6 RESPI - Bronchopneumonia.
6 RESPI - Bronchopneumonia.
6 RESPI - Bronchopneumonia.
#6 RSP
Bronchopneumonia
Created by : Tim Draft SOOCA-PROX
BHP : PHOP :
1. (Beneficence) Penggunaan flue vaccine yang dilakukan 1. Primary level, pada negara berkembang - MTBS ( Management Terpadu Balita Sakit)
secara regular, apakah wajar atau tidak? 2. National level, untuk mengurangi mortalitas dan morbiditas Pneumonia
3. International level, untuk mengurangi mortalitas dan morbiditas Pneumonia
SakinaPS, AzizahNH, EvelineY, YasminAR, AdindaSN, FadhalMA, HasnaH, DeviA, DeaD Halo dr Proxima, semangat di tahun 3nya ya :D Semoga bisa sama-sama menjadi dr yang baik
Learning that we should know
• Explain the anatomy of upper and lower respiratory tract (Department of Anatomy).review • COPD
• Explain the histology of the respiratory tract wall and lung parenchyma (Department of Histology).REVIEW
• COPD
• Explain the growth and development of the respiratory tract (department of Biomedic).
• COPD
• Explain the gas exchange of the lung (Department of Physiology).
• Explain the physiology of respiration, pathophysiology of dyspnea and coughing (Department of • Coughing = Croup
Physiology).review
• Explain the acid-base balance of the blood and acidosis/alkalosis (Department of Biochemistry).review • COPD
• Explain the laboratory findings of pneumonia (Department of Clinical Pathology).
• Explain the microbiology findings of pneumonia (Department of Microbiology).
• Describe the anatomical pathology of pneumonia (Department of Anatomical Pathology).
• Describe the radiological findings of pneumonia (Department of Radiology).
• Explain the host defenses mechanisms of the respiratory tract (Department of Pediatric).
• Explain the clinical manifestation of pneumonia in children and adults (Department of Pediatric and Internal
Medicine).
• Explain the WHO guidelines for the management of cough or difficult breathing in under-5 child (Department
of Pediatric).
• Explain the epidemiology of pneumonia in children and adults (Department of Pediatric and Internal
Medicine).
• Explain the epidemiology of bacterial etiology of pneumonia in children and adults (Department of Pediatric
and Internal Medicine).
Learning that we should know
1. Physical barrier
Deposition: upper airway filtering system
GROWTH AND DEVELOPMENT CoughBatuk merupakan mekanisme normal untuk airway clearance. Batuk
OF RESPIRATORY TRACT dikarakteristikkan oleh 4 fase spesifik, yaitu:
Def: Merupakan perkembangan 1. Batuk dimulai dengan usaha yang cepat dan dalam dari respirasi (inspiratory phase)
dari respiratory tract (dan juga 2. Cepat dan dalamnya inspirasi dengan segera diikuti kompresi (compression phase)
organ) yang dimulai sejak minggu 3. Bukaan spontan dari glottis, high expiratory airflow, explosive sound. Collapse of the central
ke 4 di dalam kandungan. Bukan airways can occur (expressive phase)
hanya perkembangan paru-paru, 4. Relaksasi otot dan tekanan reversal (relaxation phase)
tapi juga perkembangan dari Mucocilliary escalator: trapping at mucus, moved by cilia
conducting pathways (trachea- Respiratory epithelium: punya fungsi physical barrier, antimicrobial function (mucus, Ig,
bronnchioles) lysozyme, lactoferrin, mucus proteinase inhibitor), regulatory function (neuropeptide
degrading enzymes, endothelin, NO, TGF-b), dan pro-inflammatory function (arachidonic acid
metabolites, inflammatory cytokines)
Secreted substances: ;ysozyme, surfactant-associated proteins, lactoferrin, fibronectin,
1. Prenatal Lung Growth 2. The Lung at Birth
antiproteases
1. Embryonic (days 26-52): Terjadi perubahan yang krusial pada
2. Pseudoglandular (days 52-week 16) fase ini. Epitel paru-paru berubah dari
2. Cellular-alveolar Mechanism
3. Canalicular (week 16-28) liquid secretion menjadi fluid
Phagocytosis by alveolar macrophage
4. Saccular (week 28-36) absorption. Aliran darah meningkat 20x
