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66 Cards in this Set

  • Front
  • Back
Types of ACTIVE Tb (3)
1)progressive primary Tb
2)reactivation Tb
3)Extrapulmonary Tb
Progressive Primary Tb

Reactivation Tb (2)
a)disease continues to spread and cause illness

b)1/2 of em will happen within 2yrs of primary infexn
b)most common in lung apices
Extrapulmonary Tb (2 and can occur where (3))
1)most common in immunocomp
2)MILIARY is large inoculum in blood leading to disseminated disease (emergency)

1)pleural disease
2)lymphatic
3)bone/joint
S/sx of ACTIVE Tb (6)
1)wt loss
2)fatigue
3)productive cough
4)fever
5)night sweats
6)hemoptysis
HIV presentation w/ ACTIVE Tb (4)
1)minimal CXR changes
2)negative skin test
3)decr s/sx
4)extrapulmonary disease
Basics of medication regimens for ACTIVE pulmonary Tb (3)
1)initially 4 drugs for first 8wks to prevent selection of resistant MOs
2)then con't phase w/ isoniazid and rifampin, when resistant is not a prob
3)tailor regimens to susceptibility results
4 Drug Active Tb regimen
a)initial phase
b)con't phase
a)isoniazid, rifampin, pyrazinamide, ethambutol FOR 2MONTHS (ethambutol can be cut AT ANY TIME if strain is found to be fully susceptible)

b)isoniazid and rifampin FOR 4-7MONTHS
3 Drug Active Tb regimen
a)initial phase
b)con't phase
c)when to use
a)Isoniazid, Rifampin, Ethambutol 2months (no cutting off ethambutol)
b)isoniazid, rifampin

c1)liver disease
c2)gout
c3)pregnancy
If initial phase is
a)Isoniazid
b)Rifampin
c)Ethambutol
d)Pyrazinamide
DAILY x 2months OR 5d/wk x 2months what are possible continuation phases (3)
Isoniazid and Rifampin daily x18wks or daily 5d/wk x18wks

Isoniazide and Rifampin twice weekly x18wks

Isoniazid and Rifapentin once weekly x18wks
If initial phase is
a)Isoniazid
b)Rifampin
c)Ethambutol
d)Pyrazinamide
Daily x2wks then twice weekly for 6wks OR daily 5d/wk x 2wks then twice weekly x6wks then what are possible continuation phases (2)
Isoniazid and Rifampin twice weekly for 18wks

Isoniazid and Rifapentine once weekly for 18wks
Active Tb therapies that are ALWAYS DOT (3)
1)5d/wk
2)2x weekly
3)3x weekly
1x weekly Rifapentine can only be used if pt is.... (4)
1)HIV-
2)no cavitary disease on initial CXR
3)2month sputum smear (-) for AFB
4)no extrapulmonary Tb
Who gets 7month conintuation phase (4)
1)caviatation on initial CXR (and 2month sputum culture is +)
2)HIV+
3)whose initial phase did NOT include pyrazinamide
4)treated w/ once-weekly isoniazid and rifapentine (and 2 months sputum culture is still +)
Most people get what regimen? (most = what?)
2months of isoniazid, rifampin, ethambutol, pyrazinamide daily THEN

