Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Oct;280(10):4327-4337.
doi: 10.1007/s00405-023-08091-w. Epub 2023 Jul 6.

Surgical outcome in class 4 congenital anomalies of the ossicular chain: a systematic review of the literature

Affiliations

Surgical outcome in class 4 congenital anomalies of the ossicular chain: a systematic review of the literature

S E Henkemans et al. Eur Arch Otorhinolaryngol. 2023 Oct.

Abstract

Objective: To review hearing and surgical outcomes after reconstructive middle ear surgery in class 4 congenital middle ear anomalies (CMEA), e.g., patients with oval- or round window atresia of dysplasia.

Data sources: Pubmed/Medline, Embase and Cochrane library.

Review methods: Articles containing data on hearing outcomes and complications after reconstructive ear surgery in class 4 anomalies were analyzed and critically appraised. The following data were included and reviewed: patient demographics, audiometric testing, surgical techniques, complications, revision surgeries and their outcomes. Risk of bias was determined, and GRADE certainty of evidence was assessed. Primary outcomes were postoperative air conduction thresholds (AC), change in AC, and success rates (closure of the ABG to within 20 dB), the occurrence of complications (most importantly sensorineural hearing loss) and the long-term stability of hearing results (> 6-month follow-up) and occurrence of recurrence of preoperative hearing loss.

Results: Success rates varied from 12.5 to 75% at long-term follow-up with larger cohorts reporting success rates around 50%, mean postoperative gain in AC varied from 4.7 to 30 dB and - 8.6 to 23.6 dB at, respectively, short- and long-term follow-up. No postoperative change in hearing occurred in 0-33.3% of ears, and recurrence of hearing loss occurred in 0-66.7% of ears. SNHL occurred in a total of seven ears across all studies of which three experienced complete hearing loss.

Conclusion: Reconstructive surgery can be an effective treatment option which should be considered in patients with very favorable baseline parameters, while also considering the substantial risk of recurrence of hearing loss, the possibility of unchanged hearing despite surgery and the rare occurrence of SNHL.

Level of evidence: 2c.

Keywords: Audiometry; Malformation; Minor ear anomalies; Ossicular chain; Otology; Surgery.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest; authors did not receive any funding.

Figures

Fig. 1
Fig. 1
PRISMA flowchart of study selection

Similar articles

Cited by

References

    1. Totten DJ, Marinelli JP, Carlson ML. Incidence of congenital stapes footplate fixation since 1970: a population-based study. Otol Neurotol. 2020;41(4):489–493. doi: 10.1097/MAO.0000000000002554. - DOI - PMC - PubMed
    1. Teunissen EB, Cremers WRJ. Classification of congenital middle ear anomalies report on 144 ears. Ann Otol Rhinol Laryngol. 1993;102(8):606–612. doi: 10.1177/000348949310200807. - DOI - PubMed
    1. Henkemans SE, Smit AL, Stokroos RJ, Thomeer HGXM. Congenital anomalies of the ossicular chain: surgical and audiological outcomes. Ann Otol Rhinol Laryngol. 2022;131(4):388–396. doi: 10.1177/00034894211025405. - DOI - PMC - PubMed
    1. Vincent R, Wegner I, Kamalski DMA, Bittermann AJN, Grolman W. Congenital stapes ankylosis in children: surgical findings and results in 35 cases. Otol Neurotol. 2016;37(4):367–373. doi: 10.1097/MAO.0000000000000923. - DOI - PubMed
    1. Quesnel S, Benchaa T, Bernard S, et al. Congenital middle ear anomalies: anatomical and functional results of surgery. Audiol Neurotol. 2015;20(4):237–242. doi: 10.1159/000380940. - DOI - PubMed

Publication types