ID
40608
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 Female Follow-up form. Follow-up continues every three months until either the treatment is successful and the patient is discharged from care or the patient is lost to follow-up. 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
Female Follow-up
- StudyEvent: ODM
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 8 questions of the questionnaire are not included in this version of the standard set. The ICHOM OID's are: ICIQ-FLUTSsex1 to ICIQ-FLUTSsex8 Inclusion Criteria: Female 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]
- C0086287
- UMLS CUI [1,3]
- C0278092
- UMLS CUI [1,4]
- C2964552
Descripción
Side effects and burden of treatment
Alias
- UMLS CUI-1
- C0879626
- UMLS CUI-2
- C0087111
- UMLS CUI-3
- C2828008
Descripción
Inclusion Criteria: All patients Timing: Follow-up Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0814225
- UMLS CUI [1,2]
- C0039798
- UMLS CUI [1,3]
- C0809944
- UMLS CUI [1,4]
- C0681889
Descripción
Inclusion Criteria: All patients Timing: Follow-up Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C1704410
- UMLS CUI [1,3]
- C0878773
Descripción
Treatment satisfaction
Alias
- UMLS CUI-1
- C3476649
Similar models
Female Follow-up
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
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])
C0086287 (UMLS CUI [1,2])
C0278092 (UMLS CUI [1,3])
C2964552 (UMLS CUI [1,4])
C0087111 (UMLS CUI-2)
C2828008 (UMLS CUI-3)
C0039798 (UMLS CUI [1,2])
C0809944 (UMLS CUI [1,3])
C0681889 (UMLS CUI [1,4])
C0184511 (UMLS CUI-2)
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C0347984 (UMLS CUI-2)
C0087111 (UMLS CUI-3)
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C1704410 (UMLS CUI [1,2])
C0878773 (UMLS CUI [1,3])
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C4084799 (UMLS CUI-2)
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C3476649 (UMLS CUI-2)
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