Measles
PRESENTED BY
BEEMAMOL HUSSAIN
ASWINI K S
40TH BSC NURSING
GOVERNMENT COLLEGE OF NURSING
KOZHIKODE
Measles
• It is an acute viral infection characterized by a final stage
with a maculopapular rash erupting successively over the
neck and face, trunk, arms, and legs, and accompanied
by a high fever and catarrhal symptoms of URT.
Etiology
• Measles virus, the cause of measles, is an RNA virus of the
genus Morbillivirus in the family Paramyxoviridae.
• Only one serotype is known
• It is rarely subclinical .
Epidemiology
• Measles is endemic throughout the world.
• In the past, epidemics tended to occur irregularly , appearing in
the spring in large cities at 2-4-yr intervals (3 yr interval in India)
as new groups of susceptible children were exposed
• When introduced into a virgin community more than 90% of that
community will be infected.
• Prior to the use of measles vaccine, the peak incidence was
among children 5-10 yr of age.
• Disease has high mortality and morbidity in developing
countries
Incidence
Epidemiological determinants
• Agent factors
AGENT : paramyxo virus
Cannot survive outside human body
SOURCE OF INFECTION : A case of measles
carriers are not known to occur
subclinical measles occur more often.
INFECTIVE MATERIAL : Secretion of the nose, throat and respiratory
tract of a case of measles.
COMMUNICABILITY : Highly infectious during prodomal period and
eruption
declines rapidly after appearance of rash.
SECOND ATTACK RATE : There is only one antigenic type of measles
virus
infection confers lifelong immunity
• Host factors
AGE : Infancy or childhood (6 months to 3 years of age)
SEX : Incidence equal
IMMUNITY : No inborn immunity. Immunity conferred only by attack of
measles
NUTRITION : Tends to be severe in the malnourished Children
Carrying a mortality upto 400 times higher than in well nourished children having
measles.
May be related to poor cell meditated immune response secondary to malnutrition
Additionally severely malnourished have been shown to excrete measles virus for
longer periods.
An attack of severe measles may be followed by weight loss precipitating the
child into malnutrition.
Transmission
• Measles is highly contagious ; directly from person to person
• Maximal dissemination of virus occurs by droplet infection and
droplet nuclei during the prodromal period ( catarrhal stage ).
• Transmission to susceptible contacts often occurs prior to
diagnosis of the index case
• Portal of entry is respiratory tract
• Infection through conjunctiva is considered likely
• Recipients of vaccine are non-contagious to others
Pathogenesis
• The essential lesion of measles is found in the skin ,
conjunctivae , and the mucous membranes of the nasopharynx
, bronchi , and intestinal tract .
• Serous exudate and proliferation of mononuclear cells and a
few polymorphonuclear cells occur around the capillaries
• Hyperplasia of lymphoid tissue usually occurs, particularly in
the appendix, where multinucleated giant cells of up to 100
μm in diameter ( Warthin-Finkeldey reticuloendothelial giant
cells ) may be found.
• In the skin , the reaction is particularly notable about the
sebaceous glands and hair follicles
• Koplik spots consist of serous exudate and proliferation of
endothelial cells similar to those in the skin lesions.
• A general inflammatory reaction of the buccal and pharyngeal
mucosa extends into the lymphoid tissue and the
tracheobronchial mucous membrane
• Interstitial pneumonitis resulting from measles virus takes the
form of Hecht giant cell pneumonia .
• Bronchopneumonia may occur from secondary bacterial
infection
Clinical features
1. Incubation stage
2. Prodromal stage
3. Eruptive stage
4. Post measles stage
Incubation period
• lasts approximately 10-12 days to the first prodromal symptoms
and another 2-4 days to the appearance of the rash; rarely, it
may be as short as 6-10 days .
• Body temperature may increase slightly 9-10 days from the date
of infection and then subside for 24 hr or so.
• The patient may transmit the virus by the 9th-10th day after
exposure and occasionally as early as the 7th day, before the
illness can be diagnosed
Predomal phase
• usually lasts 3-5 days and is characterized by:
• low-grade to moderate fever
• dry cough
• coryza
• conjunctivitis .
These symptoms nearly always precede the appearance of Koplik spots
, the pathognomonic sign of measles, by 2-3 days
• The conjunctival inflammation and photophobia may suggest
measles before Koplik spots appear.
• .
