Key words
SARS-CoV-2 - COVID-19 - critical care - adult respiratory distress syndrome - acute
lung injury - personal protection equipment - N95 respiratory masks
Abbreviations
ARDS:
acute respiratory distress syndrome
COVID-19:
corona virus disease 2019
CRP:
C-reactive protein
ECMO:
extracorporeal membrane oxygenation
EI:
endotracheal intubation
FFP2/FFP3:
filtering face piece (protection classes 2/3)
IL:
interleukin
LDH:
lactate dehydrogenase
NIV:
non-invasive ventilation
NSAID:
nonsteroidal anti-inflammatory drug
PPE:
personal protective equipment
RKI:
Robert Koch Institute
RT-PCR:
reverse transcriptase polymerase chain reaction
SARS-CoV-2:
severe acute respiratory syndrome-coronavirus 2
SSC:
Surviving Sepsis Campaign
TNF:
tumour necrosis factor
Introduction
The new coronavirus, known as SARS-CoV-2 (severe acute respiratory syndrome-coronavirus
2), has caused a global pandemic within a short period of time. The clinical presentation,
i.e., the disease itself, has been given the name COVID-19 (corona virus disease 2019).
Since the initial period of transmission of infections, the number of infections reported
in the Peopleʼs Republic of China and in numerous European countries has risen exponentially
[1] and significantly exceeded the capacity of healthcare systems in certain countries
such as Italy. Physicians and nursing staff are therefore in urgent need of information
about efficient ways of diagnosing the disease and evidence-based treatment.
Epidemiology
It is currently assumed that SARS-CoV-2 was present in an animal reservoir (the market
for seafood and reptiles in Wuhan, Peopleʼs Republic of China) from where it passed
to human hosts at the beginning of December 2019 [2]. The original reservoir species is still unknown, but bats are considered the most
likely source [3]. With Wuhan as the starting point, the virus spread across all of mainland China,
with a significant concentration of cases occurring in the province of Hubei [4].
Initially, the number of infections in all affected countries increased exponentially,
although the curve has since flattened following drastic measures taken by some countries
to avoid social contacts (Peopleʼs Republic of China, Taiwan, Singapore) [5]. The characteristic exponential infection curve is due to SARS-CoV-2 being highly
contagious. Based on a meta-analysis of 12 studies published until 7 February 2020,
the mean basic reproduction number for SARS-CoV-2 is currently 3.28 infections per
infected individual, a considerably higher number than that of SARS.
Data from China suggested, that every infected individual infects an average of 3.28
other people [6].
According to current calculations, the case fatality rate (= the number of infected
persons who die of the infection; lethality) of SARS-CoV-2 is just 1.4%, although
the risk of developing symptomatic infection increases with age (approx. 4% per year
for adults between the ages of 30 – 60 years) [7]. Patients over the age of 59 years have a 5-fold higher risk of dying from COVID-19.
Children are often not affected or only to a minor extent, but they can pass on the
infection. It is currently not expected that large numbers of children will be seriously
affected [8].
The average incubation period is about 5 – 6 days (range: 0 – 14 days). However, the
virus is still detectable in infected persons up to 30 days from onset of illness,
which makes it more difficult to classify asymptomatic patients as cured even if they
appear to have recovered from the infection [9].
There is currently insufficient evidence to be able to say whether persons who had
the disease develop immunity and how long this immunity persists [10]. Data from animal studies suggest that, as with other viral diseases, infected individuals
do develop immunity which subsequently prevents clinically apparent reinfection [11].
Clinical Characteristics
COVID-19 is primarily an infection of the upper and lower respiratory tract. The efficient
proliferation of the virus within the nasopharyngeal cavity is considered one of the
reasons for the high contagiousness of the virus [12]. Otherwise, the clinical characteristics of SARS-CoV-2 resemble those of other viral
diseases which affect the lungs: fever, cough, fatigue.
