CI2019 Pediatric: Poster Abstracts CI2019 Pediatric Poster Abstracts

Total Page:16

File Type:pdf, Size:1020Kb

CI2019 Pediatric: Poster Abstracts CI2019 Pediatric Poster Abstracts CI2019 Pediatric: Poster Abstracts CI2019 Pediatric Poster Abstracts Poster Number: 1 Abstract ID: 197 Title: Assessing the Benefits of Bimodal Fitting Category: Audiology Authors: Justin Aronoff, PhD 1, Abbigail Kirchner, BS 1, Jennifer Black, AuD 2, Michael Novak, MD 2, Smita Agrawal, PhD 3; 1Univ. of Illinois at Urbana-Champaign, Champaign, IL, 2Carle Fndn., Urbana, IL, 3Advanced Bionics, LLC, Valencia, CA. Abstract: Introduction: Patients with a cochlear implant in one ear and a hearing aid in the other (bimodal) are often not optimally programmed. There is typically little to no coordination between the two devices and the amplification needs of a bimodal listener are different from a patient who only has access to sound through hearing aids. Recently, a bimodal fitting system has been created (Naida Link) that aims to optimize the gains for this population by providing more gain for low frequencies and reduced gain at frequencies corresponding to potential dead regions in the cochlea. It also aligns the loudness growth and dynamic AGC characteristics of the bimodal hearing aid to that of the cochlear implant processor. Methods: The goal of the current study was to determine if bimodal fitting via the Naida Link yielded better speech understanding abilities compared to an individual’s current standard clinical fitting of a cochlear implant and hearing aid. To test this, patients were tested with unlinked and uncoordinated cochlear implant and hearing aid programs (only relative loudness for the two ears was adjusted). Patients were also tested with the Naida Link system. Speech understanding in noise was compared in the two configurations. Results: Preliminary results will be discussed. Conclusion: An efficient and effective bimodal fiiting methodology is beneficial to patients as well as clinicians. CI2019 Pediatric Poster Abstracts Poster Number: 2 Abstract ID: 83 Title: Bilingual Language Proficiency in Adolescents with Typical Hearing and Adolescents with Hearing Loss Category: Rehabilitation/Educational Aspects Authors: Alliete Alfano, PhD 1, Stacey Lim, AuD, PhD 2, Carolina Gutierrez-Rivas, PhD 2; 1Communication Sciences and Disorders, Florida Intl. Univ., Miami, FL, 2Central Michigan Univ., Mount Pleasant, MI. Abstract: Introduction: Though there is evidence demonstrating children with disabilities are able to become bilingual, there are still concerns of how children with hearing loss can learn more than one spoken language (Thomas, El-Kashlan, & Zwolan, 2008). In more recent years, it has been found that there are advantages to speaking more than one language at home, particularly if the parents are fluent in other spoken languages (Thomas, El-Kashlan, & Zwolan, 2008). In the past, however, parents of children with hearing loss were strongly encouraged to speak one language only; generally, this was the language of the majority population in the country--so for example, bilingual parents in the United States were encouraged to speak only English with their children with hearing loss, regardless of the parents’ proficiency in English. The purpose of this study was to compare English and Spanish proficiency in bilingual adolescents with and without hearing loss. Methods: Sixteen bilingual (English/Spanish) adolescents, 12-19 years old, participated in the study. Eight of the adolescents had severe to profound bilateral sensorineural hearing loss. Hearing loss was identified by 2 years of age and hearing aid fitting/cochlear implantation occurred by 2 1/2 year of age. The remaining 8 adolescents had typical hearing and were age-matched to the adolescents with hearing loss. Participants completed a bilingual history questionnaire and the Woodcock-Muñoz Language Survey in English