Visit 7: 3 months post OP/ premature discontinuation

  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
Study termination
Descripción

Study termination

Alias
UMLS CUI [1,1]
C2348570
Premature Trial termination of this patient?
Descripción

Premature Trial termination

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C5669243
Date of premature trial termination /last contact
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C4684805
UMLS CUI [1,3]
C4018905
Reason for premature end of study participation
Descripción

Reason

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C2348581
UMLS CUI [1,3]
C4018905
If other reason, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Cause of death
Descripción

Cause of death

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0007465
If other cause of death, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Date of visit
Descripción

Date of visit

Alias
UMLS CUI [1,1]
C1320303
Date of visit
Descripción

Date of visit

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1320303
Postoperative pancreativ fistua (POPF)
Descripción

Postoperative pancreativ fistua (POPF)

Alias
UMLS CUI [1,1]
C0241311
UMLS CUI [1,2]
C0030290
Postoperative pancreativ fistua (POPF) according to the ISGPS classification
Descripción

POPF ISGPS

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0241311
UMLS CUI [1,2]
C0030290
UMLS CUI [1,3]
C0008902
If POPF ocurred, please fill out eForm 'Adverse Events'
Descripción

If POPF ocurred, please fill out eForm 'Adverse Events'

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C3273494
Other postoperative morbidities
Descripción

Other postoperative morbidities

Alias
UMLS CUI [1,1]
C0241311
UMLS CUI [1,2]
C0589603
UMLS CUI [1,3]
C0009488
Postinterventional pancreatitis
Descripción

Postinterventional pancreatitis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030305
UMLS CUI [1,2]
C2347647
Perioperative sepsis
Descripción

Perioperative sepsis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1518988
UMLS CUI [1,2]
C0243026
Delayed gastric emptying (DGE)
Descripción

DGE

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0740411
Delayed gastric emptying (DGE) according to the ISGPS definitions
Descripción

DGE ISGPS

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0740411
UMLS CUI [1,2]
C1704788
Postpancreatectomy hemorrhage (PPH)
Descripción

PPH

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0687676
UMLS CUI [1,2]
C0030279
UMLS CUI [1,3]
C0019080
Postpancreatectomy hemorrhage (PPH) according to the ISGPS definitions
Descripción

PPH ISGPS

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0687676
UMLS CUI [1,2]
C0030279
UMLS CUI [1,3]
C0019080
UMLS CUI [1,4]
C1704788
Intraabdominal fluid collection
Descripción

Intraabdominal fluid collection

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C4285843
Intraabdominal fluid abscess
Descripción

Intraabdominal fluid abscess

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1512910
UMLS CUI [1,2]
C4726050
Lymphatic fistula / chylus ascites
Descripción

Lymphatic fistula / chylus ascites

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0340791
UMLS CUI [1,2]
C0008730
UMLS CUI [1,3]
C0003962
Wound infection
Descripción

Wound infection

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0043241
If yes, please specify wound infection
Descripción

specify

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1521902
Burst abdomen
Descripción

Burst abdomen

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1739397
UMLS CUI [1,2]
C2711727
If any of above-mentioned complications occurred, please fill out eForm 'Adverse Events'.
Descripción

If any of above-mentioned complications occurred, please fill out eForm 'Adverse Events'.

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C3273494
Reintervention/ -operation
Descripción

Reintervention/ -operation

Alias
UMLS CUI [1,1]
C5452916
UMLS CUI [1,2]
C0035110
Reintervention/ -operation
Descripción

Reintervention/ -operation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C5452916
UMLS CUI [1,2]
C0035110
Number of Reinterventions / Reoperations
Descripción

Number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0449788
1st reintervention / reoperation
Descripción

1st reintervention / reoperation

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C5452916
UMLS CUI [1,3]
C0035110
Date of 1st reintervention / reoperation
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
Procedures
Descripción

Procedures

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0199171
If other, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Reason (Diagnosis)
Descripción

Diagnosis

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011900
2nd reintervention / reoperation
Descripción

2nd reintervention / reoperation

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C5452916
UMLS CUI [1,3]
C0035110
Date of 2nd reintervention / reoperation
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
Procedures
Descripción

Procedures

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0199171
If other, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Reason (Diagnosis)
Descripción

Diagnosis

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011900
3rd reintervention / reoperation
Descripción

