prevention and intervention in clinical practice
TRANSCRIPT
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Ototoxicity
Prevention and intervention in clinical practice
Alida Naudé PhD 2017-10-27 Pine Lodge Conference Centre 14:00-15:00
Who?
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Treating specialist
Dose regulation
Medication changes
Audiologist
Early intervention
Communication strategies
Counselling / Education
Who?
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Emotional well-being Reasoning skills Communication
Quality of life Coping skills
Stress
Speech/language development Social-emotional development Lifetime of medical expenses
Educational achievement Reasoning skills
Where?
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• Impacts the structure and function of: oVestibular & cochlear hair cells and their
supporting structures oThe vestibulocochlear (VIIIth) nerve
Where?
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What?
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xxx
• Amikacin, Gentamicin, Neomycin, Kanamycin, Netilmicin, Streptomycin, Tobramycin
Aminoglycoside antibiotics
• Erythromycin, Vancomycin, Chloramphenicol, Furazolidone, Polymyxin B & E, Trimethoprim-sulfamethoxazole Other antibiotics
•Ethacrynic acid, Furosemide, Bumetanide Loop diuretics
•Quinine, Chloroquine, Hydroxychloroquine, Primaquine, Quinidine, Pyrimethamine
Antimalarial drugs
•Aspirin, Nonsteroidal anti-inflammatory agents Salicylates
•Cisplatin, Carboplatin, Oxaliplatin, Nitrogen mustard, Methotrexate, Vincristine, Dactinomycin
Antineoplastic drugs
What?
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xxx Over 148 ototoxic chemicals
•benzene, benzyl alcohol, butyl alcohol, carbon disulphide (rubber, cellophane), carbon, tetrachloride, heptane, hexane, styrene, toluene, trichloroethylene and xylene
Organic solvents Skin*
•arsenic, cobalt, lead, manganese,
mercury and trimethyltin Heavy metals
Adhesives, auto emissions, fungicides, glues, grease, spot removers, insecticides, insulation lacquers, liquid correction fluid, organic solvents, paint, paint thinners, resins, room deodorizers, rug cleaners, spray paint, varnishes, and wood preservatives
What?
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Combination of stressors Noise +
•Mechanical energy oscillations transferred to the human body •Anterior, posterior SCC & utricular membrane
HAV WBV
•CBV Sympathetic
vasoconstriction
•Smoking •Painkillers •BP •Cholesterol
Life style factors
What?
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• Ototoxicity o Difficult to predict; poorly correlated with dosage, peak serum
levels, development of other toxicities e.g. renal toxicity • Depends on dosage, age, genetics, and concurrent exposure to
noise or other chemicals/drugs • Effects of multiple ototoxic agents may be synergistic, antagonistic,
and nonlinear
What?
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• Audiological evaluation • Case history
• Think drugs • Concurrently taking drugs, order of taking drugs • Synergistic relationship between drugs and noise
Aspirin, Cisplatin, Chlorampehnicol, Gentamicin, Kanamycin Gain & MPO
Everyday practice: Case History
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• Thorough and complete history • Impact current status • Impact future-based medical decision making
o Get the name o Ototoxic Drugs Exposed o Index of suspicion o Ototoxic drug list
Symptoms
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• Hearing loss (permanent, temporary, varying degree, from high to low frequencies)
• Tinnitus • Hyperacusis • Aural fullness • Imbalance/dizziness
Clinical objectives
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1. Pretreatment ototoxicity risk assessment to demonstrate the anticipated hearing loss in the conventional frequency range as a result of the prescribed dosing schedule.
2. Screening for early hearing changes to identify any ASHA-significant hearing shift within each patient’s individualized SRO, as measured directly using pure-tone threshold testing or estimated using DPOAE testing.
3. Screening for outer hair cell dysfunction DPOAEs to identify early, potentially preclinical damage.
4. Screen failure follow-up testing to determine the extent that hearing changes include frequencies in the conventional audiometric frequency range as measured directly using pure-tone threshold testing or estimated using DPOAE testing.
5. Screening for tinnitus to determine whether the drug treatment is instigating or exacerbating tinnitus and the need for a tinnitus management referral.
6. Patient and provider education about ototoxic-induced hearing and tinnitus, synergistic effects of ototoxins and noise overexposure, and rehabilitative solutions to hearing loss and tinnitus.
Clinical picture
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• Hearing loss and tinnitus • Impaired central auditory processing
o Synergistic relationship between chemical and noise Arsenic, butyl alcohol, butyl nitrite, heptane, hexane,
manganese, mercury and trimethyltin 11-20 times increased risk
What?
