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Measles

Updated : December 1, 2022





Background

Measles, commonly known as rubeola, is a highly infectious, preventable febrile viral infection. It is still a significant source of worldwide mortality and morbidity, notably in Southeast Asia and Africa. Despite the availability of effective vaccination, it causes over 100,000 fatalities each year.

Officials declared measles eliminated in the United States in 2000, after one year of no continuous disease transmission, and from the Americas area in 2016. However, outbreaks continue to occur in the community due to illnesses and transmission among unvaccinated juveniles.

Epidemiology

Measles epidemiology varies around the globe and is linked to vaccination levels attained in a given location. Before implementing comprehensive immunization programs, measles was responsible for an estimated 2.6 million fatalities. Despite immunization in the modern period, the World Health Organization recorded 134,200 fatalities (15 deaths per hour) from measles in 2015.

The measles virus has no animal reservoir and exclusively affects humans. The virus is highly infectious, with each case having the potential to cause 14 to 18 secondary infections among susceptible populations. Measles is spread by respiratory droplets, particle aerosols, and intimate contact. Although more extended periods have been documented, the incubation period is 10 to 14 days.

Young children are most frequently affected by measles, which is highly contagious among unvaccinated and pregnant women. Due to rising vaccination coverage rates and changes in the levels of population immunity at various ages, there has been a recent transition to older kids

Anatomy

Pathophysiology

The virus infects the dendritic cells, lymphocytes, and alveolar macrophages of the respiratory tract. Later, it spreads throughout the circulation, causing viremia, before migrating to distant organs and adjacent lymphoid tissue. When a person coughs or sneezes, the virus in their lymphocytes and dendritic cells spreads to their respiratory tract epithelial cells, cleared and discharged as respiratory droplets, infecting others and continuing the cycle.

The early inflammation causes cough, coryza, and conjunctivitis. The onset of fever and the growth of viremia are related. Following spread, lymphocytic and perivascular infiltrates induce a cutaneous rash. The measles virus suppresses interferon production during the prodromal phase by using its nonstructural proteins, C and V, to lower host immunity. The escalating viral replication then induces humoral and cellular immune responses.

antibody production, which may be detected three to four days after the rash first emerges and last for six to eight weeks, makes up the early humoral reaction. IgG antibodies are subsequently generated, mainly against the viral nucleoprotein. Increased plasma levels of Th1-dependent interferon-gamma during the acute phase and subsequent increases in Th2-dependent interleukin 4, interleukin 13 levels, and interleukin 10 cellular immune responses are crucial for recovery. The typical Warthin-Finkeldey large cells in lymph node biopsy are seen against a paracortical hyperplasia background.

Immunosuppression brought on by the measles virus has been reported to endure for weeks, months, or even years. Due to this, individuals are more vulnerable to bacterial and other secondary illnesses. Due to the host’s increased vulnerability to subsequent infections, this causes the majority of the morbidity and death related to measles. The neutralizing IgG antibodies provide lifelong protection against hemagglutinin, which prevents host cell receptors from attaching to the virus.

Etiology

The causative agent is the measles virus, a member of the Paramyxoviridae family and genus. It is a negative-sense RNA virus that is nonsegmented, single-stranded, and enclosed. Six structural proteins and two non-structural proteins, C and V, are both encoded by the genome. The structural proteins are haemagglutinin (HA), matrix, large protein, nucleoprotein, and phosphoprotein. The virus attaches to the host cell via the HA protein.

Passive antibody transfer protects young children delivered to women with acquired immunity against measles, but when these antibodies diminish, they become vulnerable. The four days before and four days after the rash appears are when an infection is most contagious, coinciding with the highest viremia levels and the symptoms of cough, conjunctivitis, and coryza.

Genetics

Prognostic Factors

There is a risk of a poor prognosis, even though many individuals with measles will recover without any complications. Otitis media and diarrhea are two typical side effects of measles infection. Otitis media may result in hearing loss.

Infants and young children under the age of five, individuals over the age of 20, pregnant women, and those with impaired immune systems are more prone to experience serious consequences.

