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Version Date Author Comment
Lucy Lamb, Consultant Infectious
1 19/03/20 Diseases and General Medicine
Royal Free London
Manreet Nijjar, Consultant Infectious Reviewed NA
1.1 20/03/20 Diseases and General Medicine,
Barts Health
Neil Ashman, Medicine Board NICE guidance included
1.2 22/03/20
Nick Bunker, Consultant Critical Care
Martina Cummins, Infection Control Infection control review
1.3 23/03/20 Dr Caryn Rosmarin, Consultant
Microbiologist
1
23/03/20 version 1.3
Confirmed COVID-1 Bundle of Care
This document should be used as a practical guide for care of patients in association with operational
guidance for the care of patients. For all patients a treatment and escalation plan MUST be
discussed and documented with patient (if possible), family and senior decision maker.
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Clinical Syndromes
1. Mild Illness: Non-specific symptoms can include a fever, fatigue, cough (with or without sputum),
malaise, myalgia, sore throat or headache. Diarrhoea and vomiting are less common (10%).
2. Pneumonia:
I. Non-severe: Adult with pneumonia but no need for supplemental oxygen.
II. Severe: Fever or suspected respiratory infection, plus one of raised respiratory rate >30
breaths/min; severe respiratory distress or SpO2 < 93% on room air. Noting that some
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people particularly the elderly can get “silent hypoxaemia” with minimal dyspnoea.
3. Acute Respiratory Distress Syndrome: ARDS onset is within 1 week of known insult or
new/worsening respiratory symptoms with bilateral opacities on CXR or CT and no other likely
differential (eg. fluid overload). May be significant hypoxia and other organ dysfunction.
Clotting – Tends to be normal but DIC can develop associated with a poor prognosis.
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D-dimer - >1µg/ml poor prognostic marker
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C-reactive protein – tracks with disease severity and prognosis .
Renal function – limited AKI seen (<10%), except those with known CKD.
Radiological Findings:
Chest X-ray – patchy ground glass opacities (peripheral and basal) – can be subtle. Unilateral
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changes can be seen. Masses, cavitation, lymphadenopathy and pleural effusions are uncommon.
FBC, clotting, U&Es, LFTs, CK, LDH, Ferritin, CRP, glucose, HIV test, β-HCG (in women of
childbearing age), troponin, D-Dimer. Consider malaria RDT and film if appropriate travel history
NPS samples for SARS-CoV-2 and respiratory viral pathogens, sputum MCS if productive cough, and
Pneumococcal/ Legionella urinary antigens if consolidation on CXR.
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ECG, CXR , ABG (if history of type 2 resp failure/COPD/failing to maintain sats >93% on room air)
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King’s Critical Care – Evidence Summary Clinical Management of COVID-19
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Xie et al. 2020
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Yang et al 2/21.
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Zhou et al Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan,
China: a retrospective cohort study
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Mehta et al 3/20 Consider cytokine storm syndromes and immunosuppression
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23/03/20 version 1.3
1. Mild illness COVID-19
2. Pneumonia – COVID-19
On admission, assess all adults for frailty, irrespective of age and COVID-19 status. Consider
comorbidities and underlying health conditions. Use the Rockwood score below, and record the frailty
assessment in the patient's medical record.
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23/03/20 version 1.3
Clinical Management Maintain oxygen saturations >94% (unless
COPD)
Physiological targets (Based on NEWS) Monitor for clinical deterioration using NEWS
score and call 2222 if required. Inform team that
patient is COVID-19 confirmed before entering
the room
Consider medical co-morbidites to tailor
management
Conservative fluid management of patients when
no shock (BP>100 systolic). Use crystalloid
(Plasmalyte 148). If patient well encourage oral
intake
Discuss the risks, benefits and possible likely outcomes of the different treatment options with
patients, families and carers using decision support tools (where available) so that they can make
informed decisions about their treatment wherever possible.
