CF Flashcards

1
Q

clinical presentation

A

increased cough
increased sputum production
SOB
chest pain
loss of appetite
weight loss

decreased FEV1
decreased FVC

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2
Q

Common pathogens of CF

A

pseudomonas aeruginosa**
strenotrophomonas maltophilia
MRSA**
acchomocter xylosoxidans
burkhoderia cepacia complex**
nontuberculosis mycobacteria

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3
Q

initial antimicrobial selection

A

typical pathogens for age
recent culture data
recent outpatient antiimicribial use
previous abx that result in clinical improvement
allergies
advere effects

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4
Q

mucoid

A

slimy or viscous consistency of bacterial colony

caused by the adaptation that assist the bacteria with resisting antibiotic

seen w persistent pseudomonas infections

aggressive therapy in CF

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5
Q

antibiotic selection for pulmonary exacerbation

A

no clear consensus what should be prescribed

target most common organism in respiratory tract

quarterly sputum collection for empiric therapy

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6
Q

pulmonary exacerbations =

A

respiratory symptoms + decline in lung function

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7
Q

two antibiotics

A

decreased resistance
higher cost
toxicity risk

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8
Q

one antibiotic

A

increased resistance
reduced cost
reduced toxicity

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9
Q

most centers us a two antibiotic regimen for CF exacerbations to target what

A

Pseudomonas

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10
Q

what is the outcome of using two different mechanism of action

A

synergistic activity in vitro

ex: AMG+ beta lactam

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11
Q

when is acute inpatient management indicated

A

severe exacerbations
resistance to oral antibiotics
failure to resolve exacerbations

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12
Q

antibiotic selection for acute inpatient is based on

A

sensitivities
microbial culture
renal function
previous clinical response

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13
Q

routes for acute pulmonary exacerbations

A

oral
IV
aerosolized

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14
Q

first treatment options for Pseudomonas

A
  • tobramycin, amikacin
    -cirprofloxacin
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15
Q

second treatment options for Pseudomonas

A

-piperacillin/tazobactam
-ceftazidime, cefepime
-carbapenem, meropenem, imipenem

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16
Q

treatment option for stenotrophonas maltophilia

A

-sulfamethoxazole/trimethoprim
-levofloxacin
-ceftazidime
-piperacillin/tazobactam

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17
Q

treatment option for MRSA

A

vancomycin ***
linezolid **
sulfamethoxazole/trimethoprim
ceftaroline
clindamycin

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18
Q

if MSSA treatment

A

may use beta lactase except ceftazidime (poor coverage)

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19
Q

treatment option for stenotrophomonas maltopilia

A

-sulfamethoxazole/trimethoprim
-levofloxacin
-ceftazidime
-piperacillin/tazobactam

20
Q

treatment option for burkholderia cepacia complex

A

-sulfamethoxazole/trimethoprim
-doxycycline
-ceftazidime
-meropenem

21
Q

How long are CF drugs administered and what are the drugs commonly used for pseudomonas

A

longer period of time

beta lactams
-cepfepime
-ceftazidime
-imipenem
-meropenem
-piperacillin/tazobactam
-

22
Q

PK of CF

A

larger volume of distribution
faster clearance
larger antibiotic doses and shorter dosing intervals
therapeutic drug monitoring and necessary dosage and regimen adjustments are critical

23
Q

dosing strategies of AMG

A

high doses, extended interval doses

monitoring: random only
less doses and TDM
lower is of toxicity

higher doses=higher peaks

extended intervals=lower troughs= lower troughs =lower toxicity

24
Q

TOPIC study Conclusion

A

IV tobramycin had equal Efficacy given one vs three times a day for CF
once a day is less nephrotoxic

25
what is the guideline Recommendations dosing for AMG for cf pulmonary exacerbation
once a day dosing
26
what is the long time consequence of AMG in CF?
INCREASED RISK FOR VESTIBULAR LOSS (HEARING LOSS)
27
Is it sufficient to recommend an optimal duration of antibiotic treatment of an acute exacerbation of pulmonary disease?
No, but most centers treat 10-14 days
28
monitoring during pulmonary exacerbations
FEV1 to normal baseline, if possible symptoms improvement c-reactive protein procalcitonin
29
AMG monitoring
peak, trough, or random renal function panel twice weekly CBC with differential weekly 'vestibular testing (annually or those with frequent toobramycin
30
beta lactam monitoring
CDC with differential weekly renal function panel weekly liver functiobtest and bilirubin baseline and when therapy > 14 days (pip.taz, ceftriaxone, imipenem, meropenam
31
vancomycin monitoring
Target AUC: 400-600 mcg*hr/L random level and trough before dose when patient reaches steady state renal function panel twice weekly
32
Fluroquinolones monitoring
avoid use with QT prolongation
33
linezoid monitoring
CBC with differential weekly liver function tests serotonin syndrom
34
other considerations for CF pulmonary exacerbation
bronchodilator mucoytic enzyme mucolytic inhaled inhaled antibiotic
35
chronic management of CF
inhaled antibiotic Tobramycin
36
Tobramycin dose
300 mg INH BID x 28 days on , alternated with aztreonam
37
ADR of tobramycin
discolored sputum, altered voice, hearing loss
38
when is tobramycin recommended ?
>=6 yo with mild to severe lung disease w peresistent pseudomonas in sputum culture
39
when is aztreonam recommended ?
>=6 yo with mild to severe lung disease w peresistent pseudomonas in sputum culture
40
aztreonam dose
75 mg INH TID x 28 on, alternated with tobramycin
41
ADR of aztreonam
coughing weezing
42
anti-inflammatory therapy of CF
AZithromycin
43
when is azithromycin recommended in CF
>=6 yo w persistent p. aeruginosa infection utilized for antimicrobial (may decrease p. aeruginosa) and anti-inflammatory (decrease neutrophils) properties
44
what do patients need to be screened for to prevent resistance before taking azithromycin
non tuberculosis mycobacteria
45
what does the guideline stronly recommend for the prevention and eradication of initial p.aeruginosa
the use of inhaled tobramycin 300 mg BID for 28 days
46
when is prophylactic antimicrobial therapy used in CF
generally reserved for persistent p. aeruginosa infections and is recommended last during chronic pulmonary clearance therapy