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Pro f. ZHILIANG GAO

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Title: Pro f. ZHILIANG GAO


1
GENERAL PRICIPLES OF INFECTIOUS DISEASES
  • Pro f. ZHILIANG GAO
  • Department of Infectious Diseases
  • Third hospital, Sun Yet-sen University

2
SINGNIFECANCE AND IMPORTANCE OF STUDY
3
History review
  • In 14th century, Plague in European ,20 million
    people death
  • In 1718th century, smallbox in European ,150
    million people death
  • In 1918, flu in the worldwide,40 million people
    death?

4
In 1905,Nobel gainer of physiology and medicine
award Robert Koch (Germany)
In 1882, Koch discovered tubculosis bacilii
5
In 1945,Nobel gainer of physiology and medicine
award Alexander Fleming(Scotland)
In 1928?, Fleming Discorvered Penicillin Into
antibiotics era
6
  • WHO reports
  • ? Among 52 million of death in the worldwide
    annually, 17 million(32) of death from
    infectious diseases and parasite
  • ? In developing country,a half of death by
    infectious diseases
  • ? About 15 million of death by infectious
    diseases per hour in the worldwide,most occurred
    in developing country?

7
Pattern of Infection in Developed Countries
  • In 20th century, fall in the incidence of
    communicable diseases in developed countries
  • due to factors such as
  • Immunization
  • antimicrobial chemotherapy
  • improved nutrition
  • and better sanitation and housing.

8
Re-emergence of old infectious disease
  • ?(Tuberculosis)
  • ?(Viral hepatitis)
  • ?(Sexually transmitted diseases)
  • ?others cholera?charcoal

9
Re-emergence of old infectious disease
  • 2 million death of TB in the worldwide annually
  • 78 million infected by TB in the worldwide
    annually
  • March 24,for World TB Day

10
Emerging infectious diseases
  • WHO information
  • near 30 years,
  • about 30 kinds of infectious diseases
    discovered in the worldwide
  • Emerging infectious diseases

11
Emerging infectious diseases
  • ? 40 million of HIV/AIDS cases 4000? worldwide
  • ? HIV infection rates16000persons/per day,6
    million persons/annually,11 cases/minute?
  • ? 95 in developing country
  • ? Maximal nation Africa,infection rate about 10
  • ? Dec.1 for World AIDS Day

12
Emerging infectious diseases
  • In 1985,First case of AIDS in china, it is
    american tourer to china ?
  • To 2003,about 840 thousands HIV in china,80
    thousands of AIDS cases
  • HIV increase 30 annually in china

13
Emerging infectious diseases
  • SARS (SARSCoV)
  • From 2002.11.16 to 2003.7,SARS spreaded 6
    continent, 32 countries,cases of 8437,death of
    916
  • In china, cases of 5327,death of 349
  • SARS most serious emerging infectious diseases
    in 21 century

14
Emerging infectious diseases
Avian influenza H5N1 virus
15
Antibiotics
  • Antibiotics, within the last 60 years,
  • Resulted in the cure of many previously lethal
    infections, wonder drugs.
  • Only several years , drug-resistant emerged.
  • pathogenic staphylococci were found to have
    the ability to produce enzymes (penicillinases)
    that destroyed penicillin, thus rendering the
    drug useless against these strains
  • Overuse and misuse of these, wonder drugs will
    eventually reder them useless.

16
Hospital infections
  • Antibiotics resistance in hospitals
  • Organ transplantation, prosthetic devices,
    artificial organs, indwelling pace makers, and
    neonatal and adult intensive care

17
COMMUNICABLE DISEASES
18
  • CONCEPT OF COMMUNICABLE DISEASES
  • Caused by pathogens virus?chlamydia?richettsia?pr
    ion?bacteria?spirochete?fungus and
    parasite(helminth?protozoa)or medical insect
  • Infectious disease involve any organ or system
    of the body and thus embraces all medical
    disciplines.
  • Communicability is another factor which
    differentiates infections from non-infectious
    diseases. Transmission of pathogenic organisms
    to other people, directly or indirectly, may lead
    to an epidemic.

