ID
40611
Beskrivning
ICHOM Overactive bladder data collection Version 1.2.2 Revised: April 10th, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. For Overactive Bladder, the following treatment approaches (or interventions) are covered by our Standard Set. Treatment Approaches : Patient education | Behavioral modification | Pharmacological management | Intradetrusor Botox, PTNS, SNS | Surgery This document contains the Male Baseline Measures form. It has to be filled in at Baseline. This document also should also be filled out repeatedly in the event of symptom recurrence. Collecting Clinician and Patient-Reported Outcome Measures: ICIQ-OAB, ICIQ-MLUTSsex and ICIQ-FLUTSsex. For all: Free for use in clinical practice, routine outcomes measurement, and clinical research. As permission from the developer is required, only the total score will be included in this version of the standard set. To obtain permission and an offical copy and scoring guide or to inquire about translations see http://www.iciq.net/userpolicy.html OAB-q SF (4-week recall). As a license is needed for use of this questionnaire, only the total score will be included in this version of the standard set. TBS. Free for use without a license. Please see Colman S et al (2008) Validation of the treatment benefit scale for assessing subjective outcomes in Treatment of Overactive Bladder. Urology 72:803-807 ICHOM's Standard set was supported by IUGA (international urogynecological association), National Association for Continence, The Canadian Continence Foundation, Continence Foundation of Australia Publication: Foust-Wright C, Wissig S, Stowell C, et al. Development of a core set of outcome measures for OAB treatment. Int Urogynecol J. 2017;28(12):1785–1793. doi:10.1007/s00192-017-3481-6 For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Nyckelord
Versioner (3)
- 2019-06-11 2019-06-11 -
- 2019-06-17 2019-06-17 -
- 2020-04-30 2020-04-30 - Sarah Riepenhausen
Rättsinnehavare
ICHOM
Uppladdad den
30 april 2020
DOI
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Creative Commons BY-NC 4.0
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ICHOM Overactive bladder
Male Baseline Measures
- StudyEvent: ODM
Beskrivning
Demographics
Alias
- UMLS CUI-1
- C1704791
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Numerical Response Options: YYYY
Datatyp
partialDate
Alias
- UMLS CUI [1]
- C2826771
- UMLS CUI [2]
- C0001779
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1]
- C0079399
Beskrivning
Baseline clinical factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Beskrivning
Supporting Definition: For calculating BMI Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient‐reported Type: Numerical Response Options: Numerical value of height in metric or imperial system
Datatyp
integer
Alias
- UMLS CUI [1]
- C0005890
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient‐reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Beskrivning
Supporting Definition: For calculating BMI Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer Response Options: Numerical value of weight in metric or imperial system
Datatyp
float
Alias
- UMLS CUI [1]
- C0005910
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0549184
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022104
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0021390
- UMLS CUI [3]
- C0010346
- UMLS CUI [4]
- C0009324
Beskrivning
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0233794
Beskrivning
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1298908
Beskrivning
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1704272
Beskrivning
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C0033581
Beskrivning
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0186080
Beskrivning
Inclusion Criteria: To all patients with score >0 on HXPELVICSURG Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0186080
- UMLS CUI [1,2]
- C0205156
- UMLS CUI [1,3]
- C0449243
Beskrivning
Explanatory variable
Alias
- UMLS CUI-1
- C0681841
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0442735
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0542299
- UMLS CUI [3]
- C0429791
- UMLS CUI [4]
- C0150474
- UMLS CUI [5]
- C0262718
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0262718
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0175795
- UMLS CUI [3]
- C0991556
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2,1]
- C0700702
- UMLS CUI [2,2]
- C1533685
- UMLS CUI [2,3]
- C0005682
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0013787
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C3805249
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C2609267
Beskrivning
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0543467
Beskrivning
OAB symptom severity and burden
Alias
- UMLS CUI-1
- C1319166
- UMLS CUI-2
- C2828008
Beskrivning
As permission is required, the actual 8 questions of this questionnaire are not included in this version of the standard set. The ICHOM OID's are:ICIQ-OAB1 to ICIQ-OAB8 Inclusion Criteria: All patients Timing: Baseline and follow‐up Reporting Source: Patient‐reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beskrivning
Health Related Quality of Life
Alias
- UMLS CUI-1
- C4279947
Beskrivning
As license is needed for use this questionaire, the actual 8 questions are not included in this version of the standard set. The ICHOM OID's are: OAB-q SF1 to OAB-q SF13 Inclusion Criteria: All patients Timing: Baseline and follow‐up Reporting Source: Patient‐reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C4279947
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beskrivning
Sexual function
Alias
- UMLS CUI-1
- C0278092
Beskrivning
As permission is required, the actual 9 questions of the questionnaire are not included in this version of the standard set. The ICHOM OID's are: ICIQ-MLUTSsex1 to ICIQ-MLUTSsex9 Inclusion Criteria: Male patients Timing: Baseline and follow‐up Reporting Source: Patient‐reported Type: Single answer
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C1706180
- UMLS CUI [1,3]
- C0278092
- UMLS CUI [1,4]
- C2964552
Similar models
Male Baseline Measures
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
(Comment:en)
(Comment:en)
C1442488 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0549184 (UMLS CUI [2])
C0011849 (UMLS CUI [2])
C0022104 (UMLS CUI [2])
C0021390 (UMLS CUI [2])
C0010346 (UMLS CUI [3])
C0009324 (UMLS CUI [4])
C0233794 (UMLS CUI [2])
C0442800 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2])
C0442800 (UMLS CUI [1,2])
C1704272 (UMLS CUI [2])
C0442800 (UMLS CUI [1,2])
C0033581 (UMLS CUI [2])
C0186080 (UMLS CUI [1,2])
(Comment:en)
C0034896 (UMLS CUI-2)
C0021853 (UMLS CUI-3)
(Comment:en)
(Comment:en)
C0205156 (UMLS CUI [1,2])
C0449243 (UMLS CUI [1,3])
(Comment:en)
C0205452 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205447 (UMLS CUI-5)
C0439234 (UMLS CUI-6)
(Comment:en)
C0205451 (UMLS CUI-2)
C0439234 (UMLS CUI-3)
(Comment:en)
C0205456 (UMLS CUI-2)
C0439234 (UMLS CUI-3)
(Comment:en)
(Comment:en)
C0878773 (UMLS CUI [1,2])
C0442735 (UMLS CUI [2])
C0878773 (UMLS CUI [1,2])
C0542299 (UMLS CUI [2])
C0429791 (UMLS CUI [3])
C0150474 (UMLS CUI [4])
C0262718 (UMLS CUI [5])
C0878773 (UMLS CUI [1,2])
C0262718 (UMLS CUI [2])
C0878773 (UMLS CUI [1,2])
C0175795 (UMLS CUI [2])
C0991556 (UMLS CUI [3])
C0878773 (UMLS CUI [1,2])
C0700702 (UMLS CUI [2,1])
C1533685 (UMLS CUI [2,2])
C0005682 (UMLS CUI [2,3])
C0878773 (UMLS CUI [1,2])
C0013787 (UMLS CUI [2])
C0878773 (UMLS CUI [1,2])
C3805249 (UMLS CUI [2])
C0878773 (UMLS CUI [1,2])
C2609267 (UMLS CUI [2])
C0878773 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2])
C2828008 (UMLS CUI-2)
C0878773 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C0878773 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C1706180 (UMLS CUI [1,2])
C0278092 (UMLS CUI [1,3])
C2964552 (UMLS CUI [1,4])