Loading…

Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients

Liposomal amphotercin B was compared with conventional amphotericin B for empirical antifungal therapy in febrile neutropenic patients in a randomized, double-blind, multicentre trial. Using a composite end-point, the two drugs were equivalent in overall efficacy. However, the liposomal amphotericin...

Full description

Saved in:
Bibliographic Details
Published in:Journal of antimicrobial chemotherapy 2002, Vol.49 (suppl_1), p.81-86
Main Author: CAGNONI, Pablo J
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c428t-9830d35e1c63d3a25dacf991a3a7d50370b4fcc40ec022e021f91e6304b000293
cites
container_end_page 86
container_issue suppl_1
container_start_page 81
container_title Journal of antimicrobial chemotherapy
container_volume 49
creator CAGNONI, Pablo J
description Liposomal amphotercin B was compared with conventional amphotericin B for empirical antifungal therapy in febrile neutropenic patients in a randomized, double-blind, multicentre trial. Using a composite end-point, the two drugs were equivalent in overall efficacy. However, the liposomal amphotericin B treatment group had fewer proven fungal infections, fewer infusion-related side effects and less nephrotoxicity. Patient data from that study were analysed to compare the pharmacoeconomics of liposomal versus conventional amphotericin B therapy. Itemized billing data from 414 patients were collected and analysed. Hospital costs from first dose were significantly higher for all patients who received liposomal amphotericin B ($48,962 versus $43,183, P = 0.02). However, hospital costs were very sensitive to the cost of the study medication ($39,648 versus $43,048, when acquisition costs are not included, P = 0.4). Using decision analysis models and sensitivity analyses to vary the cost of study medications and risk of nephrotoxicity, the break-even points for the cost of liposomal therapy were calculated to range from $72 to $87 per 50 mg for all patients, and $83 to $112 per 50 mg in allogeneic bone marrow transplant patients. Therefore, the drug acquisition costs and the risk of nephrotoxicity are important factors in determining the cost-effectiveness of liposomal amphotericin B as empirical therapy in persistently febrile neutropenic patients. In a recent randomized double-blind study comparing liposomal amphotericin B at 3 or 5 mg/kg/day with amphotericin B lipid complex (ABLC) 5 mg/kg/day as empirical antifungal treatment in patients with febrile neutropenia, liposomal amphotericin B was associated with less toxicity than ABLC, both in terms of infusion-related reactions and nephrotoxicity. The incidence of study drug discontinuation due to toxicity was: liposomal amphotericin B 3 mg/kg/day, 14%; liposomal amphotericin B 5 mg/kg/day, 15%; and ABLC, 42% (P < 0.001).
doi_str_mv 10.1093/jac/49.suppl_1.81
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_18642945</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18642945</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-9830d35e1c63d3a25dacf991a3a7d50370b4fcc40ec022e021f91e6304b000293</originalsourceid><addsrcrecordid>eNplkU-LFDEQxYMo7jj6AbxIEPTWs6kknU6OuvgPBrzoOWTS1WyG7k5M0gt79osb2YEFvVSo1K8e1HuEvAZ2AGbE9dn5a2kOZUtptnDQ8ITsQCrWcWbgKdkxwfpukL24Ii9KOTPGVK_0c3IFoBn0etiR38eQYomLm6lb0m2smIMPK_1I7zCXrVAf1ztca4jr_0gr9RYpLim0rzavGV1dGk7jRFMTCKW2br6nE55ymJGuuNUcE67B0-RqaNPykjyb3Fzw1eXdk5-fP_24-dodv3_5dvPh2HnJde2MFmwUPYJXYhSO96PzkzHghBvGnomBneTkvWToGefIOEwGUAkmT-1ybsSevH_QTTn-2rBUu4TicZ7dinErFrSS3DS79uTtP-A5brkZUCyHQSktlW4QPEA-x1IyTjblsLh8b4HZv_HYFo-Vxl7isRrazpuL8HZacHzcuOTRgHcXwJVm6JTd6kN55MSgeqG5-AONL52b</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217668468</pqid></control><display><type>article</type><title>Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients</title><source>Oxford Journals Online</source><creator>CAGNONI, Pablo J</creator><creatorcontrib>CAGNONI, Pablo J</creatorcontrib><description>Liposomal amphotercin B was compared with conventional amphotericin B for empirical antifungal therapy in febrile neutropenic patients in a randomized, double-blind, multicentre