Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis
Study Objectives. To determine if apparent protective mortality benefits of intravenous active vitamin D in patients undergoing hemodialysis extend across all groups defined by dialysis duration; if higher monthly dose and dosing regularity are associated with reduced mortality; and if intravenous a...
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Veröffentlicht in: | Pharmacotherapy 2009-02, Vol.29 (2), p.154-164 |
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description | Study Objectives. To determine if apparent protective mortality benefits of intravenous active vitamin D in patients undergoing hemodialysis extend across all groups defined by dialysis duration; if higher monthly dose and dosing regularity are associated with reduced mortality; and if intravenous active vitamin D use is associated with reduced cardiovascular, infectious, and cancer‐related mortality.
Study Design. Retrospective cohort study
Data Source. Centers for Medicare and Medicaid Services End‐Stage Renal Disease database.
Patients. A total of 193,830 patients undergoing hemodialysis during 1999–2000, of whom 94,208 (48.6%) were taking intravenous active vitamin D in the baseline period.
Measurements and Main Results. Time‐varying Cox proportional hazards models were used to assess the effects of monthly vitamin D dose and dosing regularity over 3‐month intervals on risk of all‐cause and cause‐specific death, by dialysis duration groups (< 1 yr, 1 to < 3 yrs, 3 to < 5 yrs, and ≤ 5 yrs from dialysis initiation). Models were adjusted for baseline characteristics, time‐varying hospital days, monthly epoetin alfa dose, mean hemoglobin level, and urea reduction ratio in the 3‐month intervals. Maximum follow‐up time was 5.25 years. Adjusted all‐cause mortality risk was reduced 7–17% among patients receiving vitamin D each month of the 3‐month interval, with the highest reduction among patients with shorter dialysis duration. However, regular vitamin D dosing did not show consistent benefit across dialysis duration groups for cardiovascular, infectious, cancer, or other (all deaths not attributable to cardiovascular disease, infection, or cancer) mortality.
Conclusion. Mortality benefits of intravenous vitamin D cannot be easily explained by currently proposed biologic mechanisms. Randomized controlled trials are needed to show definitively whether intravenous vitamin D can reduce all‐cause and cause‐specific mortality in patients undergoing dialysis compared with placebo. |
doi_str_mv | 10.1592/phco.29.2.154 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66856814</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66856814</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4691-e12b23a4ae202ad9625768599970c084d744abee29f8bc9739856bcc024595063</originalsourceid><addsrcrecordid>eNp9kEFv0zAYhi0EYmVw5IpyYbcU27Hj-FhtYx0asE0UJC6W63zpDIldbHeQK78cR622Gyfrs573-ewXodcEzwmX9N32zvg5lXOaR_YEzUgjeCkJYU_RDFMhSoxxc4RexPgDY0pqRp-jIyKJwLzhM_T3vOvApFj4rvjoXbrrx-LMRyi0a4tb2Ox6HaYL6zYTculS0Pfg_C4WC5PsPRRfbdKDdcVZscox77ImJN3bNBaLwefYtU4WXF6xci2EjZ9USxh8a3U_Rhtfomed7iO8OpzHaPX-_Mvpsrz6fHF5urgqDaslKYHQNa0000Ax1a2sKRd1w6WUAhvcsFYwptcAVHbN2khRyYbXa2MwZVxyXFfH6GTv3Qb_awcxqcFGA32vHeT_qDrb6oawDJZ70AQfY4BObYMddBgVwWoqXU2lKyoVzePEvzmId-sB2kf60HIG3h4AHY3uu6CdsfGBowQ3kmKZuWrP_bY9jP_fqq6Xi1vCCXl8ro0J_jykdPipalEJrr59ulCSLz_g7zc3ilb_ABgXqi4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66856814</pqid></control><display><type>article</type><title>Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Peter, Wendy L. St ; Li, Shuling ; Liu, Jiannong ; Gilbertson, David T. ; Arneson, Thomas J. ; Collins, Allan J.</creator><creatorcontrib>Peter, Wendy L. St ; Li, Shuling ; Liu, Jiannong ; Gilbertson, David T. ; Arneson, Thomas J. ; Collins, Allan J.</creatorcontrib><description>Study Objectives. To determine if apparent protective mortality benefits of intravenous active vitamin D in patients undergoing hemodialysis extend across all groups defined by dialysis duration; if higher monthly dose and dosing regularity are associated with reduced mortality; and if intravenous active vitamin D use is associated with reduced cardiovascular, infectious, and cancer‐related mortality.
