Measles virus: Difference between revisions
From IDWiki
m (Text replacement - "Clinical Presentation" to "Clinical Manifestations") |
(ββ: updated) |
||
Line 1: | Line 1: | ||
* |
*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 |
|||
*Enveloped RNA ''Morbillivirus'' in the Paramyxoviridae family |
|||
=== Pathophysiology === |
|||
**Family includes parainfluenza, RSV, measles, mumps |
|||
* Airborne droplets can remain in the air up to 2 hours after a person with measles has coughed |
|||
*Eight structural proteins: F, C, H (haemagglutination), L (large), M (matrix), N (nucleoprotein), P (phosphopolymerase), and V |
|||
** It is droplet, but just very small droplet |
|||
**N, P, and L complex with RNA |
|||
* Innoculated through respiratory mucosa, enters lymphoid cells via SLAM receptor |
|||
**C and V interact with cellular proteins and regulate replication |
|||
** SLAM (CDw150) is present on lymphocytes and antigen-presenting cells |
|||
**M, H, and F are viral envelope proteins |
|||
* Spreads to entire respiratory systems, as well as intestines, bladder, skin, and spleen, lymph nodes, liver, conjunctiva, and brain |
|||
**H helps with host cell attachment, and F helps with spread between cells |
|||
* 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 |
|||
=== |
===Pathophysiology=== |
||
* 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 |
|||
*Airborne droplets can remain in the air up to 2 hours after a person with measles has coughed |
|||
== Clinical Manifestations == |
|||
**It is droplet, but just very small droplet |
|||
* Incubation period 10-14 days (range up to 21 days), followed by several days of prodrome that includes fever, anorexia, cough, coryza, and conjunctivitis |
|||
*Innoculated through respiratory mucosa, enters lymphoid cells via SLAM receptor |
|||
** Can be mistaken for common cold or for Kawasaki disease |
|||
**SLAM (CDw150) is present on lymphocytes and antigen-presenting cells |
|||
** Koplik spots appear at end of prodrome |
|||
*Spreads to entire respiratory systems, as well as intestines, bladder, skin, and spleen, lymph nodes, liver, conjunctiva, and brain |
|||
*** Bluish gray specks on a red base in the oral mucosa ("like grains of sand") |
|||
*Propagates within T and B lymphocytes and monocytes, but also endothelial, epithelial, and dendritic cells |
|||
* Rash follows Koplik spots |
|||
*Host response success causes disappearance of serology and appearance of rash |
|||
** Spreads from face to body, including palms and soles |
|||
**Possibly the rash represents a hypersensitivity reaction to the virus mediated by cellular immunity |
|||
** 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 |
|||
=== |
===Epidemiology=== |
||
* 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 |
|||
*Infection confers lifelong immunity, though vaccination may not |
|||
=== Subacute sclerosing panencephalitis (SSPE) === |
|||
*Worldwide distribution |
|||
* Degenerative neurological condition caused by persistent CNS infection despite immune response |
|||
*Prior to vaccination, there were epidemics every 2 to 5 years lasting 3 to 4 months |
|||
* 5-10 years after infection |
|||
*Vaccine hesitancy is becoming more common |
|||
* Higher risk if infection before age 2 years |
|||
**Parts of Europe |
|||
* Inevitably ends in death |
|||
==Clinical Manifestations== |
|||
=== 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 |
|||
*Incubation period 10-14 days (range up to 21 days), followed by several days of prodrome that includes fever, anorexia, cough, coryza, and conjunctivitis |
|||
==== Atypical measles ==== |
|||
**Can be mistaken for common cold or for Kawasaki disease |
|||
* Patients with prior immunization with killed vaccine (no longer on market, since 1960s) may have an atypical presentation |
|||
**Koplik spots appear at end of prodrome |
|||
* Prodrome of fever and pain for 1 to 2 days |
|||
***Bluish gray specks on a red base in the oral mucosa ("like grains of sand") |
|||
* Rash follows, but moves peripherally to centrally, and have varied form (urticarial, maculopapular, hemorrhagic, vesicular) |
|||
*Rash follows Koplik spots |
|||
** Can mimic vaicella, RMSF, HSP, drug eruption, or toxic shock syndrome |
|||
**Spreads from face to body, including palms and soles |
|||
* Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion |
|||
**Fevers resolve soon after rash appears |
|||
* More prolonged course, with very high antibody titres |
|||
**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=== |
||
* 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 |
|||
*Respiratory involvement, either as primary infection of with bacterial superinfection |
|||
==== Pregnancy ==== |
|||
**Otitis media, pneumonia (on CXR, even if uncomplicated) |
|||
* Can be severe |
|||
*Acute encephalitis, which can have sequelae |
|||
* Can cause spontaneous abortion and premature delivery |
|||
**Blindness, corneal scarring |
|||
* Newborn can be infected; they should get immune globulin at birth |
|||
*Hepatitis |
|||
*Complications are more common in adults who are infected |
|||
===Subacute sclerosing panencephalitis (SSPE)=== |
|||
== Differential Diagnosis == |
