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นพ.อินทนนท์ อิมสุวรรณ
                             ่
โครงการจัดตังภาควิชาเวชศาสตร์ฉุกเฉิน
            ้
        คณะแพทยศาสตร์ มหาวิทยาลัย
                         ธรรมศาสตร์
Ä   On October 2, 2001
0   a 63-year-old Caucasian photo editor
    working for a Florida newspaper
o   awoke early with nausea, vomiting, and
    confusion and was taken to a local
    emergency room for evaluation
P   His illness, which started on September
    27 during a trip to North Carolina
    characterized by malaise, fatigue, fever,
    chills, anorexia, and sweats
,   No history of headache, cough, chest
    pain, myalgias, dyspnea, abdominal
    pain, diarrhea, or skin lesions
Π  Patient was alert and interactive but
    spoke nonsensically
l   He was not oriented to person, place, or
    time
t   BT 39.2°C HR 109/min BP 110/80 RR
    14/min
0   Initial pulmonary, heart, and abdominal
    examinations were normal
e   No nuchal rigidity
CBC: Hct 45.7 WBC 9400 N 76% L15%
    Plt 109,000
C   Na 132 K 3.5 Cl 110 HCO3 24
1   UA :no RBC,WBC
l   prominent superior mediastinum and
    small left pleural effusion
0   WBC count 4,750/µL (81% neutrophils)
µ   RBC count 1,375/µL
µ   glucose 57 mg/dL (serum glucose 174
    mg/dL)
    protein 666 mg/dL
Microscopy examination of the CSF
showed many gram-positive bacilli
Shortly after admission
m   He had generalized seizures and was
    intubated for airway protection
The patient died on October 5
Autopsy findings
hemorrhagic mediastinal lymphadenitis
immunohistochemical staining showed
 disseminated B. anthracis in multiple organs
l   a 59-year-old Caucasian man, contract
    employee at a U.S. State Department
    mail sorting facility that received mail
    from the District of Columbia postal
    facility became ill
He had drenching sweats
    2 days of fever with chills,severe
    myalgias
w   cough with scant white sputum
    substernal chest pain
    nausea, vomiting, abdominal pain
BT 38.2°C HR 116/min BP 120/70 RR
    16/min
/   oxygen saturation 94% (room air)
n    He appeared ill and had decreased
    breath sounds at the right base
    The rest of the examination was
    unremarkable
ì   Hematocrit 48.1%
ì   WBC count 9,500/mm3 ( 81% N, 9% L
    9% M)
m   Platelet count 196,000/ mm3
9   Normal electrolytes and creatinine
Widening mediastinum
Mediastinal adenopathy with evidence of
 hemorrhage
Normal lung parenchyma
Small bilateral pleural effusions
Suspected small pericardial effusion
°   Intravenous penicillin
c   Rifampin
c   Ciprofloxacin
c   Vancomycin
Features that should alert possibility
of bioterrorism-related outbreak
r   A rapidly increasing disease incidence
    (e.g., within hours or days) in a normally
    healthy population
o    An epidemic curve that rises and falls
    during a short period of time
t   especially with fever, respiratory, or
    gastrointestinal complaints
Features that should alert possibility
of bioterrorism-related outbreak
    An endemic disease rapidly emerging at an
    uncharacteristic time or in an unusual pattern
    Lower attack rates among people who had
    been indoors
    especially in areas with filtered air or closed
      ventilation systems compared with people who
      had been outdoors
s   Clusters of patients arriving from a single locale
Features that should alert possibility
of bioterrorism-related outbreak
     Large numbers of rapidly fatal cases
s    Any patient presenting with uncommon
    disease and has bioterrorism potential
    Pulmonary anthrax
    Tularemia
    Plague
Ä   The U.S. Public health system and primary
    healthcare providers must be prepared to
    address various biological agents
b   pathogens that are rarely seen in the united
    states
r   High-priority agents include organisms that
    pose a risk to national security
P   Category A agents
    Can be easily disseminated or transmitted
     from person to person
    Result in high mortality rates and have the
