ID
40665
Descrizione
ICHOM Paediatric Facial Palsy data collection Version 1.0.0 Revised: August 31st, 2018 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 Paediatric Facial Palsy, the following conditions and treatment approaches (or interventions) are covered by ICHOM‘s Standard Set. Conditions: Congenital/Syndromic | Acquired Unilateral (single- and multi-territory) | Bilateral (single- and multi-territory) Treatment approaches: Medical treatment | Surgery | Eye care Physiotherapy/Occupational therapy | Botulinum toxin | Psychological support This document contains the Pre-Intervention - Patient Form. It has to be filled in prior to any new treatment (any invasive or non-invasive). Valid for 6 months if multiple interventions started within this period. If patient < 8 years, please take the parentreported Form. Collecting Patient-Reported Outcome Measure: eFACE – Clinician. For more information see: Banks CA, Bhama PK, Park J, Hadlock CR, Hadlock TA. Clinician-Graded Electronic Facial Paralysis Assessment: The eFACE, August 2015. doi: 10.1097/PRS.0000000000001447 FACE-Q Kids. As there is a license for use of this questionnaire, the questions will not be included in this version of the standard set, only subscores. Snellen Chart – Clinician. PROMIS Paediatric Global Health 7 and PROMIS Pediatric Peer Relationships SF 8a. As there is an official distribution site, only the total score of these questionnaires will be included in this version of the standard set. For more information see: http://www. healthmeasures.net/explore-measurement-systems/promis/ obtain-administer-measures Reference: Butler DP, De la Torre A, Borschel GH, et al. An International Collaborative Standardizing Patient-Centered Outcome Measures in Pediatric Facial Palsy. JAMA Facial Plast Surg. Published online May 09, 2019. doi:10.1001/jamafacial.2019.0224 The Standard set of ICHOM was supported by the royal free charity and the Dianne and Michael Bienes Charitable Foundation Inc. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
collegamento
Keywords
versioni (3)
- 27/08/19 27/08/19 -
- 05/09/19 05/09/19 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright
ICHOM
Caricato su
30 aprile 2020
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 4.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
ICHOM Paediatric Facial Palsy
Pre-Intervention - Patient Form
- StudyEvent: ODM
Descrizione
Degree of Health
Alias
- UMLS CUI-1
- C0018759
Descrizione
Inclusion Criteria: All patients Timing: On all forms Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0586406
- UMLS CUI [2,1]
- C0085732
- UMLS CUI [2,2]
- C0005757
Descrizione
Inclusion Criteria: All patients Timing: On all forms Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0586406
- UMLS CUI [2,1]
- C0085732
- UMLS CUI [2,2]
- C0509489
Descrizione
Inclusion Criteria: All patients Timing: On all forms Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0586406
- UMLS CUI [2,1]
- C3257803
- UMLS CUI [2,2]
- C1456711
- UMLS CUI [3,1]
- C3257803
- UMLS CUI [3,2]
- C0043187
Descrizione
Inclusion Criteria: All patients Timing: On all forms Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0586406
- UMLS CUI [2,1]
- C0036658
- UMLS CUI [2,2]
- C2266644
- UMLS CUI [2,3]
- C0314719
- UMLS CUI [2,4]
- C0332183
Descrizione
Inclusion Criteria: All patients Timing: On all forms Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0586406
- UMLS CUI [2,1]
- C0015392
- UMLS CUI [2,2]
- C0332575
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Pre-Intervention, Post-Intervention,5 and 11 ages follow-up, End of study Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0037822
Descrizione
Inclusion Criteria: Age >8y Timing: On all forms Data Source: Patient-reported Type: Single answer Response Options: Numeric rating scale (0 - 10) or Visual Analog Scale
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C0015450
Descrizione
As there is a license for use of this questionnaire, the actual 15 questions are not part of this version of the standard set. ICHOMs OID's are: FACEQF_Q01 to FACEQF_Q15 Inclusion Criteria: Age 8-18 Timing: On all forms Data Source: Patient-reported
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0700364
- UMLS CUI [1,2]
- C0015450
- UMLS CUI [1,3]
- C0008059
- UMLS CUI [1,4]
- C0449820
