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ANATOMI,PEMERIKSAAN FISIK

TELINGA DAN TES PENALA


01
ANATOMI TELINGA
• Telinga luar terdiri dari
daun telinga dan liang
telinga sampai membran
timpani
• Telinga Tengah benbentuk kubus dengan :
- batas luar : membrane timpani
- batas depan : tuba eustachius
- batas bawah : vena jugularis (bulbus jugularis)
- batas belakang : aditus ad antrum, kanalis fasialis
pars vertikalis
- batas atas : tegmen timpani (meningen/otak)
- batas dalam : berturut-turut dari atas ke bawah
kanalis sirkularis horizontal, kanalis fasialis, tingkap
lonjong (oval window), tingkap bundar (round window)
dan promontorium
• Telinga dalam terdiri dari koklea
(rumah siput) yang berupa dua
setengah lingkaran dan
vestibuler yang terdiri dari 3
buah kanalis semisirkularis.
02
PEMERIKSAAN FISIK TELINGA
Alat yang diperlukan untuk pemeriksaan telinga :
1. Lampu kepala
2. Corong telinga
3. Otoskop
4. Pelilit kapas
5. Pengait serumen
6. Pinset telinga
7. Garputala
 Pasien duduk dengan posisi badan condong sedikit ke
depan dan kepala lebih tinggi sedikit dad kepala
pemeriksa untuk memudahkan melihat liang telinga
dan membran timpani.
 Mula-mula dilihat keadaan dan bentuk daun telinga,
daerah belakang daun telinga (retro-aurikuler) apakah
terdapat tanda peradangan atau sikatriks bekas
operasi.
 Dengan menarik daun telinga ke atas dan ke
belakang, liang telinga menjadi lebih lurus dan akan
mempermudah untuk melihat keadaan liang telinga
dan membran timpani.
 Pakailah otoskop untuk melihat lebih jelas bagian-
bagian membran timpani.
 Otoskop dipegang dengan tangan kanan untuk
memeriksa telinga kanan pasien dan dengan tangan
kiri bila memeriksa telinga kiri.
 Supaya posisi otoskop ini stabil maka jari kelingking
tangan yang memegang otoskop ditekankan pada pipi
pasien.
03
Tes penala
• Tes Rinne  tes untuk membandingkan hantaran
melalui udara dan hantaran melalui tulang pada
telinga yang diperiksa.
• Tes Weber  tes pendengaran untuk
membandingkan hantaran tulang telinga kiri
dengan telinga kanan.
• Tes Schwabach  membandingkan hantaran
tulang orang yang diperiksa dengan pemeriksa
yang pendengarannya normal.
• Tes Bing (tes Oklusi)
- Cara pemeriksaan : Tragus telinga yang
diperiksa ditekan sampai menutup liang
telinga, sehingga terdapat tuli konduktif kira-
kira 30 dB. Penala digetarkan dan diletakkan
pada pertengahan kepala (seperti pada tes
Veber).
- Penilaian : Bila terdapat lateralisasi ke telinga
yang ditutup, berarti telinga tersebut normal.
Bila bunyi pada telinga yang ditutup tidak
bertambah keras, berarti telinga tersebut
menderita tuli konduktif.
• Tes Stenger  digunakan pada pemeriksaan
MACAM-MACAM PENALA

• Penala terdiri dari 1 set (5 buah) dengan


frekuensi 128 H2,256 Hz, 512 Hz, 1024 Hz dan
2048 Hz.

• Pada umumnya dipakai 3 macam penala  512


Hz, 1024 Hz, 2048 Hz.

