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Particularitățile clinice,

evoluția, diagnosticul,
diagnosticul diferențial
al gripei sezoniere,
IACRS, SARI și COVID-
19 la adulți
IACRS
Rinita acută – obstrucție nazală cu secreții. Etiologie – rinovirusuri,
coronavirusuri, VSR, adenovirusuri, v.influenzae, v.parainfluenzae,
metapneumovirusuri. Incubația 1-3 zile. Alte semne: odinofagie (dureri la
deglutiție), după 1-2 zile pot apărea cefalea și tusea.
Faringita și angina acută – infecții acute ale orofaringelui și amigdalelor
palatine cu febră, sindrom faringian inflamator (eritem, edem, asociate uneori
cu exsudat, disfagie, odinofagie) , CMV, HIV. Etiologie – virusuri 60-80%
cazuri, aceleași ca și în rinita acută (a. eritematoase)+ VEB (a.
pseudomembranoasă) , Herpes Simplex și enterovirusuri (a. veziculare, mai
des vara); bacterii – streptococul beta-hemolitic grup A (a. eritemopultacee),
streptococi gr.B,C,E,G, fuzospirili (a. ulceronecrotice, unilaterale, cu depozit
cenușiu), corinebacterium diphteriae (a. pseudomembranoasă), neisseria
meningitidis, Haemophilus influenzae, etc. Alte semne: adenopatii cervicale.
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• Laringita – răgușeală până la afonie. De obicei, apare în contextul
IACRS virale (adenovirus, v. Gripal, paragripal, VSR, coronavirus).
Bacteriene: corynebacterium diphteriae, streptococ gr. A, moraxela
catarralis. Crupul – obstrucție laringiană, care produce tuse
lătrătoare, stridor inspirator, retracție sternală cu progresie spre
insuficiența respiratorie acută.
• Epiglotita – Hemophilus influenzae gr.B major ca etiologie, dar și
streptococ beta-hemolitic, pneumococ, Staph. Aureus. Debut brusc
spre obstrucție respiratorie, prin edemațierea roșiatică a epglotei, cu
odinofagie, disfagie, salivație intensă. Poziția copilului cu capul
înainte aplicat în față. La examinare cu laringoscopul epiglota apare
ca o cireașă roșie, iar Rx arată o inflamație a laringelui subglotic.

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SARI (Severe Acute Respiratory Infection)
conform ordinului nr.1103 MSMPS RM din 02.10.2019

• O infecție respiratorie acută cu:


- Istoric de febră sau febră măsurată de minimum 38*C
ȘI
- Tuse
Și
-Debut în perioada de 10 zile anterioare
Și
-Necesită spitalizare

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Pneumoniile reprezinta un
ansamblu de leziuni care
intereseaza parenchimul
pulmonar (alveolita) si
interstitiul pulmonar datorat
unor factori infectiosi
(virusuri, bacterii,
fungi,protozoare).

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Gripa sezonieră (...dar și despre gripa pandemică)

• A,B,C.

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Effectiveness of a new bioequivalent formulation of oseltamivir (Enfluvir®) on 2010–2011 seasonal influenza viruses:
An open phase IV studyFebruary 2012. International journal of infectious diseases: IJID: official publication of the
International Society for Infectious Diseases 16(4):e273-8.DOI:10.1016/j.ijid.2011.12.008/SourcePubMed
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9/14/2022 Bohn et al.: Molecular, serological, and biochemical diagnosis and monitoring of COVID-19 15
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Omicron has many key mutations
compared
to Delta Fig: Delta compared to Omicron with mutations in the S1 domain of the spike
protein

Delta Omicron

• On 26 November 2021, WHO


designated SARS-CoV-2 variant
B.1.1.529 a variant of concern (VOC)
and named it Omicron
• Omicron has > 30 genetic mutations of
the spike protein. The SARS-CoV-2
spike protein acts like a ‘key” and Spike protein
allows the virus to bind to ACE-2 of SARS-
CoV-2
receptor and enter and infect cells in Areas with mutations

humans. More than 70% 40 to 70% 15 to 40% 5 to 15% 1 to 5%

• The spike protein of SARS-CoV-2 is Image: AFP


https://www.who.int/news/item/26-11-2021-classification-of-omicron-(b.1.1.529)-sars-cov-2-variant-of-
targeted by some currently approved concern

