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Intrathecal Application of a Fluorescent Dye for the Identification of Cerebrospinal Fluid Leaks in Cochlear Malformation
Published on: February 29, 2020
[Cochlear implantation and early outcomes in children with incompletely partition type Ⅲ malformation]
Insights
Cochlear implantation (CI) effectively treats children with incompletely partitioned type III (IP-III) malformation, showing similar hearing thresholds to controls. However, speech development in these children is slower than in those with normal cochleas.
Area of Science:
- Otolaryngology
- Pediatric Audiology
- Neurosurgery
Context:
- Incompletely partitioned type III (IP-III) malformation is a complex inner ear anomaly.
- Cochlear implantation (CI) is a potential treatment for hearing loss in children with IP-III.
- Surgical challenges and outcomes in IP-III malformations require further investigation.
Purpose:
- To evaluate the early effects of cochlear implantation (CI) in children diagnosed with incompletely partitioned type III (IP-III) malformation.
- To compare hearing thresholds, auditory performance, and speech intelligibility in IP-III patients post-CI with a control group.
Summary:
- Ten children with IP-III malformation underwent cochlear implantation (CI).
- Post-implantation, pure tone average (PTA) thresholds in the IP-III group were comparable to the control group.
- While auditory performance (CAP scores) showed no significant difference, speech intelligibility (SIR scores) was significantly lower in the IP-III group at 6, 9, and 12 months.
Impact:
- Cochlear implantation is a beneficial treatment for hearing loss associated with IP-III malformation.
- Despite surgical challenges, CI can be performed with low complication rates with skilled surgeons.
- Children with IP-III malformation receiving CI demonstrate slower speech and hearing development compared to peers with normal cochlear anatomy.
Abstract:
Objective:To analyze the early effect of the cochlear implantation (CI) in children with cochlear incompletely partition type Ⅲ malformation (IP-Ⅲ). Method:Ten children with IP-Ⅲ malformation who underwent CI were recruited in this study. The hearing characteristics, preoperative speech performance and surgery were analyzed retrospectively. The aided hearing threshold with CI, the categories of auditory performance (CAP) score, speech intelligibility rating (SIR) score and speech perception were designed to access the benefits of CI. Ten children with normal cochlea were also enrolled as the control group. Demographic information of children in the control group including hearing loss and speech level before implantation, age at implantation, hearing aids using history, duration with CI were matched with those in the IP-Ⅲ group. The hearing threshold, CAP score and SIR score in the IP-Ⅲ group were compared with the control group using the SPSS 20.0 software. Result:The computed tomography of temporal bones showed typical IP-Ⅲ malformation in all patients. The electrode arrays were properly and totally implanted in all children. Cerebrospinal fluid gusher occurred intra-operatively, and no other complications in all patients. The pure tone average (PTA) threshold at the 3rd, 6th, 9th and 12th month after implantation were (40.8±8.5) dB HL, (36.1±9.1) dB HL, (32.5±6.8) dB HL and (33.0±7.3) dB HL, respectively. The PTA thresholds in the IP-Ⅲ group were similar to those in the control group at all tested time points (P>0.05). At the 3rd, 6th, 9th and 12th month after implantation, the CAP scores in the IP-Ⅲ group were lower than those in the control group, but there was no significantly difference (P>0.05). Furthermore, the SIR scores were lower than those in the control group, and there were significantly difference at the 6 th, 9 th and 12 th month after implantation (P<0.05). Conclusion:CI was an effective treatment for children with IP-Ⅲ malformation. Surgery on IP-Ⅲ was challenging, however, seldom complication would occur with excellent surgical skills. Though the CI was benefit for IP-Ⅲ, the development of hearing and speech ability were slower than children with normal cochlea.
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