Pregnancy Outcome

  1. StudyEvent: ODM
    1. Pregnancy Outcome
Demographics
Beskrivning

Demographics

Study ID
Beskrivning

Study ID

Datatyp

text

Alias
UMLS CUI [1]
C2826693
Study site name
Beskrivning

Study site

Datatyp

text

Alias
UMLS CUI [1]
C2825164
Subject ID
Beskrivning

Subject ID

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Pregnancy History
Beskrivning

Pregnancy History

Date pregnancy outcome obtained (m m/dd/yyyy):
Beskrivning

Date pregnancy outcome

Datatyp

date

Alias
UMLS CUI [1]
C0032972
Was the outcome of the participant’s/subject’s most recent pregnancy a live born infant?
Beskrivning

If No, complete the following and then STOP, you are finished

Datatyp

integer

Alias
UMLS CUI [1]
C0032972
Pregnancy outcome
Beskrivning

Pregnancy outcome

Datatyp

text

Alias
UMLS CUI [1]
C0032972
Outcome Date
Beskrivning

Pregnancy outcome

Datatyp

date

Alias
UMLS CUI [1]
C0032972
Was the fetus normal?
Beskrivning

Pregnancy outcome

Datatyp

integer

Alias
UMLS CUI [1]
C0032972
Was the fetus normal? If no, please describe
Beskrivning

Pregnancy outcome

Datatyp

text

Alias
UMLS CUI [1]
C0032972
Delivery type
Beskrivning

Delivery type

Datatyp

integer

Alias
UMLS CUI [1]
C2114511
Delivery type Induced; specify reason (Choose all that apply)
Beskrivning

Delivery type

Datatyp

integer

Alias
UMLS CUI [1]
C2114511
Delivery type Induced; Other, specify
Beskrivning

Delivery type

Datatyp

text

Alias
UMLS CUI [1]
C2114511
Delivery route
Beskrivning

Delivery route

Datatyp

integer

Alias
UMLS CUI [1]
C3654234
Delivery route Cesarean section reason
Beskrivning

Delivery route

Datatyp

text

Alias
UMLS CUI [1]
C3654234
Delivery route Cesarean section timing
Beskrivning

Delivery route

Datatyp

integer

Alias
UMLS CUI [1]
C3654234
Delivery modality type
Beskrivning

Delivery modality type

Datatyp

integer

Alias
UMLS CUI [1]
C2114311
Did the participant/subject experience any complications during labor/delivery?
Beskrivning

Complications

Datatyp

integer

Alias
UMLS CUI [1]
C0009566
Did the participant/subject experience any complications during labor/delivery? If yes, please specify
Beskrivning

Complications

Datatyp

text

Alias
UMLS CUI [1]
C0009566
Did the participant/subject require tocolytic agents during preterm labor?
Beskrivning

Tocolytic agent

Datatyp

integer

Alias
UMLS CUI [1]
C0040349
Did the participant/subject require tocolytic agents during preterm labor? If yes, please specify
Beskrivning

Tocolytic agent

Datatyp

text

Alias
UMLS CUI [1]
C0040349
Details of Most Recent Live Birth
Beskrivning

Details of Most Recent Live Birth

Birth Date
Beskrivning

Birth Date

Datatyp

date

Alias
UMLS CUI [1]
C0421451
Birth sex
Beskrivning

Birth sex

Datatyp

integer

Alias
UMLS CUI [1]
C4019317
Birth weight
Beskrivning

Birth weight

Datatyp

float

Alias
UMLS CUI [1]
C0005612
Please specify units used for birth weight
Beskrivning

Unit of measurement

Datatyp

integer

Alias
UMLS CUI [1]
C1519795
Birth length
Beskrivning

Birth length

Datatyp

integer

Alias
UMLS CUI [1]
C0419415
Please specify units used for birth length
Beskrivning

Unit of measurement

Datatyp

integer

Alias
UMLS CUI [1]
C1519795
Was the child delivered full-term
Beskrivning

Full-term delivery

Datatyp

integer

Alias
UMLS CUI [1]
C0438070
Indicate gestational age GA (weeks):
Beskrivning

Gestational age

Datatyp

integer

Alias
UMLS CUI [1]
C0017504
APGAR 5 Minute score
Beskrivning

APGAR

Datatyp

integer

Alias
UMLS CUI [1]
C0003533
APGAR 10 Minute score
Beskrivning

APGAR

Datatyp

integer

Alias
UMLS CUI [1]
C0003533
Mother’s weight at the time of birth
Beskrivning

Body weight

Datatyp

float

Alias
UMLS CUI [1]
C0005910
Please specify units used for body weight
Beskrivning

