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...

Full description

Saved in:
Bibliographic Details
Published inValue in health Vol. 13; no. 4; pp. 418 - 423
Main Authors Johnson, F. Reed, Hauber, A. Brett, Özdemir, Semra, Lynd, Larry
Format Journal Article
LanguageEnglish
Published Malden, USA Elsevier Inc 01.06.2010
Blackwell Publishing Inc
Subjects
Online AccessGet full text
ISSN1098-3015
1524-4733
1524-4733
DOI10.1111/j.1524-4733.2010.00694.x

Cover

Loading…
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.
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
BookMark eNqVks1u1DAUhS1URH_gFVB2XWXwT-IkEkIwVWkrVRpgCkhsLI9zjTzNOMV2aGfHO_CGPAk3TJkFEmLwxlf2d47te3xI9nzvgZCM0QnD8Ww5YSUv8qISYsIprlIqm2Jy94AcbDf2sKZNnQvKyn1yGOOSIiV4-Yjsc8oFLUt6QD69HbRPzq6d_5x97Ffgj2M2TzpBm03Bg3Xpx7fv71y8zq6CbiGfWZu9CWAhgDcQM9uH7GI6x13QCeUpmw3JoFF8TB5a3UV4cj8fkfevT69OzvPL2dnFyavL3EhOixy4rFnNFryparHAJZyZtYwtQALXWLdsJIA1dV0XsmokElAWtCi5lVockeON703ovwwQk1q5aKDrtId-iKoqCyYqLti_SVFQwWUhkHx6Tw6LFbTqJriVDmv1u3EI1BvAhD5G7McWYVSNGamlGqNQYxRqzEj9ykjdofTFH1LjsOGu9ylo1-1i8HxjcOs6WO98sPpwfooFyqcbOWAoXx0EFY0bw2xdAJNU27v_eMTWxHTOO6O7a1hDXPZD8Bi6YipyRdV8_IrjT2RUUlrJBg1e_t1gtzv8BJMh5nc
CitedBy_id crossref_primary_10_1007_s00520_014_2309_x
crossref_primary_10_1089_acm_2011_0015
crossref_primary_10_1111_apt_16917
crossref_primary_10_1111_papr_12100
crossref_primary_10_1371_journal_pone_0219905
crossref_primary_10_1007_s40273_014_0211_5
crossref_primary_10_1111_apt_16816
crossref_primary_10_1177_23743735221147762
crossref_primary_10_1016_j_pain_2013_03_024
crossref_primary_10_3389_fmed_2020_543046
crossref_primary_10_1007_s43441_020_00197_1
crossref_primary_10_1097_j_pain_0000000000001952
crossref_primary_10_1007_s40258_013_0028_y
crossref_primary_10_1111_hex_12256
crossref_primary_10_1007_s10198_022_01512_3
crossref_primary_10_1016_j_jocm_2014_12_001
crossref_primary_10_1007_s40271_014_0048_1
crossref_primary_10_1177_1558944720974123
crossref_primary_10_1111_nmo_14269
crossref_primary_10_1016_j_cgh_2022_02_016
crossref_primary_10_1136_bmjopen_2015_009387
crossref_primary_10_1007_s00345_017_2066_9
crossref_primary_10_1097_j_pain_0000000000002475
crossref_primary_10_1007_s40273_017_0518_0
crossref_primary_10_1161_CIRCOUTCOMES_114_001013
crossref_primary_10_1186_s12913_022_08464_7
crossref_primary_10_2147_PPA_S375062
crossref_primary_10_1007_s40290_014_0059_1
crossref_primary_10_1111_head_12142
crossref_primary_10_1111_jep_12635
Cites_doi 10.1089/jwh.2006.0218
10.1002/pds.1319
10.1001/archinte.165.12.1363
10.1001/archinte.161.14.1733
10.1111/j.1365-2133.2006.07535.x
10.1111/j.1572-0241.2001.03626.x
10.1016/j.jhealeco.2006.01.001
10.2307/3152127
10.1509/jmkr.39.2.214.19080
10.1097/MLR.0b013e318040ad90
10.1053/j.gastro.2007.04.075
10.2307/3151882
10.1016/S0140-6736(00)02033-X
10.1046/j.1365-2036.1999.00010.x
ContentType Journal Article
Copyright 2010 International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
2010, International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
Copyright_xml – notice: 2010 International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
– notice: International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
– notice: 2010, International Society for Pharmacoeconomics and Outcomes Research (ISPOR)
DBID 6I.
