Meningococcal Meningitis
(Cerebrospinal Fever)
Dr. Yan Lin Aung
Medical Officer
Central Epidemiology Unit
Department of Public Health
Meningococcal Disease:
Overview of a Rare but
Potentially Deadly Infection
Meningitis
Meningococcal Disease
 A bacterial infection
– Neisseria meningitidis
 An unpredictable disease
– 98% of cases are sporadic; fewer than 2% are related to
outbreaks
– Typically occurs among previously healthy children and
adolescents
 Approximately 2100-3400 cases occurred annually
in the 1990s
– Approximately 370-1000 per year during 2009-2015
Getty Images/ROYALTYSTOCKPHOTO
Causal Organism
 Several different bacteria can cause meningitis
– Neisseria meningitidis is the one with the potential
to cause large epidemics
– Twelve serogroups of N. meningitidis have been
identified, six of which (A, B, C, W135, X and Y)
can cause epidemics
– Groups A, B and C accounts for at least 90% of
cases worldwide
– Group B and C in most European and many Latin
American countries
– Group A is the main cause in Africa and Asia
– Geographic distribution and epidemic potential
differ according to serogroup.
Neisseria meningitidis
 Family - Neisseriaceae
 Gram-negative
 Non-spore forming
 Non-motile
 Encapsulated
 Non acid-fast diplococci
Kidney bean shape
under microscope
 At least 12 serogroups
Invasive: serogroups A,
B, C, W-135, and Y
Epidemiology
Bacterial form of meningitis
Serious infection of the meninges
that affects the brain membrane
 It can cause severe brain damage
 Fatal in 50% of cases if untreated
Meningitis belt of sub-Saharan
Africa
– Gambia, Senegal, Mali, Burkina
Faso, Ghana, Niger, Nigeria, Camero
on, Chad, Central African
Republic, Sudan, South
Sudan, Uganda, Kenya, Ethiopia, Eritrea
Dynamics of Disease Transmission
Rash in Meningitis
 Meningococcacemia – rash
 Tumbler Test
Meningitis the rash can be
very scanty or even absent
Look for the rash, and a non-
blanching rash should therefore
be treated as an emergency
Modes of Transmission
 Spread through respiratory and throat secretions
– Coughing, Sneezing
– Kissing
– Sharing eating utensils, water bottles, etc
 Crowded settings facilitate transmission
– College dormitory
– Crowded household
– Military barracks
– Nightclubs, bars
Getty Images/Nick Daly
Risk groups
 Household contacts of case patients, Military recruits,
College freshmen who live in dormitories,
Microbiologists, Persons traveling to a country where
meningococcal disease is epidemic or highly endemic,
and Patients without spleens or with terminal
complement component deficiencies.
 Infants less than one year of age and adolescents ages
16 through 21 years have higher rates of disease than
other age groups, but cases occur in all age groups
including the elderly.
Carrier
 Reservoir - Humans
The bacteria can be carried in the throat and
sometimes-
It is believed that 10% to 20% of the population
carries Neisseria meningitidis in their throat at any
given time
However, the carriage rate may be higher in epidemic
situations
The mean duration of temporary carriers is about 10
months
During epidemics, the carrier rate may go up to 70 –
80 percent
Incubation Period
 Incubation period – 3-4 days (2-10 days)
 Neisseria meningitidis only infects in humans;
 There is no animal reservoir
Symptoms
 Commonest: High Fever, Stiff neck, sensitivity to
Light, Confusion, Headaches and Vomiting
 Diagnosed early and adequate treatment is started -
5% to 10% of patients die
- typically within 24 to 48 hours after the onset of symptoms
 A less common but even more severe (often fatal)
form of meningococcal disease is meningococcal
septicaemia,
- characterized by a haemorrhagic rash and rapid circulatory
collapse.