     potential for major public health impact
    Might cause public panic and social
     disruption
    Require special action for public health
     preparedness
•   Anthrax (bacillus anthracis)
i   Botulism (clostridium botulinum toxin)
1   Plague (yersinia pestis)
H   Smallpox (variola major)
a   Tularemia (francisella tularensis)
r   Viral hemorrhagic fever
    filoviruses [Ebola, marburg]
    arenaviruses [Lassa, machupo]
Biological weapon
In year 2001, US
Anthrax was deliberately spread through the
 postal system by sending letters with powder
 containing anthrax
22 cases of anthrax infection
P   Bacillus anthracis
i    a gram-positive spore-forming
    bacterium
s   “woolsorters'disease”
a   a disease of sheep, cattle, and horses
The spores are extremely hardy and can
    survive for years
s   The disease is caused by exposure to
    the spores, not the bacilli in their
    vegetative state
The spores germinate into bacilli inside
    macrophages
n   Releasing toxins
    protective antigen
    edema factor
    lethal factor
O   cause edema and cell death
Skin : cutaneous anthrax
x   Lung : inhalation anthrax
    Breathing in anthrax spores from infected
     animal products like wool
l   GI tract : gastrointestinal anthrax
    Eating undercooked meat from infected
     animals
Incubation period
d   ranges from 1day to 8 weeks (average
    5days) depending on the exposure route
    and dose
     2-60 days following pulmonary exposure
     1-7 days following cutaneous exposure
     1-7 days following ingestion
0   the most lethal form of the disease
f   caused by inhaling spores into the lungs
n   the spores germinate and are
    transported to the tracheobronchial
    lymph nodes
Initial phase
ð flulike illness with malaise
 w nonproductive cough, chest discomfort
 u initial phase can be delayed for more
   than a month in some patients
 s 50% of patients develop hemorrhagic
   meningitis
Within 24 to 48 hours
h   abrupt deterioration
    Overwhelming sepsis
    Dyspnea, stridor
    Shock
    Hemorrhagic mediastinitis
Π  Chest radiograph show a widened
    mediastinum and hilar adenopathy
Mediastinal widening and pleural effusion
CT chest is more sensitive
Bloody pleural effusions
consolidation of the lung fields
H   Clinical diagnosis
    Flulike or septic illness
c   A reason to consider anthrax in the first
    place
    Current outbreak, warning from authorities
,   Sputum culture, gram stain, and blood
    cultures are not helpful until late in the
    course of the disease
Tests to confirm the diagnosis
    PCR for identification of anthrax markers
    in pleural fluid
i   serologic detection of immunoglobulin to
    protective antigen
e   Immunohistochemical testing of biopsy
    specimens
l   Influenza
spores are introduced into the skin
    through open wounds or abrasions
n   After I.P. 1 to 5 days
5   Begins as a papule usually on an
    exposed area
    the head, neck, or an upper extremity
o   The papule may resemble an insect or
    spider bite and may itch
a papule progressing to form a large
    vesicle over the next several days
e   Severe edema occurs around the lesion
    with regional lymphadenitis
m   The lesions are not tender
m   patient may or may not be febrile
Day 2   Day 4
Day 4 : edema   Day 4 : Eschar formation
After about 1 week
ü   the lesion ruptures, forming a black
    eschar
r   surrounding erythema and edema
    increase
h   The necrotic ulcer is usually painless
Ulcer and vesicle ringblack eschar
Forearm lesion on day 7
n   vesiculation and ulceration of initial macular or
    papular anthrax skin lesion
h   Eschar of the neck on day 15, typical of the
    last day of lesion
In the next 2 to 3 weeks
ü   the eschar sloughs off
f   the organism disseminates and the
    patient dies
The mortality rate
     20% without treatment
     1% with treatment
t   Antibiotics do not affect the course of
    local disease
e   but are used to prevent dissemination
    and death
H   Clinical diagnosis.
