Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach—an Indian experience
Purpose Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard’s Bayesian algorithms use information from model and individual multivariate determinants of IFX concentr...
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Veröffentlicht in: | European journal of clinical pharmacology 2021, Vol.77 (1), p.55-62 |
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creator | Dave, Mihika B. Dherai, Alpa J. Desai, Devendra C. Mould, Diane R. Ashavaid, Tester F. |
description | Purpose
Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard’s Bayesian algorithms use information from model and individual multivariate determinants of IFX concentration and can predict dose and dosing interval.
Aim
To compare measured IFX concentrations in our laboratory with values predicted by iDose dashboard system and report its efficacy in managing patients not responding to conventional dosing schedule.
Method
Clinical history, demographic details, and laboratory findings such as albumin and C-reactive protein (CRP) data of IBD patients (
n
= 30; median age 23 years (IQR: 14.25 – 33.5)) referred for IFX drug monitoring in our laboratory from November 2017 to November 2019 were entered in iDose software. The IFX concentration predicted by iDose based on this information was compared with that measured in our laboratory. In addition, a prospective dashboard-guided dosing was prescribed in 11 of these 30 patients not responding to conventional dosing and was followed to assess their clinical outcome.
Result
IFX monitoring in our 30 patients had shown therapeutic concentration in 12, supratherapeutic in 2 and subtherapeutic concentration in 16 patients. The iDose predicted concentration showed concordance in 21 of these 30 patients. Of 11 patients managed with iDose-assisted prospective dosing, 8 achieved clinical remission, 2 showed partial response, and one developed antibodies.
Conclusion
Retrospective data analysis showed concordance between laboratory measured and iDose-predicted IFX level in 70% of patients. iDose-assisted management achieved clinical remission and cost reduction. |
doi_str_mv | 10.1007/s00228-020-02975-0 |
format | Article |
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Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard’s Bayesian algorithms use information from model and individual multivariate determinants of IFX concentration and can predict dose and dosing interval.
Aim
To compare measured IFX concentrations in our laboratory with values predicted by iDose dashboard system and report its efficacy in managing patients not responding to conventional dosing schedule.
Method
Clinical history, demographic details, and laboratory findings such as albumin and C-reactive protein (CRP) data of IBD patients (
n
= 30; median age 23 years (IQR: 14.25 – 33.5)) referred for IFX drug monitoring in our laboratory from November 2017 to November 2019 were entered in iDose software. The IFX concentration predicted by iDose based on this information was compared with that measured in our laboratory. In addition, a prospective dashboard-guided dosing was prescribed in 11 of these 30 patients not responding to conventional dosing and was followed to assess their clinical outcome.
Result
IFX monitoring in our 30 patients had shown therapeutic concentration in 12, supratherapeutic in 2 and subtherapeutic concentration in 16 patients. The iDose predicted concentration showed concordance in 21 of these 30 patients. Of 11 patients managed with iDose-assisted prospective dosing, 8 achieved clinical remission, 2 showed partial response, and one developed antibodies.