4months of isoniazid/rifampin daily or 2x/wk

specimen collected @ end of initial phase is NOT + or is + but pt is NOT HIV+ or had cavitation on initial CXR
Active Therapy for Tb is ultimately determined by...
NUMBER OF DOSES GIVEN
Pts are no longer considered infectious if: (3)
1)are on adequate therapy
2)have a sig clinical response to therapy
3)have had 3 straight (-) sputum smears
HIV+ considerations in Active Tb tx (5)
1)9months total of tx
2)NO 2x/wk therapy if CD4 is under 100
3)CI to 1x/wk rifapentine
4)use rifabutin in place of rifampin if pt is on retrovirals
5)have poorer prognosis
Pregnancy/lactation considerations in Active Tb tx (5)
1)9months of tx (w/o pyrazinamide)
2)NO use of AG's
3)caution w/ ethionamide and FQ's
4)LTB can be deferred until 2nd trimester
5)most antimycobacterial's are in breast milk, but are safe
Kids considerations in Active Tb tx (3)
1)tx similar to adults
2)therapy often extended for 9months
3)all first line agents except rifapentine are safe
Tb Tx Failure if: (and what to do) (3)
1)sputum (+) after 5-6mon
2)reassess susceptibility and add 3 NEW bactericidal drugs
3)DOT is advised
If Tb Tx Relapse do what? (3)
1)perform sensitivity
2)consider DOT
3)use same regimen; change as C&S show resistance
General info about resistance in Tb (4)
1)multi drug therapy needed to prevent resistance
2)resistance higher in HIV+
3)resistance higher in foreigners
4)isoniazid and rifampin are best meds for preventing resistance
Suspect the following pts of Tb resistance (7)
1)prior Tb tx
2)pt from high prevalence areas (NYC, mexico)
3)homeless
4)institutionalized
5)IVDU
6)HIV+
7)exposure to resistant strain
Tests that tell you pt is Tb resistant (3)
1)AFB smears + @ 2mon of tx
2)AFB cultures + @ 2-4mon of tx
3)pt who fail or relapse
MDR-Tb is resistant to... (2)

XDR-Tb is resistant to... (4)
Isoniazid and Rifampin

Isoniazid, rifampin, FQ's, AG's
Tx of MDR/XDR Tb (3)
1)REQUIRES CARE FROM A SPECIALIST****
2)no standard regimen
3)generally prolonged isolation and tx
Monitoring Pts w/ AFB+ Smears (4)
1)smears should be repeated every 1-2wks until 2 strait (-) smears
2)sputum cultures performed monthly until 2 strait (-) cultures
3)if smears are (+) after 2wks, susceptibility should be repeated
4)Chem/LFT/CBC @ baseline and periodically
Monitoring Pts w/
a)(-) pretx smears
b)other monitoring parameters (3)
a1)check CXR and s/sx improvement

b1)audiometric testing @ baseline/monthly for streptomycin pts
b2)vision testing on all pts who receive ethambutol
b3)all pts (+) for Tb should be tested for HIV******
Most important monitoring parameter
ADHERENCE AT EVERY CONTACT W/ PT
Isoniazid ADR's (5)
1)hepatoxicity
2)peripheral neuropathy
3)CNS effects
4)lupus-like syndrome
5)hypersensitivity
Rifampin ADR
Ethambutol ADR
Rifabutin ADR
red-orange discoloration (will stain contacts)

retrobulbar neuritis (decr red-green discrimination)

uveitis (hazy vision, floaters)
Hepatoxicity in isoniazid, pyrazinamide and rifampin manifests how? (6)
1)ab pain
2)incr LFTs
3)n/v
4)loss of appetits
5)fatigue
6)dark colored urine
Peripheral neuropathy in isoniazid manifests how? (3)
1)tingling/burning in hands/feet
2)numbness
3)weakness
How to prevent peripheral neuropathy w/ isoniazid and in whom is at risk (6)
PYRIDOXINE 25-50MG/D******

1)DM
2)HIV
3)renal failure
4)alcoholism
5)nutritional deficiency
6)pregnancy
Isoniazid Hepatotoxicity
a)is worse in... (4)
b)avoid in...
a1)pre-existing liver disease
a2)elderly
a3)postpartum/pregnancy
a4)combined w/ rifampin

b)baseline LFTs 6-8x normal
Characterisitcs of Non-tuberculous mycobacteria (4)
1)in environment (soil, water, animals)
2)inhalation or direct inoculation from environment
3)no evidence of person to person spread
4)less virulent than Tb (opportunistic infexn)
Non-tuberculous mycobacteria
a)slow growing MOs (2)
b)rapid growing MOs (3)
a1)M.avium
a2)M.interacellulare

