Measles virus: Difference between revisions
From IDWiki
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*Prodrome of fever and pain for 1 to 2 days |
*Prodrome of fever and pain for 1 to 2 days |
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*Rash follows, but moves peripherally to centrally, and have varied form (urticarial, maculopapular, hemorrhagic, vesicular) |
*Rash follows, but moves peripherally to centrally, and have varied form (urticarial, maculopapular, hemorrhagic, vesicular) |
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**Can mimic |
**Can mimic [[varicella]], [[RMSF]], [[HSP]], [[drug eruption]], or [[toxic shock syndrome]] |
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*Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion |
*Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion |
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*More prolonged course, with very high antibody titres |
*More prolonged course, with very high antibody titres |
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{| class="wikitable" |
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!rowspan=2 |Population |
! rowspan="2" |Population |
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!colspan=2 |Time since measles exposure |
! colspan="2" |Time since measles exposure |
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!β€72 hours |
!β€72 hours |
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|Susceptible infants <6 months old |
|Susceptible infants <6 months old |
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|colspan=2|IMIg 0.5 mL/kg |
| colspan="2" |IMIg 0.5 mL/kg |
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|Susceptible immunocompetent infants 6-12 months old |
|Susceptible immunocompetent infants 6-12 months old |
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|Susceptible immunocompetent people β₯12 months old |
|Susceptible immunocompetent people β₯12 months old |
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|colspan=2|MMR |
| colspan="2" |MMR |
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|Susceptible pregnant people |
|Susceptible pregnant people |
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|colspan=2|IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
| colspan="2" |IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
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|Immunocompromised individuals β₯6 months old |
|Immunocompromised individuals β₯6 months old |
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|colspan=2|IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
| colspan="2" |IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
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|Susceptible immunocompetent people β₯12 months old |
|Susceptible immunocompetent people β₯12 months old |
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|colspan=2|MMR |
| colspan="2" |MMR |
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|People with confirmed immunity |
|People with confirmed immunity |
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|colspan=2|None |
| colspan="2" |None |
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*Vaccination in the presence of passive antibody |
*Vaccination in the presence of passive antibody |
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== |
==Further Reading== |
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* |
*[https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-4-active-vaccines/page-12-measles-vaccine.html#pep Measles vaccine: Canadian Immunization Guide]. Public Health Agency of Canada. |
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[[Category:Paramyxoviridae]] |
[[Category:Paramyxoviridae]] |
Revision as of 22:22, 16 August 2020
- Highly contagious virus that causes a triad of cough, coryza, and conjunctivitis
Background
Microbiology
- Enveloped RNA Morbillivirus in the Paramyxoviridae family
- Family includes parainfluenza, RSV, measles, mumps
- Eight structural proteins: F, C, H (haemagglutination), L (large), M (matrix), N (nucleoprotein), P (phosphopolymerase), and V
- N, P, and L complex with RNA
- C and V interact with cellular proteins and regulate replication
- M, H, and F are viral envelope proteins
- H helps with host cell attachment, and F helps with spread between cells
Pathophysiology
- Airborne droplets can remain in the air up to 2 hours after a person with measles has coughed
- It is droplet, but just very small droplet
- Innoculated through respiratory mucosa, enters lymphoid cells via SLAM receptor
- SLAM (CDw150) is present on lymphocytes and antigen-presenting cells
- Spreads to entire respiratory systems, as well as intestines, bladder, skin, and spleen, lymph nodes, liver, conjunctiva, and brain
- Propagates within T and B lymphocytes and monocytes, but also endothelial, epithelial, and dendritic cells
- Host response success causes disappearance of serology and appearance of rash
- Possibly the rash represents a hypersensitivity reaction to the virus mediated by cellular immunity
Epidemiology
- Infection confers lifelong immunity, though vaccination may not
- Worldwide distribution
- Prior to vaccination, there were epidemics every 2 to 5 years lasting 3 to 4 months
- Vaccine hesitancy is becoming more common
- Parts of Europe
Clinical Manifestations
- Incubation period 10 to 14 days (range up to 21 days), followed by several days of prodrome that includes fever, anorexia, cough, coryza, and conjunctivitis
- Can be mistaken for common cold or for Kawasaki disease
- Koplik spots appear at end of prodrome
- Bluish gray specks on a red base in the oral mucosa ("like grains of sand")
- Rash follows Koplik spots
- Spreads from face to body, including palms and soles
- Fevers resolve soon after rash appears
- Rash is erythematous and maculopapular, and my desquamate as it begins to heal
- Usually lasts 5 days, clearing in the same pattern that it appeared
