Mannitol for the prevention of cisplatin-induced nephrotoxicity: A retrospective comparison of hydration plus mannitol versus hydration alone in inpatient and outpatient regimens at a large academic medical center

Background Cisplatin-induced nephrotoxicity is a dose limiting adverse effect that occurs in nearly one-third of patients. Mannitol administration has been used as a means to negate this toxicity. Data regarding the efficacy of mannitol use in this context are conflicting and limited. Objective The...

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Veröffentlicht in:Journal of oncology pharmacy practice 2017-09, Vol.23 (6), p.422-428
Hauptverfasser: Williams, Robert P, Ferlas, Brandon W, Morales, Paul C, Kurtzweil, Andy J
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container_end_page 428
container_issue 6
container_start_page 422
container_title Journal of oncology pharmacy practice
container_volume 23
creator Williams, Robert P
Ferlas, Brandon W
Morales, Paul C
Kurtzweil, Andy J
description Background Cisplatin-induced nephrotoxicity is a dose limiting adverse effect that occurs in nearly one-third of patients. Mannitol administration has been used as a means to negate this toxicity. Data regarding the efficacy of mannitol use in this context are conflicting and limited. Objective The aim of this study is to evaluate the effect of mannitol on renal function and describe the incidence of cisplatin-induced nephrotoxicity. Methods This study is a quasi-experimental retrospective analysis approved by the Institutional Review Board of inpatient and outpatient adults receiving cisplatin doses ≥40 mg/m2. The primary outcome was mean change in serum creatinine from baseline. Secondary outcomes included incidences of various grades of nephrotoxicity. Results A total of 313 patients (95 treated with mannitol and 218 without) were evaluated. The average increase in serum creatinine (mg/dL) was lower in patients who received mannitol versus those who did not (0.30 vs. 0.47; 95% confidence interval for difference, 0.03 to 0.31; P = 0.02). Grade 2 or higher nephrotoxicity occurred less frequently in patients who received mannitol versus those who did not (8% vs. 17%; P = 0.04). Non-gynecologic regimens and those who received doses ≥70 mg/m2 of cisplatin had lower rates of grade 2 or higher nephrotoxicity with mannitol (6% vs. 23%; P = 0.001, and 7% vs. 22%; P = 0.03, respectively). Conclusion The use of mannitol reduces the incidence and severity of nephrotoxicity in patients treated with cisplatin. The results of the study suggest mannitol may be most effective when used with non-gynecologic regimens and with cisplatin doses ≥70 mg/m2.
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Mannitol administration has been used as a means to negate this toxicity. Data regarding the efficacy of mannitol use in this context are conflicting and limited. Objective The aim of this study is to evaluate the effect of mannitol on renal function and describe the incidence of cisplatin-induced nephrotoxicity. Methods This study is a quasi-experimental retrospective analysis approved by the Institutional Review Board of inpatient and outpatient adults receiving cisplatin doses ≥40 mg/m2. The primary outcome was mean change in serum creatinine from baseline. Secondary outcomes included incidences of various grades of nephrotoxicity. Results A total of 313 patients (95 treated with mannitol and 218 without) were evaluated. The average increase in serum creatinine (mg/dL) was lower in patients who received mannitol versus those who did not (0.30 vs. 0.47; 95% confidence interval for difference, 0.03 to 0.31; P = 0.02). Grade 2 or higher nephrotoxicity occurred less frequently in patients who received mannitol versus those who did not (8% vs. 17%; P = 0.04). Non-gynecologic regimens and those who received doses ≥70 mg/m2 of cisplatin had lower rates of grade 2 or higher nephrotoxicity with mannitol (6% vs. 23%; P = 0.001, and 7% vs. 22%; P = 0.03, respectively). Conclusion The use of mannitol reduces the incidence and severity of nephrotoxicity in patients treated with cisplatin. The results of the study suggest mannitol may be most effective when used with non-gynecologic regimens and with cisplatin doses ≥70 mg/m2.