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Mumps and Pertuses

Dr.shihab ahmed

Lecturer in TUCOM


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OBJECTIVES

Clarify the epidemiology of mumps.

Identify the clinical features of mumps.

Outline the management of mumps.

List the complications of mumps.

Identify the stages of pertuses.

Clarify who to diagnose pertuses.

Outline the prevention of pertuses.


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Mumps 

Mumps is an important childhood disease that was 
historically widespread but now occur very 
infrequently. It is an acute viral infection 
characterized by painful enlargement of salivary 
glands, chiefly the parotids, as the usual presenting 
sign.

Mumps caused by RNA virus paramyxovirus in the 
family paramyxoviridae, which also includes the Para 
influenza viruses. Only one serotype is known.


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Epidemiology 

Mumps is endemic in most unvaccinated 
populations; the virus is spread from human 
reservoir by direct contact, airborne droplets, fomites 
contaminated by saliva, and possibly by urine.

It is distributed worldwide and affects both sexes 
equally.

Before the introduction of vaccine, the peak 
incidence of the disease occurred in children 5-9 
years of age; now must cases occur in young adults.


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Cilnical manifestations

The incubation period range from 14-24 days, with a peak at 17-18 
days. Approximately 30-40% of cases are sub clinical. In children, 
prodromal manifestations are rare but may be manifested by fever, 
muscular pain ( especially in the neck ) , headache and malaise.

Salivary glands; pain and swelling in one or more parotid glands. 
Edema of the skin and soft tissues usually extends further and obscure 
the limit of the glandular swelling, so that the swelling is more readily 
appreciated by sight more than by palpation, the swelling is proceed 
gradually and reach the peak within 1-3 days pushing the earlobe 
upward and outward and the angle of the mandible is on longer be 
visible, the swelling slowly subside within 3-7 days but occasionally 
stay longer. One parotid gland usually swell a day ore two before the 
other, but in approximately quarter of cases the disease remains 
unilateral. The swollen area is tender and painful especially when 
tasting sour liquids such us lemon juice. Redness and swelling around 
opening of stensen duct is common. Edema of the homolateral 
pharnyx and displace the tonsil medially.

In 10-15% of patients only the sub mandibular glands may be swollen, 
redness and swelling of Wharton duct common in such a case.


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Diagnosis and differential diagnosis

Diagnosis is usually by clinical symptoms and physical 
examination.

Routine laboratory tests are nonspecific such as leucopenia 
and relative lymphocytosis.

The microbiological diagnosis is by serology and viral culture.

Serology; seroconersion , four folds rise of IgG titer is 
diagnostic.

DIFFERENTIAL DIAGNOSIS.

Other viral causes of parotitis include HIV, influenza and Para 
influenza virus, CMV , coxsackieviruses.

Acute suppurative parotitis is bacterial infection caused by 
staphylococcus aureus in which pus can be expressed from the 
duct. A salivary calculus obstructing either parotid or sub 
mandibular duct may also leads to dland swelling.


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treatment

No specific anti viral therapy.

Treatment is entirely supportive.

Antipyretics, such as acetaminophen and ibuprofen 
are indicated for fever.

Bed rest should be guided by patients needs.

Diet should be adjusted according to ability to chew.

Mumps arthritis may be treated by 2 weeks of non-
steroidal anti inflammatory agents or corticosteroids, 
salicylates don

’t appear to be effective.


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Complications of mumps

Meningoencephalomylitis, which is the most frequent 
complication in childhood, it occurs either as a primary viral 
infection to the neurons, or post infectious demylinating 
encephalitis.

Orchitis and epididymitis.

Oophoritis.

Pancreatitis.

Myocarditis.

Arthritis.

Thyroditis.

Deafness.

Ocular complications; dacryoadenitis and optic neuritis.


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pertussis

Pertussis is an acute respiratory tract infection 
caused by Bordetella pertussis and pordetella para 
pertussis, its preferable than whooping couph 
because most infected individuals don

’t whoop.

Bordetella organisms are tiny gram negative 
coccobacilli that grow aerobically on starch blood 
agar, and producing pertussis toxin which is the most 
virulent protein. 


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Clinical manifestations

Classically, pertussis is a 6 weeks disease, divided into catarrhal, 
paroxysmal, and convalescent stages.

Catarrhal stage begins after an incubation period 3-12 days of non 
specific symptoms of congestion and rhinorrhea accompanied by low 
grade fever, sneezing, lacrimation and conjactival injection. As initial 
symptoms wane, coughing marks the onset of the disease.

Paroxysmal stage; the cough at first is dry, intermittent and irritative 
evolve to severe paroxysms that are the hallmark of pertussis. 

Whoop (forceful inspiratory gasp) infrequently occur in infants less 
than 3 months of age who are exhausted or lack of muscular strength 
to create a sudden negative intra thoracic pressure.

Post tussive emesis is common in pertussis at all ages and is a 
specific clue to the diagnosis.

Convalescent stage; as paroxysmal stage fade, the number, severity 
and duration of episodes diminished.


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Contd.

Paradoxically in infants, cough and whoops may become more 
louder and classic in convalescent stage.

Immunized children have shortening of all stages of pertussis. 
In infants younger than 3 months, the catarrhal phase is few 
days or even not recognized at all when apnea, chocking, or 
gasping coughing herald the onset of the disease; 
convalescence include intermittent paroxysms of coughing 
throughout the fist year of life including exacerbations with 
subsequent respiratory illnesses; these are not due to 
reinfection or reactivation of B. pertussis.

Finding on physical examination are non specific, signs of lower 
respiratory tract disease are not expected. Conjunctival 
hemorrhage and petechiae on the upper body are common.


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Diagnosis 

Pertussis should be suspected in any patient who predominant 
complaint of cough especially if the following are absent: fever, 
malaise or myalgia, exanthem or enanthem, sore throat, 
hoarseness, whease or tachypnea and rales.

Cough more than 14 days with at least on associated symptom 
of paroxysms, whoop, or post tussive emesis has sensitivity of 
81%.

Apnea or cyanosis ( before appreciation of cough) is a clue in 
infant less than 3 months.

Leukocytosis (15,000-20,000) due to absolute lymphocytosis is 
characteristic in catarrhal stage.

Isolation of B.pertussis in culture remain the gold stander for 
diagnosis.


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Treatment

Goals of treatment are to limit the number of 
paroxysms, maximize nutrition, rest, and recovery 
without sequelae.

Erythromycin 40-50 mg/kg 4 times a day for 14 days. 
Clarithromycin 15-20 mg/kg/day twice daily for 7 
days. Azithromycin 10 mg/kg once daily for 5 days.

Isolation; patients are placed in respiratory isolation 
for more than 5 days after initiation of erythromycin 
therapy.

Children should be excluded from school until 
erythromycin has been taken for 5 days .


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Prevention 

Universal immunization of children less than 7 years 
of age with pertussis vaccine, beginning in infancy.

ACELLULAR VACCINE. Multiple diphtheria and 
tetanus toxoids combined with acellular pertussis 
vaccine (DTaP) vaccines currently are licensed in the 
united state and are preferred over those containing 
whole cell pertussis vaccine because of fewer 
adverse reactions.




رفعت المحاضرة من قبل: Bakr Zaki
المشاهدات: لقد قام عضو واحد فقط و 124 زائراً بقراءة هذه المحاضرة








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