AAFTH
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7QJ
DOI 10.1111/j.1524-4733.2010.00694.x
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
Applied Social Sciences Index & Abstracts (ASSIA)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
Applied Social Sciences Index and Abstracts (ASSIA)
DatabaseTitleList MEDLINE - Academic

Applied Social Sciences Index and Abstracts (ASSIA)


MEDLINE

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Pharmacy, Therapeutics, & Pharmacology
EISSN 1524-4733
EndPage 423
ExternalDocumentID 20230550
10_1111_j_1524_4733_2010_00694_x
VHE694
S1098301510600769
1_s2_0_S1098301510600769
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations United States
GeographicLocations_xml – name: United States
GroupedDBID ---
--K
--M
.1-
.3N
.FO
.GA
.Y3
.~1
0R~
10A
123
1OC
1P~
1~.
29Q
31~
36B
4.4
44B
457
4G.
51W
51X
52N
52P
52R
52S
52X
53G
5LA
5VS
66C
6PF
7-5
7PT
8-1
8P~
8UM
AAEDT
AAEDW
AAFJI
AAFWJ
AAIKJ
AAKOC
AALRI
AAMMB
AAOAW
AAPFB
AAQFI
AAQXK
AATTM
AAWTL
AAXKI
AAXUO
AAYWO
ABBQC
ABCQN
ABDBF
ABEML
ABIVO
ABJNI
ABMAC
ABMMH
ABMZM
ABWVN
ABXDB
ACDAQ
ACGFS
ACHQT
ACIEU
ACPRK
ACRLP
ACRPL
ACUHS
ACVFH
ACXQS
ADBBV
ADCNI
ADEZE
ADFHU
ADMUD
ADNMO
ADVLN
AEBSH
AEFGJ
AEIPS
AEKER
AENEX
AEUPX
AEVXI
AEXQZ
AEYQN
AFBPY
AFEBI
AFJKZ
AFPUW
AFRHN
AFTJW
AFXIZ
AFZJQ
AGCQF
AGHFR
AGQPQ
AGTHC
AGUBO
AGXDD
AGYEJ
AIDQK
AIDYY
AIEXJ
AIGII
AIIAU
AIIUN
AIKHN
AITUG
AJAOE
AJRQY
AJUYK
AKBMS
AKRWK
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
ANKPU
ANZVX
AOMHK
APXCP
ASPBG
AVARZ
AVWKF
AXJTR
AXLSJ
AZFZN
BAWUL
BFHJK
BKOJK
BLXMC
BNPGV
BY8
CAG
CO8
COF
CS3
DCZOG
DIK
DU5
EAD
EAP
EBS
EFJIC
EFKBS
EJD
EMB
EMK
EMOBN
ESX
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
GBLVA
HF~
HVGLF
HZI
HZ~
IHE
IXB
KOM
LH4
M41
MO0
N9A
O-L
O9-
OAUVE
OIG
OK1
OVD
P-8
P-9
P2P
PC.
PQQKQ
PRBVW
Q38
QB0
R2-
ROL
SDF
SEL
SES
SPCBC
SSB
SSF
SSH
SSO
SSZ
SV3
T5K
TEORI
TUS
W99
WIN
WYUIH
XG1
YFH
Z5R
~G-
0SF
6I.
