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  3. Vol. 11 No. 4 (2020): Autumn
  4. Review Article

Vol. 11 No. 4 (2020)

October 2020

Evaluation of Efficacy of Low-Level Laser Therapy

  • Vahid Mansouri
  • Babak Arjmand
  • Mostafa Rezaei-Tavirani
  • Mohammadreza Razzaghi
  • Mohammad Rostami-Nejad
  • Mostafa Hamdieh

Journal of Lasers in Medical Sciences, Vol. 11 No. 4 (2020), 3 October 2020 , Page 369-380
Published: 2020-10-03

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Abstract

Introduction: Given the inconsistencies in the literature regarding laser performance in non-surgical treatments, this study investigated the available literature to determine the advantages and disadvantages of low-power lasers in treating non-surgical complications and diseases.
Methods: Authentic information from articles was extracted and evaluated to assess low-power laser performance for non-surgical treatments. A systematic search of studies on low-level laser therapy (LLLT) for non-surgical treatments was conducted mainly in PubMed and google scholar articles.
Results: Four categories of diseases, including brain-related diseases, skin-related diseases, cancers, and bone-related disorders, which were treated by LLLT were identified and introduced. The various types of LLLT regarding the studied diseases were discussed.
Conclusion: Positive aspects of LLLT versus a few disadvantages of its application imply more investigation to find better and efficient new methods.

Keywords:
  • Low level laser therapy
  • Photobiomodulation
  • disorders
  • treatment
  • side affects
  • PDF

How to Cite

Mansouri, V. ., Arjmand, B., Rezaei-Tavirani, M., Razzaghi, M. ., Rostami-Nejad, M., & Hamdieh, M. (2020). Evaluation of Efficacy of Low-Level Laser Therapy. Journal of Lasers in Medical Sciences, 11(4), 369–380. Retrieved from https://journals.sbmu.ac.ir/jlms/article/view/32252
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References

Khalkhal E, Razzaghi M, Rostami-Nejad M, Rezaei-Tavirani M, Heidari Beigvand H, Rezaei Tavirani M. Evaluation of laser effects on the human body after laser therapy. J Lasers Med Sci. 2020;11(1):91-7. doi: 10.15171/jlms.2020.15.

Rezaei-Tavirani M, Tavirani MR, Zamanian Azodi M, Moravvej Farshi H, Razzaghi M. Evaluation of skin response after Erbium:yttrium–aluminum–garnet laser irradiation: a network analysis approach. J Lasers Med Sci. 2019;10(3):194-99. doi: 10.15171/jlms.2019.31.

Mansouri V, Rezaei-Tavirani M, Zadeh-Esmaeel MM, Rezaei-Tavirani S, Razzaghi M, Okhovatian F, et al. Analysis of laser therapy effects on squamous cell carcinoma patients: A system biology study. J Lasers Med Sci. 2019;10(Suppl 1):S1-S6. doi: 10.15171/jlms.2019.S1.

Safaei A, Rezaei Tavirani M, Zamanian Azodi M, Lashay A, Mohammadi SF, Broumand MG, et al. Diabetic retinopathy and laser therapy in rats: A protein-protein interaction network analysis. J Lasers Med Sci. 2017;8(Suppl 1):S20-S21. doi: 10.15171/jlms.2017.s4.

Seifi M, Shafeei HA, Daneshdoost S, Mir M. Effects of two types of low-level laser wave lengths (850 and 630 nm) on the orthodontic tooth movements in rabbits. Lasers Med Sci. 2007;22(4):261-4. doi: 10.1007/s10103-007-0447-9.

Kabnick LS. Outcome of different endovenous laser wavelengths for great saphenous vein ablation. J Vasc Surg. 2006;43(1):88-93. doi: 10.1016/j.jvs.2005.09.033.

Esnouf A, Wright PA, Moore JC, Ahmed S. Depth of penetration of an 850nm wavelength low level laser in human skin. Acupunct Electrother Res. 2007;32(1-2):81-6. doi: 10.3727/036012907815844165.

Ferreira DM, Zângaro RA, Villaverde AB, Cury Y, Frigo L, Picolo G, et al. Analgesic effect of He-Ne (632.8 nm) low-level laser therapy on acute inflammatory pain. Photomed Laser Surg. 2005;23(2):177-81. doi: 10.1089/pho.2005.23.177.

Navratil L, Kymplova J. Contraindications in noninvasive laser therapy: truth and fiction. J Clin Laser Med Surg. 2002;20(6):341-3. doi: 10.1089/104454702320901134.

Kitchen SS, Partridge CJ. A review of low level laser therapy: Part I: background, physiological effects and hazards. Physiotherapy. 1991;77(3):161-8. doi: 10.1016/S0031-9406(10)61694-X.

Walker J. Relief from chronic pain by low power laser irradiation. Neurosci Lett. 1983;43(2-3):339-44. doi: 10.1016/0304-3940(83)90211-2.

Shooshtari SMJ, Badiee V, Taghizadeh SH, Nematollahi AH, Amanollahi AH, Grami MT. The effects of low level laser in clinical outcome and neurophysiological results of carpal tunnel syndrome. Electromyogr Clin Neurophysiol. 2008;48(5):229-31.

Van Dinten LC, Wassenaar AL, Gorbalenya AE, Spaan WJ, Snijder EJ. Processing of the equine arteritis virus replicase ORF1b protein: identification of cleavage products containing the putative viral polymerase and helicase domains. J Virol. 1996;70(10):6625-33. doi: 10.1128/jvi.70.10.6625-6633.1996.

Garavello-Freitas I, Baranauskas V, Joazeiro PP, Padovani CR, Dal Pai-Silva M, da Cruz-Höfling MA. Low-power laser irradiation improves histomorphometrical parameters and bone matrix organization during tibia wound healing in rats. J Photochem Photobiol B. 2003;70(2):81-9. doi: 10.1016/s1011-1344(03)00058-7.

Hawkins D, Houreld N, Abrahamse H. Low level laser therapy (LLLT) as an effective therapeutic modality for delayed wound healing. Ann N Y Acad Sci. 2005;1056(1):486-93. doi: 10.1196/annals.1352.040.