i   Confirmation
    Culturing of the lesion, punch biopsy,or
     serologic testing
l   Rare manifestations
o   The ingestion of insufficiently cooked,
    contaminated meat
t   the spores are transported to regional
    lymphatic tissue
r   I.P 2- 5 day
r   The mortality rate is 50%
0   Present with sore throat and neck
    swelling from cervical and
    submandibular lymphadenitis
m   The tonsils are frequently involved
i   Fever and toxicity
t   Dysphagia
t   Respiratory distress
Π  Begins with nausea, vomiting, and fever
e   Hematemesis
e   Ascites
e   Bloody diarrhea
e   Mesenteric lymphadenitis
a   Present with an acute abdomen
Rosen's Emergency Medicine: Concepts and Clinical Practice, 6th Ed
,   Death usually results within 3 days
s   The mortality rate was thought to
    exceed 90%
Π  Inactivated, cell-free anthrax vaccine
l   There is a vaccine to prevent anthrax, but it
    is not yet available for the general public
a   Anyone who may be exposed to anthrax
    Certain members of the US
    Armed forces
    Laboratory workers
    Workers who may enter contaminated areas
    In the event of an attack using anthrax as a
      weapon, people exposed would get the vaccine
ˆ   Human-to-human transmission has not
    been reported with inhalational anthrax
t   Airborne transmission does not occur,
    but direct contact with skin lesions may
    result in cutaneous infection
è   Yersinia pestis
à   gram-negative bacterium
c   Zoonotic disease is transmitted to
    humans by the bites of infected rodent
    fleas
Male Xenopsylla cheopis (oriental rat flea) engorged with
blood. This flea is the primary vector of plague in most large
plague epidemics in Asia, Africa, and South America
è   suggestive of exposure to rodents,
    rodent fleas, wild rabbits, sick or dead
    carnivores, or patients with pneumonic
    plague.
a   Incubation period is 1–6 days
,   Specimens
    bubo aspirates, blood cultures, sputum
     culture if pneumonic
o   Microscopic identification
t   culture confirmation
t   Serologic tests
    fourfold change in antibody titer to f1 antigen
     between acute- and convalescent-phase sera
Physicians should report all suspected
plague cases to state or local health
departments and/or consult with CDC to
obtain information and access
diagnostic services.
(   Parenteral antibiotic therapy
    Streptomycin
O   Alternatively
    Gentamicin
¤   Oral therapy
    Doxycycline
ì   No vaccine is currently available in the
    united states.
i   aimed at reducing contact with fleas and
    potentially infected rodents and other
    wildlife
Generated by the infected patient during
coughing, sneezing, talking during
respiratory-care procedures
Healthcare providers and others should
    wear a surgical-type mask when within 3
    feet of the infected patient
c   Some healthcare facilities require a
    mask be worn to enter the room of a
    patient on droplet precautions
Maintained until patient has completed
72 hours of antimicrobial therapy
Maintaining spatial separation of at least
    3 feet between infected patients and
    others when cohorting is not achievable.
r   Avoiding placement in the same room
    with an immunocompromised patient.
m   Special air handling is not necessary
    and doors may remain open
0   Prophylactic antibiotic treatment in
    person who exposure to
    bites of wild rodent fleas during an outbreak
    tissues of a plague-infected animal
    person or animal with suspected plague
     pneumonia
Contact precautions
Wear clean gloves upon entry into patient
 room.
Wear gown for all patient contact and for all
 contact with the patient’s environment.
Require a gown be worn to enter the room of
 a patient.
Gown must be removed before leaving the
 patient’s room.
