The effect of diabetes and severe ischaemia on the penetration of ceftazidime into tissues of the limb

SUMMARY Aims  To determine the effect of diabetes and of different degrees of ischaemia on the penetration of ceftazidime into different tissues. Methods  Sixteen patients (10 with diabetes mellitus) undergoing lower extremity amputation for severe ischaemia (in 12 in combination with infection), re...

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Veröffentlicht in:Diabetic medicine 2001-03, Vol.18 (3), p.229-234
Hauptverfasser: Raymakers, J. T., Houben, A. J., Heyden, J. J. vd, Tordoir, J. H., Kitslaar, P. J., Schaper, N. C.
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container_end_page 234
container_issue 3
container_start_page 229
container_title Diabetic medicine
container_volume 18
creator Raymakers, J. T.
Houben, A. J.
Heyden, J. J. vd
Tordoir, J. H.
Kitslaar, P. J.
Schaper, N. C.
description SUMMARY Aims  To determine the effect of diabetes and of different degrees of ischaemia on the penetration of ceftazidime into different tissues. Methods  Sixteen patients (10 with diabetes mellitus) undergoing lower extremity amputation for severe ischaemia (in 12 in combination with infection), received 2000 mg ceftazidime intravenously as a bolus 30 min prior to the operation. Skin perfusion was determined by transcutaneous oxygen pressure measurements (TcPO2) on the dorsal side of the midfoot. After amputation bone, skin and muscle samples were obtained from the forefoot, midfoot and proximal tibia. Tissue and plasma concentrations were determined by HPLC. The tissue concentrations were corrected for blood contamination. Results  No differences were observed in skin, muscle or bone ceftazidime levels between diabetic and non‐diabetic patients. Multiple regression analysis suggested that tissue perfusion was a major determinant of skin and bone ceftazidime concentrations, predicting 40–47% of the ceftazidime concentrations at several biopsy sites. Conclusions  The present study suggests that tissue perfusion is the major determinant of the penetration of a third generation cephalosporin into the tissues of the ischaemic (diabetic) foot. Diabetes alone however, has no major effects upon this penetration.
doi_str_mv 10.1046/j.1464-5491.2001.00460.x
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T. ; Houben, A. J. ; Heyden, J. J. vd ; Tordoir, J. H. ; Kitslaar, P. J. ; Schaper, N. C.</creator><creatorcontrib>Raymakers, J. T. ; Houben, A. J. ; Heyden, J. J. vd ; Tordoir, J. H. ; Kitslaar, P. J. ; Schaper, N. C.</creatorcontrib><description>SUMMARY Aims  To determine the effect of diabetes and of different degrees of ischaemia on the penetration of ceftazidime into different tissues. Methods  Sixteen patients (10 with diabetes mellitus) undergoing lower extremity amputation for severe ischaemia (in 12 in combination with infection), received 2000 mg ceftazidime intravenously as a bolus 30 min prior to the operation. Skin perfusion was determined by transcutaneous oxygen pressure measurements (TcPO2) on the dorsal side of the midfoot. After amputation bone, skin and muscle samples were obtained from the forefoot, midfoot and proximal tibia. Tissue and plasma concentrations were determined by HPLC. The tissue concentrations were corrected for blood contamination. Results  No differences were observed in skin, muscle or bone ceftazidime levels between diabetic and non‐diabetic patients. Multiple regression analysis suggested that tissue perfusion was a major determinant of skin and bone ceftazidime concentrations, predicting 40–47% of the ceftazidime concentrations at several biopsy sites. Conclusions  The present study suggests that tissue perfusion is the major determinant of the penetration of a third generation cephalosporin into the tissues of the ischaemic (diabetic) foot. Diabetes alone however, has no major effects upon this penetration.