</description><identifier>ISSN: 1078-1552</identifier><identifier>EISSN: 1477-092X</identifier><identifier>DOI: 10.1177/1078155216656927</identifier><identifier>PMID: 27352615</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Academic Medical Centers ; Adult ; Aged ; Antineoplastic Agents - adverse effects ; Chemotherapy ; Cisplatin ; Cisplatin - adverse effects ; Creatinine ; Drug therapy ; Female ; Health care facilities ; Humans ; Hydration ; Incidence ; Inpatients ; Kidney Diseases - chemically induced ; Kidney Diseases - prevention &amp; control ; Male ; Mannitol ; Mannitol - administration &amp; dosage ; Middle Aged ; Outpatients ; Renal function ; Retrospective Studies ; Studies ; Toxicity</subject><ispartof>Journal of oncology pharmacy practice, 2017-09, Vol.23 (6), p.422-428</ispartof><rights>The Author(s) 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-8a04a445252071af4f182a51f3f05537a2e48f5c8983e42e53836f9d1820e7ab3</citedby><cites>FETCH-LOGICAL-c431t-8a04a445252071af4f182a51f3f05537a2e48f5c8983e42e53836f9d1820e7ab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1078155216656927$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1078155216656927$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27352615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, Robert P</creatorcontrib><creatorcontrib>Ferlas, Brandon W</creatorcontrib><creatorcontrib>Morales, Paul C</creatorcontrib><creatorcontrib>Kurtzweil, Andy J</creatorcontrib><title>Mannitol for the prevention of cisplatin-induced nephrotoxicity: A retrospective comparison of hydration plus mannitol versus hydration alone in inpatient and outpatient regimens at a large academic medical center</title><title>Journal of oncology pharmacy practice</title><addtitle>J Oncol Pharm Pract</addtitle><description>Background Cisplatin-induced nephrotoxicity is a dose limiting adverse effect that occurs in nearly one-third of patients. Mannitol administration has been used as a means to negate this toxicity. Data regarding the efficacy of mannitol use in this context are conflicting and limited. Objective The aim of this study is to evaluate the effect of mannitol on renal function and describe the incidence of cisplatin-induced nephrotoxicity. Methods This study is a quasi-experimental retrospective analysis approved by the Institutional Review Board of inpatient and outpatient adults receiving cisplatin doses ≥40 mg/m2. The primary outcome was mean change in serum creatinine from baseline. Secondary outcomes included incidences of various grades of nephrotoxicity. Results A total of 313 patients (95 treated with mannitol and 218 without) were evaluated. The average increase in serum creatinine (mg/dL) was lower in patients who received mannitol versus those who did not (0.30 vs. 0.47; 95% confidence interval for difference, 0.03 to 0.31; P = 0.02). Grade 2 or higher nephrotoxicity occurred less frequently in patients who received mannitol versus those who did not (8% vs. 17%; P = 0.04). Non-gynecologic regimens and those who received doses ≥70 mg/m2 of cisplatin had lower rates of grade 2 or higher nephrotoxicity with mannitol (6% vs. 23%; P = 0.001, and 7% vs. 22%; P = 0.03, respectively). Conclusion The use of mannitol reduces the incidence and severity of nephrotoxicity in patients treated with cisplatin. The results of the study suggest mannitol may be most effective when used with non-gynecologic regimens and with cisplatin doses ≥70 mg/m2.</description><subject>Academic Medical Centers</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Cisplatin - adverse effects</subject><subject>Creatinine</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Health care facilities</subject><subject>Humans</subject><subject>Hydration</subject><subject>Incidence</subject><subject>Inpatients</subject><subject>Kidney Diseases - chemically induced</subject><subject>Kidney Diseases - prevention &amp; control</subject><subject>Male</subject><subject>Mannitol</subject><subject>Mannitol - administration &amp; dosage</subject><subject>Middle Aged</subject><subject>Outpatients</subject><subject>Renal function</subject><subject>Retrospective Studies</subject><subject>Studies</subject><subject>Toxicity</subject><issn>1078-1552</issn><issn>1477-092X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1Uc1rFDEUD6LYWr17koDnqfmYTDLeSlErVLwoeBteMy-7KTPJmGSW7h_q_2PqdlUEIZC8_L5e8gh5ydk551q_4UwbrpTgXae6XuhH5JS3WjesF98e13OFm3v8hDzL-ZYxZrQwT8mJ0FKJjqtT8uMThOBLnKiLiZYt0iXhDkPxMdDoqPV5maD40PgwrhZHGnDZpljinbe-7N_SC5qwpJgXtMXvkNo4L5B8Pui3-zHBL7NlWjOdj2k7TLnWf2CYYkDqQ11LvakdUAgjjWs5lgk3fsaQKVSITpA2SMHCiLO3dMbRW5iorUxMz8kTB1PGFw_7Gfn6_t2Xy6vm-vOHj5cX141tJS-NAdZC2yqhBNMcXOu4EaC4k44pJTUIbI1T1vRGYitQSSM714-VxVDDjTwjrw--S4rfV8xluI1rCjVy4L3kPZdamcpiB5at35QTumFJfoa0Hzgb7uc4_DvHKnn1YLze1Kf9FhwHVwnNgZBhg3-l_s_wJ6Znqrg</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Williams, Robert P</creator><creator>Ferlas, Brandon W</creator><creator>Morales, Paul C</creator><creator>Kurtzweil, Andy J</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20170901</creationdate><title>Mannitol for the prevention of cisplatin-induced nephrotoxicity: