ID
40611
Descripción
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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Versiones (3)
- 11/6/19 11/6/19 -
- 17/6/19 17/6/19 -
- 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor
ICHOM
Subido en
30 de abril de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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ICHOM Overactive bladder
Male Baseline Measures
- StudyEvent: ODM
Descripción
Demographics
Alias
- UMLS CUI-1
- C1704791
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Numerical Response Options: YYYY
Tipo de datos
partialDate
Alias
- UMLS CUI [1]
- C2826771
- UMLS CUI [2]
- C0001779
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0079399
Descripción
Baseline clinical factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Descripción
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
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0005890
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descripción
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
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0005910
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0549184
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022104
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0021390
- UMLS CUI [3]
- C0010346
- UMLS CUI [4]
- C0009324
Descripción
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0233794
Descripción
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1298908
Descripción
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C1704272
Descripción
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0033572
- UMLS CUI [1,2]
- C0442800
- UMLS CUI [2]
- C0033581
Descripción
Inclusion Criteria: Male patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0186080
Descripción
Inclusion Criteria: To all patients with score >0 on HXPELVICSURG Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0186080
- UMLS CUI [1,2]
- C0205156
- UMLS CUI [1,3]
- C0449243
Descripción
Explanatory variable
Alias
- UMLS CUI-1
- C0681841
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0442735
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
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
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0262718
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0175795
- UMLS CUI [3]
- C0991556
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
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
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0013787
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C3805249
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C2609267
Descripción
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0543467
Descripción
OAB symptom severity and burden
Alias
- UMLS CUI-1
- C1319166
- UMLS CUI-2
- C2828008
Descripción
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
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Descripción
Health Related Quality of Life
Alias
- UMLS CUI-1
- C4279947
Descripción
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
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C4279947
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Descripción
Sexual function
Alias
- UMLS CUI-1
- C0278092
Descripción
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
Tipo de datos
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])