Intraocular Penetration of Systemic Antibiotics in Eyes with Penetrating Ocular Injury
To determine whether penetrating scleral or corneal injury can enhance intraocular penetration of systemic moxifloxacin, vancomycin, and ceftazidime. Thirty rabbits were divided into 3 groups for each antibiotic and then further subdivided to receive either scleral or corneal injury to the right eye...
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Veröffentlicht in: | Journal of ocular pharmacology and therapeutics 2014-12, Vol.30 (10), p.823-830 |
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creator | AHMED, Shareef KURUVILLA, Oscar CHIN YEE, David AGGARWAL, Himanshu YUE LI EDWARDS, Paul XIAOXI QIAO HUA GAO |
description | To determine whether penetrating scleral or corneal injury can enhance intraocular penetration of systemic moxifloxacin, vancomycin, and ceftazidime.
Thirty rabbits were divided into 3 groups for each antibiotic and then further subdivided to receive either scleral or corneal injury to the right eye. The left eye served as a control. Intravenous antibiotics were given following injury, and eyes were subsequently enucleated. Vitreous antibiotic concentration was determined by high-performance liquid chromatography analysis. Plasma concentration was measured for comparison.
Intravitreal moxifloxacin concentration was unchanged by injury. Minimum inhibitory concentration (MIC90) was achieved in the vitreous against the most common gram-positive endophthalmitis-causing organisms. Intravitreal vancomycin levels were not enhanced by injury and did not reach the MIC90 for gram-positive organisms commonly causing intraocular infection. Intravitreal ceftazidime was increased in the injured eyes, 67% and 73% higher in scleral and corneal injury eyes. It reached MIC90 of many gram-negative bacteria.
Intravitreal antibiotic penetration of systemic antibiotics with or without penetrating ocular injury varies depending on the antibiotic. For prevention or treatment of gram-positive-bacteria-causing endophthalmitis, intravitreal vancomycin is necessary and provides the most reliable coverage. Systemic ceftazidime can be used for many gram-negative bacteria, but intravitreal injection is recommended for better coverage, especially for more-potent organisms. Systemic moxifloxacin can be considered for most gram-positive and -negative infections due to its excellent intraocular penetration and broad coverage, but the patient's previous history of its topical use and increasing resistance patterns must be considered. |
doi_str_mv | 10.1089/jop.2014.0056 |
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Thirty rabbits were divided into 3 groups for each antibiotic and then further subdivided to receive either scleral or corneal injury to the right eye. The left eye served as a control. Intravenous antibiotics were given following injury, and eyes were subsequently enucleated. Vitreous antibiotic concentration was determined by high-performance liquid chromatography analysis. Plasma concentration was measured for comparison.
Intravitreal moxifloxacin concentration was unchanged by injury. Minimum inhibitory concentration (MIC90) was achieved in the vitreous against the most common gram-positive endophthalmitis-causing organisms. Intravitreal vancomycin levels were not enhanced by injury and did not reach the MIC90 for gram-positive organisms commonly causing intraocular infection. Intravitreal ceftazidime was increased in the injured eyes, 67% and 73% higher in scleral and corneal injury eyes. It reached MIC90 of many gram-negative bacteria.