Lubart R, Friedmann H, Lavie R, Longo L, Jacobi J, Baruchin O, et al. A reasonable mechanism for visible light-induced skin rejuvenation. Lasers Med Sci. 2007;22(1):1-3. doi: 10.1007/s10103-006-0406-x.

Vaghardoost R, Momeni M, Kazemikhoo N, Mokmeli S, Dahmardehei M, Ansari F, et al. Effect of low-level laser therapy on the healing process of donor site in patients with grade 3 burn ulcer after skin graft surgery (a randomized clinical trial). Lasers Med Sci. 2018;33(3):603-7. doi: 10.1007/s10103-017-2430-4.

Bhagwanani NS, Bhatia CC, Sharma N, Hemvani N, Chitnis DS. Low level nitrogen laser therapy in pulmonary tuberculosis. Laser ther. 2015;24(3):209-14. doi: 10.5978/islsm.15-OR-14.

Nakashima T, Ueda H, Misawa H, Suzuki T, Tominaga M, Ito A, et al. Transmeatal low-power laser irradiation for tinnitus. Otol Neurotol. 2002;23(3):296-300. doi: 10.1097/00129492-200205000-00011.

Bjordal JM, Lopes-Martins RA, Joensen J, Couppe C, Ljunggren AE, Stergioulas A, et al. A systematic review with procedural assessments and meta-analysis of low level laser therapy in lateral elbow tendinopathy (tennis elbow). BMC Musculoskelet Disord. 2008;9(1):75. doi: 10.1186/1471-2474-9-75.

Kerr CM, Lowe PB, Spielholz NI. Low level laser for the stimulation of acupoints for smoking cessation: a double blind, placebo controlled randomised trial and semi structured interviews. Journal of Chinese Medicine. 2008;86:46.

Tumilty S, McDonough S, Hurley DA, Baxter GD. Clinical effectiveness of low-level laser therapy as an adjunct to eccentric exercise for the treatment of Achilles' tendinopathy: a randomized controlled trial. Arch Phys Med Rehabil. 2012;93(5):733-9. doi: 10.1016/j.apmr.2011.08.049.

Gur A, Karakoc M, Cevik R, Nas K, Sarac AJ, Karakoc M. Efficacy of low power laser therapy and exercise on pain and functions in chronic low back pain. Lasers Surg Med. 2003;32(3):233-8. doi: 10.1002/lsm.10134.

Ordahan B, Karahan AY, Kaydok E. The effect of high-intensity versus low-level laser therapy in the management of plantar fasciitis: a randomized clinical trial. Lasers Med Sci. 2018;33(6):1363-9. doi: 10.1007/s10103-018-2497-6.

Dincer U, Cakar E, Kiralp MZ, Kilac H, Dursun H. The effectiveness of conservative treatments of carpal tunnel syndrome: splinting, ultrasound, and low-level laser therapies. Photomed Laser Surg. 2009;27(1):119-25. doi: 10.1089/pho.2008.2211.

Hirschl M, Katzenschlager R, Francesconi C, Kundi M. Low level laser therapy in primary Raynaud's phenomenon--results of a placebo controlled, double blind intervention study. J Rheumatol. 2004;31(12):2408-12.

Cullum N, Nelson EA, Flemming K, Sheldon T. Systematic reviews of wound care management: (5) beds; (6) compression; (7) laser therapy, therapeutic ultrasound, electrotherapy and electromagnetic therapy. Health Technol Assess. 2001;5(9):1-221. doi: 10.3310/hta5090.

Meireles SM, Jones A, Jennings F, Suda AL, Parizotto NA, Natour J. Assessment of the effectiveness of low-level laser therapy on the hands of patients with rheumatoid arthritis: a randomized double-blind controlled trial. Clin Rheumatol. 2010;29(5):501-9. doi: 10.1007/s10067-009-1347-0.

Tauber S, Schorn K, Beyer W, Baumgartner R. Transmeatal cochlear laser (TCL) treatment of cochlear dysfunction: a feasibility study for chronic tinnitus. Lasers Med Sci. 2003;18(3):154-61. doi: 10.1007/s10103-003-0274-6.

Vlassov VV, Pechatnikov LM, MacLehose HG. Low level laser therapy for treating tuberculosis. Cochrane Database of Syst Rev. 2002(3).

Coates VH, Turkelson CM, Chapell R, Bruening W, Mitchell MD, Reston JT, et al. Diagnosis and treatment of worker-related musculoskeletal disorders of the upper extremity. Evid Rep Technol Assess (Summ). 2002(62):1-12.

Salvioli S, Guidi M, Marcotulli G. The effectiveness of conservative, non-pharmacological treatment, of plantar heel pain: A systematic review with meta-analysis. Foot (Edinb). 2017;33:57-67. doi: 10.1016/j.foot.2017.05.004.

Salehpour F, Mahmoudi J, Kamari F, Sadigh-Eteghad S, Rasta SH, Hamblin MR. Brain photobiomodulation therapy: a narrative review. Mol Neurobiol. 2018;55(8):6601-36. doi: 10.1007/s12035-017-0852-4.

Wan S, Parrish JA, Anderson RR, Madden M. Transmittance of nonionizing radiation in human tissues. Photochem Photobiol. 1981;34(6):679-81. doi: 10.1111/j.1751-1097.1981.tb09063.x.

Eells JT, Henry MM, Summerfelt P, Wong-Riley MTT, Buchmann EV, Kane M, et al. Therapeutic photobiomodulation for methanol-induced retinal toxicity. Proc Natl Acad Sci U S A. 2003;100(6):3439-44. doi: 10.1073/pnas.0534746100.

Wong-Riley MTT, Liang HL, Eells JT, Chance B, Henry MM, Buchmann E, et al. Photobiomodulation directly benefits primary neurons functionally inactivated by toxins: role of cytochrome c oxidase. J Biol Chem. 2005;280(6):4761-71. doi: 10.1074/jbc.M409650200.