and Spanish. Results: An independent-samples t-test was run to determine if there were differences in language proficiency scores in English and Spanish between bilingual adolescents with typical hearing and bilingual adolescents with hearing loss. English Listening proficiency was higher for adolescents with typical hearing (101.2± 9.6) than for adolescents with hearing loss (76.1 ± 18.1), a statistically significant difference of 4.9, t(19) = 6.331, p = .000. English Oral Language proficiency was higher for adolescents with typical hearing (101.8± 7.7) than for adolescents with hearing loss (71.0 ± 14.7), a statistically significant difference of 6.0, t(19) = 4.293, p = .000. Spanish Listening proficiency was higher for adolescents with typical hearing (79.0± 16.5) than for adolescents with hearing loss (25.4 ± 22.1) a statistically significant difference of 8.4, t(19) = 6.356, p = .000. Spanish Oral Language proficiency was higher for adolescents with typical hearing (67.9± 17.9) than for adolescents with hearing loss (33.5 ± 23.5) a statistically significant difference of 9.1, t(19) = 3.081, p = .001. Conclusion: Results indicate that bilingual adolescents with typical hearing have higher language proficiency in both English and Spanish when compared to bilingual adolescents with hearing loss. Additionally, English proficiency was higher for both groups. CI2019 Pediatric Poster Abstracts Poster Number: 3 Abstract ID: 224 Title: Quality of Life Outcomes After Cochlear Implantation in Older Adults: A Systematic Review Category: Audiology Authors: Ellen Andries, Drs, MSc AUD, Griet Mertens, PhD, MSc AUD, Paul Van de Heyning, MD, PhD;Department of Otorhinolaryngology, Univ. Hosp. Antwerp, Antwerp, Belgium. Abstract: Introduction: According to the WHO, one third of adults aged 65 or older has disabling hearing loss. Those with severe to profound sensorineural hearing loss could benefit from cochlear implants (CI) as it is shown in several studies that CI can significantly improve auditory gains, cognition and quality of life (QOL). There is growing interest in older CI recipients and their QOL, as QOL is an issue especially of reimbursement strategies. To assess QOL in CI recipients, clinical psycho-acoustic measures such as speech recognition and pure tone audiometry alone are not all-embracing. QOL also needs to be evaluated in a more general way, taking into account personal factors and functional benefits that cannot be described by (speech) audiometry. Therefore, numerous QOL measurement instruments have been developed, divided in two categories: disease-specific and generic instruments. Generic instruments can be used in various diseases as they assess general health states, while disease-specific measures assess particular diseases. Nevertheless, there is lack of consensus regarding QOL measures in CI recipients. Moreover, there are less data in QOL changes available in recent articles compared to data in psycho-acoustic measures changes in CI. Therefore, the aim of this study is to critically review current literature concerning QOL in CI recipients. Methods: Studies were selected by searching MEDLINE (PubMed) and Cochrane Library and by checking reference lists of relevant articles. No restrictions were imposed regarding language, publication date or publication status. Inclusion criteria were as follows: (1) The study sample were adults aged 50 and older with bilateral severe to profound hearing loss with postlingual onset (2) All subjects received a multi- electrode CI (3) QOL was assessed before and after implantation. The following search string was used: (‘Cochlear Implants’[Mesh] OR ‘Cochlear Implantation’[Mesh] OR (cochlear implant*)) AND (‘Quality Of Life’[Mesh] OR quality[Text Word] OR life[Text Word] OR benefit[Text Word] OR self-report[Text Word] OR self-reported[Text Word] OR selfreported[Text Word] OR patient-report[Text Word] OR patient- reported[Text