|||
* [[Rubella]] |
|||
* [[Kawasaki syndrome]] |
|||
* [[Scarlet fever]] |
|||
* [[Roseola]] |
|||
* Infectious [[mononucleosis]] |
|||
* [[Rickettsia species|Risckettsial infections]] |
|||
* [[Enterovirus|Enteroviral infections]] |
|||
* [[Adenovirus|Adenoviral infections]] |
|||
*Degenerative neurological condition caused by persistent CNS infection despite immune response |
|||
== Diagnosis == |
|||
*5-10 years after infection |
|||
* Typically diagnosed clinically; CBC may show leukopenia |
|||
*Higher risk if infection before age 2 years |
|||
* If uncertain of the diagnosis, can use serology or molecular tests to confirm |
|||
*Inevitably ends in death |
|||
** 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 |
|||
===Special Populations=== |
|||
== Management == |
|||
====Modified measles==== |
|||
* 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 |
|||
*Patients with passive immunity to measles may present with a milder form |
|||
== Prevention == |
|||
**Babies with mom's immunoglobulin, or patients who have received immune globulin |
|||
=== Infection control === |
|||
*The prodrome, Koplik spots, and rash are often absent, and it is sometimes subclinical |
|||
* 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 |
|||
====Atypical measles==== |
|||
=== Post-exposure prophylaxis (PEP) === |
|||
* Indications for passive immunization with immune globulin |
|||
** High risk for severe or fatal measles and are susceptible |
|||
** Includes children with malignancy, cell-mediated immunodeficiency (including AIDS), and possibly babies <1 year |
|||
** Must be given within 6 days of exposure |
|||
** Infants <1 year: IMIg 0.25 mL/kg once |
|||
** Other children: IMIg 0.5 mL/kg once (maximum of 15 mL) |
|||
* Immunization for post-exposure prophylaxis can be done in other, immunocompetent patients |
|||
** Can shorten the time to rash, suggesting a shorter period of infectiousness |
|||
*Patients with prior immunization with killed vaccine (no longer on market, since 1960s) may have an atypical presentation |
|||
=== Vaccination === |
|||
*Prodrome of fever and pain for 1 to 2 days |
|||
* Live vaccine given in MMR at 12-15 months, with a booster later in childhood |
|||
*Rash follows, but moves peripherally to centrally, and have varied form (urticarial, maculopapular, hemorrhagic, vesicular) |
|||
* Don't vaccinate for 5-6 months after receiving immune globulin |
|||
**Can mimic vaicella, RMSF, HSP, drug eruption, or toxic shock syndrome |
|||
* No adverse effects of revaccination |
|||
*Fever continues, with edema, interstitial pneumonia, hepatitis, and occasionally pleural effusion |
|||
* Rates need to be >95% to prevent imported cases from causing outbreaks |
|||
*More prolonged course, with very high antibody titres |
|||
* 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 |
|||
** 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 |
|||
==== |
====Immunocompromised==== |
||
* Improper storage >4ΒΊ C |
|||
*Chemotherapy, transplantation, AIDS, and congenital cellular immunodefieciency are all risk factors for severe measles |
|||
* Failure to use proper diluent for lyophilized vaccine |
|||
**Possibly also malnutrition |
|||
* Exposure to light or heat |
|||
*Can develop giant cell pneumonia, without rash, as well as a chronic encephalitis |
|||
* Vaccination in the presence of passive antibody |
|||
**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]] |
|||
*[[Rickettsia species|Risckettsial infections]] |
|||
*[[Enterovirus|Enteroviral infections]] |
|||
*[[Adenovirus|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 |
|||
{| class="wikitable" |
|||
!Population |
|||
!β€72 hours |
|||
!73 hours to 6 days |
|||
|- |
|||
|Susceptible infants <6 months old |
|||
|IMIg 0.5 mL/kg |
|||
|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 |
|||
|MMR |
|||
|- |
|||
|Susceptible pregnant people |
|||
|IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
|||
|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 |
|||
|IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
|||
|- |
|||
|Susceptible immunocompetent people β₯12 months old |
|||
|MMR |
|||
|MMR |
|||
|- |
|||
|People with confirmed immunity |
|||
|None |
|||
|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 == |
|||
* [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. |
|||
[[Category:Paramyxoviridae]] |
[[Category:Paramyxoviridae]] |
Revision as of 00:08, 20 July 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 10-14 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 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
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 | β€72 hours | 73 hours to 6 days |
---|---|---|
Susceptible infants <6 months old | IMIg 0.5 mL/kg | 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 | MMR |
Susceptible pregnant people | IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg | 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 | IVIg 400 mg/kg (preferred) or IMIg 0.5 mL/kg |
Susceptible immunocompetent people β₯12 months old | MMR | MMR |
People with confirmed immunity | None | 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.