Outcomes of Neonatal Bulbar Weakness

Author:

Baudon Jean-Jacques1,Renault Francis2,Flores-Guevara Roberto23,Vazquez Marie-Paule45

Affiliation:

1. Faculté de Médecine Pierre et Marie Curie, Université Paris 6, Paris, France;

2. Clinical Neurophysiology Unit, Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Paris, France;

3. Facultad de Medicina, Universidad Nacional Mayor de San Marcos, Lima, Peru;

4. Faculté de Médecine René Descartes, Université Paris 5, Paris, France; and

5. Department of Maxillofacial Surgery, Hôpital Necker-Enfants Malades, Assistance Publique – Hôpitaux de Paris, Paris, France

Abstract

BACKGROUND AND OBJECTIVE: Neonatal bulbar weakness (BW) has various etiologies and a broad prognostic range. We aimed to report outcomes in a large series of children with neonatal BW and explore the association of orofacial electrodiagnostic data with outcome. METHODS: We retrospectively reviewed the files of children who presented with facial, lingual, laryngeal, or pharyngeal weakness at birth and who underwent electrodiagnostic studies combining conventional needle electromyography (EMG) of orofacial muscles, blink responses, and EMG during bottle-feeding. Outcome measures included the need for prolonged respiratory assistance and enteral feeding, as well as sensorimotor and cognitive impairments. RESULTS: Of 175 patients, 73% had developmental disorders, 25% suffered from acquired brain damage, and 2% had no apparent underlying disorders. Motor or mental impairment was observed in 71%; death occurred in 16%. Outcomes were not significantly different when comparing developmental disorders versus acquired brain damage or neurogenic versus normal detection EMG. Abnormal blink responses were associated with higher frequencies of respiratory assistance (P = .03), gastrostomy (P = .025), and death (P = .009); moderate or severe oropharyngeal incoordinations were associated with higher frequencies of respiratory assistance (P = .006), prolonged enteral feeding (P < .0001), and gastrostomy (P = .0002). CONCLUSIONS: Orofacial electrodiagnostic studies provide supplementary information to help the pediatrician anticipate the management and prognosis of young infants with BW.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Reference23 articles.

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Orofacial motor dysfunction in Moebius syndrome;Developmental Medicine & Child Neurology;2019-11-12

2. Neurological Examination;Volpe's Neurology of the Newborn;2018

3. Pediatric Cranial Neuropathies;Pediatric Electromyography;2017

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