Critical care Covid-19 management protocol

Critical care Covid-19 management protocol

EVMS Critical care Covid-19 management protocol

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also great treatment homepage info: https://covid19criticalcare.com/treatment-protocol/

This is our recommended approach to COVID-19 based on the best (and most recent) literature. We should not re-invent the wheel but learn from the experience of others. This is a very dynamic situation; therefore, we will be updating the guideline as new information emerges. Please check on the EVMS website for updated versions of this protocol.

“We have zero success for patients who were intubated. Our thinking is changing to postpone intubation to as long as possible, to prevent mechanical injury from the ventilator. These patients tolerate arterial hypoxia surprisingly well. Natural course seems to be the best.”

EVMS Critical care Covid-19 management protocol

THIS IS A STEROID RESPONSE DISEASE: HOWEVER TIMING IS CTRITICAL

Prophylaxis


While there is very limited data (and none specific for COVID-19), the following “cocktail” may have a role in the prevention/mitigation of COVID-19 disease. While there is no high-level evidence that this
cocktail is effective; it is cheap, safe and widely available.

  • Vitamin C 500 mg BID and Quercetin 250-500 mg BID
  • Zinc 75-100 mg/day (acetate, gluconate or picolinate). Zinc lozenges are preferred. After 1 month, reduce the dose to 30-50 mg/day.
  • Melatonin (slow release): Begin with 0.3mg and increase as tolerated to 2 mg at night
  • Vitamin D3 1000-4000 u/day

Symptomatic patients (at home):

  • Vitamin C 500 mg BID and Quercetin 250-500 mg BID
  • Zinc 75-100 mg/day
  • Melatonin 6-12 mg at night (the optimal dose is unknown)
  • Vitamin D3 1000-4000 u/day
  • Optional: ASA 81 -325 mg/day
  • Optional: Hydroxychloroquine 400mg BID day 1 followed by 200mg BID for 4 days
  • Optional: In highly symptomatic patients, monitoring with home pulse oximetry is recommended

Mildly Symptomatic patients (on floor):

  • Vitamin C 500mg q 6 hourly and Quercetin 250-500 mg BID (if available)
  • Zinc 75-100 mg/day
  • Melatonin 6-12 mg at night (the optimal dose is unknown)
  • Vitamin D3 1000-4000 u/day
  • Enoxaparin 60 mg daily
  • Methylprednisolone 40 mg daily; increase to 40mg q 12 hourly in patients with progressive symptoms and increasing CRP
  • Famotidine 40mg daily (20mg in renal impairment)
  • Optional: Hydroxychloroquine 400mg BID day 1 followed by 200mg BID for 4 days
  • Optional: Remdesivir, if available
  • N/C 2L /min if required (max 4 L/min; consider early t/f to ICU for escalation of care).
  • Avoid Nebulization and Respiratory treatments. Use “Spinhaler” or MDI and spacer if required.
  • Avoid non-invasive ventilation
  • T/f EARLY to the ICU for increasing respiratory signs/symptoms and arterial desaturation

Respiratory symptoms (SOB; hypoxia- requiring N/C ≥ 4 L min: admit to ICU):

Essential Treatment (dampening the STORM)

1. Methylprednisolone 80 mg loading dose then 40mg q 12 hourly for at least 7 days and until transferred out of ICU. In patients with an increasing CRP or worsening clinical status increase the dose to 80mg q 12 hourly, then titrate down as appropriate.

2. Ascorbic acid (Vitamin C) 3g IV q 6 hourly for at least 7 days and/or until transferred out of ICU. Note caution with POC glucose testing (see below).

3. Full anticoagulation: Unless contraindicated we suggest FULL anticoagulation (on admission to the ICU) with enoxaparin, i.e 1 mg kg s/c q 12 hourly (dose adjust with Cr Cl < 30mls/min). Heparin is suggested with CrCl < 15 ml/min. Alternative approach: Half-dose rTPA: 25mg of tPA over 2 hours followed by a 25mg tPA infusion administered over the subsequent 22 hours, with a dose not to exceed 0.9 mg/kg followed by full anticoagulation.