AACTN
AAFTH
AAHHS
ABVKL
ACCFJ
AEEZP
AEQDE
AFCTW
AFKWA
AIWBW
AJBDE
AJOXV
AMFUW
NCXOZ
RIG
SUPJJ
AAIAV
ABLVK
ABYKQ
AJBFU
AKYCK
EFLBG
IXIXF
LCYCR
AAYXX
AGRNS
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7QJ
ID FETCH-LOGICAL-c6204-e268181b29783b6209781ff11be6e2a81fd16818e1988846796978e540452f6a3
IEDL.DBID .~1
ISSN 1098-3015
1524-4733
IngestDate Fri Sep 05 14:49:07 EDT 2025
Fri Sep 05 13:09:56 EDT 2025
Mon Jul 21 06:03:50 EDT 2025
Tue Jul 01 02:49:12 EDT 2025
Thu Apr 24 23:05:48 EDT 2025
Wed Jan 22 17:04:08 EST 2025
Fri Feb 23 02:30:28 EST 2024
Sun Feb 23 10:18:50 EST 2025
Tue Aug 26 16:34:16 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords irritable bowel syndrome
maximum acceptable risk
incremental net benefits
benefit–risk analysis
conjoint analysis
Language English
License http://www.elsevier.com/open-access/userlicense/1.0
https://www.elsevier.com/tdm/userlicense/1.0
https://www.elsevier.com/open-access/userlicense/1.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c6204-e268181b29783b6209781ff11be6e2a81fd16818e1988846796978e540452f6a3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.sciencedirect.com/science/article/pii/S1098301510600769
PMID 20230550
PQID 734032643
PQPubID 23479
PageCount 6
ParticipantIDs proquest_miscellaneous_754137231
proquest_miscellaneous_734032643
pubmed_primary_20230550
crossref_primary_10_1111_j_1524_4733_2010_00694_x
crossref_citationtrail_10_1111_j_1524_4733_2010_00694_x
wiley_primary_10_1111_j_1524_4733_2010_00694_x_VHE694
elsevier_sciencedirect_doi_10_1111_j_1524_4733_2010_00694_x
elsevier_clinicalkeyesjournals_1_s2_0_S1098301510600769
elsevier_clinicalkey_doi_10_1111_j_1524_4733_2010_00694_x
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate June/July 2010
PublicationDateYYYYMMDD 2010-06-01
PublicationDate_xml – month: 06
  year: 2010
  text: June/July 2010
PublicationDecade 2010
PublicationPlace Malden, USA
PublicationPlace_xml – name: Malden, USA
– name: United States
PublicationTitle Value in health
PublicationTitleAlternate Value Health
PublicationYear 2010
Publisher Elsevier Inc
Blackwell Publishing Inc
Publisher_xml – name: Elsevier Inc
– name: Blackwell Publishing Inc
References Kanninen (bib140) 2002; 39
Mangel, Northcutt (bib220) 1999; 13
Johnson, Özdemir, Mansfield (bib90) 2009; 133
Camilleri, Chey, Mayer (bib200) 2001; 161
Camilleri, Northcutt, Kong (bib210) 2000; 355
Johnson, Ozdemir, Manjunath (bib60) 2007; 45
Ryan, Netten, Skatun, Smith (bib70) 2006; 25
(bib180) 2005
Zwerina K, Huber J, Kuhfeld WF. A general method for constructing efficient choice designs. SAS Working Paper, 2006.