Unit of measurement

Datatyp

integer

Alias
UMLS CUI [1]
C1519795
Any abnormal fetal diagnostic tests performed during pregnancy?
Beskrivning

Fetal diagnostic tests abnormal

Datatyp

integer

Alias
UMLS CUI [1,1]
C0947980
UMLS CUI [1,2]
C0205161
Any abnormal fetal diagnostic tests? If yes please fill in the dates of testing and the test results
Beskrivning

Fetal diagnostic tests abnormal

Datatyp

text

Alias
UMLS CUI [1,1]
C0947980
UMLS CUI [1,2]
C0205161
Were there any congenital anomalies?
Beskrivning

Congenital anomalies

Datatyp

integer

Alias
UMLS CUI [1]
C0000768
Were there any congenital anomalies?If Yes, specify
Beskrivning

Complete an adverse event form if the participant/subject was enrolled in the study at the time of the birth.

Datatyp

text

Alias
UMLS CUI [1]
C0000768
Were there other newborn complications?
Beskrivning

Newborn complications

Datatyp

integer

Alias
UMLS CUI [1]
C1148391
Were there other newborn complications? If Yes, specify
Beskrivning

Newborn complications

Datatyp

text

Alias
UMLS CUI [1]
C1148391
Did the newborn experience any abnormalities of placenta or umbilical cord?
Beskrivning

Abnormalities of placenta or umbilical cord

Datatyp

integer

Alias
UMLS CUI [1]
C4025798
Did the newborn experience any abnormalities of placenta or umbilical cord? If Yes, specify
Beskrivning

