2. INTRODUCTION
Respiratory tract infection refers to any of a
number of infectious diseases involving
the respiratory tract
It is classified in to 2 types they are:
UPPER RESPIRATORY TRACT INFECTION
LOWER RESPIRATORY TRACT INFECTION
A respiratory tract infection (RTI) is any of a number
of infectious diseases involving the respiratory tractinfection
of this type is normally further classified as an upper
respiratory tract infection (URI or URTI) or a lower
respiratory tract infection (LRI or LRTI). Lower respiratory
infections, such as pneumonia, tend to be far more serious
conditions than upper respiratory infections, such as
the common cold.
3.
4. PATHOGENESIS
Host Factors
Nasal hairs
Convoluted passage
Mucus lining
Secretary IgA
Nonspecific antibacterial substances
Cilia
Reflexes such as coughing, sneezing & swallowing.
Microorganism Factors
Adherence
Colonization
Fimbriae
Toxins
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9. Viral infections : e.g
Influenza A
Respiratory syncytial virus (RSV)
Human metapneumovirus (hMPV)
Varicella-zoster virus (VZV)
Chickenpox
10. symptom
Cough (especially if lasting for 3 weeks or longer) with or without sputum production
•Coughing up blood (hemoptysis)
•Chest pain
•Loss of appetite
•Unexplained weight loss
•Night sweats
•Fever
•Fatigue
11.
12. Medical history, physical examination
Test for TB infection (TB skin test or TB blood
test)
Chest radiograph (X- ray), and
Appropriate laboratory tests
Diagnosis of TB disease
13. LABORATORY DIAGNOSIS
Specimen collection and Transport
A. Sputum
1. Expectorated
Food should not have been ingested for 1-2 hours before
expectoration.
Mouth should be rinsed with saline or water just before
expectoration.
The patient should be standing, if possible or sitting upright in bed.
He or she should take deep breath to full the lungs, and empty then in
one
breath, coughing as hard and as deeply as possible.
Sputum brought up should be spit into screw capped container.
Visually inspect the specimen.
Tighten the cap of the container and send immediately to lab
14. Collection of sample of sputum (Day1)
1-before collecting sputum the mouth should be prerinsed and this removes
contaminants from oral cavity.
2- give the patients a clean dry wide necked leak-proof container and request
him or her to cough deeply to produce a sputum specimen.
3-for the best result early morning freshly expectorated sputum specimen
should be collected.
15. Examination
Volume:
A 24 hr volume of sputum is measured in patient with chronic bronchitis , lung
abscess or bronchial asthma. A rising volume indicates worsening & decreasing
volume indicates improvement
16. Appearance:-
Purulent: Green looking, mostly pus
Mucopurulent: green looking with pus & mucus.
Mucoid: mostly mucus
Mucoslivary: mucus with small amount of saliva.
17. Lab diagnosis for AFB patients
CBC (Complete Blood Count ) is normal
Usually moderate normochromic or
slightly hypochromic anemia
Thrombocytosis may be seen
Anemia may be there due to the
chronic debiliting nature of the disease
ESR & CRP are raised
18.
19. Used when few Bacilli are present
Reduces time needed for testing
Beter conclusion with one or two specimens unlike Ziehl Neelsen method needing 3 or more
specimen
Florescent microscopy
20.
21.
22.
23.
24. Result
AFB Red, straight or slightly curved rods, occurring singly or in a
small groups, may appear beaded.
Cells Green
Background material Green
27. Culture of the specimen
To obtain as pure a culture as possible of respiratory pathogens it is necessary
to reduce the number of commensals inoculated. Ways of reducing
commensal number include washing the sputum free from saliva or liquefying
and diluting it. The technique using saline- washed sputum described. The
dilution technique requires a liquid agent such as dithiothreitol (sputolysin
sputasol) wich is expensive and unstable.
28. Culturing Mycobacterium
Culturing on1- Lowenstein Jenson remain the affordable , economical method in developing world
Mycobacterium spp are slow growing needed for 6-8 weeks for growing, so the sample can be
contaminated while growing.
As even few bacilli can be grown in spite of smear negativity
2-liquid medium
3- agar medium
29. Each specimen received for culture
should be plated on agar
Different agar:-
1- blood agar
2- chocolate agar
3-macConkey agar
4- Thioglycolate broth
30. blood agar and chocolate agar
1 – wash a purulent part of sputum in about 5ml of sterile physiological saline
2- inoculate the washed sputum on plate of :
Blood agar
Chocolate agar
3- add on optochin disc to the blood plate within the area of 2 nd spread.
This will help to identify Sterptococcus pneumonia
4- incubate the blood agar plate aerobically and the chocolate agar plate in a
carbon dioxide enriched atmosphere.
31. Day2 and onward
Examine and report the culture
Blood agar and chocolate agar cultures
Look specially for a significant growth of :
Stre. Pneumonia
Haemo. Influenzae
Staph. aureus