peds resp. Flashcards

1
Q

def. asthma

A

inflammatory disorder of the airway char by paroxysmal or persistnet Sx associated with variable degree of airflow limitations and responsiveness of the airway to stim.

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2
Q

Sx suggestive of athsma

A
  • freq. breathlessness, wheeze or cough
  • Sx worse at night or in early AM
  • dev with infection, excercise, exposure to allergens
  • after playing or laughing
  • better with roids or dilators
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3
Q

2 requirements for asthma diagnosis

A
  1. FEV1/FVC 12% with dilators (in adults must be over 200ml)
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4
Q

how to diagnose in preschoolers

A
  • not able to do PFTs

- need careful Hx and PHx

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5
Q

what is in asthma predictive index

A
>4 wheezing episodes in past year
PLUS
ONE major crit.:
- parent with astma
- atopic dermatitis
- allergen sens
OR
2 minor crti.:
-food sens
- peripheral eosinophilia
- wheezing not related to infection
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6
Q

what is goal of asthma Sx management

A

want them to be asymtomatic

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7
Q

what are two main therapeutic targets

A
  1. smooth muscle dysfunction

2. airway inflammation

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8
Q

2 main types of meds and their types

A
  1. controllers
    - roids
    - LTRA
    - amalizumab
  2. relievers
    - SABA
    - LABA
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9
Q

what are guidelines for controller therapy

A
  1. regular controller therapy indicated for those with poor asthma control
  2. ICS are first line for all ages
    - second line is LTRA
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10
Q

if taking low dose ICA, what are three options to increase

A
  1. increase to mod or high dose
  2. add LABA
  3. add LTRA
    - not enough evidecne for
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11
Q

what is reccomendation for adults with low dose ICS for escalation

A

add a LABA

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12
Q

what is reccomendations for children on low dose ICS

A

mod or high dose

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13
Q

what is recc for children on mod-high dose ICS

A

add a LABA

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14
Q

what is CF

A
  • auto recc. disorder
  • affects lung, panc, intestines, liver
  • affects CF transmembrae regulator
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15
Q

what is CFTR needed for

A

allows Cl out to keep a good layer of airway surface fluid

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16
Q

what are 6 classes of CF

A
  1. no protein
  2. poor folding- not on surface
  3. gets to surface, doesn’t work
  4. doesn’t work well
  5. not very many
  6. less stable
17
Q

what are 2 types of CF and what classes in each

A
  1. panc. insuff
    - !,2,3
  2. panc suff
    4,5,6
18
Q

3 things that influence CF outcomes

A
  1. genes
  2. env.
  3. time
19
Q

what is needed for CF diagnosis

A
clinical features compatible OR CF in sib OR +ve newborn screeen
PLUS
lab evidence
- sweat test
- nasal PD
- 2 disease causing mutations
20
Q

what is levels for sweat test

A

sweat Cl > 60 is pos
30-60 intermediate
panc. insuff. have lower mean sweats

21
Q

what are newborn screening steps

A
  1. check for trypsinogen on blood spot
  2. if elevated, check for 35 DNA mutations
  3. is mutations found - sweat test
22
Q

Tx of pulm. manifestations for CF

A
  • chest physio
  • mucolytics
  • ABs
  • SABA
  • ICS
  • O2
  • lung transplant
23
Q

Tx of extra-pulm manifestations

A
  • enzyme replacement
  • ADEK vits
  • high cal, high fat diet
  • ursodiol
24
Q

def. Obst. Sleep Apnea

A

recurrent events of full or partial complete upper airway obst. during sleep

25
Q

what defines severe OSA

A

apnea-hyponea index >100/hour

26
Q

2 general issues that make the balance

A
  1. neuromuscular activation

2. structural narrowing

27
Q

2 ways to diagnose

A
  1. Hx and Phx - poor accuracy

2. polysomnogram

28
Q

Tx for OSA

A

adenotonsillectomy

- cures 80%