Infectious Disease Flashcards
(70 cards)
Fever without source
fever of one week or less
history, physical, labs don’t show source
Fever of Unknown Origin (FUO)
Fever for at least 8 days
history, physical, labs don’t show source
PNA triad
tachypnea + high fever+ cough
Rigors
sudden feeling of cold, shivering, rise in temp, sweating
-higher probability of SBI
-can indicate serious non-bacterial
-dengue, malaria, chikungunya
Localizing signs of SBI in Children
- lethargy, irritability, change in mental status
- tachycardia disproportinate to degree of temp elevation
- tachypnea or labored respirations
- bulging or depressed anterior fontanel
- nuchal rigidity
- petechiae
- localized erythema, tenderness, or swelling
- abdominal or flank tenderness
- fever
risk factors for occult bacteremia
- 36 mts or younger
- > 39.5 C or 103.1F
- WBC ≥ 15,000 or ≤ 5,000
- total band cells ≥1500
- ESR ≥ 30 mm/hr
- underlying chronic disease (malignancy, immunodefeciency, sickle cell, malnutrition)
- clinial appearance (irritability, lethargy, toxic appearance)
Diagnostic work up: ≤90 days
Fever criteria- 100.4 or higher
CBC w/ diff, cath urine, blood/urine culture, CRP, procalcitonin
if ≤29 days or if concerns- lumbar puncture
stool studies/ culture- if diarrhea
WBC alone not reliable, viral PCR can be helpful but don’t stand alone
chest x ray if respiratory sysmptoms- tachypnea, hypoxia, rales, wheezes, increased WOB
Diagnostic work up: 3-36 mts
3-24 mts- 102.2 w/o clear source
24-36 mts- 103.1 w/o clear source
- if not at increased risk, at least 2 doses of prevnar PCV12- do not need blood testing
- if at increased risk because unimmunized, unknown vaccine status, or 1 dose prenar- may need screen eval w/ CBC, blood and urine cx
infants w/ temp >102.2
- urine testing- females < 2, uncircumcised < 1 yr, circumcised < 6 mts
infants w/ temp >103.1 & WBC > 20,000- chest x ray to detect occult pna
Diagnostic work up: > 36 mts
- lab eval dependent on H&P
- work up for chronic disease - sickle cell, cancer, immunodeficiency, nephrotic syndrome, cardiac transplant
- children w/ CP- higher chance of UTI
- chidlren w/ CF- increased risk of respiratory infection
- cognitive impairment- higher chance of LRT d/t decreased ability to clear airway
Common organisms for SBI/ Occult Bacteremia- ≤ 3 mts
E coli
Group B strep
streptococcus pneumoniae
listeria monocytogenes
salmonella (> 1 mt)
haemophilus influenzae type b (> 1 mt)
Common organisms for SBI/ Occult Bacteremia- 3-36 mts
s. pneumoniae
neisseria meningitidis
salmonella
staphylococcus aureus
HIB
Meningitis
Inflammation of the meninges
CSF -elevated protein count, low glucose
Meningitis Etiology 2 weeks
Group B Strep
E Coli
Enterococcus
Listeria monocytogenes
Meningitis Etiology 3-6 wks
group b strep
HIB
Streptococcus pneumoniae
Neisseria meningitides
E. coli
Listeria monocytogenes
Meningitis Etiology 7 weeks-15 yrs
HIB
Streptococcus pneumoniae
Neisseria meningitides
Meningitis etiology > 15 yrs
Streptococcus pneumoniae
Neisseria meningitides
streptococcus
Meningitis clinical signs
hyper/hypothermia, jaundice, hepatomegaly, lethargy, poor feeding, vomiting
bulging fontanel in 1/4 - late onset, rarely nuchal rigidity
Meningitis - early onset
- first 5 days, death rate 20-50%
- acquired at delivery
- typically secondary to septicemia from maternal infection (vertical transfer)
- e coli or GBS
Meningitis-late onset
- after 5-7 days, death rate 20%
- post natal symptom onset
- e coli, GBS, enterococci, gram negative enteric bacilli (i.e klebsiella), listeria moncytogenes
Meningitis treatment- newborn
- ampicillin & aminoglycocide (gentamycin) or cefotaxime
- +/- acyclovir
- older than 1 week - vancomycin + gentamycin
- treat for 2 weeks at least beyond sterile CSF (typically 14-21 days)
- sequelae: hydrocephalus, CP, epilepsy, cognitive impairment, deafness
Erythema Infectiosum (fifth disease) etiology, transmission, incubation
parovirus B19
respiratory route, blood, blood products
incubation 4-28 days
Parovirus clinical manifestations
- prodromal phase - LGF (15-30%), HA, Mild URI
- Rash (afebrile)- hall mark characteristic
- begins w/ facial flushing (slapped cheek)
- spreads to trunk and extremeties as diffuse macular erythema
- central clearing- lacy, reticulated appearance
- waxes & wanes for 1-3 wks
- can recur w/ exposure to sunlight, heat, exercise, stress
Erythema Infectiosum complications
- arthropathy - more common in adults and older adolscents after infections, joints most affected are hands, wrists, knees, ankles
- transient aplastic crisis - increased risk for sickle cell pts
- immunocompromised pts at risk for chronic infection- chronic anemia, neutropenia, thrombocytopena, or complete bone marrow suppression, treated w/ IVIG
- primary maternal infection associated w/ fetal hydrops and IUFD
Erythema Infectiousum diagnosis/ differentials/ treatment
Diagnosis
- typically based on clinical symptoms
- antibody testing available, usually not done in peds
- PCR testing
Differntials
-rubella, measles, enterovirus infections, drug rx
arthralgias- JRA, SLE
Treatment- symptomatic