Conclusion
Retrospective data analysis showed concordance between laboratory measured and iDose-predicted IFX level in 70% of patients. iDose-assisted management achieved clinical remission and cost reduction.</description><identifier>ISSN: 0031-6970</identifier><identifier>EISSN: 1432-1041</identifier><identifier>DOI: 10.1007/s00228-020-02975-0</identifier><identifier>PMID: 32803288</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Bayesian analysis ; Biomedical and Life Sciences ; Biomedicine ; C-reactive protein ; Dosage ; Immunotherapy ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Infliximab ; Intestine ; Laboratories ; Monoclonal antibodies ; Pharmacokinetics and Disposition ; Pharmacology/Toxicology ; Remission ; Therapeutic drug monitoring ; TNF inhibitors ; Tumor necrosis factor-α</subject><ispartof>European journal of clinical pharmacology, 2021, Vol.77 (1), p.55-62</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020. corrected publication September 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020. corrected publication September 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-8edffa3443c6b0b716df6a3a86184f7f08d2f009731bfabb32ec6e8ffff278f33</citedby><cites>FETCH-LOGICAL-c375t-8edffa3443c6b0b716df6a3a86184f7f08d2f009731bfabb32ec6e8ffff278f33</cites><orcidid>0000-0002-5574-3798</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00228-020-02975-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00228-020-02975-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27915,27916,41479,42548,51310</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32803288$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dave, Mihika B.</creatorcontrib><creatorcontrib>Dherai, Alpa J.</creatorcontrib><creatorcontrib>Desai, Devendra C.</creatorcontrib><creatorcontrib>Mould, Diane R.</creatorcontrib><creatorcontrib>Ashavaid, Tester F.</creatorcontrib><title>Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach—an Indian experience</title><title>European journal of clinical pharmacology</title><addtitle>Eur J Clin Pharmacol</addtitle><addtitle>Eur J Clin Pharmacol</addtitle><description>Purpose
Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard’s Bayesian algorithms use information from model and individual multivariate determinants of IFX concentration and can predict dose and dosing interval.
Aim
To compare measured IFX concentrations in our laboratory with values predicted by iDose dashboard system and report its efficacy in managing patients not responding to conventional dosing schedule.
Method
Clinical history, demographic details, and laboratory findings such as albumin and C-reactive protein (CRP) data of IBD patients (
n
= 30; median age 23 years (IQR: 14.25 – 33.5)) referred for IFX drug monitoring in our laboratory from November 2017 to November 2019 were entered in iDose software. The IFX concentration predicted by iDose based on this information was compared with that measured in our laboratory. In addition, a prospective dashboard-guided dosing was prescribed in 11 of these 30 patients not responding to conventional dosing and was followed to assess their clinical outcome.
Result
IFX monitoring in our 30 patients had shown therapeutic concentration in 12, supratherapeutic in 2 and subtherapeutic concentration in 16 patients. The iDose predicted concentration showed concordance in 21 of these 30 patients. Of 11 patients managed with iDose-assisted prospective dosing, 8 achieved clinical remission, 2 showed partial response, and one developed antibodies.
Conclusion
Retrospective data analysis showed concordance between laboratory measured and iDose-predicted IFX level in 70% of patients. iDose-assisted management achieved clinical remission and cost reduction.</description><subject>Bayesian analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>C-reactive protein</subject><subject>Dosage</subject><subject>Immunotherapy</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Infliximab</subject><subject>Intestine</subject><subject>Laboratories</subject><subject>Monoclonal antibodies</subject><subject>Pharmacokinetics and Disposition</subject><subject>Pharmacology/Toxicology</subject><subject>Remission</subject><subject>Therapeutic drug monitoring</subject><subject>TNF inhibitors</subject><subject>Tumor necrosis factor-α</subject><issn>0031-6970</issn><issn>1432-1041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1u1TAQhS0EopfCC7BAltiwCYztJHaWqOKnUqVuYG2Nk3Gvq8QJdiJ6u-IheEKeBNNbQGLBSKORZr45Hvkw9lzAawGg32QAKU0FEkp2uqngAduJWslKQC0esh2AElXbaThhT3K-BhBNB-oxO1HSQEmzY-lyWcMUbnENc-Sz5yH6MdyECR1f95RwOZTWXRenCdc5Hbibv9LIh5AJM_Eth3jFkQ-Y927GNHBcljRjv__x7TtGfh6HUArdLJQCxZ6eskcex0zP7usp-_z-3aezj9XF5Yfzs7cXVa90s1aGBu9R1bXqWwdOi3bwLSo0rTC11x7MID1Ap5VwHp1TkvqWjC8htfFKnbJXR91yzZeN8mqnkHsaR4w0b9nKWtW6qduuKejLf9DreUuxXFco3YBSujWFkkeqT3POibxdUvmodLAC7C9H7NERWxyxd45YKEsv7qU3N9HwZ-W3BQVQRyCXUbyi9Pft_8j-BBIjmWY</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Dave, Mihika B.