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COVID-19 Protocol Version 10 - Charlotte Maxeke Johannesburg Academic Hospital / Gauteng ICU Group

COVID treatment protocol devised at CMJAH and which is being used by the Gauteng ICU group. Version 10

The following document represents the treatment protocol devised at CMJAH and which is being used by the Gauteng ICU group. This schema is subject to change as new evidence emerges.

EMGuidance confirms that it is not the owner of the information provided, nor does it intend to present it as such.

The Gauteng ICU group: Therapy of CoVID 19 - Version 10 (14 July 2020)  

*** UPDATED REFRACTORY HYPOXAEMIA AND CORTICOSTEROID DOSE RECOMMENDATIONS ***


Prophylaxis: we believe there is no value in chloroquine prophylaxis.

There may be value in nutritional supplementation.

  • Vitamin D 4 000 IU daily or 50 000 weekly x 4 then monthly
  • Nicotinic acid 25-50mg daily
  • Zinc 20-50mg daily

Have added colchicine though small study and uncertain benefit- however we have been using it for a while.

We believe that the benefit of dexamethasone is a class effect and that it doesn’t matter which steroid issued: 

Dexamethasone comes in 8mg ampoules:

8mg dexamethasone = 30mg methylpred= 40mg mg prednisone = Hydrocortisone 200mg daily

The tocilizumab or polygam will be for a small percentage of patients that are not improving despite Standard of care but in particular corticosteroids and anticoagulation. Tocilizumab use is off label and requires patient or family consent. If used, the Roche form for off label use must be filled in and please can Brian Levy brian@plexsys.co.za  be informed as he is collecting data retrospectively

 

Asymptomatic
Presentation -
Supportive treatment
None: Monitor
Antiviral treatment None
Anti-inflammatory symptoms -
URT Symptoms
Presentation Fever, sore throat, cough;
no dyspnea
or tachypnea;
saturation normal
Supportive treatment Vitamin D 50 000 units stat
Zinc 20 - 50mg daily x 5 days
Nicotinic 25mg - 50mg daily
Vit C 500mg tds
Thiamine 100mg daily

 
Antiviral treatment None
Anti-inflammatory treatment Paracetamol
URT symptoms +age>65 ± comorbidity
OR
LRT symptoms ±pneumonia on CXR
Presentation Fever, dyspnea, tachypnea, crackles
saturation <90%
P/F ratio <300
Hypokalaemia
Supportive treatment
Supportive treatment as above
Oxygen therapy
Antiviral treatment Plasmoquine is unlikely to be of any benefit
Anti-inflammatory treatment
Paracetamol
Full anticoagulation - Factor Xa guided (0.6-0.8)
Corticosteroid: Hydrocortisone 100mg stat
then 50mg 6hrly
OR
Dex 8mg BD x 1 then 8mg dly
OR
Methylpred 40mg BD x 1 then 40mg dly
OR
Prednisone 40mg BD x 1 then 40mg daily
Colchicine 1.5mg stat then 0.5mg BD
Consider heparin/dornase nebs
Severe symptoms
Presentation Tachypnea, cyanosis,
saturation< 90%,
P/F ratio < 200;
Mechanical ventilation
Hypotension, Hypokalaemia,
organ dysfunction
CRP >150 and rising;
D-Dimer rising
Il-6 > 80 if available
IL-6 (pg/ml) / lymphocyte (106/ml) ratio> 50
APACHE II >17
Supportive treatment Supportive treatment as above
ICU: High flow nasal
Try self proning

Mechanical ventilation

ECMO if resources allow -
Mostly will not be possible
Antiviral treatment Remdesivir when available
Anti-inflammatory treatment Therapy as above
If deteriorating: CRP rising; sats worsening or requires intubation on admission consider in addition to above:
Tocilizumab 400mg IVI over 60 mins x one dose
Or if unavailable
Polygam 24g x 1-2 days
Review with expert group
Cardiac failure / myocarditis
Presentation Gallop
Reduced EF
Troponin elevated
Supportive treatment As for severe symptoms above
Antiviral treatment As for severe symptoms above
Anti-inflammatory treatment Polygam 24g daily x 3
Methylprednisone 250 daily x 3

Refractory Hypoxaemia:

Aim to reduce FiO2 which may increase reactive oxidant production and cause pulmonary fibrosis

If on HFN and resp rate >26 or sat <90% consider mechanical ventilation

  1. With persistently elevated CRP/IL-6: If infection excluded
    Increase dose of steroid dose-methylprednisolone 125mg 8hrly x 2 days and assess response
    Consider adding heparin nebs 5000U BD (monitor Xa and aPTT)
  2. With low inflammatory markers:
    Consider adding heparin nebs 5000U BD with physio and aggressive suctioning
    Consider bronchoscopy to assess if plugs

NB

  1. Not all therapy is evidence based
  2. Correct hypokalaemia which is common and may be exacerbated by CHQ
  3. Resources may restrict availability of ventilated beds
  4. Initiate corticosteroids early in all with pneumonic changes and hypoxaemia to avoid mechanical ventilation if possible
  5. If mechanical ventilation required: distress, acidosis, cognitive deterioration, progressive decline in sats, etc. do not withhold it on the assumption that it may do harm

Limit fluid intake but maintain nutrition - avoid oedema (sacral) 

Assist control 

Initiate with PEEP 10

Peak pressure 26 

FiO2 to maintain sat > 90%

If still hypoxaemic or FiO2 > 0.6 

Prone patient and increase mean airway pressure

PEEP may be higher if obese or considerable extrathoracic effect on compliance 

Maximal Peak pressure 30 or if obese 34 

OR 

APRV: (Our preferred mode) 

Pressure high 26-30 

Pressure low 0 

Time high 4 secs

Time low set on the flow tracing- inspiration occurs at 40% of Peak expiratory flow: usually 0.8secs; shorter may create excessive autoPEEP with an increase in pCO2 and decrease in PaO2

No Pressure support

Allow spontaneous respiration: Trigger should be at the lowest setting.

If pCO2 elevated to the extent that pH drops to < 7.3 shorten time high to 3- i.e. increasing the respiratory rate

NOTE: sedation is usually not necessary on this mode unless the tube is critical and extubation would rapidly be fatal 

 

 

GA Richards Emeritus Professor Critical Care 

083 266 8378

Guy.richards@wits.ac.za

M Mer Associate Professor Critical Care 

083 488 1200

Mervyn.Mer@wits.ac.za

Click here for the ORIGINAL document  


Version 10 (14 July 2020)  

Drugs mentioned

NeoHealth® ID 18990 · updated 9/21/2023