Analyzer · Sparsifire

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

Dataset

SAE Model

Document

Active Features

1523

MIN ACTIVATION

0.0

Details List

#1244 Feature #1244

#102 Feature #102

#2650 Feature #2650

#1006 Feature #1006

#2232 Medical Case Reports & Cancer Research

#2414 Feature #2414

#2810 Feature #2810

#1025 Feature #1025

#676 Feature #676

#288 Feature #288

#1768 Feature #1768

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#2529 Feature #2529

#881 Feature #881

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#1984 Feature #1984

#3022 Feature #3022

#1009 Feature #1009

#2255 Feature #2255

#3068 Feature #3068

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#111 Feature #111

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#1437 Feature #1437

#88 Feature #88

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#565 Feature #565

#2792 Feature #2792

#400 Feature #400

#877 Feature #877

#1686 Feature #1686

#1595 Feature #1595

#698 Feature #698

#1687 Feature #1687

#1203 Feature #1203

#919 Feature #919

#2635 Feature #2635

#1452 Feature #1452

#85 Feature #85

#2716 Feature #2716

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#23 Neuronal Circuitry and Cellular Processes

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#708 Drug Resistance Mechanisms in Cancer

#1695 Feature #1695

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#1792 Metastatic Cancer

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#374 Medical Imaging and Oncology

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Document Content

Important factors for pain during photodynamic therapy for actinic keratosis.
Photodynamic therapy (PDT) is an efficient treatment for actinic keratosis. A common problem, however, is pain. The aim of this study was to investigate pain during PDT for actinic keratosis. The possibility of using capsaicin cream for pain relief was also assessed. Pain was investigated during aminolaevulinic acid PDT in 91 patients. Size, redness, scaling and induration of the lesions were recorded. Maximum pain during treatment was registered, using a visual analogue scale (0-10). The pain-reducing efficacy of capsaicin was tested in a pilot study in six patients (10 lesions). These patients were pre-treated with capsaicin cream for one week before commencing PDT. Pain was found to be normally distributed around a mean value of visual analogue scale 4.6. Larger lesions gave more pain (p=0.001). The redness of the actinic lesions was found to be related to PDT-induced pain (p=0.01), the reduction of actinic area (p=0.007), and the cure rate (p=0.01). The redder the actinic area, the better the treatment outcome and the more pain experienced. Patients with the largest reduction in the actinic area experienced more pain (p=0.053). The most important factors for presence of pain seem to be the size and the redness of the lesion. No significant pain relief was experienced after pre-treatment with capsaicin.

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