ID
36865
Beschrijving
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/ 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
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Trefwoorden
Versies (3)
- 11-06-19 11-06-19 -
- 17-06-19 17-06-19 -
- 30-04-20 30-04-20 - Sarah Riepenhausen
Houder van rechten
ICHOM
Geüploaded op
17 juni 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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ICHOM Overactive bladder
Male Baseline Measures
- StudyEvent: ODM
Beschrijving
Demographics
Alias
- UMLS CUI-1
- C1704791
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Numerical Response Options: YYYY
Datatype
partialDate
Alias
- UMLS CUI [1]
- C2826771
- UMLS CUI [2]
- C0001779
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Baseline clinical factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1]
- C0005890
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Beschrijving
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
Datatype
float
Alias
- UMLS CUI [1]
- C0005910
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0549184
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022104
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0021390
- UMLS CUI [3]
- C0010346
- UMLS CUI [4]
- C0009324
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0233794
Beschrijving
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1298908
Beschrijving
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1704272
Beschrijving
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C0033581
Beschrijving
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0186080
Beschrijving
Inclusion Criteria: To all patients with score >0 on HXPELVICSURG Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0186080
- UMLS CUI [1,2]
- C0205156
- UMLS CUI [1,3]
- C0449243
Beschrijving
Explanatory variable
Alias
- UMLS CUI-1
- C0681841
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0442735
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
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
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0262718
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0175795
- UMLS CUI [3]
- C0991556
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
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
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0013787
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C3805249
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C2609267
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0543467
Beschrijving
OAB symptom severity and burden
Alias
- UMLS CUI-1
- C1319166
- UMLS CUI-2
- C2828008
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beschrijving
Health Related Quality of Life
Alias
- UMLS CUI-1
- C4279947
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4279947
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beschrijving
Sexual function
Alias
- UMLS CUI-1
- C0278092
Beschrijving
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
Datatype
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])