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1.
J Int Adv Otol ; 16(3): 395-410, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33136024

RESUMO

Summarise outcomes following cochlear implantation (CI) in patients with post-meningitis deafness. Systematic review and narrative synthesis. Databases searched: Medline, Pubmed, Embase, Web of Science, Cochrane Collection and ClinicalTrials.gov. No limits placed on language or year of publication. Studies with a minimum of 20 individuals with post-meningitis deafness were included. Review conducted in accordance with the PRISMA statement. Searches identified 906 abstracts and 291 full texts. Of these, 19 studies met the inclusion criteria, reporting outcomes in 610 patients with 650 implants. Audiological outcomes improved across all studies following cochlear implantation. 7 studies demonstrated a statistically significant difference between pre and post-CI outcomes. Patients with no cochlear ossification, full electrode insertion, shorter duration of deafness and no neurological sequelae generally appeared to perform best. A total of 31 minor and 19 major complications were reported, with 15 cases of reimplantation. The methodological quality of the included studies was sufficient, predominantly consisting of cohort studies. 15 studies were OCEBM grade III and 4 studies were OCEBM grade IV. All studies had a minimum of 20 individuals with post-meningitic deafness and used multi-channel cochlear implant devices. Audiological outcomes following cochlear implantation in meningitis are satisfactory, providing functional levels of speech perception and intelligibility. Improvement in hearing is dependent on the amount of cochlear ossification, duration of deafness prior to implantation, electrode insertion depth and presence of neurological sequalae. Cochlear implantation in meningitis patients can be challenging due to the presence of ossification and inaccuracies of pre-operative imaging. Therefore, early and bilateral implantation is recommended in all patients with post-meningitis hearing loss to improve the likelihood of full electrode insertion.


Assuntos
Implante Coclear , Implantes Cocleares , Surdez , Meningite , Percepção da Fala , Adulto , Pré-Escolar , Estudos de Coortes , Surdez/cirurgia , Humanos , Lactente , Recém-Nascido , Estudos Prospectivos , Estudos Retrospectivos , Resultado do Tratamento
2.
Neuropharmacology ; 143: 49-62, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30240782

RESUMO

Ongoing, spontaneous pain is characteristic of inflammatory joint pain and reduces an individual's quality of life. To understand the neural basis of inflammatory joint pain, we made a unilateral knee injection of complete Freund's adjuvant (CFA) in mice, which reduced their natural digging behavior. We hypothesized that sensitization of knee-innervating dorsal root ganglion (DRG) neurons underlies this altered behavior. To test this hypothesis, we performed electrophysiological recordings on retrograde labeled knee-innervating primary DRG neuron cultures and measured their responses to a number of electrical and chemical stimuli. We found that 24-h after CFA-induced knee inflammation, knee neurons show a decreased action potential generation threshold, as well as increased GABA and capsaicin sensitivity, but have unaltered acid sensitivity. The inflammation-induced sensitization of knee neurons persisted for 24-h in culture, but was not observed after 48-h in culture. Through immunohistochemistry, we showed that the increased knee neuron capsaicin sensitivity correlated with enhanced expression of the capsaicin receptor, transient receptor potential vanilloid 1 (TRPV1) in knee-innervating neurons of the CFA-injected side. We also observed an increase in the co-expression of TRPV1 with tropomyosin receptor kinase A (TrkA), which is the receptor for nerve growth factor (NGF), suggesting that NGF partially induces the increased TRPV1 expression. Lastly, we found that systemic administration of the TRPV1 antagonist, A-425619, reversed the decrease in digging behavior induced by CFA injection, further confirming the role of TRPV1, expressed by knee neurons, in acute inflammatory joint pain.


Assuntos
Artralgia/metabolismo , Gânglios Espinais/metabolismo , Inflamação/metabolismo , Atividade Motora/fisiologia , Células Receptoras Sensoriais/metabolismo , Canais de Cátion TRPV/metabolismo , Animais , Anti-Inflamatórios não Esteroides/farmacologia , Artralgia/tratamento farmacológico , Artralgia/patologia , Capsaicina , Células Cultivadas , Modelos Animais de Doenças , Feminino , Adjuvante de Freund , Gânglios Espinais/efeitos dos fármacos , Gânglios Espinais/patologia , Membro Posterior , Inflamação/tratamento farmacológico , Inflamação/patologia , Isoquinolinas/farmacologia , Camundongos Endogâmicos C57BL , Atividade Motora/efeitos dos fármacos , Receptor trkA/metabolismo , Células Receptoras Sensoriais/efeitos dos fármacos , Canais de Cátion TRPV/antagonistas & inibidores , Ureia/análogos & derivados , Ureia/farmacologia , Ácido gama-Aminobutírico/metabolismo
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