lipat. Cairan yang ada di dalam paru Identifyinitiation transmission from receptor efector collecting
5. Alveolar (week 36-term) pseudopodia pseupodia phagocyte fusion
akan diresorpsi oleh darah dan limfatik
Peningkatan pada phagocytosis, makrofag sekresi H2O2, kills bacteria
3. Postnatal Lung Growth Immunologic reactions
1. diameter trakea melebar sekitar kali lipat (triple) Macrophage initiate humoral and cellular immune system, B and T lymphocyte
2. jumlah alveolar meningkat sekitar 10 kali lipat antibody and cell mediated
3. massa tubuh meningkat sekitar 20 kali lipat. Immunoglobulins
4. hubungan anatomi lainnya dari paru-paru bayi dan anak adalah sama dengan Ig are present in the secretion of the upper and lower airways. In the upper
those in the adult’s lung. airways IgA accounts for 10% of the protein content. IgG is minimal (1%), and IgE is
5. Jumlah alveoli meningkat pesat dari 20 million sampai 200 million pada tahun found in trace amounts unless allergic rhinitis or autopsy presents. IgA seems to be
ketiga kehidupan, tetapi kemudian alveolar multiplication slows. most important for host defense, it is not clear how it functions.
6. Pada mature adult lung, , jumlah alveoli bervariasi 200-600 million, dan
individual diameter alveolus is 250-350 μm.
Common Cold
Definition : Management :
Common cold adalah penyakit yang disebabkan akibat infeksi - Istirahat
virus yang menyebabkan adanya runny nose, sore throat, - Mucolytic untuk mengurangi batuk
sneezing, dan coughing. - NO antibiotic
Etiology :
Viral Infection
- Rhinovirus (40%)
- Coronavirus (20%)
- RSV (20%)
- Parainfluenza
Risk Factor :
- Age (bayi 4-6 minggu memiliki risiko tertinggi)
- Orang sekitar yang sedang terinfeksi
Prevention :
ASI (untuk bayi), PHBS, dan tidur yang cukup
Microbial aspect of Streptococcus pneumonia Clinical Science of Pneumonia
• NORMAL FLORA PADA URT Rute Infeksi:
• Merupakan gram positif diplococci - Microaspiration dari sekresi oropharyngeal yang
• Berbentuk rantai, dilindungi oleh kapsul Def: Inflamasi akut pada terdapat koloni mikroorganisme
polisakarida. parenchym paru yang - Gross aspiration (biasanya pada CNS disorder)
• Di dalam solid media, sensitif terhadap menyebabkan adanya - Aerosolization
optochin test. infiltrasi sel-sel inflammatory - Hematogenous route
• Alfa-hemolitik. pada alveoli. - Contiguous spread
• Grows well on sheep blood agar.
Mempunyai pneumolysin : melisiskan Epidemiology
red blood cell pada kondisi anaerob (alfa- o Pneumonia is a common disease. The overall attack rate is about 12 cases per 1000 persons
hemolisis) per year.
o Pneumonia merupakan pembunuh utama anak dibawah usia lima tahun (Balita) di duniaDi
Virulence factor :
Indonesia berdasarkan hasil Riset Kesehatan Dasar (Riskesdas) tahun 2007, menunjukkan;
1. Polysaccharide capsule : melindungi dari phagocytosis, prevalensi nasional ISPA: 25,5% (16 provinsi di atas angka nasional), angka kesakitan
menghambat complement pathway (morbiditas) pneumonia pada Bayi: 2.2 %, Balita: 3%, angka kematian (mortalitas) pada bayi
2. Cell wall polysaccharide : inflammatory effect (enhance 23,8%, dan Balita 15,5%
vascular permeability, mast cell degranulation, etc)
3. Pneumolysin : cytotoxin. Menyebabkan cell lysis
Pathogenesis :
Pneumococci masuk via inhalasi, menempel pada epitel saluran pernafasan atas dengan
sebelumnya terkena infeksi virus (biasanya). Epithelial damage, disebabkan oleh infeksi
sebelumnya oleh virus di pernafasan atas, memudahkan pneumococci untuk menempel dan
berkolonisasi di epitel. Kegagalan dari mekanisme pertahanan tubuh spesifik (secretory IgA)
dan nonspesifik (cough, mucosal secretion, dan cilia transport) dapat memfasilitasi bakteri
untuk pindah menuju lower respi (bronchi and lung). Epithelial damage juga memungkinkan
pneumococci untuk menembus bloodstream. Dari darah mengalir menuju meningen dan
menyebabkan meningitis. Bisa juga secara langsung lewat nasopharynx.
