ID

15819

Description

NINDS Common Data Elements (Pregnancy Outcome; Headache) Used from the National Institute of Neurological Disorders and Stroke Common Data Elements (https://www.commondataelements.ninds.nih.gov/) References: Grinnon ST, Miller K, Marler JR, Lu Y, Stout A, Odenkirchen J, Kunitz S. National Institute of Neurological Disorders and Stroke Common Data Element Project - approach and methods. Clin Trials. 2012;9(3):322-9.

Lien

https://www.commondataelements.ninds.nih.gov/

Mots-clés

  1. 15/06/2016 15/06/2016 -
Téléchargé le

15 juin 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

NINDS CDE Pregnancy Outcome Headache

Pregnancy Outcome

  1. StudyEvent: ODM
    1. Pregnancy Outcome
Demographics
Description

Demographics

Study ID
Description

Study ID

Type de données

text

Alias
UMLS CUI [1]
C2826693
Study site name
Description

Study site

Type de données

text

Alias
UMLS CUI [1]
C2825164
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Pregnancy History
Description

Pregnancy History

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

Date pregnancy outcome

Type de données

date

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

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

Type de données

integer

Alias
UMLS CUI [1]
C0032972
Pregnancy outcome
Description

Pregnancy outcome

Type de données

text

Alias
UMLS CUI [1]
C0032972
Outcome Date
Description

Pregnancy outcome

Type de données

date

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

Pregnancy outcome

Type de données

integer

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

Pregnancy outcome

Type de données

text

Alias
UMLS CUI [1]
C0032972
Delivery type
Description

Delivery type

Type de données

integer

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

Delivery type

Type de données

integer

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

Delivery type

Type de données

text

Alias
UMLS CUI [1]
C2114511
Delivery route
Description

Delivery route

Type de données

integer

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

Delivery route

Type de données

text

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

Delivery route

Type de données

integer

Alias
UMLS CUI [1]
C3654234
Delivery modality type
Description

Delivery modality type

Type de données

integer

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

Complications

Type de données

integer

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

Complications

Type de données

text

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

Tocolytic agent

Type de données

integer

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

Tocolytic agent

Type de données

text

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

Details of Most Recent Live Birth

Birth Date
Description

Birth Date

Type de données

date

Alias
UMLS CUI [1]
C0421451
Birth sex
Description

Birth sex

Type de données

integer

Alias
UMLS CUI [1]
C4019317
Birth weight
Description

Birth weight

Type de données

float

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

Unit of measurement

Type de données

integer

Alias
UMLS CUI [1]
C1519795
Birth length
Description

Birth length

Type de données

integer

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

Unit of measurement

Type de données

integer

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

Full-term delivery

Type de données

integer

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

Gestational age

Type de données

integer

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

APGAR

Type de données

integer

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

APGAR

Type de données

integer

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

Body weight

Type de données

float

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

Unit of measurement

Type de données

integer

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

Fetal diagnostic tests abnormal

Type de données

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
Description

Fetal diagnostic tests abnormal

Type de données

text

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

Congenital anomalies

Type de données

integer

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

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

Type de données

text

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

Newborn complications

Type de données

integer

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

Newborn complications

Type de données

text

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

Abnormalities of placenta or umbilical cord

Type de données

integer

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

Abnormalities of placenta or umbilical cord

Type de données

text

Alias
UMLS CUI [1]
C4025798

Similar models

Pregnancy Outcome

  1. StudyEvent: ODM
    1. Pregnancy Outcome
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial