This page summarises and signposts to medicine related guidance we’re aware of from professional and government bodies relating to coronavirus and infection and infectious diseases.
Our advice is constantly reviewed as the pandemic situation evolves.
Whilst we have tried to ensure that the information on this page is complete, please report a concern if you feel anything is omitted or inaccurate.
To see our professional guidance summaries for other clinical areas, click here
Advice in this area includes:
Published 23 March 2021, updated 3 June 2021
This comprehensive guideline covers the management of COVID-19 for children, young people and adults in all care settings. Within the section on treatment within the hospital setting there is guidance on escalating and de-escalating treatment and delivering care on critical care and respiratory support units. Therapeutic guidance and evidence overviews are provided on the use of antibiotics (not to be used unless evidence of bacterial co-infection), azithromycin (not to be used as a treatment for COVID-19), colchicine (not to be used), corticosteroids, low molecular weight heparin, remdesivir, tocilizumab, and sarilumab.
Published 14 June 2021
- This policy sets out the interim clinical commissioning position for the use of remdesivir for patients with COVID-19.
- Key changes from previous version (V2) are that patients with end stage renal disease are now eligible for treatment if they meet other eligibility criteria and that patients who are significantly immunocpmpromised are eligible for an extended course of treatment of up to 10 days.
Last updated 1 July 2021
This document sets out the interim clinical commissioning position for passive immunisation with palivizumab against respiratory syncytial virus (RSV) in at-risk pre-term infants as follows
- Infants who meet the current JCVI recommendations will continue to be eligible for palivizumab.
- In addition, during the COVID-19 pandemic, the following additional access criteria are permitted:
• Infants born at ≤34+0 weeks gestation; AND
• Diagnosed with CLD6; AND
• Discharged from hospital on home oxygen in the 9 months prior to the start of the RSV season.
NICE: COVID 19 rapid evidence summary: Anakinra for COVID-19 associated secondary haemophagocytic lymphohistiocytosis [ES26]
Published date: 21 May 2020
In this review no studies were found that considered the effectiveness, safety or cost effectiveness of anakinra in adults and children with secondary haemophagocytic lymphohistiocytosis (SHLH) triggered by SARS-CoV-2 or a similar coronavirus.
However overall NICE conclude:
- anakinra has been used (off label) for cytokine storm syndromes triggered by other viruses (such as herpes viruses), including sHLH, and is reported to be relatively well tolerated, with a favourable safety profile.
- caution is advised when using immunomodulating therapies in critically ill people with known or suspected infections because they increase the risk of infectious complications. However, it has been proposed that anakinra may be an option if such a treatment is considered necessary because it has a relatively short half-life and can be discontinued quickly if an adverse effect or concern for worsening infection arises.
- anakinra can be given intravenously (off label) or subcutaneously and has a large therapeutic window.
- when anakinra is effective for cytokine storm syndromes, it reportedly works within 2 or 3 days
Issued 17 December 2020
NICE encourages people to follow UK government advice to take a Vitamin D supplement. They do not support the use of Vitamin D to either treat or prevent Covid-19 infection excpet as part of a clinical trial.
Published 14 April 2020
The available evidence suggests that, although the anti-inflammatory effects of NSAIDs reduce acute symptoms (such as fever), they may either have no effect on, or worsen, long-term outcomes, possibly by masking symptoms of worsening acute respiratory tract infection. Further evidence is needed to confirm this, and to determine whether these results also apply to infections such as COVID-19.
Published date: 21 May 2020
No evidence was found to suggest that people taking NSAIDs for a long-term condition should be advised to stop treatment in the context of COVID‑19. Stopping or switching NSAID treatment could have a negative impact on some people.
Published date: 21 May 2020
Despite biological plausibility for the role of ACEIs and ARBs in both increasing and decreasing the risk of COVID-19 and its complications, this evidence review has not found any observational or experimental data to support these hypotheses. However, the risks of stopping treatment with an ACEI or an ARB, such as worsening heart failure or hypertension, are well understood.
