COVID-19 Flashcards

1
Q

Pathogenesis.

a) Viral cause
b) Receptor
c) Risk of mild illness (flu-like), severe (pneumonia) and critical (ARDS)
d) Incubation period
e) Transmission
f) Median time from symptom onset to: i) ICU admission, ii) death or recovery to discharge

A

a) Severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2)

b) Angiotensin converting enzyme 2 (ACE-2)
- Same as for SARS-Cov (i.e. SARS)
- Found in lungs, heart, kidneys, etc.
- Up-regulated by ACE inhibitors and NSAIDs (so patients on these may have more severe disease)

c) Mild - 80%
Severe - 15%
Critical - 5%

  • Note: risk higher in older patients/ those with comorbidities such as as diabetes, heart failure, etc.
    d) 5 - 11 days

e) - Aerosol - coughing, sneezing, contaminated particles on surfaces (direct contact)
- Also found in blood and stool in lower quantities

f) i) 10 days (1 -2 weeks)
ii) 2 - 3 weeks

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2
Q

Presentation.

a) Main symptoms core features
b) Other common features
c) Less common features
d) Signs o/e

A

a) • Fever (37.8 C or higher), +/- chills, rigors
• Cough (new and continuous; usually dry)
• Dyspnoea - may warrant hospital admission
• Altered sense/loss of smell/taste

b) • Headache
• Myalgia
• Fatigue
• Sore throat
• Anorexia

c) • Resp - Sputum production, haemoptysis
• GI symptoms - Diarrhoea, nausea/vomiting, abdo pain
• Neuro - Confusion, dizziness
• Rhinorrhoea, conjunctival congestion
• Chest pain/ palpitations (may indicate myocarditis)

d) - Fever, tachycardia
- Pneumonia/ARDS - hypoxia, tachypnoea, cyanosis, confusion, crackles/bronchial breathing/etc.
- Pharyngitis/ tonsillar enlargement
- “Silent hypoxia” - hypoxia without any SOB

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3
Q

Preventive measures: community

A

Hygiene.
- Hand washing, cough/sneeze hygiene

Containment.

  • Isolation of confirmed/suspected cases
  • Contact tracing
  • Household/close contact quarantine

Mitigation/suppression.

  • Social distancing
  • School/university/workplace closures
  • Closure of public places (eg. pubs, restaurants, shops)
  • Banning public gathering
  • ?Vaccine
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4
Q

Preventing nosocomial infection

A
  • Isolation of suspected cases
  • Wear PPE
  • Hand-washing
  • Dispose of clinical waste
  • Limit visitors/ contact
  • Sterilise rooms/ equipment used by COVID-19 cases
  • Testing of staff
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5
Q

Investigations in hospital

a) Diagnostic investigations
b) Bedside/bloods
c) Imaging

A

Diagnosis.
- Nasopharyngeal and oropharyngeal swabs*
(+/- sputum samples if obtainable)
- Send for reverse transcriptase PCR (RT-PCR) - 75% senstive
- If negative but high suspicion of infection, take further samples for testing
- May also be positive for influenza A/B or other viruses
- Stool samples may be positive for COVID

    • Can be taken as: a) individual nose and throat swabs in separate collection tubes; OR, b) Combined nose and throat swab in one collection tube containing universal transport medium; OR, c) single swab used for throat then nose
  • In patients with severe lower respiratory symptoms, consider taking broncho-alveolar sample but ensure full PPE (including visor and FFP3 mask) as this is likely an aerosol generating procedure

Bedside.

  • Pulse oximetry
  • ABG (low PaO2, ?raised PaCO2)
  • Blood cultures
  • Sputum cultures

Bloods.
• FBC (cytopenia*, eg. thrombocytopenia or lymphopenia, - poor prognostic indicator)
• U+E (calculate CURB-65 score, AKI, deranged electrolytes - e.g. hypoK/hypoCa)
• LFTs (elevated ALT and bilirubin, low albumin)
• Coagulation screen (raised D-dimer common, if also raised PT/low fibrinogen -?DIC)
• Inflammatory markers (CRP, procalcitonin)
• Serum troponin (raised)
• Serum ferritin (raised)
• Serum lactate dehydrogenase (raised)
• Serum creatine kinase (raised)

*Cytopenia + unremitting fever + raised ferritin = cytokine storm

Imaging.