Koplicks spot
• An enanthem or red mottling is usually present on the hard and soft
palates
• the pathognomonic sign of measles
• are grayish white dots , usually as small as grains of sand, that have slight,
reddish areolae ; occasionally they are hemorrhagic .
• tend to occur opposite the lower molars but may spread irregularly over
the rest of the buccal mucosa.
• Rarely they are found within the midportion of the lower lip , on the palate ,
and on the lacrimal caruncle .
• They appear and disappear rapidly , usually within 12-18 hr .
• As they fade , a red , spotty discoloration of the mucosa may remain
Predomal phase (cont.)
• Occasionally , the prodromal phase may be severe , being
ushered in by a sudden high fever , sometimes with convulsions
and even pneumonia .
• Usually the coryza, fever, and cough are increasingly severe up
to the time the rash has covered the body.
• The temperature rises abruptly as the rash appears and often
reaches 40°C (104°F) or higher.
• In uncomplicated cases , as the rash appears on the legs and
feet, the symptoms subside rapidly within about 2 days , usually
with an abrupt drop in temperature to normal.
Eruptive stage
Usually starts as faint macules on the:
 upper lateral parts of the neck
 behind the ears
 along the hairline
 posterior parts of the cheek .
The rash
The individual lesions become increasingly maculopapular as the
rash spreads rapidly over the:
• entire face
• neck
• upper arms
• upper part of the chest
within approximately the first 24 hr <
• During the succeeding 24 hr the rash spreads over the back,
abdomen, entire arm, and thighs.
• As it finally reaches the feet on the 2nd-3rd day , it begins to
fade on the face.
• The rash fades downward in the same sequence in which it
appeared.
• The severity of the disease is directly related to the extent and
confluence of the rash.
• In mild measles the rash tends not to be confluent , and in very
mild cases there are few, if any, lesions on the legs
• In severe cases the rash is confluent , the skin is completely
covered, including the palms and soles, and the face is swollen
and disfigured.
• The rash is often slightly hemorrhagic ; in severe cases with a
confluent rash, petechiae may be present in large numbers, and
there may be extensive ecchymoses
• Complete absence of rash is rare except :
• 1. in patients who have received immunoglobulin (Ig) during the
incubation period
• 2. in some patients with HIV infection
• 3. occasionally in infants younger than 9 mo of age who have
appreciable levels of maternal antibody
• In the hemorrhagic type of measles ( black measles ), bleeding
may occur from the mouth, nose, or bowel.
• In mild cases the rash may be less macular and more nearly
pinpoint , somewhat resembling that of scarlet fever or rubella
• Itching is generally slight .
• As the rash fades , branny desquamation and brownish
discoloration occur and then disappear within 7-10 days.
Diagnosis
• The diagnosis is usually apparent from the characteristic
clinical picture ; laboratory confirmation is rarely needed
• Testing for measles IgM antibodies is recommended in
some situations
• Measles IgM is detectable for 1 mo after illness , but
sensitivity of IgM assays may be limited in the first 72 hr of
the rash illness.
• Isolation of measles virus from clinical samples is also
useful in identifying the genotype of the strain to track
transmission patterns.
• All suspected measles cases should be reported
immediately to local or health departments.
• During the prodromal stage multinucleated giant cells can
be demonstrated in smears of the nasal mucosa
• Antibodies become detectable when the rash appears ;
• Testing of acute and convalescent sera demonstrates the
diagnostic seroconversion or fourfold increase in titer.
• Measles virus can be isolated by tissue culture in human
embryonic or rhesus monkey kidney cells
• Cytopathic changes , visible in 5-10 days, consist of
multinucleated giant cells with intranuclear inclusions .
• The white blood cell count tends to be low with a relative
lymphocytosis
• Cerebrospinal fluid in patients with measles encephalitis
usually shows an increase in protein and a small increase in
lymphocytes . The glucose level is normal.
• The rash of rubeola must be differentiated from that of:
• Rubella
• Roseola infantum (human herpesvirus 6
• Infections resulting from:
• echovirus
• coxsackievirus
• adenovirus
• Infectious mononucleosis
• Toxoplasmosis
• Meningococcemia
• Scarlet fever
• Rickettsial diseases
• Kawasaki disease
• Serum sickness
• Drug rashes

Measles .pptx

  • 1.