trial. Using a composite end-point, the two drugs were equivalent in overall efficacy. However, the liposomal amphotericin B treatment group had fewer proven fungal infections, fewer infusion-related side effects and less nephrotoxicity. Patient data from that study were analysed to compare the pharmacoeconomics of liposomal versus conventional amphotericin B therapy. Itemized billing data from 414 patients were collected and analysed. Hospital costs from first dose were significantly higher for all patients who received liposomal amphotericin B ($48,962 versus $43,183, P = 0.02). However, hospital costs were very sensitive to the cost of the study medication ($39,648 versus $43,048, when acquisition costs are not included, P = 0.4). Using decision analysis models and sensitivity analyses to vary the cost of study medications and risk of nephrotoxicity, the break-even points for the cost of liposomal therapy were calculated to range from $72 to $87 per 50 mg for all patients, and $83 to $112 per 50 mg in allogeneic bone marrow transplant patients. Therefore, the drug acquisition costs and the risk of nephrotoxicity are important factors in determining the cost-effectiveness of liposomal amphotericin B as empirical therapy in persistently febrile neutropenic patients. In a recent randomized double-blind study comparing liposomal amphotericin B at 3 or 5 mg/kg/day with amphotericin B lipid complex (ABLC) 5 mg/kg/day as empirical antifungal treatment in patients with febrile neutropenia, liposomal amphotericin B was associated with less toxicity than ABLC, both in terms of infusion-related reactions and nephrotoxicity. The incidence of study drug discontinuation due to toxicity was: liposomal amphotericin B 3 mg/kg/day, 14%; liposomal amphotericin B 5 mg/kg/day, 15%; and ABLC, 42% (P &lt; 0.001).</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/49.suppl_1.81</identifier><identifier>PMID: 11801587</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Amphotericin B - administration &amp; dosage ; Amphotericin B - adverse effects ; Amphotericin B - economics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal agents ; Antifungal Agents - administration &amp; dosage ; Antifungal Agents - adverse effects ; Antifungal Agents - economics ; Biological and medical sciences ; Drug Combinations ; Humans ; Liposomes ; Medical sciences ; Neutropenia - drug therapy ; Neutropenia - economics ; Pharmacology. Drug treatments ; Phosphatidylcholines - administration &amp; dosage ; Phosphatidylcholines - adverse effects ; Phosphatidylcholines - economics ; Phosphatidylglycerols - administration &amp; dosage ; Phosphatidylglycerols - adverse effects ; Phosphatidylglycerols - economics</subject><ispartof>Journal of antimicrobial chemotherapy, 2002, Vol.49 (suppl_1), p.81-86</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Jan 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-9830d35e1c63d3a25dacf991a3a7d50370b4fcc40ec022e021f91e6304b000293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,4023,4049,4050,23929,23930,25139,27922,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13765382$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11801587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CAGNONI, Pablo J</creatorcontrib><title>Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Liposomal amphotercin B was compared with conventional amphotericin B for empirical antifungal therapy in febrile neutropenic patients in a randomized, double-blind, multicentre trial. Using a composite end-point, the two drugs were equivalent in overall efficacy. However, the liposomal amphotericin B treatment group had fewer proven fungal infections, fewer infusion-related side effects and less nephrotoxicity. Patient data from that study were analysed to compare the pharmacoeconomics of liposomal versus conventional amphotericin B therapy. Itemized billing data from 414 patients were collected and analysed. Hospital costs from first dose were significantly higher for all patients who received liposomal amphotericin B ($48,962 versus $43,183, P = 0.02). However, hospital costs were very