Naeser MA, Hamblin MR. Potential for transcranial laser or LED therapy to treat stroke, traumatic brain injury, and neurodegenerative disease. Photomed Laser Surg. 2011;29(7):443-6. doi: 10.1089/pho.2011.9908.

Lapchak PA. Taking a light approach to treating acute ischemic stroke patients: transcranial near-infrared laser therapy translational science. Ann Med. 2010;42(8):576-86. doi: 10.3109/07853890.2010.532811.

Ebrahimi H, Najafi S, Khayamzadeh M, Zahedi A, Mahdavi A. Therapeutic and analgesic efficacy of laser in conjunction with pharmaceutical therapy for trigeminal neuralgia. J lasers Med Sci. 2018;9(1):63-8. doi: 10.15171/jlms.2018.13.

de Leeuw R, editor. Orofacial pain: guidelines for assessment, Diagnosis and Management. 4th ed. Chicago: Quintessence Publishing; 2008.

Ohno T. Pain suppressive effect of low power laser irradiation. A quantitative analysis of substance P in the rat spinal dorsal root ganglion. Nihon Ika Daigaku Zasshi. 1997;64(5):395-400. [In Japanese]. doi: 10.1272/jnms1923.64.395.

Brondon P, Stadler I, Lanzafame RJ. Melanin density affects photobiomodulation outcomes in cell culture. Photomed Laser Surg. 2007;25(3):144-9. doi: 10.1089/pho.2007.2045.

Asnaashari M, Safavi N. Application of low level lasers in dentistry (endodontic). J Lasers Med Sci. 2013;4(2):57-66.

Taylor CA, Greenspan AI, Xu L, Kresnow MJ. Comparability of national estimates for traumatic brain injury-related medical encounters. J Head Trauma Rehabil. 2015;30(3):150-9. doi: 10.1097/HTR.0000000000000105.

Ross ST, Soltesz I. Selective depolarization of interneurons in the early posttraumatic dentate gyrus: involvement of the Na+/K+-ATPase. J Neurophysiol. 2000;83(5):2916-30. doi: 10.1152/jn.2000.83.5.2916.

Bramlett HM, Dietrich WD. Pathophysiology of cerebral ischemia and brain trauma: similarities and differences. J Cereb Blood Flow Metab. 2004;24(2):133-50. doi: 10.1097/01.WCB.0000111614.19196.04.

Zinman LH, Ngo M, Ng ET, Nwe KT, Gogov S, Bril V. Low-intensity laser therapy for painful symptoms of diabetic sensorimotor polyneuropathy: a controlled trial. Diabetes Care. 2004;27(4):921-4. doi: 10.2337/diacare.27.4.921.

Gustafsson H, Flood K, Berge OG, Brodin E, Olgart L, Stiller CO. Gabapentin reverses mechanical allodynia induced by sciatic nerve ischemia and formalin-induced nociception in mice. Exp Neurol. 2003;182(2):427-34. doi: 10.1016/s0014-4886(03)00097-9.

Ali-Asgarzadeh A, Agha-Mohammadi D, Movasaghi R, Shahsavari P. [Effect of low-intensity laser on lower limb neuropathic pain in patients with diabetes mellitus]. Journal of Anesthesiology and Pain. 2011;1(4):48-60. [In Persian]

Bertolini GRF, Artifon EL, da Silva TS, Cunha DM, Vigo PR. Low-level laser therapy, at 830 nm, for pain reduction in experimental model of rats with sciatica. Arq Neuropsiquiatr. 2011;69(2B):356-9. doi: 10.1590/s0004-282x2011000300017.

Kalinina OV, Alekseeva NV, Burtsev EM. Infrared laser therapy in distal diabetic polyneuropathy. Zh Nevrol psikhiatr Im S S Korsakova. 1998;98(6):23-5. [In Russian]

Alcântara CC, Gigo‐Benato D, Salvini TF, Oliveira AL, Anders JJ, Russo TL. Effect of low‐level laser therapy (LLLT) on acute neural recovery and inflammation‐related gene expression after crush injury in rat sciatic nerve. Lasers Surg Med. 2013;45(4):246-52. doi: 10.1002/lsm.22129.

Bjordal JM, Johnson MI, Iversen V, Aimbire F, Lopes-Martins RAB. Low-level laser therapy in acute pain: a systematic review of possible mechanisms of action and clinical effects in randomized placebo-controlled trials. Photomed Laser Surg. 2006;24(2):158-68. doi: 10.1089/pho.2006.24.158.

Jimbo K, Noda K, Suzuki K, Yoda K. Suppressive effects of low-power laser irradiation on bradykinin evoked action potentials in cultured murine dorsal root ganglion cells. Neurosci Lett. 1998;240(2):93-6.

Chow R, Armati P, Laakso EL, Bjordal JM, Baxter GD. Inhibitory effects of laser irradiation on peripheral mammalian nerves and relevance to analgesic effects: a systematic review. Photomed Laser Surg. 2011;29(6):365-81. doi: 10.1089/pho.2010.2928.

Hagiwara S, Iwasaka H, Hasegawa A, Noguchi T. Pre-irradiation of blood by gallium aluminum arsenide (830 nm) low-level laser enhances peripheral endogenous opioid analgesia in rats. Anesth Analg. 2008;107(3):1058-63. doi: 10.1213/ane.0b013e31817ee43e.

Yan W, Chow R, Armati PJ. Inhibitory effects of visible 650‐nm and infrared 808‐nm laser irradiation on somatosensory and compound muscle action potentials in rat sciatic nerve: implications for laser‐induced analgesia. J Peripher Nerv Syst. 2011;16(2):130-5. doi: 10.1111/j.1529-8027.2011.00337.x.

Masoumipoor M, Jameie S, Janzadeh A, Nasirinezhad F, Soleimani M, Kerdary M. Effects of 660-and 980-nm low-level laser therapy on neuropathic pain relief following chronic constriction injury in rat sciatic nerve. Lasers Med Sci. 2014;29(5):1593-8. doi: 10.1007/s10103-014-1552-1.