</creator><creator>Dherai, Alpa J.</creator><creator>Desai, Devendra C.</creator><creator>Mould, Diane R.</creator><creator>Ashavaid, Tester F.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7U9</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>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</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><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5574-3798</orcidid></search><sort><creationdate>2021</creationdate><title>Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach—an Indian experience</title><author>Dave, Mihika B. ; Dherai, Alpa J. ; Desai, Devendra C. ; Mould, Diane R. ; Ashavaid, Tester F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-8edffa3443c6b0b716df6a3a86184f7f08d2f009731bfabb32ec6e8ffff278f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bayesian analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>C-reactive protein</topic><topic>Dosage</topic><topic>Immunotherapy</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Infliximab</topic><topic>Intestine</topic><topic>Laboratories</topic><topic>Monoclonal antibodies</topic><topic>Pharmacokinetics and Disposition</topic><topic>Pharmacology/Toxicology</topic><topic>Remission</topic><topic>Therapeutic drug monitoring</topic><topic>TNF inhibitors</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dave, Mihika B.</creatorcontrib><creatorcontrib>Dherai, Alpa J.</creatorcontrib><creatorcontrib>Desai, Devendra C.</creatorcontrib><creatorcontrib>Mould, Diane R.</creatorcontrib><creatorcontrib>Ashavaid, Tester F.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</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><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dave, Mihika B.</au><au>Dherai, Alpa J.</au><au>Desai, Devendra C.</au><au>Mould, Diane R.</au><au>Ashavaid, Tester F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach—an Indian experience</atitle><jtitle>European journal of clinical pharmacology</jtitle><stitle>Eur J Clin Pharmacol</stitle><addtitle>Eur J Clin Pharmacol</addtitle><date>2021</date><risdate>2021</risdate><volume>77</volume><issue>1</issue><spage>55</spage><epage>62</epage><pages>55-62</pages><issn>0031-6970</issn><eissn>1432-1041</eissn><abstract>Purpose
Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard’s Bayesian algorithms use information from model and individual multivariate determinants of IFX concentration and can predict dose and dosing interval.
Aim
To compare measured IFX concentrations in our laboratory with values predicted by iDose dashboard system and report its efficacy in managing patients not responding to conventional dosing schedule.
Method
Clinical history, demographic details, and laboratory findings such as albumin and C-reactive protein (CRP) data of IBD patients (
n
= 30; median age 23 years (IQR: 14.25 – 33.5)) referred for IFX drug monitoring in our laboratory from November 2017 to November 2019 were entered in iDose software. The IFX concentration predicted by iDose based on this information was compared with that measured in our laboratory. In addition, a prospective dashboard-guided dosing was prescribed in 11 of these 30 patients not responding to conventional dosing and was followed to assess their clinical outcome.
Result
IFX monitoring in our 30 patients had shown therapeutic concentration in 12, supratherapeutic in 2 and subtherapeutic concentration in 16 patients. The iDose predicted concentration showed concordance in 21 of these 30 patients. Of 11 patients managed with iDose-assisted prospective dosing, 8 achieved clinical remission, 2 showed partial response, and one developed antibodies.
Conclusion
Retrospective data analysis showed concordance between laboratory measured and iDose-predicted IFX level in 70% of patients. iDose-assisted management achieved clinical remission and cost reduction.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32803288</pmid><doi>10.1007/s00228-020-02975-0</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5574-3798</orcidid></addata></record> |
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source | Springer Nature - Complete Springer Journals |
subjects | Bayesian analysis Biomedical and Life Sciences Biomedicine C-reactive protein Dosage Immunotherapy Inflammatory bowel disease Inflammatory bowel diseases Infliximab Intestine Laboratories Monoclonal antibodies Pharmacokinetics and Disposition Pharmacology/Toxicology Remission Therapeutic drug monitoring TNF inhibitors Tumor necrosis factor-α |
title | Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach—an Indian experience |
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