Infectious process

Содержание

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Content

Infectious diseases. Infectious process
Biological basis of infectious process
Syndromes of infectious diseases.
Diagnosis

Content Infectious diseases. Infectious process Biological basis of infectious process Syndromes of
(etiology)
Microscopy,
Bacteriological investigation ,
Serological investigations
Primary and secondary immune response
To prove etiological diagnosis: Ab; Ig; Ag
Phases of the process
Treatment
Etiotropic treatment
Pathogenetic (syndromic) treatment
Basic regiment

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Infectious PROCESS is
an interaction between
micro- and macro-organisms
(under the impact

Infectious PROCESS is an interaction between micro- and macro-organisms (under the impact
of natural and social factors of the environment).
Infectious DISEASE is
a clinically marked part of this process.

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Infectious diseases

There is an agent =>
Contagious: can be transmitted to another macro-organism

Infectious diseases There is an agent => Contagious: can be transmitted to
=> possibility of an outbreak.
Cyclic course (timing).

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Infectious process.

got
inf.

Disease:
Severe. Moderate.
Mild. Sub-clinical.
Carriage.

incub

relapse

Clinical recovery:
sanitation or chronic form

onset

Infectious process. got inf. Disease: Severe. Moderate. Mild. Sub-clinical. Carriage. incub relapse

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Biological basis of infectious process

Agent’s factors:
pathogenic power; portal of

Biological basis of infectious process Agent’s factors: pathogenic power; portal of entry
entry of infection; dose
Host’s factors:
genetically determined: non-specific
and specific resistance (HLA)
acquired: nutrition, intoxications, ecologic factors, behavior patterns, vaccination, treatment.

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Complications

Specific: typical to the disease (perforation of ulcers of small intestine in

Complications Specific: typical to the disease (perforation of ulcers of small intestine
typhoid fever patients)
Non specific (sepsis of another origin due to prolonged presence of intravenous catheter).

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Symptoms and signs of infectious diseases

Fever
Rash
Lymphadenopathy
Liver /spleen enlargement
Respiratory syndrome
Diarrhea
Hepatitis
Meningeal syndrome,

Symptoms and signs of infectious diseases Fever Rash Lymphadenopathy Liver /spleen enlargement
etc

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Syndromes

Congunctivitis,
Tonsillitis, pharyngitis, stomatitis, …
Pneumonia, bronchitis…
Gastro-entero-colitis…
Hepatitis…
Kidney insufficiency (acute, chronic)
Meningitis…
DIC,
etc

Syndromes Congunctivitis, Tonsillitis, pharyngitis, stomatitis, … Pneumonia, bronchitis… Gastro-entero-colitis… Hepatitis… Kidney insufficiency

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Diagnosis

Anamnesis, symptoms and signs => syndromes.
Prove the syndrome: biochemical tests,

Diagnosis Anamnesis, symptoms and signs => syndromes. Prove the syndrome: biochemical tests,
ECG, X-ray, USI, etc.
Anamnesis, association of syndromes => suggestion of etiology.
Clinical etiologic diagnosis is always hypothetical => how to check it?

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Etiologic diagnosis

To prove or to disapprove it: to find the supposed agent

Etiologic diagnosis To prove or to disapprove it: to find the supposed
or to find its markers.
Markers: Ag of the agent or Ab to it.
Methods depend on the agent:
bacteria, virus, rickettsia, clamydia, mycoplasma, protozoa, helminthes, fungi.

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Microscopy

Pluses:
- fast
- the main method for protozoa, helminthes, fungi.
Minuses: for bacterial

Microscopy Pluses: - fast - the main method for protozoa, helminthes, fungi.
infections in the most cases it is a tentative method.
But sometimes can be very informative (N.meningitidis in CSF).

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Bacteriological investigation

Pluses: accurate; sensitivity to antibiotics
Minus: needs time (several days

Bacteriological investigation Pluses: accurate; sensitivity to antibiotics Minus: needs time (several days
or more)
Negative result does not always turn down a supposed diagnose:
- defects of sample taking, transportation, media and lab technique;
- recovery stage (spontaneous or due to correct treatment).
Absence of correct suggestion! => media

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Serological investigations

To detect antibodies to a suggested agent
Antibodies – in serum (CSF).
Pluses:

Serological investigations To detect antibodies to a suggested agent Antibodies – in
simple; reliable; cheap; often – the only confirmation of a diagnosis.
Minuses:
“window period”;
investigation itself is fast, but results are always retrospective.

