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Covid -19 Management Protocol - Narayana Health

For a patient with RT-PCR or Trunat confirmed Covid-19 infection or strong clinical suspi-
cion with CT of Corads 4 or 5 at least in absence of a positive RT-PCR or Trunat.
Step 1:
First determine the severity of the illness using the following table.
MILD MODERATE SEVERE

Clinical Criteria
SpO2 > 94 % on Room Air 90 - 94 % on Room Air < 90 % on Room Air
RR (/min) < 24 24 – 30 > 30

Symptoms Fever +/- Fever plus breathing difficultyFever with respiratory distress

Pneumonia involving 1 or Pneumonia involving more


Chest Xray (evaluate
Normal
3 zones in each lung upper, mid and lower zones)
two zones than 2 zones

CT Chest Criteria

Average of the % involvement


Normalof
oreach
< 25 lobe
% < 50% > 50%

Laboratory Findings

< 3.2 > 3.2 >17


NLR
CRP < 20 > 40 >40

Ferritin <500 > 500 > 800

D-dimer <0.5 0.5-1.0 > 1.0

LDH < 300 300 – 400 > 400

IL6 < 5.0 5 – 50 > 50, or rising

LFT Normal Slight Derangement Moderate Derangement


SE-
MILD MODERATE
VERE

Treatment

T. Paracetamol 500 mg QID; in high fever not settling can give 1 gm Q8H; DO
NOT exceed 3 g/day. NB: Caution in persons with liver dysfunction
Anti-tussives SOS Anti-tussives SOS Anti-tussives SOS
T. Vitamin C 500 mg
Symptomatic T. Vitamin C 500 mg BD Inj Vit C 1.5 G q8h in ICU
OD
and supportive
care T. Zinc 50 mg BD T. Zinc 50 mg BD T. Zinc 50 mg BD
Inj. Pantoprazole 40 mg IV
Consider Sucralfate OD; titrate up or down de-
C. Esomeprazole 40 mg OD, if symptomatic pending on symptoms and
response
Adequate but conservative hydration - oral or
Fluids Conservative Fluids
parenteral

DOXYCYCLINE
• COLCHICINE
100mg BD for 5 days
• Loading dose: 1.5 mg followed by 0.5 mg of
+
colchicine 60 minutes later if no adverse gastroin-
IVERMECTIN
testinal effects
Antiviral 12mg OD for 5 days
• Maintenance dosage: 0.5 mg BD until discharge
and/or or a maximum of 21 days (reduce to OD if body
OR
Anti-inflamma- weight <60 kg)
tory • Contra indicated if eGFR <30 ml/min/1.73m2
FAVIPIRAVIR 1800mg
• Inj REMDESIVIR
1-0-1 on Day 1
• 200 mg IV on day 1 followed, by 100 mg IV daily
then 800mg 1-0-1 for
for 4 days (total 5 days)
6 days (total 7 days;
• Consider CONVALESCENT PLASMA
can be extended to 14
days on expert ad-
vice)
Inj. Piperacillin-
Tazobactam 4.5 G IV
infusion over 4 hours,
Inj Co-amoxiclav 1.2 G q6h for 7 days.
Not indicated; can be infusion q8h Escalate/deescalate /
Antibiotics prescribed with ex- or change if indicated by
pert consultation Inj Ceftriaxone 2 G iv in- infection biomarkers or
fusion OD by C/S
Seek expert opinion if
allergic to PipTazo or
resistant on culture
Anticoagula-
tion
Inj. Enoxaparin 40 Inj. Enoxaparin 40 mg SC
Inj. Enoxaparin 1 mg/ BD x 5 Days (can be started
Contraindicated mg SC OD x 5 Days kg SC OD x 5 Days as prophylactic without D
in ESRD, active if D-dimer elevated
bleeding, or DIMER)
emergency Inj. Dalteparin 2500 IU Inj. Dalteparin 5000 IU SC
surgery, SC OD ×5 days OD × 5 day
platelets < Alternatively, Tab
3 Dabigatran 110 mg In ESRD, Unfractionated
In ESRD, Unfractionated
BD Heparin – 5000U SC BD
Heparin – 5000U SC BD
20,000/mm ,
BP > 200/120
SE-
MILD MODERATE
VERE

Inj. Dexamethasone 0.1


– Inj. Dexamethasone 0.2 –
0.2 mg /kg ≈ 6 mg IV 0.4 mg
OD x 5 Days /kg ≈ 6 mg IV BD x 10
Steroids Not recommended or Days or
inj. Methyl Prednisolone Inj. Methyl Prednisolone 1.0
0.5 -2.0 mg/kg ≈ 80 mg OD x
-1 mg/kg ≈ 60mg OD x 5 10 Days
Days
Oxygen Sup-
Not Required Maintain Target sPO2 of Maintain Target SPo2
port
92 to 96 % > 90 %
Nasal Prongs (4 lit / min) NRM (10 -15 lit / min)
↓ ↓
Face Mask (5-10 lit / min) HFNC (10 - 60 lit / min)
↓ ↓
NRM (10 -15 lit / min) NIV