Note: A falling SaO2 despite respiratory symptoms should be a trigger to start anti-inflammatory treatment (see Figure 2). Note: Early termination of ascorbic acid and corticosteroids will likely result in a rebound effect with clinical deterioration (see Figure 3).

EVMS Critical care Covid-19 management protocol

Additional Treatment Components (the Full Monty)

  1. Melatonin 6-12 mg at night (the optimal dose is unknown).
  2. Famotidine 40mg daily (20mg in renal impairment)
  3. Vitamin D 400u PO daily
  4. Magnesium: 2 g stat IV. Keep Mg between 2.0 and 2.4 mmol/l. Prevent hypomagnesemia (which increases the cytokine storm and prolongs Qtc).
  5. Optional: Azithromycin 500 mg day 1 then 250 mg for 4 days (has immunomodulating properties including downregulating IL-6; in addition, Rx of concomitant bacterial pneumonia).
  6. Optional: Atorvastatin 40-80 mg/day. Of theoretical but unproven benefit. Statins have been demonstrated to reduce mortality in the hyper-inflammatory ARDS phenotype. Statins have
    pleotropic anti-inflammatory, immunomodulatory, antibacterial and antiviral effects. In addition, statins decrease expression of PAI-1
  7. Broad-spectrum antibiotics if superadded bacterial pneumonia is suspected based on procalcitonin levels and resp. culture (no bronchoscopy). Due to the paradox of hyperinflammation and immune suppression (a major decrease of HLA-DR on CD14 monocytes) secondary bacterial infection is not uncommon.
  8. Maintain EUVOLEMIA (this is not non-cardiogenic pulmonary edema). Due to the prolonged “symptomatic phase” with flu-like symptoms (6-8 days) patients may be volume depleted. Cautious rehydration with 500 ml boluses of Lactate Ringers may be warranted, ideally guided by noninvasive hemodynamic monitoring. Diuretics should be avoided unless the patient has obvious intravascular volume overload. Avoid hypovolemia.
  9. Early norepinephrine for hypotension.
  10. Escalation of respiratory support (steps); Try to avoid intubation if at all possible, (see Figure 4)
  • Accept “permissive hypoxemia” (keep O2 Saturation > 84%); follow venous lactate and Central Venous O2 saturations (ScvO2) in patents with low arterial O2 saturations
  • N/C 1-6 L/min • High Flow Nasal canula (HFNC) up to 60-80 L/min
  • Trial of inhaled Flolan (epoprostenol)
  • Attempt proning (cooperative repositioning-proning)
  • Intubation … by Expert intubator; Rapid sequence. No Bagging; Full PPE. Crash/emergency intubations should be avoided.
  • Volume protective ventilation; Lowest driving pressure and lowest PEEP as possible. Keep driving pressures < 15 cmH2O.
  • Moderate sedation to prevent self-extubation
  • Trial of inhaled Flolan (epoprostenol)
  • Prone positioning.

There is widespread concern that using HFNC could increase the risk of viral transmission. There is however, no evidence to support this fear. HFNC is a better option for the patient and the health care system than intubation and mechanical ventilation. CPAP/BiPAP may be used in select
patients, notably those with COPD exacerbation or heart failure.

A sub-group of patients with COVID-19 deteriorates very rapidly. Intubation and mechanicalventilation may be required in these patients.