    Measles PRESENTED BY BEEMAMOL HUSSAIN ASWINIK S 40TH BSC NURSING GOVERNMENT COLLEGE OF NURSING KOZHIKODE
  • 2.
    Measles • It isan acute viral infection characterized by a final stage with a maculopapular rash erupting successively over the neck and face, trunk, arms, and legs, and accompanied by a high fever and catarrhal symptoms of URT.
  • 4.
    Etiology • Measles virus,the cause of measles, is an RNA virus of the genus Morbillivirus in the family Paramyxoviridae. • Only one serotype is known • It is rarely subclinical .
  • 5.
    Epidemiology • Measles isendemic throughout the world. • In the past, epidemics tended to occur irregularly , appearing in the spring in large cities at 2-4-yr intervals (3 yr interval in India) as new groups of susceptible children were exposed • When introduced into a virgin community more than 90% of that community will be infected.
  • 6.
    • Prior tothe use of measles vaccine, the peak incidence was among children 5-10 yr of age. • Disease has high mortality and morbidity in developing countries
  • 7.
  • 8.
    Epidemiological determinants • Agentfactors AGENT : paramyxo virus Cannot survive outside human body SOURCE OF INFECTION : A case of measles carriers are not known to occur subclinical measles occur more often. INFECTIVE MATERIAL : Secretion of the nose, throat and respiratory tract of a case of measles.
  • 9.
    COMMUNICABILITY : Highlyinfectious during prodomal period and eruption declines rapidly after appearance of rash. SECOND ATTACK RATE : There is only one antigenic type of measles virus infection confers lifelong immunity
  • 10.
    • Host factors AGE: Infancy or childhood (6 months to 3 years of age) SEX : Incidence equal IMMUNITY : No inborn immunity. Immunity conferred only by attack of measles
  • 11.
    NUTRITION : Tendsto be severe in the malnourished Children Carrying a mortality upto 400 times higher than in well nourished children having measles. May be related to poor cell meditated immune response secondary to malnutrition Additionally severely malnourished have been shown to excrete measles virus for longer periods. An attack of severe measles may be followed by weight loss precipitating the child into malnutrition.
  • 12.
    Transmission • Measles ishighly contagious ; directly from person to person • Maximal dissemination of virus occurs by droplet infection and droplet nuclei during the prodromal period ( catarrhal stage ).
  • 13.
    • Transmission tosusceptible contacts often occurs prior to diagnosis of the index case • Portal of entry is respiratory tract • Infection through conjunctiva is considered likely • Recipients of vaccine are non-contagious to others
  • 14.
    Pathogenesis • The essentiallesion of measles is found in the skin , conjunctivae , and the mucous membranes of the nasopharynx , bronchi , and intestinal tract . • Serous exudate and proliferation of mononuclear cells and a few polymorphonuclear cells occur around the capillaries
  • 15.
    • Hyperplasia oflymphoid tissue usually occurs, particularly in the appendix, where multinucleated giant cells of up to 100 μm in diameter ( Warthin-Finkeldey reticuloendothelial giant cells ) may be found. • In the skin , the reaction is particularly notable about the sebaceous glands and hair follicles
  • 16.
    • Koplik spotsconsist of serous exudate and proliferation of endothelial cells similar to those in the skin lesions. • A general inflammatory reaction of the buccal and pharyngeal mucosa extends into the lymphoid tissue and the tracheobronchial mucous membrane
  • 17.
    • Interstitial pneumonitisresulting from measles virus takes the form of Hecht giant cell pneumonia . • Bronchopneumonia may occur from secondary bacterial infection
  • 18.
    Clinical features 1. Incubationstage 2. Prodromal stage 3. Eruptive stage 4. Post measles stage
  • 19.
    Incubation period • lastsapproximately 10-12 days to the first prodromal symptoms and another 2-4 days to the appearance of the rash; rarely, it may be as short as 6-10 days . • Body temperature may increase slightly 9-10 days from the date of infection and then subside for 24 hr or so. • The patient may transmit the virus by the 9th-10th day after exposure and occasionally as early as the 7th day, before the illness can be diagnosed
  • 20.
    Predomal phase • usuallylasts 3-5 days and is characterized by: • low-grade to moderate fever • dry cough • coryza • conjunctivitis . These symptoms nearly always precede the appearance of Koplik spots , the pathognomonic sign of measles, by 2-3 days
  • 21.
    • The conjunctivalinflammation and photophobia may suggest measles before Koplik spots appear. • .
