Should be ordered in all patients with suspected Ebola infection while the patient is in isolation.
Returns result 24 to 48 hours before ELISA testing.
Several different commercial PCR kits are available with varying sensitivity, specificity, and limits of detection.
In Western settings, the test may only be available in regional or national laboratories that have category 4 facilities. In epidemic settings and some countries, category 4 laboratories are set up locally and results are available 4 hours after the sample has arrived.
Viral RNA can be detected in the patient’s blood by RT-PCR from day 3 up to days 6 to 17 of symptom onset. A positive PCR result implies that the patient is potentially infective, particularly if he or she has active diarrhoea, vomiting, or bleeding.
If negative, the test should be repeated within 48 hours since viral load is low and can be undetectable early in the course of the illness. Negative tests should be repeated to rule out a diagnosis if it is strongly suspected (or confirm resolution of infection).
positive for Ebola virus RNA
Giemsa-stained thick and thin blood smears and rapid diagnostic tests are the tests of choice for malaria screening.
A negative result makes Ebola virus infection more likely in the appropriate epidemiological context; however, co-infection with malaria was seen in up to 5% of patients in West Africa during the 2014 outbreak, so the possibility of dual infection should be considered in all patients.
negative (may be positive if dual infection)
Important test to order (if available) in areas where other investigations are limited.
May indicate acute kidney injury.
Especially useful in patients with diarrhoea and vomiting.
Hypokalaemia or hyperkalaemia, due to vomiting and diarrhoea or acute kidney injury, was seen in approximately 33% of cases in the 2014 outbreak.
Hypocalcaemia has been associated with fatal infection.
Useful to guide correction of electrolytes and fluid replacement.
may be abnormal
Important test to order (if available) in areas where other investigations are limited.
Elevated lactate is a marker of tissue hypoperfusion and is an indicator of shock. It is useful in acutely ill patients with signs of sepsis to identify the degree of systemic hypoperfusion and to guide fluid resuscitation.
Elevated lactate was one indicator of gram-negative sepsis at day 15 in a patient treated in Germany.
Arterial or venous blood pH and bicarbonate are useful in acutely ill patients with signs of sepsis to identify the degree of systemic hypoperfusion and guide fluid resuscitation.
Decrease in platelet count and marked lymphopenia can be seen in the initial stages of infection; however, this is not diagnostic. Often followed by neutrophil leukocytosis in the later stages of patients who eventually recover, along with normalisation of thrombocytopenia. Leukocytosis may persist and show immature forms.
Patients with severe disease may show a progressive decline in platelet count as a manifestation of disseminated intravascular coagulation (DIC).
thrombocytopenia, marked lymphopenia; decreased haemoglobin (if bleeding manifestations)
Prolonged prothrombin time (PT) or activated partial thromboplastin time (aPTT) is associated with more severe infection and bleeding manifestations such as DIC.
Patients with fatal infection have been found to have D-dimer levels four-fold higher on days 6 to 8 of infection compared with patients who survive.
prolonged PT or aPTT, elevated D-dimer level (if bleeding manifestations)
Haematuria or proteinuria may be seen in severe disease.
Oliguria that does not respond to fluid resuscitation is a poor prognostic sign.
may show haematuria or proteinuria
Both ALT and AST are usually elevated; however, most studies show that AST rises out of proportion to ALT, and this is more suggestive of systemic tissue damage rather than hepatocellular injury.
Bilirubin, GGT, and ALP are often slightly elevated. Highly elevated ALT and severe jaundice suggests an alternative diagnosis (e.g., viral hepatitis).
high AST:ALT ratio; bilirubin, GGT, and ALP may be slightly elevated
Elevated levels have been reported in several studies and indicates the presence of pancreatitis, an indicator of severe infection.
may be elevated
Negative blood cultures are helpful as they rule out other non-viral infectious causes (e.g., sepsis, enteric fever).
Gram-negative bacteraemia, presumably from gut translocation, has been identified as a complication of the disease course in two patients. However, a study in Sierra Leone where blood cultures were taken from patients on admission to an Ebola treatment centre found that only one of the 22 cultures was positive with a presumed contaminant.
Therefore, blood should be collected for culture at baseline and/or at the time of the onset of gastrointestinal symptoms or other clinical deterioration.
Useful diagnostic test with high specificity; however, it is not universally available. Can be used to confirm the diagnosis along with a positive RT-PCR result.
Most likely to give a positive result from day 3 until day 6 of infection, and can give widely variable results from days 7 to 16.
positive for Ebola virus antibodies
Useful in later stages of the infection.
IgM antibodies can appear in serum as early as day 2 post infection, but can give variable results up to day 9. They become negative between 30 and 168 days after symptom onset. IgG response develops between day 6 and 18 and can persist for several years.
A positive IgM or a rising IgG titre is strong evidence for recent Ebola virus infection.
Useful in patients with respiratory symptoms.
Pulmonary infiltrates are not typical of infection and suggest an alternative (or comorbid) diagnosis.
May be difficult to arrange in an isolation unit and should only be ordered judiciously to avoid contamination.
Rapid PCR testing for Ebola virus infection remains a major hurdle for effective, targeted isolation of affected patients. Current tests take an average of 4 hours to perform with a fully equipped laboratory close at hand, but results may take several days to arrive in remote areas. This means that, until they are confirmed negative, patients with febrile illnesses other than Ebola virus infection are confined to isolation and often unwittingly exposed to the virus.
Rapid bedside tests can therefore make a very significant contribution to infection control in treatment centres.
Several different technologies are being evaluated by WHO for use in field conditions. These include numerous RT-PCR-based assays that have been made simpler to use with a shorter turnaround time of <1 hour. The WHO has listed ReEBOV™ Antigen Rapid Test Kit for potential use; however, it currently only recommends its use in special situations. World Health Organization (WHO): interim guidance on the use of rapid Ebola antigen detection tests external link opens in a new window
The alternatives are ELISA-based antigen-detection assays that could be quicker and simpler with the possible advantage of only needing a drop of blood. Their major disadvantage is a reduced sensitivity, particularly in the initial stages of illness.
A GeneXpert® diagnostic tool (Xpert® Ebola) has been trialled in the field, and is an automated cartridge-based system that requires minimal laboratory skill. An inactivated sample is placed into a single-use cartridge, which is then entered into the enclosed machine. Sample preparation, nucleic acid amplification and detection, and production of a result are automated processes minimising staff training requirements, risk of infection, and cross contamination.This test was used in the field during the 2018 outbreak in the Democratic Republic of the Congo.
The US Food and Drug Administration has approved a rapid, single-use test for the detection of Zaire ebolavirus. It is the second rapid antigen fingerstick test available under an emergency use authorisation, but is the first that uses a portable battery-operated reader which can provide results outside of laboratories.It has also approved the single-use OraQuick® Ebola Rapid Antigen Test to detect Ebola virus antigens in human blood from certain living individuals, as well as samples from certain recently deceased individuals suspected to have died from Ebola (cadaveric oral fluid). It is the first rapid diagnostic test to be marketed in the US, and provides a rapid, presumptive diagnosis that must be later confirmed.
This is a rapidly evolving field and different kits are approved according to the country and settings in which they are to be deployed. WHO and Food and Drug Administration (FDA) recommendations are available: World Health Organization (WHO): Ebola vaccines, therapies, and diagnostics external link opens in a new window Food and Drug Administration (FDA): 2014 Ebola virus emergency use authorizations external link opens in a new window
positive for Ebola virus
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