Word]) AND (adult[Text Word] OR adults[Text Word]) AND (‘Aging’[Mesh] OR ‘Aged’[Mesh] OR ‘Geriatrics’[Mesh] OR elder[Text Word] OR elderly[Text Word] OR elders[Text Word] OR old[Text Word] OR older[Text Word] OR aged [Text Word] OR aging[Text Word] OR ageing[Text Word] OR senior[Text Word] OR seniors[Text Word] OR geriatric[Text Word] OR geriatrics[Text Word]) Results: Title and abstract of 475 articles were screened and 35 articles were selected for full-text assessment. The general results will be presented at CI 2019. Conclusion: Current literature shows that QOL improves post CI. However, no instruments or methods are generally accepted to assess QOL in CI recipients. The overall results will be presented at CI 2019. CI2019 Pediatric Poster Abstracts Poster Number: 4 Abstract ID: 300 Title: Comparing Measures of the Cochlear Implant Electrode-Neuron Interface to Clinical Measures in Listeners with Enlarged Vestibular Aqueduct Category: Audiology Authors: Julie G. Arenberg, PhD, Kelly Jahn, AuD, Molly Bergen, BS;Speech and Hearing Sciences, Univ. of Washington, Seattle, WA. Abstract: Introduction: Etiology of hearing loss can lead to varying development and formation of the inner ear, resulting in differing qualities of the interface between individual, cochlear implant (CI) electrodes and the auditory nerve. However, the relation between etiology and psychophysical and impedance measures is not well understood. The goal of the present study was to compare detailed psychophysical and impedance measures obtained in a small sample of subjects with enlarged vestibular aqueduct (EVA) to those obtained clinically in a much larger sample of patients. Methods: Detailed psychophysical measures were obtained in 16 CI listeners that received their first implant during childhood. Four participants were diagnosed with enlarged vestibular aqueduct (EVA), which is characterized
Recommended publications
  • Mudr. Kaliariková Seminar for Medical Students 2019/20
    MUDr. Kaliariková Seminar for medical students 2019/20 Deformity of shape, cosmetic defect Therapy: plastic correction – otoplasty: Children from the age of 6 years Congenital defect of auricle development (microtia) or missing auricle (anotia) is often combined with the congenital defect of the EAC (stenosis, atresia) Auditory canal stenosis means that it is narrower than 4 mm Dg: CT, objective hearing examination (exclusion of congenital defect of the middle and inner ear or the auditory track) Conductive hearing loss HRCT of the Temporal Bone Right side – stenosis of EAC Left side – atresia of EAC It depends on examination results and on hearing affliction extent (unilateral or bilateral affliction) Aim: provide communication Hearingaid devices (BAHA) Surgery: tympanoplasty, plastic of external auditory canal or auricle External opening is placed near the tragus and the inner opening between cartilaginous and bone part of the EAC Complication – inflammation (secretion, swelling or erythema) Th: Exstirpation, ATB (inflammation) Usually connected with atresia of EAC and anomalies of auricle Isolated / part of syndroms (more common, e.g. Treacher Collins) Usually unilateral Hearing-impairment Dg: CT, objective hearing examination Th: hearing-aid devices, tympanoplasty 20% of children with SNHL (sensorineural hearing loss) have CT anomalies of inner ear Cochlear anomalies Enlarged vestibular aqueduct (EVA) Semicircular canal dysplasia Michel deformity or complete labyrinthine aplasia (cochlea + vestibulum) Cochlear aplasia Common cavity malformation to the cochlea and vestibule Cochlear hypoplasia Cochlear incomplete partition type I (including cystic cochleovestibular anomaly) Cochlear incomplete partition type II (Mondini dysplasia) 1,5 screw of cochlea, dilated aqueductus Normal cochlea 2,5-2,75 screw Dilated vestibulum Normal vestibulum Ø 60% congenital • Damage of auditory organ during development (1.