Sensitively discuss a possible 'do not attempt cardiopulmonary resuscitation' decision with all adults
with capacity and a CFS score suggestive of increased frailty (for example of 5 or more). Include in
the discussion:
Useful aids:
https://www.nice.org.uk/guidance/ng159/resources/information-to-support-decision-making-pdf-
8708913901
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23/03/20 version 1.3
3. Management of Critical Care COVID-19 Acute Respiratory Distress Syndrome (ARDS)
6,8
Clinical Management Recognise severe hypoxaemic respiratory failure:
RR>30, despite FiO2 0.60
Non-invasive ventilation is not advised in the
treatment of COVID-19. There may be patients
with co-existing disease who should still be
considered for NIV (eg sleep apnoea/COPD)
Consider early endotracheal intubation, using
COVID-19 specific intubation check list
Critical care interventions to be considered
include; neuromuscular blockade, lung protective
ventilation, high PEEP, prone positioning,
Negative fluid balance
NGT & feeding
VTE Prophylaxis
PPI
Physiological targets
Hb >70 g/dL
Vt 6 ml/kg IBW
Plat Press < 30 cmH20
Sats 94 - 96%
PaO2 > 8.0 kPa
PaCO2 < 6.0 kPa
MAP > 60 mmHg
UO > 0.5 ml/kg/hr
K+ 4.0 – 5.0 mmol/L
Mg+ > 1.0 mmol/L
Glu 6.0 – 12.0 mmol/L
Observations Hourly: O2 Sats, EtCO2, ECG, Invasive BP monitoring,
Temp, Neuro obs, RASS score, BM, consider CO
monitoring
Investigations CXR, ECG, FBC, U&Es, LFTs, Clotting, Fibrinogen, Blood
Film, Ferritin, CK, LDH, CRP, triglycerides, troponin, Blood
Cultures, Sputum Cultures, CSU if indicated
Consider repeat viral NPA/ETA for SARS-CoV-2 viral PCR
Consider echo
Interventions Antibiotic treatment guided by MicroGuide
At this time there are no specific therapies advised for the
treatment of COVID-19.
Currently we advise against the use of steroids, IVIG,
chloroquine/hydroxychloroquine, remdesivir and Kaletra
outside of a clinical trial.
In patients with evidence of cytokine storm/HLH treatment
with an anti-cytokine agent such as Tocilizumab may be
consider on a named patient basis.
The guidance for treatment of patients with COVID-19 is continually evolving and as it does so
the evidence is being assessed by a multi-disciplinary group. When the evidence changes this
document will evolve. This is the assessment of the current position at version 1.2.
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World Health Organisation. Clinical Management of severe acute respiratory infection (SARI) when
COVID-19 disease is suspected. Interim guidance dated 13 March 2020.
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Clinical guide for the management of critical care patients during the coronavirus pandemic dated 16
March 2020 version 1.
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23/03/20 version 1.3
Basic Rules for Managing Confirmed COVID19 patients:
Appropriate PPE. Equip yourself and check your colleagues before entering the patient environment.
Minimise number of staff exposed. Don’t take equipment/notes/personal belongings into the room.
Breathing: is RR rising? Are sats falling? Does pt have a new 0 2 requirement? Sputum? If concerned
consider need for repeat CXR/ABG and senior/ICU review.
Circulation: assess cap refill, JVP, BP and pulse. Is patient passing adequate urine? If known heart
failure, review fluid balance and consider need for diuresis. AVOID IV FLUIDS where possible.
Disability: Assess GCS. Check blood glucose if diabetes or decreased GCS. Discuss with diabetes
team if BMs >15. Consider patient’s psychological state – are they coping with isolation and anxiety?
Exposure: check pressure areas, assess for signs of DVT. Review CVC/peripheral cannula
site/urinary catheters. Remove or change if inflammation at site.
Feed/Family: Can the patient drink? Eating adequately? Bowels open? Consider need for laxatives,
nutritional support or supplements. Is the patient able to communicate current status to family/friends
by telephone independently or do team need to call next of kin to update?
Infection: Review drug chart – are antibiotics indicated? IV to po switch? Any drug interactions? Send
further samples if indicated (eg. blood cultures if febrile, sputum if cough now productive).
Lab: review results available. Are further routine bloods required for monitoring? (If on antibiotics,
FBC/U&E/LFTs/CRP at least every 72hrs).
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23/03/20 version 1.3