Cumulative Study Flashcards
WHICH ORGANISMS
cause
AOM
1 = STREPTOCOCCUS PNEUMONIAE
- *VIRUS = MOST COMMON**
- advocate to VACCINATE –> Influenze & Pneumococcal*
Moraxella Catarrhalis + HaemoPhilus Influenza
- Staphylococcus Aureus*
- rare but need for CLINDA for this*
When to consider:
OBSERVATION
Based on:
Age & Severity
Healthy Children:
6mo - 2y/o w/ non-severe illness & unilateral involvement
or
> 2 y/o** w/ **non-severe** illness & **no otorrhea (ear discharge)
Observation is:
Defer AB therapy for 48-72 hours
Schedule an RE-Evalulation // Communication
SNAP –> don’t fill RX until DR. conformation
2nd Line Treatment
For
SEVERE AOM
BILATERAL infection / OTORRHEA
Fever > 39*C (102.2*F)
- *CEFTRIAXONE**
- *IM QD x 3 days**
or
Cefdinir
QD - BID
Cefuroxime
BID
1st Line Treatment
For
NON-SEVERE AOM
Mild Symptoms / Unilateral Infxn / No Otorrhea
Fever < 39* (102.2F)
AMOXICILLIN** @ **80-90 mg/kg/day BID
HIGH DOSE –> needs to reach MIDDLE EAR
OR
OBSERVATION
defer AB for 48-72 hours
if observed & failed after 48-72 hours –> AMOX 80-90
Treatment if PCN allergy
For
NON-SEVERE AOM
Mild Symptoms / Unilateral Infxn / No Otorrhea
Fever < 39* (102.2F)
Cefuroxime - BID
or
Cefdinir - QD or BID
3rd Line Treatment
For
NON-SEVERE AOM
Mild Symptoms / Unilateral Infxn / No Otorrhea
Fever < 39* (102.2F)
After Failing AMOXICILLIN +/- Observation:
&
Failing AUGMENTIN:
CEFTRIAXONE - IM QD F3D
- *CLINDAMYCIN**
- may need ADDITIONALLY to cover* H.Influenzae
TYMPANOCENTESIS
TUBE to withdraw fluid or pus from middle ear
1st Line Treatment
For
SEVERE AOM
BILATERAL infection / OTORRHEA
Fever > 39*C (102.2*F)
AUGMENTIN** @ **80-90 mg/kg/day BID
When to Suggest < 10 day therapy
for
AOM
7 DAY THERAPY for:
2-5 y/ow/mild-Moderate AOM
- *5-7 Day Therapy** for:
- *>** 6y/o
Outpatient CAP Treatment
No recent AB therapy
<90 days
MACROLIDE** or **DOXYCYCLINE
-
ZPAK (500mg x1day -> 250mg x4days)
- 5 days, stays INSIDE cellls
-
Azithromycin XR Suspension 2gm
- one dose
-
Clarithromycin 250-500mg BID or XR 1gm daily
- no renal adjustment
- GI upset / Ototoxicity / 3A4 inhibitor
-
DOXYCYCLINE 100mg q12h
- 7-14 days
- no renal adjustment
- Teeth discoloration / GI Upset
- antacids / magnesium / iron / calcium
INPATIENT CAP Treatment
NON-ICU
B-LACTAM
cefuroxime / ceftriaxone / ertepenem / amp-sulbactam
+
MACROLIDE** or **DOXYCYLINE** or **RESPIRATORY FLUOROQUINOLONE
levofloxacin / moxifloxacin
INPATIENT CAP Treatment
ICU + PCN ALLERGY
RESPIRATORY FLUOROQUINOLONE
Levofloxacin + Moxifloxacin
+
AZTREONAM
1-2gm IVPB q8
instead of B-Lactam (ceftriaxone etc.)