Study Design. Retrospective cohort study
Data Source. Centers for Medicare and Medicaid Services End‐Stage Renal Disease database.
Patients. A total of 193,830 patients undergoing hemodialysis during 1999–2000, of whom 94,208 (48.6%) were taking intravenous active vitamin D in the baseline period.
Measurements and Main Results. Time‐varying Cox proportional hazards models were used to assess the effects of monthly vitamin D dose and dosing regularity over 3‐month intervals on risk of all‐cause and cause‐specific death, by dialysis duration groups (< 1 yr, 1 to < 3 yrs, 3 to < 5 yrs, and ≤ 5 yrs from dialysis initiation). Models were adjusted for baseline characteristics, time‐varying hospital days, monthly epoetin alfa dose, mean hemoglobin level, and urea reduction ratio in the 3‐month intervals. Maximum follow‐up time was 5.25 years. Adjusted all‐cause mortality risk was reduced 7–17% among patients receiving vitamin D each month of the 3‐month interval, with the highest reduction among patients with shorter dialysis duration. However, regular vitamin D dosing did not show consistent benefit across dialysis duration groups for cardiovascular, infectious, cancer, or other (all deaths not attributable to cardiovascular disease, infection, or cancer) mortality.
Conclusion. Mortality benefits of intravenous vitamin D cannot be easily explained by currently proposed biologic mechanisms. Randomized controlled trials are needed to show definitively whether intravenous vitamin D can reduce all‐cause and cause‐specific mortality in patients undergoing dialysis compared with placebo.</description><identifier>ISSN: 0277-0008</identifier><identifier>EISSN: 1875-9114</identifier><identifier>DOI: 10.1592/phco.29.2.154</identifier><identifier>PMID: 19170585</identifier><identifier>CODEN: PHPYDQ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Centers for Medicare and Medicaid Services (U.S.) ; Cohort Studies ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Emergency and intensive care: renal failure. Dialysis management ; Female ; Follow-Up Studies ; hemodialysis ; Humans ; Injections, Intravenous ; Intensive care medicine ; Kidney Failure, Chronic - therapy ; Male ; Medical sciences ; Middle Aged ; mortality ; Pharmacology. Drug treatments ; Proportional Hazards Models ; Renal Dialysis - mortality ; Retrospective Studies ; United States ; vitamin D ; Vitamin D - administration & dosage ; Vitamin D - therapeutic use ; Vitamins - administration & dosage ; Vitamins - therapeutic use ; Young Adult</subject><ispartof>Pharmacotherapy, 2009-02, Vol.29 (2), p.154-164</ispartof><rights>2009 Pharmacotherapy Publications Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4691-e12b23a4ae202ad9625768599970c084d744abee29f8bc9739856bcc024595063</citedby><cites>FETCH-LOGICAL-c4691-e12b23a4ae202ad9625768599970c084d744abee29f8bc9739856bcc024595063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1592%2Fphco.29.2.154$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1592%2Fphco.29.2.154$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21089209$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19170585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peter, Wendy L. St</creatorcontrib><creatorcontrib>Li, Shuling</creatorcontrib><creatorcontrib>Liu, Jiannong</creatorcontrib><creatorcontrib>Gilbertson, David T.</creatorcontrib><creatorcontrib>Arneson, Thomas J.</creatorcontrib><creatorcontrib>Collins, Allan J.</creatorcontrib><title>Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis</title><title>Pharmacotherapy</title><addtitle>Pharmacotherapy</addtitle><description>Study Objectives. To determine if apparent protective mortality benefits of intravenous active vitamin D in patients undergoing hemodialysis extend across all groups defined by dialysis duration; if higher monthly dose and dosing regularity are associated with reduced mortality; and if intravenous active vitamin D use is associated with reduced cardiovascular, infectious, and cancer‐related mortality.
Study Design. Retrospective cohort study
Data Source. Centers for Medicare and Medicaid Services End‐Stage Renal Disease database.
