Almost all States/UTs of the country are affected by COVID-19. Given the seasonal pattern of epidemic prone diseases observed every year in our country, it diseases like Dengue, Malaria, Seasonal Influenza, Leptospirosis, Chikungunya, Enteric fever, etc. can not only present as a diagnostic dilemma but may co-exist in COVID cases. This poses challenges in clinical and laboratory diagnosis of COVID , and have a bearing on clinical management and patient outcomes.
The scope of this document is to provide clear guidelines on prevention and treatment of co-infections of COVID with diseases like Dengue, Malaria, Seasonal Influenza (H1N1), Leptospirosis, Chikungunya etc.
As per the World Health Organization (WHO) case definition, a COVID case may present with:
This case definition, although sensitive, is not very specific. Seasonal epidemic prone diseases, as cited in the foregoing paragraphs may all present as febrile illness, with symptoms that mimic COVID-19. If there is a co-infection, then apart from the febrile illness there may be constellation of signs and symptoms that may lead to difficulty in diagnosis. A comparative analysis of disease onset, symptoms, signs, warning signs, complications and diagnosis is given at Annexure.
A high index of suspicion must be maintained for epidemic prone diseases (e.g. Dengue, Malaria, Chikungunya, Seasonal influenza, Leptospirosis) prevalent in a particular geographic region during monsoon and post-monsoon seasons. Bacterial co-infections must also be suspected in moderate or severe cases of COVID-19 not responding to treatment.
Despite the possibility of above mentioned co-infections, in present times of the pandemic, approach to diagnosis for COVID-19 essentially remains the same. Testing protocol as per MoHFW/ICMR guidelines will be followed. However, in addition, further tests for a likely co-infection will also be undertaken, whenever suspected.
While each of these infections are antigenically distinct with specific serological responses, yet in the eventuality of co-infections, cross-reactions (resulting in false-positive /false negative results) cannot be totally ruled out, especially if the testing kits used are not having requisite sensitivity and specificity. Hence the tests recommended by ICMR (for COVID-19) and that recommended by the concerned programme divisions (NVBDCP for vector borne diseases [Malaria, Dengue, Chikungunya]) and NCDC (Seasonal Influenza, Leptospirosis, Scrub Typhus)] needs to be followed. Availability of rapid diagnostic kits for malaria, dengue, scrub typhus should be ensured in such
COVID treatment facilities.
The table below summarizes the various (confirmatory) test to be undertaken for possible coinfections.
Laboratory Testing: Co-infection of COVID 19 with other seasonal epidemic prone diseases
Diseases | Tests | Sample |
Dengue | NS1 antigen ELISA or RT PCR: For < 5 days of illness IgM capture ELISA (MAC-ELISA): For >5 days of illness | Blood/Serum |
Chikungunya | Early disease: RT PCR After first week of illness: IgM capture ELISA |
Blood/Serum |
HINI | Acute Phase: RT PCR | Naso/Oropharyngeal swab |
COVID 19 | Acute phase: RT PCR | Nasopharyngeal/Oropharyngeal swab |
Malaria |
RDT (bi-valent both Pf/Pv detection) Quality microscopy for slide positivity confirmation |
Blood Blood |
Leptospirosis | In endemic areas: IgM ELISA and MAT tests Non-endemic areas: IgM ELISA followed by MAT test for confirmation | |
Scrub Typhus |
Detection of IgM antibodies by Weil-Felix Test (WFT) Enzyme linked Immunosorbent assay (ELISA) |
Serum Serum |
Bacterial co-infections | Gram stain and culture, Blood culture | Sputum/Bronchial aspirate/Blood |
Management of co-infection of COVID-19 with dengue, Influenza and bacterial co-infections may however be challenging and are dealt with in greater detail here.