Signs & Symptoms
• Rash (8-9 hrs)
• Shock
• Septicemia
• Impair consciousness
• Neck stiffness
• Sign of meningism
Time Is of the Essence
 Early symptoms are nonspecific
– Fever, Headache, Nausea, Vomiting, Loss of Appetite
– Mimic symptoms of common Viral illnesses
 Characteristic symptoms occur later
– Hemorrhagic rash, neck stiffness,
photophobia
– Typically develop approximately 12-15 hours
after symptoms begin
 Rapid progression
– Death may occur within 24 hours of symptom onset
Diagnosis
 Initial diagnosis - Clinical Examination followed by
Lumbar Puncture (LP)
 LP- purulent spinal fluid (CSF)
 The bacteria can sometimes be seen in microscopic
examinations of the spinal fluid.
 Confirmed by growing the bacteria from specimens
of spinal fluid or blood - by agglutination tests or by
Polymerase Chain Reaction (PCR).
 Serogroups and susceptibility testing to antibiotics -
important
Differential Diagnosis??
 Acute Disseminated Encephalomyelitis
 Aseptic Meningitis
 Haemophilus Meningitis
 Herpes Simplex Encephalitis
 Intracranial Epidural Abscess
 Lyme Disease
 Neonatal Meningitis
 Staphylococcal Meningitis
 Subdural Empyema
 Tuberculous Meningitis
 Viral Meningitis
Treatment
 Potentially fatal & Medical emergency
 Admission to a hospital or health centre is necessary
 Isolation of the patient is not necessary
 Respiratory isolation for 24 hours after start of chemotreatment
Appropriate antibiotic treatment must be started as soon as
possible, ideally after LP
 Penicillin, Ampicillin, Chloramphenicol and Ceftriaxone
– Benzylpenicillin 1200 mg (Adult & aged 10 or older)
• Child 1-9 years: 600 mg
• Infant: 300 mg
Outcomes Can Be Severe,
Even with Treatment
 Serious outcomes include meningitis (most common
clinical presentation) and meningococcemia (bloodstream
infection)
 Death rate of 10%-15%, even with antibiotic therapy
Death rate even higher (up to
50%) for patients who develop
meningococcemia
. Up to 20% of people who
survive meningococcal
disease suffer lifelong
disability
–Amputation of arms or legs,
hearing loss, brain damage
Courtesy of National Meningitis Association
Prevention
 Cough etiquette
– Cover your mouth and nose with a tissue when you
cough or sneeze.
– Put your used tissue in the waste basket.
– If you don't have a tissue, cough or sneeze into your
upper sleeve or elbow, not your hands.
 Respiratory Hygiene
– You may be asked to put on a facemask to protect
others.
– Wash your hands often with soap and warm water for
20 seconds.
– If soap and water are not available, use an alcohol-
based hand rub.
Chemoprophylaxis
 Close contact (>8hrs + <3feet)
Standard regimens for antimicrobial prophylaxis:
Ciprofloxacin, Ceftriaxone, and Rifampin
 Adults - single oral dose of 500 mg of Ciprofloxacin
 250 mg of Intramuscular (IM) Ceftriaxone
 Under age 15 - a single dose of 150 mg of IM
Ceftriaxone.
Vaccination
 Polysaccharide vaccines have been available to
prevent the disease for over ?30 years.
 Bivalent (groups A and C)
 Trivalent (groups A, C and W)
 Tetravalent (groups A, C, Y and W135)
 For group B, polysaccharide vaccines cannot be
developed, due to antigenic mimicry with
polysaccharide in human neurologic tissues.
Epidemic response
 Prompt and appropriate case management with only
Chloramphenicol or Ceftriaxone
 Reactive mass vaccination of populations not already
protected through vaccination.
Key Points which should be taken
to your home
 Meningococcal disease is rare but potentially deadly for
people
 You are at increased risk from your mid-to-late teens into
your early 20s
 Disease can come on suddenly, without warning, and can
quickly become life-threatening
 The disease can result in severe, lifelong disability, such as
hearing loss, amputation of arms or legs, and brain damage
 Meningococcal vaccine is safe and effective
 For routine vaccination, 2 doses are recommended
Principles of Outbreak
Investigations
Be systematic!
