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MENINGOCOCCAL INFECTION
BHAVYA KOGANTI
GROUP 3
TSMU
MENINGOCOCCAL INFECTION
 Neisseria meningitidis (meningococcus)
 gm (-) diplococcus usually found
within PMN leucocytes
13 serogroups by surface
capsular polysaccharide
A, B, C, W135 and Y- frequent
isolates.
 Disease may occur following exposure
to carriers or infected patients within
the family, day care and military camps
 occurs most frequent:(< 5 yrs old )
peak attack rate : 6-12 months old
 2nd peak attack rate: 15-19 y/o of age
MENINGOCOCCAL INFECTION
Meningococci colonize the nasopharynx

penetrate mucosal surface

transported by leukocytes to blood stream

hematogenous dissemination

localizes: heart, CNS, skin, mucous and
serous membranes adrenals
Release of IL
and TNF
hypotension
multi-organ
system
failure
Diffuse *Complement DIC
vasculitis activation
H’ge and necrosis in
any organ
bleeding into adrenals
in patients with
septicemia and
shock
Waterhouse-
Friderichsen
syndrome
 Clinic.The incubation period is from 2 to 10
days (usually 4-6 days).
 Clinical classification:
 Localized forms (acute nasopharyngitis)
 Generalized forms
(meningococcemia, meningitis)
 Rare form (endocarditis, arthritis,
pneumonia, iridocyclitis)
 spectrum range from asx’c colonization to
fulminant sepsis
1. Bacteremia without sepsis
2. Meningococcemia (sepsis) without meningitis
3. Meningitis with or without meningococcemia
 Manifested a moderate and short-term (1-3
days)
 increase in temperature,
 mild symptoms of intoxication
 rhinopharyngitis (nasal congestion, flushing,
dryness, swelling of the posterior pharyngeal
wall with hyperplasia of lymphoid follicles
affected mucosa "dry", sometimes bluish).
 From acute viral disease meningococcal
nasopharyngitis different is that the mucous
membrane of the soft and hard palate, and
tonsils are not impaired or only slightly
hyperaemic, but major changes are located
on the back of the throat.
 Nasopharyngitis preceded meningococcemia
at an average of 78% of patients.
 Meningococcemia is inherently
meningococcal sepsis, which, like other
septic conditions, appears febrile fever and
severe intoxication syndrome with
manifestations of multiple organ pathology.
 The most important diagnostic symptom is a
“RASH”.
 after 5-15 hours of onset
 single or multiple polymorphic elements
ranging in size from 2.1 mm to 5 cm or more
in diameter and has a hemorrhagic character.
 asymmetrically, mainly on the skin of the
thighs and buttocks, at least - on the trunk
and face.
 Initially with pharyngitis, fever, myalgias,
arthralgias, headache, and GI complaints
within hours--> (+) petechial, purpuric
(purpura fulminanas)
