E Hagni Wardoyo-Respiratory Tract Infections Blok Respirasi

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    Respiratory tract infectionE. Hagni Wardoyo

    Clinical MicrobiologyMataram, 4 Juni 2014

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    Anatomy

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    Functional perspective

    deliver air from the outside to the alveoli ALL THE TIME Increase the risk of microorganisms colonization and infectio

    Anatomical barrier of infection

    Normal biota barrier

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    Anatomical barrier

    nasal hair, mucociliary cells

    coughing,

    secretory immunoglobulin,

    defensins,

    phagocytic inflammatory cells

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    Normal biota

    The normal biota of the nasopharynx and oropharynx helpsthe host by preventing colonization by pathogenic organism

    for the same nutrients

    and the same receptor sites on host cells.

    produce bacteriocins: bacterial products that are toxic to popathogens

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    Normal biota stimulate natural immunesystem of the host

    Preventscolonization

    of pathogen

    keeps the immunesystem primed fora rapid response

    to invading

    organisms

    stimulates crosprotective

    immune facto

    known as natu

    antibodies

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    Normal biota bacteria usually present

    Streptococcus mitisand other -hemolytic streptococci

    Nongroup A -hemolyticstreptococci

    Streptococcus pneumoniae

    Streptococcus pyogenes

    Streptococcus salivarius

    Veillonellaspp.

    Bacteroidesspp.

    Fusobacteriumspp.

    Prevotellaspp.

    Porphyromonasspp.

    Coagulase-negative staph

    Neisseriaspp.

    Nonhemolytic streptococ

    Diphtheroids Micrococcusspp.

    Eikenellaspp.

    Capnocytophagaspp.

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    Normal biota

    bacteria occasionally present

    Haemophilus influenzae

    Haemophilus parainfluenzae

    Peptostreptococcus

    Actinomycetes

    Staphylococcus aureus

    Mycoplasma

    Fungus and virus

    Candida spp

    Herpes simplex virus

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    Normal biota shifting

    Common normalbiota

    Differentpharyngeal biota

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    Detect microorganism: colonize or infec

    Microorganismsisolated from the

    pharynx

    Colonization?Infection?

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    Things to consider

    Microorganism detection primary or possible pathogen?

    A high-quality sample improve the clinical value of tculture results

    A high-quality sample [i.e sputum] meaning minimizes contamination by oral biota

    is collected before initiation of antibiotic

    Interpretation of the result must be based on several factors Characteristics of the specimen

    Which compatible clinical syndrome should be present

    the presence of a potential pathogen is clinically relevant

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    Selected Nonviral Pathogens in theRespiratory Tract

    Primary Pathogens Streptococcus

    pneumoniae

    Group A -hemolyticstreptococci

    Neisseriameningitidis

    Neisseriagonorrhoeae

    Bordetella pertussis

    Mycobacteriumkansasii

    Mycobacteriumtuberculosis

    Legionellapneumophila

    Toxin-producingCorynebacteriumdiphtheriae

    Mycoplasmapneumoniae

    Chlamydiatrachomatis

    Chlamydophilapneumoniae

    Pneumocystis jiroveci(carinii)

    Possible Pathogens Acinetobacter spp.

    Enterics and other gram-negative b

    Fungi

    Nocardiaspp.

    Staphylococcus aureus

    Haemophilus influenzae

    -Hemolytic streptococci, nongrou

    Moraxella catarrhalis

    Anaerobes

    Mycobacteriumspp.

    Actinomycetes

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    Case analysis 1

    Microbiology diagnostic flow

    few colonies

    Staphylococcusaureus from a

    sputum specimen

    Quality of sputum

    Low leukocyte, high

    epithelial cells

    Clinically relevant

    Young man with

    mild symptoms ofcoughing

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    Case analysis 2

    Microbiology diagnostic flow

    heavy growth

    coloniesStaphylococcus

    aureus from a

    sputum specimen

    Quality of sputum

    High leukocyte, low

    epithelial cells

    Clinically relevant

    an elderly man with

    post-influenzapneumonia

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    Seasonal and Community Trends in Infe

    Viral: seasonal infections of the respiratory tract

    Mycoplasma pneumonia occur throughout the year, withouseasonal variability

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    Microbial diagnostic flow

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    Alur prosedur Lab MK

    Pra-

    analitik

    Intra-

    analitik

    Pasca-

    analitik

    Mikrobiologi Klinik

    Klinisi terkait Klinisi terkait

    Konsensus prosedur laboratorium Mikrobiologi klinik-PAMKI 2

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    Diagnosis mikrobiologi

    Keterangan klinis pasien dapat mengarahkan jenis mikroorgyang diharapkan: bakteri, virus, jamur

    Jika diagnosis menjurus pada bacterial Direct smeardiagnosis presumtif pemilihan antibiotika empi

    pemilihan media pembenihan

    Diferensiasi kolonisasi dan infeksi kualitas specimen

    Proses pembenihan only strong suggested pathogen will highlygrowth expected

    Identifikasi

    Uji AST memerlukan pertumbuhan ulang pada media MHA dengankuman terstandar

    TAT antara 36-72 jam

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    Viral

    Direct smear tidak aplikatif

    Kultur virus (tidak rutin)

    Memerlukan media telur, sel HeLa

    Lama

    Polymerase chain reaction (TAT 3-4 jam)

    Lebih cepat dan sensitive Uji AST (tidak rutin)

    Infeksi virus HIV

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    Fungal

    Direct smear

    Hyphae

    Filamen

    Spora

    Budding yeast

    Kultur

    Menggunakan media Saborroud agar

    Pertumbuhan 1-2 minggu

    Uji sensitivitas antifungal (tidak rutin)

    Hanya pada infeksi jamur dimorfik atau yeast (Candida spp)

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    Upper Respiratory TractInfections

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    Case

    Seorang anak laki-laki usia 4 tahun yang tidak menerima vak

    rutin dibawa ke klinik dengan riwayat demam sejak 6 jam ylkesulitan menelan. Pemeriksaan fisik ditemukan stridor inspVisualisasi epiglottis dengan proteksi airway menunjukkan akemerahan dan edema

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    Direct swab cultures of the epiglottis

    Blood cultures

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    d h l

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    Proceed with culture

    Id ifi i

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    Identification

    A ibi i ibili i

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    Antibiotic susceptibility testing

    T i k ih

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    Terimakasih

    CR Mahon, DC Lehman, G Manusellis. Textbook of Diagnost

    Microbiology. 4th edition. 2011. WB Saunders. Missouri

    Konsensus Mikrobiologi. 2005. Jakarta