Johnson, Ozdemir, Hauber, Kauf (bib100) 2007; 16
Kuhfeld, Garratt, Tobias (bib110) 1994; 31
Hensher, Rose, Greene (bib190) 2005
Institute of Medicine (bib30) 2007
Huber, Zwerina (bib130) 1996; 33
Wysowski, Swartz (bib10) 2005; 165
Lynd, Najafzadeh, Colley (bib50) 10 September 2009
Hirst, Cook, Dai (bib20) 2006; 15
Ashcroft, Seston, Griffiths (bib80) 2006; 155
Train (bib170) 2003
Dey (bib120) 1985
Ipsos Observer (bib160)
Wolfe, Chey, Washington (bib40) 2001; 96
2002; 39
2001; 161
2005; 165
2000; 355
2006; 25
2006; 15
2009
1999; 13
2009; 133
2007
1985
2006
2005
2003
2007; 45
2001; 96
2006; 155
2007; 16
1994; 31
1996; 33
10.1111/j.1524-4733.2010.00694.x_bib150
Johnson (10.1111/j.1524-4733.2010.00694.x_bib90) 2009; 133
Camilleri (10.1111/j.1524-4733.2010.00694.x_bib200) 2001; 161
Camilleri (10.1111/j.1524-4733.2010.00694.x_bib210) 2000; 355
Hirst (10.1111/j.1524-4733.2010.00694.x_bib20) 2006; 15
Hensher (10.1111/j.1524-4733.2010.00694.x_bib190) 2005
Wolfe (10.1111/j.1524-4733.2010.00694.x_bib40) 2001; 96
Train (10.1111/j.1524-4733.2010.00694.x_bib170) 2003
Ashcroft (10.1111/j.1524-4733.2010.00694.x_bib80) 2006; 155
Mangel (10.1111/j.1524-4733.2010.00694.x_bib220) 1999; 13
Institute of Medicine (10.1111/j.1524-4733.2010.00694.x_bib30) 2007
Ipsos Observer (10.1111/j.1524-4733.2010.00694.x_bib160)
Ryan (10.1111/j.1524-4733.2010.00694.x_bib70) 2006; 25
Dey (10.1111/j.1524-4733.2010.00694.x_bib120) 1985
Kuhfeld (10.1111/j.1524-4733.2010.00694.x_bib110) 1994; 31
Lynd (10.1111/j.1524-4733.2010.00694.x_bib50) 2009
Johnson (10.1111/j.1524-4733.2010.00694.x_bib100) 2007; 16
Kanninen (10.1111/j.1524-4733.2010.00694.x_bib140) 2002; 39
(10.1111/j.1524-4733.2010.00694.x_bib180) 2005
Wysowski (10.1111/j.1524-4733.2010.00694.x_bib10) 2005; 165
Huber (10.1111/j.1524-4733.2010.00694.x_bib130) 1996; 33
Johnson (10.1111/j.1524-4733.2010.00694.x_bib60) 2007; 45
References_xml – volume: 45
  start-page: 545
  year: 2007
  end-page: 552
  ident: bib60
  article-title: Factors that affect adherence to bipolar disorder treatments—a stated-preference approach
  publication-title: Med Care
– volume: 16
  start-page: 1028
  year: 2007
  end-page: 1040
  ident: bib100
  article-title: Women's willingness to accept perceived risks for vasomotor symptom relief
  publication-title: J Womens Health
– volume: 15
  start-page: 839
  year: 2006
  end-page: 849
  ident: bib20
  article-title: A call for international harmonization in therapeutic risk management
  publication-title: Pharmacoepidemiol Drug Saf
– volume: 133
  start-page: 769
  year: 2009
  end-page: 779
  ident: bib90
  article-title: Crohn's disease patients' risk-benefit preferences: serious adverse event risks versus treatment efficacy
  publication-title: Gastroenterology
– year: 2005
  ident: bib180
  publication-title: Gauss 7.0 [Computer Program]
– ident: bib160
  article-title: Data Collection
– year: 2005
  ident: bib190
  publication-title: Applied Choice Analysis: A Primer
– volume: 355
  start-page: 1035
  year: 2000
  end-page: 1040
  ident: bib210
  article-title: Efficacy and safety of alosetron in women with irritable bowel syndrome: a randomised, placebo-controlled trial
  publication-title: Lancet
– volume: 25
  start-page: 927
  year: 2006
  end-page: 944
  ident: bib70
  article-title: Using discrete choice experiments to estimate a preference-based measure of outcome—an application to social care for older people
  publication-title: J Health Econ
– volume: 31
  start-page: 545
  year: 1994
  end-page: 557
  ident: bib110
  article-title: Efficient experimental design with marketing research applications
  publication-title: J Mark Res
– year: 2003