 ( slate gray satellite shaped ) or morbilliform
lesions with hypotension, DIC, acidosis, adrenal
h’ge, renal/heart failure, coma
 If fulminant--> rapidly progressive purpura,
relentless shock, adrenal H’ge, extensive
hematogenous dissemination unresponsive to
therapy
 if with meningitis, (most common clinical
manifestation) indistinguishable from those
2° to other bacteria
 (+) petechial < 12° prior to admission
 (+) hypotension
 absence of meningitis
 WBC < 10,000/mm3
 ESR < 10 mm/hr.
Interpretation:
(+) 3 or > features: 90% mortality
> 2 features; 9% mortality
 Rapid progression of petechia to ecchymoses
or purpura
 Wakefulness
 skin perfusion
 respiratory distress
 thrombocytopenia
 advanced age
 Seen in children and adults
 low grade fever, non toxic appearance, arthralgias,
headache , rash,
 (+) blood culture
 mean duration of illness: 6-8 weeks
 Waxing and waning sx
purulent arthritis
acute non suppurative polyarthritis
erythema nodosum
URI
subacute endocarditis
 assoc with C5 deficiency
CHRONIC
MENINGOCOCCEMIA
1. Maintain a high index of suspicion
(fever, petechial rash, abn mental status)
2. Gm stain of petechial scrapings
CSF
buffy coat of blood;
gm (-) diplococci
3. Culture of blood, CSF, petechial scraping, synovial
fluid, sputum and other body fluids
4. Antigen detection tests (CSF, urine, serum)
CIE, latex agglutination,
lack adequate sensitivity and specificity
Aq Penicillin G 250,000 -300,000 u/k/day IV
6 div doses x 7 days
Alternatives :
Cefotaxime
Ceftriazone
200 mg/k/d
100-150 mg/k/day
If allergic to B-lactams :
Chloramphenicol 75-100 mg/kg d
Chemoprophylaxis
 for all household, school or day care contacts
ASAP
 NOT ROUTINELY recommended for medical
personnel EXCEPT those with INTIMATE
exposure (mouth to mouth resuscitation,
intubation, suctioning)
Chemoprophylaxis
 DOC: Rifampicin 10 mg/kg (max 600 mg) q 12° x
2 days
 other drugs: Ceftriaxone
Ciprofloxacin
 meningococcal vaccine can be used with
chemoprophylaxis since 2° cases may occur several
weeks later
Vaccines available
monovalent A
bivalent A and C
quadrivalent A, C, Y, W135
 no effective vaccine against serogroup B
 not routinely recommended
Recommended:
1. children > 2 yrs.
2. In high risk grps.
(+) functional /anatomic asplenia,
(+) terminal complement component defect +
as adjunct to chemoprophylaxis
For Meningitis:
deafness
ataxia
Sz
blindness
paresis of CN 3,4,6,7,
hemi or quadriparesis
obstructive hydrocephalus
COMPLICATIONS
For Meningococcemia:
Adrenal H’ge, arthritis,
myocarditis, pericarditis,
pneumonia, lung abscess,
peritonitis, renal infarcts, DIC,
peripheral neuropathy
Vasculitis - 2° bacterial infection  tissue necrosis
 gangrene  skin loss