Cidral‐Filho FJ, Martins DF, Moré AOO, Mazzardo‐Martins L, Silva MD, Cargnin‐Ferreira E, et al. Light‐emitting diode therapy induces analgesia and decreases spinal cord and sciatic nerve tumour necrosis factor‐α levels after sciatic nerve crush in mice. Eur J Pain. 2013;17(8):1193-204. doi: 10.1002/j.1532-2149.2012.00280.x.

Catarino HR, de Godoy NP, Scharlack NK, Neves LM, de Gaspi FO, Esquisatto MA, et al. InGaP 670-nm laser therapy combined with a hydroalcoholic extract of Solidago chilensis Meyen in burn injuries. Lasers Med Sci. 2015;30(3):1069-79. doi: 10.1007/s10103-014-1707-0.

Ezzati A, Bayat M, Taheri S, Mohsenifar Z. Low-level laser therapy with pulsed infrared laser accelerates third-degree burn healing process in rats. J Rehabil Res Dev. 2009;46(4):543-54. doi: 10.1682/jrrd.2008.09.0121.

Brassolatti P, Bossini PS, Oliveira MCD, Kido HW, Tim CR, Almeida‐Lopes L, et al. Comparative effects of two different doses of low‐level laser therapy on wound healing third‐degree burns in rats. Microsc Res Tech. 2016;79(4):313-20. doi: 10.1002/jemt.22632.

Chiarotto GB, Neves LMG, Esquisatto MAM, do Amaral MEC, dos Santos GMT, Mendonça FAS. Effects of laser irradiation (670-nm InGaP and 830-nm GaAlAs) on burn of second-degree in rats. Lasers Med Sci. 2014;29(5):1685-93. doi: 10.1007/s10103-014-1573-9.

Fu L, Zhang Y, Li C, Wu Z, Zhuo Q, Huang X, et al. Skin tissue repair materials from bacterial cellulose by a multilayer fermentation method. J Mater Chem. 2012;22(24):12349-57. doi: 10.1039/c2jm00134a.

Fiório FB, Albertini R, Leal-Junior ECP, de Carvalho Pde T. Effect of low-level laser therapy on types I and III collagen and inflammatory cells in rats with induced third-degree burns. Lasers Med Sci. 2014;29(1):313-9. doi: 10.1007/s10103-013-1341-2.

de Vasconcelos Catão MHC, Nonaka CFW, de Albuquerque RLC, Bento PM, de Oliveira Costa R. Effects of red laser, infrared, photodynamic therapy, and green LED on the healing process of third-degree burns: clinical and histological study in rats. Lasers Med Sci. 2015;30(1):421-8. doi: 10.1007/s10103-014-1687-0.

Bayat M, Vasheghani MM, Razavi N, Taheri S, Rakhshan M. Effect of low-level laser therapy on the healing of second-degree burns in rats: a histological and microbiological study. J Photochem Photobiol B. 2005;78(2):171-7. doi: 10.1016/j.jphotobiol.2004.08.012.

Avci P, Gupta A, Sadasivam M, Vecchio D, Pam Z, Pam N, et al. Low-level laser (light) therapy (LLLT) in skin: stimulating, healing, restoring. Semin Cutan Med Surg. 2013;32(1):41-52.

Ezzati A, Bayat M, Khoshvaghti A. Low-level laser therapy with a pulsed infrared laser accelerates second-degree burn healing in rat: a clinical and microbiologic study. Photomed Laser Surg. 2010;28(5):603-11. doi: 10.1089/pho.2009.2544.

Karu TI, Pyatibrat LV, Afanasyeva NI. Cellular effects of low power laser therapy can be mediated by nitric oxide. Lasers Surg Med. 2005;36(4):307-14. doi: 10.1002/lsm.20148.

Ranjbar R, Ashrafzadeh Takhtfooladi M. The effects of low level laser therapy on Staphylococcus aureus infected third-degree burns in diabetic rats. Acta Cir Bras. 2016;31(4):250-5. doi: 10.1590/S0102-865020160040000005.

Núñez SC, França CM, Silva DFT, Nogueira GEC, Prates RA, Ribeiro MS. The influence of red laser irradiation timeline on burn healing in rats. Lasers Med Sci. 2013;28(2):633-41. doi: 10.1007/s10103-012-1105-4.

Karu T, Pyatibrat L, Kalendo G. Irradiation with He-Ne laser increases ATP level in cells cultivated in vitro. J Photochem Photobiol B. 1995;27(3):219-23. doi: 10.1016/1011-1344(94)07078-3.

Renno ACM, Iwama AM, Shima P, Fernandes KR, Carvalho JG, De Oliveira P, et al. Effect of low-level laser therapy (660 nm) on the healing of second-degree skin burns in rats. J Cosmet Laser Ther. 2011;13(5):237-42. doi: 10.3109/14764172.2011.606466.

Gupta A, Keshri GK, Yadav A, Gola S, Chauhan S, Salhan AK, et al. Superpulsed (Ga‐As, 904 nm) low‐level laser therapy (LLLT) attenuates inflammatory response and enhances healing of burn wounds. J Biophotonics. 2015;8(6):489-501. doi: 10.1002/jbio.201400058.

Meireles GC, Santos JN, Chagas PO, Moura AP, Pinheiro AL. Effectiveness of laser photobiomodulation at 660 or 780 nanometers on the repair of third-degree burns in diabetic rats. Photomed Laser Surg. 2008;26(1):47-54. doi: 10.1089/pho.2007.2051.

Moreno‐Arias G, Castelo‐Branco C, Ferrando J. Paradoxical effect after IPL photoepilation. Dermatol Surg. 2002;28(11):1013-6. doi: 10.1046/j.1524-4725.2002.02101.x.

Leavitt M. Evaluation of the activity of laser light doses compared to an inactive control dose on ex vivo hair growth. J Am Acad Dermatol. 2010;62(3): P2109.