14. Salvage Treatments

  • Plasma exchange
  • High dose corticosteroids; 120mg methylprednisolone q 6-8 hourly
  • Siltuximab and Tocilizumab (IL-6 inhibitors)
  • ?? CVVH with cytokine absorbing/filtering filters
  • ?? ECMO < 60 yrs. and no severe commodities/organ failure

15.Treatment of Macrophage Activation Syndrome (MAS)

  • A sub-group of patients will develop MAS. This appears to be driven by SARS-CoV-2 induced inflammasome activation and increased IL-1 β production (see Figure 5).
  • A ferritin > 4400 ng/ml is considered diagnostic of MAS. Other diagnostic features include increasing AST/ALT and increasing CRP.
  • “High dose corticosteroids.” Methylprednisolone 120 mg q 6-8 hourly for at least 3 days, then wean according to Ferritin, CRP, AST/ALT (see Figure 6). Ferritin should decrease by at least 15% before weaning corticosteroids.
  • Consider plasma exchange.
  • Anakinra (competitively inhibits IL-1 binding to the interleukin-1 type I receptor) can be considered in treatment failures.

16.Monitoring

  • Daily: PCT, CRP, IL-6, BNP, Troponins, Ferritin, Neutrophil-Lymphocyte ratio, D-dimer and Mg. CRP, IL-6 and Ferritin track disease severity closely (although ferritin tends to lag behind CRP). Thromboelastogram (TEG) on admission and repeated as indicated.
  • In patients receiving IV vitamin C, the Accu-Chek™ POC glucose monitor will result in spuriously high blood glucose values. Therefore, a laboratory glucose is recommended to confirm the blood glucose levels.
  • Monitor QTc interval if using chloroquine/hydrochloroquine and azithromycin and monitor Mg++ (torsades is uncommon in monitored ICU patients)
  • No routine CT scans, follow CXR and chest ultrasound.
  • Follow ECHO closely; Pts develop a severe cardiomyopathy.

17. Post ICU management

a. Enoxaparin 40-60 mg s/c daily
b. Methylprednisone 40 mg day, the wean slowly
c. Vitamin C 500 mg PO BID
d. Melatonin 3-6 mg at night

Figure 3. Premature discontinuation of corticosteroids and IV vitamin C (after 4 day) and the effect of reinitiation of this combination on the CRP 9clinical course followed CRP profile.

EVMS Critical care Covid-19 management protocol
EVMS Critical care Covid-19 management protocol

Figure 5. COVID-19 Subtypes of Infections (Phenotypes)

EVMS Critical care Covid-19 management protocol

Figure 6. SARS-CoV-2 induced Macrophage Activation Syndrome (MAS) treated with Vitamin C 3g IV q 6 and increased methylprednisolone (125 mg q 8 hourly)

EVMS Critical care Covid-19 management protocol

Scientific Rational for MATH+ Treatment Protocol

Three core pathologic processes lead to multi-organ failure and death in COVID-19:

1) Hyper-inflammation (“Cytokine storm”) – a dysregulated immune system whose cells infiltrate and damage multiple organs, namely the lungs, kidneys, and heart. It is now widely accepted that SARS-CoV-2 causes aberrant T lymphocyte and macrophage activation resulting in a “cytokine storm.”.


2) Hyper-coagulability (increased clotting) – the dysregulated immune system damages the endothelium and activates blood clotting, causing the formation of micro and macro blood clots. These blood clots impair blood flow.


3) Severe Hypoxemia (low blood oxygen levels) –lung inflammation caused by the cytokine storm, together with microthrombosis in the pulmonary circulation severely impairs oxygen absorption resulting in oxygenation failure.

The above pathologies are not novel, although the combined severity in COVID-19 disease is considerable. Our long-standing and more recent experiences show consistently successful treatment if traditional therapeutic principles of early and aggressive intervention is achieved, before the onset of advanced organ failure.

It is our collective opinion that the historically high levels of morbidity and mortality from COVID-19 is due to a single factor: the widespread and inappropriate reluctance amongst
intensivists to employ anti-inflammatory and anticoagulant treatments, including corticosteroid therapy early in the course of a patient’s hospitalization.

