Readmission To Hospital (repeatable instrument)

  1. StudyEvent: PREBOT Pilot
    1. Visit 1: Enrollment and Randomization
    2. Visit 2: Endoscopic intervention
    3. Visit 3: Operation
    4. Visit 4: POD 3
    5. Visit 5: Day of discharge
    6. Visit 6: POD 30
    7. Visit 7: 3 months post OP/ premature discontinuation
    8. Signature
  2. StudyEvent: Complications
    1. Complications
  3. StudyEvent: Readmission To Hospital (repeatable instrument)
    1. Readmission To Hospital (repeatable instrument)
  4. StudyEvent: Adverse Events (repeatable instrument)
    1. Adverse Events (repeatable instrument)
  5. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  6. StudyEvent: Protocol Violation (repeatable instrument)
    1. Protocol Violation (repeatable instrument)
  7. StudyEvent: Patient report: EORTC QLQ-C30
  8. StudyEvent: Patient report: EORTC QLQ-PAN26
Readmission to hospital
Beschreibung

Readmission to hospital

Alias
UMLS CUI [1,1]
C0600290
Reason for readmission
Beschreibung

Reason

Datentyp

integer

Alias
UMLS CUI [1,1]
C0566251
If other, please specify
Beschreibung

specify

Datentyp

text

Alias
UMLS CUI [1,1]
C1521902
Start of hospitalisation
Beschreibung

Start

Datentyp

date

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0808070
Ongoing hospital stay at end of study
Beschreibung

Ongoing hospital stay

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3489408
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C2983670
End of hospitalisation
Beschreibung

End

Datentyp

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0019993
Procedure / treatment
Beschreibung

procedure

Datentyp

integer

Alias
UMLS CUI [1,1]
C0087111
If other procedure, please specify
Beschreibung

specify

Datentyp

text

Alias
UMLS CUI [1,1]
C1521902
ICU/ IMC stay
Beschreibung

ICU/ IMC stay

Alias
UMLS CUI [1,1]
C4489279
UMLS CUI [1,2]
C0021708
UMLS CUI [1,3]
C3489408
Number of days in ICU / IMC
Beschreibung

Number of days

Datentyp

integer

Alias
UMLS CUI [1,1]
C3640790

Ähnliche Modelle

Readmission To Hospital (repeatable instrument)

  1. StudyEvent: PREBOT Pilot
    1. Visit 1: Enrollment and Randomization
    2. Visit 2: Endoscopic intervention
    3. Visit 3: Operation
    4. Visit 4: POD 3
    5. Visit 5: Day of discharge
    6. Visit 6: POD 30
    7. Visit 7: 3 months post OP/ premature discontinuation
    8. Signature
  2. StudyEvent: Complications
    1. Complications
  3. StudyEvent: Readmission To Hospital (repeatable instrument)
    1. Readmission To Hospital (repeatable instrument)
  4. StudyEvent: Adverse Events (repeatable instrument)
    1. Adverse Events (repeatable instrument)
  5. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  6. StudyEvent: Protocol Violation (repeatable instrument)
    1. Protocol Violation (repeatable instrument)
  7. StudyEvent: Patient report: EORTC QLQ-C30
  8. StudyEvent: Patient report: EORTC QLQ-PAN26
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Readmission to hospital
C0600290 (UMLS CUI [1,1])
Item
Reason for readmission
integer
C0566251 (UMLS CUI [1,1])
Code List
Reason for readmission
CL Item
complications due to DP surgery (1)
C0009566 (UMLS CUI [1,1])
C0176940 (UMLS CUI [1,2])
CL Item
complications due to BOTOX® injection/endoscopic procedure (2)
C0009566 (UMLS CUI [1,1])
C0700702 (UMLS CUI [1,2])
C1533685 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
C0014245 (UMLS CUI [1,5])
CL Item
complications due to tumor disease (3)
C0009566 (UMLS CUI [1,1])
C2826292 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
CL Item
complications due to oncologic treatment other than surgery (4)
C0009566 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0597030 (UMLS CUI [1,3])
C1518388 (UMLS CUI [1,4])
CL Item
complications due to concomitant disease (e.g. pancreatitis) (5)
C0009566 (UMLS CUI [1,1])
C0243087 (UMLS CUI [1,2])
CL Item
medical comorbidity (6)
C4540934 (UMLS CUI [1,1])
CL Item
other (7)
C0205394 (UMLS CUI [1,1])
CL Item
unknown (8)
C0439673 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Start
Item
Start of hospitalisation
date
C0019993 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Ongoing hospital stay
Item
Ongoing hospital stay at end of study
boolean
C3489408 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C2983670 (UMLS CUI [1,3])
End
Item
End of hospitalisation
date
C0806020 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
Item
Procedure / treatment
integer
C0087111 (UMLS CUI [1,1])
Code List
Procedure / treatment
CL Item
surgery (1)
C0543467 (UMLS CUI [1,1])
CL Item
conservative (2)
C0459914 (UMLS CUI [1,1])
CL Item
other (3)
C0205394 (UMLS CUI [1,1])
specify
Item
If other procedure, please specify
text
C1521902 (UMLS CUI [1,1])
Item Group
ICU/ IMC stay
C4489279 (UMLS CUI [1,1])
C0021708 (UMLS CUI [1,2])
C3489408 (UMLS CUI [1,3])
Number of days
Item
Number of days in ICU / IMC
integer
C3640790 (UMLS CUI [1,1])