Infection prevention and control for healthcare professionals
Always consult local infection prevention and control protocols; only basic principles are detailed here.
Immediately isolate all suspected or confirmed cases in an area that is separate from other patients. Place patients in adequately ventilated single rooms if possible. When single rooms are not available, place all cases together in the same room and ensure there is at least 1 metre (3 feet) between patients.
Implement standard precautions at all times:
Practice hand and respiratory hygiene
Give patients a medical mask to wear
Wear appropriate personal protective equipment
Practice safe waste management and environmental cleaning.
Implement additional contact and droplet precautions before entering a room where cases are admitted:
Wear a medical mask, gloves, an appropriate gown, and eye/facial protection (e.g., goggles or a face shield)
Use single-use or disposable equipment.
Implement airborne precautions when performing aerosol-generating procedures, including placing patients in a negative pressure room.
Some countries and organisations recommend airborne precautions for any situation involving the care of a COVID-19 patient.
All specimens collected for laboratory investigations should be regarded as potentially infectious.
Appropriate personal protective equipment gives healthcare workers a high level of protection against COVID-19. A cross-sectional study of 420 healthcare workers deployed to Wuhan with appropriate personal protective equipment tested negative for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on molecular and serological testing when they returned home, despite all participants having direct contact with COVID-19 patients and performing at least one aerosol-generating procedure. Standard surgical masks are as effective as respirator masks for preventing infection of healthcare workers in outbreaks of viral respiratory illnesses such as influenza, but it is unknown whether this applies to COVID-19.
Detailed infection prevention and control guidance is available:
Telehealth for primary care physicians
It is important that primary care physicians avoid in-person assessment of patients with suspected COVID-19 in primary care when possible to avoid infection. Most patients can be managed remotely by telephone or video consultations. Algorithms for dealing with these patients are available:
General prevention measures for the general public
Wash hands often with soap and water for at least 20 seconds or an alcohol-based hand sanitiser (that contains at least 60% alcohol), especially after being in a public place, blowing their nose, or coughing/sneezing. Avoid touching the eyes, nose, and mouth with unwashed hands
Avoid close contact with people (i.e., maintain a distance of at least 1 metre [3 feet]) including shaking hands, particularly those who are sick, have a fever, or are coughing or sneezing. Avoid going to crowded places. It is important to note that recommended distances differ between countries (for example, 2 metres is recommended in the US and UK) and you should consult local guidance. However, there is no evidence to support a distance of 2 metres
Practice respiratory hygiene (i.e., cover mouth and nose when coughing or sneezing, discard tissue immediately in a closed bin, and wash hands)
Seek medical care early if they have a fever, cough, and difficulty breathing, and share their previous travel and contact history (travellers or suspected/confirmed cases) with their healthcare provider
Stay at home and self-isolate if they are sick, even with mild symptoms, until they recover (except to get medical care)
Clean and disinfect frequently touched surfaces daily (e.g., light switches, door knobs, countertops, handles, phones).
Face masks for the general public
Recommendations on the use of face masks in community settings vary between countries. It is mandatory to wear a mask in public in certain countries or in certain situations, and masks may be worn in some countries according to local cultural habits. Consult local guidance for more information.
There is no high-quality or direct scientific evidence to support the widespread use of masks by healthy people in the community setting, and there are risks and benefits that must be considered. Evidence for mask effectiveness for respiratory tract infection prevention is stronger in healthcare settings compared with community settings; direct evidence on comparative effectiveness in SARS-CoV-2 infection is lacking.
The World Health Organization (WHO) recommends that people with symptoms of COVID-19 should wear a medical mask, self-isolate, and seek medical advice as soon as possible. The WHO also now encourages the general public to wear medical or cloth masks in specific situations and settings (e.g., areas with known or suspected widespread transmission and limited or no capacity to implement other containment measures such as social distancing, contact tracing, and testing; settings where social distancing cannot be achieved, particularly in vulnerable populations). This recommendation is based on observational evidence only.
The Centers for Disease Control and Prevention (CDC) recommends that homemade cloth face coverings can be worn in public settings where social distancing measures are difficult to maintain (e.g., pharmacies, supermarkets), especially in areas where there is significant community transmission.
Use of a mask alone is insufficient to provide adequate protection, and they should be used in conjunction with other infection prevention and control measures such as frequent hand hygiene and social distancing. It is important to wash your hands with soap and water (or an alcohol-based sanitiser) prior to putting on a face mask, and to remove it correctly. Used masks should be disposed of properly.