19
  • The goal of studying infectious disease
  • to study these disease occurrence, development,
    spreading and prevention inside or outside of host

20
  • Infection and immunity

21
  • ?. Concept of infection
  • The course of struggle between pathogens and
    human or animal bodies (host).
  • Absolutely necessary condition

22
Kinds of infections
  • Commensals
  • opportunistic infection
  • Primary infection
  • Repeated infection
  • Mixed infection
  • Superinfection
  • Secondary infection

23
  • Commensalism Pathogens live in the host
    but dont induce pathologic changes.
    Escherichia coli in the colon
    Epstein-Barr virus

24
  • Opportunistic infection Pathogens within
    the host can induce pathologic changes if host
    immunity is suppressed by some factors.
    Cryptococcus neoformans Cytomegalovirus
    Candida albicans

25
  • Primary infection measles, chicken box
  • Repeated infection
  • malaria, schistosomiasis, ancylostomiasis
  • Mixed infection rare
  • Superinfection HBV overlap HEV
  • Secondary infection HBV following bacilli

26
Infections status(infection spectrum) Entrance
and colonization of pathogens will lead to the
following results
  • Eliminate pathogen
  • inapparent/sub-clinical infection
  • apparent/clinical infection
  • Carrier status
  • Latent infection

27
  • ? Elimination pathogens were excluded
    out by host nonspecific or specific immunity.
    Such as Candida albicans
    Hepatitis A virus

28
  • ? inapparent/sub-clinical infection
    most frequently occurs in healthy
    individuals. The outcomes will be
    A. Immunity acquired. HAV B. Carrier
    state healthy carriers. HBV

29
  • ? apparent/clinical infection infection
    The outcomes will be A. Recovery.
    Shigella B. Chronic carrier.
    Salmonella typhi

30
  • ? Carrier state Definition of different
    types of carriers . incubation carrier
    . acute carrier . convalescent carrier .
    chronic carrier

31
? Latent infection After infection,
pathogens remain latent inside the body.
Develop clinical manifestations when the host
immunity has been impaired. Pathogens
usually will notbe excreted by the host during
period of latency. Herpes simplex
32
  • The infection status may change each other in
    some conditions.
  • Latent infection
  • Apparent
  • Carrier status
  • Inapparent
  • eliminate

frequency/ratio
33
?? Role of Pathogens in Infection Process?
Invasiveness adhesion, penetration ability.
Shigella ? Virulence toxins, enzymes, and
histolytic ability. E. histolytica ? Infection
dose minimal dose that can cause an
infection. S. typhi ? Variability change in
structure of the pathogen to evade from host
immunity. Influenza virus
34
?? The Role of Immune Response in Infection
Process Differentiation between protective
immunity and allergy. . Protective immunity
beneficial . Allergy(anaphylactic reaction)
harmful
35
  • ? Nonspecific immunity A. Natural barriers
    external (skin, mucous membrane, cilia), internal
    (blood-brain barrier).B. Phagocytosis
    monocytes, macrophages, and granulocytes.C.
    Humoral factors complements, lysozyme,
    interferons (a ß ?), cytokines

36
  • ? Specific immunity Immune respond to
    specific recognizable antigens. A.
    Cell-mediated immunity Important in
    intracellular infections by viruses, fungi,
    protozoa and certain bacteria.B. Humoral
    immunity Different kinds of antibodies
    (immune globulins, A D E G M) and their
    functions.

37
  • Pathogenic Mechanisms of Infectious Diseases
  • Establishment and development of infection
    process can be divided into three stages

38
  • 1. Portal of entry Each pathogen has its
    specific portal of entry. Mycobacterium
    tuberculosis, Meningococcus
  • ----via breath tract. Shigella--- via
    digestive tract.

39
  • 2. localization and Dissemination in the host
    Specific for each pathogen. . Mumps virus in
    parotid gland. . Hepatitis C virus in the
    liver. . Shigella in the intestine.

40
  • 3. Channels of excretion Important factor
    for host infectivity. As the source of
    infection. . Hepatitis A in the stool.
    . Hepatitis B in the blood. . Measles virus
    in expiratory air.

41
?? Mechanism of Tissue Damages 1. Direct
invasion Cytolysis, tissue necrosis,
inflammation.2.The actions of toxins and
cytokines Resulting in septic shock,
Disseminated intravascular coagulation, DIC
etc.3. Immunopathogenesis Immunosuppression,
T-cell destruction, immune complexes induce
cytotoxicities.
42
  • Shock is a special problem in severe infections.
  • Endotoxin from Gram-negative bacteria caused by
    other cell wall components and by lipoteichoic
    acid
  • Several mediators including kinins, components,
    histamines, cytokines, and endogeneous opiate
  • Results from reduced systemic vascular resistance
    brought about by dilated small vessels and leaky
    capillaries
  • The cycle of shock, tissue anoxia, and organ
    failure is difficult to break and may kill the
    patient within hours.