Patients. A total of 193,830 patients undergoing hemodialysis during 1999–2000, of whom 94,208 (48.6%) were taking intravenous active vitamin D in the baseline period.
Measurements and Main Results. Time‐varying Cox proportional hazards models were used to assess the effects of monthly vitamin D dose and dosing regularity over 3‐month intervals on risk of all‐cause and cause‐specific death, by dialysis duration groups (< 1 yr, 1 to < 3 yrs, 3 to < 5 yrs, and ≤ 5 yrs from dialysis initiation). Models were adjusted for baseline characteristics, time‐varying hospital days, monthly epoetin alfa dose, mean hemoglobin level, and urea reduction ratio in the 3‐month intervals. Maximum follow‐up time was 5.25 years. Adjusted all‐cause mortality risk was reduced 7–17% among patients receiving vitamin D each month of the 3‐month interval, with the highest reduction among patients with shorter dialysis duration. However, regular vitamin D dosing did not show consistent benefit across dialysis duration groups for cardiovascular, infectious, cancer, or other (all deaths not attributable to cardiovascular disease, infection, or cancer) mortality.
Conclusion. Mortality benefits of intravenous vitamin D cannot be easily explained by currently proposed biologic mechanisms. Randomized controlled trials are needed to show definitively whether intravenous vitamin D can reduce all‐cause and cause‐specific mortality in patients undergoing dialysis compared with placebo.</description><subject>Adult</subject><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Centers for Medicare and Medicaid Services (U.S.)</subject><subject>Cohort Studies</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>hemodialysis</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Intensive care medicine</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>mortality</subject><subject>Pharmacology. Drug treatments</subject><subject>Proportional Hazards Models</subject><subject>Renal Dialysis - mortality</subject><subject>Retrospective Studies</subject><subject>United States</subject><subject>vitamin D</subject><subject>Vitamin D - administration & dosage</subject><subject>Vitamin D - therapeutic use</subject><subject>Vitamins - administration & dosage</subject><subject>Vitamins - therapeutic use</subject><subject>Young Adult</subject><issn>0277-0008</issn><issn>1875-9114</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv0zAYhi0EYmVw5IpyYbcU27Hj-FhtYx0asE0UJC6W63zpDIldbHeQK78cR622Gyfrs573-ewXodcEzwmX9N32zvg5lXOaR_YEzUgjeCkJYU_RDFMhSoxxc4RexPgDY0pqRp-jIyKJwLzhM_T3vOvApFj4rvjoXbrrx-LMRyi0a4tb2Ox6HaYL6zYTculS0Pfg_C4WC5PsPRRfbdKDdcVZscox77ImJN3bNBaLwefYtU4WXF6xci2EjZ9USxh8a3U_Rhtfomed7iO8OpzHaPX-_Mvpsrz6fHF5urgqDaslKYHQNa0000Ax1a2sKRd1w6WUAhvcsFYwptcAVHbN2khRyYbXa2MwZVxyXFfH6GTv3Qb_awcxqcFGA32vHeT_qDrb6oawDJZ70AQfY4BObYMddBgVwWoqXU2lKyoVzePEvzmId-sB2kf60HIG3h4AHY3uu6CdsfGBowQ3kmKZuWrP_bY9jP_fqq6Xi1vCCXl8ro0J_jykdPipalEJrr59ulCSLz_g7zc3ilb_ABgXqi4</recordid><startdate>200902</startdate><enddate>200902</enddate><creator>Peter, Wendy L. St</creator><creator>Li, Shuling</creator><creator>Liu, Jiannong</creator><creator>Gilbertson, David T.</creator><creator>Arneson, Thomas J.</creator><creator>Collins, Allan J.</creator><general>Blackwell Publishing Ltd</general><general>Pharmacotherapy</general><scope>BSCLL</scope><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>200902</creationdate><title>Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis</title><author>Peter, Wendy L. St ; Li, Shuling ; Liu, Jiannong ; Gilbertson, David T. ; Arneson, Thomas J. ; Collins, Allan J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4691-e12b23a4ae202ad9625768599970c084d744abee29f8bc9739856bcc024595063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Centers for Medicare and Medicaid Services (U.S.)</topic><topic>Cohort Studies</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>hemodialysis</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Intensive care medicine</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>mortality</topic><topic>Pharmacology. Drug treatments</topic><topic>Proportional Hazards Models</topic><topic>Renal Dialysis - mortality</topic><topic>Retrospective Studies</topic><topic>United States</topic><topic>vitamin D</topic><topic>Vitamin D - administration & dosage</topic><topic>Vitamin D - therapeutic use</topic><topic>Vitamins - administration & dosage</topic><topic>Vitamins - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peter, Wendy L. St</creatorcontrib><creatorcontrib>Li, Shuling</creatorcontrib><creatorcontrib>Liu, Jiannong</creatorcontrib><creatorcontrib>Gilbertson, David T.