SARS-CoV-2: Difference between revisions
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*For patients no requiring supplemental oxygen, the focus is on supportive care |
*For patients no requiring supplemental oxygen, the focus is on supportive care |
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**[[Remdesivir]] 200 mg IV once followed by 100 mg IV daily for 2 more days may be used within 7 days of symptom onset who have at least one risk factor for disease progression (age ≥60 years, obesity, or other medical conditions)[[CiteRef::gottlieb2021ea]] |
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** |
**Consideration of monoclonal antibodies such as [[casirivimab-imdevimab]] (Regeneron), depending on the variant |
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***Use in patients who are anti-spike protein seronegative and within 9 days of symptom onset |
***Use in patients who are anti-spike protein seronegative and within 9 days of symptom onset |
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***May reduce hospitalization of high risk patients (hypertension, diabetes, chronic lung disease, congestive heart failure, of immunodeficiency) with ARR of 2 to 3% |
***May reduce hospitalization of high risk patients (hypertension, diabetes, chronic lung disease, congestive heart failure, of immunodeficiency) with ARR of 2 to 3% |
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*For patients requiring supplemental oxygen or with oxygen saturation less than 94%: |
*For patients requiring supplemental oxygen or with oxygen saturation less than 94%: |
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**[[Dexamethasone]] 6 mg PO/IV daily for 10 days, which has a mortality benefit |
**[[Dexamethasone]] 6 mg PO/IV daily for 10 days, which has a mortality benefit |
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**[[Remdesivir]] 200 mg |
**[[Remdesivir]] 200 mg IV once on day one followed by 100 mg PO daily for 5-10 days, which has not been shown to have a mortality benefit |
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**[[Tocilizumab]] indicated if progressing despite [[dexamethasone]], still requiring oxygen and CRP ≥75 mg/L, per RECOVERY trial |
**[[Tocilizumab]] indicated if progressing despite [[dexamethasone]], still requiring oxygen and CRP ≥75 mg/L, per RECOVERY trial |
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***ARR for 28-day mortality of about 4% |
***ARR for 28-day mortality of about 4% |
Revision as of 12:31, 21 January 2022
Background
Microbiology
- Coronavirus related to SARS-CoV
- Virion consists of:
- Spike glycoprotein (S), which appears to be an important virulence factor
- Vaccines may target either the full protein or only its distal receptor binding domain
- Membrane protein (M)
- Nucleocapsid protein (N)
- Hemagglutinin esterase (He)
- Envelope protein (E)
- Spike glycoprotein (S), which appears to be an important virulence factor
Epidemiology
- Transmitted mostly by respiratory droplets, with some amount transmission via aerosols and little to no transmission via contact
- First cases detected Dec 2019 related to likely exposure in wet market in Wuhan, Hubei, China, and declared a pandemic in 2020
- Secondary household attack rate of 12-17%
- Possibility of animal reservoirs, including cats (possibly), dogs (unlikely), deer (probably)
- Difficult to prove transmission to humans
- Unlikely to contribute to household transmission, since human-to-human transmission is far more likely
Risk Factors for Mortality
- Greater age
- Male sex
- COPD
- Dyslipidemia
- Diabetes
Clinical Manifestations
- Incubation period 4 to 5 days (range 2 to 11 days), possibly as long as 14 days in some cases
- Main presenting symptoms were fever and cough, followed by myalgia, fatigue, headache, dyspnea
- Other symptoms include dyspnea, rhinorrhea, vomiting, diarrhea, anosmia/hyposmia
- Lymphopenia is common, as is hypoalbuminemia, elevated D-dimer, CRP, LDH, AST/ALT
- Viral load detectable before symptom onset and peaks around the time of symptom onset
Pregnancy
- Please refer to a living systematic review on the topic
- Slightly less reported fever and myalgias
- Slightly more ICU admissions and mechanical ventilation
- Risk factors included age, obesity, hypertension, and diabetes
- With regards to the fetus, there were more preterm deliveries (6%) and more needed NICU admission (25%)
Severity
- Mild: no oxygen
- Moderate: supplemental oxygen
- Severe: non-invasive mechanical ventilation
- Critical: invasive mechanical ventilation
Bacterial Coinfection
- True coinfection is rare, detected in about 5% of patients1
- See https://www.tarrn.org/covid for a living systematic review
- Most commonly Mycoplasma pneumonia, Pseudomonas aeruginosa, and Haemophilus influenzae
- May be at risk of post-infectious or secondary bacterial infections
- Also possibly need to consider Aspergillus fumigatus and even Pneumocystis jirovecii
Complications
- In critically ill patients:
- ARDS (75%)
- AKI (40%)
- Thrombosis (10%)
Investigations
- CT chest imaging may show:2
- Typical appearance:, classic for COVID-19
- Peripheral, bilateral ground-glass opacity with out without consolidation or visible intralobular lines (crazy paving)