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• Audiological evaluation o Otoscopic examination o Tympanometry (incl acoustic reflexes) o Behavioral audiometry o Speech audiometry o OAEs o Staggered spondaic word test (SSW) o ABR
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<8 000 Hz (36% - Fausti et al., 2003)
Monitoring: Sensitivity range for ototoxicity air conduction (SRO), Otoscopy & tympanometry
Length of test, lack of equipment OAE
I/O function fine step frequency measures Test-retest reference limits Limited, protocol consistency
One method limitations Formal tinnitus monitoring procedures
No results for universal Grading of hearing loss
Chang Scale, Brock’s hearing loss grades, NCI CTCAE grades for children
QOL
Reflection on practices
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Reflection on practices
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Reflection on practices QOL
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The perception (physical and mental well-being) of the individual and not just their functional status
• Hearing handicap inventory for adults (HHIA) • Health-related quality of life questionnaire (HRQOL) • PedsdQLTM ( 6-18y) • Hearing handicap inventory for the elderly (HHIE-S) • Youth quality of life instrument – Deaf and hard of hearing module • Dizziness handicap inventory (DHI)
When?
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Baseline
M1 M2 M3
Post treatment
Long-term follow-up
TREATMENT
Design individualized monitoring programme
Adapted from Kathleen Campbell
Identify patients needing ototoxicity monitoring
Responsive Limited Responsive Non-Responsive
Soundproof booth Soundproof booth Soundproof booth Ward Ward Ward
Control noise Control noise Control noise
Full Audiometric Assessment Subjective measures Objective measures
Limited time: Subjective + Objective measures Objective measures
BASELINE MEASUREMENT
IN TREATMENT MONITORING / FOLLOW UP MEASUREMENT
POST TREATMENT MONITORING / FOLLOW UP MEASUREMENT
Tinnitus, noise and hearing surveys Otoscopy (video vs normal) Tympanometry and reflexes
Pulsed Pure tone AC/BC (extended high freq) Establish sensitivity range for ototoxicity (SRO)
Speech audiometry / DPOAE or ABR
Otoscopy Tympanometry and reflexes
DPOAE or ABR
Tinnitus, noise and hearing surveys Otoscopy
Tympanometry and reflexes Pure tone AC/BC and establish SRO
DPOAE (DP/TE/SF) or ABR
Tinnitus and noise surveys Otoscopy
Tympanometry and reflexes SRO (top freq ≤100dB + 6 below
DPOAE or ABR screen If changes – repeat
Tinnitus and noise surveys Otoscopy
Tympanometry and reflexes SRO
DPOAE or ABR screen If changes - repeat
Otoscopy Tympanometry and reflexes
DPOAE or ABR screen If changes - repeat
Inform team of any changes, continue monitoring
Monitoring protocol: 1 month / 3 months Baseline protocol: 6 months
Asha 1994
Repeated change ≥20 dB PTT change at 1 freq
≥10 dB PTT change at 2 adj freq Loss of response at 3 adj freq
2.4 dB 2002 / 7dB 2003 / 3-6dB 2011
Sensitive (> hit rate) Specific (< false positive rate)
Reliable (< test-retest variability)
Terminate, change or alter dose
Q U A L I T Y O F L I F E
Age
Threshold detection method Earphones Calibration
Intersubject variability
How?
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Assessment of hearing Assessment of balance
Baseline: PT pulsed 0.5, 1,2,3,4,6,8,9,10,11.2,12.5,14,16,18,20
Bedside DVA vHIT Head shake Postural control VNG Rotational testing
Documenting: Threshold detection method,
earphones
Why?
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1. Educate: Patients, caregivers, physicians 2. Counseling
• Potential impacts on auditory system • Signs and symptoms • Potential effects of noise exposure • Communication strategies
3. Early intervention critical for maintenance of QOL 4. Rehabilitation with use of amplification 5. Vestibular rehabilitation 6. TOMI
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Informed consent: Aware of side effects Alternative treatment Children
Implementation: Lack of education Time-consuming procedures Equipment / resources / staff Averse to vestibular testing Discharge from hospital Medical aid / keeping cost in check Cooperation Professional skill
(subjective complaints + risk identification, CPD)
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Record keeping – documentation
Research
Quality of life: returning to work etc
Under reporting due to fear of medico-legal issues
Infection control
Ototoxicity
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xxx
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