Microbiology 2 Flashcards
What are the host defences associated with the nasopharynx?
Nasal hairs
Ciliate epithelia
IgA
What are the host defences associated with the oropharynx?
Saliva
Sloughing
Cough
What is the common organism associated with epiglottitis?
Haemophilus influenzae type B (HiB)
What are some of the risk factors for getting epiglottitis?
being immunocompromised /immunosuppressed
Transmission of capsulated strain to unvaccinated host
How can you test which organism is causing the epiglottis?
Blood culture
Not throat swab due to irritating the throat and causing resp failure
What antibiotic do you treat epiglottitis with?
Ceftriaxone
What is Haemophilus influenza in terms of stain etc?
Gram negative coccobacillus
What are the host defences in the conducting airways? (trachea and bronchi)
Mucociliary escalator
Cough
AMP’s
Cellular and humoral immunity
How may you get infection in your conducting airways?
By trauma or incubation
Abnormalities with the ciliary elevator for example etc
What type of infections are more common in people with COPD?
Bacterial 50%
Viral 30%
Why are people with COPD more prone to infections?
Over time the inflammation leads to impaired cilliary clearance, effectively reduces the host’s normal defence and leads to increased susceptibility to infection. Which in turn leads to acute exacerbations of COPD. Causes of these exacerbations can be viral or bacterial, and the normal culprets are organisms we routinely associate with standard chest infections
What is one of the most commonly encountered organisms for COPD patients?
Moraxella catarrhalis. Which is a gram negative coccus
How would you test and treat infections in COPD?
Testing
- sputum culture
- sputum purulence
- CXR
Treatment
- only treat if increase in sputum purulence of new CXR change or pneumonia
What is the specific treatment for acute exacerbation of COPD?
- 1st line Amoxicillin 500 mg TDS (5 days)
- 2nd line Doxycycline 200mg D1 > 100 mg D2-5
Aim to cover in 1st instance H. influenzae, M. catarrhalis & S. pneumoniae
What is Cystic Fibrosis?
Inherited disease leads to abnormally viscous mucous – blockages of many tubular structures including conducting airways & lungs.