Potential harms and disadvantages of wearing masks include: potential increased risk of self-contamination due to manipulation of face mask and touching face/eyes, or when non-medical masks are not changed when wet or soiled; headache and/or breathing difficulties; facial skin lesions, irritant dermatitis, or worsening acne; discomfort; difficulty communicating; false sense of security; poor compliance; waste management issues; and difficulties for patients with chronic respiratory conditions or breathing problems. Masks may also create a humid habitat where the virus can remain active and this may increase viral load in the respiratory tract; deeper breathing caused by wearing a mask may push the virus deeper into the lungs.
In a study comparing the use of cloth masks to surgical masks in healthcare workers, the rates of all infection outcomes were highest in the cloth mask arm, with the rate of influenza-like illness statistically significantly higher in this group. Moisture retention, reuse of cloth masks, and poor filtration may result in increased risk of infection. The filtration, fit, effectiveness, and performance of cloth masks are inferior to medical masks and respirators. Protection may be improved by selecting appropriate material, increasing the number of mask layers, and using masks with a design that provides filtration and fit.
Alcohol-based hand sanitisers
The CDC has issued a warning about alcohol-based sanitisers containing methanol (which may be labelled as containing ethanol). Methanol poisoning should be considered in patients who present with relevant signs and symptoms (e.g., headache, impaired vision, nausea/vomiting, abdominal pain, loss of co-ordination, decreased level of consciousness) who report ingestion of hand sanitiser or frequent repeated topical use. Cases of permanent blindness and death have been reported.
Frequent use of hand sanitisers may result in antimicrobial resistance. Accidental ingestion, especially by children, has been reported.
Screening and quarantine
People travelling from areas with a high risk of infection may be screened using questionnaires about their travel, contact with ill persons, symptoms of infection, and/or measurement of their temperature. Combined screening of airline passengers on exit from an affected area and on arrival elsewhere has been relatively ineffective when used for other infections such as Ebola virus infection, and has been modelled to miss up to 50% of cases of COVID-19, particularly those with no symptoms during the incubation period. Symptom-based screening processes have been reported to be ineffective in detecting SARS-CoV-2 infection in a small number of patients who were later found to have evidence of SARS-CoV-2 in a throat swab.
Enforced quarantine is being used to isolate easily identifiable cohorts of people at potential risk of recent exposure (e.g., groups evacuated by aeroplane from affected areas, people returning to their home countries before border closures, or groups on cruise ships with infected people on board). The psychosocial effects of enforced quarantine may have long-lasting repercussions. Despite limited evidence, a Cochrane review found quarantine to be important in reducing the number of people infected and deaths, especially when started earlier and when used in combination with other prevention and control measures.
Travellers who arrive in the UK are required to self-isolate for 14 days. PHE: coronavirus (COVID-19) – how to self-isolate when you travel to the UK external link opens in a new window
Many countries have implemented mandatory social distancing measures in order to reduce and delay transmission (e.g., city lockdowns, stay-at-home orders, curfews, non-essential business closures, bans on gatherings, school and university closures, travel restrictions and bans, remote working, quarantine of exposed people/travellers).
Although the evidence for social distancing for COVID-19 is limited, it is emerging, and the best available evidence appears to support social distancing measures to reduce the transmission and delay spread. The timing and duration of these measures appears to be critical.
Researchers in Singapore found that social distancing measures (isolation of infected individuals and family quarantine, school closures, and workplace distancing) significantly decreased the number of infections in simulation models.
Shielding extremely vulnerable people
Shielding is a measure used to protect vulnerable people (including children) who are at very high risk of severe illness from COVID-19 because they have an underlying health condition. Shielding involves minimising all interactions between those who are extremely vulnerable and other people to protect them from coming into contact with the virus.
Extremely vulnerable groups include:
Solid organ transplant recipients
People with specific cancers
People with severe respiratory conditions (e.g., cystic fibrosis, severe asthma, or severe COPD)
People with rare diseases that significantly increase the risk of infections (e.g., sickle cell anaemia, severe combined immunodeficiency)
People on immunosuppression therapies sufficient to significantly increase the risk of infection
Women who are pregnant with significant heart disease (congenital or acquired)
Other people who have also been classed as clinically extremely vulnerable based on clinical judgement and an assessment of their needs.
The UK government currently recommends shielding for certain groups of people until 31 July, and will pause shielding from 1 August unless community transmission begins to rise significantly. Consult current guidance for specific recommendations (recommendations may differ between countries).
Shielding advice for children and young adults is available; children can be divided into group A (conditions that require shielding) or group B (conditions that require discussion between the clinician and the child and their family/carer to establish whether shielding is necessary). The majority of children currently considered extremely clinical vulnerable will be able to be removed from the shielded patient list from 1 August after discussion with their paediatric specialist or general practitioner.