According to data from the Peopleʼs Republic of China, more than 80% of affected patients
are asymptomatic or present with only mild symptoms, around 15% develop more serious
general symptoms including pneumonia, and around 5% of patients become critically
ill and develop sepsis, septic shock or multi-organ failure [13], [14], [15], [16], [17], [18] ([Table 1]). The lethality is between 1 – 2%. Men are affected significantly more often than
women [16], [23]. The figures may vary, depending on the intensity and time of testing. This appears
to be the case in Italy.
Table 1 Classification of symptoms and severity in persons with COVID-19 (data from [18]).
Severity
|
Symptoms
|
Mild (outpatient/ normal ward)
|
Fever
Cough
Fatigue
|
Severe (IMC = intermediate care)
|
Dyspnoea
Respiratory rate ≥ 30/min
SaO2 ≤ 93%
paO2/FiO2 < 300
Lung infiltrates > 50% within 24 – 48 h
|
Critically ill (ICU = intensive care unit)
|
Lung failure
Septic shock
Multi-organ failure
|
Critically ill patients present with the classic features of ARDS including hyaline
membrane formation, consolidated areas in the lungs and atelectasis [19]. Images of the thorax obtained with computed tomography show ground-glass opacity
in more than 50% of cases and bilateral shadows [16]; bilateral shadowing was also found in > 50% of cases with conventional X-ray imaging
[20].
On admission to hospital, more than 80% of patients were found to have lymphocytopenia;
laboratory tests in a cohort of 173 patients from Wuhan with severe disease showed
elevated CRP (≥ 10 mg/l, 81.5%), LDH (≥ 250 U/l, 58.1%) and D-dimer (≥ 0.5 mg/l, 59.8%)
levels in a majority of patients, while only 13.7% of patients had elevated procalcitonin
levels of more than ≥ 0.5 ng/l [16]. Elevated D-dimer and serum ferritin levels have also been reported in other cohorts
[21], [22].
In general, it appears that older men with comorbidities are more likely to fall ill
and more likely to die.
Around half of patients with COVID-19 have chronic comorbidities; the majority have
cardiovascular or cerebrovascular comorbidities or diabetes mellitus [23]. Some patients with severe course of disease had coinfections with bacteria and
fungi. Examination of cultures has identified Acinetobacter baumannii, Klebsiella pneumoniae, Aspergillus flavus, Candida glabrata and Candida albicans among others [23].
Diagnosis
In cases suspicious for infection with SARS-CoV-2, the Robert Koch Institute (RKI)
recommends obtaining parallel samples from the upper and lower respiratory tract,
depending on the clinical situation. It is important to use swabs suitable for detecting
the virus (virus swabs with an appropriate transport medium or, if necessary, dry
swabs moistened with a small amount of NaCl solution; no agar swabs).
The material should be examined with RT-PCR for the presence of viral RNA [24]. If the material needs to be preserved for longer periods, it must be stored at
a temperature of 4 °C.
According to the recommendations of the RKI (www.rki.de/covid-19-falldefinition; as per: 28.03.2020), testing should focus on symptomatic persons and individuals
suspected of having the virus based on a differential diagnosis.
A clinical suspicion of infection is based on an individualʼs previous history, symptoms
or findings consistent with COVID-19 disease, and whether a diagnosis for a different
disease exists which could adequately explain the presenting symptoms and clinical
picture [25].
In practice, the recurrent issue for medical staff is which contacts should lead to
testing.
A category 1 contact person is defined a person who had face-to-face contact for a
cumulative period of at least 15 minutes with a known COVID-19 patient, e.g. during
a conversation [25]. Persons who had this type of contact should initially be sent home to self-isolate
(quarantine) for 14 days. For medical staff, this category has been subdivided further
into category 1a and 1b contact persons.
A category 1a contact is a person with high-risk exposure, e.g. someone who had unprotected
exposure to secretions and aerosols from COVID-19 patients (intubation and extubation
of the patient, bronchoscopy, aspiration, nebulisation, manual ventilation prior to
endotracheal anaesthesia, proning the patient, noninvasive ventilation (NIV), tracheotomy
and cardiopulmonary resuscitation) [26]. This group of people should usually be required to quarantine themselves at home
for a period of 14 days. As medical staff are a very limited resource, in view of
the shortage of relevant staff, the RKI has recommended a shorter isolation period
of 7 days for this group.