- The rash disappears about 7 to 10 days after late prodromal period, with cough being the last symptom to disappear
Complications
- Respiratory involvement, either as primary infection of with bacterial superinfection
- Otitis media, pneumonia (on CXR, even if uncomplicated)
- Acute encephalitis, which can have sequelae
- Blindness, corneal scarring
- Hepatitis
- Complications are more common in adults who are infected
Subacute sclerosing panencephalitis (SSPE)
- Degenerative neurological condition caused by persistent CNS infection despite immune response
- 5-10 years after infection
- Higher risk if infection before age 2 years
- Inevitably ends in death
Special Populations
Modified measles
- Patients with passive immunity to measles may present with a milder form
- Babies with mom's immunoglobulin, or patients who have received immune globulin
- The prodrome, Koplik spots, and rash are often absent, and it is sometimes subclinical
Atypical measles
- Patients with prior immunization with killed vaccine (no longer on market, since 1960s) may have an atypical presentation
- Prodrome of fever and pain for 1 to 2 days
- Rash follows, but moves peripherally to centrally, and have varied form (urticarial, maculopapular, hemorrhagic, vesicular)
- Can mimic varicella, RMSF, HSP, drug eruption, or toxic shock syndrome
- Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion
- More prolonged course, with very high antibody titres
Immunocompromised
- Chemotherapy, transplantation, AIDS, and congenital cellular immunodefieciency are all risk factors for severe measles
- Possibly also malnutrition
- Can develop giant cell pneumonia, without rash, as well as a chronic encephalitis
- Can detect measles RNA in brain tissue
Pregnancy
- Can be severe
- Can cause spontaneous abortion and premature delivery
- Newborn can be infected; they should get immune globulin at birth
Differential Diagnosis
- Rubella
- Kawasaki syndrome
- Scarlet fever
- Roseola
- Infectious mononucleosis
- Risckettsial infections
- Enteroviral infections
- Adenoviral infections
Diagnosis
- Typically diagnosed clinically; CBC may show leukopenia
- If uncertain of the diagnosis, can use serology or molecular tests to confirm
- NP swab PCR within 7 days of rash onset
- Urine PCR within 14 days of rash onset
- ELISA IgG serology, repeated after 1 week; fourfold titre increase is diagnostic
- Or IgM, if available, to diagnose on one sample
- IgM can persist for up to a month
- Viral culture is also possible
- For SSPE, can demonstrate high titres in serum and CSF
Management
- Most infectious just before rash; quickly becomes non-infectious after end of prodrome
- Supportive care
- Vitamin A can be given, especially if the child is deficien
- In children >1 year, vitamin A 200,000 IU daily for 2 days
- If 6-12 months old, use 100,000 IU for 2 days
- Less than 6 months, use 50,000 IU
- If deficient, give another dose at 2 to 4 weeks
- Ribavirin unhelpful but sometimes given
Prevention
Infection control
- Infectious period is 5 days prior to until 4 days after onset of rash
- Need to do contact tracing, including people up to two hours after any room they were in
- All contacts should be quarantined at home regardless of symptoms
Post-exposure prophylaxis (PEP)
- Use either MMR vaccine or immune globulin in susceptible people
- Immunization
- Should be offered to all susceptible, immunocompetent people age 6 months and older
- Give within 72 hours of exposure
- Can shorten the time to rash, suggesting a shorter period of infectiousness
- Immunoglobulin can provide short-term protection to certain susceptible, immunocompromised people
- Given to people with high risk for severe or fatal measles and are susceptible:
- Susceptible pregnant women
- Susceptible immunocompromised people
- Regardless of prior vaccination, should also be considered in advanced HIV
- Regardless of prior vaccination, should also be consider in all patients with hematopoietic stem cell transplantation until they have been revaccinated post-transplant with confirmed adequate antibody titres
- Susceptible infants <6 months of age
- Susceptible immunocompetent infants from 6 to 11 months of age who present after 72 hours
- Give within 6 days of exposure
- Given to people with high risk for severe or fatal measles and are susceptible:
Population | Time since measles exposure | |
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β€72 hours | 73 hours to 6 days | |
Susceptible infants <6 months old | IMIg 0.5 mL/kg | |
Susceptible immunocompetent infants 6-12 months old | MMR | IMIg 0.5 mL/kg |
Susceptible immunocompetent people β₯12 months old | MMR | |
Susceptible pregnant people | IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg | |
Immunocompromised individuals β₯6 months old | IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg | |
Susceptible immunocompetent people β₯12 months old | MMR | |
People with confirmed immunity | None |
Vaccination
- Live vaccine (given in MMR or MMRV) at 12-15 months, with a booster later in childhood between 18 months and school entry
- Wait at least 5-6 months after receiving immunoglobulin
- Wait at least 4 weeks from a dose given before 12 months for post-exposure prophylaxis
- No adverse effects of revaccination
- Rates need to be >95% to prevent imported cases from causing outbreaks
- Rates less than 80% allow endemic transmission with cyclical outbreaks every 3-5 years
- Vaccination is contraindicated in advanced HIV, other cell-mediated immunodeficiency, and in pregnancy
- Wait 3 months after chemotherapy
- Don't use MMRV, since no safety data are available
- Can be associated with anaphylaxis in patients with true egg allergy
Vaccine failure
- Improper storage >4ΒΊ C
- Failure to use proper diluent for lyophilized vaccine
- Exposure to light or heat
- Vaccination in the presence of passive antibody
Further Reading
- Measles vaccine: Canadian Immunization Guide. Public Health Agency of Canada.