3rd reintervention / reoperation

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C5452916
UMLS CUI [1,3]
C0035110
Date of 3rd reintervention / reoperation
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
Procedures
Descripción

Procedures

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0199171
If other, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Reason (Diagnosis)
Descripción

Diagnosis

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011900
4th reintervention / reoperation
Descripción

4th reintervention / reoperation

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C5452916
UMLS CUI [1,3]
C0035110
Date of 4th reintervention / reoperation
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
Procedures
Descripción

Procedures

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0199171
If other, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Reason (Diagnosis)
Descripción

Diagnosis

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011900
5th reintervention / reoperation
Descripción

5th reintervention / reoperation

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C5452916
UMLS CUI [1,3]
C0035110
Date of 5th reintervention / reoperation
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
Procedures
Descripción

Procedures

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0199171
If other, please specify
Descripción

specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1521902
Reason (Diagnosis)
Descripción

Diagnosis

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011900
Questionnaires
Descripción

Questionnaires

Alias
UMLS CUI [1,1]
C0034394
EORTC QLQ-C30 completed
Descripción

EORTC QLQ-C30

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3641780
UMLS CUI [1,2]
C2826970
EORTC QLQ-PAN26 completed
Descripción

EORTC QLQ-PAN26

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C4288326
UMLS CUI [1,2]
C2826970
Concomitant Medication
Descripción

Concomitant Medication

Alias
UMLS CUI [1,1]
C2347852
Any changes in Concomitant Medication since last visit
Descripción

changes in Concomitant Medication since last visit

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3872643
UMLS CUI [1,2]
C0580105
If yes, please fill out eForm 'Concomitant Medication'.
Descripción

If yes, please fill out eForm 'Concomitant Medication'.

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C3273494
Adverse Events
Descripción

Adverse Events

Alias
UMLS CUI [1,1]
C0877248
Any new Adverse Events occurred since last visit
Descripción

Any new Adverse Events occurred since last visit

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C3872643
If yes, please fill out eForm 'Adverse Events'.
Descripción

If yes, please fill out eForm 'Adverse Events'.

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C3273494
Protocol violations
Descripción

Protocol violations

Alias
UMLS CUI [1,1]
C1709750
Any protocol violations occurred since last visit
Descripción

Any protocol violations occurred since last visit

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1709750
UMLS CUI [1,2]
C3872643
If yes, please fill out eForm 'Protocol Violation'.
Descripción

If yes, please fill out eForm 'Protocol Violation'.

