Efficacy of narrow-band ultraviolet B on atopic dermatitis / Eman Mohammed Mohammed Talkhan ; Supervised Amal Mohamed Abdelbaky , Abeer Mohamed Abdelaziz Elkholy , Rokaia Ali Zain Elabedeen Mohamed Toson
Material type: TextLanguage: English Publication details: Cairo : Eman Mohammed Mohammed Talkhan , 2021Description: 61 P. : charts , facsimiles ; 25cmOther title:- فاعلية الاشعه فوق البنفسجيه الضيقه النطاق ب على مرضى الجلد التأتبى [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.21.07.M.Sc.2021.Em.E (Browse shelf(Opens below)) | Not for loan | 01010110083913000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.21.07.M.Sc.2021.Em.E (Browse shelf(Opens below)) | 83913.CD | Not for loan | 01020110083913000 |
Thesis (M.Sc.) - Cairo University - Faculty of Physical Therapy - Department of Physical Therapy for Surgery
Purpose of the study: To evaluate the current role of narrow band ultraviolet B in the treatment of atopic dermatitis.Subjects: Thirty children suffering from atopic dermatitis participated and completed the procedure of the study.Their ages ranged from 5 to 17 years,They were selected from Mansoura hospital, Department of dermatology. Methods: All patients were assessed by recording data sheet, SCORAD scale and Dermoscopy before and after the end of treatment procedures. All patients were randomly assigned into two equal groups (15 patients for each group): Group A (Study group):This group was composed of fifteen children suffering from atopic dermatitis and they were received topical emollient daily and narrow-band ultraviolet B 3 times /week for 12 weeks.Group B (Control group): This group was composed of fifteen children suffering from atopic dermatitis and they were received topical emollient daily for 12 weeks. Results: In study group, the mean values of pre- and post-treatment of Dermoscopy assessment were 8.27 ±0.70 and 1.80 ±0.67, respectively, with improvement percentage 78.23%.While in control group, the mean values of pre- and post-treatment of Dermoscopy assessment were 8.40 ±0.73 and 6.33 ±0.90, respectively, with improvement percentage 24.64%. In study group, the mean values of pre- and post-treatment of SCORAD scale assessment were 47.58 ±5.49 and 12.13 ±1.95, respectively, with improvement percentage 74.51%. In control group, the mean values of pre- and post-treatment of SCORAD scale assessment were 43.60 ±7.46 and 36.13 ±7.36, respectively, with improvement percentage 17.13%
Issued also as CD
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