Wash hands using an antimicrobial agent
Healthcare facilities without patient
    rooms appropriate for Airborne
    Precautions
e   should have a plan for transfer of
    suspected or confirmed smallpox
    patients to neighboring facilities with
    appropriate isolation rooms
Ð   Fever, headache and stiff neck
a   sepsis and rash in meningococcemia
H   N. meningitidis colonizes mucosal
    surfaces of nasopharynx
p   direct contact with large droplet
    respiratory secretions from the patients
    or asymptomatic carriers
c   Humans are the only host
H   Patients with meningococcemia should
    be placed in respiratory isolation for at
    least 24 hours.
H   Close contacts should receive antibiotic
    prophylaxis.
h   Household, nursery school, and daycare
    center contacts
r   Intimate contacts and health care workers
    with intimate exposure
    mouth-to-mouth resuscitation, intubation,suctioning
Rifampin, 10 mg/kg (up to 600 mg)
    orally every 12 hours for four doses
h   The dose for infants younger than 1
    month is 5 mg/kg.
.   Rifampin discolors the urine
r   Contact lenses should be removed to
    avoid permanent staining.
Ceftriaxone IM is effective against group
    A strains.
    125 mg for children younger than 12 years
    250 mg for those older than 12 years
    alternative for pregnant women and for
     people in whom compliance cannot be
     ensured.
o   Ciprofloxacin (500 mg orally)
È   Meningococcal vaccine should be
    considered
    adjunct to prophylaxis in epidemics
    close contacts in sporadic cases
n   The currently available vaccine is a
    quadrivalent vaccine
    containing purified capsular polysaccharides
     for groups A, C, Y, W
No vaccine exists for group B
the most prevalent serogroup in the United
 States.
The quadrivalent vaccine is not
    recommended for routine use
r   but should be administered to
    children 2 years of age
    older in high-risk groups
    functional or anatomic asplenia
    terminal complement deficiency
The vaccine is currently administered to
    U.S. military recruits.
c   Consideration in people traveling to
    endemic areas of the world such as sub-
    Saharan Africa.
Bioterrorism Present
Bioterrorism Present

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Bioterrorism Present

  • 1. นพ.อินทนนท์ อิมสุวรรณ ่ โครงการจัดตังภาควิชาเวชศาสตร์ฉุกเฉิน ้ คณะแพทยศาสตร์ มหาวิทยาลัย ธรรมศาสตร์
  • 2. Ä On October 2, 2001 0 a 63-year-old Caucasian photo editor working for a Florida newspaper o awoke early with nausea, vomiting, and confusion and was taken to a local emergency room for evaluation
  • 3. P His illness, which started on September 27 during a trip to North Carolina characterized by malaise, fatigue, fever, chills, anorexia, and sweats , No history of headache, cough, chest pain, myalgias, dyspnea, abdominal pain, diarrhea, or skin lesions
  • 4. Œ Patient was alert and interactive but spoke nonsensically l He was not oriented to person, place, or time t BT 39.2°C HR 109/min BP 110/80 RR 14/min 0 Initial pulmonary, heart, and abdominal examinations were normal e No nuchal rigidity
  • 5.
  • 6. CBC: Hct 45.7 WBC 9400 N 76% L15% Plt 109,000 C Na 132 K 3.5 Cl 110 HCO3 24 1 UA :no RBC,WBC
  • 7.
  • 8. l prominent superior mediastinum and small left pleural effusion
  • 9. 0 WBC count 4,750/µL (81% neutrophils) µ RBC count 1,375/µL µ glucose 57 mg/dL (serum glucose 174 mg/dL) protein 666 mg/dL
  • 10. Microscopy examination of the CSF showed many gram-positive bacilli
  • 11.
  • 12.
  • 13.
  • 14. Shortly after admission m He had generalized seizures and was intubated for airway protection
  • 15.
  • 16. The patient died on October 5 Autopsy findings hemorrhagic mediastinal lymphadenitis immunohistochemical staining showed disseminated B. anthracis in multiple organs
  • 17.