• Follow the same steps for every type of outbreak
• Write down case definitions
• Ask the same questions of everybody
Stop often to re-assess what you know
• Line-listing and epidemic curve provide valuable
information;
Coordinate with partners (e.g., environmental and
epidemiology)
10 Steps of an Outbreak
Investigation
 Identify investigation team and resources
 Establish existence of an outbreak
 Verify the diagnosis
 Construct case definition
 Find cases systematically and develop line listing
Perform descriptive epidemiology/develop hypotheses
Evaluate hypotheses/perform additional studies as
necessary
 Implement control measures
 Communicate findings
 Maintain surveillance
Threshold
 A threshold approach according to the epidemiology of
the country is used in many countries to differentiate
endemic disease from outbreaks
 Alert threshold: 5 cases per 100,000 population or
increased in relation to previous non-epidemic years.
 Once the alert threshold is reached: mandatory
investigation, confirmation of agent, reinforcing of
surveillance, enhancing of preparedness, and treatment
of patients
Threshold (cont.)
 Epidemic threshold: 10 cases per 100,000 population or
15 cases per 100,000 population or weekly doubling of
cases each week or 2 cases at a mass gathering or
among refugees or displaced persons
 Once epidemic threshold is reached: mass vaccination,
provision of drugs to health units, treatment of cases,
and public education
Distribution of Reported Meningococcal
Meningitis by State and Region (2015,
2016 and 2017)
Percent Distribution of Reported
Meningococcal Meningitis by State and
Region (2017)
Distribution of Reported Meningococcal
Meningitis by State and Region (2017)
Thank You
For
Your Kind Attention

Meningococcal meningitis (dr.yla)

  • 1.
    Meningococcal Meningitis (Cerebrospinal Fever) Dr.Yan Lin Aung Medical Officer Central Epidemiology Unit Department of Public Health
  • 2.
    Meningococcal Disease: Overview ofa Rare but Potentially Deadly Infection
  • 3.
  • 4.
    Meningococcal Disease  Abacterial infection – Neisseria meningitidis  An unpredictable disease – 98% of cases are sporadic; fewer than 2% are related to outbreaks – Typically occurs among previously healthy children and adolescents  Approximately 2100-3400 cases occurred annually in the 1990s – Approximately 370-1000 per year during 2009-2015 Getty Images/ROYALTYSTOCKPHOTO
  • 5.
    Causal Organism  Severaldifferent bacteria can cause meningitis – Neisseria meningitidis is the one with the potential to cause large epidemics – Twelve serogroups of N. meningitidis have been identified, six of which (A, B, C, W135, X and Y) can cause epidemics – Groups A, B and C accounts for at least 90% of cases worldwide – Group B and C in most European and many Latin American countries – Group A is the main cause in Africa and Asia – Geographic distribution and epidemic potential differ according to serogroup.
  • 6.
    Neisseria meningitidis  Family- Neisseriaceae  Gram-negative  Non-spore forming  Non-motile  Encapsulated  Non acid-fast diplococci Kidney bean shape under microscope  At least 12 serogroups Invasive: serogroups A, B, C, W-135, and Y
  • 7.
    Epidemiology Bacterial form ofmeningitis Serious infection of the meninges that affects the brain membrane  It can cause severe brain damage  Fatal in 50% of cases if untreated Meningitis belt of sub-Saharan Africa – Gambia, Senegal, Mali, Burkina Faso, Ghana, Niger, Nigeria, Camero on, Chad, Central African Republic, Sudan, South Sudan, Uganda, Kenya, Ethiopia, Eritrea
  • 8.
    Dynamics of DiseaseTransmission
  • 9.
    Rash in Meningitis Meningococcacemia – rash  Tumbler Test Meningitis the rash can be very scanty or even absent Look for the rash, and a non- blanching rash should therefore be treated as an emergency
  • 10.
    Modes of Transmission Spread through respiratory and throat secretions – Coughing, Sneezing – Kissing – Sharing eating utensils, water bottles, etc  Crowded settings facilitate transmission – College dormitory – Crowded household – Military barracks – Nightclubs, bars Getty Images/Nick Daly
  • 11.