INPATIENT CAP Treatment
ICU
B-LACTAM
cefuroxime / ceftriaxone / ertepenem / amp-sulbactam
ceftriaxone could be dosed 1gm IVPB q12
+
MACROLIDE** or **RESPIRATORY FLUOROQUINOLONE
levofloxacin / moxifloxacin, same doses
Common Organisms (6)
CAP
“SMH - MILC”
SMH = Same as AOM
STREPtococcus PNEUMoniae
M. Catarrhalis
H. Influenzae
Legionella + Influenza
Mycoplasma + Chlamydophilia
Outpatient CAP Treatment
Recent AB therapy (90days) or Comorbid Conditions
Chronic: Liver / Heart / Renal / Lung Disease
Diabetes / Malignancy
Diabetes / Asplenia / IMS disease-drugs
RESPIRATORY FLUOROQUINOLONE
Levofloxacin / Moxifloxacin / Gemifloxacin
OR
MACROLIDE + B-LACTAM
Zpak or Clarithromycin
Augmentin / Amoxicillin / Cefuroxime / Cefpodoxime
- *CURB-65**
- *PNEUMONIA TREATMENT**
Score:
0-1 = Outpatient
2 = Inpatient
> 3 = ICU
20 - 30/60/90
Confusion
Uremia = BUN > 20mg/dl
Respiratory Rate > 30
Blood Pressure < 90/60 mmHg
Age > 65
CAP Treatment
Length of Therapy
7-14 Days total
except for zpak (5days) / levofloxacin (750mg 5days)
Legionella = 7-10 days
When to COVER MRSA?
HAP
Risk factor for MDR
ABx <90 days / >5day hospitalization
VAP - Septic Shock / ARDS / Acute renal replacement therapy
Unit where patient is residing has:
>10% incidence of MRSA
Prevelence of MRSA NOT KNOWN
and/or
patient is INTUBATED
and/or
SEPTIC SHOCK
HAP Treatment if
MSSA ISOLATED
2-N-O-C
Nafcillin
2gm IVPB q4h
Oxacillin
2gm IVPB q4h
Cefazolin
2gm q8h
What HAP drug has DRUG INTERACTIONS?
& What drugs?
LINEZOLID
600mg q12h for MRSA Coverage
SSRI’s - Fluoxetine
TCA’s / Venlafaxine
Mirtazapine
TRAZADONE
HAP TREATMENT
2 DRUGS
for
Pseudomonas or Resistant Gram-NEG-
SECOND DRUG
“CCBM + FAP”
Antipseudomonal Fluoroquinolone
- *Levofloxacin** - 750mg IVPB qd
- *Ciprofloxacin** - 400mg IVPB q8h
- *AminoGlycoside**
- *Gentamicin / Tobramycin / Amikacin**
- *Polymixin**
- *Colistin** - 5mg/kg x1dose -> 2.5mg/kg IVPB q12h
- *Polymixin B -** 2.5-3mg/kg/day IVPB in TDD
HAP TREATMENT if
NO MRSA RISK FACTORS / No factors for Resistance
Empirically Cover with MONOTHERAPY“CLIP-M”
Cefepime
Levofloxacin
Imipenem
Piperacillin-Tazobactam
Meropenem
When to use
2 DRUGS
for
Pseudomonas or Resistant Gram-NEG-
Risk Factor for MDR
ABx <90 days / >5day hospitalization
VAP - Septic Shock / ARDS / Acute renal replacement therapy
Unit where patient is residing has a:
>10% incidence of RESISTANCE to the ANTBIOTIC
that is being considered for monotherapy
Prevelance is NOT KNOWN & INTUBATED
Or
patient has structural lung disease –> ↑risk of G- infxns
CYSTIC FIBROSIS**or**BRONCHIECTASIS
Risk Factors for
MULTI DRUG RESISTANT PATHOGENS
HAP
<90 day Antimicrobial Therapy
> 5 days of Hospitalization
Septic Shock @ time of VAP
ARDS preceding VAP
Acute Renal Replacement Therapy prior to VAP
HAP TREATMENT
2 DRUGS
for
Pseudomonas or Resistant Gram-NEG-
FIRST DRUG
“CCBM + FAP”
Antipseudomonal Cephalosporin
- *CEFtazadime** - 2gm IVPB q8h
- *CEFipime** - 2gm IVPB q8h
Antipseudomonal Carbapenem
- *Imipenem** - 500mg IVPB q6h
- *Meropenem** - 1gm IVPB q8h
- *B-Lactam_/_B-lactamase inhibitor**
- *Piperacillin / Tazobactam** - 4.5gm IVPB q6h
- *Monobactam**
- *Aztreonam** - 2gm IVPB q8h
Which TB Drug based on Target?