HFNC (10 - 40 lit / min) ↓


↓ MV (ARDS Protocol)
NIV
Awake Proning
- 30 to 120 mins prone
- 30 to 120 mins left lat- Prone Ventila-
eral tion 16 to 18
- 30 to 120 mins right lat- hrs / Day
Encourage early
Proning eral
awake proning
- 30 to 120 mins upright – Caution in altered mental
– Caution in altered status and hemodynamic
mental status and he- instability, pregnancy
modynamic instability,
pregnancy
Inj. Itolizumab- Start at
1.6 mg/kg dose iv infu- Inj. Itolizumab- Start at 1.6
sion, if well tolerated mg/kg dose iv infusion, if
and improvement in well tolerated and im-
Cytokine patient observed, clini- provement in patient ob-
Storm* cian has the discretion served, clinician has the
(Criteria for use to continue with 1.6 mg/ discretion to continue with
and contraindi- kg dose every 2 weeks 1.6 mg/kg dose every 2
cations listed at or 0.8 mg/kg weekly weeks or 0.8 mg/kg weekly
-
the bottom of or or
the table) Inj. Toculizumab 400 Inj. Toculizumab 400 mg
If in doubt, mg (max 800 mg) slow (max 800 mg) slow IV in
please seek IV in 100 ml NS over 1 100 ml NS over 1 Hour
expert opinion. Hour Repeat Dose after 12
Repeat Dose after 12 hours if needed
hours if needed -Informed consent is need-
Informed consent is ed
needed
COMORBIDITIES AND COMPLICATIONS

Comorbidi6es
and Complica- Treat Appropriately; seek expert opinion where needed
6ons

MONITORING
BP / HR Daily 6th Hourly 4th Hourly

RR / WOB /spO2 6th Hourly 2nd Hourly ConAnuously

CBC / NLR / RFT / Baseline Every 2 Days Daily


LFT
COVID Profile Baseline Once every 4 days Once every 2 days

D Dimer Repeat every 4 days Once every 4 days Once every 2 days

Troponin / CK Repeated 24 hours & Once every 2 days Once everyday


MB 36 hours
ECG Baseline Once every 2 days Daily
ABG - - Daily
X Ray - If Clinical DeterioraAon

DISCHARGE POLICY

MILD MODERATE SEVERE

DISCHARGE CRITERIA
Afebrile > 3 Days without anApyreAcs + No Breathlessness

10 Days from Symptom 10 Days from Symp- Clinical Recovery


Onset tom Onset
- No O2 Requirement
for 3 Days
RT-PCR not Required RT-PCR not Required Repeat RT-PCR if Swab NegaAve
Transfer to Non Covid Care
Ward – if clinical recovery is de-
layed
DISCHARGE POLICY

DISCHARGE ADVICE

MILD MODERATE SEVERE

Tab Dabigatran 150 mg twice daily


AnAcoagula- Tab Dabigatran 110 mg twice daily for 15-30 days or for 15-30 days
Aon Tab Apixaban 2.5 mg BD for 15-20 days Tab Apixaban 5 mg BD for 15-20
days

Supportive ther-
• Tab Zinc 50 mg 1-0-1 X 7 DAYS
apy ( unevi-
• Tab Vitamin C 500 mg 1-0-1 X 7 DAYS
denced)
• Tab N Acetylcysteine 600mg 1-1-1 If Patient has cough with thick sputum

Isola6on + Self Monitoring for 7 Days

Take all necessary precauAons (e.g. single room with good venAlaAon, face-mask
wear, reduced close contact with family members, separate meals, good hand sani-
taAon, no outdoor acAviAes, personal hygiene) in order to protect family members
and the community from infecAon and further spread of SARS-CoV-2.

Discuss blood donaAon acer full recovery for convalescent plasma collecAon
* Indications for the onset of the cytokine storm and for use of itolizumab or tocilizumab
are:
• Male or non-pregnant female, ≥60 years of age
OR
• ≥30 years of age with at least one known risk factor (arterial hypertension, diabetes
mellitus, coronary heart disease, heart failure, pre-existing chronic pulmonary disease)
• Signed Informed Consent Form
• CRP ≥50mg/L PLUS 3 out of the following 5 criteria need to be fulfilled:
• Respiration Rate ≥25
• SpO2 ≤ 93% (on ambient air)
• PaO2 <65 mmHg
• Persistent or increasing dyspnoea as defined by a one point increase on the mMRC
dyspnoea scale (over 1 hour)
• Persistent or increasing oxygen demand (over 1 hour)

Exclusion Criteria:
• Patients >80 years of age
• Treatment with tocilizumab or itolizumab in previous 4 weeks
• Uncontrolled bacterial superinfection according to treating clinician
• History of severe allergic reaction to monoclonal antibodie
• History of diverticulitis requiring antibiotic treatment or history of colon perforation
• History of primary immunodeficiency (e.g. CVID) or progressing malignancy
• History of chronic liver disease (>Child-Pugh A)
• ALT/AST >5 X ULN
• Hemoglobin <8.0 g/dL
• Leukocytes <2000/mL
• Absolute neutrophil count <1000
• Platelets < 50000

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