1 in 1000 infected children may develop encephalitis, and 1-2 of all infected children may die from measles-related neurologic or respiratory difficulties.

Clinical History

Physical Examination

Age group

Associated comorbidity

Associated activity

Acuity of presentation

Differential Diagnoses

Laboratory Studies

Imaging Studies

Procedures

Histologic Findings

Staging

Treatment Paradigm

by Stage

by Modality

Chemotherapy

Radiation Therapy

Surgical Interventions

Hormone Therapy

Immunotherapy

Hyperthermia

Photodynamic Therapy

Stem Cell Transplant

Targeted Therapy

Palliative Care

Medication

 

immune globulin IM (IGIM) 

Indicates a susceptible person who has not had measles before and has not been vaccinated :

0.25

mL/kg

Intramuscular (IM)


Comments:  
Avoid taking the measles vaccine at the same time.  



measles mumps and rubella vaccine, live 

Indicated for Immunization against mumps, and rubella :

0.5

ml

Subcutaneous (SC)


Administer the second dose 28 days later



 

immune globulin IM (IGIM) 

Indicates a susceptible person who has not had measles before and has not been vaccinated  :

0.25

mL/kg

Intravenous (IV)


Comments:  
Avoid taking the measles vaccine at the same time.



measles mumps and rubella vaccine, live 

Indicated for Immunization against mumps, and rubella :

0.5

ml

of first dose subcutaneously (SC)


Administer the 2nd dose between 4-6 years



measles, mumps, rubella, and varicella vaccine, live (Rx) 

Indicated for Measles, Rubella, Mumps,& Varicella Vaccination:


Two-step dose vaccination: 
1st dose- 0.5ml subcutaneous, at age 12-15 months 
2nd dose- 0.5ml subcutaneous, at age 4-6 years 



measles, mumps, rubella, and varicella vaccine, live (Rx) 

Indicated for Measles, Rubella, Mumps,& Varicella Vaccination:


Two-step dose vaccination: 
1st dose- 0.5ml subcutaneous, at age 12-15 months 
2nd dose- 0.5ml subcutaneous, at age 4-6 years 



vitamin A 

World Health Organization (WHO) recommends administration orally once a day for two days:


Age (<6 months): 50,000 IU
Age(6–11 months): 100,000 IU
Age(> 12 months): 200,000 IU



 

Media Gallary

References

from: https://www.ncbi.nlm.nih.gov/books/NBK448068/

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Measles

Updated : December 1, 2022




Measles, commonly known as rubeola, is a highly infectious, preventable febrile viral infection. It is still a significant source of worldwide mortality and morbidity, notably in Southeast Asia and Africa. Despite the availability of effective vaccination, it causes over 100,000 fatalities each year.

Officials declared measles eliminated in the United States in 2000, after one year of no continuous disease transmission, and from the Americas area in 2016. However, outbreaks continue to occur in the community due to illnesses and transmission among unvaccinated juveniles.

Measles epidemiology varies around the globe and is linked to vaccination levels attained in a given location. Before implementing comprehensive immunization programs, measles was responsible for an estimated 2.6 million fatalities. Despite immunization in the modern period, the World Health Organization recorded 134,200 fatalities (15 deaths per hour) from measles in 2015.

The measles virus has no animal reservoir and exclusively affects humans. The virus is highly infectious, with each case having the potential to cause 14 to 18 secondary infections among susceptible populations. Measles is spread by respiratory droplets, particle aerosols, and intimate contact. Although more extended periods have been documented, the incubation period is 10 to 14 days.

Young children are most frequently affected by measles, which is highly contagious among unvaccinated and pregnant women. Due to rising vaccination coverage rates and changes in the levels of population immunity at various ages, there has been a recent transition to older kids

The virus infects the dendritic cells, lymphocytes, and alveolar macrophages of the respiratory tract. Later, it spreads throughout the circulation, causing viremia, before migrating to distant organs and adjacent lymphoid tissue. When a person coughs or sneezes, the virus in their lymphocytes and dendritic cells spreads to their respiratory tract epithelial cells, cleared and discharged as respiratory droplets, infecting others and continuing the cycle.

