In December 2019, the first patients presenting with a pneumonia of unknown origin were reported in the Wuhan province of the People’s Republic of China. Over the subsequent months, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has rapidly spread across the globe, resulting in the COVID-19 pandemic. As of 23 April 2020, there have been over 2.4 million confirmed cases worldwide in over 213 countries, areas or territories, resulting in 169 000 deaths.1
Early clinical experiences in China demonstrated the wide spectrum of SARS-CoV-2 severity: from asymptomatic infection or mild upper respiratory tract illness, to severe viral pneumonia with respiratory failure and death. Patients with severe pneumonia are often hospitalised and a small proportion of these patients require mechanical ventilation and critical care support.2
The typical presentation of COVID-19 relates to the pathophysiology of the SARS-CoV-2 infection. SARS-CoV-2 is principally spread by aerosol transmission and is taken up into airway epithelial cells, and therefore the disease primarily affects the lungs. Research into SARS-CoV-2 has shown that in early stages of infection, only ciliated cells in the conducting airways are infected. In the 80% of patients with mild disease, only these conducting airways are affected, however 20% of patients will develop severe disease when the virus infects alveolar type II cells.3 Viral replication in these cells results in direct pathological insult to the lung parenchyma by causing inflammation and apoptosis. This damage typically results in pneumonia but can also progress to an acute respiratory distress syndrome (ARDS), which may lead to life-threatening respiratory failure.
Viral replication throughout the body may lead to an excessive immune reaction or ‘cytokine storm’ due to haemophagocytic lymphohistiocytosis (HLH) in some patients.4 In most patients, there is an acute phase response which manifests as the systemic features of COVID-19, including fever, cytopenias and myalgias, and can result in multiple organ failure in a small proportion.
Like many infectious and inflammatory conditions, there are a myriad of clinical presentations resulting from SARS-CoV-2, hence many atypical features require a high level of clinical suspicion. This article discusses presentations of COVID-19 and presents some of the atypical presentations and mimic conditions to give an overview of the diagnostic nuances of this new virus.
Typical presentations of COVID-19
The case definition adopted by the UK has been developed using the typical presentation of COVID-19.5 This is defined as patients who have required hospital admission and meet one of three clinical criteria (figure 1).
This case definition aligns with data from China outlining the most common presenting features of COVID-19 (table 1).6 Usual symptoms at onset of illness were fever, cough, myalgia or fatigue; whereas less common symptoms were headache, vomiting and diarrhoea.
In patients with suspicious symptoms, confirmation of a COVID-19 diagnosis requires evidence of active SARS-CoV-2 infection. At present, laboratories require either an upper respiratory tract sample (nasopharyngeal and/or oropharyngeal swab) or a lower respiratory tract sample (sputum or tracheal aspirate) for testing. The presence of SARS-CoV-2 RNA is detected using reverse transcriptase PCR (RT-PCR). However, the performance of the biomolecular assay depends on both the stage of the disease and the site and operator accuracy of the sampling. When coupled with sampling errors, the overall sensitivity of the RT-PCR test is approximately 75%.7
Atypical presentations of COVID-19
Reports of atypical presentations of COVID-19 have been emerging as the SARS-CoV-2 pandemic has grown across the globe. Atypical presenting features refer to patients where the constitutional or respiratory symptoms are absent or minimal, and other non-respiratory symptoms or signs are early or predominant features.
COVID-19 in the elderly: including delirium
Studies have shown that the greatest risk factor for severe COVID-19 is increasing age, particularly patients with multimorbidity and/or higher frailty scores.3 8 9
Like many infections affecting elderly patients, COVID-19 can present as a non-specific decline. While most studies report elderly patients presenting with a fever and productive cough, this may be related to the case definition criteria being used to diagnose COVID-19. Elderly patients may in fact not develop the typical fever seen in SARS-CoV-2 infection due to a blunted response caused by immune senescence.10 ‘Silent hypoxaemia’, the phenomenon whereby patients develop hypoxaemia and respiratory failure without dyspnoea or respiratory distress, is another unusual presentation of COVID-19 that appears to particularly affect the elderly population.11 This is an especially worrying presentation as patients may feel well and therefore not present to hospital, and then subsequently precipitously deteriorate due to their hypoxaemia, thus leading to treatment delay and adverse outcomes.