A retrospective comparison of hydration plus mannitol versus hydration alone in inpatient and outpatient regimens at a large academic medical center</title><author>Williams, Robert P ; Ferlas, Brandon W ; Morales, Paul C ; Kurtzweil, Andy J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-8a04a445252071af4f182a51f3f05537a2e48f5c8983e42e53836f9d1820e7ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Academic Medical Centers</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Chemotherapy</topic><topic>Cisplatin</topic><topic>Cisplatin - adverse effects</topic><topic>Creatinine</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Health care facilities</topic><topic>Humans</topic><topic>Hydration</topic><topic>Incidence</topic><topic>Inpatients</topic><topic>Kidney Diseases - chemically induced</topic><topic>Kidney Diseases - prevention &amp; control</topic><topic>Male</topic><topic>Mannitol</topic><topic>Mannitol - administration &amp; dosage</topic><topic>Middle Aged</topic><topic>Outpatients</topic><topic>Renal function</topic><topic>Retrospective Studies</topic><topic>Studies</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, Robert P</creatorcontrib><creatorcontrib>Ferlas, Brandon W</creatorcontrib><creatorcontrib>Morales, Paul C</creatorcontrib><creatorcontrib>Kurtzweil, Andy J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>Journal of oncology pharmacy practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, Robert P</au><au>Ferlas, Brandon W</au><au>Morales, Paul C</au><au>Kurtzweil, Andy J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mannitol for the prevention of cisplatin-induced nephrotoxicity: A retrospective comparison of hydration plus mannitol versus hydration alone in inpatient and outpatient regimens at a large academic medical center</atitle><jtitle>Journal of oncology pharmacy practice</jtitle><addtitle>J Oncol Pharm Pract</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>23</volume><issue>6</issue><spage>422</spage><epage>428</epage><pages>422-428</pages><issn>1078-1552</issn><eissn>1477-092X</eissn><abstract>Background Cisplatin-induced nephrotoxicity is a dose limiting adverse effect that occurs in nearly one-third of patients. Mannitol administration has been used as a means to negate this toxicity. Data regarding the efficacy of mannitol use in this context are conflicting and limited. Objective The aim of this study is to evaluate the effect of mannitol on renal function and describe the incidence of cisplatin-induced nephrotoxicity. Methods This study is a quasi-experimental retrospective analysis approved by the Institutional Review Board of inpatient and outpatient adults receiving cisplatin doses ≥40 mg/m2. The primary outcome was mean change in serum creatinine from baseline. Secondary outcomes included incidences of various grades of nephrotoxicity. Results A total of 313 patients (95 treated with mannitol and 218 without) were evaluated. The average increase in serum creatinine (mg/dL) was lower in patients who received mannitol versus those who did not (0.30 vs. 0.47; 95% confidence interval for difference, 0.03 to 0.31; P = 0.02). Grade 2 or higher nephrotoxicity occurred less frequently in patients who received mannitol versus those who did not (8% vs. 17%; P = 0.04). Non-gynecologic regimens and those who received doses ≥70 mg/m2 of cisplatin had lower rates of grade 2 or higher nephrotoxicity with mannitol (6% vs. 23%; P = 0.001, and 7% vs. 22%; P = 0.03, respectively). Conclusion The use of mannitol reduces the incidence and severity of nephrotoxicity in patients treated with cisplatin. The results of the study suggest mannitol may be most effective when used with non-gynecologic regimens and with cisplatin doses ≥70 mg/m2.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>27352615</pmid><doi>10.1177/1078155216656927</doi><tpages>7</tpages></addata></record>
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1477-092X
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subjects Academic Medical Centers
Adult
Aged
Antineoplastic Agents - adverse effects
Chemotherapy
Cisplatin
Cisplatin - adverse effects
Creatinine
Drug therapy
Female
Health care facilities
Humans
Hydration
Incidence
Inpatients
Kidney Diseases - chemically induced
Kidney Diseases - prevention & control
Male
Mannitol
Mannitol - administration & dosage
Middle Aged
Outpatients
Renal function
Retrospective Studies
Studies
Toxicity
title Mannitol for the prevention of cisplatin-induced nephrotoxicity: A retrospective comparison of hydration plus mannitol versus hydration alone in inpatient and outpatient regimens at a large academic medical center
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