Studying and Comparing the Effects of Cetirizine, Gabapentin, and Coconut Oil on Reducing Skin Itching after Burn Wound Healing

Document Type : Original Article

Authors

1 Assistant Professor of General Surgery, Shiraz University of Medical Sciences, Burn & Wound Healing Research Center, Amir-Al-Momenin Burn Hospital, Shiraz, Iran

2 Assistant Professor, Department of General Surgery, Shiraz University of Medical Sciences, Burn and Wound Healing Research Center, Amiralmomenin Hospital (AS)

3 Assistant Professor, Department of Plastic and Cosmetic Surgery, Shiraz University of Medical Sciences, Burn and Wound Healing Research Center

4 Master of Science in Microbiology, Shiraz University of Medical Sciences, Burn and Wound Healing Research Center, Amiralmomenin Hospital (AS)

5 Associate Professor, Department of Biotechnology, Institute of Advanced Science and Technology and Environmental Sciences, Kerman University of Advanced Technology

Abstract
Introduction & Objective: Burns is one of the most severe forms of trauma that cause damage to the skin and subcutaneous tissues in different ways with different severity and extent. Effective reduction of itching symptoms after burns is a major problem in rehabilitating all burn patients. However, although there are many potential treatments for pruritus, there is still no consensus on the best treatment. This study was conducted to investigate and compare the effects of cetirizine, gabapentin, and coconut oil in reducing skin itching after burn wound healing. Materials & Methods: The present research population was selected from among the patients of Amir-Al-Momenin burn hospital affiliated with Shiraz University of Medical Sciences who suffered from mild to severe burns that are resistant to treatment and sometimes have bleeding. In this study, after the approval of the ethical committee of the University Research Council and the consent of the patients, 150 people were selected by random sampling. To collect data from the studied sample, the questionnaire of Khars Yusipovich et al. (2001) was used. The obtained data were statistically analyzed using t-correlated and covariance analysis and with the help of SPSS. Results: The average and standard deviation of the itchiness of the burn site before the cetirizine drug is 4.32 and 0.74. Also, the average and standard deviation of the itchiness of the burn site after the cetirizine drug is equal to 3.04 and 1.57. The mean and standard deviation of the itchiness of the burn site before the gabapentin drug are equal to 4.98 and 0.82. Also, the average and standard deviation of the itchiness of the burn site after the gabapentin drug is equal to 1.66 and 0.47. The average and standard deviation of the itchiness of the burn site before coconut oil is equal to 4.40 and 1.76. Also, the mean and standard deviation of the itchiness of the burn site after coconut oil is equal to 1.60 and 0.49. The intensity of itching was measured before and after the administration of cetirizine, gabapentin, and coconut oil, and there was a significant difference between all three groups. Conclusions: This study showed that all three drugs, cetirizine, gabapentin, and coconut oil, reduce itching after burns and coconut oil showed the greatest effect, followed by gabapentin and finally cetirizine. The long-term follow-up of patients after discharge from the hospital showed that after transplant surgery, itching was less and that patients who lived in cold areas experienced less itching after burns.