Persons classified as contact category 1b had contact with a confirmed COVID-19 case
in the context of delivering care or undertaking a medical examination (> 15 min,
≤ 2 m distance) without personal protective equipment but also without carrying out
a high-risk procedure. Because of the shortage of staff, this group of persons may
continue working but should use a surgical mask to cover their mouth and nose for
a period of 14 days.
No special precautions are required for category 3 contact persons; this category
covers medical staff who were in the same room as a confirmed COVID-19 case and were
not wearing adequate personal protective equipment but were never closer than 2 metres,
did not come into direct contact with secretions or excretions of the patient and
were not exposed to aerosols as well as medical staff who were closer than 2 m to
the patient but were wearing adequate personal protective equipment throughout the
entire contact period [26].
The overview below summarises the contact categories and appropriate response for
each category.
Overview
The 3 contact categories for medical staff
There are 3 different contact categories for medical staff.
Category Ia
Risky contact with aerosol production.
→ If there are staff shortages: 7 days self-isolation at home followed by testing.
Category Ib
Risky contact without aerosol exposure, distance to patient was < 2 metres, duration
of contact was > 15 minutes.
→ If there are staff shortages: can return directly to work with patients if wearing
a surgical mask covering mouth and nose.
Category III
No aerosol contact, distance to patient was > 2 metres, duration of contact was < 15
minutes or aerosol + adequate personal protective equipment.
→ No particular measures required.
Hygiene Measures
Cave
Data from Wuhan and Italy show that around 4 – 20% of medical staff were infected
with the virus while caring for COVID-19 patients [18], [27].
In addition to strict observance of the rules of basic hygiene, it is critically important
to ensure that staff are adequately provided with personal protective equipment. Because
the disease is highly contagious, use of a FFP2/FFP3 (face filtering piece) respirator
mask is recommended for all aerosol-generating procedures performed when caring for
patients. Staff must additionally wear protective goggles and a waterproof apron or
gown [28].
Class 2 and 3 FFP masks are characterised by a very low levels of overall leakage,
which is why they offer good protection against aerosols (droplet infection); however,
working while wearing FFP2/FFP3 respirator masks is only possible for limited periods
of time because of the high breathing resistance [29].
As it is expected that supplies of FFP2/FFP3 respirator masks will be insufficient
during the pandemic, it is necessary to also think about alternative approaches in
an emergency. In its recently published recommendations on the treatment of patients
with COVID-19, the Surviving Sepsis Campaign (SSC) cited a current meta-analysis which
did not find special respiratory masks (analogous to our FFP2/FFP3 masks) to be superior
to conventional surgical masks with regard to preventing the infection from spreading
to healthcare staff who treated infectious patients [30]. A randomised study on the treatment of patients which included a number of patients
infected with the coronavirus also reported that surgical masks were noninferior to
N95 respirator masks [31]. This means that, in exceptional situations, providing patients and healthcare staff with surgical masks could be a useful means of reducing the risk
of infection for medical staff, at least when treating spontaneously breathing patients.
However, during all aerosol-generating procedures, it is absolutely essential that
medical staff wear a FFP2 mask at the very least, or better still a FFP3 mask (see
above) for their own protection. The German Society for Pneumology and Respiratory
Medicine recently published detailed recommendations [32]. To reduce the use of FFP2/FFP3 masks, it is recommended that medical staff wear
personal protective equipment (PPE) during as many of their encounters with patients
as possible. When treating patients with the virus who are on the same ward, several
patients can be treated while wearing the same PPE. Between contacts with patients,
the FFP mask can be placed between 2 low-microbe disposable cardboard kidney dishes
if it is possible to prevent the inside of the mask from being contaminated.
To ensure that sufficient PPE is available for all medical staff despite the increased
demand during the pandemic, tests are currently being carried out to see whether it
would be possible to re-use used FFPS masks using suitable reprocessing methods. Before
the reprocessed masks are released for use, it will be necessary to test whether the
masks continue to fulfil their protective function after reprocessing.