COVID-19 Therapeutics Advice & Support Group (CTAG): Position Statement: Use of investigational antiviral agents for COVID-19 in adults. Interim Support for hospital clinicians in England
Last updated 24 December 2020
Remdesivir is approved for the treatment of COVID-19 in adults and adolescents requiring supplemental oxygen and should used in line with the interim Clinical Commissioning Policy which sets out inclusion and exclusion criteria for the use of remdesivir in the UK
Investigative antiviral agents should be used in the context of a clinical trial
Provides details of RECOVERY, REMAP-CAP, ACTT, GS-5774, GS-5773 and SNG016 clinical trials of treatments (and schematic as to how the trials fit in terms of treatment setting and disease severity). Also provides details of ISARIC-CCP and GenOMICC observational trials and the expanded access programme for remdesivir
MHRA. CAS Alert: Corticosteroids in the treatment of suspected or confirmed COVID-19
Issued 3 Sept 2020
Based on the results of the REMAP-CAP trial for hydrocortisone and a meta-analysis of corticosteroids (that included results from 7 RCTs including REMAP-CAP and the RECOVERY study of dexamethasone). The MHRA has advised that corticosteroids have been demonstrated to have a clear place in the management of patients with severe or critical COVID-19 disease (as defined by WHO – definitions provided within CAS) but should not be used in patients with non-severe disease. It is stated the guidance applies primarily to patients who are hospitalised and receiving supplemental oxygen but may apply to some non-hospitalised patients.
The following dose regimens for adults are recommended
- The recommended regimen in adults is dexamethasone 6mg (orally or by injection) once daily for 7-10 days or hydrocortisone 50mg (by injection) three times daily for 7 -10 days. Treatment should stop if discharged from hospital within 10 days.
- A longer low-dose hydrocortisone regimen (lasting up to 28 days) may be considered for use in patients with septic shock.
- Prescribers are referred to relevant SPC for use in children, pregnancy or breastfeeding women.
- Co- prescription of a PPI should be considered for gastroprotection according to local policies
- Interaction advice wrt to remdesivir updated to state: “Coadministration has not been studied but based on metabolism and clearance a clinically significant interaction is unlikely”
COVID-19 Therapeutics Advice & Support Group (CTAG): Position Statement: Use of investigational immunomodulatory agents for COVID-19 in adults. Interim Support for hospital clinicians in England
Last updated 22 Jan 2021
A subset of patients with COVID-19 experience an exaggerated host hyperinflammatory response associated with hypercytokinaemia following or associated with the initial viral response phase. This predominately affects the lung but can progress to multi-organ disease.
Several investigative immunomodulatory agents have potential to be repurposed for the management of COVID-19 associated hyperinflammation (including and not limited to anakinra, interferon-beta, tocilizumab, sarilumab, canakinumab and ruxolitinib). The evidence base for these agents and a number of others is described briefly.
There are no licenced immunomodulatory therapies to treat COVID-19 associated hyperinflammation. The standard of care in managing COVID-19 associated hyperinflammation is yet to be defined. Randomised controlled trials to address this are ongoing. RECOVERY, REMAP-CAP and COVACTA trials have got immunomodulatory arms incorporated into their design. Details of other proposed trials are also provided.
It is noted that the existing supplies of these medicines within the NHS supply chain are needed for patients receiving them for conventional indications and use outside of the context of a clinical trial will compromise the feasibility of the trial.
Suspected side effects to medicines used in coronavirus treatment should be reported via the Yellow Card COVID-19 reporting site: https://coronavirus-yellowcard.mhra.gov.uk
Updated to include new evidence and guidance on corticosteroids from WHO and letter from the CMO office. Additional advice from CTAG to consider dexamethasone in patients with a new oxygen requirement)
British HIV Association: Coronavirus (COVID-19) and HIV – Responses to common questions
Last updated 19 March 2020
- Recommended treatment with antiretrovirals should be continued at the same dose. Dose increases do not help protect against Covid-19 or make the infection less severe and could be harmful.
- Do not share antiretrovirals with anyone who has Covid-19 or is worried about catching it.
- The antiretrovirals used in PREP are not active against coronavirus
British Infection Association: Links to national guidance, academic publications and professional societies
- A series of links to useful resources about the treatment of Covid-19 but no specific advice
- Updated to include updated interim commissioning policy on palivizumab
- Updated to include revised interim commissioning policy on remdesivir.
- Updated to highlight new recommendations from NICE on colchicine and azithromycin and the revised guidance on remdesivir.
- Updated to include comprehensive COVID treatment guideline from NICE and any superseded guidance deleted.