  • CXR - in those with pneumonia, you will likely see lung infiltrates (25% unilateral, 75% bilateral)
  • ?CT - bilateral ground glass opacity/ consolidation, crazy paving pattern, interlobular septal thickening
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6
Q

Management of suspected cases.

a) Immediate
b) Supportive treatments in non-ICU environment
c) ICU treatments
d) Experimental treatments

A

a) - Immediately isolate and don PPE, etc.
- Take observations and swabs for RT-PCR
- High-flow oxygen
- Consider need for critical care (SpO2 < 94% on 40% oxygen and rising RR = ARDS) and appropriateness (clinical frailty scale, CFS)
- Once confirmed - notify PHE
- Severe COVID-19 (RR > 30, requiring oxygen/ ventilation) = dexamethasone 6mg daily PO/IV for 10/7
- Select patients with severe COVID-19 = remdesevir 100mg IV daily for 5-10 days

b) - Oxygen (initially aim for >94%, once stable aim for > 90%)
- RECOVERY-RS - CPAP/HFNO
- ?trial of NIV in T2RF
- Conservative fluid management - encourage mod oral intake, run “on the dry side” (no more than 2L/day); if shocked, avoid aggressive fluid resus to avoid ARDS
- Paracetamol for fever/ pain
- Antibiotics - empirical for chest sepsis (Sepsis 6), and follow Start Smart/Then Focus (review at 48 - 72h)
- Neuraminidase inhibitor (eg. Tamiflu) if flu cannot be ruled out
- Thromboprophylaxis - raised VTE risk in COVID
- Monitoring - vital signs, ACVPU, fluid status, pain, etc.
- Treatment of underlying conditions (eg. asthma, diabetes and heart failure)
- Consider ceilings of care - decide if candidates for critical care (if > 65 without long-term disability, use CFS, with threshold of < 5 and other factors)
- End of life care

c) - Intubation (PPE to protect from aerosol generation)
- Neuromuscular paralysis
- Mechanical ventilation
- Haemofiltration
- Vasopressor therapy
- ECMO

d) Do not administer unless part of clinical trial:
- RECOVERY - azithromycin, convalescent plasma, tocilizumab, monoclonal antibody
- Lopinavir/ ritonavir (antiretroviral)
- Chloroquine/ hydroxychloroquine
- IVIG (children)

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7
Q

Clinical frailty scale (CFS).

a) Score 1 = ? Score 5 = ? Score 9 = ?
b) Score of 4 or less in Covid patient indicates…?
c) Score of 5+ in Covid patient indicates…?
d) Should only be used in patients who are…

A

a) 1 = Very fit for age
5 = mildly frail (may need some support with high order ADLs, eg. finances, transport, medication)
9 = Terminally ill

b) Likely to benefit from critical care support
c) Unlikely to benefit from critical care support

d) - 65 years old and over
- Without long-term physical or learning disability (eg. cerebral palsy, intellectual impairment, autism) - do an individualised assessment of frailty

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8
Q

Principles of ventilating Covid-19 patients.

a) In intubated ICU patient
b) In non-intubated patient

A

a) ARDS management.
- Low tidal volumes
- Consider neuromuscular paralysis
- Consider prone ventilation

b) - High-flow oxygen: NRB or HFNC
- CPAP/BiPAP

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9
Q

ARDS.

a) Define
b) Severe according to PaO2: FiO2 ratio
c) Pathogenesis
d) Causes

A

a) An acute inflammatory syndrome manifesting as:
- diffuse pulmonary oedema, and
- respiratory failure