</description><identifier>ISSN: 0742-3071</identifier><identifier>EISSN: 1464-5491</identifier><identifier>DOI: 10.1046/j.1464-5491.2001.00460.x</identifier><identifier>PMID: 11318845</identifier><identifier>CODEN: DIMEEV</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Aged ; Amputation ; antibiotic ; Associated diseases and complications ; Biological and medical sciences ; ceftazidime ; Ceftazidime - pharmacokinetics ; Cephalosporins - pharmacokinetics ; Diabetes Mellitus - physiopathology ; Diabetes. Impaired glucose tolerance ; Diabetic Angiopathies - physiopathology ; diabetic foot ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Gangrene - surgery ; Humans ; ischaemia ; Ischemia - physiopathology ; Leg - blood supply ; Leg - surgery ; Male ; Medical sciences ; penetration ; Peripheral Vascular Diseases - physiopathology ; Peripheral Vascular Diseases - surgery ; Tissue Distribution</subject><ispartof>Diabetic medicine, 2001-03, Vol.18 (3), p.229-234</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4300-b3fc33d1dcf12008f359a9404f1c7b2da63665c1f507aa661d6201bf5a28abd73</citedby><cites>FETCH-LOGICAL-c4300-b3fc33d1dcf12008f359a9404f1c7b2da63665c1f507aa661d6201bf5a28abd73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1464-5491.2001.00460.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1464-5491.2001.00460.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=972139$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11318845$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raymakers, J. T.</creatorcontrib><creatorcontrib>Houben, A. J.</creatorcontrib><creatorcontrib>Heyden, J. J. vd</creatorcontrib><creatorcontrib>Tordoir, J. H.</creatorcontrib><creatorcontrib>Kitslaar, P. J.</creatorcontrib><creatorcontrib>Schaper, N. C.</creatorcontrib><title>The effect of diabetes and severe ischaemia on the penetration of ceftazidime into tissues of the limb</title><title>Diabetic medicine</title><addtitle>Diabet Med</addtitle><description>SUMMARY Aims  To determine the effect of diabetes and of different degrees of ischaemia on the penetration of ceftazidime into different tissues. Methods  Sixteen patients (10 with diabetes mellitus) undergoing lower extremity amputation for severe ischaemia (in 12 in combination with infection), received 2000 mg ceftazidime intravenously as a bolus 30 min prior to the operation. Skin perfusion was determined by transcutaneous oxygen pressure measurements (TcPO2) on the dorsal side of the midfoot. After amputation bone, skin and muscle samples were obtained from the forefoot, midfoot and proximal tibia. Tissue and plasma concentrations were determined by HPLC. The tissue concentrations were corrected for blood contamination. Results  No differences were observed in skin, muscle or bone ceftazidime levels between diabetic and non‐diabetic patients. Multiple regression analysis suggested that tissue perfusion was a major determinant of skin and bone ceftazidime concentrations, predicting 40–47% of the ceftazidime concentrations at several biopsy sites. Conclusions  The present study suggests that tissue perfusion is the major determinant of the penetration of a third generation cephalosporin into the tissues of the ischaemic (diabetic) foot. Diabetes alone however, has no major effects upon this penetration.</description><subject>Aged</subject><subject>Amputation</subject><subject>antibiotic</subject><subject>Associated diseases and complications</subject><subject>Biological and medical sciences</subject><subject>ceftazidime</subject><subject>Ceftazidime - pharmacokinetics</subject><subject>Cephalosporins - pharmacokinetics</subject><subject>Diabetes Mellitus - physiopathology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic Angiopathies - physiopathology</subject><subject>diabetic foot</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Gangrene - surgery</subject><subject>Humans</subject><subject>ischaemia</subject><subject>Ischemia - physiopathology</subject><subject>Leg - blood supply</subject><subject>Leg - surgery</subject><subject>Male</subject><subject>Medical sciences</subject><subject>penetration</subject><subject>Peripheral Vascular Diseases - physiopathology</subject><subject>Peripheral Vascular Diseases - surgery</subject><subject>Tissue Distribution</subject><issn>0742-3071</issn><issn>1464-5491</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE9v1DAQxS0EotvCV0CWkLgl2HFiJxIXVEqL1AUORUhcrIk9Vr3kz2J7Ycunx2FXy5WT7ZnfezN-hFDOSs5q-XpT8lrWRVN3vKwY4yXLVVbuH5HVqfGYrJiqq0Iwxc_IeYybDFad6J6SM84Fb9u6WRF3d48UnUOT6Oyo9dBjwkhhsjTiTwxIfTT3gKMHOk80ZXyLE6YAyed31hh0CX5768fMTmmmyce4yx65t-CDH_tn5ImDIeLz43lBvry_uru8KW4_XX-4fHtbmFowVvTCGSEst8bx_K_WiaaDrma140b1lQUppGwMdw1TAFJyKyvGe9dA1UJvlbggrw6-2zD_yDskPeb1cRhgwnkXtWJqsWMZbA-gCXOMAZ3eBj9CeNCc6SVjvdFLlHqJUi8Z678Z632WvjjO2PUj2n_CY6gZeHkEIBoYXIDJ-HjiOlVx0WXqzYH65Qd8-O_x-t36Kl-yvDjIfUy4P8khfNdSCdXorx-vdbPu-Df2ea1b8QfAQ6X0</recordid><startdate>200103</startdate><enddate>200103</enddate><creator>Raymakers, J. 