Hamblin M. Evaluation of activity of laser doses on ex-vivo hair growth. http://www.hairmax.com/downloads/PDF/EX_VIVO_ STUDY_SLIDES_7_09.pdf [accessed October 19th, 2014]

Zarei M, Wikramanayake TC, Falto-Aizpurua L, Schachner LA, Jimenez JJ. Low level laser therapy and hair regrowth: an evidence-based review. Lasers Med Sci. 2016;31(2):363-71. doi: 10.1007/s10103-015-1818-2.

Wikramanayake TC, Rodriguez R, Choudhary S, Mauro LM, Nouri K, Schachner LA, et al. Effects of the Lexington LaserComb on hair regrowth in the C3H/HeJ mouse model of alopecia areata. Lasers Med Sci. 2012;27(2):431-6. doi: 10.1007/s10103-011-0953-7.

Wikramanayake TC, Villasante AC, Mauro LM, Nouri K, Schachner LA, Perez CI, et al. Low-level laser treatment accelerated hair regrowth in a rat model of chemotherapy-induced alopecia (CIA). Lasers Med Sci. 2013;28(3):701-6. doi: 10.1007/s10103-012-1139-7.

King Jr LE, Silva KA, Kennedy VE, Sundberg JP. Lack of response to laser comb in spontaneous and graft-induced alopecia areata in C3H/HeJ mice. J Invest Dermatol. 2014;134(1):264-66. doi: 10.1038/jid.2013.252.

Satino JL, Markou M. Hair regrowth and increased hair tensile strength using the HairMax LaserComb for low-level laser therapy. Int J Cosmet Surg Aesthetic Dermatol. 2003;5(2):113-7. doi: 10.1089/153082003769591209.

Leavitt M, Charles G, Heyman E, Michaels D. HairMax LaserComb laser phototherapy device in the treatment of male androgenetic alopecia: A randomized, double-blind, sham device-controlled, multicentre trial. Clin Drug Investig. 2009;29(5):283-92. doi: 10.2165/00044011-200929050-00001.

Kim H, Choi JW, Kim JY, Shin JW, Lee Sj, Huh CH. Low‐level light therapy for androgenetic alopecia: A 24‐week, randomized, double‐blind, sham device–controlled multicenter trial. Dermatol Surg. 2013;39(8):1177-83. doi: 10.1111/dsu.12200.

Lanzafame RJ, Blanche RR, Bodian AB, Chiacchierini RP, Fernandez‐Obregon A, Kazmirek ER. The growth of human scalp hair mediated by visible red light laser and LED sources in males. Lasers Surg Med. 2013;45(8):487-95. doi: 10.1002/lsm.22173.

Lanzafame RJ, Blanche RR, Chiacchierini RP, Kazmirek ER, Sklar JA. The growth of human scalp hair in females using visible red light laser and LED sources. Lasers Surg Med. 2014;46(8):601-7. doi: 10.1002/lsm.22277.

Jimenez JJ, Wikramanayake TC, Bergfeld W, Hordinsky M, Hickman JG, Hamblin MR, et al. Efficacy and safety of a low-level laser device in the treatment of male and female pattern hair loss: a multicenter, randomized, sham device-controlled, double-blind study. Am J Clin Dermatol. 2014;15(2):115-27. doi: 10.1007/s40257-013-0060-6.

Munck A, Gavazzoni MF, Trüeb RM. Use of low-level laser therapy as monotherapy or concomitant therapy for male and female androgenetic alopecia. Int J Trichology. 2014;6(2):45-49. doi: 10.4103/0974-7753.138584.

Nguyen VT, Ndoye A, Grando SA. Pemphigus vulgaris antibody identifies pemphaxin a novel keratinocyte annexin-like molecule binding acetylcholine. J Biol Chem. 2000;275(38):29466-76. doi: 10.1074/jbc.M003174200.

Scully C, Challacombe SJ. Pemphigus vulgaris: update on etiopathogenesis, oral manifestations, and management. Crit Rev Oral Biol Med. 2002;13(5):397-408. doi: 10.1177/154411130201300504.

Minicucci EM, Miot HA, Barraviera SRCS, Almeida-Lopes L. Low-level laser therapy on the treatment of oral and cutaneous pemphigus vulgaris: case report. Lasers Med Sci. 2012;27(5):1103-6. doi: 10.1007/s10103-012-1101-8.

Scully C, De Almeida OP, Porter SR, Gilkes JJ. Pemphigus vulgaris: the manifestations and long‐term management of 55 patients with oral lesions. Br J Dermatol. 1999;140(1):84-9. doi: 10.1046/j.1365-2133.1999.02612.x.

Davenport S, Chen SY, Miller AS. Pemphigus vulgaris: clinicopathologic review of 33 cases in the oral cavity. Int J Periodontics Restorative Dent. 2001;21(1):85-90.

Yousef M, Mansouri P, Partovikia M, Esmaili M, Younespour S, Hassani L. The effect of low level laser therapy on Pemphigus vulgaris lesions: A Pilot Study. J Lasers Med Sci. 2017;8(4):177-80. doi: 10.15171/jlms.2017.32.

Jeffcoate WJ, Harding KG. Diabetic foot ulcers. Lancet. 2003;361(9368):1545-51. doi: 10.1016/S0140-6736(03)13169-8.

Kajagar BM, Godhi AS, Pandit A, Khatri S. Efficacy of low level laser therapy on wound healing in patients with chronic diabetic foot ulcers—a randomised control trial. Indian J Surg. 2012;74(5):359-63. doi: 10.1007/s12262-011-0393-4.

Beckmann KH, Meyer-Hamme G, Schröder S. Low level laser therapy for the treatment of diabetic foot ulcers: a critical survey. Evid Based Complement Alternat Med. 2014;2014:626127. doi: 10.1155/2014/626127.

Lipsky BA, Berendt AR, Cornia PB, Pile JC, Peters EJ, Armstrong DG, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012;54(12):e132-e73.

Rüttermann M, Maier-Hasselmann A, Nink-Grebe B, Burckhardt M. Local treatment of chronic wounds: in patients with peripheral vascular disease, chronic venous insufficiency, and diabetes. Dtsch Arztebl Int. 2013;110(3):25-31. doi: 10.3238/arztebl.2013.0025.

