ID

17816

Description

Intermittent prone positioning in the treatment of severe and moderate posttraumatic lung injury (1999). Background: Severe posttraumatic lung injury is characterized by impairment of gas exchange and pulmonary densities. The influence of intermittent prone positioning on pulmonary gas exchange and parenchymal densities was investigated prospectively in patients with pulmonary injury after multiple trauma with blunt chest trauma. Publication granted by Claudia Ose, ZKS UK Essen. Multizentrische prospektive randomisierte Studie zur Überprüfung der prognostischen und therapeutischen Effektivität der dorsoventralen Wechsellagerung bei Patienten mit posttraumatischem akutem Lungenversagen. Freigegeben durch Frau Claudia Ose, ZKS Essen.

Keywords

Versions (1)
  1. 10/4/16 10/4/16 -
Uploaded on

October 4, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Adverse Events Intermittent Prone Positioning Posttraumatic Lung Injury Study

German

Adverse Events Intermittent Prone Positioning Posttraumatic Lung Injury Study

1 forms  
Patientenidentifikation
Description

Patientenidentifikation

Alias
UMLS CUI-1
C1269815
Patientennr.:
Description

Patient ID

Data type

integer

Alias
UMLS CUI [1]
C2348585
Initialen:
Description

Patient Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Zentrumsnr.:
Description

number of study centre

Data type

integer

Alias
UMLS CUI [1,1]
C2825181
UMLS CUI [1,2]
C1300638
Unerwünschte Ereignisse
Description

Unerwünschte Ereignisse

Alias
UMLS CUI-1
C0877248
Ereignis/Symptom
Description

event/symptom

Data type

text

Alias
UMLS CUI [1]
C0877248
UMLS CUI [2]
C1457887
Datum des Auftretens
Description

date of appearance

Data type

date

Alias
UMLS CUI [1]
C2585732
Intensität
Description

Intensity

Data type

integer

Alias
UMLS CUI [1]
C0522510
Aktion
Description

treatment action

Data type

integer

Alias
UMLS CUI [1]
C0441472
Zusammenhang mit der Lagerung
Description

coherent to patients position

Data type

integer

Alias
UMLS CUI [1,1]
C0449850
UMLS CUI [1,2]
C0542559
Klinischer Verlauf
Description

clinical course

Data type

integer

Alias
UMLS CUI [1]
C0449259
Datum des Endes
Description

end date

Data type

date

Alias
UMLS CUI [1]
C0806020
Dauer (falls <24h)
Description

duration of symptom

Data type

time

Measurement units
  • hh:mm
Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C1457887
hh:mm
sUE
Description

Serious Adverse Event

Data type

boolean

Alias
UMLS CUI [1]
C1519255
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Similar models

Adverse Events Intermittent Prone Positioning Posttraumatic Lung Injury Study

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patientenidentifikation
C1269815 (UMLS CUI-1)
Patient ID
Item
Patientennr.:
integer
C2348585 (UMLS CUI [1])
Patient Initials
Item
Initialen:
text
C2986440 (UMLS CUI [1])
number of study centre
Item
Zentrumsnr.:
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Unerwünschte Ereignisse
C0877248 (UMLS CUI-1)
event/symptom
Item
Ereignis/Symptom
text
C0877248 (UMLS CUI [1])
C1457887 (UMLS CUI [2])
date of appearance
Item
Datum des Auftretens
date
C2585732 (UMLS CUI [1])
Item
Intensität
integer
C0522510 (UMLS CUI [1])
Intensity
Code List
Intensität
CL Item
leicht (1)
CL Item
mittel (3)
CL Item
schwer (3)
Item
Aktion
integer
C0441472 (UMLS CUI [1])
treatment action
Code List
Aktion
CL Item
keine (1)
CL Item
nur symptomatische (2)
CL Item
Behandlung  (3)
CL Item
Lagerungsmethode (3)
CL Item
zeitweise abgesetzt (5)
CL Item
Lagerungsmethode (4)
CL Item
abgesetzt (7)
Item
Zusammenhang mit der Lagerung
integer
C0449850 (UMLS CUI [1,1])
C0542559 (UMLS CUI [1,2])
coherent to patients position
Code List
Zusammenhang mit der Lagerung
CL Item
gesichert (1)
CL Item
wahrscheinlich (2)
CL Item
möglich (3)
CL Item
unwahrscheinlich (4)
CL Item
keiner (5)
CL Item
Beurteilung nicht möglich (6)
Item
Klinischer Verlauf
integer
C0449259 (UMLS CUI [1])
clinical course
Code List
Klinischer Verlauf
CL Item
wiederhergestellt (1)
CL Item
verbessert (2)
CL Item
gleich geblieben (3)
CL Item
verschlechtert (4)
CL Item
schwerwiegend (sUE) (5)
CL Item
Tod (sUE) (6)
end date
Item
Datum des Endes
date
C0806020 (UMLS CUI [1])
duration of symptom
Item
Dauer (falls <24h)
time
C0449238 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
Serious Adverse Event
Item
sUE
boolean
C1519255 (UMLS CUI [1])
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