Trace Element Loss in Urine and Effluent Following Traumatic Injury
Background: Few data are available to establish recommendations for trace element supplementation during critical illness. This study quantified the loss of several elements and assessed the adequacy of manganese and selenium in parenteral nutrition (PN). Methods: Men with traumatic injuries were gr...
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creator | Klein, Catherine J. Nielsen, Forrest H. Moser-Veillon, Phylis B. |
description | Background: Few data are available to establish recommendations
for trace element supplementation during critical illness. This study
quantified the loss of several elements and assessed the adequacy of manganese
and selenium in parenteral nutrition (PN). Methods: Men with
traumatic injuries were grouped by renal status: adequate (POLY; n = 6), acute
failure with continuous venovenous hemofiltration (CVVH; n = 2), or continuous
venovenous hemodiafiltration (CVVHD; n = 4). PN supplied 300 μg/d manganese
and 60 μg/d selenium. Urine and effluent (from artificial kidneys) were
collected for 3 days and analyzed for boron, manganese, nickel, and silicon
using inductively coupled plasma atomic emission spectrometry, and for
selenium using atomic absorption spectrometry. Results: POLY
manganese and selenium excretion averaged (standard deviation [SD]) 7.9 (3.3)μ
g/d and 103.5 (22.4) μg/d, respectively. All elements except selenium
were detected in dialysate (prior to use). CVVHD effluent contained 3.5 and
7.3 times more manganese and nickel than CVVH ultrafiltrate, respectively.
Loss of manganese averaged 2.6%, 21%, and 73% of PN amounts for POLY, CVVH,
and CVVHD groups, respectively. Discussion: Minimal loss of manganese
compared with the amount in PN suggests that excessive amounts are retained.
POLY patients excreted more selenium than was in PN, indicating negative
balance. POLY losses of boron and silicon were less than that published for
healthy adults, reflecting less than typical intake, whereas loss during CVVH
was in the normal reference range, possibly because of added intake from boron
contamination of replacement fluids. All patients lost more nickel than
amounts published for healthy adults. Conclusions: Current guidelines
of 60-100 μg/d of parenteral manganese may be excessive for trauma
patients. The uptake of manganese and nickel from contaminants in CVVHD
dialysate should be investigated.
Trauma patients excrete substantial urinary nickel and selenium but little manganese. Current guidelines of 60-100 μg/d of parenteral manganese may be excessive, especially if bile secretion and fecal excretion are impaired. The uptake of manganese and nickel from contaminants in dialysate during continuous renal replacement therapy should be investigated. |
doi_str_mv | 10.1177/0148607108314762 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_230204174</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_0148607108314762</sage_id><sourcerecordid>1543587051</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4099-d66e71a77cb447839a4c53afe20c4e6aea40dcae0c08dfdecbc318ae52c284383</originalsourceid><addsrcrecordid>eNqFkEFLw0AQhRdRbK3ePcniPTq7O81ujlJSrRT10J7DdjMpKWlSNw2l_96EFAqCeJrDe9-bmcfYvYAnIbR-BoEmBC3AKIE6lBdsKCIUgUTESzbs5KDTB-ymrjcAoEKAazYQBkFHMB6yycJbRzwuaEvlns-ruuZ5yZc-L4nbMuVxlhVNJ02roqgOebnmLdJs7T53fFZuGn-8ZVeZLWq6O80RW07jxeQtmH--ziYv88AhRFGQhiFpYbV2K0RtVGTRjZXNSIJDCi1ZhNRZAgcmzVJyK6eEsTSWThpURo3YY5-789V3Q_U-2VSNL9uViVQgAYXG1gS9yfn2F09ZsvP51vpjIiDpSkt-l9YiD6fcZrWl9AycWmoNYW845AUd_w1M3r_iDxAyasGgB2u7pvO1f17yA7M0gm4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230204174</pqid></control><display><type>article</type><title>Trace Element Loss in Urine and Effluent Following Traumatic Injury</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Klein, Catherine J. ; Nielsen, Forrest H. ; Moser-Veillon, Phylis B.</creator><creatorcontrib>Klein, Catherine J. ; Nielsen, Forrest H. ; Moser-Veillon, Phylis B.</creatorcontrib><description>Background: Few data are available to establish recommendations
for trace element supplementation during critical illness. This study
quantified the loss of several elements and assessed the adequacy of manganese
and selenium in parenteral nutrition (PN). Methods: Men with
traumatic injuries were grouped by renal status: adequate (POLY; n = 6), acute
failure with continuous venovenous hemofiltration (CVVH; n = 2), or continuous
venovenous hemodiafiltration (CVVHD; n = 4). PN supplied 300 μg/d manganese
and 60 μg/d selenium. Urine and effluent (from artificial kidneys) were
collected for 3 days and analyzed for boron, manganese, nickel, and silicon
using inductively coupled plasma atomic emission spectrometry, and for
selenium using atomic absorption spectrometry. Results: POLY
manganese and selenium excretion averaged (standard deviation [SD]) 7.9 (3.3)μ
g/d and 103.5 (22.4) μg/d, respectively. All elements except selenium
were detected in dialysate (prior to use). CVVHD effluent contained 3.5 and
7.3 times more manganese and nickel than CVVH ultrafiltrate, respectively.
Loss of manganese averaged 2.6%, 21%, and 73% of PN amounts for POLY, CVVH,
and CVVHD groups, respectively. Discussion: Minimal loss of manganese
compared with the amount in PN suggests that excessive amounts are retained.
POLY patients excreted more selenium than was in PN, indicating negative
balance. POLY losses of boron and silicon were less than that published for
healthy adults, reflecting less than typical intake, whereas loss during CVVH
was in the normal reference range, possibly because of added intake from boron
contamination of replacement fluids. All patients lost more nickel than
amounts published for healthy adults. Conclusions: Current guidelines
of 60-100 μg/d of parenteral manganese may be excessive for trauma
patients. The uptake of manganese and nickel from contaminants in CVVHD
dialysate should be investigated.
Trauma patients excrete substantial urinary nickel and selenium but little manganese. Current guidelines of 60-100 μg/d of parenteral manganese may be excessive, especially if bile secretion and fecal excretion are impaired. The uptake of manganese and nickel from contaminants in dialysate during continuous renal replacement therapy should be investigated.</description><identifier>ISSN: 0148-6071</identifier><identifier>EISSN: 1941-2444</identifier><identifier>DOI: 10.1177/0148607108314762</identifier><identifier>PMID: 18407905</identifier><identifier>CODEN: JPENDU</identifier><language>eng</language><publisher>United States: SAGE Publications</publisher><subject>Acute Kidney Injury - metabolism ; Acute Kidney Injury - therapy ; acute renal failure ; Adolescent ; Adult ; boron ; Boron - analysis ; Boron - urine ; Critical Illness - therapy ; Female ; Food Contamination - analysis ; Humans ; Male ; manganese ; Manganese - administration & dosage ; Manganese - analysis ; Manganese - urine ; Middle Aged ; nickel ; Nickel - administration & dosage ; Nickel - analysis ; Nickel - urine ; Nutritional Requirements ; Parenteral Nutrition - adverse effects ; Renal Replacement Therapy ; selenium ; Selenium - administration & dosage ; Selenium - analysis ; Selenium - urine ; silicon ; Silicon - administration & dosage ; Silicon - analysis ; Silicon - urine ; trace elements ; Trace Elements - administration & dosage ; Trace Elements - analysis ; Trace Elements - urine ; trauma</subject><ispartof>JPEN. Journal of parenteral and enteral nutrition, 2008-03, Vol.32 (2), p.129-139</ispartof><rights>American Society for Parenteral and Enteral Nutrition</rights><rights>2008 by The American Society for Parenteral and Enteral Nutrition</rights><rights>Copyright American Society for Parenteral and Enteral Nutrition Mar/Apr 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4099-d66e71a77cb447839a4c53afe20c4e6aea40dcae0c08dfdecbc318ae52c284383</citedby><cites>FETCH-LOGICAL-c4099-d66e71a77cb447839a4c53afe20c4e6aea40dcae0c08dfdecbc318ae52c284383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1177%2F0148607108314762$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1177%2F0148607108314762$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18407905$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klein, Catherine J.</creatorcontrib><creatorcontrib>Nielsen, Forrest H.</creatorcontrib><creatorcontrib>Moser-Veillon, Phylis B.</creatorcontrib><title>Trace Element Loss in Urine and Effluent Following Traumatic Injury</title><title>JPEN. Journal of parenteral and enteral nutrition</title><addtitle>JPEN J Parenter Enteral Nutr</addtitle><description>Background: Few data are available to establish recommendations
for trace element supplementation during critical illness. This study
quantified the loss of several elements and assessed the adequacy of manganese
and selenium in parenteral nutrition (PN). Methods: Men with
traumatic injuries were grouped by renal status: adequate (POLY; n = 6), acute
failure with continuous venovenous hemofiltration (CVVH; n = 2), or continuous
venovenous hemodiafiltration (CVVHD; n = 4). PN supplied 300 μg/d manganese
and 60 μg/d selenium. Urine and effluent (from artificial kidneys) were
collected for 3 days and analyzed for boron, manganese, nickel, and silicon
using inductively coupled plasma atomic emission spectrometry, and for
selenium using atomic absorption spectrometry. Results: POLY
manganese and selenium excretion averaged (standard deviation [SD]) 7.9 (3.3)μ
g/d and 103.5 (22.4) μg/d, respectively. All elements except selenium
were detected in dialysate (prior to use). CVVHD effluent contained 3.5 and
7.3 times more manganese and nickel than CVVH ultrafiltrate, respectively.
Loss of manganese averaged 2.6%, 21%, and 73% of PN amounts for POLY, CVVH,
and CVVHD groups, respectively. Discussion: Minimal loss of manganese
compared with the amount in PN suggests that excessive amounts are retained.
POLY patients excreted more selenium than was in PN, indicating negative
balance. POLY losses of boron and silicon were less than that published for
healthy adults, reflecting less than typical intake, whereas loss during CVVH
was in the normal reference range, possibly because of added intake from boron
contamination of replacement fluids. All patients lost more nickel than
amounts published for healthy adults. Conclusions: Current guidelines
of 60-100 μg/d of parenteral manganese may be excessive for trauma
patients. The uptake of manganese and nickel from contaminants in CVVHD
dialysate should be investigated.