Litscher G. Integrative laser medicine and high-tech acupuncture at the Medical University of Graz, Austria, Europe. Evid Based Complement Alternat Med. 2012;2012:103109. doi: 10.1155/2012/103109.

Ebrahimi T, Moslemi N, Rokn A, Heidari M, Nokhbatolfoghahaie H, Fekrazad R. The influence of low-intensity laser therapy on bone healing. J Dent (Tehran). 2012;9(4):238-48.

Sobanko JF, Alster TS. Efficacy of low‐level laser therapy for chronic cutaneous ulceration in humans: A review and discussion. Dermatol Surg. 2008;34(8):991-1000. doi: 10.1111/j.1524-4725.2008.34197.x.

de Paula Eduardo C, Aranha ACC, Simões A, Bello-Silva MS, Ramalho KM, Esteves-Oliveira M, et al. Laser treatment of recurrent herpes labialis: a literature review. Lasers Med Sci. 2014;29(4):1517-29. doi: 10.1007/s10103-013-1311-8.

Al-Maweri SA, Kalakonda B, AlAizari NA, Al-Soneidar WA, Ashraf S, Abdulrab S, et al. Efficacy of low-level laser therapy in management of recurrent herpes labialis: a systematic review. Lasers Med Sci. 2018;33(7):1423-30. doi: 10.1007/s10103-018-2542-5.

Pinto AC, De Azambuja E. Improving quality of life after breast cancer: dealing with symptoms. Maturitas. 2011;70(4):343-8. doi: 10.1016/j.maturitas.2011.09.008.

Cormier JN, Askew RL, Mungovan KS, Xing Y, Ross MI, Armer JM. Lymphedema beyond breast cancer: A systematic review and meta‐analysis of cancer‐related secondary lymphedema. Cancer. 2010;116(22):5138-49. doi: 10.1002/cncr.25458.

Fu MR. Breast cancer-related lymphedema: Symptoms, diagnosis, risk reduction, and management. World J Clin Oncol. 2014;5(3):241-7. doi: 10.5306/wjco.v5.i3.241.

Nouri K, Jimenez GP, Harrison‐Balestra C, Elgart GW. 585‐nm pulsed dye laser in the treatment of surgical scars starting on the suture removal day. Dermatol Surg. 2003;29(1):65-73. doi: 10.1046/j.1524-4725.2003.29014.x.

Assis L, Moretti AIS, Abrahão TB, de Souza HP, Hamblin MR, Parizotto NA. Low-level laser therapy (808 nm) contributes to muscle regeneration and prevents fibrosis in rat tibialis anterior muscle after cryolesion. Lasers Med Sci. 2013;28(3):947-55. doi: 10.1007/s10103-012-1183-3.

Jang DH, Song DH, Chang EJ, Jeon JY. Anti-inflammatory and lymphangiogenetic effects of low-level laser therapy on lymphedema in an experimental mouse tail model. Lasers Med Sci. 2016;31(2):289-96. doi: 10.1007/s10103-015-1854-y.

Maiya AG, Olivia E, Dibya A. Effect of low energy laser therapy in the management of post-mastectomy lymphoedema. Physiotherapy Singapore. 2008;11(1):2-5.

Tumilty S, Munn J, McDonough S, Hurley DA, Basford JR, Baxter GD. Low level laser treatment of tendinopathy: a systematic review with meta-analysis. Photomed Laser Surg. 2010;28(1):3-16. doi: 10.1089/pho.2008.2470.

Epstein JB, Thariat J, Bensadoun RJ, Barasch A, Murphy BA, Kolnick L, et al. Oral complications of cancer and cancer therapy: from cancer treatment to survivorship. CA Cancer J Clin. 2012;62(6):400-22. doi: 10.3322/caac.21157.

Hunter KU, Schipper M, Feng FY, Lyden T, Haxer M, Murdoch-Kinch CA, et al. Toxicities affecting quality of life after chemo-IMRT of oropharyngeal cancer: prospective study of patient-reported, observer-rated, and objective outcomes. Int J Radiat Oncol Biol Phys. 2013;85(4):935-40. doi: 10.1016/j.ijrobp.2012.08.030.

Zecha JA, Raber-Durlacher JE, Nair RG, Epstein JB, Elad S, Hamblin MR, et al. Low-level laser therapy/photobiomodulation in the management of side effects of chemoradiation therapy in head and neck cancer: part 2: proposed applications and treatment protocols. Support Care Cancer. 2016;24(6):2793-805. doi: 10.1007/s00520-016-3153-y.

Elting LS, Keefe DM, Sonis ST, Garden AS, Spijkervet F, Barasch A, et al. Patient‐reported measurements of oral mucositis in head and neck cancer patients treated with radiotherapy with or without chemotherapy: demonstration of increased frequency, severity, resistance to palliation, and impact on quality of life. Cancer. 2008;113(10):2704-13. doi: 10.1002/cncr.23898.

Clarkson JE, Worthington HV, Furness S, McCabe M, Khalid T, Meyer S. Interventions for treating oral mucositis for patients with cancer receiving treatment. Cochrane Database Syst Rev. 2010(8):CD001973.

Riley P, Glenny AM, Worthington HV, Littlewood A, Clarkson JE, McCabe MG. Interventions for preventing oral mucositis in patients with cancer receiving treatment: oral cryotherapy. Cochrane Database of Syst Rev. 2015(12):CD011552. doi: 10.1002/14651858.CD011552.pub2.

Bayer S, Kazancioglu HO, Acar AH, Demirtas N, Kandas NO. Comparison of laser and ozone treatments on oral mucositis in an experimental model. Lasers Med Sci. 2017;32(3):673-7. doi: 10.1007/s10103-017-2166-1.

Burdelya LG, Gleiberman AS, Toshkov I, Aygun-Sunar S, Bapardekar M, Manderscheid-Kern P, et al. Toll-like receptor 5 agonist protects mice from dermatitis and oral mucositis caused by local radiation: implications for head-and-neck cancer radiotherapy. Int J Radiat Oncol Biol Phys. 2012;83(1):228-34. doi: 10.1016/j.ijrobp.2011.05.055.