43
  • Bacteramia and Septicaemia
  • Bacteraemia, the presence of living organisms in
    the blood, can occur in healthy people without
    causing symptoms
  • Unless there is a focus on which they can settle
    and multiply, e. g. an abnormal heart valve,
    these organisms are normally cleared very rapidly
    from the blood.
  • Other organisms invading the blood stream, such
    as staphylococcus aureus and Escherichia coli. ,
    are less likely to be dealt with by the immune
    system and more likely to cause disease

44
  • Septicaemia
  • Caused by Gram-positive, Gram-negative, or fungal
    organisms.
  • Complicated by septic lesions in organs or
    tissues.
  • Such as pneumococcal pneumonia and meningococcal
    meningitis.
  • Cirulatory failure, the septic shock syndrome, is
    the most dangerous complication
  • Blood cultures are the most important initial
    investigation

45
?? Important Patho-physiologic Changes in
infection
46
  • 1. Fever (pyrexia) Exogenous and endogenous
    pyrogens.. Exogenous pyrogens virus etc. .
    Endogenous pyrogens IL-1, IL-6, TNF, interferon
    etc.

47
  • 2. Metabolism changes(1) Protein metabolism
    higher proteins catabolism.(2) Carbohydrate
    metabolism acceleration of
    glucolysis.(3) Water and electrolytes
    metabolism dehydration, hypokalemia. (4)
    Endocrine disturbances higher anabolism,
    hyper-corticosteroidemia

48
Epidemiological Process of Infectious
49
  • Diseases and Influencing Factors Epidemiological
    Process(course) include

50
Sources of infection Definition. Human,
animal.? Patients acute, chronic typical,
atypical(mild, severe).? Subclinical infection
no symptoms. poliomyelitis.? Carriers
chronictyphoid, shigellosis.? Infected
animals(natural source) rabies, plague,
schistosomiasis.
51
2. Routes of transmission? Air, droplets, dusts
e.g. measles, diphtheria.? Water, food,
flies(fecal-oral infection) e.g.
typhoid, cholera.? Fingers, utensils (contact
infection) e.g. shigellosis, influenza.
52
  • ? Arthropods A. Biologic intermediate
    hosts, e.g. mosquitoes in malaria,
    chiggers in scrub typhus. B. Mechanical
    passive transfer. e.g. flies in amebiasis

53
?Bloob,body liquid transmission
  • Such as HBV,HIV
  • ?Vertical transmission mother to baby
  • ?Horizontal transmission others

54
3.susceptibility
  • Susceptible person

55
?? Factors Influencing Epidemiological Process
56
  • 1. Natural factors . Climatic season, rain,
    humidity.. Geographic endemicity,
    schistosomiasis clonorchiasis sinensis fresh
    fish

57
  • 2. Social factors Social system,
    social-economic condition, cultural background

58
Characteristics of Infectious Diseases
59
  • 1. Basic characteristics(1) Presence of
    pathogens.(2) Infectivity duration of
    infection, chronic carrier.(3) Epidemiological
    features age, sex, season imported or
    endemic sporadic or epidemic and pandemic
    epidemic outbreaks.(4) Post-infection
    immunity.

60
2. Clinical Characteristics(1) Stages of
development A. Incubation period.B. Prodromal
period.C. Symptomatic period.D. Convalescent
period.E. Recrudescence, relapse.F. Sequelae.
61
? incubation period Incubation period is the
period between the invasion of the tissues by
pathogens and the appearance of clinical features
of infection. infectivity to others. ?
prodromal period from onset of diseases to
apparent clinical features
62
? Symptomatic period. Apparent of clinical
manifestations.? convalescent period
lighten and disappear clinical manifestations,Lab.
normal
63
  • relapse  re-appear symptom after recovering of
    diseases. S.typhi
  • recrudescence  re-increasing and re-appear ,
    when lighting of clinical symptom and decreasing
    of temperature.S.typhi.

64
? sequela body function abnormal after
recovering of diseases
65
Characteristic of infectious disease
66
3. Common symptoms and signs. ? Fever(pyrexia)
A. Effervescence early stage. B. Fastigium
full-blown stage.C. Defervescence
improvement stage
67
Fever formsA. Sustained fever Difference
of body temperature less than 1 degree
centigrade within 24 hours, over 39?.
e.g. Second week of typhoid
68
sustained fever
69
  • B. Remittent fever Change of body
    temperature more than 1 degree
    centigrade within 24 hours, the base line
    higher than normal. e.g. Septicemia.