</creatorcontrib><creatorcontrib>Arneson, Thomas J.</creatorcontrib><creatorcontrib>Collins, Allan J.</creatorcontrib><collection>Istex</collection><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>Pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peter, Wendy L. St</au><au>Li, Shuling</au><au>Liu, Jiannong</au><au>Gilbertson, David T.</au><au>Arneson, Thomas J.</au><au>Collins, Allan J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis</atitle><jtitle>Pharmacotherapy</jtitle><addtitle>Pharmacotherapy</addtitle><date>2009-02</date><risdate>2009</risdate><volume>29</volume><issue>2</issue><spage>154</spage><epage>164</epage><pages>154-164</pages><issn>0277-0008</issn><eissn>1875-9114</eissn><coden>PHPYDQ</coden><abstract>Study Objectives. To determine if apparent protective mortality benefits of intravenous active vitamin D in patients undergoing hemodialysis extend across all groups defined by dialysis duration; if higher monthly dose and dosing regularity are associated with reduced mortality; and if intravenous active vitamin D use is associated with reduced cardiovascular, infectious, and cancer‐related mortality.
Study Design. Retrospective cohort study
Data Source. Centers for Medicare and Medicaid Services End‐Stage Renal Disease database.
Patients. A total of 193,830 patients undergoing hemodialysis during 1999–2000, of whom 94,208 (48.6%) were taking intravenous active vitamin D in the baseline period.
Measurements and Main Results. Time‐varying Cox proportional hazards models were used to assess the effects of monthly vitamin D dose and dosing regularity over 3‐month intervals on risk of all‐cause and cause‐specific death, by dialysis duration groups (< 1 yr, 1 to < 3 yrs, 3 to < 5 yrs, and ≤ 5 yrs from dialysis initiation). Models were adjusted for baseline characteristics, time‐varying hospital days, monthly epoetin alfa dose, mean hemoglobin level, and urea reduction ratio in the 3‐month intervals. Maximum follow‐up time was 5.25 years. Adjusted all‐cause mortality risk was reduced 7–17% among patients receiving vitamin D each month of the 3‐month interval, with the highest reduction among patients with shorter dialysis duration. However, regular vitamin D dosing did not show consistent benefit across dialysis duration groups for cardiovascular, infectious, cancer, or other (all deaths not attributable to cardiovascular disease, infection, or cancer) mortality.
Conclusion. Mortality benefits of intravenous vitamin D cannot be easily explained by currently proposed biologic mechanisms. Randomized controlled trials are needed to show definitively whether intravenous vitamin D can reduce all‐cause and cause‐specific mortality in patients undergoing dialysis compared with placebo.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19170585</pmid><doi>10.1592/phco.29.2.154</doi><tpages>11</tpages></addata></record> |
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subjects | Adult Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Centers for Medicare and Medicaid Services (U.S.) Cohort Studies Dose-Response Relationship, Drug Drug Administration Schedule Emergency and intensive care: renal failure. Dialysis management Female Follow-Up Studies hemodialysis Humans Injections, Intravenous Intensive care medicine Kidney Failure, Chronic - therapy Male Medical sciences Middle Aged mortality Pharmacology. Drug treatments Proportional Hazards Models Renal Dialysis - mortality Retrospective Studies United States vitamin D Vitamin D - administration & dosage Vitamin D - therapeutic use Vitamins - administration & dosage Vitamins - therapeutic use Young Adult |
title | Effects of Monthly Dose and Regular Dosing of Intravenous Active Vitamin D Use on Mortality Among Patients Undergoing Hemodialysis |
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