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Menigocccal

  • 2. MENINGOCOCCAL INFECTION  Neisseria meningitidis (meningococcus)  gm (-) diplococcus usually found within PMN leucocytes 13 serogroups by surface capsular polysaccharide A, B, C, W135 and Y- frequent isolates.
  • 3.  Disease may occur following exposure to carriers or infected patients within the family, day care and military camps  occurs most frequent:(< 5 yrs old ) peak attack rate : 6-12 months old  2nd peak attack rate: 15-19 y/o of age MENINGOCOCCAL INFECTION
  • 4. Meningococci colonize the nasopharynx  penetrate mucosal surface  transported by leukocytes to blood stream  hematogenous dissemination  localizes: heart, CNS, skin, mucous and serous membranes adrenals
  • 5. Release of IL and TNF hypotension multi-organ system failure Diffuse *Complement DIC vasculitis activation H’ge and necrosis in any organ bleeding into adrenals in patients with septicemia and shock Waterhouse- Friderichsen syndrome
  • 6.  Clinic.The incubation period is from 2 to 10 days (usually 4-6 days).  Clinical classification:  Localized forms (acute nasopharyngitis)  Generalized forms (meningococcemia, meningitis)  Rare form (endocarditis, arthritis, pneumonia, iridocyclitis)
  • 7.  spectrum range from asx’c colonization to fulminant sepsis 1. Bacteremia without sepsis 2. Meningococcemia (sepsis) without meningitis 3. Meningitis with or without meningococcemia
  • 8.  Manifested a moderate and short-term (1-3 days)  increase in temperature,  mild symptoms of intoxication  rhinopharyngitis (nasal congestion, flushing, dryness, swelling of the posterior pharyngeal wall with hyperplasia of lymphoid follicles affected mucosa "dry", sometimes bluish).
  • 9.  From acute viral disease meningococcal nasopharyngitis different is that the mucous membrane of the soft and hard palate, and tonsils are not impaired or only slightly hyperaemic, but major changes are located on the back of the throat.
  • 10.  Nasopharyngitis preceded meningococcemia at an average of 78% of patients.  Meningococcemia is inherently meningococcal sepsis, which, like other septic conditions, appears febrile fever and severe intoxication syndrome with manifestations of multiple organ pathology.
  • 11.  The most important diagnostic symptom is a “RASH”.  after 5-15 hours of onset  single or multiple polymorphic elements ranging in size from 2.1 mm to 5 cm or more in diameter and has a hemorrhagic character.  asymmetrically, mainly on the skin of the thighs and buttocks, at least - on the trunk and face.
  • 12.  Initially with pharyngitis, fever, myalgias, arthralgias, headache, and GI complaints within hours--> (+) petechial, purpuric (purpura fulminanas)  ( slate gray satellite shaped ) or morbilliform lesions with hypotension, DIC, acidosis, adrenal h’ge, renal/heart failure, coma
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.  If fulminant--> rapidly progressive purpura, relentless shock, adrenal H’ge, extensive hematogenous dissemination unresponsive to therapy  if with meningitis, (most common clinical manifestation) indistinguishable from those 2° to other bacteria
  • 19.  (+) petechial < 12° prior to admission  (+) hypotension  absence of meningitis  WBC < 10,000/mm3  ESR < 10 mm/hr. Interpretation: (+) 3 or > features: 90% mortality > 2 features; 9% mortality
  • 20.  Rapid progression of petechia to ecchymoses or purpura  Wakefulness  skin perfusion  respiratory distress  thrombocytopenia  advanced age
  • 21.  Seen in children and adults  low grade fever, non toxic appearance, arthralgias, headache , rash,  (+) blood culture  mean duration of illness: 6-8 weeks
  • 22.  Waxing and waning sx purulent arthritis acute non suppurative polyarthritis erythema nodosum URI subacute endocarditis  assoc with C5 deficiency CHRONIC MENINGOCOCCEMIA
  • 23. 1. Maintain a high index of suspicion (fever, petechial rash, abn mental status) 2. Gm stain of petechial scrapings CSF buffy coat of blood; gm (-) diplococci
  • 24.
  • 25. 3. Culture of blood, CSF, petechial scraping, synovial fluid, sputum and other body fluids 4. Antigen detection tests (CSF, urine, serum) CIE, latex agglutination, lack adequate sensitivity and specificity
  • 26. Aq Penicillin G 250,000 -300,000 u/k/day IV 6 div doses x 7 days Alternatives : Cefotaxime Ceftriazone 200 mg/k/d 100-150 mg/k/day If allergic to B-lactams : Chloramphenicol 75-100 mg/kg d
  • 27. Chemoprophylaxis  for all household, school or day care contacts ASAP  NOT ROUTINELY recommended for medical personnel EXCEPT those with INTIMATE exposure (mouth to mouth resuscitation, intubation, suctioning)
  • 28. Chemoprophylaxis  DOC: Rifampicin 10 mg/kg (max 600 mg) q 12° x 2 days  other drugs: Ceftriaxone Ciprofloxacin  meningococcal vaccine can be used with chemoprophylaxis since 2° cases may occur several weeks later
  • 29. Vaccines available monovalent A bivalent A and C quadrivalent A, C, Y, W135  no effective vaccine against serogroup B  not routinely recommended
  • 30. Recommended: 1. children > 2 yrs. 2. In high risk grps. (+) functional /anatomic asplenia, (+) terminal complement component defect + as adjunct to chemoprophylaxis
  • 31. For Meningitis: deafness ataxia Sz blindness paresis of CN 3,4,6,7, hemi or quadriparesis obstructive hydrocephalus
  • 32. COMPLICATIONS For Meningococcemia: Adrenal H’ge, arthritis, myocarditis, pericarditis, pneumonia, lung abscess, peritonitis, renal infarcts, DIC, peripheral neuropathy Vasculitis - 2° bacterial infection  tissue necrosis  gangrene  skin loss