COVID-19 vaccines; therefore,


mutations in the spike protein need to 21
be closely monitored
Omicron shows preference for
upper respiratory tract infection
• Omicron appears to show preference for Fig: Upper respiratory tract
infecting and replicating in the upper respiratory
tract, compared to Delta and other strains which
prefer the lower respiratory tract.
• This may confer a transmission advantage
independent of immune evasion
• Preliminary studies suggest that Omicron
appears to have decreased ability to infect lung
tissue, which may be a reason why people
infected with Omicron have a less severe
disease compared to Delta
• Early studies from animal models show that
Omicron-infected animals show fewer
clinical signs and have less severe disease

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Omicron has reduced risk of
hospitalization
• Omicron has reduced risk of hospitalization
compared to Delta, suggest early studies from
several countries including Denmark, South
Africa, UK, Canada and the USA
• There is decoupling between case reports and
hospitalization in places of high levels of
population immunity
• Omicron infection appears to be associated with
lower severity and lower proportion of
hospitalized patients compared to previous ©WHO
variants, but the large number of people being
infected with it translates into significant number
of patients requiring hospital admission, putting
strain on healthcare systems.

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Routine diagnostics continue to
detect Omicron
• Routinely used diagnostic tests,
including PCR and antigen detection
rapid diagnostic tests (Ag-RDT),
continue to detect infection with
Omicron

• Studies of the comparative


sensitivity of Ag-RDTs are ongoing

©WHO

Source:
Enhancing Readiness for Omicron (B.1.1.529): Technical Brief and Priority Actions for Member States
(who.int)

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Omicron shows increased re-
infection risk after previous SARS-
CoV-2 infection
• There is evidence that Omicron has some immune evasion*
• Increased trend in re-infection** cases have been reported by some countries including South
Africa, UK, Denmark, Israel
• The risk of reinfection with the Omicron variant was estimated to be 5.4 fold higher in comparison
with the Delta variant in England, show UK studies
• Significant reduction in antibody neutralization*** with Omicron may contribute to increased
risk of re-infection

Public health and safety measures such as:


wearing a mask properly, keeping distance and
washing
hands regularly , continue to protect against infection by
all SARS-CoV-2 variants
*Immune evasion refers to the ability of the virus to evade a person’s protective immune system
**Re-infection refers to infection after previous SARS-CoV-2 infection, while breakthrough infection refers to infection after
vaccination.
***Test to detect levels of antibodies that bind the virus and prevent its infection

Source: Enhancing Readiness for Omicron (B.1.1.529): Technical Brief and Priority Actions for Member States (who.int)

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Preserved cellular immune process
protects against severe disease
• Protection through cellular immunity*
appears to be preserved in Omicron
infection
• In those who have been previously
infected, and/or previously vaccinated, 70-
80% of certain cells involved in the
protective immune process (CD4+ and
CD8+) were maintained for Omicron
infection
• This likely translates to protection against
severe disease and death after vaccination
and after previous infection, remaining high

Image: Juan Gaertner / Science Photo Library

*Cellular immunity is a protective (non-antibody) immune process involving immune cells which kill virus-infected cells.

Source: Enhancing Readiness for Omicron (B.1.1.529): Technical Brief and Priority Actions for Member States (who.int)

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Therapeutics and
Omicron
• Interleukin-6 receptor blockers and
corticosteroids are expected to remain effective
in the management of patients with severe
and critical disease
• Preliminary data from non-peer reviewed
publications suggest that some of the
monoclonal antibodies developed against SARS-
CoV-2 may have impaired neutralization against
Omicron

©WHO

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Older people and those with
underlying conditions remain at
risk
• Older people continue to be at greater risk for
developing severe disease
• Those with underlying conditions, of any age, are also
at risk for developing severe disease

People at greater risk of COVID-19 include those:


unvaccinated, with obesity, people over the age of 60,
hypertension, Diabetes mellitus, cardiac disease,
chronic lung disease, cerebrovascular disease,
dementia, mental disorders, chronic kidney disease,
immunosuppression, cancer, HIV/AIDS,
pregnancy.

©WHO

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