Etiology
The effects of pneumolysin on ciliary beating of epithelial cells and the effects of the IgA1
protease secreted by pneumococci (see the section on virulence factors, above) might
impair these defense mechanisms.
Clinical Science of Pneumonia
Keterangan
Risk Factor
The type of agent (typical or atypical) causing the
infection,
• Typical pneumonias result from infection by bacteria
that multiply
extracellularly in the alveoli and cause inflammation and
exudation of fluid into the air-filled spaces of tthe alveoli
Clinical manifestation
Most children with pneumonia present with cough or difficulty breathing, • Aypical pneumonias are caused by viral and
but only the minority of children with these symptoms have pneumonia. mycoplasma infections that involve the alveolar
Bacterial pneumonia should be considered in children <3 years of age who septum and the interstitium of the lung. They produce
present with fever > 38.5, chest recession and increased respiratory rate less striking symptoms and physical findings than
>50 breaths/minute. If chest indrawing, nasal flaring, grunting or bacterial pneumonia; there is a lack of alveolar
crepitations are also present then the probability of pneumonia is increased infiltration and purulent sputum, leukocytosis, and lobar
further consolidation on the radiograph
Children with fast breathing pneumonia with Children age 2–59 Children aged 2–59 months with severe pneumonia1
no chest indrawing or general danger sign months with chest should be treated with parenteral ampicillin
should be treated with oral amoxicillin: at indrawing (or penicillin) and gentamicin as a first-line
least 40 mg/kg/dose twice daily pneumonia4 treatment.
(80mg/kg/day) for five days. should be treated — Ampicillin: 50 mg/kg, or benzyl penicillin: 50 000
In areas with low HIV prevalence, give with oral units per kg IM/IV every six hours for at
amoxicillin for three days. amoxicillin: at least five days
Children with fast-breathing pneumonia who least — Gentamicin: 7.5 mg/kg IM/IV once a day for at
fail on first-line treatment with amoxicillin 40mg/kg/dose least five days
should twice daily Ceftriaxone should be used as a second-line
have the option of referral to a facility where (80mg/kg/day) for treatment in children with severe pneumonia having
there is appropriate second-line treatment five days. failed on the first-line treatment.
Recommendation 4 Recommendation 5
Ampicillin (or penicillin when ampicillin is not available) plus Empiric cotrimoxazole treatment for suspected Pneumocystis
gentamicin or ceftriaxone are recommended as a first-line jirovecii (previously Pneumocystis carinii) pneumonia (PCP) is
antibiotic regimen for HIV-infected and -exposed infants and recommended as an additional treatment for HIV-infected and -
for children under 5 years of age with chest indrawing exposed infants aged from 2 months up to 1 year with severe or
pneumonia or severe pneumonia. very severe pneumonia.
For HIV-infected and -exposed infants and for children with Empirical cotrimoxazole treatment for Pneumocystis jirovecii
chest indrawing pneumonia or severe pneumonia (PCP) is not recommended for HIV-infected and -
pneumonia, who do not respond to treatment with ampicillin exposed children over 1 year of age with chest indrawing or severe
or penicillin plus gentamicin, ceftriaxone alone is pneumonia.
recommended for use as second-line treatment
Management of Children Illness or ‘ManajementerpaduBalitaSakit (MTBS)’ in Eradication of Acute Respiratory Infection Program
(Program Pemberantasan ISPA)