Alias
UMLS CUI [1,1]
C3273494
UMLS CUI [1,2]
C1709750

Similar models

Visit 7: 3 months post OP/ premature discontinuation

  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
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Study termination
C2348570 (UMLS CUI [1,1])
Premature Trial termination
Item
Premature Trial termination of this patient?
boolean
C5669243 (UMLS CUI [1,1])
Date
Item
Date of premature trial termination /last contact
date
C0011008 (UMLS CUI [1,1])
C4684805 (UMLS CUI [1,2])
C4018905 (UMLS CUI [1,3])
Item
Reason for premature end of study participation
integer
C0392360 (UMLS CUI [1,1])
C2348581 (UMLS CUI [1,2])
C4018905 (UMLS CUI [1,3])
Code List
Reason for premature end of study participation
CL Item
patient's withdrawal of informed consent (1)
C1707492 (UMLS CUI [1,1])
CL Item
DP not performed (2)
C0176940 (UMLS CUI [1,1])
C0749191 (UMLS CUI [1,2])
CL Item
death (3)
C1306577 (UMLS CUI [1,1])
CL Item
lost to follow up (4)
C1302313 (UMLS CUI [1,1])
CL Item
other (5)
C0205394 (UMLS CUI [1,1])
specify
Item
If other reason, please specify
text
C1521902 (UMLS CUI [1,1])
Item
Cause of death
integer
C0007465 (UMLS CUI [1,1])
Code List
Cause of death
CL Item
related to DP surgery (1)
C0176940 (UMLS CUI [1,1])
C1704787 (UMLS CUI [1,2])
CL Item
related to BOTOX injection / endoscopic procedure (2)
C0700702 (UMLS CUI [1,1])
C1533685 (UMLS CUI [1,2])
C0014245 (UMLS CUI [1,3])
C1704787 (UMLS CUI [1,4])
CL Item
related to tumor disease (3)
C1704787 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
CL Item
related to oncologic treatment other than surgery (4)
C1704787 (UMLS CUI [1,1])
C0597030 (UMLS CUI [1,2])
CL Item
other (5)
C0205394 (UMLS CUI [1,1])
CL Item
unknown (6)
C0439673 (UMLS CUI [1,1])
specify
Item
If other cause of death, please specify
text
C1521902 (UMLS CUI [1,1])
Item Group
Date of visit
C1320303 (UMLS CUI [1,1])
Date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1,1])
Item Group
Postoperative pancreativ fistua (POPF)
C0241311 (UMLS CUI [1,1])
C0030290 (UMLS CUI [1,2])
Item
Postoperative pancreativ fistua (POPF) according to the ISGPS classification
integer
C0241311 (UMLS CUI [1,1])
C0030290 (UMLS CUI [1,2])
C0008902 (UMLS CUI [1,3])
Code List
Postoperative pancreativ fistua (POPF) according to the ISGPS classification
CL Item
No POPF (1)
C1298908 (UMLS CUI [1,1])
CL Item
Biochemical Leak (2)
C0205474 (UMLS CUI [1,1])
C0332234 (UMLS CUI [1,2])
CL Item
Grade B POPF (3)
C0441806 (UMLS CUI [1,1])
CL Item
Grade C POPF (4)
C0441807 (UMLS CUI [1,1])
Item Group
If POPF ocurred, please fill out eForm 'Adverse Events'
C0877248 (UMLS CUI [1,1])
C3273494 (UMLS CUI [1,2])
Item Group
Other postoperative morbidities
C0241311 (UMLS CUI [1,1])
C0589603 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Postinterventional pancreatitis
Item
Postinterventional pancreatitis
boolean
C0030305 (UMLS CUI [1,1])
C2347647 (UMLS CUI [1,2])
Perioperative sepsis
Item
Perioperative sepsis
boolean
C1518988 (UMLS CUI [1,1])
C0243026 (UMLS CUI [1,2])
DGE
Item
Delayed gastric emptying (DGE)
boolean
C0740411 (UMLS CUI [1,1])
Item
Delayed gastric emptying (DGE) according to the ISGPS definitions
integer
C0740411 (UMLS CUI [1,1])
C1704788 (UMLS CUI [1,2])
Code List
Delayed gastric emptying (DGE) according to the ISGPS definitions
CL Item
no DGE (1)
C1298908 (UMLS CUI [1,1])
CL Item
Grade A (2)
C0309195 (UMLS CUI [1,1])
CL Item
Grade B (3)
C0441806 (UMLS CUI [1,1])
CL Item
Grade C (4)
C0441807 (UMLS CUI [1,1])
PPH
Item
Postpancreatectomy hemorrhage (PPH)
boolean
C0687676 (UMLS CUI [1,1])
C0030279 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,3])
Item
Postpancreatectomy hemorrhage (PPH) according to the ISGPS definitions
integer
C0687676 (UMLS CUI [1,1])
C0030279 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,3])
C1704788 (UMLS CUI [1,4])
Code List
Postpancreatectomy hemorrhage (PPH) according to the ISGPS definitions
