><issn>1533-3159</issn><issn>2150-1149</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkctOwzAQRS0EgvLYs0KW2LAJ9SNx4iVCQCshsQG2luNOWleJHWwXxCfw17i8Fqw8njl3dDUXoVNKLrkgtZiO4_qSEcqmtJqWjdxBE0YrUlBayl00oRXnBaeVPECHMa4J4UJKvo8O2LYphZigj7lOwS_BWYNX7yME40Oy0fc2Dtj4Yeyt0cm6JU7B6sFY53vvAGsDyTu7AGzdGkyy3sVc4jHD4FLEbzat8Gz-jL3DwWZWv9pQtN7HBAs8Bp9Ax616Zds8DvEY7XW6j3Dy8x6hp9ubx-tZcf9wN7--ui9Mdp-KekGopJ1u2kZWtKadqGU2Q9pGdJD7UhLWsUZwUna8bIXMP2gN0bIWDErDj9DF997s4WUDManBRgN9rx34TVSU1o1oakZ4Rs__oWu_CS67U0xUgpB8xy1FvikTfIwBOjUGO-jwrihRXzGpHJPaxqRopXJMWXL2s3jTDrD4E_zmwj8BNoGRzQ</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Fessler, David</creator><creator>Beach, Jennifer</creator><creator>Keel, John</creator><creator>Stead, Wendy</creator><general>American Society of Interventional Pain Physician</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20121101</creationdate><title>Iatrogenic hypercortisolism complicating triamcinolone acetonide injections in patients with HIV on ritonavir-boosted protease inhibitors</title><author>Fessler, David ; Beach, Jennifer ; Keel, John ; Stead, Wendy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-7d0191fa8b895171f679ace0b86fe1fa9902f286304f34b692f2ebc0a9762e4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Back Pain - drug therapy</topic><topic>Case reports</topic><topic>Cushing Syndrome - chemically induced</topic><topic>Drug Interactions</topic><topic>Epidural</topic><topic>Female</topic><topic>Glucocorticoids - administration & dosage</topic><topic>Glucocorticoids - adverse effects</topic><topic>HIV</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Protease Inhibitors - therapeutic use</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Iatrogenesis</topic><topic>Iatrogenic Disease</topic><topic>Injections, Epidural</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Ritonavir - therapeutic use</topic><topic>Steroids</topic><topic>Triamcinolone Acetonide - administration & dosage</topic><topic>Triamcinolone Acetonide - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fessler, David</creatorcontrib><creatorcontrib>Beach, Jennifer</creatorcontrib><creatorcontrib>Keel, John</creatorcontrib><creatorcontrib>Stead, Wendy</creatorcontrib><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>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</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 Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pain physician</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fessler, David</au><au>Beach, Jennifer</au><au>Keel, John</au><au>Stead, Wendy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iatrogenic hypercortisolism complicating triamcinolone acetonide injections in patients with HIV on ritonavir-boosted protease inhibitors</atitle><jtitle>Pain physician</jtitle><addtitle>Pain Physician</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>15</volume><issue>6</issue><spage>489</spage><epage>493</epage><pages>489-493</pages><issn>1533-3159</issn><eissn>2150-1149</eissn><abstract>Epidural corticosteroid injection is a commonly used approach for managing back pain of several etiologies. The risk of clinical complications from systemic absorption is felt to be rare. Ritonavir is a protease inhibitor whose potent cytochrome P450 3A4 inhibition is exploited for pharmacologic boosting in human immunodeficiency virus (HIV) infection. It has been associated with systemic hypercortisolism when used in combination with nasal and inhaled corticosteroids. This is a case series describing 2 patients with HIV on ritonavir-containing regimens who developed iatrogenic hypercortisolism following epidural injection of triamcinolone acetonide. The 2 patients developed cushingoid symptoms, with detectable serum triamcinolone acetonide levels weeks after their epidural injections. Their symptoms took several weeks to resolve, in one case necessitating a change to an HIV regimen that did not contain ritonavir. Iatrogenic hypercortisolism is a rarely reported, but potentially devastating complication of injectable corticosteroids. Individuals receiving ritonavir-based therapy appear to be at increased risk for this process due to pharmacologic boosting of the corticosteroid. The preponderance of reported cases of iatrogenic hypercortisolism following injectable corticosteroids has involved triamcinolone acetonide, which may be due to the relatively rapid absorption characteristics and high serum levels of this compound compared with other preparations. For individuals on ritonavir-containing HIV therapy, we recommend close coordination with the involved HIV clinicians prior to use of injectable corticosteroids, and avoidance of injections with triamcinolone acetonide whenever possible. Choosing an alternative corticosteroid preparation to triamcinolone acetonide may reduce the risk of systemic absorption, though more research is needed to confirm this hypothesis.</abstract><cop>United States</cop><pub>American Society of Interventional Pain Physician</pub><pmid>23159966</pmid><doi>10.36076/ppj.2012/15/489</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Back Pain - drug therapy Case reports Cushing Syndrome - chemically induced Drug Interactions Epidural Female Glucocorticoids - administration & dosage Glucocorticoids - adverse effects HIV HIV Infections - drug therapy HIV Protease Inhibitors - therapeutic use Human immunodeficiency virus Humans Iatrogenesis Iatrogenic Disease Injections, Epidural Male Middle Aged Ritonavir - therapeutic use Steroids Triamcinolone Acetonide - administration & dosage Triamcinolone Acetonide - adverse effects |
title | Iatrogenic hypercortisolism complicating triamcinolone acetonide injections in patients with HIV on ritonavir-boosted protease inhibitors |
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