  ident: bib170
  publication-title: Discrete Choice Methods with Simulation
– year: 1985
  ident: bib120
  publication-title: Orthogonal Fractional Factorial Designs
– volume: 165
  start-page: 1363
  year: 2005
  end-page: 1369
  ident: bib10
  article-title: Adverse drug event surveillance and drug withdrawals in the United States, 1969–2002: the importance of reporting suspected reactions
  publication-title: Arch Intern Med
– year: 2007
  ident: bib30
  publication-title: The Future of Drug Safety: Promoting and Protecting the Health of the Public
– volume: 155
  start-page: 1236
  year: 2006
  end-page: 1241
  ident: bib80
  article-title: Trade-offs between the benefits and risks of drug treatment for psoriasis: a discrete choice experiment with UK dermatologists
  publication-title: Br J Dermatol
– volume: 161
  start-page: 1733
  year: 2001
  end-page: 1740
  ident: bib200
  article-title: A randomized controlled clinical trial of the serotonin type 3 receptor antagonist alosetron in women with diarrhea-predominant irritable bowel syndrome
  publication-title: Arch Intern Med
– volume: 13
  start-page: 77
  year: 1999
  end-page: 82
  ident: bib220
  article-title: Review article: the safety and efficacy of alosetron, a 5-HT
  publication-title: Aliment Pharmacol Ther
– volume: 96
  start-page: 803
  year: 2001
  end-page: 811
  ident: bib40
  article-title: Tolerability and safety of alosetron during long-term administration in female and male irritable bowel syndrome patients
  publication-title: Am J Gastroenterol
– year: 10 September 2009
  ident: bib50
  article-title: Using the incremental net benefit framework for quantitative benefit–risk analysis in regulatory decision-making—a case study of alosetron in irritable bowel syndrome
  publication-title: Value Health
– volume: 33
  start-page: 307
  year: 1996
  end-page: 317
  ident: bib130
  article-title: The importance of utility balance in efficient choice designs
  publication-title: J Mark Res
– volume: 39
  start-page: 214
  year: 2002
  end-page: 227
  ident: bib140
  article-title: Optimal design for multinomial choice experiments
  publication-title: Journal of Marketing Research
– reference: Zwerina K, Huber J, Kuhfeld WF. A general method for constructing efficient choice designs. SAS Working Paper, 2006.
– year: 1985
– volume: 39
  start-page: 214
  year: 2002
  end-page: 27
  article-title: Optimal design for multinomial choice experiments
  publication-title: Journal of Marketing Research
– volume: 31
  start-page: 545
  year: 1994
  end-page: 57
  article-title: Efficient experimental design with marketing research applications
  publication-title: J Mark Res
– volume: 133
  start-page: 769
  year: 2009
  end-page: 79
  article-title: Crohn's disease patients' risk‐benefit preferences: serious adverse event risks versus treatment efficacy
  publication-title: Gastroenterology
– volume: 13
  start-page: 77
  issue: 2
  year: 1999
  end-page: 82
  article-title: Review article: the safety and efficacy of alosetron, a 5‐HT receptor antagonist, in female irritable bowel syndrome patients
  publication-title: Aliment Pharmacol Ther
– volume: 15
  start-page: 839
  year: 2006
  end-page: 49
  article-title: A call for international harmonization in therapeutic risk management
  publication-title: Pharmacoepidemiol Drug Saf
– year: 2005
– volume: 155
  start-page: 1236
  year: 2006
  end-page: 41
  article-title: Trade‐offs between the benefits and risks of drug treatment for psoriasis: a discrete choice experiment with UK dermatologists
  publication-title: Br J Dermatol
– volume: 33
  start-page: 307
  year: 1996
  end-page: 17