70
remittent fever
71
  • C. Intermittent fever Fluctuation between
    normal temperature and high fever within 24
    hours. e.g. Malaria.

72
intermittent fever
73
  • D. Relapsing fever Fever lasting 57 days
    with relapse after several days. e.g.
    Relapsing fever, brucellosis.

74
relapsing fever
75
  • E. Irregular fever Curve of body
    temperature is irregular. e.g.
    Brucellosis, septicemia

76
  • E. Irregular fever Curve of body
    temperature is irregular. e.g.
    Brucellosis, septicemia

77
? Skin rash or eruption Note appearance
type and day of the disease.
78
  • Eraption time
  • first day chickenbox.
  • second day scarlatina
  • third day smallbox.
  • forth day measles..
  • Fifth day ship fever
  • sixth day typhoid fever

79
  • A. Enanthem Rash on mucous membrane
    (mucosa). e.g. Koplik spots in measles.
  • B. Exanthem Rash on skin surface,
    e.g. chickenpox, smallpox.
  • C. Maculopapular rash e.g. Macula and
    papule (Maculopapule) in measles
    rose spots in typhoid fever.

80
macula
81
papule
82
herpes
83
pustule
84
  • d. Urticaria Seen in serum sickness,
    tetenus antitoxin (TAT) parasitic
    diseases, schistosomiasis drug
    hypersensitivity, piperacillin, etc.

85
  • (3) Toxemic symptoms A. General
    presentations malaise headache
    anorexia pain in muscles, joints and
    bones disturbance in consciousness
    meningeal irritation septic shock liver
    and kidney failure, etc.

86
  • B. Mononuclear-phagocyte system
    (Reticulo-endothelial system) reactions
    hepatomegaly, splenomegaly,
    lymphadenopathy.

87
4. Clinical forms(1) development Acute,
subacute and chronic forms. (2) forms of
clinical manifestation mild, moderate
(typical) or severe forms of the disease.
ambulatory form in typhoid (without
symptom and signs).
88
  • Acute
  • Fever anoxia, protein catabolism, negative
    nitrogen balance, acute-phase protein response,
    albuminaemia, low serum iron, anemia,
    neutrophilia
  • Inflammation pain, dysfunction, tissue damage
  • Convulsion especially in children
  • Shock
  • Hemorrhage hemolytic anemia, intravascular
    coagulation
  • Organ failure kidneys, liver, lung, heart,
    brain, necrosis of skin

89
  • Chronic
  • Weight loss and muscle-wasting
  • Malnutrition especially associated with diarrhea
  • Retardation of growth and intellect in children
  • Anemia iron sequestration
  • Tissue destruction e. g. lung in pneumonia or
    tuberculosis, liver in hepatitis B
  • Post-infective syndromes e.gpost-viral fatigue
    syndrome

90
Diagnosis of Infectious Diseases
91
  • Clinical manifestations(1) Mode of onset(2)
    Type of fever(3) Accompanying symptoms
    headache, myalgia, arthalgia etc.(4) Signs
    Consciousness, jaundice, skin rash, Koplik
    spot, eschar, subcutaneous
  • hemorrhage, liver, spleen,
    lymph nodes.

92
Pathognomonic signs
  • Measles Koplik spots
  • Mumps swelling of parotid gland
  • Scrub typhus eschar
  • Leptospirosis myalgia, calf muscle
  • Typhoid rose spots
  • Cysticercosis subcutaneous nodules
  • Hepatoencephalopathy flapping tremor
  • Schistosomiasis urticaria
  • Shigellosis mucus-pus-bloody stool
  • Amebic dysentery strawberry jam-like stool
  • Rabies hydrophobia

93
  • 2. Epidemiological Data(1) History of contact
    with similar cases.(2) Occupation,
    living environment and life style.(3)
    History of vaccination.(4) History of
    transfusion of blood or blood products.

94
?? Laboratory Examinations(1) Routine
examinations blood, urine, stool.
Leukocytosis, leukopenia, eosinopenia,
eosinophilia. Biochemical analysis of the
blood for liver functions and kidney
functions, etc.
95
Leukocytosis
  • Infection with virus
  • epidemic hemorrhagic fever
  • Japanese B encephalitis
  • infectious mononucleosis
  • rabies
  • Infection with bacteria, etc.