CL Item
no PPH (1)
C1298908 (UMLS CUI [1,1])
CL Item
Grade A (2)
C0309195 (UMLS CUI [1,1])
CL Item
Grade B (3)
C0441806 (UMLS CUI [1,1])
CL Item
Grade C (4)
C0441807 (UMLS CUI [1,1])
Intraabdominal fluid collection
Item
Intraabdominal fluid collection
boolean
C4285843 (UMLS CUI [1,1])
Intraabdominal fluid abscess
Item
Intraabdominal fluid abscess
boolean
C1512910 (UMLS CUI [1,1])
C4726050 (UMLS CUI [1,2])
Lymphatic fistula / chylus ascites
Item
Lymphatic fistula / chylus ascites
boolean
C0340791 (UMLS CUI [1,1])
C0008730 (UMLS CUI [1,2])
C0003962 (UMLS CUI [1,3])
Wound infection
Item
Wound infection
boolean
C0043241 (UMLS CUI [1,1])
Item
If yes, please specify wound infection
integer
C1521902 (UMLS CUI [1,1])
Code List
If yes, please specify wound infection
CL Item
superficial incisional surgical site infection (1)
C3662309 (UMLS CUI [1,1])
CL Item
deep incisional surgical site infection (2)
C3662302 (UMLS CUI [1,1])
Burst abdomen
Item
Burst abdomen
boolean
C1739397 (UMLS CUI [1,1])
C2711727 (UMLS CUI [1,2])
Item Group
If any of above-mentioned complications occurred, please fill out eForm 'Adverse Events'.
C0877248 (UMLS CUI [1,1])
C3273494 (UMLS CUI [1,2])
Item Group
Reintervention/ -operation
C5452916 (UMLS CUI [1,1])
C0035110 (UMLS CUI [1,2])
Reintervention/ -operation
Item
Reintervention/ -operation
boolean
C5452916 (UMLS CUI [1,1])
C0035110 (UMLS CUI [1,2])
Item
Number of Reinterventions / Reoperations
integer
C0449788 (UMLS CUI [1,1])
Code List
Number of Reinterventions / Reoperations
CL Item
1 (1)
C0205447 (UMLS CUI [1,1])
CL Item
2 (2)
C0205448 (UMLS CUI [1,1])
CL Item
3 (3)
C0205449 (UMLS CUI [1,1])
CL Item
4 (4)
C0205450 (UMLS CUI [1,1])
CL Item
5 (5)
C0205451 (UMLS CUI [1,1])
Item Group
1st reintervention / reoperation
C0205435 (UMLS CUI [1,1])
C5452916 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
Date
Item
Date of 1st reintervention / reoperation
date
C0011008 (UMLS CUI [1,1])
Item
Procedures
integer
C0199171 (UMLS CUI [1,1])
Code List
Procedures
CL Item
completion pancreatectomy (1)
C0040511 (UMLS CUI [1,1])
CL Item
relaprotomy without completion pancreatectomy (2)
C0205341 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
C0332288 (UMLS CUI [1,3])
C0040511 (UMLS CUI [1,4])
CL Item
interventional abdominal drainage (3)
C0184661 (UMLS CUI [1,1])
C1167781 (UMLS CUI [1,2])
CL Item
esophagogastroduodenoscopy (4)
C0079304 (UMLS CUI [1,1])
CL Item
radiologic management of postoperative bleeding (5)
C0344093 (UMLS CUI [1,1])
C0032788 (UMLS CUI [1,2])
CL Item
other (6)
C0205394 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Diagnosis
Item
Reason (Diagnosis)
text
C0011900 (UMLS CUI [1,1])
Item Group
2nd reintervention / reoperation
C0205435 (UMLS CUI [1,1])
C5452916 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
Date
Item
Date of 2nd reintervention / reoperation
date
C0011008 (UMLS CUI [1,1])
Item
Procedures
integer
C0199171 (UMLS CUI [1,1])
Code List
Procedures
CL Item
completion pancreatectomy (1)
C0040511 (UMLS CUI [1,1])
CL Item
relaprotomy without completion pancreatectomy (2)
C0205341 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
C0332288 (UMLS CUI [1,3])
C0040511 (UMLS CUI [1,4])
CL Item
interventional abdominal drainage (3)
C0184661 (UMLS CUI [1,1])
C1167781 (UMLS CUI [1,2])
CL Item
esophagogastroduodenoscopy (4)
C0079304 (UMLS CUI [1,1])
CL Item
radiologic management of postoperative bleeding (5)
C0344093 (UMLS CUI [1,1])
C0032788 (UMLS CUI [1,2])
CL Item
other (6)
C0205394 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Diagnosis
Item
Reason (Diagnosis)
text
C0011900 (UMLS CUI [1,1])
Item Group
3rd reintervention / reoperation
C0205435 (UMLS CUI [1,1])
C5452916 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
Date
Item
Date of 3rd reintervention / reoperation
date
C0011008 (UMLS CUI [1,1])
Item
Procedures
integer