Keywords


1. Benson HA. Skin structure, function, and permeation. Topical and transdermal drug delivery: Principles and practice. 2012: 1-22.
2. Iskrant AP. Statistics and epidemiology of burns. Bulletin of the New York Academy of Medicine. 1967; 43(8): 636.
3. Evers LH, Bhavsar D, Mailänder P. The biology of burn injury. Experimental dermatology. 2010; 19(9): 777-83.
4. Kuan P, Chua S, Safawi E, Wang H, Tiong W. A comparative study of the classification of skin burn depth in human. Journal of Telecommunication, Electronic and Computer Engineering (JTEC). 2017; 9(2-10): 15-23.
5. Eming SA, Martin P, Tomic-Canic M. Wound repair and regeneration: mechanisms, signaling, and translation. Science translational medicine. 2014;6(265):265sr6-sr6.
6. Gauglitz GG, Williams F. Overview of the management of the severely burned patient. UpToDate, Waltham, MA (Accessed on March 29, 2016). 2020.
7. Stoddard FJ, Saxe G, MK D. Ten-year research review of physical injuries. Journal of the American Academy of Child & Adolescent Psychiatry. 2001; 40(10): 1128-45.
8. Benly P. Role of histamine in acute inflammation. Journal of Pharmaceutical Sciences and Research. 2015; 7(6): 373.
9. Dhand A, Aminoff MJ. The neurology of itch. Brain. 2014; 137(2): 313-22.
10.    Lyell A. The itching patient: a review of the causes of pruritus. Scottish medical journal. 1972; 17(10): 334-47.
11.    Yosipovitch G, Kwatra SG. Living with itch: A patient's guide: JHU Press; 2013.
12.    Sheffer AL, Samuels LL. Cetirizine: antiallergic therapy beyond traditional H1 antihistamines. Journal of allergy and clinical immunology. 1990; 86(6): 1040-6.
13.    Marron SE, Tomas-Aragones L, Boira S,
Campos-Rodenas R. Quality of life, emotional wellbeing and family repercussions in dermatological patients experiencing chronic itching: a pilot study. Acta dermato-venereologica. 2016; 96(3): 331-5.
14.    Campoli-Richards DM, Buckley MM-T, Fitton A. Cetirizine: a review of its pharmacological properties and clinical potential in allergic rhinitis,
pollen-induced asthma, and chronic urticaria. Drugs. 1990; 40: 762-81.
15.    Thurmond RL, Gelfand EW, Dunford PJ.
The role of histamine H1 and H4 receptors in
allergic inflammation: the search for new antihistamines. Nature reviews Drug discovery. 2008; 7(1): 41-53.
16.    Chen C. Physicochemical, pharmacological and pharmacokinetic properties of the zwitterionic antihistamines cetirizine and levocetirizine. Current medicinal chemistry. 2008; 15(21): 2173-91.
17.    Benedetti MS, Whomsley R, Poggesi I, Cawello W, Mathy F-X, Delporte M-L, et al. Drug metabolism and pharmacokinetics. Drug metabolism reviews. 2009; 41(3): 344-90.
18.    Rose M, Kam P. Gabapentin: pharmacology and its use in pain management. Anaesthesia. 2002; 57(5): 451-62.
19.    Nicholson B. Gabapentin use in neuropathic pain syndromes. Journal of the Peripheral Nervous System. 2000; 5(4): 245.
20.    Rosenquist RW. Gabapentin. JAAOS-Journal of the American Academy of Orthopaedic Surgeons. 2002; 10(3): 153-6.
21.    Fife B. Virgin Coconut Oil: Nature's Miracle Medicine: Piccadilly Books, Ltd.; 2006.
22.    Omura Y, O'Young B, Jones M, Pallos A, Duvvi H, Shimotsuura Y. Caprylic acid in the effective treatment of intractable medical problems of frequent urination, incontinence, chronic upper respiratory infection, root canalled tooth infection, ALS, etc., caused by asbestos & mixed infections of Candida albicans, Helicobacter pylori & cytomegalovirus with or without other microorganisms & mercury. Acupuncture & electro-therapeutics research. 2011; 36(1-2): 19-64.
23.    Chew Y-L. The beneficial properties of virgin coconut oil in management of atopic dermatitis. Pharmacognosy Reviews. 2019; 13(25): 24.
24.    Nasrabadi Z, Rakhshani MH, Ebadi H, Akbarzadeh R. Comparison of the effect of gabapentin and evening primrose oil on peripheral neuropathy pain in patients with type 2 diabetes. Clin Med. 2019; 26(1): 5-11.
25.    Hamid Naushad SNK. Comparison of the therapeutic effects of gabapentin and antihistamines in the treatment of uremic pruritus and psychological disorders caused by it. Journal of Medical Sciences Studies. 2019; 21(3): 286-92.
26.    Hamid Noshad SS, Ramona Molodi, Mahshid Moulai Far, Hassan Organi, Mohammad Reza Ardalan, Sima Abedi Azar. A placebo-controlled clinical trial to investigate the efficacy of gabapentin in the treatment of uremic pruritus. Journal of Medical Sciences Studies. 2008; 18(5): 29-33.
27.    Visha M, Karunagaran M. A review on wound healing. International Journal of Clinicopathological Correlation. 2019; 3(2): 50-9.
28.    Ghomi ER, Shakiba M, Ardahaei AS, Kenari MA, Faraji M, Ataei S, et al. Innovations in drug delivery for chronic wound healing. Current Pharmaceutical Design. 2022; 28(5): 340-51.
 
 
 
 
 
29.    Reinke J, Sorg H. Wound repair and regeneration. European surgical research. 2012; 49(1): 35-43.
30.    Biswas TK, Mukherjee B. Plant medicines of Indian origin for wound healing activity: a review. The international journal of lower extremity wounds. 2003; 2(1): 25-39.
31.    Rogha M, Hashemi SM, Okhovat SA, Saied
Abasi H. The Effect of Intraturbinal Injection of Triamcinolon in Comparison with Oral
Cetirizin in the Treatment of Allergic Rhinitis. Journal of Isfahan Medical School. 2009;
27(92): 9-14.
32.    Rennekampff H-O, Rabbels J, Reinhard V, Becker ST, Schaller H-E. Comparing the Vancouver Scar Scale with the cutometer in the assessment of donor site wounds treated with various dressings in a randomized trial. Journal of burn care & research. 2006; 27(3): 345-51.
33.    Chung BY, Kim HB, Jung MJ, Kang SY, Kwak
I-S, Park CW, et al. Post-burn pruritus. International journal of molecular sciences. 2020; 21(11): 3880.
34.    Zachariah JR, Rao AL, Prabha R, Gupta AK, Paul MK, Lamba S. Post burn pruritus-a review of current treatment options. Burns. 2012; 38(5): 621-9.