  • 18. l a 59-year-old Caucasian man, contract employee at a U.S. State Department mail sorting facility that received mail from the District of Columbia postal facility became ill
  • 19. He had drenching sweats 2 days of fever with chills,severe myalgias w cough with scant white sputum substernal chest pain nausea, vomiting, abdominal pain
  • 20. BT 38.2°C HR 116/min BP 120/70 RR 16/min / oxygen saturation 94% (room air) n He appeared ill and had decreased breath sounds at the right base The rest of the examination was unremarkable
  • 21. ì Hematocrit 48.1% ì WBC count 9,500/mm3 ( 81% N, 9% L 9% M) m Platelet count 196,000/ mm3 9 Normal electrolytes and creatinine
  • 22.
  • 24.
  • 25. Mediastinal adenopathy with evidence of hemorrhage Normal lung parenchyma Small bilateral pleural effusions Suspected small pericardial effusion
  • 26. ° Intravenous penicillin c Rifampin c Ciprofloxacin c Vancomycin
  • 27.
  • 28. Features that should alert possibility of bioterrorism-related outbreak r A rapidly increasing disease incidence (e.g., within hours or days) in a normally healthy population o An epidemic curve that rises and falls during a short period of time t especially with fever, respiratory, or gastrointestinal complaints
  • 29. Features that should alert possibility of bioterrorism-related outbreak An endemic disease rapidly emerging at an uncharacteristic time or in an unusual pattern Lower attack rates among people who had been indoors especially in areas with filtered air or closed ventilation systems compared with people who had been outdoors s Clusters of patients arriving from a single locale
  • 30. Features that should alert possibility of bioterrorism-related outbreak Large numbers of rapidly fatal cases s Any patient presenting with uncommon disease and has bioterrorism potential Pulmonary anthrax Tularemia Plague
  • 31. Ä The U.S. Public health system and primary healthcare providers must be prepared to address various biological agents b pathogens that are rarely seen in the united states r High-priority agents include organisms that pose a risk to national security
  • 32. P Category A agents Can be easily disseminated or transmitted from person to person Result in high mortality rates and have the potential for major public health impact Might cause public panic and social disruption Require special action for public health preparedness
  • 33. Anthrax (bacillus anthracis) i Botulism (clostridium botulinum toxin) 1 Plague (yersinia pestis) H Smallpox (variola major) a Tularemia (francisella tularensis) r Viral hemorrhagic fever filoviruses [Ebola, marburg] arenaviruses [Lassa, machupo]
  • 34. Biological weapon In year 2001, US Anthrax was deliberately spread through the postal system by sending letters with powder containing anthrax 22 cases of anthrax infection
  • 35. P Bacillus anthracis i a gram-positive spore-forming bacterium s “woolsorters'disease” a a disease of sheep, cattle, and horses
  • 36.
  • 37. The spores are extremely hardy and can survive for years s The disease is caused by exposure to the spores, not the bacilli in their vegetative state
  • 38. The spores germinate into bacilli inside macrophages n Releasing toxins protective antigen edema factor lethal factor O cause edema and cell death
  • 39. Skin : cutaneous anthrax x Lung : inhalation anthrax Breathing in anthrax spores from infected animal products like wool l GI tract : gastrointestinal anthrax Eating undercooked meat from infected animals
  • 40.
