ID
36868
Beschreibung
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 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
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Stichworte
Versionen (3)
- 11.06.19 11.06.19 -
- 17.06.19 17.06.19 -
- 30.04.20 30.04.20 - Sarah Riepenhausen
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ICHOM
Hochgeladen am
17. Juni 2019
DOI
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Creative Commons BY-NC 3.0
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ICHOM Overactive bladder
Male Follow-up
- StudyEvent: ODM
Beschreibung
Explanatory variable
Alias
- UMLS CUI-1
- C0681841
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0442735
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
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
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0262718
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0175795
- UMLS CUI [3]
- C0991556
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
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
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0013787
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C3805249
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C2609267
Beschreibung
Inclusion Criteria: All patients Timing: Baseline and follow-up Reporting Source: Patient‐reported Type: Multiple answers
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2827774
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [2]
- C0543467
Beschreibung
OAB symptom severity and burden
Alias
- UMLS CUI-1
- C1319166
- UMLS CUI-2
- C2828008
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beschreibung
Health Related Quality of Life
Alias
- UMLS CUI-1
- C4279947
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C4279947
- UMLS CUI [1,2]
- C0878773
- UMLS CUI [1,3]
- C2964552
Beschreibung
Sexual function
Alias
- UMLS CUI-1
- C0278092
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2711268
- UMLS CUI [1,2]
- C1706180
- UMLS CUI [1,3]
- C0278092
- UMLS CUI [1,4]
- C2964552
Beschreibung
Side effects and burden of treatment
Alias
- UMLS CUI-1
- C0879626
- UMLS CUI-2
- C0087111
- UMLS CUI-3
- C2828008
Beschreibung
Inclusion Criteria: All patients Timing: Follow-up Reporting Source: Patient-reported Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0814225
- UMLS CUI [1,2]
- C0039798
- UMLS CUI [1,3]
- C0809944
- UMLS CUI [1,4]
- C0681889
Beschreibung
Inclusion Criteria: All patients Timing: Follow-up Reporting Source: Patient-reported Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C1704410
- UMLS CUI [1,3]
- C0878773
Beschreibung
Treatment satisfaction
Alias
- UMLS CUI-1
- C3476649
Ähnliche Modelle
Male 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])
C1706180 (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)
(Comment:en)
C1704410 (UMLS CUI [1,2])
C0878773 (UMLS CUI [1,3])
(Comment:en)
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C4084799 (UMLS CUI-2)
(Comment:en)
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C3476649 (UMLS CUI-2)
(Comment:en)