Recover burn ointment for managing acute radiodermatitis in patients with breast cancer: A double blind randomized controlled trial
Background: Radiodermatitis is the most common complication of radiotherapy. There is no gold standard for managing the radiodermatitis. This study aimed to evaluate the effect of topical Recove® burn ointment; basically compounded of sesame oil, camphor, and zinc oxide; in preventing acute radioder...
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Babol University of Medical Sciences,
2022-02-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_5f0c6876d5d54dd78b25ed43b82b943b | ||
042 | |a dc | ||
100 | 1 | 0 | |a Nargeuss Abbaszade Marzbali |e author |
700 | 1 | 0 | |a Ebrahim Zabihi |e author |
700 | 1 | 0 | |a Nicolas Magne |e author |
700 | 1 | 0 | |a Alexis Vallard |e author |
700 | 1 | 0 | |a Mohammad Moslemi |e author |
700 | 1 | 0 | |a Dariush Moslemi |e author |
245 | 0 | 0 | |a Recover burn ointment for managing acute radiodermatitis in patients with breast cancer: A double blind randomized controlled trial |
260 | |b Babol University of Medical Sciences, |c 2022-02-01T00:00:00Z. | ||
500 | |a 2008-6164 | ||
500 | |a 2008-6172 | ||
520 | |a Background: Radiodermatitis is the most common complication of radiotherapy. There is no gold standard for managing the radiodermatitis. This study aimed to evaluate the effect of topical Recove® burn ointment; basically compounded of sesame oil, camphor, and zinc oxide; in preventing acute radiodermatitis. Methods: This double blind RCT (IRCT No.: 201204047136N2) was performed on 71 patients that referred for radiotherapy after mastectomy to Shahid Rajaee Hospital (Babolsar-Iran) during 2013-2017. Patients were allocated into 2 groups; 34 in control group and 37 in Recove® group. Patients applied the ointment 2 times a day, before every radiation therapy session for 5 weeks. The radiation oncologist assessed the severity of dermatitis weekly for 5 weeks and graded it from 0 to 4 according to the RTOG criteria. Results:Baseline characteristics including age, and BMI had no significant difference between groups. The Recover group patients experienced significantly less severe dermatitis compared to the controls (p<0.001). None of the patients in Recove® group encountered more than grade 2 of RTOG criteria, however, in the control group, 4 (12.9%)patients experienced grade 3 of RTOG and 3 (9.7%)patients developed grade 4 of RTOG at the end of the 5th week. Conclusion: Our results indicate that Recove® ointment significantly reduces the severity of acute radiodermatitis. | ||
546 | |a EN | ||
690 | |a breast cancer | ||
690 | |a radiotherapy | ||
690 | |a radiodermatitis | ||
690 | |a recove ointment | ||
690 | |a radiation therapy oncology group. | ||
690 | |a Internal medicine | ||
690 | |a RC31-1245 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Caspian Journal of Internal Medicine, Vol 13, Iss 2, Pp 349-355 (2022) | |
787 | 0 | |n http://caspjim.com/article-1-2568-en.html | |
787 | 0 | |n https://doaj.org/toc/2008-6164 | |
787 | 0 | |n https://doaj.org/toc/2008-6172 | |
856 | 4 | 1 | |u https://doaj.org/article/5f0c6876d5d54dd78b25ed43b82b943b |z Connect to this object online. |