Pediatric Vaccines Flashcards

1
Q

5 types of vaccines

A
  1. Live attenuated
  2. Inactivated
  3. Viral particles
  4. Subunit
  5. toxoid
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2
Q

what 3 vaccines are live attenuated

A

MMR
Flu Mist
Varicella

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3
Q

Toxoid vaccine example

A

tetneus

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4
Q

what are the 4 groups in which a vaccine is contraindicated

A
  1. Pregnant
  2. Compramised immune system
  3. anaphylactic reaction
  4. Moderate or severe illness currently
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5
Q

what is the allergy that should not get the flu vaccine

A

Egg or chicken allergy

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6
Q

Common Misconceptions These are NOT contraindications 3

A

fever
breast feeding
antibiotics

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7
Q

when do you want to give 2 live virus

A

same time if not 28 days apart

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8
Q

what you should know for vaccines

A
  1. 1st does
  2. Last does
  3. Contraindications
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9
Q

Meningococcal Conjugate Vaccine is also called

A

MCV 4

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10
Q

MCV4 first does

A

11

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11
Q

MCV 4 booster

A

16

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12
Q

high risk Meningococcal

A

2-10 year old

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13
Q

Contraindications to MCV4 3

A

i. Latex allergy
ii. History of life-threatening allergic reaction to diphtheria toxoid
iii. Previous history of Guillain-Barré Syndrome (GBS)

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14
Q

what ages gets the flu shot

A

2-49

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15
Q

who should NOT get the flu vaccine 5

A

i. children 2-17 years receiving aspirin or aspirin-containing products persons who are allergic to eggs
ii. pregnant women
iii. immunosuppressed persons
iv. children 2-4 years of age with asthma or who had wheezing in the past 12 months
v. persons who have taken influenza antiviral medications in the previous 48 hours

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16
Q

what is the vaccine for RSV

A

Synagis

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17
Q

what is the most serious normal reaction to a vaccine

A

i. Low grade fevers (<101.5F)

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18
Q

what are the abnormal reaction to a vaccine 4

A

i. crying for >3 hr
ii. High fever >104-105F
iii. Seizure
v. Anaphylactic reaction

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19
Q

Roseola infantum caused by what

A

Human Herpes Virus 6 or 7

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20
Q

Roseola infantum ages

A

6 months - 3 years

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21
Q

Roseola infantum textbook

A
  1. fever > 104 3 days
  2. rash that starts on trunk and spreads to head
  3. adenopathy
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22
Q

Roseola infantum treatment

A

supportive

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23
Q

a. Erythema Infectiosum “Fifth’s disease”

cause

A

. Parvo B-19

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24
Q
  1. Lace-like rash (trunk/limbs) follows slapped cheeks

What disease

A

Erythema Infectiosum “Fifth’s disease”

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25
Fifth’s disease treatment
supportive
26
i. Candida albicans yeast infection of the oral mucosa
Oral Candidiasis “thrush"
27
Oral Candidiasis “thrush" treatment
Nystatin suspension | Treat mom PRN
28
a. Enterobiasis (Enterobus vermicularis) “Pinworms” | symptoms 2
1. Asymptomatic | 2. Anal itching
29
nterobiasis (Enterobus vermicularis) “Pinworms” treatment 2
1. Mebendazole | 2. Treat the whole family
30
a. Molluscum Contogiosum | what virus
Pox
31
i. Bacterial infection of the meninges of the brain and spinal cord
a. Bacterial Meningitis
32
i. Suspected bacterial meningitis = emergency; untreated mortality almost 100%
TRUE
33
Bacterial Meningitis | 1-3 months
a. Group B streptococcus
34
Bacterial Meningitis | 3 months - 10 years
a. S. pneumonia
35
Bacterial Meningitis | 10 years - 19 years
a. N. meningitides
36
i. Petechial rash of N. meningitides:
does NOT blanch
37
i. Keep index of suspicion high in children…it may look A LOT like many other Peds infections
TRUTH
38
i. Bottom line: it’s bacterial meningitis until proven otherwise
truth
39
Defined as disorders resulting from inherited defects of the immune system (both isolated and combined defects)
1. Primary Immunodeficiency | - a. Defect may be present in any part (or multiple parts) of the immune system, including the humoral immune system
40
Humoral immunodeficiency
impaired antibody (Ig) production
41
Recurrent, severe URI/LRTI, including OM, sinusitis, pneumonia Infection w/ encapsulated bacteria (Hib, S pneumo, N menigitidis, Group B strep, Klebsiella pneumoniae, Salmonella typhi)
Primary immunodeficiency
42
Most common immunodeficiency
Selective IgA Deficiency
43
Deficiency of serum IgA (w/ normal IgG & IgM) in a child > 4 yo
Selective IgA Deficiency
44
Selective IgA Deficiency MC symptoms
asymptomatic
45
Any of the following: Giardiasis (GI infection w Giardia lamblia, intestinal protozoan) Family Hx of any primary immunodeficiency
Selective IgA Deficiency
46
Impaired B-cell, T-cell and dendritic cell production impaired Ig production
Common Variable Immunodeficiency
47
``` Criteria: Reduced serum IgA, IgG & IgM Presence of B-cells Poor response (or no response) to vaccines Absence of other immunodeficiency ```
Common Variable Immunodeficiency
48
S/S: Chronic or recurrent URI/LRTI May develop bronchiectasis (even in peds!), watch for abnormal CXRs GI infections Diarrhea, malabsorption, weight loss FTT Atopic triad
Common Variable Immunodeficiency
49
A severe defect in both the T- & B-lymphocyte systems, which leads to early death from overwhelming infection, typically in the first year of life
Severe Combined Immunodeficiency
50
Multiple forms- most common form is X-linked (males only) “bubble boy” disease Part of newborn screening in all states
Severe Combined Immunodeficiency
51
Children may become ill from live vaccines: varicella, MMR, OPV or RV Infant may not have a visible thymus on CXR
Severe Combined Immunodeficiency
52
Manifestations: Persistent mucocutaneous candidiasis (thrush) Death from common viral infections (CMV, VZV, EBV, HSV, flu, etc.) P. jirovecii infection Intrauterine graft-vs-host disease- caused by transplacental maternal T-cells Lymphoma and other malignancies
Severe Combined Immunodeficiency
53
Therapy managed by Immunology | Stem cell transplantation
Severe Combined Immunodeficiency
54
Chromosomal deletion (22q11.2) affecting multiple body systems
DiGeorge Syndrome
55
The most prevalent microdeletion syndrome in the US (up to 1/4000
DiGeorge Syndrome
56
Immune dysfunction (hypoplastic thymus gland) T-cell deficits; severity varies Most severe form is considered a SCID Cleft palate & other craniofacial abnormalities Hypocalcemia (parathyroid hypoplasia)
DiGeorge Syndrome
57
X-linked disorder caused by mutation in WASp protein
Wiskott-Aldrich Syndrome
58
Classic presentation Susceptibility to infections (bacterial, viral, fungal) Thrombocytopenia (plts are also SMALL) Eczema
Wiskott-Aldrich Syndrome
59
SCT only curative treatment (stem cell transplant)
Wiskott-Aldrich Syndrome
60
Homozygous presentation: progressive cerebellar ataxia (first sign), abnormal eye movements, other neurologic abnormalities, oculocutaneous telangiectasias, immune deficiency (esp. pulmonary infection), and malignancy
Ataxia-Telangiectasia
61
- Walk at normal age but don’t develop fluidity of gait, wobbly - Telangiectasias of the conjunctive, face, neck
Ataxia-Telangiectasia