ID

31293

Descrizione

CATARACTS DATA COLLECTION Version 2.0.1 Revised: March 8th, 2017, International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Conditions: Symptomatic Cataract | Asymptomatic Cataract Treatment Approaches: Phacoemulsification | Sutured Extracapsular Cataract Extraction | Sutureless Extracapsular Cataract Extraction | Intracapsular Cataract Extraction Scores: Catquest-9SF - The Catquest-9SF is free for all health care organizations, and a license is not needed for use. By Mats Lundström et al. This ODM-file contains the post-operative clinical form. The items are to be filled in with clinical or administrative data, collected within three months after cataract surgery.

collegamento

http://www.ichom.org/

Keywords

versioni (2)
  1. 09/08/18 09/08/18 - Sarah Riepenhausen
  2. 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright

ICHOM

Caricato su

9 agosto 2018

DOI

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Licenza

Creative Commons BY-NC 3.0
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ICHOM Cataracts

Inglese

Post-operative Clinical Form - Outcomes

1 moduli  
Administrative Data
Descrizione

Administrative Data

Alias
UMLS CUI-1
C1320722
Indicate the patient's medical record number
Descrizione

This number will not be shared with ICHOM. In the case patient-level data is submitted to ICHOM for benchmarking or research purposes, a separate ICHOM Patient Identifier will be created and cross-linking between the ICHOM Patient Identifier and the medical record number will only be known at the treating institution INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical RESPONSE OPTIONS: According to institution

Tipo di dati

integer

Alias
UMLS CUI [1]
C1269815
Post-operative visual status
Descrizione

Post-operative visual status

Alias
UMLS CUI-1
C2095821
Indicate the distance visual acuity measured uncorrected in the right eye between 7 days and 3 months post operatively
Descrizione

Details such as distance, chart type, and specific equipment will be left to each institution INCLUSION CRITERIA: All patients undergoing cataract surgery (independent of method of surgery), excluding patients that cannot cooperate TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Results reported in format chosen by institution

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0429539
UMLS CUI [1,2]
C4072785
UMLS CUI [1,3]
C2112579
Indicate the distance visual acuity measured best corrected in the right eye between 7 days and 3 months post operatively
Descrizione

Details such as distance, chart type, and specific equipment will be left to each institution INCLUSION CRITERIA: All patients undergoing cataract surgery (independent of method of surgery), excluding patients that cannot cooperate TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Results reported in format chosen by institution

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0429539
UMLS CUI [1,2]
C4072794
UMLS CUI [1,3]
C2112579
Indicate the distance visual acuity measured uncorrected in the left eye between 7 days and 3 months post operatively
Descrizione

Details such as distance, chart type, and specific equipment will be left to each institution INCLUSION CRITERIA: All patients undergoing cataract surgery (independent of method of surgery), excluding patients that cannot cooperate TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Results reported in format chosen by institution

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0429538
UMLS CUI [1,2]
C4072785
UMLS CUI [1,3]
C2112579
Indicate the distance visual acuity measured best corrected in the left eye between 7 days and 3 months post operatively
Descrizione

Details such as distance, chart type, and specific equipment will be left to each institution INCLUSION CRITERIA: All patients undergoing cataract surgery (independent of method of surgery), excluding patients that cannot cooperate TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Results reported in format chosen by institution

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0429538
UMLS CUI [1,2]
C4072794
UMLS CUI [1,3]
C2112579
Indicate the distance visual acuity units
Descrizione

INCLUSION CRITERIA: All patients undergoing cataract surgery (independent of method of surgery), excluding patients that cannot cooperate TIMING: Post-operative period REPORTING SOURCE: Clinical TYPE: Single Answer

Tipo di dati

integer

Alias
UMLS CUI [1,1]
C0429537
UMLS CUI [1,2]
C0439148
UMLS CUI [1,3]
C2112579
Indicate the record, within 3 months post operatively, of the spherical target refraction, which has been agreed pre-operatively, in the right eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Spherical target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176047
Indicate the record, within 3 months post operatively, of the spherical target refraction, which has been agreed pre-operatively, in the left eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Spherical target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176052
Indicate the record, within 3 months post operatively, of the cylinder target refraction, which has been agreed pre-operatively, in the right eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Cylinder target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176049
Indicate the record, within 3 months post operatively, of the cylinder target refraction, which has been agreed pre-operatively, in the left eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Cylinder target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176054
Indicate the record, within 3 months post operatively, of the axis target refraction, which has been agreed pre-operatively, in the right eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Axis target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176048
Indicate the record, within 3 months post operatively, of the axis target refraction, which has been agreed pre-operatively, in the left eye
Descrizione

For surgical eye INCLUSION CRITERIA:All patients undergoing cataract surgery (independent of method of surgery) TIMING: Post-operative period REPORTING SOURCE: Clinical RESPONSE OPTIONS: Axis target refraction

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034949
UMLS CUI [1,2]
C3176053
Post-operative complications
Descrizione

Post-operative complications

Alias
UMLS CUI-1
C0032787
Indicate if there was any return to an operating theater within 3 months of initial cataract surgery date
Descrizione

Only include those cases caused by either an intra-operative or post-operative complication following cataract surgery INCLUSION CRITERIA: Excluding cases when the reason for return to theater is not related to either an intra-operative or post-operative complication of initial cataract surgery TIMING: Post-operative period REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Tipo di dati

integer

Alias
UMLS CUI [1]
C0035110
Indicate if there was post-operative severe intra-ocular inflammation within 3 months of initial cataract surgery date
Descrizione