    [Show full text]
  • EUROCAT Syndrome Guide
    JRC - Central Registry european surveillance of congenital anomalies EUROCAT Syndrome Guide Definition and Coding of Syndromes Version July 2017 Revised in 2016 by Ingeborg Barisic, approved by the Coding & Classification Committee in 2017: Ester Garne, Diana Wellesley, David Tucker, Jorieke Bergman and Ingeborg Barisic Revised 2008 by Ingeborg Barisic, Helen Dolk and Ester Garne and discussed and approved by the Coding & Classification Committee 2008: Elisa Calzolari, Diana Wellesley, David Tucker, Ingeborg Barisic, Ester Garne The list of syndromes contained in the previous EUROCAT “Guide to the Coding of Eponyms and Syndromes” (Josephine Weatherall, 1979) was revised by Ingeborg Barisic, Helen Dolk, Ester Garne, Claude Stoll and Diana Wellesley at a meeting in London in November 2003. Approved by the members EUROCAT Coding & Classification Committee 2004: Ingeborg Barisic, Elisa Calzolari, Ester Garne, Annukka Ritvanen, Claude Stoll, Diana Wellesley 1 TABLE OF CONTENTS Introduction and Definitions 6 Coding Notes and Explanation of Guide 10 List of conditions to be coded in the syndrome field 13 List of conditions which should not be coded as syndromes 14 Syndromes – monogenic or unknown etiology Aarskog syndrome 18 Acrocephalopolysyndactyly (all types) 19 Alagille syndrome 20 Alport syndrome 21 Angelman syndrome 22 Aniridia-Wilms tumor syndrome, WAGR 23 Apert syndrome 24 Bardet-Biedl syndrome 25 Beckwith-Wiedemann syndrome (EMG syndrome) 26 Blepharophimosis-ptosis syndrome 28 Branchiootorenal syndrome (Melnick-Fraser syndrome) 29 CHARGE
    [Show full text]
  • Thieme: Imaging of the Temporal Bone
    fm 1/7/09 12:23 PM Page i Imaging of the Temporal Bone Fourth Edition fm 1/7/09 12:23 PM Page ii fm 1/7/09 12:23 PM Page iii Imaging of the Temporal Bone Fourth Edition Joel D. Swartz, MD President Germantown Imaging Associates Gladwyne, Pennsylvania Laurie A. Loevner, MD Professor of Radiology and Otorhinolaryngology—Head and Neck Surgery Department of Radiology Neuroradiology Section University of Pennsylvania School of Medicine and Health System Philadelphia, Pennsylvania Thieme New York • Stuttgart fm 1/7/09 12:23 PM Page iv Thieme Medical Publishers, Inc. 333 Seventh Ave. New York, NY 10001 Executive Editor: Timothy Hiscock Editorial Assistant: David Price Vice President, Production and Electronic Publishing: Anne T. Vinnicombe Production Editor: Heidi Pongratz, Maryland Composition Vice President, International Marketing and Sales: Cornelia Schulze Chief Financial Officer: Peter van Woerden President: Brian D. Scanlan Compositor: Thomson Digital Printer: The Maple-Vail Book Manufacturing Group Library of Congress Cataloging-in-Publication Data Imaging of the temporal bone / [edited by] Joel D. Swartz, Laurie A. Loevner.– 4th ed. p. ; cm. Rev. ed. of: Imaging of the temporal bone / Joel D. Swartz, H. Ric Harnsberger. 3rd ed. 1998. Includes bibliographical references and index. ISBN 978-1-58890-345-7 1. Temporal bone—Imaging. 2. Temporal bone—Diseases—Diagnosis. I. Swartz, Joel D. II. Loevner, Laurie A. [DNLM: 1. Temporal Bone—radiography. 2. Magnetic Resonance Imaging. 3. Temporal Bone—pathology. 4. Tomography, X-Ray Computed. WE 705 I31 2008] RF235.S93 2008 617'.514–dc22 2008026874 Copyright © 2009 by Thieme Medical Publishers, Inc.
    [Show full text]
  • Large Vestibular Aqueduct and Congenital Sensorineural Hearing Loss
    Large Vestibular Aqueduct and Congenital Sensorineural Hearing Loss Mahmood F. Mafee, 1 Dale Char/etta, Arvind Kumar, and Hera/do Belmonf From the Department of Radiology, University of Illinois at Chicago (MAM), the Department of Radiology, Rush-Presbyterian-St. Luke's Medical Center (DC), and the Department of Otolaryngalogy-Head and Neck Surgery, University of Illinois at Chicago (AK) The inner ear is composed of the membranous All of the structures of the membranous laby­ labyrinth and the osseous labyrinth (1). The mem­ rinth are enclosed within hollowed-out bony cav­ branous labyrinth has two major subdivisions, a ities that are considerably larger than their mem­ sensory portion called the sensory labyrinth and branous contents. These bony cavities assume a nonsensory portion designated the nonsensory the same shape as the membranous chambers labyrinth. and are referred to as the osseous labyrinth. The The sensory labyrinth lies within the petrous bony cavities of the osseous labyrinth are lined portion of the temporal bone. It contains two by periosteum and contain fluid, known as peri­ intercommunicating portions: 1) the cochlear lab­ lymph, that bathes the external surface of the yrinth that consists of the cochlea and is con­ membranous labyrinth. The perilymph is rich in cerned with hearing, and 2) the vestibular laby­ . sodium ions and poor in potassium ions and is rinth that contains the utricle, saccule, and sem­ roughly comparable with extracellular tissue fluid icircular canals, all of which are concerned with or cerebrospinal fluid (CSF). It appears to act as equilibrium. These hollow chambers are filled a hydraulic shock absorber to protect the mem­ with fluid, known as endolymph, that resembles branous labyrinth.