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C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4300-b3fc33d1dcf12008f359a9404f1c7b2da63665c1f507aa661d6201bf5a28abd73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Aged</topic><topic>Amputation</topic><topic>antibiotic</topic><topic>Associated diseases and complications</topic><topic>Biological and medical sciences</topic><topic>ceftazidime</topic><topic>Ceftazidime - pharmacokinetics</topic><topic>Cephalosporins - pharmacokinetics</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diabetic Angiopathies - physiopathology</topic><topic>diabetic foot</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Gangrene - surgery</topic><topic>Humans</topic><topic>ischaemia</topic><topic>Ischemia - physiopathology</topic><topic>Leg - blood supply</topic><topic>Leg - surgery</topic><topic>Male</topic><topic>Medical sciences</topic><topic>penetration</topic><topic>Peripheral Vascular Diseases - physiopathology</topic><topic>Peripheral Vascular Diseases - surgery</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raymakers, J. T.</creatorcontrib><creatorcontrib>Houben, A. J.</creatorcontrib><creatorcontrib>Heyden, J. J. vd</creatorcontrib><creatorcontrib>Tordoir, J. H.</creatorcontrib><creatorcontrib>Kitslaar, P. J.</creatorcontrib><creatorcontrib>Schaper, N. 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C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of diabetes and severe ischaemia on the penetration of ceftazidime into tissues of the limb</atitle><jtitle>Diabetic medicine</jtitle><addtitle>Diabet Med</addtitle><date>2001-03</date><risdate>2001</risdate><volume>18</volume><issue>3</issue><spage>229</spage><epage>234</epage><pages>229-234</pages><issn>0742-3071</issn><eissn>1464-5491</eissn><coden>DIMEEV</coden><abstract>SUMMARY Aims  To determine the effect of diabetes and of different degrees of ischaemia on the penetration of ceftazidime into different tissues. Methods  Sixteen patients (10 with diabetes mellitus) undergoing lower extremity amputation for severe ischaemia (in 12 in combination with infection), received 2000 mg ceftazidime intravenously as a bolus 30 min prior to the operation. Skin perfusion was determined by transcutaneous oxygen pressure measurements (TcPO2) on the dorsal side of the midfoot. After amputation bone, skin and muscle samples were obtained from the forefoot, midfoot and proximal tibia. Tissue and plasma concentrations were determined by HPLC. The tissue concentrations were corrected for blood contamination. Results  No differences were observed in skin, muscle or bone ceftazidime levels between diabetic and non‐diabetic patients. Multiple regression analysis suggested that tissue perfusion was a major determinant of skin and bone ceftazidime concentrations, predicting 40–47% of the ceftazidime concentrations at several biopsy sites. Conclusions  The present study suggests that tissue perfusion is the major determinant of the penetration of a third generation cephalosporin into the tissues of the ischaemic (diabetic) foot. Diabetes alone however, has no major effects upon this penetration.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11318845</pmid><doi>10.1046/j.1464-5491.2001.00460.x</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Aged
Amputation
antibiotic
Associated diseases and complications
Biological and medical sciences
ceftazidime
Ceftazidime - pharmacokinetics
Cephalosporins - pharmacokinetics
Diabetes Mellitus - physiopathology
Diabetes. Impaired glucose tolerance
Diabetic Angiopathies - physiopathology
diabetic foot
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Female
Gangrene - surgery
Humans
ischaemia
Ischemia - physiopathology
Leg - blood supply
Leg - surgery
Male
Medical sciences
penetration
Peripheral Vascular Diseases - physiopathology
Peripheral Vascular Diseases - surgery
Tissue Distribution
title The effect of diabetes and severe ischaemia on the penetration of ceftazidime into tissues of the limb
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