  article-title: The importance of utility balance in efficient choice designs
  publication-title: J Mark Res
– volume: 355
  start-page: 1035
  year: 2000
  end-page: 40
  article-title: Efficacy and safety of alosetron in women with irritable bowel syndrome: a randomised, placebo‐controlled trial
  publication-title: Lancet
– year: 2007
– year: 2006
– year: 2003
– volume: 25
  start-page: 927
  year: 2006
  end-page: 44
  article-title: Using discrete choice experiments to estimate a preference‐based measure of outcome—an application to social care for older people
  publication-title: J Health Econ
– volume: 16
  start-page: 1028
  year: 2007
  end-page: 40
  article-title: Women's willingness to accept perceived risks for vasomotor symptom relief
  publication-title: J Womens Health
– volume: 161
  start-page: 1733
  year: 2001
  end-page: 40
  article-title: A randomized controlled clinical trial of the serotonin type 3 receptor antagonist alosetron in women with diarrhea‐predominant irritable bowel syndrome
  publication-title: Arch Intern Med
– volume: 45
  start-page: 545
  year: 2007
  end-page: 52
  article-title: Factors that affect adherence to bipolar disorder treatments—a stated‐preference approach
  publication-title: Med Care
– volume: 165
  start-page: 1363
  year: 2005
  end-page: 9
  article-title: Adverse drug event surveillance and drug withdrawals in the United States, 1969–2002: the importance of reporting suspected reactions
  publication-title: Arch Intern Med
– year: 2009
  article-title: Using the incremental net benefit framework for quantitative benefit–risk analysis in regulatory decision‐making—a case study of alosetron in irritable bowel syndrome
  publication-title: Value Health
– volume: 96
  start-page: 803
  year: 2001
  end-page: 11
  article-title: Tolerability and safety of alosetron during long‐term administration in female and male irritable bowel syndrome patients
  publication-title: Am J Gastroenterol
– year: 1985
  ident: 10.1111/j.1524-4733.2010.00694.x_bib120
– year: 2005
  ident: 10.1111/j.1524-4733.2010.00694.x_bib190
– volume: 16
  start-page: 1028
  year: 2007
  ident: 10.1111/j.1524-4733.2010.00694.x_bib100
  article-title: Women's willingness to accept perceived risks for vasomotor symptom relief
  publication-title: J Womens Health
  doi: 10.1089/jwh.2006.0218
– volume: 15
  start-page: 839
  year: 2006
  ident: 10.1111/j.1524-4733.2010.00694.x_bib20
  article-title: A call for international harmonization in therapeutic risk management
  publication-title: Pharmacoepidemiol Drug Saf
  doi: 10.1002/pds.1319
– year: 2003
  ident: 10.1111/j.1524-4733.2010.00694.x_bib170
– volume: 165
  start-page: 1363
  year: 2005
  ident: 10.1111/j.1524-4733.2010.00694.x_bib10
  article-title: Adverse drug event surveillance and drug withdrawals in the United States, 1969–2002: the importance of reporting suspected reactions
  publication-title: Arch Intern Med
  doi: 10.1001/archinte.165.12.1363
– volume: 161
  start-page: 1733
  year: 2001
  ident: 10.1111/j.1524-4733.2010.00694.x_bib200
  article-title: A randomized controlled clinical trial of the serotonin type 3 receptor antagonist alosetron in women with diarrhea-predominant irritable bowel syndrome
  publication-title: Arch Intern Med
  doi: 10.1001/archinte.161.14.1733
– ident: 10.1111/j.1524-4733.2010.00694.x_bib150
– volume: 155
  start-page: 1236
  year: 2006
  ident: 10.1111/j.1524-4733.2010.00694.x_bib80
  article-title: Trade-offs between the benefits and risks of drug treatment for psoriasis: a discrete choice experiment with UK dermatologists
  publication-title: Br J Dermatol