INHIBIT:
Mycolic Acid Synthesis - C60-90 alpha alkyl
&
target inhA = long chain NAD-dependent enoyl-ACP reductase
INH covalently attaches to nicotinamide ring of NADH@ side of hydride exhange
- *ISONIAZID** = INH
- *ETHIONAMIDE = ETH**
Hepatotoxicity** & **PERIPHERAL NEURITIS –> give B6
Both are:
Bacterial-Activated Prodrugs
Isoniazid is activated by Catalase Peroxidase = katG
Ethionamide is activated by Monooxygenase = etA
Which TB Drug based on Target?
binds to:
beta-subunit rpoB of RNA polymerase
changes conformation -> prevents binding of nucleotides & inhibits initiation of transcription
RIFAMYCINS
HEPATITIS + RED URINE
INDUCTION OF CYP450 ENZYMES –> ↓Half-Life of:
steroids / anticoagulants / macrolides / imidazoles
Protease inhibitors / NNRTIs
Rifampin
- *Rifabutin**
- less p450 activation –> recommended for HIV/TB co-infection*
- *Rifapentine**
- LONG HALF LIFE –> can be dosed WEEKLY in continuation phase*
Which TB Drug based on Target?
only active in vitro at low pH <6
Requires:
pncA
to generate the active agent = pyrazinoic acid
Sterilizing Activity
treatment 9mo –> 6mo
PYRAZINAMIDE
Significant HEPATOTOXICITY
↑ALT ↑AST
MOA IS UNCERTAIN
TB-SPECIFIC DRUG:
TB has deficient efflux compared to some naturally resistant mycobacteria
Which TB Drug based on Target?
inhibits:
ARABINOSYL TRANSFERASE
affecting the synthesis of:
arabinogalactan & lipoarabinomannan in cell wall
ETHAMBUTOL
OPTIC NEURITIS
visual acuity –> red-green differentiation
Isoniazid Resistance
PERIPHERAL NEURITIS –> GIVE B6
HEPATOTOXICITY
65% in
- *katG** = activating enzyme
- *Missense** or Large deletions in catalase peroxidase
20% in
- *inhA** = final target
- *mutations in NADH binding site**
Rifamycin Resistance
HEPATITIS + RED URINE
P450 INDUCER
Single AA substitutions in hotspot in:
rpoB
RNA polymerase subunit
Ethambutol Resistance
OPTIC NEURITIS
very low resistance
OVERexpression of:
embA**+**embB**+**embC
- *Rifabutin Uses**
- in comparison to RIFAMPIN*
- LESS ACTIVATION OF P450*
- rifampin –> strong p450 INDUCER*
Rifamycin of choice for:
HIV/TB Co-infection when using protease inhibitors
Active vs some:
Rifampin-resistant strains of M. TB
use for:
M.AVIUM - intracellulare infection
- *Rifapentine Uses**
- in comparison to RIFAMPIN*
- *LONGER HALF LIFE**
- *intermittent dosing** –> 2x a week for initial phase
ONCE A WEEK in Continuation phase
not active against Rifampin-resistant strains of M. TB
DiarylQuinoline = Bedaquiline
Uses for TB
Targets: ATP-SYNTHASE
5 month half life –> single dose
highly potent vs:
NON-REPLICATING M.TB = LATENT TB
FDA approved for MDR-TB when no other options available
Adr:
Prolonged QT Interval + Hepatotoxicities
Treatment for:
STAPH Aureus
Coagulase-Negative Staphylococci
PVE
(Prosthetic)
No resistance / Susceptible Strains
PVE STAPH = 3 DRUGS + >6 week treatment
Nafcillin** or **Oxacillin
12g per 24h
> 6 WEEKS
++++
Rifampin
900mg per 24 hours
> 6 WEEKS
+++
Gentamicin
3mg/kg per 24 hours
2 WEEKS
Treatment for:
STREP
Veridans / Gallolyticus / Abiotrophia / Granulicatella
NVE
(native valve endocarditis)
- *PCN - Intermediate Resistance**
- *MIC > 0.12 , <0.5**
- *Penicillin G Sodium**
- *24 million** units per 24 hours
- *4 WEEKS**
++PLUS++
- *Gentamicin**
- *3mg/kg** per 24 hours
- *2 WEEKS**
Treatment for:
STREP
Veridans / Gallolyticus / Abiotrophia / Granulicatella
NVE
(native valve endocarditis)
PCN ALLERGY
- *Vancomycin**
- *30mg/kg** per 24 hours in 2divdoses
- *4 WEEKS**
for
PVE –> 6 Week treatment