sensitive to the cost of the study medication ($39,648 versus $43,048, when acquisition costs are not included, P = 0.4). Using decision analysis models and sensitivity analyses to vary the cost of study medications and risk of nephrotoxicity, the break-even points for the cost of liposomal therapy were calculated to range from $72 to $87 per 50 mg for all patients, and $83 to $112 per 50 mg in allogeneic bone marrow transplant patients. Therefore, the drug acquisition costs and the risk of nephrotoxicity are important factors in determining the cost-effectiveness of liposomal amphotericin B as empirical therapy in persistently febrile neutropenic patients. In a recent randomized double-blind study comparing liposomal amphotericin B at 3 or 5 mg/kg/day with amphotericin B lipid complex (ABLC) 5 mg/kg/day as empirical antifungal treatment in patients with febrile neutropenia, liposomal amphotericin B was associated with less toxicity than ABLC, both in terms of infusion-related reactions and nephrotoxicity. The incidence of study drug discontinuation due to toxicity was: liposomal amphotericin B 3 mg/kg/day, 14%; liposomal amphotericin B 5 mg/kg/day, 15%; and ABLC, 42% (P &lt; 0.001).</description><subject>Amphotericin B - administration &amp; dosage</subject><subject>Amphotericin B - adverse effects</subject><subject>Amphotericin B - economics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - administration &amp; dosage</subject><subject>Antifungal Agents - adverse effects</subject><subject>Antifungal Agents - economics</subject><subject>Biological and medical sciences</subject><subject>Drug Combinations</subject><subject>Humans</subject><subject>Liposomes</subject><subject>Medical sciences</subject><subject>Neutropenia - drug therapy</subject><subject>Neutropenia - economics</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphatidylcholines - administration &amp; dosage</subject><subject>Phosphatidylcholines - adverse effects</subject><subject>Phosphatidylcholines - economics</subject><subject>Phosphatidylglycerols - administration &amp; dosage</subject><subject>Phosphatidylglycerols - adverse effects</subject><subject>Phosphatidylglycerols - economics</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNplkU-LFDEQxYMo7jj6AbxIEPTWs6kknU6OuvgPBrzoOWTS1WyG7k5M0gt79osb2YEFvVSo1K8e1HuEvAZ2AGbE9dn5a2kOZUtptnDQ8ITsQCrWcWbgKdkxwfpukL24Ii9KOTPGVK_0c3IFoBn0etiR38eQYomLm6lb0m2smIMPK_1I7zCXrVAf1ztca4jr_0gr9RYpLim0rzavGV1dGk7jRFMTCKW2br6nE55ymJGuuNUcE67B0-RqaNPykjyb3Fzw1eXdk5-fP_24-dodv3_5dvPh2HnJde2MFmwUPYJXYhSO96PzkzHghBvGnomBneTkvWToGefIOEwGUAkmT-1ybsSevH_QTTn-2rBUu4TicZ7dinErFrSS3DS79uTtP-A5brkZUCyHQSktlW4QPEA-x1IyTjblsLh8b4HZv_HYFo-Vxl7isRrazpuL8HZacHzcuOTRgHcXwJVm6JTd6kN55MSgeqG5-AONL52b</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>CAGNONI, Pablo J</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>2002</creationdate><title>Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients</title><author>CAGNONI, Pablo J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-9830d35e1c63d3a25dacf991a3a7d50370b4fcc40ec022e021f91e6304b000293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amphotericin B - administration &amp; dosage</topic><topic>Amphotericin B - adverse effects</topic><topic>Amphotericin B - economics</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - administration &amp; dosage</topic><topic>Antifungal Agents - adverse effects</topic><topic>Antifungal Agents - economics</topic><topic>Biological and medical sciences</topic><topic>Drug Combinations</topic><topic>Humans</topic><topic>Liposomes</topic><topic>Medical sciences</topic><topic>Neutropenia - drug therapy</topic><topic>Neutropenia - economics</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphatidylcholines - administration &amp; dosage</topic><topic>Phosphatidylcholines - adverse effects</topic><topic>Phosphatidylcholines - economics</topic><topic>Phosphatidylglycerols - administration &amp; dosage</topic><topic>Phosphatidylglycerols - adverse effects</topic><topic>Phosphatidylglycerols - economics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAGNONI, Pablo