Delirium—the clinical manifestation of encephalopathy—is an important feature in COVID-19. Elderly patients infected with SARS-CoV-2 may present with delirium or subsequently develop delirium during the illness. However, the development of delirium is not exclusive to geriatric patients and may be seen in any patient with severe infection, particularly those on critical care. Delirium in its hyperactive motor form presents significant additional challenges in the context of management of admitted patients with COVID-19, due to increased risk of transmission to other patients and possible reduction in staffing levels. The British Geriatric Society recommends increased screening of high-risk groups (including patients with COVID-19) using the 4 ‘A’s Test tool, and avoidance of common precipitants of delirium.12
Smell and taste dysfunction has been reported in 34%–59% of patients with COVID-19.13 Anosmia (lack of the sense of smell) was an early observation in the pandemic and can present with or without taste disturbance (dysgeusia). It commonly arises early in the disease process or in patients with mild or no constitutional symptoms.14 The British Association of Otorhinolaryngology is now recommending anosmia and dysgeusia are added to the primary screening symptoms for COVID-19.15
Other rhinological symptoms typically seen in other respiratory viruses, such as rhinorrhoea or nasal congestion, are often absent in patients with COVID-19.14 Coronaviruses are known to be neurotropic,16 17and therefore isolated anosmia suggests SARS-CoV-2 invades the nervous system via the olfactory system specifically.
Myocardial injury occurs early in SARS-CoV-2 infections, reflected in the rise of high-sensitivity troponin and natriuretic peptides, even in patients without known cardiovascular disease.18 However, it has been noted the pattern of rise of high-sensitivity troponin follows with other inflammatory markers (such as D-dimer, ferritin, lactate dehydrogenase), therefore this may be due to a ‘cytokine storm’ or secondary HLH, rather than organic myocardial injury from the virus.19 A report produced by the National Health Commission of China shows that some patients with COVID-19 present with chest tightness and palpitations without fever and cough.18 This suggests the possibility of viral myocarditis or stress cardiomyopathy caused by the virus. Inflammation in the vascular system caused by SARS-CoV-2 can result in diffuse microangiopathy with microthrombosis. Likewise, inflammation in the myocardium can result in myocarditis, heart failure, cardiac arrhythmias, acute coronary syndrome, rapid deterioration and sudden death.20 Case reports from China showed mimics of ST-elevation myocardial infarctions without coronary obstruction in patients who are SARS-CoV-2 positive, with normalisation of ejection fraction and troponins as the patient recovered from COVID-19.21
Distinguishing the cause of these cardiac presentations as being due to SARS-CoV-2 or organic cardiovascular disease is difficult. Indeed, it is likely that SARS-CoV-2 both induces new cardiac pathologies and may exacerbate underlying cardiovascular diseases,22 in some cases leading to orthostatic hypotension and syncope.23
It remains imperative that appropriate treatment for heart failure, arrhythmias, acute coronary syndrome and thrombosis must be initiated regardless of the aetiology. However, clinicians should be aware of SARS-CoV-2 infection as a possible cause and investigate accordingly.
Gastrointestinal and hepatic features
Nausea and vomiting occur in approximately 5% of patients with COVID-19 and diarrhoea occurs in approximately 4%.6 In early case series, including the first case of COVID-19 in the USA,24 gastrointestinal symptoms often predated any respiratory symptoms and, in some cases, have been the predominant feature of the illness.25 SARS-CoV-2 RNA has been isolated on anal swabs of patients with COVID-19, even after the virus has been cleared from the respiratory tract.26 This suggests that SARS-CoV-2 can replicate and cause symptoms in the gastrointestinal tract.
SARS-CoV-2 may cause liver injury, thus elevating liver aminotransferase enzyme levels in 16%–53% of patients with COVID-19.6 27–31 However, these results are usually discovered as a coexistent feature in more severe disease and not as the presenting feature.32 There are many potential causes for elevated aminotransferase levels including hypoxic hepatitis from respiratory compromise or drug-induced liver injury from current some of the COVID-19 treatments. Collateral liver damage may be caused by virally induced cytotoxic T cells, and the induction of a dysregulated innate immune response by the virus, explaining the association between deranged liver markers and COVID-19 severity.33 Therefore, clinicians should focus on treatment of the virus as this will improve the hepatic picture.