Intravitreal antibiotic penetration of systemic antibiotics with or without penetrating ocular injury varies depending on the antibiotic. For prevention or treatment of gram-positive-bacteria-causing endophthalmitis, intravitreal vancomycin is necessary and provides the most reliable coverage. Systemic ceftazidime can be used for many gram-negative bacteria, but intravitreal injection is recommended for better coverage, especially for more-potent organisms. Systemic moxifloxacin can be considered for most gram-positive and -negative infections due to its excellent intraocular penetration and broad coverage, but the patient's previous history of its topical use and increasing resistance patterns must be considered.</description><identifier>ISSN: 1080-7683</identifier><identifier>EISSN: 1557-7732</identifier><identifier>DOI: 10.1089/jop.2014.0056</identifier><identifier>PMID: 25167230</identifier><language>eng</language><publisher>Larchmont, NY: Liebert</publisher><subject><![CDATA[Animals ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - pharmacokinetics ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Ceftazidime - administration & dosage ; Ceftazidime - pharmacology ; Corneal Injuries - drug therapy ; Corneal Injuries - metabolism ; Corneal Injuries - microbiology ; Endophthalmitis - microbiology ; Endophthalmitis - prevention & control ; Eye Injuries, Penetrating - drug therapy ; Eye Injuries, Penetrating - metabolism ; Eye Injuries, Penetrating - microbiology ; Eye Injuries, Penetrating - pathology ; Fluoroquinolones - administration & dosage ; Fluoroquinolones - pharmacokinetics ; Gram-Positive Bacterial Infections - prevention & control ; Intravitreal Injections ; Medical sciences ; Pharmacology. Drug treatments ; Rabbits ; Sclera - injuries ; Sclera - metabolism ; Sclera - microbiology ; Vancomycin - administration & dosage ; Vancomycin - pharmacokinetics ; Vitreous Body - metabolism]]></subject><ispartof>Journal of ocular pharmacology and therapeutics, 2014-12, Vol.30 (10), p.823-830</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-2b48caef6229e7d95a927ce20e08c09129ef7782a8f6257649a5eb53c716ed643</citedby><cites>FETCH-LOGICAL-c323t-2b48caef6229e7d95a927ce20e08c09129ef7782a8f6257649a5eb53c716ed643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=29062853$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25167230$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>AHMED, Shareef</creatorcontrib><creatorcontrib>KURUVILLA, Oscar</creatorcontrib><creatorcontrib>CHIN YEE, David</creatorcontrib><creatorcontrib>AGGARWAL, Himanshu</creatorcontrib><creatorcontrib>YUE LI</creatorcontrib><creatorcontrib>EDWARDS, Paul</creatorcontrib><creatorcontrib>XIAOXI QIAO</creatorcontrib><creatorcontrib>HUA GAO</creatorcontrib><title>Intraocular Penetration of Systemic Antibiotics in Eyes with Penetrating Ocular Injury</title><title>Journal of ocular pharmacology and therapeutics</title><addtitle>J Ocul Pharmacol Ther</addtitle><description>To determine whether penetrating scleral or corneal injury can enhance intraocular penetration of systemic moxifloxacin, vancomycin, and ceftazidime.
Thirty rabbits were divided into 3 groups for each antibiotic and then further subdivided to receive either scleral or corneal injury to the right eye. The left eye served as a control. Intravenous antibiotics were given following injury, and eyes were subsequently enucleated. Vitreous antibiotic concentration was determined by high-performance liquid chromatography analysis. Plasma concentration was measured for comparison.
Intravitreal moxifloxacin concentration was unchanged by injury. Minimum inhibitory concentration (MIC90) was achieved in the vitreous against the most common gram-positive endophthalmitis-causing organisms. Intravitreal vancomycin levels were not enhanced by injury and did not reach the MIC90 for gram-positive organisms commonly causing intraocular infection. Intravitreal ceftazidime was increased in the injured eyes, 67% and 73% higher in scleral and corneal injury eyes. It reached MIC90 of many gram-negative bacteria.