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Primary immune response

Onset

10

“Window”
period

20

IgG

IgM

Antibodies

30

40

Primary immune response Onset 10 “Window” period 20 IgG IgM Antibodies 30 40

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Secondary immune response

Onset

10

No “window” period; no IgM

20

IgG
only

Antibodies

30

40

Secondary immune response Onset 10 No “window” period; no IgM 20 IgG only Antibodies 30 40

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To prove etiological diagnosis: Ab

4 times increase in titers of Ab to

To prove etiological diagnosis: Ab 4 times increase in titers of Ab
the agent (primary or secondary immune response):
Samples should be taken twice in time!
- 1-st time: the 1-st week (zero is expected),
- 2-nd time: in 2 weeks (maximum level).
Diagnosis is late: after 2-3 weeks; can be even later under effective treatment =>
- the 3d sample at week 5-6 of the disease.
The only test can be (+) due to previous disease, vaccination, poly-agglutination. “Min diagnostic level of Ab” is not reliable.

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To prove etiological diagnosis: Ig

Ig M (+) to the agent even once

To prove etiological diagnosis: Ig Ig M (+) to the agent even
means
the primary immune response.
Ig M can be usually found since the 5-th day of the disease up to the 4-6 weeks.
Rare IgM can persist much longer (HBV).
Ig G(+): >10 days of the disease (peak, recovery, chronic stage, previous disease or vaccination)–similar to Ab significance.

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To prove etiological diagnosis: Ag

Ag can be found in any substrate.
No “window”

To prove etiological diagnosis: Ag Ag can be found in any substrate.
period =>
- Express-techniques to reveal the Ag (Ab with some additional mark to make immune complex visible): plague, etc.
PCR – to reveal DNA/RNA of the agent. In blood PCR(+): replication; PCR(-): no replication; sanitation -? => biopsy.
Ag disappear in the process of sanitation in recovery stage => Ab.

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Phases of the process

The end of incubation and the first part of

Phases of the process The end of incubation and the first part
the disease – presence of Ag; no Ab: the most contagious and dangerous part.
Recovery with clearing from the agent: all Ag disappear, Ab become (+).
Chronic form: presence of Ag, or Ag+Ab; sometimes – only Ab (anti-HBcor Ab).
Life prognosis depends mostly on tissues functions (biochemical tests, ECG, etc).

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Mixed infections, combination of different diseases

Confirmation of the one disease does not

Mixed infections, combination of different diseases Confirmation of the one disease does
allow us to exclude another one.
To exclude (or confirm) a disease we should investigate for this disease.

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C

B

D

inf

1

2

3

4

5

6

7

8

C B D inf 1 2 3 4 5 6 7 8

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Exact diagnosis:

Prognosis
spontaneous course (subclinical, mild, moderate, severe),
under the treatment
Treatment
etiology,
phase

Exact diagnosis: Prognosis spontaneous course (subclinical, mild, moderate, severe), under the treatment
of the process,
severity

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Infectious process.

got
inf.

Disease:
Severe. Moderate.
Mild. Sub-clinical.
Carriage.

incub

relapse

Clinical recovery:
sanitation or chronic form

onset

Infectious process. got inf. Disease: Severe. Moderate. Mild. Sub-clinical. Carriage. incub relapse

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Treatment

Etiotropic – to affect the agent.
Pathogenetic (syndromic)– to improve or to replace

Treatment Etiotropic – to affect the agent. Pathogenetic (syndromic)– to improve or
tissues functions.
Symptomatic – to suppress symptoms.

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Etiotropic treatment

Antibacterial, antiviral, antiprotozoal, etc.
Result of therapy depends mostly on
- correct choice

Etiotropic treatment Antibacterial, antiviral, antiprotozoal, etc. Result of therapy depends mostly on
of spectrum and activity of preparations (if not correct: disease and treatment go own ways);
when the treatment is started (the first 1-2 days => just stop the disease);
duration of the treatment.

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Pathogenetic (syndromic) treatment

Can be life-saving (rehydration in cholera, hemodialysis in HFRS,

Pathogenetic (syndromic) treatment Can be life-saving (rehydration in cholera, hemodialysis in HFRS,
dehydration in brain edema, intubation in laryngeal diphtheria).
Often it is the main part of the treatment: DS is too late to start etiotropic treatment (HAV, HF), or etiotropic treatment is not correct, etc.

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Basic regiment

Bed rest
Diet: in acute diseases – according to appetite; boiled and

Basic regiment Bed rest Diet: in acute diseases – according to appetite;
cultured milk foods can be used in any situation. Liquids.
Clinical observation (behavior, t, pulse, BP, RR, diuresis, symptoms and signs).
Symptomatic treatment - can be useful.
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