Measles virus: Difference between revisions
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*Highly contagious virus that causes a '''triad of cough, coryza, and conjunctivitis''' |
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==Background== |
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= Microbiology = |
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===Microbiology=== |
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* |
*Enveloped RNA ''Morbillivirus'' in the Paramyxoviridae family |
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** |
**Family includes parainfluenza, RSV, measles, mumps |
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* |
*Eight structural proteins: F, C, H (haemagglutination), L (large), M (matrix), N (nucleoprotein), P (phosphopolymerase), and V |
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** |
**N, P, and L complex with RNA |
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** |
**C and V interact with cellular proteins and regulate replication |
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** |
**M, H, and F are viral envelope proteins |
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** |
**H helps with host cell attachment, and F helps with spread between cells |
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= |
===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== |
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= Differential Diagnosis = |
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*Incubation period [[Usual incubation period::10 to 14 days]] (range [[Incubation period range::up to 21 days]]), followed by several days of prodrome that includes fever, anorexia, cough, coryza, and conjunctivitis |
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* [[Rubella]] |
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**Can be mistaken for common cold or for Kawasaki disease |
|||
* [[Kawasaki syndrome]] |
|||
**Koplik spots appear at end of prodrome |
|||
* [[Scarlet fever]] |
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***Bluish gray specks on a red base in the oral mucosa ("like grains of sand") |
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* [[Roseola]] |
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*Rash follows Koplik spots |
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* Infectious [[mononucleosis]] |
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**Spreads from face to body, including palms and soles |
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* [[Rickettsia species|Risckettsial infections]] |
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**Fevers resolve soon after rash appears |
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* [[Enterovirus|Enteroviral infections]] |
|||
**Rash is erythematous and maculopapular, and my desquamate as it begins to heal |
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* [[Adenovirus|Adenoviral infections]] |
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**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 |
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===Complications=== |
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= Clinical Presentation = |
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*Respiratory involvement, either as primary infection of with bacterial superinfection |
|||
* Incubation period 10-14 days (range up to 21 days), followed by several days of prodrome that includes fever, anorexia, cough, coryza, and conjunctivitis |
|||
**[[Otitis media]], [[pneumonia]] (on CXR, even if uncomplicated) |
|||
** Can be mistaken for common cold or for Kawasaki disease |
|||
*Acute [[encephalitis]] in 1 in 1000-2000 patients, with new fevers, headaches, seizures, and altered level of consciousness |
|||
** Koplik spots appear at end of prodrome |
|||
**Likely from hypersensitivity to virus in the brain rather than from direct infection |
|||
*** Bluish gray specks on a red base in the oral mucosa ("like grains of sand") |
|||
**Sequelae include blindness, corneal scarring |
|||
* Rash follows Koplik spots |
|||
*Chronic encephalitis, also called subacute sclerosing panencephalitis |
|||
** Spreads from face to body, including palms and soles |
|||
*[[Hepatitis]] |
|||
** Fevers resolve soon after rash appears |
|||
*Complications are more common in adults who are infected |
|||
** 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 |
|||
===Subacute Sclerosing Panencephalitis (SSPE)=== |
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== Complications == |
|||
*Degenerative neurological condition caused by persistent CNS infection despite immune response |
|||
* Respiratory involvement, either as primary infection of with bacterial superinfection |
|||
*5-10 years after infection |
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** Otitis media, pneumonia (on CXR, even if uncomplicated) |
|||
*Higher risk if infection before age 2 years |
|||
* Acute encephalitis, which can have sequelae |
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*Inevitably ends in death |
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** Blindness, corneal scarring |
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* Hepatitis |
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* Complications are more common in adults who are infected |
|||
===Special Populations=== |
|||
== Subacute sclerosing panencephalitis (SSPE) == |
|||
====Modified Measles==== |
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*Patients with passive immunity to measles may present with a milder form |
|||
* Degenerative neurological condition caused by persistent CNS infection despite immune response |
|||
**Babies with mom's immunoglobulin, or patients who have received immune globulin |
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* 5-10 years after infection |
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*The prodrome, Koplik spots, and rash are often absent, and it is sometimes subclinical |
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* Higher risk if infection before age 2 years |
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* Inevitably ends in death |
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====Atypical Measles==== |
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== Special Populations == |
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*Patients with prior immunization with killed vaccine (no longer on market, since 1960s) may have an atypical presentation |
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== Modified measles == |
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*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]] |
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*Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion |
|||
*More prolonged course, with very high antibody titres |
|||
====Immunocompromised==== |
|||
* 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 |
|||
*Chemotherapy, transplantation, AIDS, and congenital cellular immunodefieciency are all risk factors for severe measles |
|||
== Atypical 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==== |
|||
* 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 vaicella, 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 |
|||
*Can be severe |
|||
== Immunocompromised == |
|||
*Can cause spontaneous abortion and premature delivery |
|||
*Newborn can be infected; they should get immune globulin at birth |
|||
==Differential Diagnosis== |
|||
* 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 |
|||
*[[Rubella]] |
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== Pregnancy == |
|||
*[[Kawasaki syndrome]] |
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*[[Scarlet fever]] |
|||
*[[Roseolavirus|Roseola]] |
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*[[Infectious mononucleosis]] |
|||
*[[Rickettsioses]] |
|||
*[[Enterovirus|Enteroviral infections]] |
|||
*[[Adenovirus|Adenoviral infections]] |
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==Diagnosis== |
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* Can be severe |
|||
* Can cause spontaneous abortion and premature delivery |