Preliminary studies report that approximately 40% of patients with COVID-19 develop neurological symptoms: including headache, impaired consciousness and acute cerebrovascular disease.34 SARS-CoV-2 has neurotropic properties and has been found in cerebrospinal fluid (CSF) and brain tissue on autopsy.35
There is an increased risk of development of cerebrovascular events in patients with COVID-19.34 COVID-19 infection results in cytokine storm syndrome, which alongside coagulation dysfunction (resulting in abnormal D-dimer and platelet levels), increases the risk of cerebrobasilar disease.36 Therefore, patients at an increased risk of cerebrovascular disease should be informed of their risk from SARS-CoV-2 and monitored during a COVID-19 infection.
Viruses are a well-recognised cause of encephalitis, hence raising the possibility that SARS-CoV-2 can induce encephalitis in patients with COVID-19. Case reports from Wuhan describe classical signs of encephalitis in context of a typical COVID-19 presentation, without any evidence of other bacterial or viral infection.37 However, there may be difficulty in diagnosing SARS-CoV-2-induced encephalitis due to the dissemination of the virus throughout the CSF resulting in a low CSF viral titre. There have also been reports of acute haemorrhagic necrotising encephalopathy induced by the SARS-CoV-2 virus.38 Clinicians should be aware of patients who are SARS-CoV-2 positive who present with focal neurological signs and be prepared to treat as viral encephalitis.
There are several reports of Guillain-Barré syndrome (GBS) associated with SARS-CoV-2 infection from both China and Italy.39 40 The onset of symptoms was 5–10 days after onset of viral symptoms, which is a time period similar to other infections which cause GBS.41 Clinicians should be aware of the possibility of GBS caused by SARS-CoV-2 infection and give appropriate treatment.
Coincidental finding of infection
Due to the incubation period and nosocomial spread of the virus, COVID-19 must be considered as a potential causative agent in new diagnoses of hospital-acquired pneumonia during this pandemic. Patients admitted to hospital for other causes may become positive for SARS-CoV-2 infection during their stay, and therefore all patients must be regularly monitored for development of symptoms.
During the early phases of the pandemic, incidental findings of typical COVID-19 infection were found in imaging studies undertaken for other indications. For example, positron emission tomography-CT undertaken for standard oncological indications in a high prevalence region of Italy found a high number of incidental interstitial pneumonias consistent with COVID-19.42 Similar findings of incidental pneumonic changes consistent with COVID-19 were found in our own centre with trauma CT series undertaken for road traffic accidents and other injuries in previously asymptomatic patients.
Due to the rapid case transmission within the pandemic setting, any new cases of acute-onset respiratory illness may be treated as COVID-19 as default. Given the 75% sensitivity of RT-PCR detection and therefore presence of false negatives,7 in our hospital we adopted an edict that ‘if it looks like COVID-19, it probably is COVID-19, so treat it as COVID-19’. This approach was adopted primarily to protect staff and allow for appropriate isolation precautions to be adopted in all suspected patients. However, as we continue into the later stages of the pandemic, this approach may lead to availability bias and thus misdiagnosis of COVID-19 in patients without the virus.
Availability bias is the tendency to judge diagnoses as more or less likely depending on how easily they come to mind, which is often influenced by recent patients seen.43 44 In the context of the COVID-19 pandemic, patients fitting the typical case presentation but without a SARS-CoV-2 infection may be misdiagnosed due to this availability bias. This may lead to delayed treatment of the true aetiology, and thus an increased risk of adverse outcomes. Throughout this pandemic situation and despite the varied presentations of COVID-19, it is important that availability bias does not blind clinicians and lead to diagnostic oversight of other non-COVID-19 conditions during this time.
Potential issues related to this diagnostic uncertainty include: misdiagnosis of exacerbations of asthma and chronic obstructive pulmonary disease and delay in treatment with oral prednisolone; community-acquired pneumonia not caused by SARS-CoV-2 being misdiagnosed and patient subsequently placed on a ‘positive’ ward; misdiagnosis of dyspnoea caused by pulmonary oedema secondary to heart failure and delay in diuretic treatment. Therefore, it is imperative that clinicians do not ignore their normal diagnostic processes and continue to consider a variety of differential diagnosis during this pandemic.