  • 22.
    Koplicks spot • Anenanthem or red mottling is usually present on the hard and soft palates • the pathognomonic sign of measles • are grayish white dots , usually as small as grains of sand, that have slight, reddish areolae ; occasionally they are hemorrhagic . • tend to occur opposite the lower molars but may spread irregularly over the rest of the buccal mucosa. • Rarely they are found within the midportion of the lower lip , on the palate , and on the lacrimal caruncle . • They appear and disappear rapidly , usually within 12-18 hr . • As they fade , a red , spotty discoloration of the mucosa may remain
  • 24.
    Predomal phase (cont.) •Occasionally , the prodromal phase may be severe , being ushered in by a sudden high fever , sometimes with convulsions and even pneumonia . • Usually the coryza, fever, and cough are increasingly severe up to the time the rash has covered the body. • The temperature rises abruptly as the rash appears and often reaches 40°C (104°F) or higher.
  • 25.
    • In uncomplicatedcases , as the rash appears on the legs and feet, the symptoms subside rapidly within about 2 days , usually with an abrupt drop in temperature to normal.
  • 26.
    Eruptive stage Usually startsas faint macules on the:  upper lateral parts of the neck  behind the ears  along the hairline  posterior parts of the cheek .
  • 27.
    The rash The individuallesions become increasingly maculopapular as the rash spreads rapidly over the: • entire face • neck • upper arms • upper part of the chest within approximately the first 24 hr <
  • 29.
    • During thesucceeding 24 hr the rash spreads over the back, abdomen, entire arm, and thighs. • As it finally reaches the feet on the 2nd-3rd day , it begins to fade on the face.
  • 30.
    • The rashfades downward in the same sequence in which it appeared. • The severity of the disease is directly related to the extent and confluence of the rash. • In mild measles the rash tends not to be confluent , and in very mild cases there are few, if any, lesions on the legs
  • 31.
    • In severecases the rash is confluent , the skin is completely covered, including the palms and soles, and the face is swollen and disfigured. • The rash is often slightly hemorrhagic ; in severe cases with a confluent rash, petechiae may be present in large numbers, and there may be extensive ecchymoses
  • 32.
    • Complete absenceof rash is rare except : • 1. in patients who have received immunoglobulin (Ig) during the incubation period • 2. in some patients with HIV infection • 3. occasionally in infants younger than 9 mo of age who have appreciable levels of maternal antibody
  • 33.
    • In thehemorrhagic type of measles ( black measles ), bleeding may occur from the mouth, nose, or bowel. • In mild cases the rash may be less macular and more nearly pinpoint , somewhat resembling that of scarlet fever or rubella
  • 34.
    • Itching isgenerally slight . • As the rash fades , branny desquamation and brownish discoloration occur and then disappear within 7-10 days.
  • 35.
    Diagnosis • The diagnosisis usually apparent from the characteristic clinical picture ; laboratory confirmation is rarely needed • Testing for measles IgM antibodies is recommended in some situations • Measles IgM is detectable for 1 mo after illness , but sensitivity of IgM assays may be limited in the first 72 hr of the rash illness.
  • 36.
    • Isolation ofmeasles virus from clinical samples is also useful in identifying the genotype of the strain to track transmission patterns. • All suspected measles cases should be reported immediately to local or health departments. • During the prodromal stage multinucleated giant cells can be demonstrated in smears of the nasal mucosa
  • 37.
    • Antibodies becomedetectable when the rash appears ; • Testing of acute and convalescent sera demonstrates the diagnostic seroconversion or fourfold increase in titer. • Measles virus can be isolated by tissue culture in human embryonic or rhesus monkey kidney cells
  • 38.
    • Cytopathic changes, visible in 5-10 days, consist of multinucleated giant cells with intranuclear inclusions . • The white blood cell count tends to be low with a relative lymphocytosis • Cerebrospinal fluid in patients with measles encephalitis usually shows an increase in protein and a small increase in lymphocytes . The glucose level is normal.
  • 39.
    • The rashof rubeola must be differentiated from that of: • Rubella • Roseola infantum (human herpesvirus 6 • Infections resulting from: • echovirus • coxsackievirus • adenovirus • Infectious mononucleosis • Toxoplasmosis • Meningococcemia • Scarlet fever • Rickettsial diseases • Kawasaki disease • Serum sickness • Drug rashes