There is currently no vaccine available. Vaccines are in development, but it may take at least 12 to 18 months before one is available. Several vaccine candidates are currently approved for human testing through clinical trials, including mRNA and DNA platform vaccines, adenovirus vector vaccines, and inactivated virus vaccines.
Previous trials of coronavirus vaccines identified cellular immunopathology and antibody-dependent enhancement (ADE) as potential safety issues, so there are concerns over ADE of SARS-CoV-2 due to prior exposure to other coronaviruses (such as those that cause the common cold).
Results from preliminary animal and human studies are beginning to emerge, but scientists urge caution over the results.
Ad5-nCoV: a recombinant adenovirus type-5 (Ad5) vectored vaccine expressing the SARS-CoV-2 spike glycoprotein. Results from a single-centre, open-label, non-randomised, dose-escalation phase 1 trial in China report that the vaccine was immunogenic, inducing humoral responses (peaking 28 days after vaccination) and T-cell responses (peaking 14 days after vaccination) in most participants. Participants were healthy and had no underlying diseases. At least one adverse reaction was reported within the first 7 days after vaccination in 83% (low- and medium-dose groups) and 75% (high-dose group) of participants. The most common adverse reactions reported included injection-site reactions, fever, fatigue, headache, and muscle pain. No serious adverse events were noted within 28 days of vaccination. A phase 2 trial is ongoing.
ChAdOx1 nCoV-19: an adenovirus vector vaccine that carries the SARS-CoV-2 spike protein. Preliminary results (not peer reviewed) from animal studies found that a single dose induced a humoral and cellular response in mice and rhesus macaques. However, while viral loads in bronchoalveolar lavage fluid and lung tissues of vaccinated animals were significantly reduced compared with unvaccinated animals, reduction in viral shedding from the nose was not observed. Despite this, researchers are moving to human trials.
Inactivated SARS-CoV-2 virus (Sinovac®): contains a more traditional chemically inactivated version of the virus. The vaccine was found to induce immunity in mice, rats, and non-human primates. When challenged with the virus, monkeys who were vaccinated with the highest dose of the vaccine did not develop infection, and no virus was recovered from the throat, lung, or rectum.
mRNA-1273: a novel vaccine that uses mRNA technology not previously approved for use in humans. The mRNA encodes for a full-length prefusion stabilised spike protein of SARS-CoV-2 and is encapsulated in a lipid nanoparticle. Animal studies in mice have been completed, but testing in other animals such as hamsters, ferrets, and non-human primates has been skipped in order to expedite the vaccine development process. Results from a phase 1 trial indicated that all 45 healthy adults (ages 18-55 years) seroconverted by day 15 after the first dose, according to a press release issued by the manufacturer. Of the cohort of 15 patients who received the highest dose (250 micrograms), 20% of participants experienced grade adverse events following the second dose (the press release does not say what these were). Of the two cohorts who received the 25 microgram and 100 microgram doses, only one patient experienced a grade 3 adverse event (erythema at injection site). No grade 4 adverse events were reported in this small cohort. The study did not include people with underlying conditions. mRNA-1273 has been granted fast-track designation by the US Food and Drug Administration, and phase 2 trials are expected to start soon.
BNT162b1: a lipid nanoparticle-formulated, nucleoside-modified, mRNA vaccine that encodes spike glycoprotein RBD. Preliminary (not peer-reviewed) phase 1/2 study results in healthy adults aged 18 to 55 years have been published. RBD-binding immunoglobulin G antibodies and SARS-CoV-2 neutralising antibodies were detected in all subjects at 28 days after two doses. Adverse reactions were dose-dependent and reported in 50% of subjects who received the 10 microgram or 30 microgram dose, and by 58% of subjects who received the 100 microgram dose.
Some governments are discussing or implementing certifications for people who have contracted and recovered from COVID-19 based on antibody tests (sometimes called ‘immunity passports’). Possession of a passport would allow people to have a greater range of privileges (e.g., work, education, travel). However, the WHO does not support these certifications as there is currently no evidence that people who have recovered from infection and have antibodies are protected from reinfection. Other potential issues include lack of public support for these measures, potential for discrimination of groups of people, testing errors (including cross-reactivity with other human coronaviruses), access to testing, fraud, legal and ethical objections, and people getting infected intentionally in order to obtain a certification.
Past or current smokers have nearly double the risk for severe disease, and smoking cessation should be encouraged. The WHO recommends that tobacco users stop using tobacco given the well-established harms associated with tobacco use and second-hand smoke exposure. Public Health England also recommends stopping smoking. PHE: COVID-19 – advice for smokers and vapers external link opens in a new window
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