Martins Olivia de Freitas Mendes, Chaves Junior Cauby Maia, Rossi Rowdley Robert Pereira, Cunali Paulo Afonso, Dal-Fabbro Cibele, Bittencourt Lia
Universidade Federal do Piauí, Curso de Especialização em Ortodontia (Teresina/PI, Brazil).
Centro Universitário UNINOVAFAPI, Curso de Especialização em Ortodontia (Teresina/PI, Brazil).
Dental Press J Orthod. 2018 Aug 1;23(4):45-54. doi: 10.1590/2177-6709.23.4.045-054.oar.
Occlusal side effects or development of pain and/or functional impairment of the temporomandibular complex are potential reasons for poor compliance or abandonment of mandibular advancement splints treatment for snoring and obstructive sleep apnea.
This study aimed at providing a comprehensive review evaluating the craniofacial side effects of oral appliance therapy for snoring and obstructive sleep apnea.
An electronic search was systematically conducted in PubMed and Virtual Health Library from their inception until October 2016. Only Randomized Controlled Trials whose primary aim was to measure objectively identified side effects on craniofacial complex of a custom-made oral appliance for treating primary snoring or obstructive sleep apnea were included. Studied patients should be aged 20 or older. The risk of bias in the trials was assessed in accordance with the recommendations of The Cochrane Risk of Bias criteria.
A total of 62 full-text articles were assessed for eligibility. After the review process, only 6 met all the inclusion criteria. All studies were rated as having a high risk of bias. The most uniformly reported mandibular advancement splint side effects were predominantly of dental nature and included a decrease in overjet and overbite. The risk of developing pain and function impairment of the temporomandibular complex appeared limited with long-term mandibular advancement splint use.
The limited available evidence suggests that mandibular advancement splint therapy for snoring and obstructive sleep apnea results in changes in craniofacial morphology that are predominantly dental in nature, specially on a long-term basis. Considering the chronic nature of obstructive sleep apnea and that oral appliance use might be a lifelong treatment, a thorough customized follow-up should therefore be undertaken to detect possible side effects on craniofacial complex. It is also important to provide adequate information to the patients regarding these possible changes, especially to those in whom larger occlusal changes are to be expected or in whom they are unfavorable. Long-term assessments of adverse effects of oral appliance therapy, with larger study samples and recruitment of homogenous patient population are still required.
咬合方面的副作用或颞下颌关节复合体疼痛和/或功能障碍的出现是下颌前移矫治器治疗打鼾和阻塞性睡眠呼吸暂停时依从性差或放弃治疗的潜在原因。
本研究旨在全面综述评估口腔矫治器治疗打鼾和阻塞性睡眠呼吸暂停的颅面副作用。
从创刊至2016年10月,在PubMed和虚拟健康图书馆系统地进行了电子检索。仅纳入主要目的是客观测量定制口腔矫治器治疗原发性打鼾或阻塞性睡眠呼吸暂停对颅面复合体副作用的随机对照试验。研究对象应为20岁及以上的患者。根据Cochrane偏倚风险标准的建议评估试验中的偏倚风险。
共评估了62篇全文文章的 eligibility。经过审查过程,只有6篇符合所有纳入标准。所有研究均被评为具有高偏倚风险。下颌前移矫治器最一致报告的副作用主要是牙齿方面的,包括覆盖和覆牙合减小。长期使用下颌前移矫治器时,颞下颌关节复合体出现疼痛和功能障碍的风险似乎有限。
有限的现有证据表明,下颌前移矫治器治疗打鼾和阻塞性睡眠呼吸暂停会导致颅面形态改变,主要是牙齿方面的,特别是在长期使用时。考虑到阻塞性睡眠呼吸暂停的慢性性质以及口腔矫治器的使用可能是一种终身治疗,因此应进行全面的定制随访,以检测对颅面复合体可能的副作用。向患者提供有关这些可能变化的充分信息也很重要,特别是对于那些预期会有较大咬合变化或变化不利的患者。仍需要对口腔矫治器治疗的不良反应进行长期评估,样本量要更大,并招募同质的患者群体。