  • 41. Incubation period d ranges from 1day to 8 weeks (average 5days) depending on the exposure route and dose  2-60 days following pulmonary exposure  1-7 days following cutaneous exposure  1-7 days following ingestion
  • 42. 0 the most lethal form of the disease f caused by inhaling spores into the lungs n the spores germinate and are transported to the tracheobronchial lymph nodes
  • 43. Initial phase ð flulike illness with malaise w nonproductive cough, chest discomfort u initial phase can be delayed for more than a month in some patients s 50% of patients develop hemorrhagic meningitis
  • 44. Within 24 to 48 hours h abrupt deterioration Overwhelming sepsis Dyspnea, stridor Shock Hemorrhagic mediastinitis
  • 45. Œ Chest radiograph show a widened mediastinum and hilar adenopathy
  • 46. Mediastinal widening and pleural effusion
  • 47. CT chest is more sensitive Bloody pleural effusions consolidation of the lung fields
  • 48. H Clinical diagnosis Flulike or septic illness c A reason to consider anthrax in the first place Current outbreak, warning from authorities , Sputum culture, gram stain, and blood cultures are not helpful until late in the course of the disease
  • 49. Tests to confirm the diagnosis PCR for identification of anthrax markers in pleural fluid i serologic detection of immunoglobulin to protective antigen e Immunohistochemical testing of biopsy specimens
  • 50. l Influenza
  • 51. spores are introduced into the skin through open wounds or abrasions n After I.P. 1 to 5 days 5 Begins as a papule usually on an exposed area the head, neck, or an upper extremity o The papule may resemble an insect or spider bite and may itch
  • 52. a papule progressing to form a large vesicle over the next several days e Severe edema occurs around the lesion with regional lymphadenitis m The lesions are not tender m patient may or may not be febrile
  • 53. Day 2 Day 4
  • 54. Day 4 : edema Day 4 : Eschar formation
  • 55. After about 1 week ü the lesion ruptures, forming a black eschar r surrounding erythema and edema increase h The necrotic ulcer is usually painless
  • 56. Ulcer and vesicle ringblack eschar
  • 57. Forearm lesion on day 7 n vesiculation and ulceration of initial macular or papular anthrax skin lesion
  • 58. h Eschar of the neck on day 15, typical of the last day of lesion
  • 59.
  • 60.
  • 61. In the next 2 to 3 weeks ü the eschar sloughs off f the organism disseminates and the patient dies
  • 62. The mortality rate  20% without treatment  1% with treatment t Antibiotics do not affect the course of local disease e but are used to prevent dissemination and death
  • 63. H Clinical diagnosis. i Confirmation Culturing of the lesion, punch biopsy,or serologic testing
  • 64. l Rare manifestations o The ingestion of insufficiently cooked, contaminated meat t the spores are transported to regional lymphatic tissue r I.P 2- 5 day r The mortality rate is 50%
  • 65. 0 Present with sore throat and neck swelling from cervical and submandibular lymphadenitis m The tonsils are frequently involved i Fever and toxicity t Dysphagia t Respiratory distress
  • 66. Œ Begins with nausea, vomiting, and fever e Hematemesis e Ascites e Bloody diarrhea e Mesenteric lymphadenitis a Present with an acute abdomen
  • 67.
  • 68. Rosen's Emergency Medicine: Concepts and Clinical Practice, 6th Ed
  • 69. , Death usually results within 3 days s The mortality rate was thought to exceed 90%
  • 70. Œ Inactivated, cell-free anthrax vaccine l There is a vaccine to prevent anthrax, but it is not yet available for the general public a Anyone who may be exposed to anthrax Certain members of the US Armed forces Laboratory workers Workers who may enter contaminated areas In the event of an attack using anthrax as a weapon, people exposed would get the vaccine
  • 71. ˆ Human-to-human transmission has not been reported with inhalational anthrax t Airborne transmission does not occur, but direct contact with skin lesions may result in cutaneous infection
  • 72.
  • 73.
  • 74.
  • 75.
  • 76. è Yersinia pestis à gram-negative bacterium c Zoonotic disease is transmitted to humans by the bites of infected rodent fleas
  • 77. Male Xenopsylla cheopis (oriental rat flea) engorged with blood. This flea is the primary vector of plague in most large plague epidemics in Asia, Africa, and South America
  • 78. è suggestive of exposure to rodents, rodent fleas, wild rabbits, sick or dead carnivores, or patients with pneumonic plague. a Incubation period is 1–6 days
  • 79.