The early inflammation causes cough, coryza, and conjunctivitis. The onset of fever and the growth of viremia are related. Following spread, lymphocytic and perivascular infiltrates induce a cutaneous rash. The measles virus suppresses interferon production during the prodromal phase by using its nonstructural proteins, C and V, to lower host immunity. The escalating viral replication then induces humoral and cellular immune responses.

antibody production, which may be detected three to four days after the rash first emerges and last for six to eight weeks, makes up the early humoral reaction. IgG antibodies are subsequently generated, mainly against the viral nucleoprotein. Increased plasma levels of Th1-dependent interferon-gamma during the acute phase and subsequent increases in Th2-dependent interleukin 4, interleukin 13 levels, and interleukin 10 cellular immune responses are crucial for recovery. The typical Warthin-Finkeldey large cells in lymph node biopsy are seen against a paracortical hyperplasia background.

Immunosuppression brought on by the measles virus has been reported to endure for weeks, months, or even years. Due to this, individuals are more vulnerable to bacterial and other secondary illnesses. Due to the host’s increased vulnerability to subsequent infections, this causes the majority of the morbidity and death related to measles. The neutralizing IgG antibodies provide lifelong protection against hemagglutinin, which prevents host cell receptors from attaching to the virus.

The causative agent is the measles virus, a member of the Paramyxoviridae family and genus. It is a negative-sense RNA virus that is nonsegmented, single-stranded, and enclosed. Six structural proteins and two non-structural proteins, C and V, are both encoded by the genome. The structural proteins are haemagglutinin (HA), matrix, large protein, nucleoprotein, and phosphoprotein. The virus attaches to the host cell via the HA protein.

Passive antibody transfer protects young children delivered to women with acquired immunity against measles, but when these antibodies diminish, they become vulnerable. The four days before and four days after the rash appears are when an infection is most contagious, coinciding with the highest viremia levels and the symptoms of cough, conjunctivitis, and coryza.

There is a risk of a poor prognosis, even though many individuals with measles will recover without any complications. Otitis media and diarrhea are two typical side effects of measles infection. Otitis media may result in hearing loss.

Infants and young children under the age of five, individuals over the age of 20, pregnant women, and those with impaired immune systems are more prone to experience serious consequences.

1 in 1000 infected children may develop encephalitis, and 1-2 of all infected children may die from measles-related neurologic or respiratory difficulties.

immune globulin IM (IGIM) 

Indicates a susceptible person who has not had measles before and has not been vaccinated :

0.25

mL/kg

Intramuscular (IM)


Comments:  
Avoid taking the measles vaccine at the same time.  



measles mumps and rubella vaccine, live 

Indicated for Immunization against mumps, and rubella :

0.5

ml

Subcutaneous (SC)


Administer the second dose 28 days later



immune globulin IM (IGIM) 

Indicates a susceptible person who has not had measles before and has not been vaccinated  :

0.25

mL/kg

Intravenous (IV)


Comments:  
Avoid taking the measles vaccine at the same time.



measles mumps and rubella vaccine, live 

Indicated for Immunization against mumps, and rubella :

0.5

ml

of first dose subcutaneously (SC)


Administer the 2nd dose between 4-6 years



measles, mumps, rubella, and varicella vaccine, live (Rx) 

Indicated for Measles, Rubella, Mumps,& Varicella Vaccination:


Two-step dose vaccination: 
1st dose- 0.5ml subcutaneous, at age 12-15 months 
2nd dose- 0.5ml subcutaneous, at age 4-6 years 



measles, mumps, rubella, and varicella vaccine, live (Rx) 

Indicated for Measles, Rubella, Mumps,& Varicella Vaccination:


Two-step dose vaccination: 
1st dose- 0.5ml subcutaneous, at age 12-15 months 
2nd dose- 0.5ml subcutaneous, at age 4-6 years 



vitamin A 

World Health Organization (WHO) recommends administration orally once a day for two days:


Age (<6 months): 50,000 IU
Age(6–11 months): 100,000 IU
Age(> 12 months): 200,000 IU



from: https://www.ncbi.nlm.nih.gov/books/NBK448068/

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