J</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAGNONI, Pablo J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2002</date><risdate>2002</risdate><volume>49</volume><issue>suppl_1</issue><spage>81</spage><epage>86</epage><pages>81-86</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Liposomal amphotercin B was compared with conventional amphotericin B for empirical antifungal therapy in febrile neutropenic patients in a randomized, double-blind, multicentre trial. Using a composite end-point, the two drugs were equivalent in overall efficacy. However, the liposomal amphotericin B treatment group had fewer proven fungal infections, fewer infusion-related side effects and less nephrotoxicity. Patient data from that study were analysed to compare the pharmacoeconomics of liposomal versus conventional amphotericin B therapy. Itemized billing data from 414 patients were collected and analysed. Hospital costs from first dose were significantly higher for all patients who received liposomal amphotericin B ($48,962 versus $43,183, P = 0.02). However, hospital costs were very sensitive to the cost of the study medication ($39,648 versus $43,048, when acquisition costs are not included, P = 0.4). Using decision analysis models and sensitivity analyses to vary the cost of study medications and risk of nephrotoxicity, the break-even points for the cost of liposomal therapy were calculated to range from $72 to $87 per 50 mg for all patients, and $83 to $112 per 50 mg in allogeneic bone marrow transplant patients. Therefore, the drug acquisition costs and the risk of nephrotoxicity are important factors in determining the cost-effectiveness of liposomal amphotericin B as empirical therapy in persistently febrile neutropenic patients. In a recent randomized double-blind study comparing liposomal amphotericin B at 3 or 5 mg/kg/day with amphotericin B lipid complex (ABLC) 5 mg/kg/day as empirical antifungal treatment in patients with febrile neutropenia, liposomal amphotericin B was associated with less toxicity than ABLC, both in terms of infusion-related reactions and nephrotoxicity. The incidence of study drug discontinuation due to toxicity was: liposomal amphotericin B 3 mg/kg/day, 14%; liposomal amphotericin B 5 mg/kg/day, 15%; and ABLC, 42% (P &lt; 0.001).</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>11801587</pmid><doi>10.1093/jac/49.suppl_1.81</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0305-7453
ispartof Journal of antimicrobial chemotherapy, 2002, Vol.49 (suppl_1), p.81-86
issn 0305-7453
1460-2091
language eng
recordid cdi_proquest_miscellaneous_18642945
source Oxford Journals Online
subjects Amphotericin B - administration & dosage
Amphotericin B - adverse effects
Amphotericin B - economics
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antifungal agents
Antifungal Agents - administration & dosage
Antifungal Agents - adverse effects
Antifungal Agents - economics
Biological and medical sciences
Drug Combinations
Humans
Liposomes
Medical sciences
Neutropenia - drug therapy
Neutropenia - economics
Pharmacology. Drug treatments
Phosphatidylcholines - administration & dosage
Phosphatidylcholines - adverse effects
Phosphatidylcholines - economics
Phosphatidylglycerols - administration & dosage
Phosphatidylglycerols - adverse effects
Phosphatidylglycerols - economics
title Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T16%3A25%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Liposomal%20amphotericin%20B%20versus%20conventional%20amphotericin%20B%20in%20the%20empirical%20treatment%20of%20persistently%20febrile%20neutropenic%20patients&rft.jtitle=Journal%20of%20antimicrobial%20chemotherapy&rft.au=CAGNONI,%20Pablo%20J&rft.date=2002&rft.volume=49&rft.issue=suppl_1&rft.spage=81&rft.epage=86&rft.pages=81-86&rft.issn=0305-7453&rft.eissn=1460-2091&rft.coden=JACHDX&rft_id=info:doi/10.1093/jac/49.suppl_1.81&rft_dat=%3Cproquest_cross%3E18642945%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c428t-9830d35e1c63d3a25dacf991a3a7d50370b4fcc40ec022e021f91e6304b000293%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=217668468&rft_id=info:pmid/11801587&rfr_iscdi=true