b1)M.fortuitum
b2)M.chelonae
b3)M.abscessus
MAC
a)MOs
b)general characteristics (4)
a)M.avium and M.intracellualar

b1)incr'd w/ AIDS epidemic
b2)infects immunosuppressed and immunocompetent pts
b3)in environment (soil, water, food)
b4)no person to person transmission
MAC tx (3 drugs but 5 things total)
1)ATLEAST 2 DRUGS

clarithromycin/azith AND
Rifampin/rifabutin AND
ethambutol

Treat for 1yr after - culture
Prophylaxis of MAC in HIV+ pts (2)
1)if CD4 is under 50
2)azith 1200mg qweek or clarith 500mg bid
Normal amount of WBC in CSF
less than 5/mm
Common pathogens in Meningitis in:
a)Newborn to 1month (3)
b)1month to 4yrs (2)
c)5-29yrs (2)
d)30-60yrs (2)
e)over 60yrs (2)
a1)Group B strep
a2)E.coli/Kleb/Enterobacter
a3)Listeria

b1)S. pneumo
b2)N. meningitidis

c1)N. meningitidis
c2)S. pneumo

d1)S. pneumo
d2)N. meningitidis

e1)S. pneumo
e2)E.coli/Kleb/Enterobacter
Mengitis
a)s/sx (4)
b)signs (2)
a1)fever
a2)nuchal rigidity (hurts to turn head)
a3)altered mental status
CLASSIC TRIAD ARE ABOVE 3
a4)purpuric/petechial skin rash (in meningococcal infexn)

b1)Kernig sign
b2)Brudzinski sign
BACTERIAL Meningitis
a)WBC
b)Differential
c)Protein
d)Glc
a)1000-5000

b)over 80 PMNs

c)100-500

d)over 40-60% of serum
VIRAL Meningitis
a)WBC
b)Differential
c)Protein
d)Glc
a)100-1000

b)50 lymphocytes

c)30-150

d)over 30-70% of serum
Fungal Mengitis
a)WBC
b)Differential
c)Protein
d)Glc
a)40-400

b)over 50 lymphocytes

c)40-150

d)over 30-70% of serum
Initial treatments of Mengitis (2)
1)supportive care w/ f/e, analgesics/antipyretics
2)NOTHING SHOULD DELAY ABX ADMIN
Abx selection for Mengitis (2)
1)empiric coverage is needed until pathogen is found
2)based it on pt's allergies, age and medical conditions
Abx penetration into CNS (6)
1)inflammation of meninges incr abx penetration
2)low MW pass more easily
3)lipid soluble abx penetrate better
4)low protein binding pass into CSF (b/c higher free fraction)
5)maximize abx dosing to get adequate CSF penetration
6)use IV, intrathecal, intracisternal
Mengitis abx
a)dosing
b)duration of tx (2)
a1)more aggressive to achieve CSF penetration

b1)at least 48-72h or until dx of bacterial mengitis can be ruled out
b2)cont therapy should be based on clinical course, c&s
Dosing of ____ for Mengitis
a)Cefotaxime
b)Ceftriaxone
c)PenG
d)Vanco
a)8-12g daily (divided up q4-6h)

b)4g daily (divided up q12-24h)

c)24mU daily (divided up q4h)

d)30-45mg/kg daily (divided up q8-12h)
Conjunctive use of corticosteroids in mengitis
a)in who? (2)
b)benefits (2)
c)disadv
d)dosing (3)
a1)kids w/ H.flu or S.pneumo
a2)in adults w/ S. pneumo