Trauma patients excrete substantial urinary nickel and selenium but little manganese. Current guidelines of 60-100 μg/d of parenteral manganese may be excessive, especially if bile secretion and fecal excretion are impaired. The uptake of manganese and nickel from contaminants in dialysate during continuous renal replacement therapy should be investigated.</description><subject>Acute Kidney Injury - metabolism</subject><subject>Acute Kidney Injury - therapy</subject><subject>acute renal failure</subject><subject>Adolescent</subject><subject>Adult</subject><subject>boron</subject><subject>Boron - analysis</subject><subject>Boron - urine</subject><subject>Critical Illness - therapy</subject><subject>Female</subject><subject>Food Contamination - analysis</subject><subject>Humans</subject><subject>Male</subject><subject>manganese</subject><subject>Manganese - administration & dosage</subject><subject>Manganese - analysis</subject><subject>Manganese - urine</subject><subject>Middle Aged</subject><subject>nickel</subject><subject>Nickel - administration & dosage</subject><subject>Nickel - analysis</subject><subject>Nickel - urine</subject><subject>Nutritional Requirements</subject><subject>Parenteral Nutrition - adverse effects</subject><subject>Renal Replacement Therapy</subject><subject>selenium</subject><subject>Selenium - administration & dosage</subject><subject>Selenium - analysis</subject><subject>Selenium - urine</subject><subject>silicon</subject><subject>Silicon - administration & dosage</subject><subject>Silicon - analysis</subject><subject>Silicon - urine</subject><subject>trace elements</subject><subject>Trace Elements - administration & dosage</subject><subject>Trace Elements - analysis</subject><subject>Trace Elements - urine</subject><subject>trauma</subject><issn>0148-6071</issn><issn>1941-2444</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkEFLw0AQhRdRbK3ePcniPTq7O81ujlJSrRT10J7DdjMpKWlSNw2l_96EFAqCeJrDe9-bmcfYvYAnIbR-BoEmBC3AKIE6lBdsKCIUgUTESzbs5KDTB-ymrjcAoEKAazYQBkFHMB6yycJbRzwuaEvlns-ruuZ5yZc-L4nbMuVxlhVNJ02roqgOebnmLdJs7T53fFZuGn-8ZVeZLWq6O80RW07jxeQtmH--ziYv88AhRFGQhiFpYbV2K0RtVGTRjZXNSIJDCi1ZhNRZAgcmzVJyK6eEsTSWThpURo3YY5-789V3Q_U-2VSNL9uViVQgAYXG1gS9yfn2F09ZsvP51vpjIiDpSkt-l9YiD6fcZrWl9AycWmoNYW845AUd_w1M3r_iDxAyasGgB2u7pvO1f17yA7M0gm4</recordid><startdate>200803</startdate><enddate>200803</enddate><creator>Klein, Catherine J.</creator><creator>Nielsen, Forrest H.</creator><creator>Moser-Veillon, Phylis B.</creator><general>SAGE Publications</general><general>American Society for Parenteral and Enteral Nutrition</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>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200803</creationdate><title>Trace Element Loss in Urine and Effluent Following Traumatic Injury</title><author>Klein, Catherine J. ; Nielsen, Forrest H. ; Moser-Veillon, Phylis B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4099-d66e71a77cb447839a4c53afe20c4e6aea40dcae0c08dfdecbc318ae52c284383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acute Kidney Injury - metabolism</topic><topic>Acute Kidney Injury - therapy</topic><topic>acute renal failure</topic><topic>Adolescent</topic><topic>Adult</topic><topic>boron</topic><topic>Boron - analysis</topic><topic>Boron - urine</topic><topic>Critical Illness - therapy</topic><topic>Female</topic><topic>Food Contamination - analysis</topic><topic>Humans</topic><topic>Male</topic><topic>manganese</topic><topic>Manganese - administration & dosage</topic><topic>Manganese - analysis</topic><topic>Manganese - urine</topic><topic>Middle Aged</topic><topic>nickel</topic><topic>Nickel - administration & dosage</topic><topic>Nickel - analysis</topic><topic>Nickel - urine</topic><topic>Nutritional Requirements</topic><topic>Parenteral Nutrition - adverse effects</topic><topic>Renal Replacement Therapy</topic><topic>selenium</topic><topic>Selenium - administration & dosage</topic><topic>Selenium - analysis</topic><topic>Selenium - urine</topic><topic>silicon</topic><topic>Silicon - administration & dosage</topic><topic>Silicon - analysis</topic><topic>Silicon - urine</topic><topic>trace elements</topic><topic>Trace Elements - administration & dosage</topic><topic>Trace Elements - analysis</topic><topic>Trace Elements - urine</topic><topic>trauma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Klein, Catherine J.</creatorcontrib><creatorcontrib>Nielsen, Forrest H.</creatorcontrib><creatorcontrib>Moser-Veillon, Phylis B.