Due to suspected or proven intra-ocular infection attributed to the surgery INCLUSION CRITERIA: All cases of suspected endophthalmitis, whether culture-proven (e.g. positive culture) or those with a negative culture that behave clinically like infection (e.g. respond to antibiotics) TIMING: Post-operative period REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Tipo di dati

integer

Alias
UMLS CUI [1]
C0014236
Indicate if there was a corneal edema starting immediately after surgery that does not completely resolve during the 3 month follow-up period
Descrizione

INCLUSION CRITERIA: All cases of persistent corneal edema post-operatively TIMING: Post-operative period REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Tipo di dati

integer

Alias
UMLS CUI [1]
C0010037
Indicate if there was a significant post-operative complication within 3 months of initial cataract surgery date that means on-going treatment or poorer vision
Descrizione

Such as persistent elevated IOP with need for medication, uveitis with need for medication, wound problems that mean repeated visits to the clinic, etc. INCLUSION CRITERIA: Excluding complications that cause return to operating theater TIMING: Post-operative period REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Tipo di dati

integer

Alias
UMLS CUI [1,1]
C0032787
UMLS CUI [1,2]
C0205394
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Similar models

Post-operative Clinical Form - Outcomes

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID
Item
Indicate the patient's medical record number
integer
C1269815 (UMLS CUI [1])
Item Group
Post-operative visual status
C2095821 (UMLS CUI-1)
Post-operative distance visual acuity: Uncorrected, right
Item
Indicate the distance visual acuity measured uncorrected in the right eye between 7 days and 3 months post operatively
text
C0429539 (UMLS CUI [1,1])
C4072785 (UMLS CUI [1,2])
C2112579 (UMLS CUI [1,3])
Post-operative distance visual acuity: Corrected, right
Item
Indicate the distance visual acuity measured best corrected in the right eye between 7 days and 3 months post operatively
text
C0429539 (UMLS CUI [1,1])
C4072794 (UMLS CUI [1,2])
C2112579 (UMLS CUI [1,3])
Post-operative distance visual acuity: Uncorrected, left
Item
Indicate the distance visual acuity measured uncorrected in the left eye between 7 days and 3 months post operatively
text
C0429538 (UMLS CUI [1,1])
C4072785 (UMLS CUI [1,2])
C2112579 (UMLS CUI [1,3])
Post-operative distance visual acuity: Corrected, left
Item
Indicate the distance visual acuity measured best corrected in the left eye between 7 days and 3 months post operatively
text
C0429538 (UMLS CUI [1,1])
C4072794 (UMLS CUI [1,2])
C2112579 (UMLS CUI [1,3])
Item
Indicate the distance visual acuity units
integer
C0429537 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
C2112579 (UMLS CUI [1,3])
Post-operative distance visual acuity units
Code List
Indicate the distance visual acuity units
CL Item
Snellen (1)
C1827708 (UMLS CUI-1)
(Comment:en)
CL Item
Decimal (2)
C0042812 (UMLS CUI-1)
C1708071 (UMLS CUI-2)
(Comment:en)
CL Item
LogMAR (3)
C0487935 (UMLS CUI-1)
(Comment:en)
Actual refraction: Spherical, right
Item
Indicate the record, within 3 months post operatively, of the spherical target refraction, which has been agreed pre-operatively, in the right eye
text
C0034949 (UMLS CUI [1,1])
C3176047 (UMLS CUI [1,2])
Actual refraction: Spherical, left
Item
Indicate the record, within 3 months post operatively, of the spherical target refraction, which has been agreed pre-operatively, in the left eye
text
C0034949 (UMLS CUI [1,1])
C3176052 (UMLS CUI [1,2])
Actual refraction: Cylinder, right
Item
Indicate the record, within 3 months post operatively, of the cylinder target refraction, which has been agreed pre-operatively, in the right eye
text
C0034949 (UMLS CUI [1,1])
C3176049 (UMLS CUI [1,2])
Actual refraction: Cylinder, left
Item
Indicate the record, within 3 months post operatively, of the cylinder target refraction, which has been agreed pre-operatively, in the left eye
text
C0034949 (UMLS CUI [1,1])
C3176054 (UMLS CUI [1,2])
Actual refraction: Axis, right
Item
Indicate the record, within 3 months post operatively, of the axis target refraction, which has been agreed pre-operatively, in the right eye
text
C0034949 (UMLS CUI [1,1])
C3176048 (UMLS CUI [1,2])
Actual refraction: Axis, left
Item
Indicate the record, within 3 months post operatively, of the axis target refraction, which has been agreed pre-operatively, in the left eye
text
C0034949 (UMLS CUI [1,1])
C3176053 (UMLS CUI [1,2])
Item Group
Post-operative complications
C0032787 (UMLS CUI-1)
Item
Indicate if there was any return to an operating theater within 3 months of initial cataract surgery date
integer
C0035110 (UMLS CUI [1])
Return to operative theater within 3 months
Code List
Indicate if there was any return to an operating theater within 3 months of initial cataract surgery date
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Item
Indicate if there was post-operative severe intra-ocular inflammation within 3 months of initial cataract surgery date
integer
C0014236 (UMLS CUI [1])
Endophthalmitis
Code List
Indicate if there was post-operative severe intra-ocular inflammation within 3 months of initial cataract surgery date
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Item
Indicate if there was a corneal edema starting immediately after surgery that does not completely resolve during the 3 month follow-up period
integer
C0010037 (UMLS CUI [1])
Diabetic retinopathy and/or diabetic macular edema
Code List
Indicate if there was a corneal edema starting immediately after surgery that does not completely resolve during the 3 month follow-up period
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Item
Indicate if there was a significant post-operative complication within 3 months of initial cataract surgery date that means on-going treatment or poorer vision
integer
C0032787 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Diabetic retinopathy and/or diabetic macular edema
Code List
Indicate if there was a significant post-operative complication within 3 months of initial cataract surgery date that means on-going treatment or poorer vision
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
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