• Jika akan memakai hanya 1 penala, digunakan


512 Hz.

• Untuk mempermudah interpretasi secara klinik,


dipakai tes Rinne, tes Weber dan tes Schwabach
secara bersamaan
Cara pemeriksaan
• Tes Rinne :
Penala digetarkan, tangkainya diletakkan di prosesus mastoid,
setelah tidak terdengar penala dipegang di depan telinga kira-
kira2 1/2 cm. Bila masih terdengar disebut Rinne positif (+), bila
tidak terdengar disebut Rinne negatif (-).
• Tes Weber :
Penala digetarkan dan tangkai penala diletakkan di garis tengah
kepala (di verteks, dahi, pangkal hidung, di tengah-tengah gigi
seri atau di dagu). Apabila bunyi penala terdengar lebih keras
pada salah satu telinga disebut Weber lateralisasi ke telinga
tersebut. Bila tidak dapat dibedakan ke arah telinga mana bunyi
terdengar lebih keras disebut Weber tidak ada lateralisasi.
• Tes Schwabach :
Penala digetarkan, tangkai penala diletakkan pada prosesus
mastoideus sampai tidak terdengar bunyi. Kemudian tangkai
penala segera dipindahkan pada prosesus mastoideus
telinga pemeriksa yang pendengarannya normal. Bila
pemeriksa masih dapat mendengar disebut Schwabach
memendek, bila pemeriksa tidak dapat mendengar,
pemeriksaan diulang
dengan cara sebaliknya yaitu penala diletakkan pada
prosesus mastoideus pemeriksa lebih dulu. Bila pasien masih
dapat mendengar bunyi disebut Schwabach memanjang dan
bila pasien dan pemeriksa kira-kira sama-sama
mendengarnya disebut dengan Schwabach sama dengan
pemeriksa.
Referensi

Soepardi EA, Iskandar N, Bashiruddin J, Restuti RD. Buku Ajar Ilmu Kesehatan
THT-KL FK UI. Dalam: Gangguan Pendengaran dan Kelainan Telinga. Edisi ketujuh.
Jakarta: Badan Penerbit FKUI; 2012
THANKS
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TABLE OF CONTENTS

01 02 03

INTRODUCTION BACKGROUND METHODOLOGY

04 05 06

RESULTS DISCUSSION CONCLUSION


WHAT IS A MEDICAL
BREAKTHROUGH?

A medical breakthrough:
● Represents a significant advancement in the field of
medicine
● Challenges conventional medical practices
and beliefs
● Holds the potential to revolutionize treatments,
improve patient outcomes and save lives

In summary, a medical breakthrough can revolutionize


medical care and improve patient lives
INTRODUCTION

PROBLEM STATEMENT CONTEXT


Clearly state the specific problem or Provide context and emphasize the
challenge in the medical field. importance of addressing the identified
Emphasize its significance and impact, challenge. Discuss existing knowledge
highlighting gaps or limitations in or approaches, emphasizing the gaps or
current knowledge or approaches that limitations that hinder progress and
motivate the need for a breakthrough drive the need for innovative solutions
BACKGROUND

CURRENT EMERGING BREAKTHROUGH


LANDSCAPE TRENDS VISION
Highlight the current challenges Focus on emerging medical Outline a visionary goal for the
and limitations in the medical trends, technologies, or breakthrough, such as curing a
field that require a scientific discoveries that disease or revolutionizing
breakthrough. Describe the present an opportunity for a procedures. Highlight the
healthcare problems, diseases or breakthrough. Discuss the broader impact on healthcare
conditions that need innovative potential benefits, such as more and global quality of life
solutions accurate diagnostics or
preventive measures
METHODOLOGY

STUDY DESIGN DATA COLLECTION


Outline the research design for the medical Explain the methods and tools used for data
breakthrough. Describe the type of study, collection, including patient records or
sample size, inclusion criteria and ethical examinations. Emphasize data accuracy and
considerations patient privacy

DATA ANALYSIS RESULTS VALIDATION


Describe the approach for analyzing the Discuss the steps taken to validate the results.
collected data. Explain the statistical methods Explain how the findings will be reviewed,
or qualitative analysis techniques used to confirmed or peer-reviewed for scientific
derive meaningful insights rigor
RESULTS
DATA ANALYSIS QUANT. RESULTS QUAL. RESULTS
Present the analyzed data from Focus on numerical results Discuss qualitative findings from
the study. Describe the methods derived from the analysis. interviews or surveys. Present
used for analysis and highlight Present percentages, means or themes, patterns and include
key findings and trends correlations and use visual aids examples

COMPARISON LIMITATIONS CONCLUSIONS


Compare results with existing Acknowledge study limitations. Summarize the findings and their
literature or previous studies. Discuss challenges faced during implications. Discuss the impact
Highlight similarities, data collection, analysis and on medical practice, patient care
differences, and novel insights interpretation or future research
for knowledge
50%
Reduction in complications