  doi: 10.1111/j.1365-2133.2006.07535.x
– volume: 96
  start-page: 803
  year: 2001
  ident: 10.1111/j.1524-4733.2010.00694.x_bib40
  article-title: Tolerability and safety of alosetron during long-term administration in female and male irritable bowel syndrome patients
  publication-title: Am J Gastroenterol
  doi: 10.1111/j.1572-0241.2001.03626.x
– volume: 25
  start-page: 927
  year: 2006
  ident: 10.1111/j.1524-4733.2010.00694.x_bib70
  article-title: Using discrete choice experiments to estimate a preference-based measure of outcome—an application to social care for older people
  publication-title: J Health Econ
  doi: 10.1016/j.jhealeco.2006.01.001
– volume: 33
  start-page: 307
  year: 1996
  ident: 10.1111/j.1524-4733.2010.00694.x_bib130
  article-title: The importance of utility balance in efficient choice designs
  publication-title: J Mark Res
  doi: 10.2307/3152127
– volume: 39
  start-page: 214
  year: 2002
  ident: 10.1111/j.1524-4733.2010.00694.x_bib140
  article-title: Optimal design for multinomial choice experiments
  publication-title: Journal of Marketing Research
  doi: 10.1509/jmkr.39.2.214.19080
– year: 2009
  ident: 10.1111/j.1524-4733.2010.00694.x_bib50
  article-title: Using the incremental net benefit framework for quantitative benefit–risk analysis in regulatory decision-making—a case study of alosetron in irritable bowel syndrome
  publication-title: Value Health
– volume: 45
  start-page: 545
  year: 2007
  ident: 10.1111/j.1524-4733.2010.00694.x_bib60
  article-title: Factors that affect adherence to bipolar disorder treatments—a stated-preference approach
  publication-title: Med Care
  doi: 10.1097/MLR.0b013e318040ad90
– volume: 133
  start-page: 769
  year: 2009
  ident: 10.1111/j.1524-4733.2010.00694.x_bib90
  article-title: Crohn's disease patients' risk-benefit preferences: serious adverse event risks versus treatment efficacy
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2007.04.075
– volume: 31
  start-page: 545
  year: 1994
  ident: 10.1111/j.1524-4733.2010.00694.x_bib110
  article-title: Efficient experimental design with marketing research applications
  publication-title: J Mark Res
  doi: 10.2307/3151882
– ident: 10.1111/j.1524-4733.2010.00694.x_bib160
– year: 2005
  ident: 10.1111/j.1524-4733.2010.00694.x_bib180
– volume: 355
  start-page: 1035
  year: 2000
  ident: 10.1111/j.1524-4733.2010.00694.x_bib210
  article-title: Efficacy and safety of alosetron in women with irritable bowel syndrome: a randomised, placebo-controlled trial
  publication-title: Lancet
  doi: 10.1016/S0140-6736(00)02033-X
– year: 2007
  ident: 10.1111/j.1524-4733.2010.00694.x_bib30
– volume: 13
  start-page: 77
  issue: Suppl. 2
  year: 1999
  ident: 10.1111/j.1524-4733.2010.00694.x_bib220
  article-title: Review article: the safety and efficacy of alosetron, a 5-HT3 receptor antagonist, in female irritable bowel syndrome patients
  publication-title: Aliment Pharmacol Ther
  doi: 10.1046/j.1365-2036.1999.00010.x
SSID ssj0006325
Score 2.0775921
Snippet The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A scientifically valid...
Abstract Background The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision-making. A...
ABSTRACT Background:  The Food and Drug Administration, currently, is exploring quantitative benefit–risk methods to support regulatory decision‐making. A...
The Food and Drug Administration, currently, is exploring quantitative benefit-risk methods to support regulatory decision-making. A scientifically valid...
Background: The Food and Drug Administration, currently, is exploring quantitative benefit--risk methods to support regulatory decision-making. A...
