Risk factors for severe hearing loss in Susac syndrome: A national cohort study

Author:

Peyre Marion1,Mageau Arthur1,Henry Feugeas Marie‐Cécile2,Doan Serge3,Halimi Caroline4,Klein Isabelle5,Goulenok Tiphaine1,François Chrystelle1,Chauveheid Marie‐Paule1,Papo Thomas1,Sacré Karim16ORCID,

Affiliation:

1. Department of Internal Medecine, Hospital Bichat‐Claude Bernard, Assistance Publique Hôpitaux de Paris Université Paris Cité Paris France

2. Department of Radiology, Hospital Bichat‐Claude Bernard, Assistance Publique Hôpitaux de Paris Université Paris Cité Paris France

3. Department of Ophthalmology, Hospital Bichat‐Claude Bernard, Assistance Publique Hôpitaux de Paris Université Paris Cité Paris France

4. Department of Otolaryngology ‐ Head and Neck Surgery, Hospital Bichat‐Claude Bernard, Assistance Publique Hôpitaux de Paris Université Paris Cité Paris France

5. Department of Radiology Clinique Alleray‐Labrouste Paris France

6. Centre de Recherche sur l'Inflammation, INSERM UMR1149, CNRS ERL8252, Faculté de Médecine site Bichat Laboratoire d'Excellence Inflamex Paris France

Abstract

AbstractBackgroundNonreversible hearing loss (HL) is the main sequelae of Susac syndrome (SuS). We aimed to identify risk factors for HL in SuS.MethodsThe CARESS study is a prospective national cohort study that started in December 2011, including all consecutive patients with SuS referred to the French reference center. The CARESS study was designed with a follow‐up including fundoscopy, audiometry, and brain magnetic resonance imaging at 1, 3, 6, and 12 months after diagnosis and then annually for 5 years. The primary outcome was the occurrence at last follow‐up of severe HL defined as the loss of 70 dB in at least one ear on audiometry or the need for hearing aids.ResultsThirty‐six patients (female 66.7%, median age 37.5 [range 24.5–42.5] years) included in the clinical study were analyzed for the primary outcome. Thirty‐three patients (91.7%) had cochleovestibular involvement at SuS diagnosis including HL >20 dB in at least one ear in 25 cases. At diagnosis, 32 (88.9%), 11 (30.6%), and 7 (19.4%) patients had received steroids, intravenous immunoglobulin, and/or immunosuppressive (IS) drugs, respectively. After a median follow‐up of 51.8 [range 29.2–77.6] months, 19 patients (52.8%) experienced severe HL that occurred a median of 13 [range 1.5–29.5] months after diagnosis. Multivariable analysis showed that the odds of severe HL were lower in patients who received IS drugs at diagnosis (OR 0.15, 95% CI 0.01–1.07, p = 0.058).ConclusionsSevere HL in SuS is associated with the absence of IS drugs given at diagnosis. Our findings support the systematic use of IS drugs in SuS.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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