…that cannot be explained by, but may co-exist with, left-sided heart failure

b) PaO2: FiO2 ratio < 20 %
- eg. on 50% oxygen but PaO2 < 10 mmHg

c) Inflammation in the alveolar-capillary membrane, leading to distal consolidation and collapse and reducing the surface area in the lungs for gas exchange

d) - Pneumonia
- Aspiration
- Sepsis
- Inhalation injury
- Trauma/ contusion
- Pancreatitis
- Burns
- Drug overdose

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10
Q

Complications of severe infection

a) Main one (cause of death)
b) Others
c) Long-term

A

a) ARDS, causing respiratory failure

b) - Sepsis and shock (+ DIC)
- Secondary infection (super-added infection)
- Heart failure
- AKI
- Acute liver injury
- Acute cardiac injury - myocarditis and arrhythmias
- Cytokine storm syndrome (hyperinflammation): triad of unremitting fever, cytopenias, and hyperferritinaemia
- Paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS)
- Neurological - most commonly stroke

c) - “Long COVID” - 90% of hospitalised patients report at least one symptom persisting 2 months later
- Post-ICU syndrome

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11
Q

Patients at greater risk of severe infection

A
  • Male
  • Older age
  • Obesity
  • Pre-existing lung disease
  • CVD - hypertension, CHD, heart failure
  • Diabetes
  • Immunosuppression
  • ?NSAID users?
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12
Q

Public Health England.

a) Definition of ‘possible case’
b) Definition of a ‘contact’
c) Isolation period (as of October 2020)

A

a) - Influenza-type illness (Fever 37.8+ and 1 or more URTI or LRTI symptom), OR
- Clinical/radiological evidence of pneumonia or ARDS

b) A contact is a person who has experienced any one of the following exposures during the 2 days before and the 14 days after the onset of symptoms of a probable or confirmed case:
• Face-to-face contact with a probable or confirmed case within 3 feet and for more than 15 minutes
• Direct physical contact with probable/confirmed case
• Direct care for a patient with probable/confirmed COVID-19 without using recommended PPE
• Other situations as indicated by local risk assessments.

c) - Suspected/confirmed - isolate for 10 days after symptom onset plus at least 3 days without fever and respiratory symptoms

  • Contact positive - isolate for 14 days from last contact
    or obtain at least two negative RT-PCR tests on respiratory specimens collected 24 hours apart before ending isolation if a test-based strategy is used.
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13
Q

Aerosol-generating procedures.

A
  • Intubation, extubation and ventilation
  • Tracheotomy/ tracheostomy
  • BiPAP/CPAP
  • High-flow nasal cannula (NFNC)
  • Nebulisers
  • Chest compressions and BVM ventilation
  • Sputum induction
  • Bronchoscopy
  • Suctioning
  • Surgery and post-mortem procedures
  • Some ENT and dental procedures
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14
Q

High-flow nasal cannulae.

- Mnemonic: HI FLOW

A
  • Heated + humidified - so does not dry out nasal mucosa, can therefore be delivered at higher flow
  • Inspiratory demand met - in tachypnoeic patient, minute ventilation may be 20 L/min or more, so need a flow rate to exceed this in order to oxygenate properly
  • Functional residual capacity improved - probably via delivery of some PEEP - avoids atelectasis
  • Lighter - nasal cannula easier to tolerate than face mask
  • Oxygen dilution less (due to higher flow, negating dilution from mouth-breathing of room air)
  • Washout of dead space - flushes out CO2 from pharynx
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15
Q

PPE rules.

a) Fluid-resistant masks and gowns, eye and face protection
b) What should be changed between every patient?
c) When should FFP3 be worn?

A

a) ‘Single-session’ use: i.e. a period of time spent in the same setting, ending when healthcare worker leaves this setting
b) Disposable gowns and gloves
c) During aerosol-generating procedures

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16
Q

Features of more serious infection.

a) Moderate
b) Severe
c) Oxygen requirement indicating ?deterioration
d) Critical

A

a) Clinical signs of pneumonia but SpO2 > 90% on room air

b) RR > 30
- Signs of respiratory distress
- SpO2 < 90% on room air
- Lung infiltrates > 50%

c) Oxygen requirement > 4L/min (or FiO2 of 28% to maintain target sats)

b) - Unable to maintain target saturations (92–96% or 88–92% in type 2 respiratory failure risk group)
- Inspired oxygen ≥ 50% to maintain target saturations
- Respiratory Rate > 30 despite oxygen
- Acidosis: pH < 7.2
- Systolic BP < 90 mmHg
- Other organ failure (e.g. liver/kidney/heart/brain)
- Decreased conscious state

17
Q

Covid and Resuscitation.

a) Resus council guidance on full CPR
b) What may still be performed in the absence of full CPR?

A

a) Only safe to perform if wearing full PPE (including FFP3 masks), as chest compressions and BVM ventilation are aerosol-generating procedures
- This will rarely be appropriate, but may be performed in suitable individuals if staff already wearing full PPE or if notified of arrest in advance by paramedics

b) - Cardiac monitoring
- If shockable rhythm - defibrillation is permissible without the need for full PPE
- Treatment of reversible causes (eg. hypovolaemia, hypoglycaemia, hypokalaemia)

18
Q

Interpreting swab results.*

a) Positive result
b) Negative result
c) False positive rates
d) False negative rates
e) Antibody test accuracy

  • Note: Results should be interpreted in the context of the pretest probability of disease
A

a) A positive RT-PCR result confirms SARS-CoV-2 infection
- However, if pre-test probability is low, interpret the result with caution

b) If the result is negative, and there is
still a clinical suspicion of infection (e.g. an epidemiologic link, typical x-ray findings, absence of
another etiology), resample the patient and repeat the test.
- A positive second swab result confirms infection.
- If the second test is negative, consider serologic testing

c) Low - less than 5% of tests (but if low prevalence, there will be a low PPV)
d) As high as 25%

e) A Cochrane review found that antibody tests for IgG/IgM detected:
- 30% of people with COVID-19 when the test was performed 1 week after the onset of symptoms
- Week 2 = 70% detected
- Week 3 = over 90% detected.

19
Q

Differentiating COVID from:

a) CAP/HAP
b) Influenza
c) Atypical pneumonia

A

a) Bacterial pneumonia more likely to have:
- Sputum production
- Focal signs o/e or CXR
- Blood/sputum culture positive

COVID more likely to have:

  • Contact positivity
  • Anosmia/ ageusia
  • COVID swab positive

b) Influenza more likely to have:
- Symptom peak within 3-7 days (vs. COVID symptom peak around 14 days)
- Influenza swab positive
- Children more at risk

COVID more likely to have:

  • Abnormal XR or CT
  • Abnormal biomarkers (e.g. lymphopenia, raised CRP, ferritinaemia, raised ALT, raised troponins, etc.)

c) - Legionella antigen
- Immunosuppressed? - consider PCP pneumonia
- Foreign travel (non-COVID area)
- Aspiration risk

20
Q

Paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS).

a) Diagnostic criteria

A

Children and adolescents 0–19 years of age with:
- Fever > 3 days

AND two of the following:

  • Rash or bilateral non-purulent conjunctivitis or muco-cutaneous inflammation signs (oral, hands or feet).
  • Hypotension or shock.
  • Features of myocardial dysfunction, pericarditis, valvulitis, or coronary abnormalities (including ECHO findings or elevated Troponin/NT-proBNP),
  • Evidence of coagulopathy (by PT, PTT, elevated d-Dimers).
  • Acute gastrointestinal problems (diarrhoea, vomiting, or abdominal pain).

AND

Elevated markers of inflammation such as ESR, C-reactive protein, or procalcitonin.

AND

No other obvious microbial cause of inflammation, including bacterial sepsis, staphylococcal or streptococcal shock syndromes.

AND

Evidence of COVID-19 (RT-PCR, antigen test or serology positive), or likely contact with patients with COVID-19