    Risk groups  Householdcontacts of case patients, Military recruits, College freshmen who live in dormitories, Microbiologists, Persons traveling to a country where meningococcal disease is epidemic or highly endemic, and Patients without spleens or with terminal complement component deficiencies.  Infants less than one year of age and adolescents ages 16 through 21 years have higher rates of disease than other age groups, but cases occur in all age groups including the elderly.
  • 12.
    Carrier  Reservoir -Humans The bacteria can be carried in the throat and sometimes- It is believed that 10% to 20% of the population carries Neisseria meningitidis in their throat at any given time However, the carriage rate may be higher in epidemic situations The mean duration of temporary carriers is about 10 months During epidemics, the carrier rate may go up to 70 – 80 percent
  • 13.
    Incubation Period  Incubationperiod – 3-4 days (2-10 days)  Neisseria meningitidis only infects in humans;  There is no animal reservoir
  • 14.
    Symptoms  Commonest: HighFever, Stiff neck, sensitivity to Light, Confusion, Headaches and Vomiting  Diagnosed early and adequate treatment is started - 5% to 10% of patients die - typically within 24 to 48 hours after the onset of symptoms  A less common but even more severe (often fatal) form of meningococcal disease is meningococcal septicaemia, - characterized by a haemorrhagic rash and rapid circulatory collapse.
  • 15.
    Signs & Symptoms •Rash (8-9 hrs) • Shock • Septicemia • Impair consciousness • Neck stiffness • Sign of meningism
  • 16.
    Time Is ofthe Essence  Early symptoms are nonspecific – Fever, Headache, Nausea, Vomiting, Loss of Appetite – Mimic symptoms of common Viral illnesses  Characteristic symptoms occur later – Hemorrhagic rash, neck stiffness, photophobia – Typically develop approximately 12-15 hours after symptoms begin  Rapid progression – Death may occur within 24 hours of symptom onset
  • 17.
    Diagnosis  Initial diagnosis- Clinical Examination followed by Lumbar Puncture (LP)  LP- purulent spinal fluid (CSF)  The bacteria can sometimes be seen in microscopic examinations of the spinal fluid.  Confirmed by growing the bacteria from specimens of spinal fluid or blood - by agglutination tests or by Polymerase Chain Reaction (PCR).  Serogroups and susceptibility testing to antibiotics - important
  • 18.
    Differential Diagnosis??  AcuteDisseminated Encephalomyelitis  Aseptic Meningitis  Haemophilus Meningitis  Herpes Simplex Encephalitis  Intracranial Epidural Abscess  Lyme Disease  Neonatal Meningitis  Staphylococcal Meningitis  Subdural Empyema  Tuberculous Meningitis  Viral Meningitis
  • 19.
    Treatment  Potentially fatal& Medical emergency  Admission to a hospital or health centre is necessary  Isolation of the patient is not necessary  Respiratory isolation for 24 hours after start of chemotreatment Appropriate antibiotic treatment must be started as soon as possible, ideally after LP  Penicillin, Ampicillin, Chloramphenicol and Ceftriaxone – Benzylpenicillin 1200 mg (Adult & aged 10 or older) • Child 1-9 years: 600 mg • Infant: 300 mg
  • 20.
    Outcomes Can BeSevere, Even with Treatment  Serious outcomes include meningitis (most common clinical presentation) and meningococcemia (bloodstream infection)  Death rate of 10%-15%, even with antibiotic therapy Death rate even higher (up to 50%) for patients who develop meningococcemia . Up to 20% of people who survive meningococcal disease suffer lifelong disability –Amputation of arms or legs, hearing loss, brain damage Courtesy of National Meningitis Association
  • 21.
    Prevention  Cough etiquette –Cover your mouth and nose with a tissue when you cough or sneeze. – Put your used tissue in the waste basket. – If you don't have a tissue, cough or sneeze into your upper sleeve or elbow, not your hands.  Respiratory Hygiene – You may be asked to put on a facemask to protect others. – Wash your hands often with soap and warm water for 20 seconds. – If soap and water are not available, use an alcohol- based hand rub.