Case vignette from our hospital
A 54-year-old man was admitted with a 2-week history of dyspnoea, followed by a 4-day history of myalgia, lethargy and an intermittent fever. The patient had a history of diabetes and asthma, and was a regular cigarette smoker. On examination he had a temperature (T) of 37°C, blood pressure (BP) of 125/90mm Hg, heart rate of 109 beats per minute, respiratory rate (RR) of 29 breaths per minute and O2 saturations of 95% on air. On respiratory examination, there were bibasal crackles. The patient was admitted with an impression of COVID-19 infection and associated hypoxia. A chest X-ray was ordered and reported subtle multifocal air space opacification that was non-specific but could be consistent with viral pneumonitis. Importantly, he tested negative for SARS-CoV-2 on RT-PCR. The patient became unwell overnight, and was diagnosed with sepsis. A blood culture was obtained, and the patient started on intravenous amoxicillin. The following day, the patient’s condition remained unchanged. SARS-CoV-2 RT-PCR testing was repeated and again was reported as negative. The patient underwent a chest CT scan that reported diffuse ground glass opacity affecting all lobes, with relative sparing of the peripheral parenchyma. The radiologist reported that these appearances were mostly in keeping with pneumocystis pneumonia (PCP) infection. Due to the possible diagnosis of PCP, the patient was tested for HIV infection. This returned as positive for HIV, with a viral load of 92742 c/mL and a CD4 count of 26 x10ˆ6/L. His blood sample tested positive for PCP PCR.
PCP is caused by Pneumocystis jirovecii, and results in a progressive dyspnoea mainly in immunocompromised individuals. In a mild presentation, patients report exertional dyspnoea. Typically, symptoms gradually worsen over time. In severe cases, patients may develop severe hypoxaemia and ARDS with a fatal outcome. PCP is an AIDS-defining illness, thus infected patients must be tested for HIV.
Differential diagnoses and mimic conditions
As seen in the case vignette above, early symptoms of COVID-19 such as fever, cough and dyspnoea are non-specific and thus can be associated with a variety of different conditions. Any acute viral infection will present in a similar way, which may result in diagnostic uncertainty. A differential diagnosis should include the possibility of a wide range of infectious and non-infectious disorders (figure 2).
During this pandemic period, the majority of patients who present with symptoms fitting the case definition will be treated as suspected COVID-19. Therefore, it is important that rapid antigen detection for SARS-CoV-2 is performed, alongside other investigations to rule out common respiratory pathogens and non-infectious conditions.45
It is also important to remember that despite the high case load of COVID-19 in hospitals, at a similar time in previous years there will have been admissions with similar presentations, caused by other respiratory viruses, for example, influenza A/B.46 Presentation with these viruses will continue throughout this pandemic and clinicians must continue to correctly diagnose and treat these patients. Current guidance suggests that for hospitalised patients with an acute respiratory infection, there is no need to screen for influenza at the same time as SARS-CoV-2 testing. However, influenza testing should be considered where SARS-CoV-2 is negative, in severe infections and immunocompromised patients and in other cases where it is relevant for clinical management.
Infection with SARS-CoV-2 can lead to sepsis.3 However, in patients with sepsis, consideration of other causes should not be forgotten. Pancultures (urine, sputum, blood) are essential in all patients with possible sepsis to rule out bacterial causes of sepsis. The Quick Sequential Organ Failure Assessment Score identifies patients with a possible sepsis diagnosis using three criteria:47
Low BP (systolic BP ≤100 mm Hg).
High RR (≥22 breaths per minute).
Altered mentation (Glasgow Coma Scale <15).
Many patients with moderate to severe COVID-19 will meet at least two of these criteria, thus making the diagnosis of possible sepsis relatively easy. The real challenge is distinguishing COVID-19 viral sepsis from other cases of sepsis, which is often impossible in the early stages.
There is growing interest in the possible role of procalcitonin in distinguishing between viral and bacterial infections. Procalcitonin is a component of the innate proinflammatory response, which has been shown to be able to differentiate between bacterial infection and other abacterial inflammatory processes.48 However, evidence on the relevance of its role is mixed. Some studies suggest procalcitonin levels are lower in viral than bacterial infections.49 However, in a recent meta-analysis of 12 studies in 2408 patients with community-acquired pneumonia of known aetiology, the sensitivity and specificity of serum procalcitonin to differentiate between bacterial and non-bacterial pneumonia were both 55%.50 This suggests that a procalcitonin level alone is unlikely to provide enough evidence to differentiate between a viral and a bacterial infection. Current guidance by the Infectious Diseases Society of America does not recommend using procalcitonin as part of clinical judgement.51
Signs and symptoms commonly seen in sepsis can also be seen in non-infectious diseases, known as infectious mimicry. The cytokine storm seen in SARS-CoV-2 infection is due to HLH. Interestingly, a wide variety of non-infectious causes can also lead to HLH, including rheumatological and neoplastic causes.5 This infectious mimicry means that the infectious workup usually performed in sepsis does not always reveal the primary disease process. Therefore, clinicians should be aware of possible non-infectious mimics of COVID-19.