Descrizione
As there is a license for use of this questionnaire, the actual 13 questions are not part of this version of the standard set. ICHOMs OID's are: FACEQMF_Q01 to FACEQMF_Q13 Inclusion Criteria: Age 8-18 Timing: Baseline, Pre-Intervention, Post-Intervention, 5 and 11 ages follow-up, End of study Data Source: Patient-reported
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0230028
- UMLS CUI [1,2]
- C0542341
- UMLS CUI [1,3]
- C0008059
- UMLS CUI [1,4]
- C0449820
Descrizione
As there is an official distribution site, the actual 7 questions of this questionnaire are not part of this version of the standard set. ICHOMs OID's are: PROMIS-CPGH7_Q01 to PROMIS-CPGH7_Q07 Inclusion Criteria: Age 8-18 Timing: Baseline, Pre-Intervention, Post-Intervention, 5 and 11 ages follow-up, End of study Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3836333
- UMLS CUI [1,2]
- C0030755
- UMLS CUI [1,3]
- C2964552
Descrizione
As there is an official distribution site, the actual 8 questions of this questionnaire are not part of this version of the standard set. ICHOMs OID's are: PROMIS-PEER_Q01 to PROMIS-PEER_Q08 Inclusion Criteria: Age 8-18 Timing: T0, T1, T2, TDS, TE Data Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3693645
- UMLS CUI [1,2]
- C1521725
- UMLS CUI [1,3]
- C0021797
- UMLS CUI [1,4]
- C2964552
Descrizione
Supporting Definition: This question is not a health outcome it is intended to identify whether patients and their families need further support to cope with the condition Inclusion Criteria: All patients Timing: Pre-Intervention Data Source: Patient or Proxy-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0035201
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [2,1]
- C0205486
- UMLS CUI [2,2]
- C0035201
- UMLS CUI [3,1]
- C0017313
- UMLS CUI [3,2]
- C0035201
Descrizione
Supporting Definition: This question is not a health outcome it is intended to identify whether patients and their families need further information to understand their condition and promote patient activation Inclusion Criteria: All patients Timing: Pre-Intervention Data Source: Patient or Proxy-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0332118
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [2,1]
- C0332118
- UMLS CUI [2,2]
- C0087111
Descrizione
Supporting Definition: This question is not a health outcome it is intended to identify whether patients and their families need further information to understand their condition and promote patient activation Inclusion Criteria: All patients Timing: Pre-Intervention Data Source: Patient or Proxy-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0162340
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [2,1]
- C0162340
- UMLS CUI [2,2]
- C0087111
Descrizione
Supporting Definition: This question is not a health outcome it is intended to identify patient satisfaction and experience Inclusion Criteria: All patients Timing: Pre-Intervention Data Source: Patient or Proxy-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3476649
Similar models
Pre-Intervention - Patient Form
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C0085732 (UMLS CUI [2,1])
C0005757 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
C0085732 (UMLS CUI [2,1])
C0509489 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
C3257803 (UMLS CUI [2,1])
C1456711 (UMLS CUI [2,2])
C3257803 (UMLS CUI [3,1])
C0043187 (UMLS CUI [3,2])
(Comment:en)
(Comment:en)
C0036658 (UMLS CUI [2,1])
C2266644 (UMLS CUI [2,2])
C0314719 (UMLS CUI [2,3])
C0332183 (UMLS CUI [2,4])
(Comment:en)
(Comment:en)
C0015392 (UMLS CUI [2,1])
C0332575 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0015450 (UMLS CUI [1,2])
C0015450 (UMLS CUI [1,2])
C0008059 (UMLS CUI [1,3])
C0449820 (UMLS CUI [1,4])
C0542341 (UMLS CUI [1,2])
C0008059 (UMLS CUI [1,3])
C0449820 (UMLS CUI [1,4])
C0030755 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C1521725 (UMLS CUI [1,2])
C0021797 (UMLS CUI [1,3])
C2964552 (UMLS CUI [1,4])
C0012634 (UMLS CUI [1,2])
C0205486 (UMLS CUI [2,1])
C0035201 (UMLS CUI [2,2])
C0017313 (UMLS CUI [3,1])
C0035201 (UMLS CUI [3,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0012634 (UMLS CUI [1,2])
C0332118 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0012634 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)