Abnormalities of placenta or umbilical cord

Datatyp

text

Alias
UMLS CUI [1]
C4025798

Similar models

Pregnancy Outcome

  1. StudyEvent: ODM
    1. Pregnancy Outcome
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Demographics
Study ID
Item
Study ID
text
C2826693 (UMLS CUI [1])
Study site
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Item Group
Pregnancy History
Date pregnancy outcome
Item
Date pregnancy outcome obtained (m m/dd/yyyy):
date
C0032972 (UMLS CUI [1])
Item
Was the outcome of the participant’s/subject’s most recent pregnancy a live born infant?
integer
C0032972 (UMLS CUI [1])
Code List
Was the outcome of the participant’s/subject’s most recent pregnancy a live born infant?
CL Item
Yes (skip to "Delivery type") (1)
CL Item
No (Complete a-c only) (2)
CL Item
Unknown (Stop,you are finished) (3)
Item
Pregnancy outcome
text
C0032972 (UMLS CUI [1])
Code List
Pregnancy outcome
Pregnancy outcome
Item
Outcome Date
date
C0032972 (UMLS CUI [1])
Item
Was the fetus normal?
integer
C0032972 (UMLS CUI [1])
Code List
Was the fetus normal?
CL Item
Yes  (1)
CL Item
No (describe) (2)
CL Item
Unknown (3)
Pregnancy outcome
Item
Was the fetus normal? If no, please describe
text
C0032972 (UMLS CUI [1])
Item
Delivery type
integer
C2114511 (UMLS CUI [1])
Code List
Delivery type
CL Item
Spontaneous (1)
CL Item
Induced; specify reason (2)
Item
Delivery type Induced; specify reason (Choose all that apply)
integer
C2114511 (UMLS CUI [1])
Code List
Delivery type Induced; specify reason (Choose all that apply)
CL Item
Hemorrhage and Placental Complications (1)
CL Item
Hypertension, Preeclampsia or Eclampsia (2)
CL Item
Rupture of Membranes-Premature, Prolonged (3)
CL Item
Maternal Conditions Complicating Pregnancy/Delivery (4)
CL Item
Fetal Conditions Complicating Pregnancy/Delivery (5)
CL Item
Malposition and Malpresentation of Fetus (6)
CL Item
Late Pregnancy (7)
CL Item
Prior Uterine Surgery (8)
CL Item
Other, specify: (9)
CL Item
Unknown (10)
Item
Delivery type Induced; Other, specify
text
C2114511 (UMLS CUI [1])
Code List
Delivery type Induced; Other, specify
Item
Delivery route
integer
C3654234 (UMLS CUI [1])
Code List
Delivery route
CL Item
Vaginal (1)
CL Item
Cesarean section please complete the following (2)
CL Item
Unknown (3)
Delivery route
Item
Delivery route Cesarean section reason
text
C3654234 (UMLS CUI [1])
Item
Delivery route Cesarean section timing
integer
C3654234 (UMLS CUI [1])
Code List
Delivery route Cesarean section timing
CL Item
Emergency (1)
CL Item
Elective (2)
Item
Delivery modality type
integer
C2114311 (UMLS CUI [1])
Code List
Delivery modality type
CL Item
Breech (1)
CL Item
Cephalic (2)
CL Item
Unknown (3)
Item
Did the participant/subject experience any complications during labor/delivery?
integer
C0009566 (UMLS CUI [1])
Code List
Did the participant/subject experience any complications during labor/delivery?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Complications
Item
Did the participant/subject experience any complications during labor/delivery? If yes, please specify
text
C0009566 (UMLS CUI [1])
Item
Did the participant/subject require tocolytic agents during preterm labor?
integer
C0040349 (UMLS CUI [1])
Code List
Did the participant/subject require tocolytic agents during preterm labor?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Tocolytic agent
Item
Did the participant/subject require tocolytic agents during preterm labor? If yes, please specify
text
C0040349 (UMLS CUI [1])
Item Group
Details of Most Recent Live Birth
Birth Date
Item
Birth Date
date
C0421451 (UMLS CUI [1])
Item
Birth sex
integer
C4019317 (UMLS CUI [1])
Code List
Birth sex
CL Item
Male  (1)
CL Item
Female  (2)
CL Item
Unknown (3)
Birth weight
Item
Birth weight
float
C0005612 (UMLS CUI [1])
Item
Please specify units used for birth weight
integer
C1519795 (UMLS CUI [1])
Code List
Please specify units used for birth weight
CL Item
ounces  (1)
CL Item
grams (2)
Birth length
Item
Birth length
integer
C0419415 (UMLS CUI [1])
Item
Please specify units used for birth length
integer
C1519795 (UMLS CUI [1])
Code List
Please specify units used for birth length
CL Item
inches (1)
CL Item
cm (2)
Item
Was the child delivered full-term
integer
C0438070 (UMLS CUI [1])
Code List
Was the child delivered full-term
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Gestational age
Item
Indicate gestational age GA (weeks):
integer
C0017504 (UMLS CUI [1])
Item
APGAR 5 Minute score
integer
C0003533 (UMLS CUI [1])
Code List
APGAR 5 Minute score
CL Item
0 (0)
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)
CL Item
10 (10)
Item
APGAR 10 Minute score
integer
C0003533 (UMLS CUI [1])
Code List
APGAR 10 Minute score
CL Item
0 (0)
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)
CL Item
10 (10)
Body weight
Item
Mother’s weight at the time of birth
float
C0005910 (UMLS CUI [1])
Item
Please specify units used for body weight
integer
C1519795 (UMLS CUI [1])
Code List
Please specify units used for body weight
CL Item
pounds (1)
CL Item
kilograms (2)
Item
Any abnormal fetal diagnostic tests performed during pregnancy?
integer
C0947980 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Code List
Any abnormal fetal diagnostic tests performed during pregnancy?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Any abnormal fetal diagnostic tests? If yes please fill in the dates of testing and the test results
text
C0947980 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Code List
Any abnormal fetal diagnostic tests? If yes please fill in the dates of testing and the test results
Item
Were there any congenital anomalies?
integer
C0000768 (UMLS CUI [1])
Code List
Were there any congenital anomalies?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Were there any congenital anomalies?If Yes, specify
text
C0000768 (UMLS CUI [1])
Code List
Were there any congenital anomalies?If Yes, specify
Item
Were there other newborn complications?
integer
C1148391 (UMLS CUI [1])
Code List
Were there other newborn complications?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Were there other newborn complications? If Yes, specify
text
C1148391 (UMLS CUI [1])
Code List
Were there other newborn complications? If Yes, specify
Item
Did the newborn experience any abnormalities of placenta or umbilical cord?
integer
C4025798 (UMLS CUI [1])
Code List
Did the newborn experience any abnormalities of placenta or umbilical cord?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Abnormalities of placenta or umbilical cord
Item
Did the newborn experience any abnormalities of placenta or umbilical cord? If Yes, specify
text
C4025798 (UMLS CUI [1])