  • 80.
  • 81. , Specimens bubo aspirates, blood cultures, sputum culture if pneumonic o Microscopic identification t culture confirmation t Serologic tests fourfold change in antibody titer to f1 antigen between acute- and convalescent-phase sera
  • 82. Physicians should report all suspected plague cases to state or local health departments and/or consult with CDC to obtain information and access diagnostic services.
  • 83.
  • 84. ( Parenteral antibiotic therapy Streptomycin O Alternatively Gentamicin ¤ Oral therapy Doxycycline
  • 85. ì No vaccine is currently available in the united states. i aimed at reducing contact with fleas and potentially infected rodents and other wildlife
  • 86.
  • 87. Generated by the infected patient during coughing, sneezing, talking during respiratory-care procedures
  • 88. Healthcare providers and others should wear a surgical-type mask when within 3 feet of the infected patient c Some healthcare facilities require a mask be worn to enter the room of a patient on droplet precautions
  • 89. Maintained until patient has completed 72 hours of antimicrobial therapy
  • 90.
  • 91. Maintaining spatial separation of at least 3 feet between infected patients and others when cohorting is not achievable. r Avoiding placement in the same room with an immunocompromised patient. m Special air handling is not necessary and doors may remain open
  • 92. 0 Prophylactic antibiotic treatment in person who exposure to bites of wild rodent fleas during an outbreak tissues of a plague-infected animal person or animal with suspected plague pneumonia
  • 93.
  • 94.
  • 95.
  • 96.
  • 97.
  • 98.
  • 99.
  • 100.
  • 101.
  • 102.
  • 103.
  • 104.
  • 105.
  • 106.
  • 107.
  • 108.
  • 109.
  • 110. Contact precautions Wear clean gloves upon entry into patient room. Wear gown for all patient contact and for all contact with the patient’s environment. Require a gown be worn to enter the room of a patient. Gown must be removed before leaving the patient’s room. Wash hands using an antimicrobial agent
  • 111.
  • 112. Healthcare facilities without patient rooms appropriate for Airborne Precautions e should have a plan for transfer of suspected or confirmed smallpox patients to neighboring facilities with appropriate isolation rooms
  • 113.
  • 114.
  • 115. Ð Fever, headache and stiff neck a sepsis and rash in meningococcemia
  • 116. H N. meningitidis colonizes mucosal surfaces of nasopharynx p direct contact with large droplet respiratory secretions from the patients or asymptomatic carriers c Humans are the only host
  • 117. H Patients with meningococcemia should be placed in respiratory isolation for at least 24 hours.
  • 118. H Close contacts should receive antibiotic prophylaxis. h Household, nursery school, and daycare center contacts r Intimate contacts and health care workers with intimate exposure mouth-to-mouth resuscitation, intubation,suctioning
  • 119. Rifampin, 10 mg/kg (up to 600 mg) orally every 12 hours for four doses h The dose for infants younger than 1 month is 5 mg/kg. . Rifampin discolors the urine r Contact lenses should be removed to avoid permanent staining.
  • 120. Ceftriaxone IM is effective against group A strains. 125 mg for children younger than 12 years 250 mg for those older than 12 years alternative for pregnant women and for people in whom compliance cannot be ensured. o Ciprofloxacin (500 mg orally)
  • 121. È Meningococcal vaccine should be considered adjunct to prophylaxis in epidemics close contacts in sporadic cases n The currently available vaccine is a quadrivalent vaccine containing purified capsular polysaccharides for groups A, C, Y, W
  • 122. No vaccine exists for group B the most prevalent serogroup in the United States.
  • 123. The quadrivalent vaccine is not recommended for routine use r but should be administered to children 2 years of age older in high-risk groups functional or anatomic asplenia terminal complement deficiency
  • 124. The vaccine is currently administered to U.S. military recruits. c Consideration in people traveling to endemic areas of the world such as sub- Saharan Africa.