PRISMΔDB

Analyze how specific documents activate the features of the SAE. Select a dataset, a run and a document to begin.

Active Features

1517

0.0
Details List
#2194 Feature 2194
3.1
#954 Feature 954
2.9
#197 Feature 197
2.8
#841 Feature 841
2.5
#734 Feature 734
2.5
#2422 Feature 2422
2.4
#1783 Feature 1783
2.4
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2.4
#2981 Feature 2981
2.2
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2.2
#332 Feature 332
2.2
#455 Feature 455
2.2
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2.1
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2.1
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2.1
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2.1
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2.0
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2.0
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2.0
#1830 Feature 1830
1.9
#2964 Feature 2964
1.9
#232 Feature 232
1.9
#2096 Feature 2096
1.8
#333 Feature 333
1.8
#1587 Feature 1587
1.7
#2065 Feature 2065
1.7
#1787 Feature 1787
1.7
#92 Feature 92
1.7
#2724 Feature 2724
1.7
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1.7
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1.6
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1.6
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1.6
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1.5
#2522 Feature 2522
1.5
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1.5
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1.5
#1792 Metastatic Cancer
1.5
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1.5
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1.5
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1.5
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1.5
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1.5
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1.4
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1.4
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1.4
#143 Feature 143
1.4
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1.4
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1.4
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1.4
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1.4
#1865 Feature 1865
1.4
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1.4
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1.4
#1313 Feature 1313
1.4
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1.4
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1.4
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1.4
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
#820 Feature 820
1.3
#1508 Feature 1508
1.3
#756 Feature 756
1.3
#2312 Feature 2312
1.3
#1384 Feature 1384
1.3
#2014 Feature 2014
1.3
#836 Feature 836
1.3
#1594 Feature 1594
1.3
#487 Feature 487
1.3
#665 Feature 665
1.3
#2061 Feature 2061
1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
#2929 Feature 2929
1.2
#1708 Feature 1708
1.2
#1449 Feature 1449
1.2
#2972 Sensory-Motor Integration
1.2
#1968 Feature 1968
1.2
#1318 Feature 1318
1.2
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1.2
#1625 Feature 1625
1.2
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1.2
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1.2
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1.2
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1.2
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1.2
#1919 Feature 1919
1.2
#1392 Feature 1392
1.2
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1.2
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1.2
#1989 Feature 1989
1.2
#1336 Feature 1336
1.2
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1.2
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1.2
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1.2
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1.2
#95 Feature 95
1.2
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
#28 Feature 28
1.1
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1.1
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1.1
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1.1
#950 Feature 950
1.1
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1.1
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1.1
#1603 Feature 1603
1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
#1232 Feature 1232
1.0
#2584 Feature 2584
1.0
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1.0
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1.0
#1032 Feature 1032
1.0
#2772 Feature 2772
1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
#1507 Feature 1507
1.0
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1.0
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1.0
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
#1527 Feature 1527
0.9
#722 Feature 722
0.9
#2354 Feature 2354
0.9
#771 Feature 771
0.9
#1093 Feature 1093
0.9
#2750 Feature 2750
0.9
#2436 Feature 2436
0.9
#2778 Hippocampal Memory and Cognitive Function
0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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Document Content

Prediction of somatic and non-somatic depressive symptoms between inpatient rehabilitation and follow-up.
Longitudinal. We identified changes in the association of somatic and non-somatic symptoms (as measured by the Patient Health Questionnaire-9, PHQ-9) between inpatient rehabilitation after spinal cord injury (SCI) and 1 year after discharge. A specialty hospital in the Southeastern USA. A total of 584 adults with traumatic SCI were administered the PHQ-9 during inpatient rehabilitation. Of them, 227 completed the PHQ-9 by survey at 1-year follow-up. We performed time-lagged regression between times of measurement for somatic and non-somatic factors of the PHQ-9. The non-somatic factor at baseline was significantly predictive of the non-somatic (r=0.67, P=0.002) and somatic factors at follow-up (r=0.53, P=0.019). The somatic factor did not significantly predict either the somatic (r=0.10, n.s.) or non-somatic factors at follow-up (r=-0.01, NS). Factor analysis also indicated changing factor structure between inpatient rehabilitation and follow-up. Our results question the interpretation of somatic items during inpatient rehabilitation, as they are not predictive of either somatic or non-somatic symptoms at follow-up.