Chen AY, Frankowski R, Bishop-Leone J, Hebert T, Leyk S, Lewin J, et al. The development and validation of a dysphagia-specific quality-of-life questionnaire for patients with head and neck cancer: the MD Anderson dysphagia inventory. Arch Otolaryngol Head Neck Surg. 2001;127(7):870-6.

Dirix P, Nuyts S, Van den Bogaert W. Radiation‐induced xerostomia in patients with head and neck cancer: a literature review. Cancer. 2006;107(11):2525-34.

Halyard MY, Jatoi A, Sloan JA, Bearden III JD, Vora SA, Atherton PJ, et al. Does zinc sulfate prevent therapy-induced taste alterations in head and neck cancer patients? Results of phase III double-blind, placebo-controlled trial from the North Central Cancer Treatment Group (N01C4).

Int J Radiat Oncol Biol Phys. 2007;67(5):1318-22. doi: 10.1016/j.ijrobp.2006.10.046.

Ben-David MA, Diamante M, Radawski JD, Vineberg KA, Stroup C, Murdoch-Kinch C-A, et al. Lack of osteoradionecrosis of the mandible after intensity-modulated radiotherapy for head and neck cancer: likely contributions of both dental care and improved dose distributions. Int J Radiat Oncol Biol Phys. 2007;68(2):396-402. doi: 10.1016/j.ijrobp.2006.11.059.

Bensadoun RJ, Riesenbeck D, Lockhart PB, Elting LS, Spijkervet FK, Brennan MT. A systematic review of trismus induced by cancer therapies in head and neck cancer patients. Support Care Cancer. 2010;18(8):1033-8. doi: 10.1007/s00520-010-0847-4.

Hee LY, Kim YS, Chung MJ, Yu M, Jung SL, Yoo IR, et al. Soft tissue necrosis in head and neck cancer patients after transoral robotic surgery or wide excision with primary closure followed by radiation therapy. Medicine (Baltimore). 2016;95(9):e2852. doi: 10.1097/MD.0000000000002852.

Deng J, Ridner SH, Dietrich MS, Wells N, Wallston KA, Sinard RJ, et al. Prevalence of secondary lymphedema in patients with head and neck cancer. J Pain Symptom Manage. 2012;43(2):244-52. doi: 10.1016/j.jpainsymman.2011.03.019.

Campos RJ, Maciel CT, Cesca MG, Leite IC. Voice analysis after cancer treatment with organ preservation. Head Neck Oncol. 2011;3(1):19. doi: 10.1186/1758-3284-3-19.

Naidu MUR, Ramana GV, Rani PU, Mohan IK, Suman A, Roy P. Chemotherapy-induced and/or radiation therapy-induced oral mucositis—complicating the treatment of cancer. Neoplasia. 2004;6(5):423-31. doi: 10.1593/neo.04169.

Al-Dasooqi N, Sonis ST, Bowen JM, Bateman E, Blijlevens N, Gibson RJ, et al. Emerging evidence on the pathobiology of mucositis. Supportive Care Cancer. 2013;21(7):2075-83. doi: 10.1007/s00520-013-1810-y.

Bjordal JM, Bensadoun RJ, Tunèr J, Frigo L, Gjerde K, Lopes-Martins RA. A systematic review with meta-analysis of the effect of low-level laser therapy (LLLT) in cancer therapy-induced oral mucositis. Supportive Care Cancer. 2011;19(8):1069-77. doi: 10.1007/s00520-011-1202-0.

Bensadoun RJ, Nair RG. Low-level laser therapy in the prevention and treatment of cancer therapy-induced mucositis: 2012 state of the art based on literature review and meta-analysis.

Curr Opin Oncol. 2012;24(4):363-70. doi: 10.1097/CCO.0b013e328352eaa3.

Kim JH, Kolozsvary AJ, Jenrow KA, Brown SL. Mechanisms of radiation-induced skin injury and implications for future clinical trials. Int J Radiat Biol. 2013;89(5):311-8. doi: 10.3109/09553002.2013.765055.

Rezvani M, Robbins M, Hopewell J, Whitehouse E. Modification of late dermal necrosis in the pig by treatment with multi-wavelength light. Br J Radiol. 1993;66(782):145-9. doi: 10.1259/0007-1285-66-782-145.

Bensadoun RJ. Photobiomodulation or low-level laser therapy in the management of cancer therapy-induced mucositis, dermatitis and lymphedema. Curr Opin Oncol. 2018;30(4):226-32. doi: 10.1097/CCO.0000000000000452.

Russi EG, Corvo R, Merlotti A, Alterio D, Franco P, Pergolizzi S, et al. Swallowing dysfunction in head and neck cancer patients treated by radiotherapy: review and recommendations of the supportive task group of the Italian Association of Radiation Oncology. Cancer Treat Rev. 2012;38(8):1033-49. doi: 10.1016/j.ctrv.2012.04.002.

Cullins MJ, Connor NP. Reduced tongue force and functional swallowing changes in a rat model of post stroke dysphagia. Brain Res. 2019;1717:160-6. doi: 10.1016/j.brainres.2019.04.023.

El Mobadder M, Farhat F, El Mobadder W, Nammour S. Photobiomodulation Therapy in the Treatment of Oral Mucositis, Dysphagia, Oral Dryness, Taste Alteration, and Burning Mouth Sensation Due to Cancer Therapy: A Case Series. Int J Environ Res Public Health. 2019 Jan;16(22):4505. doi:10.3390/ijerph16224505

El Mobadder M, Farhat F, Nammour S. Photobiomodulation therapy in the treatment of chronic dysphagia post hormonal therapy in a breast cancer patient. Dent J (Basel). 2019;7(2):53. doi: 10.3390/dj7020053.

Huang SH, Hahn E, Chiosea SI, Xu ZY, Li JS, Shen L, et al. The role of adjuvant (chemo-) radiotherapy in oral cancers in the contemporary era. Oral Oncol. 2020;102:104563. doi: 10.1016/j.oraloncology.2019.104563.

