CLINDX¶
Table Description: Clinical Diagnosis and Management
Detailed notes for this table are included below.
View Source CRFs¶
1.0 CRFs: Click on any PAG_NAME link below to be taken to the CRF used in the PPMI 1.0 Study.
1.0 Data Dictionary¶
ITM_NAME |
DSCR_1.0 |
|---|---|
CLDXCHNG |
Change in clinical diagnosis |
DCBRADY |
Present for dx PD-Bradykinesia |
DCNOMTR |
No motor signs consistent with PS |
DCRIGID |
Present for dx PD-Rigidity |
DCRTREM |
Present for dx PD-Rest Tremor |
DFOTH |
Other signs related to PS |
DFOTHCM |
Other signs related to PS - comment |
DFPGDIST |
Postural and gait dist are typical of PD |
DXFCLSGN |
Factors in diagnosis-clinical signs |
DXFDTIMG |
Factors in diagnosis-imaging data |
DXFNATHX |
Factors in diagnosis-natural history |
DXFOTH |
Factors in diagnosis-other |
DXFOTHCM |
Factors in diagnosis-other comment |
DXFRSPMD |
Factors in diagnosis-response to PD med |
MNGCHNG |
Change in clinical management |
MNGDXTST |
Current management-diagnostic testing |
MNGNOTRT |
Current management-no treatment |
MNGTRIAL |
Current management-enrolled in trial |
MNGTRTOT |
Current management-treat other than PD |
MNGTRTSX |
Current management-treat symptoms of PD |
NEURWKDX |
Other neurologist working diagnosis |
OTHNEURO |
Other neurological disorder(s) (specify) |
OTNEURVS |
Seen another neurologist |
PRIMDIAG |
Most likely primary diagnosis |
PSLVL |
Confidence level-motor signs of PS |
1.0 Code Book¶
ITM_NAME |
CODE |
DECODE_1.0 |
|---|---|---|
CLDXCHNG |
0 |
No |
CLDXCHNG |
1 |
Yes |
DCBRADY |
0 |
No |
DCBRADY |
1 |
Yes |
DCNOMTR |
0 |
No |
DCNOMTR |
1 |
Yes |
DCRIGID |
0 |
No |
DCRIGID |
1 |
Yes |
DCRTREM |
0 |
No |
DCRTREM |
1 |
Yes |
DFOTH |
0 |
No |
DFOTH |
1 |
Yes |
DFPGDIST |
0 |
No |
DFPGDIST |
1 |
Yes |
DXFCLSGN |
0 |
No |
DXFCLSGN |
1 |
Yes |
DXFDTIMG |
0 |
No |
DXFDTIMG |
1 |
Yes |
DXFNATHX |
0 |
No |
DXFNATHX |
1 |
Yes |
DXFOTH |
0 |
No |
DXFOTH |
1 |
Yes |
DXFRSPMD |
0 |
No |
DXFRSPMD |
1 |
Yes |
MNGCHNG |
0 |
No |
MNGCHNG |
1 |
Yes |
MNGDXTST |
0 |
No |
MNGDXTST |
1 |
Yes |
MNGNOTRT |
0 |
No |
MNGNOTRT |
1 |
Yes |
MNGTRIAL |
0 |
No |
MNGTRIAL |
1 |
Yes |
MNGTRTOT |
0 |
No |
MNGTRTOT |
1 |
Yes |
MNGTRTSX |
0 |
No |
MNGTRTSX |
1 |
Yes |
OTNEURVS |
0 |
No |
OTNEURVS |
1 |
Yes |
PRIMDIAG |
1 |
Idiopathic PD |
PRIMDIAG |
2 |
Alzheimer’s disease |
PRIMDIAG |
3 |
Chromosome-17 frontotemporal dementia |
PRIMDIAG |
4 |
Corticobasal degeneration |
PRIMDIAG |
5 |
Dementia with Lewy bodies |
PRIMDIAG |
6 |
Dopa-responsive dystonia |
PRIMDIAG |
7 |
Essential tremor |
PRIMDIAG |
8 |
Hemiparkinson/hemiatrophy syndrome |
PRIMDIAG |
9 |
Juv. autosomal recessive parkinsonism |
PRIMDIAG |
10 |
Motor neuron disease with parkinsonism |
PRIMDIAG |
11 |
Multiple system atrophy |
PRIMDIAG |
12 |
Neuroleptic-induced parkinsonism |
PRIMDIAG |
13 |
Normal pressure hydrocephalus |
PRIMDIAG |
14 |
Progressive supranuclear palsy |
PRIMDIAG |
15 |
Psychogenic illness |
PRIMDIAG |
16 |
Vascular parkinsonism |
PRIMDIAG |
17 |
No PD nor other neurological disorder |
PRIMDIAG |
18 |
Spinocerebellar Ataxia (SCA) |
PRIMDIAG |
97 |
Other neurological disorder(s) (specify) |
PSLVL |
1 |
Motor abnormalities likely PS (90-100%) |
PSLVL |
2 |
Motor abnormalities may be PS (50-89%) |
PSLVL |
3 |
Non-specific motor abnormalities(10-49%) |
PSLVL |
4 |
No evidence of park. motor signs (0-9%) |
Details¶
PSLVL
This variable is not being directly captured in the PPMI Extended schema. However, a similar variable (PSGLVL) is being captured in the FEATPD table. This new variable asks about any abnormalities related to neurodegenerative parkinsonian syndrome, whereas this now inactive PSLVL variable asked more specifically about motor symptoms related to parkinsonian snydrome.