    [Show full text]
  • 21-ENT Auditory Pathway → 1St-Spiral Ganglion(Bipolar) → → 2Nd-Dorsal
    21-ENT auditory pathway 1st-spiral ganglion(bipolar)→ 2nd-dorsal,ventral cochlear nucleus→ cross to opposite side(in trapezoid body)→ 3rd-sup olivary nucleus→ lat laminiscus→ 4th-inf colliculus→ inf brachium→ 5th-med geniculate body→ audit radiat→ sublentiform part internal capsule→ audit area temporal lobe Auditory Brainstem Response Audiometry(ABRA) I-II—CNVIII(distal&proximal segment) III-cochlear nucleus IV-sup olive V-Lat Leminiscus(Largest wave) VI-VII—inf colliculus displacusis-same tone heard as notes of diff pitch in either ear-inj to n to stapedius, cong syphilis(Hennebert sign) EAC exostosis-recur prolong cold H2O exposure hyperacusis-discomfort/pain on exposure to norm sound otitic barotrauma-underH2O diving, descend in aircraft, compression in press chamber paracusis willisi-sound heard better in presence of background noise-otosclerosis Tullio phenom-attack of vertigo/dizziness by loud sound-labyrinthine fistula ds-TM ASOM-presuppurative-cartwheel, suppurative-lighthouse barotrauma-congested&retracted, air bubble, hgic effusion healed myringitis bullosa-sagograin hemotympanum, glue ear, glomus tm, hemangioma middle ear-blue keratin deposit, osmium tetroxide-snakelike myringitis bullosa(influenza virus)-hgic bleb otosclerosis-norm(90%)-translucent&pearly gray, active ds-flamingo tint(pink spot) retracted-dull lustreless serous otitis media-dull, opaque, grey/bluish, potbelly spontaneousAim4aiims.in heal-dimeric(sq epith–fibrous layer) TB otitis media-camphor ice, multiple perforation tympanosclerosis-chalky white plaque audiometry
    [Show full text]
  • Us 2018 / 0305689 A1
    US 20180305689A1 ( 19 ) United States (12 ) Patent Application Publication ( 10) Pub . No. : US 2018 /0305689 A1 Sætrom et al. ( 43 ) Pub . Date: Oct. 25 , 2018 ( 54 ) SARNA COMPOSITIONS AND METHODS OF plication No . 62 /150 , 895 , filed on Apr. 22 , 2015 , USE provisional application No . 62/ 150 ,904 , filed on Apr. 22 , 2015 , provisional application No. 62 / 150 , 908 , (71 ) Applicant: MINA THERAPEUTICS LIMITED , filed on Apr. 22 , 2015 , provisional application No. LONDON (GB ) 62 / 150 , 900 , filed on Apr. 22 , 2015 . (72 ) Inventors : Pål Sætrom , Trondheim (NO ) ; Endre Publication Classification Bakken Stovner , Trondheim (NO ) (51 ) Int . CI. C12N 15 / 113 (2006 .01 ) (21 ) Appl. No. : 15 /568 , 046 (52 ) U . S . CI. (22 ) PCT Filed : Apr. 21 , 2016 CPC .. .. .. C12N 15 / 113 ( 2013 .01 ) ; C12N 2310 / 34 ( 2013. 01 ) ; C12N 2310 /14 (2013 . 01 ) ; C12N ( 86 ) PCT No .: PCT/ GB2016 /051116 2310 / 11 (2013 .01 ) $ 371 ( c ) ( 1 ) , ( 2 ) Date : Oct . 20 , 2017 (57 ) ABSTRACT The invention relates to oligonucleotides , e . g . , saRNAS Related U . S . Application Data useful in upregulating the expression of a target gene and (60 ) Provisional application No . 62 / 150 ,892 , filed on Apr. therapeutic compositions comprising such oligonucleotides . 22 , 2015 , provisional application No . 62 / 150 ,893 , Methods of using the oligonucleotides and the therapeutic filed on Apr. 22 , 2015 , provisional application No . compositions are also provided . 62 / 150 ,897 , filed on Apr. 22 , 2015 , provisional ap Specification includes a Sequence Listing . SARNA sense strand (Fessenger 3 ' SARNA antisense strand (Guide ) Mathew, Si Target antisense RNA transcript, e . g . NAT Target Coding strand Gene Transcription start site ( T55 ) TY{ { ? ? Targeted Target transcript , e .