- Multifocal rounded GGO with or without consolidation or crazy paving
- Reverse halo sign or other findings of organizing pneumonia (later finding)
- Indeterminate appearance:
- Multifocal, diffuse, perihilar, or unilateral GGO with or without consolidation lacking a specific distribution and are non-rounded or non-peripheral
- Few very small GGO with a non-rounded and non-peripheral distribution
- Atypical appearance, which suggests unlikely to be COVID-19:
- Isolated lobar or segmental consolidation without GGO
- Discrete small nodules (centrilobular, tree-in-bud)
- Lung cavitation
- Smooth interlobular septal thickening with pleural effusion
- Typical appearance:, classic for COVID-19
Diagnosis
- PCR from NP swab
- Highest sensitivity within 5 days of symptom onset, with decreasing sensitivity as the disease enters the immune-mediated phase
- May be positive long after no longer infectious
- Diagnostic accuracy of PCR by sample site (below) has a lot of heterogeneity among the studies
Sensitivity | Specificity | |
---|---|---|
Upper Respiratory Samples | ||
Oral | 56 | 99 |
Nasal | 76 | 100 |
NP | 97 | 100 |
Nasal | 95 | 100 |
Saliva | 85 | 100 |
Mid-turbinate | 100 | 100 |
Upper Versus Lower Tract | ||
Upper respiratory tract | 57 | 100 |
Lower respiratory tract | 81 | 100 |
Single Versus Repeat Testing | ||
Single test | 71 | 100 |
Repeat testing | 100 | 100 |
- Serology (IgM and IgG)
- Total antibodies have poor sensitivity (51%) in first week, and increases to about 90% by week 3
Management
- For patients no requiring supplemental oxygen, the focus is on supportive care
- Remdesivir 200 mg IV once followed by 100 mg IV daily for 2 more days may be used within 7 days of symptom onset who have at least one risk factor for disease progression (age ≥60 years, obesity, or other medical conditions)3
- Consideration of monoclonal antibodies such as casirivimab-imdevimab (Regeneron), depending on the variant
- Use in patients who are anti-spike protein seronegative and within 9 days of symptom onset
- May reduce hospitalization of high risk patients (hypertension, diabetes, chronic lung disease, congestive heart failure, of immunodeficiency) with ARR of 2 to 3%
- For patients requiring supplemental oxygen or with oxygen saturation less than 94%:
- Dexamethasone 6 mg PO/IV daily for 10 days, which has a mortality benefit
- Remdesivir 200 mg IV once on day one followed by 100 mg PO daily for 5-10 days, which has not been shown to have a mortality benefit
- Tocilizumab indicated if progressing despite dexamethasone, still requiring oxygen and CRP ≥75 mg/L, per RECOVERY trial
- ARR for 28-day mortality of about 4%
- If tocilizumab is unavailable, then baricitinib 4 mg p.o. daily for 14 days or until hospital discharge
- If unvaccinated/no prior infection, declining clinically, and within 9 days of symptom onset, casirivimab-imdevimab (Regeneron) 8000 mg IV once
- Avoid hydroxychloroquine/chloroquine, lopinavir-ritonavir
Anticoagulation
- A multiplatform RCT combined ATTACC, REMAP-CAP, and ACTIV-4a looked at therapeutic anticoagulation (compared to prophylactic)
- Therapeutic anticoagulation with heparin derivatives, using the LMWH typical for the hospital at DVT/PE treatment doses
- Duration 14 days, or until discharge if before 14 days
- Helpful in moderately ill patients, regardless of D-dimer value
- Potentially harmful in severely or critically ill patients
Strongyloidiasis
- Patients should be screened per CATMAT guidelines and treated if appropriate
- For steroid exposure, 10 days of dexamethasone +/- tocilizumab is considered substantial risk
- See also Ivermectin treatment for Strongyloides infection in patients with COVID-19 from the CCDR
Prevention
Infection Prevention and Control
Healthcare Workers
- Awaiting results
- If symptomatic, HCWs should be off work
- If asymptomatic, HCWs may return to work while awaiting results, depending on the reason for testing and the staffing needs
- Positive but asymptomatic: in exceptional circumstances, may return to work early
Clearance
- Non-test based (preferred)
- Asymptomatic: isolate for 10 days from swab
- Mild to moderate symptoms in immunocompetent person: 10 days from onset of symptoms, as long as afebrile (without antipyretics) and clinically improving
- Severe (i.e. ICU-level care) or immunocompromised: 20 days from onset of symptoms, as long as afebrile (without antipyretics) and clinically improving
- Immunocompromise includes chemotherapy, untreated HIV with CD4 <200, primary immunodeficiency, prednisone 20 mg/day for 14 days, and other immunosuppressing medication
- Test based (alternative): 2 negative swabs at least 24 hours apart (if still positive, repeat in 3 to 4 days), as long as afebrile and clinically improving
Further Reading
- Pathophysiology, Transmission, Diagnosis, and Treatment of Coronavirus Disease 2019 (COVID-19): A Review. JAMA. doi: 10.1001/jama.2020.12839
Canadian Guidelines
References
- ^ Louise Lansbury, Benjamin Lim, Vadsala Baskaran, Wei Shen Lim. Co-infections in people with COVID-19: a systematic review and meta-analysis. Journal of Infection. 2020;81(2):266-275. doi:10.1016/j.jinf.2020.05.046.