b1)decr neurologic sequelae
b2)decr bad outcomes/death

c)decr CSF []s of abx due to decr inflammation

d1)kids 2months and older get 0.15mg/kg q6h for 4 days
d2)adults get 0.15mg/kg q6h for 2-4 days
d3)must be given 10-20min prior OR WITH first dose of abx to be effective
USE DEXAMETHASONE
EMPIRIC THERAPY for Mengitis
a)new born - 1month
b)1month-4yrs
c)5yrs-29yrs
d)30-60yrs
e)over 60yrs
a)amp plus 3rd gen cephalosporin OR AG

b)vanco plus 3rd gen cephalo

c)vanco plus 3rd gen cephalo

d)vanco plus 3rd gen cephalo

e)vanco PLUS amp PLUS 3rd gen cephalo

3RD GEN CEPHALO = CEFTRIAXONE OR CEFOTAXIME
N. Meningitidis (MENINGOCOCCUS)
a)characteristic s/sx
b)tx (3)
a)purpuric/petechiae lesion or rash (50%)

b1)pen susceptible: penG or amp
b2)pen resistant: 3rd gen cephalo
b3)other: meropenem or FQs
FOR ATLEAST 7DAYS
N. Meningitidis (MENINGOCOCCUS) PROPHYLAXIS (6)
adults) rifampin 600mg q12h x4

kids 1month and OLDER) rifampin 10mg/kg q12h x4

kids under 1month) rifampin 5mg/kg x4

ALT)IM ceftriaxone 250mg/125mg for adults/kids under 12
ALT)PO cipro 500mg in adults/kids over 12

Meningococcal vaccine
S. pneumo Meningitis tx (3)
Pen susceptible: penG or amp
Pen intermediate: 3rd gen cephalo or meropenem
Pen resistant: Vanco PLUS 3rd gen cephalo
LAST FOR 10-14D
S. pneumo Meningitis prophylaxis
a)for who? (4)
b)what?
a1)over 65yo
a2)2-62yo w/ chronic illness, live in LTC or alaska, lack fxning spleen
a3)immunocompromised over 2yo
a4)college kids in dorms

b)Heptavalent conjugate vaccine for kids 2months and older
H. flu Meningitis tx (3)
BL negative: amp
BL positive: 3rd gen cephalo
alt: cefepime/FQs
FOR ATLEAST 7DAYS
H. flu Meningitis prophylaxis
a)for who?
b)what? (4)
a1)ppl not vaccinated

b1)kids: rifampin 20mg/kg/d x4
b2)adults: rifampin 600mg/d x4
b3)kids 12-48months get 1dose
b4)kids 2-11 months get 3 doses
N. mengiditis who get prophy? (2)
1)young kids are @ greatest risk
2)all household, daycare, military contacts
Listeria Monocytogenes Meningitis
a)tx (3)
b)prophy
a1)penG or amp PLUS gentamicin
a2)alt: bactrim or meropenem
a3)tx for 2-3wks after defervesence and the AG can be stopped after 10d

b)NONE
G- Meningitis (Enterbacter/Psuedomonas/Salmonella)
a)tx (2)
a1)for pseudomonas give cefepime, ceftazidime, OR meropenem PLUS AG

a2)others MOs you give 3rd or 4th gen cephalo

TREAT FOR 21DAYS
Viral Encephalitis causes (4)
1)Coxsackievirus A/B
2)Echovirus
3)Enterovirus
4)HSV (50-85% mortality w/o tx)
Tx of viral encephalitis (2)
FOR HSV:
a)acyclovir 10mg/kg IV q8h for 2-3wks
b)if resistant give foscarnet (watch for renal toxicity)

FOR OTHERS:
supportive care fluids, antipyretics/analgesics
CNS Abscess tx (2)
1)SURGERY
2)3rd gen cephalo
HAP (hospital pneumonia)
a)org's (2)
b)drug to tx (5) (w/ best 3 starred)
a1)pseudomonas
a2)enterobacter

b1)imipenem/meropenem****
b2)pip/tazo*****
b3)tobramycin/amikacin*****
b4)cefepime
b5)ceftazadime