    [Show full text]
  • Effects of Retinoid Treatment on Cochlear Development, Connexin Expression and Hearing Thresholds in Mice
    Journal of Otorhinolaryngology, Hearing and Balance Medicine Article Effects of Retinoid Treatment on Cochlear Development, Connexin Expression and Hearing Thresholds in Mice Yeunjung Kim ID and Xi Lin * Department of Otolaryngology, Emory University School of Medicine, 615 Michael Street, Room# 543, Atlanta, GA 30322-3030, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-404-727-3723; Fax: +1-404-727-6256 Received: 5 July 2017; Accepted: 17 October 2017; Published: 23 October 2017 Abstract: Mutations in GJB2, gene coding for connexin 26 (Cx26), and GJB6, gene coding for connexin 30 (Cx30), are the most common genetic defects causing non-syndromic hereditary hearing loss. We previously reported that overexpression of Cx26 completely rescues the hearing in a mouse model of human GJB6 null mutations. The results suggest that therapeutic agents up-regulating the expression of Cx26 may potentially be a novel treatment for non-syndromic hereditary deafness caused by Cx30 null mutations. Retinoids are a family of vitamin A derivatives that exert broad and profound effects on cochlear protein expression including connexins. They are readily available and already utilized as therapeutic agents for recurrent otitis media and hearing loss due to noise exposure. In this study, we characterized the expression of Cx26 and Cx30 in the postnatal inner ear by different retinoids including retinyl palmitate (RP), the main source of vitamin A in over-the-counter (OTC) supplements, retinyl acetate (RAc) which is an isomer of RP, and all-trans-retinoic acid (ATRA), the most active retinoid derivative. The results revealed ATRA significantly increased cochlear Cx26 expression and improved hearing in Cx30 knockout (KO) mice by 10 dB suggesting its potential benefits as a therapeutic agent.
    [Show full text]
  • Those Followed by F Indicate Figures
    G-1 Page numbers followed by b indicate boxes; f, figures; t, tables. GLOSSARY B C D E F G H I J K L M N O P Q R S T U V W X Y Z A Abducens nerve. Cranial nerve VI, the nerve, that innervates the lateral rectus, the extraocular eye muscle that moves the globe laterally. 260f, 559, 614b Abductor. That which draws a body part away from the median line; typically associated with a muscle.* 241–242, 242t Abembryonic pole. The side of a blastocyst opposite the embryonic pole, that is, the side opposite the inner cell mass. 43 Abnormal spindle-like microcephaly associated microcephaly (ASPM). A gene that plays an essential role in embryonic neuroblasts in normal mitotic spindle function, and is expressed in proliferating regions of the cerebral cortex during neurogenesis. 290b–291b Abortifacient. That which causes an embryo or fetus to abort. 45b Accutane. A drug taken orally for the treatment of acne. 161–162 Acetazolamide. A carbonic anhydrase inhibitor with a wide variety of uses, including the treatment of glaucoma. 638b Acheiropodia. A disorder resulting in the absence of hands and feet. 634t, 636t Achondroplasia. The most common and most recognizable form of dwarfism. It is caused by mutations in Fibroblast growth factor receptor 3 (Fgfr3). 219b, 220f, 239b, 602b Achondroplasia/hypochondroplasia syndrome. Skeletal dysplasia caused by the Fgfr3 mutation, which results in brachydactyly (abnormal shortness of the fingers) and rhizomelia (shortening of the proximal limbs). 635t Acoustic meatus, external. The ear canal. 572 Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome.