Treatment
Around 20% of patients develop severe symptoms ([Table 1]), and around 5% require treatment in an intensive care unit. The lungs react to
the disease-causing agent SARS-CoV-2 in the same way they react to other viruses which
attack the respiratory system. Patients present with pathophysiological changes which
are known to also occur in patients with influenza or viral SARS pneumonia. This means,
specifically, that the treatment of patients with COVID-19 must be based, first and
foremost, on best standard care, i.e., on optimal compliance with evidence-based treatment
recommendations developed to treat acute lung failure (acute respiratory distress
syndrome, ARDS) [33].
The recommendations of the Surviving Sepsis Campaign (SSC) published very recently
in the context of the current corona pandemic include a total of 50 statements which
were assigned different levels of recommendation [34].
The measures listed below are the only ones given a strong recommendation (cf. also
[Fig. 1]):
Fig. 1 Summary of clinical recommendations to treat COVID-19 patients [data from: Alhazzani
W, Moller MH, Arabi YM et al. Surviving Sepsis Campaign: Guidelines on the Management
of Critically Ill Adults with Coronavirus Disease 2019 (COVID-19) (in press). doi:10.1007/s00134-020-06022-5].(Copyright © 2020 by the Society of Critical Care Medicine and the European Society
of Intensive Care Medicine)
-
Recommendation against the use of dopamine,
-
Recommendation for lung-protective ventilation: low tidal volume ventilation (Vt) of 4 – 8 ml/kg predicted body weight, PEEP > 10 cm H2O, but no incremental (stepwise) PEEP recruitment,
-
Recommendation for supplemental oxygen if SpO2 is < 90% (but SpO2 must not be > 96%).
Additional measures (e.g., proning, restrictive administration of fluids and veno-venous
ECMO as emergency therapy) may be considered.
[Fig. 2] shows the suggested approach for hypoxemia. Non-invasive ventilation is usually
an important component of treatment for acute lung failure. However, the use of non-invasive
ventilation and high-flow nasal oxygen therapy are associated with aerosol generation.
Fig. 2 Treatment algorithm for patients with acute hypoxemic respiratory insufficiency caused
by COVID-19 [data from: Alhazzani W, Moller MH, Arabi YM et al. Surviving Sepsis Campaign:
Guidelines on the Management of Critically Ill Adults with Coronavirus Disease 2019
(COVID-19) (in press). doi:10.1007/s00134-020-06022-5].(Copyright © 2020 by the Society of Critical Care Medicine and the European Society
of Intensive Care Medicine)
If these forms of treatment are used, it is important to ensure the nasal high-flow
cannula or NIV mask have an optimal fit. An NIV helmet is preferable if the patient
can tolerate it.
Because of the above-mentioned problem of aerosol generation, ventilation based on
endotracheal intubation is the preferred approach for patients with acute hypoxemic
respiratory insufficiency [35].
Transpulmonary thermodilution (PiCCO2, Pulsion-Maquet or EV1000, Edwards Life Sciences)
can be used to guide the restrictive fluid strategy as it can be used to measure extravascular
lung water, which plays an important prognostic role in acute lung failure [36], [37].
Paracetamol or metamizole can be used to reduce fever. Although the WHO has withdrawn
its warning, the data on ibuprofen is still unclear, with NSAID use associated with
an increased risk of bleeding [38].
Experimental procedures
Outside best standard care, there is also a huge interest in new and experimental
treatment procedures, although there are currently no data available for the overwhelming
majority of new procedures. A very recently published study on the use of a combination
of lopinavir and ritonavir was unable to show any survival benefits for COVID-19 patients
[39].
Remdesivir (pharmaceutical company: Gilead Sciences, Inc.) is another effective antiviral
agent which was originally developed to treat infections associated with the Ebola
virus. Remdesivir is effective to treat a wide range of different viruses, including
filoviruses, paramyxoviruses, pneumo-viruses and pathogenic coronaviruses [40]. In cell cultures inoculated with Middle East respiratory syndrome coronaviruses,
remdesivir was found to be superior to a combination of lopinavir/ritonavir [30]. The first data from Chinese patients are expected in early April. However, the
substance is currently not available in Germany outside of controlled trials.