Geiger JL, Adelstein DJ. Chemotherapy in the definitive management of oral cancers: Where do we stand today? Oral Oncol. 2020;102:104584. doi: 10.1016/j.oraloncology.2020.104584.

O’Dell K, Sinha U. Osteoradionecrosis. Oral Maxillofac Surg Clin North Am. 2011;23(3):455-64. doi: 10.1016/j.coms.2011.04.011.

Harris M. The conservative management of osteoradionecrosis of the mandible with ultrasound therapy. Br J Oral Maxillofac Surg. 1992;30(5):313-8. doi: 10.1016/0266-4356(92)90181-h.

Oh HK, Chambers MS, Martin JW, Lim HJ, Park HJ. Osteoradionecrosis of the mandible: treatment outcomes and factors influencing the progress of osteoradionecrosis. J Oral Maxillofac Surg. 2009;67(7):1378-86. doi: 10.1016/j.joms.2009.02.008.

Magalhães IA, Forte CPF, Viana TSA, Teófilo CR, Verde RDM, Magalhães DP, et al. Photobiomodulation and antimicrobial photodynamic therapy as adjunct in the treatment and prevention of osteoradionecrosis of the jaws: a case report. Photodiagnosis Photodyn Ther. 2020;31:101959. doi: 10.1016/j.pdpdt.2020.101959.

Chow R. Low level laser therapy-mechanism of action: analgesia. In: Freitas PM, Simões A, editors. Lasers in Dentistry: Guide for clinical practice. Weinheim: Wiley-Blackwell; 2015. p. 34-9.

Ribeiro GH, Minamisako MC, da Silva Rath IB, Santos AMB, Simões A, Pereira KCR, et al. Osteoradionecrosis of the jaws: case series treated with adjuvant low-level laser therapy and antimicrobial photodynamic therapy. J Appl Oral Sci. 2018;26:e20170172. doi: 10.1590/1678-7757-2017-0172.

Sierra SO, Deana AM, Ferrari RAM, Albarello PM, Bussadori SK, Fernandes KPS. Effect of low-level laser therapy on the post-surgical inflammatory process after third molar removal: study protocol for a double-blind randomized controlled trial. Trials. 2013;14(1):373. doi: 10.1186/1745-6215-14-373.

Ferrante M, Petrini M, Trentini P, Perfetti G, Spoto G. Effect of low-level laser therapy after extraction of impacted lower third molars. Lasers Med Sci. 2013;28(3):845-9. doi: 10.1007/s10103-012-1174-4.

Barbosa D, Villaverde AGJB, LoschiavoArisawa EÂ, de Souza RA. Laser therapy in bone repair in rats: analysis of bone optical density. Acta Ortop Bras. 2014;22(2):71-4. doi: 10.1590/1413-78522014220200438.

Chang WD, Wu JH, Wang HJ, Jiang JA. Therapeutic outcomes of low-level laser therapy for closed bone fracture in the human wrist and hand. Photomed Laser Surg. 2014;32(4):212-8. doi: 10.1089/pho.2012.3398.

Lucke LD, Bortolazzo FO, Theodoro V, Fujii L, Bombeiro AL, Felonato M, et al. Low‐level laser and adipose‐derived stem cells altered remodelling genes expression and improved collagen reorganization during tendon repair. Cell Prolif. 2019;52(3):e12580. doi: 10.1111/cpr.12580.

Badawy FA, ElSayed WH, Saidi AA, Wadee AN, Al Balah OF, Abd El Azim ER. Effect of different doses of low-intensity laser therapy on total active range of motion after hand flexor tendon repair. J Med Sci Res. 2019;2(1):29-35. doi: 10.4103/JMISR.JMISR_5_19.

Tezcan S, Ulu Ozturk F, Uslu N, Nalbant M, Umit Yemisci O. Carpal tunnel syndrome: evaluation of the effects of low‐level laser therapy with ultrasound strain imaging. J Ultrasound Med. 2019;38(1):113-22. doi: 10.1002/jum.14669.

Xuan W, Agrawal T, Huang L, Gupta GK, Hamblin MR. Low‐level laser therapy for traumatic brain injury in mice increases brain derived neurotrophic factor (BDNF) and synaptogenesis. J Biophotonics. 2015;8(6):502-11. doi: 10.1002/jbio.201400069.

Karu T. Primary and secondary mechanisms of action of visible to near-IR radiation on cells.

J Photochem Photobiol B. 1999;49(1):1-17. doi: 10.1016/S1011-1344(98)00219-X.

Bernstein EF. Hair growth induced by diode laser treatment. Dermatol Surg. 2005;31(5):584-6. doi: 10.1111/j.1524-4725.2005.31168.

Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMC Med. 2010;8(1):18. doi: 10.1186/1741-7015-8-18.

Schindl M, Kerschan K, Schindl A, Schön H, Heinzl H, Schindl L. Induction of complete wound healing in recalcitrant ulcers by low‐intensity laser irradiation depends on ulcer cause and size. P Photodermatol Photoimmunol Photomed. 1999;15(1):18-21. doi: 10.1111/j.1600-0781.1999.tb00047.x.

Vinck EM, Cagnie BJ, Cornelissen MJ, Declercq HA, Cambier DC. Increased fibroblast proliferation induced by light emitting diode and low power laser irradiation. Lasers Med Sci. 2003;18(2):95-9. doi: 10.1007/s10103-003-0262-x.

Pinheiro ALB, Pozza DH, Oliveira MGD, Weissmann R, Ramalho LMP. Polarized light (400–2000 nm) and non-ablative laser (685 nm): a description of the wound healing process using immunohistochemical analysis. Photomed Laser Surg. 2005;23(5):485-92. doi: 10.1089/pho.2005.23.485.

Brignardello-Petersen R, Carrasco-Labra A, Araya I, Yanine N, Beyene J, Shah PS. Is adjuvant laser therapy effective for preventing pain, swelling, and trismus after surgical removal of impacted mandibular third molars? A systematic review and meta-analysis. J Oral Maxillofac Surg. 2012;70(8):1789-801. doi: 10.1016/j.joms.2012.01.008.

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