Quantifying Women's Stated Benefit–Risk Trade-Off Preferences for IBS Treatment Outcomes
The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit–risk trade-off preferences is needed to compare risks and benefits in a common metric. The study aims...
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Published in | Value in health Vol. 13; no. 4; pp. 418 - 423 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Malden, USA
Elsevier Inc
01.06.2010
Blackwell Publishing Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1098-3015 1524-4733 1524-4733 |
DOI | 10.1111/j.1524-4733.2010.00694.x |
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Abstract | The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit–risk trade-off preferences is needed to compare risks and benefits in a common metric.
The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief.
Research design: A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs. Subjects: A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS.
Preference weights and MAR were estimated using mixed-logit methods.
Subjects were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk.
Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit–risk trade-off preferences that can be used to inform regulatory decision-making. |
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AbstractList | The Food and Drug Administration, currently, is exploring quantitative benefit-risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit-risk trade-off preferences is needed to compare risks and benefits in a common metric.BACKGROUNDThe Food and Drug Administration, currently, is exploring quantitative benefit-risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit-risk trade-off preferences is needed to compare risks and benefits in a common metric.The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief.OBJECTIVESThe study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief.A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs.RESEARCH DESIGNA stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs.A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS.SUBJECTSA Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS.Preference weights and MAR were estimated using mixed-logit methods.MEASURESPreference weights and MAR were estimated using mixed-logit methods.SUBJECTS were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk.RESULTSSUBJECTS were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk.Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit-risk trade-off preferences that can be used to inform regulatory decision-making.CONCLUSIONSVariation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit-risk trade-off preferences that can be used to inform regulatory decision-making. The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit–risk trade-off preferences is needed to compare risks and benefits in a common metric. The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief. Research design: A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs. Subjects: A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS. Preference weights and MAR were estimated using mixed-logit methods. Subjects were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk. Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit–risk trade-off preferences that can be used to inform regulatory decision-making. Background: The Food and Drug Administration, currently, is exploring quantitative benefit--risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit--risk trade-off preferences is needed to compare risks and benefits in a common metric. Objectives: The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief. Methods: Research design: A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs. Subjects: A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS. Measures: Preference weights and MAR were estimated using mixed-logit methods. Results: Subjects were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk. Conclusions: Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit--risk trade-off preferences that can be used to inform regulatory decision-making. Adapted from the source document. ABSTRACT Background: The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision‐making. A scientifically valid method for assessing patients' benefit–risk trade‐off preferences is needed to compare risks and benefits in a common metric. Objectives: The study aims to quantify the maximum acceptable risk (MAR) of treatment‐related adverse events (AEs) that women with diarrhea‐predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief. Methods: Research design: A stated‐choice survey was used to elicit trade‐off preferences among constructed treatment profiles, each defined by symptom severity and treatment‐related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild‐to‐moderate constipation and the risk of four possible serious AEs. Subjects: A Web‐enabled survey was administered to 589 female US residents at least 18 years of age with a self‐reported diagnosis of diarrhea‐predominant IBS. Measures: Preference weights and MAR were estimated using mixed‐logit methods. Results: Subjects were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted‐bowel risk, but only a 1.34% increase in perforated‐bowel risk. Conclusions: Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated‐preference methods offer a scientifically valid approach to quantifying benefit–risk trade‐off preferences that can be used to inform regulatory decision‐making. The Food and Drug Administration, currently, is exploring quantitative benefit-risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit-risk trade-off preferences is needed to compare risks and benefits in a common metric. The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief. A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs. A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS. Preference weights and MAR were estimated using mixed-logit methods. SUBJECTS were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk. Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit-risk trade-off preferences that can be used to inform regulatory decision-making. Abstract Background The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A scientifically valid method for assessing patients' benefit–risk trade-off preferences is needed to compare risks and benefits in a common metric. Objectives The study aims to quantify the maximum acceptable risk (MAR) of treatment-related adverse events (AEs) that women with diarrhea-predominant irritable bowel syndrome (IBS) are willing to accept in exchange for symptom relief. Methods Research design: A stated-choice survey was used to elicit trade-off preferences among constructed treatment profiles, each defined by symptom severity and treatment-related AEs. Symptom attributes included frequency of abdominal pain and discomfort, frequency of diarrhea, and frequency of urgency. AE attributes included frequency of mild-to-moderate constipation and the risk of four possible serious AEs. Subjects: A Web-enabled survey was administered to 589 female US residents at least 18 years of age with a self-reported diagnosis of diarrhea-predominant IBS. Measures Preference weights and MAR were estimated using mixed-logit methods. Results Subjects were willing to accept higher risks of serious AEs in return for treatments offering better symptom control. For an improvement from the lowest to the highest of four benefit levels, subjects were willing to tolerate a 2.65% increase in impacted-bowel risk, but only a 1.34% increase in perforated-bowel risk. Conclusions Variation in MARs across AE types is consistent with the relative seriousness of the AEs. Stated-preference methods offer a scientifically valid approach to quantifying benefit–risk trade-off preferences that can be used to inform regulatory decision-making. |
Author | Johnson, F. Reed Özdemir, Semra Hauber, A. Brett Lynd, Larry |
Author_xml | – sequence: 1 givenname: F. Reed surname: Johnson fullname: Johnson, F. Reed email: frjohnson@rti.org organization: RTI International, Research Triangle Park, NC, USA – sequence: 2 givenname: A. Brett surname: Hauber fullname: Hauber, A. Brett organization: RTI International, Research Triangle Park, NC, USA – sequence: 3 givenname: Semra surname: Özdemir fullname: Özdemir, Semra organization: University of North Carolina at Chapel Hill, Chapel Hill, NC, USA – sequence: 4 givenname: Larry surname: Lynd fullname: Lynd, Larry organization: University of British Columbia, Vancouver, BC, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20230550$$D View this record in MEDLINE/PubMed |
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Keywords | irritable bowel syndrome maximum acceptable risk incremental net benefits benefit–risk analysis conjoint analysis |
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SubjectTerms | Adult benefit–risk analysis Carbolines - adverse effects conjoint analysis Decision making Drug and Narcotic Control Female Gastrointestinal Agents - adverse effects Humans incremental net benefits Internal Medicine Irritable bowel syndrome Irritable Bowel Syndrome - drug therapy Logistic Models maximum acceptable risk Middle Aged Multivariate Analysis Patient Preference Preferences Quality of Life Risk Assessment - methods Risk Assessment - statistics & numerical data Severity of Illness Index Side effects Treatment preferences United States Women |
Title | Quantifying Women's Stated Benefit–Risk Trade-Off Preferences for IBS Treatment Outcomes |
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