  • 22.
    Chemoprophylaxis  Close contact(>8hrs + <3feet) Standard regimens for antimicrobial prophylaxis: Ciprofloxacin, Ceftriaxone, and Rifampin  Adults - single oral dose of 500 mg of Ciprofloxacin  250 mg of Intramuscular (IM) Ceftriaxone  Under age 15 - a single dose of 150 mg of IM Ceftriaxone.
  • 23.
    Vaccination  Polysaccharide vaccineshave been available to prevent the disease for over ?30 years.  Bivalent (groups A and C)  Trivalent (groups A, C and W)  Tetravalent (groups A, C, Y and W135)  For group B, polysaccharide vaccines cannot be developed, due to antigenic mimicry with polysaccharide in human neurologic tissues.
  • 24.
    Epidemic response  Promptand appropriate case management with only Chloramphenicol or Ceftriaxone  Reactive mass vaccination of populations not already protected through vaccination.
  • 25.
    Key Points whichshould be taken to your home  Meningococcal disease is rare but potentially deadly for people  You are at increased risk from your mid-to-late teens into your early 20s  Disease can come on suddenly, without warning, and can quickly become life-threatening  The disease can result in severe, lifelong disability, such as hearing loss, amputation of arms or legs, and brain damage  Meningococcal vaccine is safe and effective  For routine vaccination, 2 doses are recommended
  • 26.
    Principles of Outbreak Investigations Besystematic! • Follow the same steps for every type of outbreak • Write down case definitions • Ask the same questions of everybody Stop often to re-assess what you know • Line-listing and epidemic curve provide valuable information; Coordinate with partners (e.g., environmental and epidemiology)
  • 27.
    10 Steps ofan Outbreak Investigation  Identify investigation team and resources  Establish existence of an outbreak  Verify the diagnosis  Construct case definition  Find cases systematically and develop line listing Perform descriptive epidemiology/develop hypotheses Evaluate hypotheses/perform additional studies as necessary  Implement control measures  Communicate findings  Maintain surveillance
  • 28.
    Threshold  A thresholdapproach according to the epidemiology of the country is used in many countries to differentiate endemic disease from outbreaks  Alert threshold: 5 cases per 100,000 population or increased in relation to previous non-epidemic years.  Once the alert threshold is reached: mandatory investigation, confirmation of agent, reinforcing of surveillance, enhancing of preparedness, and treatment of patients
  • 29.
    Threshold (cont.)  Epidemicthreshold: 10 cases per 100,000 population or 15 cases per 100,000 population or weekly doubling of cases each week or 2 cases at a mass gathering or among refugees or displaced persons  Once epidemic threshold is reached: mass vaccination, provision of drugs to health units, treatment of cases, and public education
  • 30.
    Distribution of ReportedMeningococcal Meningitis by State and Region (2015, 2016 and 2017)
  • 31.
    Percent Distribution ofReported Meningococcal Meningitis by State and Region (2017)
  • 32.
    Distribution of ReportedMeningococcal Meningitis by State and Region (2017)
  • 33.

Editor's Notes

  • #5 Meningococcal Disease in the United States Meningococcal disease is a bacterial infection caused by Neisseria meningitidis. It is an unpredictable disease. Although outbreaks do happen, the vast majority of cases (98%) are sporadic,1 typically occurring among previously healthy children and adolescents.2 For reasons that are not known, the incidence of meningococcal disease has declined in the United States since a peak in reported cases in the mid- to late-1990s. In that decade, approximately 2100 to 3400 cases were reported annually.3 Approximately 370 to 1000 cases per year were reported in the US from 2009 through 2015.4,5 Although rare, meningococcal disease has potentially severe consequences for people who are infected. References: 1. Centers for Disease Control and Prevention (CDC). Meningococcal disease. In: Epidemiology and Prevention of Vaccine-Preventable Diseases. (The Pink Book). Hamborsky J, Kroger A, Wolfe S, eds. 13th edition. Washington, DC: Public Health Foundation, 2015:231-246. 2. CDC. Prevention and control of meningococcal disease: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 2013;62(RR-2):1-28. 3. CDC. Summary of notifiable diseases—United States, 2012. MMWR. 2014;61(53):1-121. 4. CDC. Notifiable diseases and mortality tables. MMWR. 2015;63(52):ND-719-ND-732. 5. CDC. Notifiable diseases and mortality tables. MMWR. 2016;65(37):ND-652-ND-669.