C0199171 (UMLS CUI [1,1])
Code List
Procedures
CL Item
completion pancreatectomy (1)
C0040511 (UMLS CUI [1,1])
CL Item
relaprotomy without completion pancreatectomy (2)
C0205341 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
C0332288 (UMLS CUI [1,3])
C0040511 (UMLS CUI [1,4])
CL Item
interventional abdominal drainage (3)
C0184661 (UMLS CUI [1,1])
C1167781 (UMLS CUI [1,2])
CL Item
esophagogastroduodenoscopy (4)
C0079304 (UMLS CUI [1,1])
CL Item
radiologic management of postoperative bleeding (5)
C0344093 (UMLS CUI [1,1])
C0032788 (UMLS CUI [1,2])
CL Item
other (6)
C0205394 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Diagnosis
Item
Reason (Diagnosis)
text
C0011900 (UMLS CUI [1,1])
Item Group
4th reintervention / reoperation
C0205435 (UMLS CUI [1,1])
C5452916 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
Date
Item
Date of 4th reintervention / reoperation
date
C0011008 (UMLS CUI [1,1])
Item
Procedures
integer
C0199171 (UMLS CUI [1,1])
Code List
Procedures
CL Item
completion pancreatectomy (1)
C0040511 (UMLS CUI [1,1])
CL Item
relaprotomy without completion pancreatectomy (2)
C0205341 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
C0332288 (UMLS CUI [1,3])
C0040511 (UMLS CUI [1,4])
CL Item
interventional abdominal drainage (3)
C0184661 (UMLS CUI [1,1])
C1167781 (UMLS CUI [1,2])
CL Item
esophagogastroduodenoscopy (4)
C0079304 (UMLS CUI [1,1])
CL Item
radiologic management of postoperative bleeding (5)
C0344093 (UMLS CUI [1,1])
C0032788 (UMLS CUI [1,2])
CL Item
other (6)
C0205394 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Diagnosis
Item
Reason (Diagnosis)
text
C0011900 (UMLS CUI [1,1])
Item Group
5th reintervention / reoperation
C0205435 (UMLS CUI [1,1])
C5452916 (UMLS CUI [1,2])
C0035110 (UMLS CUI [1,3])
Date
Item
Date of 5th reintervention / reoperation
date
C0011008 (UMLS CUI [1,1])
Item
Procedures
integer
C0199171 (UMLS CUI [1,1])
Code List
Procedures
CL Item
completion pancreatectomy (1)
C0040511 (UMLS CUI [1,1])
CL Item
relaprotomy without completion pancreatectomy (2)
C0205341 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
C0332288 (UMLS CUI [1,3])
C0040511 (UMLS CUI [1,4])
CL Item
interventional abdominal drainage (3)
C0184661 (UMLS CUI [1,1])
C1167781 (UMLS CUI [1,2])
CL Item
esophagogastroduodenoscopy (4)
C0079304 (UMLS CUI [1,1])
CL Item
radiologic management of postoperative bleeding (5)
C0344093 (UMLS CUI [1,1])
C0032788 (UMLS CUI [1,2])
CL Item
other (6)
C0205394 (UMLS CUI [1,1])
specify
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Diagnosis
Item
Reason (Diagnosis)
text
C0011900 (UMLS CUI [1,1])
Item Group
Questionnaires
C0034394 (UMLS CUI [1,1])
EORTC QLQ-C30
Item
EORTC QLQ-C30 completed
boolean
C3641780 (UMLS CUI [1,1])
C2826970 (UMLS CUI [1,2])
EORTC QLQ-PAN26
Item
EORTC QLQ-PAN26 completed
boolean
C4288326 (UMLS CUI [1,1])
C2826970 (UMLS CUI [1,2])
Item Group
Concomitant Medication
C2347852 (UMLS CUI [1,1])
changes in Concomitant Medication since last visit
Item
Any changes in Concomitant Medication since last visit
boolean
C3872643 (UMLS CUI [1,1])
C0580105 (UMLS CUI [1,2])
Item Group
If yes, please fill out eForm 'Concomitant Medication'.
C2347852 (UMLS CUI [1,1])
C3273494 (UMLS CUI [1,2])
Item Group
Adverse Events
C0877248 (UMLS CUI [1,1])
Any new Adverse Events occurred since last visit
Item
Any new Adverse Events occurred since last visit
boolean
C0877248 (UMLS CUI [1,1])
C3872643 (UMLS CUI [1,2])
Item Group
If yes, please fill out eForm 'Adverse Events'.
C0877248 (UMLS CUI [1,1])
C3273494 (UMLS CUI [1,2])
Item Group
Protocol violations
C1709750 (UMLS CUI [1,1])
Any protocol violations occurred since last visit
Item
Any protocol violations occurred since last visit
boolean
C1709750 (UMLS CUI [1,1])
C3872643 (UMLS CUI [1,2])
Item Group
If yes, please fill out eForm 'Protocol Violation'.
C3273494 (UMLS CUI [1,1])
C1709750 (UMLS CUI [1,2])