Drouillard M, Petroff N, Majer J, Perrot C, Quesnel S, François M
APHP Groupe hospitalier Robert Debré, Pediatric Otorhinolaryngology Department, 75019 Paris, France; Université Paris 7, Denis Diderot, 5 rue Thomas Mann, 75013 Paris, France.
APHP Groupe hospitalier Robert Debré, Pediatric Otorhinolaryngology Department, 75019 Paris, France; Université Paris 7, Denis Diderot, 5 rue Thomas Mann, 75013 Paris, France.
Int J Pediatr Otorhinolaryngol. 2014 Oct;78(10):1632-6. doi: 10.1016/j.ijporl.2014.07.010. Epub 2014 Jul 14.
The study attempts to specify the circumstances under which we should pay attention to children's pseudohypacusis. It evaluates the methods used to detect such cases and to determine hearing thresholds, according to the uni-or bilateralism of hearing loss. The study finally deals with the future of children diagnosed with pseudohypacusis.
The study was retrospective from January 1993 to November 2011 and prospective from December 2011 to April 2012. We included all the children between 3 and 16 years who were diagnosed with pseudohypacusis. We observed the reasons for them to consult, whether they had already been tested or had treatment, and what kind of hearing loss they displayed. All children were tested using standard pure tone audiometry and speech audiometry. Depending on the first results, other tests were conducted. They included transient evoked otoacoustic emissions (TEOEs), auditory brainstem responses (ABR) and auditory steady state responses. Families were finally contacted by phone over April 2012 in order to let them know about their child's results.
Fifty-four children were included: 19 boys and 35 girls, with an average age of 10 year-old (±3). The simulated hearing loss (HL) was bilateral (36), unilateral (18), of perception (37), moderate HL (33), cophosis (5). Fifteen cases were linked to a family or personal history of hearing loss, while 27 cases were due to important events like adoption, abuse, verbal aggression, school problems. Before diagnosing a pseudohypacusis, 13 children had had imaging studies, 3 had been treated with corticosteroids, and 5 had hearing aids. Most of the time the presence of pseudohypacusis was suspected a discrepancy between speech reception and air-conduction pure tone thresholds, as shown by the medical test (answer on whispered voice). The diagnosis was confirmed by ABR or TEOEs, except in cases where clinic was obvious. Then family's patient and patient were reassured and informed. An audiological follow-up during either 6 months or 1 year was proposed, as well as a psychological consultation.
Complementary examinations have to be performed to rule out a pseudohypacusis case before suggesting an invasive or expensive treatment (surgery or hearing aids) of children.
本研究试图明确在何种情况下我们应关注儿童的伪听力减退。它根据听力损失的单侧或双侧性,评估用于检测此类病例和确定听力阈值的方法。该研究最终探讨被诊断为伪听力减退的儿童的未来情况。
本研究在1993年1月至2011年11月为回顾性研究,在2011年12月至2012年4月为前瞻性研究。我们纳入了所有3至16岁被诊断为伪听力减退的儿童。我们观察了他们就诊的原因、是否已经接受过测试或治疗,以及他们表现出何种类型的听力损失。所有儿童均接受了标准纯音听力测试和言语听力测试。根据首次结果,进行了其他测试。这些测试包括瞬态诱发耳声发射(TEOEs)、听性脑干反应(ABR)和听觉稳态反应。最终在2012年4月通过电话联系了这些家庭,以便让他们了解孩子的检查结果。
共纳入54名儿童:19名男孩和35名女孩,平均年龄为10岁(±3岁)。模拟听力损失(HL)为双侧(36例)、单侧(18例)、感音性(37例)、中度HL(33例)、癔症性(5例)。15例与听力损失的家族或个人史有关,而27例是由于收养、虐待、言语攻击、学校问题等重大事件导致。在诊断伪听力减退之前,13名儿童进行了影像学检查,3名接受了皮质类固醇治疗,5名佩戴了助听器。大多数情况下,伪听力减退的存在是通过医学检查(对低语声音的反应)发现言语接受和气导纯音阈值之间存在差异而被怀疑的。除了临床症状明显的病例外,通过ABR或TEOEs确诊。然后让患儿家属和患儿放心并告知结果。建议进行6个月或1年的听力学随访,以及心理咨询。
在建议对儿童进行侵入性或昂贵的治疗(手术或助听器)之前,必须进行补充检查以排除伪听力减退病例。