Intravitreal antibiotic penetration of systemic antibiotics with or without penetrating ocular injury varies depending on the antibiotic. For prevention or treatment of gram-positive-bacteria-causing endophthalmitis, intravitreal vancomycin is necessary and provides the most reliable coverage. Systemic ceftazidime can be used for many gram-negative bacteria, but intravitreal injection is recommended for better coverage, especially for more-potent organisms. Systemic moxifloxacin can be considered for most gram-positive and -negative infections due to its excellent intraocular penetration and broad coverage, but the patient's previous history of its topical use and increasing resistance patterns must be considered.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Biological and medical sciences</subject><subject>Ceftazidime - administration & dosage</subject><subject>Ceftazidime - pharmacology</subject><subject>Corneal Injuries - drug therapy</subject><subject>Corneal Injuries - metabolism</subject><subject>Corneal Injuries - microbiology</subject><subject>Endophthalmitis - microbiology</subject><subject>Endophthalmitis - prevention & control</subject><subject>Eye Injuries, Penetrating - drug therapy</subject><subject>Eye Injuries, Penetrating - metabolism</subject><subject>Eye Injuries, Penetrating - microbiology</subject><subject>Eye Injuries, Penetrating - pathology</subject><subject>Fluoroquinolones - administration & dosage</subject><subject>Fluoroquinolones - pharmacokinetics</subject><subject>Gram-Positive Bacterial Infections - prevention & control</subject><subject>Intravitreal Injections</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Rabbits</subject><subject>Sclera - injuries</subject><subject>Sclera - metabolism</subject><subject>Sclera - microbiology</subject><subject>Vancomycin - administration & dosage</subject><subject>Vancomycin - pharmacokinetics</subject><subject>Vitreous Body - metabolism</subject><issn>1080-7683</issn><issn>1557-7732</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkD1PwzAQhi0EoqUwsqIsSCwpZzv-yFhVBSpVKhIfq-W4DrhKnWInQvn3JGqB6e5ePfcOD0LXGKYYZH6_rfdTAjibAjB-gsaYMZEKQclpv4OEVHBJR-gixi0ApsDxORoRhrkgFMbofemboGvTVjokz9bb_mpc7ZO6TF662NidM8nMN65wdeNMTJxPFp2NybdrPv8f_EeyPnQs_bYN3SU6K3UV7dVxTtDbw-J1_pSu1o_L-WyVGkpok5Iik0bbkhOSW7HJmc6JMJaABWkgx31aCiGJlj3CBM9yzWzBqBGY2w3P6ATdHXr3of5qbWzUzkVjq0p7W7dRYU4zMhiAHk0PqAl1jMGWah_cTodOYVCDStWrVINKNajs-ZtjdVvs7OaP_nXXA7dHQEejqzJob1z853LgRDJKfwCuhnw2</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>AHMED, Shareef</creator><creator>KURUVILLA, Oscar</creator><creator>CHIN YEE, David</creator><creator>AGGARWAL, Himanshu</creator><creator>YUE LI</creator><creator>EDWARDS, Paul</creator><creator>XIAOXI QIAO</creator><creator>HUA GAO</creator><general>Liebert</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>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Intraocular Penetration of Systemic Antibiotics in Eyes with Penetrating Ocular Injury</title><author>AHMED, Shareef ; KURUVILLA, Oscar ; CHIN YEE, David ; AGGARWAL, Himanshu ; YUE LI ; EDWARDS, Paul ; XIAOXI QIAO ; HUA GAO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-2b48caef6229e7d95a927ce20e08c09129ef7782a8f6257649a5eb53c716ed643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Biological and medical sciences</topic><topic>Ceftazidime - administration & dosage</topic><topic>Ceftazidime - pharmacology</topic><topic>Corneal Injuries - drug therapy</topic><topic>Corneal Injuries - metabolism</topic><topic>Corneal Injuries - microbiology</topic><topic>Endophthalmitis - microbiology</topic><topic>Endophthalmitis - prevention & control</topic><topic>Eye Injuries, Penetrating - drug therapy</topic><topic>Eye Injuries, Penetrating - metabolism</topic><topic>Eye Injuries, Penetrating - microbiology</topic><topic>Eye Injuries, Penetrating - pathology</topic><topic>Fluoroquinolones - administration & dosage</topic><topic>Fluoroquinolones - pharmacokinetics</topic><topic>Gram-Positive Bacterial Infections - prevention & control</topic><topic>Intravitreal Injections</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Sclera - injuries</topic><topic>Sclera - metabolism</topic><topic>Sclera - microbiology</topic><topic>Vancomycin - administration & dosage</topic><topic>Vancomycin - pharmacokinetics</topic><topic>Vitreous Body - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AHMED, Shareef</creatorcontrib><creatorcontrib>KURUVILLA, Oscar</creatorcontrib><creatorcontrib>CHIN YEE, David</creatorcontrib><creatorcontrib>AGGARWAL, Himanshu</creatorcontrib><creatorcontrib>YUE LI</creatorcontrib><creatorcontrib>EDWARDS, Paul</creatorcontrib><creatorcontrib>XIAOXI QIAO</creatorcontrib><creatorcontrib>HUA GAO</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>MEDLINE - Academic</collection><jtitle>Journal of ocular pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>AHMED, Shareef</au><au>KURUVILLA, Oscar</au><au>CHIN YEE, David</au><au>AGGARWAL, Himanshu</au><au>YUE LI</au><au>EDWARDS, Paul</au><au>XIAOXI QIAO</au><au>HUA GAO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraocular Penetration of Systemic Antibiotics in Eyes with Penetrating Ocular Injury</atitle><jtitle>Journal of ocular pharmacology and therapeutics</jtitle><addtitle>J Ocul Pharmacol Ther</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>30</volume><issue>10</issue><spage>823</spage><epage>830</epage><pages>823-830</pages><issn>1080-7683</issn><eissn>1557-7732</eissn><abstract>To determine whether penetrating scleral or corneal injury can enhance intraocular penetration of systemic moxifloxacin, vancomycin, and ceftazidime.
Thirty rabbits were divided into 3 groups for each antibiotic and then further subdivided to receive either scleral or corneal injury to the right eye. The left eye served as a control. Intravenous antibiotics were given following injury, and eyes were subsequently enucleated. Vitreous antibiotic concentration was determined by high-performance liquid chromatography analysis. Plasma concentration was measured for comparison.
Intravitreal moxifloxacin concentration was unchanged by injury. Minimum inhibitory concentration (MIC90) was achieved in the vitreous against the most common gram-positive endophthalmitis-causing organisms. Intravitreal vancomycin levels were not enhanced by injury and did not reach the MIC90 for gram-positive organisms commonly causing intraocular infection. Intravitreal ceftazidime was increased in the injured eyes, 67% and 73% higher in scleral and corneal injury eyes. It reached MIC90 of many gram-negative bacteria.
Intravitreal antibiotic penetration of systemic antibiotics with or without penetrating ocular injury varies depending on the antibiotic. For prevention or treatment of gram-positive-bacteria-causing endophthalmitis, intravitreal vancomycin is necessary and provides the most reliable coverage. Systemic ceftazidime can be used for many gram-negative bacteria, but intravitreal injection is recommended for better coverage, especially for more-potent organisms. Systemic moxifloxacin can be considered for most gram-positive and -negative infections due to its excellent intraocular penetration and broad coverage, but the patient's previous history of its topical use and increasing resistance patterns must be considered.</abstract><cop>Larchmont, NY</cop><pub>Liebert</pub><pmid>25167230</pmid><doi>10.1089/jop.2014.0056</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - pharmacokinetics Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Ceftazidime - administration & dosage Ceftazidime - pharmacology Corneal Injuries - drug therapy Corneal Injuries - metabolism Corneal Injuries - microbiology Endophthalmitis - microbiology Endophthalmitis - prevention & control Eye Injuries, Penetrating - drug therapy Eye Injuries, Penetrating - metabolism Eye Injuries, Penetrating - microbiology Eye Injuries, Penetrating - pathology Fluoroquinolones - administration & dosage Fluoroquinolones - pharmacokinetics Gram-Positive Bacterial Infections - prevention & control Intravitreal Injections Medical sciences Pharmacology. Drug treatments Rabbits Sclera - injuries Sclera - metabolism Sclera - microbiology Vancomycin - administration & dosage Vancomycin - pharmacokinetics Vitreous Body - metabolism |
title | Intraocular Penetration of Systemic Antibiotics in Eyes with Penetrating Ocular Injury |
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