SourceID proquest
pubmed
crossref
wiley
elsevier
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 418
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
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1098301510600769
https://www.clinicalkey.es/playcontent/1-s2.0-S1098301510600769
https://dx.doi.org/10.1111/j.1524-4733.2010.00694.x
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1524-4733.2010.00694.x
https://www.ncbi.nlm.nih.gov/pubmed/20230550
https://www.proquest.com/docview/734032643
https://www.proquest.com/docview/754137231
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9NAEB5VRUJcEJSXeVR7QOXSJfZ6bWfFqalaJaC2gbYo4rJar3elCJRWOJHoBfEf-If8Emb8ClEQisTNcWYUZ2Z25tv1PABe2r71uXKGx9IUHPFtyJURnkc2plYpRhhPxcknp-nwUr6dJJMtOGxrYSitsvH9tU-vvHVzp9dIs3c9nfbOo1D10TzRqKjHekpFfFJm1D__9fdlmkcaV4NXiZgT9Wo2TyIkl1kcdzleSrZNkNZD1DoEXUW0VUg6vgd3GyzJDurHvQ9bbrYDt0-at-U7sDeu-1Lf7LOLZZlVuc_22HjZsfrmAXx6vzCUNEQlT6yaafmqZBUMLdgAnaGfzn_9-PlhWn5mGNsKx8-8Z-NuQknJEPmy0eAcv23S1tnZYo4ideVDuDw-ujgc8mboArfUmp47kWIMj3JBZ0I53qKmWN5HUe5SJwxeFxFRuEjh5lnSMRRSOAR-MhE-NfEj2J5dzdwTYMK7LC2kVcrm0lnVLxAc2Sw2_TwNC5UEkLVy1rbpSE6DMb7oP3YmqCFNGtKkIV1pSH8LIOo4r-uuHBvwqFaVuq06RT-pMXRswJv9jdeVzYIvdaRLoUO9ZpQBvOk4V-x6w99lrc1pXPb0LsfM3NWi1FksQ0TeMv4HSYIAJUP8HsDj2lw7WQnaeeLeNICkst-Nhag_Do_w4ul__atncKfOwaCzrOewPf-6cC8Q2s3z3Wrt7sKtg9G74Sl-Gk0GvwHBYkJb
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9NAEB6VVgIuCMrLPPeAyqWr-LG2s-LUVq0c2qSBpqjislrbu1IESiucSPTGf-Af8kuYsdcuURCKxM2ydxRnZnb22_XMNwBvin5hc2k0j4QuOeJbn0sdWh4UEVGl6FBbKk4ejpLsXLy_iC824KCthaG0Shf7m5heR2t3p-e02buaTntngS_76J7oVMSxnshbsEXsVOjsW3uD42zUBeQkqnuv0nhOAssJPXEoOEpFXZqXFC0P0uoqtYpCl0FtvSod3Yd7Dk6yveaNH8CGmW3D7aH7YL4NO-OGmvp6l01uKq2qXbbDxjek1dcP4fOHhaa8Iap6YnVby7cVq5FoyfYxHtrp_NePnx-n1ReGy1tp-Km1bNw1KakYgl822D_Dpy5znZ0u5qhVUz2C86PDyUHGXd8FXhA7PTdhgst4kId0LJTjLeLFsjYIcpOYUON1GdAIE0jcPws6icIRBrGfiEOb6OgxbM4uZ-YpsNCaNClFIWWRC1PIfon4qEgj3c8Tv5SxB2mrZ1U4UnLqjfFV_bE5QQspspAiC6naQuq7B0EnedUQc6whI1tTqrbwFEOlwtVjDdn0b7KmcnO-UoGqQuWrFb_04F0nueTaa_4ua31O4cynzzl6Zi4XlUoj4SP4FtE_hsSIUVKE8B48ady101VIm0_cnnoQ1_67thLVp-wQL5791796DXeyyfBEnQxGx8_hbpOSQUdbL2Bz_m1hXiLSm-ev3Ez-DTSRRAg
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Quantifying+Women%27s+Stated+Benefit%E2%80%93Risk+Trade-Off+Preferences+for+IBS+Treatment+Outcomes&rft.jtitle=Value+in+health&rft.au=Johnson%2C+F.+Reed%2C+PhD&rft.au=Hauber%2C+A.+Brett%2C+PhD&rft.au=%C3%96zdemir%2C+Semra%2C+MS&rft.au=Lynd%2C+Larry%2C+PhD&rft.date=2010-06-01&rft.issn=1098-3015&rft.volume=13&rft.issue=4&rft.spage=418&rft.epage=423&rft_id=info:doi/10.1111%2Fj.1524-4733.2010.00694.x&rft.externalDBID=ECK1-s2.0-S1098301510600769&rft.externalDocID=1_s2_0_S1098301510600769
thumbnail_m http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F10983015%2FS1098301510X60089%2Fcov150h.gif