96
  • (2) Detection and isolation of pathogens
    A. Adequate collection and transportation
    of specimens.

97
  • B. Direct examination Recognition of causative
    agent
  • malaria in blood slides, Vibrio cholerae in
    stool, diphtheria in throat swab, bacilli in
    urine
  • Entamoeba in rectal scrape, schistosome ova in
    rectal snip, rickettsia in rash aspirate, fungi
    in skin scrapings, pneumococci in purulent
    sputum, leprosy bacilli and leishmania in slit
    skin smear
  • By electron microscopy viruses in stool herpes
    viruses from skin
  • By histology of biopsy specimen acid fast
    bacilli in leprosy and tuberculosis, hepatitis B
    in liver, rabies virus in brain

98
  • C. Culture by artificialCulture of causative
    organism
  • From blood typhoid, brucellosis, Gram-negative
    speticaemia, pneumococcal pneumonia, HIV
  • From bone marrow tuberculosis, brucellosis,
    leishmaniasis, histoplasmosis
  • From other body fluids, feces or tissues urinary
    tract infection, bacillary dysentery, sputum in
    pneumonia, liver in tuberculosis

99
  • D. Animal inoculation
  • Intraperitoneal inoculation Rickettsia
    tsutsugamushi.
  • Intracerebral inoculation encephalitis
    virus.

100
  • E. Specific Immunological detection
  • Detection of microbial antigen
  • Meingococcal and pneumococcal disease
    (blood, cerebrospinal fluid, sputum, urine)
  • Detection of antibody of IgM class
  • Toxoplasmosis, hepatitis A
  • Demonstration of antibody
  • Rising titre typhoid, brucellosis, HIV
    infection
  • Closely linked to clinical syndrome amoebic
    abscess, visceral leishmaniasis
  • Screening for latent disease
    schistosomiasis,
  • Skin testing Tuberculosis, histoplasmosis,
    leishmaniasis Nonspecific

101
  • F. Molecular biologic assay Using isotope
    or non-isotope probes Polymerase chain
    reaction (PCR). Mycobacterium
    tuberculosis, hepatitis C virus, etc.

102
  • ? other examination
  • X raylobar pneumonia, renal tuberculosis,
    muscular cysticercosis
  • Isotope detection of abscess
  • Ultrasound abscess hydatid cyst
  • Computed tomography (CT) or magnetic resonance
    imaging (MRI) intracranial infection, visceral
    abscesses, mediastinal lymph node enlargement

103
Treatment of Infectious Diseases
104
  • Principles of therapy
  • 1. Aim of treatment . for alleviation of
    symptoms and signs
  • . for isolation of patients
  • . Comprehensive treatmentincludes drug
    therapy, nursing care and isolation. . Pay
    attention to both specific and symptomatic
    treatments.

105
2. Therapeutic methods? General and supportive
treatment. ? Etiologic (specific)
treatment.? Symptomatic treatment.?
Rehabilitation therapy for sequelae.?
Traditional Chinese medicine and acupuncture.
106
Prevention of Infectious Diseases
107
1. Measures against the source of infection
? Report of cases According to the Law
for Controlling Infectious Diseases
issued by the central government.
108
  • Three kinds of case reportKind A plague,
    cholera, smallpox, SARS.
    lt6hs. Kind B AIDS, hepatitis, etc.
    lt12hs.Kind C influenza, mumps,
    etc. lt48hs.

109
  • ? Isolation of patients until the patient
    becomes non-infectious.

110
3. Quarantine of contacts until the
incubation period of the infectious
disease is over.
111
  • ? Identification and treatment of carriers.
  • ? Control of infected animals Eradication
    or therapy

112
  • 2. Interrupt the routes of transmission

113
  • ? General hygienic measures Clean drinking
    water supply, Food hygiene, Correct sewage
    disposal.

114
  • ? Disinfection and eradication of insect
    vectors.

115
  • ? Intervention of parasite life cycles.e.g.
    eradication of snails in endemic area of
    schistosomiasis.

116
  • 3. Protection of the susceptible persons

117
  • ? Immunological prophylaxis . Active
    (vaccination) intracutaneous inoculation
    with smallpox vaccine. subcutaneous
    inoculation with hepatitis B vaccine. .
    passive (immunoglobulins) intramuscular
    injection with antibodies against tetanus
    bacillus.

118
  • ? Protection from environmental factors
    e.g. mosquitoes bites, skin penetration by
    Leptospira and hookworm larvae.

119
Thank you very much.
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