10x faster
This treatment is 10 times faster than previous treatments

85%
Success rate for the breakthrough
95%
Use percentages in your breakthrough presentation to quantify
and communicate the frequency or proportion of an important
finding
COLUMN CHART
UNDERSTANDING
THE NUMBERS
Use this slide to present data on the
outcomes of patients who have
received treatment for a particular
condition or disease. A column chart
can be an effective way to illustrate
changes in patient outcomes over
time. Consider including data from
clinical trials or real-world patient
populations to showcase the impact

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MILESTONES

Discovery Preclinical research Early phase Phase I clinical trial


clinical trial

Phase II clinical trial Phase III clinical trial FDA review Post-market monitoring
TREATMENT OPTIONS
TREATMENT OPTION EFFICACY RATE SIDE EFFECTS COST AVAILABILITY

Medication A 80% Mild $$ Widely available

Medication B 70% Moderate $$$ Available only with prescription

Surgery 90% High $$$$ Requires specialized facilities

Radiation therapy 75% Moderate $$ Available in most hospitals

Immunotherapy 65% Moderate $$$$ Available only in select medical centers

Physical therapy 60% Mild $$ Widely available


CLINICAL TRIAL PHASES
PHASE 1: SAFETY AND DOSAGE PHASE 2: SIDE EFFECTS

● Participants: 20-100 healthy volunteers ● Participants: up to several hundred people with the condition
● Objective: to determine safe dosage and identify side effects ● Objective: to determine effectiveness and further evaluate
● Duration: 6 months safety
● Success rate: 80% of participants completed the trial without ● Duration: 12 months
experiencing significant side effects ● Success rate: 65% of participants experienced a significant
improvement in symptoms

PHASE 3: LARGE-SCALE TESTING PHASE 4: POST-MARKET MONITORING

● Participants: from several hundred to thousands of people ● Participants: thousands of people with the condition who are
with the condition taking the drug
● Objective: to confirm effectiveness, monitor side effects, and ● Objective: to monitor long-term safety and effectiveness and
compare to detect rare side effects
standard treatments ● Duration: ongoing
● Duration: 24 months ● Success rate: no safety concerns identified in the two years
● Success rate: new treatment was better in 75% cases since the approval for market use
DATA AND STATISTICS
KEY PERFORMANCE INDICATOR NUMBER TREND IN PATIENT OUTCOMES
Patients treated 2,500
● Illustrate the trend in patient outcomes
Success rate 95% over time
● Highlight the impact of the medical breakthrough on
Average recovery time 3 days patient outcomes
● Describe any significant changes or improvements
observed in the graph
● List the key performance indicators (KPIs)
relevant to the medical breakthrough
● Enter the values or metrics for each KPI in the
table
● Discuss the significance of each KPI and its
relation to the breakthrough
● Highlight any notable achievements or milestones
reflected in the table

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IMPLICATIONS
“It's been a true lifesaver for me. I can enjoy life again without any discomfort”

—JOHN SMITH, PATIENT

“I've seen a significant improvement in patient outcomes. This breakthrough makes treatment more
efficient and personalized”

—DR. JANE DOE, MEDICAL PROFESSIONAL

“We are impressed with the safety and effectiveness of this breakthrough. It will greatly benefit patients
and healthcare systems”

—SANJAY PATEL, REGULATORY BODY REPRESENTATIVE


KEY MEMBERS
MARK JONES SARAH JAMES
Use a sentence that describes Use a sentence that describes
their job their job

Role: Lead researcher Role: Clinical trial manager

Contributions: Contributions:
● You can enter a description of the contributions ● You can enter a description of the contributions
here here
● You can enter a description of the contributions ● You can enter a description of the contributions
here here
● You can enter a description of the contributions ● You can enter a description of the contributions
here here
RESULTS AND CONCLUSIONS
BACKGROUND CONCLUSIONS
Briefly introduce the context of the investigation, such as the medical condition or Briefly summarize the main findings of
problem being addressed and the goals 1 the study or analysis
STUDY DESIGN
Discuss the implications of the findings
Describe the design of the study, such as whether it was a randomized controlled 2 and how they relate to the original
trial or observational study, the sample size and the inclusion and exclusion criteria
research question

FINDINGS REFERENCES
Summarize the main findings of the investigation, including statistical results and
any important trends or patterns observed
Include a reference page with the sources used
in your presentation. List the sources in
IMPACT alphabetical order and include the author's
name, the title of the source, the publication
Discuss the implications of the findings for patients, healthcare providers and other date and the publisher or URL
stakeholders.
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