    [Show full text]
  • Hearing Impaired Handbook
    24412_KP_ccc_hearing_cvrFNL.qxp:kp_ccc_cvr.qxd 10/6/08 7:46 AM Page 2 A Provider’s Handbook on Culturally Competent Care PEOPLE WITH HEARING LOSS 1ST EDITION Kaiser Permanente National Diversity Council and the Kaiser Permanente National Diversity Office 24412_KP_ccc_hardhear_3.qxp:KP_ccc_guts_web.qxd 10/7/08 9:17 AM Page 1 A PROVIDER’S HANDBOOK ON CULTURALLY COMPETENT CARE 24412_KP_ccc_hardhear_3.qxp:KP_ccc_guts_web.qxd 10/7/08 9:17 AM Page 2 TABLE OF CONTENTS INTRODUCTION......................................................................................................................1 DEFINITIONS AND DEMOGRAPHICS ...........................................................................2 Who are People with Hearing Loss? Definitions and Terminology: Past & Present How We Hear Causes of Hearing Loss Types of Hearing Loss Degrees of Hearing Loss Functional Aspects of Hearing Loss Demographics and Trends Health Care Provider Tips CULTURAL PERSPECTIVES, BELIEFS, AND BEHAVIORS....................................18 The Costs of Hearing Loss Stigma and Barriers to Treatment Loss and Grief Coping Beliefs Adherence Stages of Change Health Care Provider Tips COMMUNICATING WITH PEOPLE WITH HEARING LOSS ................................24 Effective Communication Behaviors in Communication Legal, Regulatory, and Accreditation Requirements Physical Settings Health Care Provider Tips RISK FACTORS ........................................................................................................................33 Perinatal Issues Congenital
    [Show full text]
  • Intervention Strategies for Air‐ and Bone‐ Conduction Unilateral Hearing Loss (UHL)
    2020-09-29 Intervention strategies for air‐ and bone‐ conduction unilateral hearing loss (UHL) Susan A. Small, PhD Associate Professor Hamber Professor of Clinical Audiology University of British Columbia Virtual Speech & Hearing BC Conference 2020 October 23, 2020, 10:30 am ‐ 12:00 pm Disclosure statement . NSERC Discovery Grant . BC Early Hearing Program (consultant): receive funds & equipment that contribute to my research program . Hamber Chair position: small contribution to research program . Interacoustics: equipment on loan Other funding . UBC Faculty of Medicine: general funds for research . Eric W. Hamber Professorship: partial salary award TOPIC AREAS TO BE ADDRESSED Prevalence of UHL Loss of binaural hearing benefits with UHL‐‐ effects on spatial hearing + other consequences Review of current data re: intervention for UHL across the lifespan‐‐ infants to adults Bone‐conduction hearing loss: Unilateral & binaural 1 2020-09-29 BC EHP Definitions Unilateral hearing loss (UHL) Normal hearing in one ear (considered to be the majority of thresholds ≤ 20 dB HL) Majority of air‐conduction (AC) thresholds >20 dB HL in the ear with permanent hearing loss Historically, audiologists most concerned with effects of severe‐to‐profound hearing loss on speech & language development Rubella outbreak in US Severe/profound clinical in 1964/5: 12,000 babies focus for years after born deaf UHL (& minimal bilateral hearing loss) might have Studies in negative effects on academic early 1980’s progress & psychosocial skills of school‐aged children ** Renewed research focus in last 3-5 years Unilateral hearing loss Focus of recent international conferences ‐ BCEHP Workshop 2017, Oct 17, 2017, Vancouver: R. McCreery, J. Lieu & S.A.