Early on, the suggestion was made that chloroquine could be a potentially effective
antiviral drug; however, positive results in cell cultures and animal experiments
could not be replicated or confirmed in clinical practice [41]. A recent Letter to the Editor [42] reported positive effects in 100 patients in a Chinese multicentre study. In the
group which received the drug, it was found to prevent exacerbation of pneumonia,
improve X-ray findings and shorten the overall course of disease. No relevant side
effects were noted. There are currently no peer-reviewed publications on its use in
this context; a recent systematic review into the use of chloroquine to treat COVID-19
disease recommended that chloroquine should only be administered in accordance with
the Monitored Emergency Use of Unregistered Interventions (MEURI) protocol [43].
Based on the available evidence, it is currently not possible to recommend any of
these therapies. In each case, an individual risk-benefit assessment is necessary
prior to initiating the off-label use of particular substances, as serious side effects
have been reported [44].
There is also considerable interest in the use of extracorporeal membrane oxygenation
(ECMO) as an emergency therapy [45]. Veno-venous ECMO (vv-ECMO) is already an established procedure to treat refractory
respiratory failure and appears to be associated with a survival benefit in a subgroup
of patients [46], [47]. There is general agreement that this therapy should only be carried out in experienced
centres. As with other medical procedures, a minimum of 20 veno-venous ECMO runs per
year is considered the minimum entry criterion [20].
A small subgroup of COVID-19 patients experience a cytokine storm during infection,
which is caused by an overwhelming and excessive release of proinflammatory cytokines
(e.g. IL-2, IL-7, interferon-γ, TNF-α) [22]. Serum ferritin and IL-6 levels were found to be significantly elevated in samples
obtained from deceased individuals from this subgroup of patients [48]. This is the rationale behind specific anti-inflammatory treatments, for example,
the administration of interferon β-1b, the IL-1 blocker anakinra, the IL-6 receptor
blocker tocilizumab or corticosteroids. There are no evidence-based data for any of
the therapies mentioned here; analogously to the recommendations on the treatment
of septic shock, corticosteroids may be considered as a hydrocortisone therapy (200 mg/24 h)
in patients with high vasopressor doses.
Improved outcomes were reported in a case series of patients with septic shock and
high cytokine concentrations (e.g. an IL-6 of ≥ 1000 pg/ml) following the use of a
cytokine filter (Cytosorbents, Berlin, Germany) [49]. This requires an extracorporeal circulation (hemofiltration and/or ECMO) in which
the filter can be incorporated. Cytokine removal could be an interesting treatment
option for patients who meet the criteria. Antibiotic dosages may need to be adjusted
accordingly.
Core Statements
-
COVID-19 is a new viral disease that affects the respiratory system. The currently
available data suggest that around 20% of cases develop severe symptoms, and around
5% of all cases require intensive care. Mortality is between 1 and 2% of all persons
who develop the disease.
-
Adequate protection of medical staff is essential to prevent nosocomial infection.
Medical staff must therefore wear personal protective equipment consisting of an FFP2/FFP3
mask, safety goggles and a waterproof overall during all aerosol-generating procedures.
-
Intensive care treatment of patients with lung failure is based on established recommendations
for the treatment of patients with ARDS issued by the relevant professional societies.
The focus is on lung-protective ventilation, prone positioning, restrictive fluid
management and adequate management of other organ insufficiencies. Patients requiring
extracorporeal membrane oxygenation must be treated in centres experienced in providing
this type of organ support.
-
New and experimental treatment options are being discussed. However, based on the
currently available evidence, it is not yet possible to recommend any of these approaches.
In every case, an individual risk-benefit assessment is necessary prior to initiating
the off-label use of particular substances as serious side effects have been reported.
Information
This is a translation of “SARS CoV-2/COVID-19: Evidence-Based Recommendations on Diagnosis
and Therapy” published in: Anästhesiol Intensivmed Notfallmed Schmerzther 2020; 55:
257 – 265