Secondary bacterial infection
To add to the difficulty of distinguishing sepsis due to a viral cause from other causes, coexistent infections are not uncommon. SARS-CoV-2 infection is known to cause a dysregulated immune response, with lymphopenia being a common feature, indicating a probable immune suppression stage.52 Therefore, in a manner similar to other respiratory viral infections, patients with COVID-19 are at high risk of developing secondary bacterial infections. These secondary infections must be identified and appropriately managed.
The prospect of another condition appearing alongside COVID-19 has been described as a ‘medical chameleon’, defined as when a condition is overlooked as it blends in with background disease.53 The background disease in this instance is COVID-19. For example, if a patient who was known positive for SARS-COV-2 infection developed sepsis, it would be understandable if the medical team attributed the cause to the virus and did not investigate further. However, if the patient had an undiagnosed coexistent bacterial infection contributing to their sepsis, the opportunity to treat with antibiotics would have been missed. Clearly this would lead to deterioration and an increased risk of adverse events.
Clinicians collect, process and interpret patient information to form a diagnosis and develop a management plan. The dual-process model of clinical reasoning was hypothesised by Dr Pat Croskerry, and outlines the processes by which clinicians reach a diagnosis. This model has been adapted to fit a diagnosis of COVID-19 for this article (figure 3).54
When analysing all available information from a patient, clinicians use pattern processing; they may or may not recognise the disease pattern. If recognised, type 1 (intuitive) processes rapidly lead to a provisional diagnosis. However, if the pattern is not recognised, type 2 (rational or analytical) processes are used. This involves slower, deliberate hypothesis based on deductive clinical reasoning to form a diagnosis.
In COVID-19, a typical pattern of fever, cough and myalgia would fit the case definition and many clinicians would immediately form the provisional diagnosis of a SARS-CoV-2 infection via type 1 thought processes. However, the atypical presentations discussed in this article would result in a type 2 thought process, in order to distinguish between an atypical presentation of COVID-19 or a completely separate disease by full consideration of history, examination and investigation results.
As discussed, many conditions may mimic COVID-19 and therefore diagnostic errors could be made if clinicians rely fully on the immediate type 1 processes of pattern recognition. Dysrationalia over-ride is a switch from type 1 to type 2 thinking, when a presentation results in deliberation as to whether this is truly COVID-19 or another mimic disease. Executive over-ride occurs when type 2 analysis leads to consideration of whether this may be an atypical presentation of COVID-19. Over time, repetition of atypical presentations (such as anosmia) may lead to pattern recognition and switching from a type 2 to a type 1 process and rapid diagnosis of COVID-19 infection.
While SARS-CoV-2 is likely to remain on the differential diagnostic list for a plethora of presentations for the foreseeable future, clinicians should be cautious of ignoring other potential diagnoses. An awareness of atypical presentations allows SARS-CoV-2 to be a differential so that it can be appropriately investigated. A knowledge of infectious mimics prevents COVID-19 from overshadowing other diagnoses, hence preventing delayed diagnosis or even misdiagnosis and consequent adverse outcomes for patients.
In the postpandemic period, it is important to remember that a patient presenting with apparent COVID-19 infection may or may not have COVID-19. Clinicians must continue to investigate fully and treat appropriately, as making assumptions can significantly hinder patient outcomes.
COVID-19 presents to acute care as a viral pneumonia, and is easily identified by pattern recognition of the typical respiratory symptoms.
A number of atypical presentations affecting a variety of organ systems have become apparent, including anosmia, diarrhoea and neurological features.
Diagnostic reasoning using intuitive processes can rapidly identify typical COVID-19 cases in a pandemic situation, but alternative cognitive processes are required to consider other COVID-19 mimic diagnoses.
Current research questions
How are the usual diagnostic reasoning processes affected during a pandemic situation such as COVID-19?
To what extent is the diagnosis of COVID-19 missed as a result of atypical presentations?
What impact does the treatment delay or omission in patients misdiagnosed with COVID-19 have on morbidity and mortality of the true diagnosis?
What is already known on the subject
Many disease processes have both atypical features and mimics that complicate diagnosis
Clinicians use Type 1 and Type 2 processes for diagnostic reasoning
COVID-19 is an emerging viral infection caused by SARS-CoV-2 that has a wide range of presentations