    [Show full text]
  • DIAGNOSTIC GENETIC TESTING REQUISITION SPECIMENS: 1428 Madison Ave., Rm AB2-25, New York, NY 10029 MAIL: One Gustave L
    DIAGNOSTIC GENETIC TESTING REQUISITION SPECIMENS: 1428 Madison Ave., Rm AB2-25, New York, NY 10029 MAIL: One Gustave L. Levy Place, Box 1497, New York, NY 10029-6574 Phone: 800-298-6470 / Fax: 646-859-6870 Tax ID# 47-5349024/ CLIA# 33D2097541 ACCESSION NO. DATE / / PATIENT INFORMATION ORDERING PROVIDER INFORMATION PATIENT LAST NAME PATIENT FIRST NAME DOB BIOLOGICAL GENDER ETHNICITY / / M F TELEPHONE EMAIL ADDRESS CITY/STATE/ZIP BIOLOGICAL MOTHER LAST NAME BIOLOGICAL FATHER LAST NAME PROVIDER SIGNATURE OF CONSENT (REQUIRED): I certify that this patient (and/or their legal guardian, as necessary) has been informed of the benefits, risks, and limitations of the laboratory test(s) requested. I have answered this person’s questions. I have obtained a signed informed BIOLOGICAL MOTHER FIRST NAME BIOLOGICAL FATHER FIRST NAME consent from this patient or their legal guardian for this testing in accordance with applicable laws and regulations, including N.Y. Civil Rights Law Section 79-L, and will retain this consent in the patient’s medical record. SIGNATURE DATE / / BIOLOGICAL MOTHER DATE OF BIRTH BIOLOGICAL FATHER DATE OF BIRTH (PLEASE FILL OUT ADDITIONAL INDICATIONS ON BACK) / / CLINICAL INDICATION / / SPECIMEN TYPE: Patient: Peripheral Blood Saliva Other: Date of Collection:____/____/____ BILLING INFORMATION Bill Clinic Bill Insurance Below Self Pay Biological mother: Peripheral Blood Saliva Other: Date of Collection:____/____/____ POLICYHOLDER LAST NAME POLICYHOLDER FIRST NAME POLICYHOLDER DOB Biological father: Peripheral Blood Saliva Other: Date of Collection:____/____/____ / / Parental samples will be used as needed in follow-up to patient testing INSURANCE CARRIER INSURANCE ID GROUP NO.
    [Show full text]
  • Abstracts from the 52Nd European Society of Human Genetics (ESHG) Conference: Posters
    European Journal of Human Genetics (2019) 27:1814–1920 https://doi.org/10.1038/s41431-019-0493-3 ABSTRACTS COLLECTION Abstracts from the 52nd European Society of Human Genetics (ESHG) Conference: Posters Published online: 10 October 2019 © European Society of Human Genetics 2019 Volume 27 | Supplement 2 The Swedish Exhibition & Congress Center, Gothenburg, Sweden June 15–18, 2019 Sponsorship: Publication of this supplement was sponsored by the European Society of Human Genetics. All content was reviewed and approved by the ESHG Scientific Programme Committee, which held full responsibility for the abstract selections. Disclosure Information: In order to help readers form their own judgments of potential bias in published abstracts, authors 1234567890();,: 1234567890();,: are asked to declare any competing financial interests. Contributions of up to EUR 10 000.- (Ten thousand Euros, or equivalent value in kind) per year per company are considered “Modest”. Contributions above EUR 10 000.- per year are considered “Significant”. Electronic Posters Introduction: Carbamoyl phosphate synthetase 1 (CPS1) is a liver-specific enzyme with the lowest enzymatic rate, E-P01 which determines the overall rate of the other reactions in Reproductive Genetics/Prenatal Genetics the pathway that converts ammonia to carbamoyl phosphate in the first step of the urea cycle. Carbamoyl-phosphate E-P01.01 synthetase 1 deficiency which usually presents as lethal A Novel Missense Mutation in the CPS1 Gene Causes hyperammonemia, is a rare autosomal recessive hereditary arbamoyl phosphate synthetase 1 deficiency identified disease. Here we report a case of a two-day-old female by next generation sequencing neonate with lethal hyperammonemia. The newborn infant presented with hyperammonemia.
    [Show full text]