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Dr. Fatma Mohammed Alfeky :: Publications:

Title:
Comparison between efficacy of High Level LASER Therapy and Low Level LASER Therapy in Treatment of Radiation- Induced Oral Mucositis: A Randomized Controlled Trial.
Authors: Fatma Mohammed Alfeky, Heba Mohamed Abd Elshafi, Esraa Hany Rostom, Ehab Saad Abdelnaby, Doaa Tammam Atia, Shimaa T.Abu El kasem
Year: 2023
Keywords: Head and Neck Cancer; High Level LASER Therapy; Low Level LASER Therapy; RadiationInduced Oral Mucositis
Journal: Journal of Pharmaceutical Negative Results
Volume: 14
Issue: 1
Pages: 10-20
Publisher: Journal of Pharmaceutical Negative Results
Local/International: International
Paper Link:
Full paper Fatma Mohammed Alfeky_RIOM.pdf
Supplementary materials Fatma Mohammed Alfeky_RIOM.pdf
Abstract:

Background: Radiation- Induced Oral Mucositis (RIOM) is a frequent debilitating side effect in patients with Head and Neck Cancer (HNC) received Radiotherapy (RT). Objectives: to evaluate and compare between the efficacy of High Level LASER Therapy (HLLT) and Low Level LASER Therapy (LLLT) in treatment of RIOM in patients with HNC. Methods: Sixty patients of both genders with RIOM were enrolled in the study and distributed randomly into 3 groups: Study group (A): 20 patients (8 male and 12 females) were received HLLT by Gallium Arsenide (GA-AS) laser class IV (wavelength 904 nm, average power 3.3W, frequency 1-2000 Hz and energy density 6.04 J/cm2 ). Scanning mode was used extraorally all over the oral cavity in one minute for five consecutive days, once a day for 2 weeks. Study group (B): 20 patients (6 male and 14 females) were received LLLT GA-AS laser class 3B with a small hand held probe intraorally both in ulcerated and erythematous areas (wavelength 904 nm, average power 70.5mW and energy density 5 J/cm2 for one minute on each point) for five consecutive days, once a day for 2 weeks. Control group (C): 20 patients (9 males and 11 females) were received shame LASER. All patients in the 3 groups were received routine medical care in the form of local antifungal, analgesics and mouth wash. Outcome measures: Patients were evaluated for OM severity according to World Health Organization (WHO) grading scale. Pain intensity was assessed by visual analogue scale (VAS). Assessment of the dependent variables was performed at two occasions; first at baseline, second after two weeks (ten LASER sessions). Results: Within group analysis, there were statistical significant difference between pre and post treatment at all variables in both study groups A and B in favor to group A (p

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