|||
* Newborn can be infected; they should get immune globulin at birth |
|||
*Typically diagnosed clinically; CBC may show leukopenia |
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= Diagnosis = |
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*If uncertain of the diagnosis, can use serology or molecular tests to confirm |
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**NP swab PCR within 7 days of rash onset |
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**Urine PCR within 14 days of rash onset |
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**ELISA IgG serology, repeated after 1 week; fourfold titre increase is diagnostic |
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***Or IgM, if available, to diagnose on one sample |
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***IgM can persist for up to a month |
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**Viral culture is also possible |
|||
*For SSPE, can demonstrate high titres in serum and CSF |
|||
==Management== |
|||
* 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 |
|||
*Most infectious just before rash; quickly becomes non-infectious after end of prodrome |
|||
= Management = |
|||
*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 |
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**Less than 6 months, use 50,000 IU |
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**If deficient, give another dose at 2 to 4 weeks |
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*Ribavirin unhelpful but sometimes given |
|||
==Prevention== |
|||
* Most infectious just before rash; quickly becomes non-infectious after end of prodrome |
|||
===Infection Control=== |
|||
* 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 |
|||
*Infectious period is 5 days prior to until 4 days after onset of rash |
|||
== Infection control == |
|||
*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 |
|||
**Susceptible contacts should be placed in airborne precautions from 5 days after first exposure to 21 days after last exposure |
|||
===Post-Exposure Prophylaxis (PEP)=== |
|||
* Infectious period is 5 days prior to rash and 4 days after, in general, though infectiousness starts with respiratory involvement |
|||
* 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 |
|||
*Use either MMR vaccine or immune globulin in susceptible people |
|||
== Post-exposure prophylaxis (PEP) == |
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*'''Immunization''' |
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**Should be offered to all susceptible, immunocompetent people age 6 months and older |
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**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 |
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***Susceptible immunocompetent infants from 6 to 11 months of age who present after 72 hours |
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**Give within 6 days of exposure |
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{| class="wikitable" |
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* Indications for passive immunization with immune globulin |
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! rowspan="2" |Population |
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** High risk for severe or fatal measles and are susceptible |
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! colspan="2" |Time since measles exposure |
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** Includes children with malignancy, cell-mediated immunodeficiency (including AIDS), and possibly babies <1 year |
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|- |
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** Must be given within 6 days of exposure |
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!β€72 hours |
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** Infants <1 year: IMIg 0.25 mL/kg once |
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!73 hours to 6 days |
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** Other children: IMIg 0.5 mL/kg once (maximum of 15 mL) |
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|- |
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* Immunization for post-exposure prophylaxis can be done in other, immunocompetent patients |
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|Susceptible infants <6 months old |
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** Can shorten the time to rash, suggesting a shorter period of infectiousness |
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| colspan="2" |IMIg 0.5 mL/kg |
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|- |
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|Susceptible immunocompetent infants 6-12 months old |
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|MMR |
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|IMIg 0.5 mL/kg |
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|- |
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|Susceptible immunocompetent people β₯12 months old |
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| colspan="2" |MMR |
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|- |
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|Susceptible pregnant people |
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| colspan="2" |IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
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|- |
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|Immunocompromised individuals |
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| colspan="2" |IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
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|- |
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|People with confirmed immunity |
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| colspan="2" |None |
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|} |
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= |
===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 |
|||
*No adverse effects of revaccination |
|||
* Rates need to be >95% to prevent imported cases from causing outbreaks |
|||
* |
*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 AIDS, other cell-mediated immunodeficiency, and in pregnancy |
|||
*Vaccination is contraindicated in advanced [[HIV]], other cell-mediated immunodeficiency, and in [[pregnancy]] |
|||
** Wait 3 months after chemotherapy |
|||
**Wait 3 months after chemotherapy |
|||
** Don't use MMRV, since no safety data are available |
|||
**Don't use MMRV, since no safety data are available |
|||
* Can be associated with anaphylaxis in patients with true egg allergy |
|||
*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 |
||
====Catch-Up==== |
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= Further Reading = |
|||
*2 doses of MMR at least 4 weeks apart |
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[[Category:RNA viruses]] |
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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]] |
Latest revision as of 22:37, 27 September 2023
- 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 in 1 in 1000-2000 patients, with new fevers, headaches, seizures, and altered level of consciousness
- Likely from hypersensitivity to virus in the brain rather than from direct infection
- Sequelae include blindness, corneal scarring
- Chronic encephalitis, also called subacute sclerosing panencephalitis
- 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
- Rickettsioses
- 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
- Susceptible contacts should be placed in airborne precautions from 5 days after first exposure to 21 days after last exposure
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 | |
---|---|---|
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 | IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg | |
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
Catch-Up
- 2 doses of MMR at least 4 weeks apart
Further Reading
- Measles vaccine: Canadian Immunization Guide. Public Health Agency of Canada.