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
Hauptverfasser: Peter, Wendy L. St, Li, Shuling, Liu, Jiannong, Gilbertson, David T., Arneson, Thomas J., Collins, Allan J.
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container_end_page 164
container_issue 2
container_start_page 154
container_title Pharmacotherapy
container_volume 29
creator Peter, Wendy L. St
Li, Shuling
Liu, Jiannong
Gilbertson, David T.
Arneson, Thomas J.
Collins, Allan J.
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.
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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 (&lt; 1 yr, 1 to &lt; 3 yrs, 3 to &lt; 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. 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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 (&lt; 1 yr, 1 to &lt; 3 yrs, 3 to &lt; 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. 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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. 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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 (&lt; 1 yr, 1 to &lt; 3 yrs, 3 to &lt; 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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