</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>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>British Nursing Database</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</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>Medical Database</collection><collection>Nursing & Allied Health Premium</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><jtitle>JPEN. Journal of parenteral and enteral nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Klein, Catherine J.</au><au>Nielsen, Forrest H.</au><au>Moser-Veillon, Phylis B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trace Element Loss in Urine and Effluent Following Traumatic Injury</atitle><jtitle>JPEN. Journal of parenteral and enteral nutrition</jtitle><addtitle>JPEN J Parenter Enteral Nutr</addtitle><date>2008-03</date><risdate>2008</risdate><volume>32</volume><issue>2</issue><spage>129</spage><epage>139</epage><pages>129-139</pages><issn>0148-6071</issn><eissn>1941-2444</eissn><coden>JPENDU</coden><abstract>Background: Few data are available to establish recommendations
for trace element supplementation during critical illness. This study
quantified the loss of several elements and assessed the adequacy of manganese
and selenium in parenteral nutrition (PN). Methods: Men with
traumatic injuries were grouped by renal status: adequate (POLY; n = 6), acute
failure with continuous venovenous hemofiltration (CVVH; n = 2), or continuous
venovenous hemodiafiltration (CVVHD; n = 4). PN supplied 300 μg/d manganese
and 60 μg/d selenium. Urine and effluent (from artificial kidneys) were
collected for 3 days and analyzed for boron, manganese, nickel, and silicon
using inductively coupled plasma atomic emission spectrometry, and for
selenium using atomic absorption spectrometry. Results: POLY
manganese and selenium excretion averaged (standard deviation [SD]) 7.9 (3.3)μ
g/d and 103.5 (22.4) μg/d, respectively. All elements except selenium
were detected in dialysate (prior to use). CVVHD effluent contained 3.5 and
7.3 times more manganese and nickel than CVVH ultrafiltrate, respectively.
Loss of manganese averaged 2.6%, 21%, and 73% of PN amounts for POLY, CVVH,
and CVVHD groups, respectively. Discussion: Minimal loss of manganese
compared with the amount in PN suggests that excessive amounts are retained.
POLY patients excreted more selenium than was in PN, indicating negative
balance. POLY losses of boron and silicon were less than that published for
healthy adults, reflecting less than typical intake, whereas loss during CVVH
was in the normal reference range, possibly because of added intake from boron
contamination of replacement fluids. All patients lost more nickel than
amounts published for healthy adults. Conclusions: Current guidelines
of 60-100 μg/d of parenteral manganese may be excessive for trauma
patients. The uptake of manganese and nickel from contaminants in CVVHD
dialysate should be investigated.
Trauma patients excrete substantial urinary nickel and selenium but little manganese. Current guidelines of 60-100 μg/d of parenteral manganese may be excessive, especially if bile secretion and fecal excretion are impaired. The uptake of manganese and nickel from contaminants in dialysate during continuous renal replacement therapy should be investigated.</abstract><cop>United States</cop><pub>SAGE Publications</pub><pmid>18407905</pmid><doi>10.1177/0148607108314762</doi><tpages>11</tpages></addata></record> |
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source | Wiley Online Library - AutoHoldings Journals; MEDLINE; Alma/SFX Local Collection |
subjects | Acute Kidney Injury - metabolism Acute Kidney Injury - therapy acute renal failure Adolescent Adult boron Boron - analysis Boron - urine Critical Illness - therapy Female Food Contamination - analysis Humans Male manganese Manganese - administration & dosage Manganese - analysis Manganese - urine Middle Aged nickel Nickel - administration & dosage Nickel - analysis Nickel - urine Nutritional Requirements Parenteral Nutrition - adverse effects Renal Replacement Therapy selenium Selenium - administration & dosage Selenium - analysis Selenium - urine silicon Silicon - administration & dosage Silicon - analysis Silicon - urine trace elements Trace Elements - administration & dosage Trace Elements - analysis Trace Elements - urine trauma |
title | Trace Element Loss in Urine and Effluent Following Traumatic Injury |
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