  • #10 What is the tumbler test? Press a clear glass tumbler firmly against the rash. If you can see the marks clearly through the glass seek urgent medical help immediately. Check the entire body. Look out for tiny red or brown pin-prick marks which can change into larger red or purple blotches and blood blisters
  • #11 Modes of Transmission Help Explain Vulnerability of Adolescents and Young Adults Meningococcal bacteria colonize the mucosal surfaces of the nose and throat and are transmitted through direct contact with respiratory and throat secretions.1,2 Close and prolonged contact, such as coughing or sneezing on someone, kissing, or sharing eating or drinking utensils, can spread the disease.2 Being in a crowded setting or living in close quarters with an infected person, such as in a college dormitory or crowded household, also facilitates transmission.2,3 Nightclubs, bars, and military barracks are other settings where transmission may more readily occur. References: 1. CDC. Prevention and control of meningococcal disease: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 2013;62(RR-2):1-28. 2. World Health Organization. Meningococcal meningitis (fact sheet no. 141). November 2015. http://www.who.int/mediacentre/factsheets/fs141/en. Accessed March 1, 2017. 3. Immunization Action Coalition. Meningococcal: questions and answers: Information about the disease and vaccines. http://www.immunize.org/catg.d/p4210.pdf. Accessed March 1, 2017.
  • #17 Time Is of the Essence Meningococcal disease is difficult to diagnose in its early stages. Early symptoms—such as fever, headache, nausea, vomiting, and loss of appetite—are nonspecific, and similar to those of common viral illnesses, such as influenza. The symptoms characteristic of meningococcal disease—such as hemorrhagic rash, neck stiffness, and sensitivity to light—develop later, typically around 12 to 15 hours after the onset of symptoms.1 The disease progresses rapidly. Shock, unconsciousness, and death may occur within 24 hours of symptom onset,1,2 leaving little time for recognition and intervention. Supplemental note: In a study of 448 children 16 years of age or younger with meningococcal disease,1 most had nonspecific symptoms in the first 4 to 6 hours, but many were near death within 24 hours. Hospitalization occurred a median of 19 hours after onset of symptoms, ranging from 13 hours in children younger than 1 year of age to 22 hours in those 15 through 16 years of age. The time window for early clinical diagnosis is thus a narrow one. In this report, 103 of 448 cases were fatal. References: 1. Thompson MJ, Ninis N, Perera R, et al. Clinical recognition of meningococcal disease in children and adolescents. Lancet. 2006;367(9508):397-403. 2. World Health Organization. Meningococcal meningitis (fact sheet no. 141). November 2015. http://www.who.int/mediacentre/factsheets/fs141/en. Accessed March 1, 2017.
  • #21 Outcomes Can Be Severe, Even with Treatment The most common clinical presentation of meningococcal disease is meningitis. In a majority of persons with meningitis, meningococcal bacteria can be isolated from the blood. This bloodstream infection, known as meningococcemia, is especially dangerous.1 Overall, the death rate in patients with meningococcal disease is between 10% and 15%—even if appropriate antibiotic treatment is provided.1 In cases of meningococcemia, as many as 4 in 10 patients die.1 Up to 20% of survivors of meningococcal disease will suffer long-term impairment, such as amputation of arms or legs, hearing loss, or brain damage.2 References: 1. CDC. Meningococcal disease. In: Epidemiology and Prevention of Vaccine-Preventable Diseases. (The Pink Book). Hamborsky J, Kroger A, Wolfe S, eds. 13th edition. Washington, DC: Public Health Foundation, 2015:231-246. 2. CDC. Prevention and control of meningococcal disease: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 2013;62(RR-2):1-28.