It is essential to recognize that it is not the virus that is
killing the patient, rather it is the patient’s overactive immune system. The flames of the “cytokine fire” are out of control and need to be extinguished. Providing supportive care (with ventilators that themselves stoke the fire) and waiting for the cytokine fire to burn itself out simply does not work… this approach has FAILED and has led to the death of tens of thousands of patients.

The systematic failure of critical care systems to adopt corticosteroid therapy resulted from the published recommendations against corticosteroids use by the World Health Organization (WHO), the Centers for Disease Control and Prevention (CDC), and the American Thoracic Society (ATS) amongst others. A very recent publication by the Society of Critical Care Medicine and authored one of the members of the Front Line COVID-19 Critical Care (FLCCC) group (UM), identified the errors made by
these organizations in their analyses of corticosteroid studies based on the findings of the SARS and H1N1 pandemics.

Their erroneous recommendation to avoid corticosteroids in the treatment of COVID19 has led to the development of myriad organ failures which have overwhelmed critical care systems across the world.

Our treatment protocol targeting these key pathologies has achieved near uniform success, if begun within 6 hours of a COVID19 patient presenting with shortness of breath or needing ≥ 4L/min of oxygen. If such early initiation of treatment could be systematically achieved, the need for mechanical ventilators and ICU beds will decrease dramatically.

It is important to recognize that “COVID-19 pneumonia” does not cause ARDS. The initial phase of “oxygenation failure” is characterized by normal lung compliance, with poor recruitability and near normal lung water (as measured by transpulmonary thermodilution).

This is the “L phenotype” as reported by Gattonini and colleagues. Treating these patients with early intubation and the ARDNSnet treatment protocol will cause the disease you are trying to prevent i.e. ARDS. These patients tolerate hypoxia remarkable well, without an increase in blood lactate concentration nor a fall in central venous

oxygen saturation. We therefore suggest the liberal us of HFNC, with frequent patient repositioning (proning) and the acceptance of “permissive hypoxemia”. However, this approach entails close patient observation.

Patients in whom the cytokine storm is not “dampened” will progress into the “H phenotype” characterized by poor lung compliance, severe oxygenation failure and PEEP recruitability (see Figure 7). Progression to this phase is exacerbated by ventilator induced lung injury (VILI). The histologic pattern of the “H Phenotype” is characterized by an acute fibrinous and organizing pneumonia (AFOP), with extensive intra-alveolar fibrin deposition called fibrin “balls” with absent hyaline membranes.

Corticosteroids seem to be of little benefit in established AFOP. High dose methylprednisolone should be attempted in the “early phase” of AFOP, however many patients will progress to irreversible pulmonary fibrosis with prolonged ventilator dependency and ultimately death.

it is important to recognize that COVID-19 patients present with a variety of phenotypes, likely dependent on genetic heterogeneity, age, viral load, immunological and nutritional status, and comorbidities (see Figure 5).

COVID-19 patients may develop a “thrombophilic phenotype” presenting with severe thrombo-embolic disease with little evidence of lung parenchymal involvement. This suggests that mildly symptomatic patients may benefit from anticoagulation. Furthermore, Vitamin D insufficiency exacerbates the cytokine storm and likely increases the risk of death.

Finally, it is important to acknowledge that there is no known therapeutic intervention that has unequivocally been proven to improve the outcome of COVID-19. This, however, does not mean we should adopt a nihilist approach and limit treatment to “supportive care”. Furthermore, it is likely that there will not be a single “magic bullet” to cure COVID-19.

Rather, we should be using multiple drugs/interventions that have synergistic and overlapping biological effects that are safe, cheap and “readily” available. The impact of COVID-19 on middle- and low-income countries will be enormous; these countries will not be able to afford expensive designer molecules

Figure 7. The consequences of “steroid” avoidance”. CT scan after 23 days of
“supportive care” demonstrating the late fibroproliferative (irreversible) phase of COVID-19 lung disease (Image kindly provide by Dr. Pierre Kory, from NYC).

Source: EVMS pdf

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