Pathogenesis
Dengue Fever and COVID-19 share many pathogenic and clinical features which might make it very difficult to differentiate the two infections (1). The phenomenon of ADE (Antibody Dependent Enhancement) has been described for both dengue virus as well as for SARS-CoV-2 virus resulting in escalation in degree of infection and number of complications. Both being RNA viruses they share certain common features in pathogenesis, eventually leading to subsequent cytokines and chemokine release and also affecting the integrity of the vascular endothelium leading to vasculopathy, coagulopathy and capillary leak. Various mechanisms can explain the signs and symptoms observed in co-infected patients but most will have the following,
Clinical Features
The clinical features of both the infections are overlapping, both present as acute febrile illness of short duration and may have thrombocytopenia and shortness of breath, although respiratory symptoms are more common in COVID-19 and bleeding manifestations more common in Dengue. Routine testing for both diseases shows leucopenia or normal leucocyte count. Decrease in platelet count which is a defining feature of dengue infection but can also be seen in significant number of covid cases. There are reports in literature, where dengue serology was positive initially and later on, it was found that cases were positive by RT-PCR for COVID-19 thereby suggesting that dengue serology can be falsely positive in COVID-19 patients. Therefore, there is a need to rely on more specific tests for each disease like throat swab RT-PCR for COVID-19 and ELISA based Dengue NS1 Antigen or serology test for dengue diagnosis. Serum sample for NS1 antigen within first 5 day of onset of fever were negative in above study suggesting that positive dengue serology was more likely to be false positive result and not co-infection. Hence, one needs to be careful while making diagnosis of co-infection.
There are now enough evidences to support that severe dengue is associated with cytokine storm and high levels of various circulating cytokine are associated with poor outcome in most cases. COVID19 infects alveolar epithelial cells leading to pneumonia and ARDS, it also infects monocytes/macrophages leading to cytokine storm associated with multi organ failure and death. This cytokine storm seen in severe cases has led to increased use of steroids and other immunosuppressive therapy in moderate to severe cases.
Both COVID-19 and Dengue infection are accompanied by coagulopathy and vasculopathy with coagulopathy being predominant in formal leading to widespread use of Low Molecular Weight Heparin (LMWH). There have been numerous evidences to suggest the increased burden of thrombosis in COVID-19 based on which recommendations have been made for the use of LMWH in moderate to severe cases. But in the presence of Dengue co-infection which is usually accompanied by thrombocytopenia and increased risk of bleeding , the use of LMWH becomes a challenging issue. Similarly, because of increased capillary leak and increased third space fluid loss, fluid administration which forms the cornerstone in management of dengue might not be recommended with clarity as conservative fluid administration has been recommended for COVID-19 in absence of shock.
Clinical management consideration for Dengue and COVID-19 co-infection
Following are some general measures to followed in case of Dengue and COVID-19 co-infection:
These measures will help to prevent the progression of illness to severe dengue and deaths, which in turn will also help to reduce the number of patients that need to be referred to hospitals, thus avoiding saturation of these facilities as well as the intensive care units.
Specific therapeutic considerations
Points related with specific therapeutic options and their use in cases with co-infection:
Co-infection with SARS-CoV-2 and other respiratory viruses has been described in a number of studies. Most prominent among these are Respiratory Syncytial Virus, Enteroviruses and Influenza A virus. With the approaching winter season, the seasonal Influenza cases may show an upward trend, and there could be cases of coinfection with COVID-19.
Pathogenesis
COVID-19 and Influenza share many pathogenic feature. Both diseases involve the respiratory system, manifesting widely from ILI to SARI. Both diseases cause pneumonitis. The histopathological manifestation of Interstitial inflammation and diffuse alveolar damage and intraalveolar edema followed by fibrin deposition, hyaline membrane, and leukocyte infiltration of the alveolar septa are seen in both COVID and Influenza. The radiological appearance is not of much help either as both diseases may have presence of opacities or consolidations.
Both being RNA viruses they share certain common features in pathogenesis, eventually leading to subsequent cytokine release and acute respiratory distress syndrome.
Diagnosis
Whenever suspected, especially in areas reporting seasonal Influenza cases, samples should also be sent and tested for SARS-CoV-2 and Influenza.
Clinical Features
The clinical features of both the infections are overlapping, both present as acute febrile illness of short duration and may have fever, cough and shortness of breath. Similarly, laboratory investigations are also not very helpful in differentiating between the two, both show leucopenia or normal leucocyte count. Co-infection should be ruled out when suspected with proper diagnostic method at the early stage to initiate proper specific management to reduce morbidity and mortality.
Specific therapeutic considerations
Points related with specific therapeutic options and their use in cases with co-infection:
Evidence shows that small proportion of COVID-19 patients may have coinfection with bacteria. Patients with community-acquired co-infections and hospital-acquired superinfections had worse outcomes. A recent systemic review on co-infections in people with COVID-19 has found that the commonly associated pathogens in such cases are Mycoplasma pnuemoniae, Psuedomonas aeroginosa, Hemophilus influenzae, Klebsiella pneumoniae etc. The occurrence of healthcare associated infections like hospital acquired pneumonia (particularly in ICU settings), urinary tract infection, skin/soft tissue infection, abdominal infections, etc.) need to be considered.
Antibiotics should not be prescribed routinely unless there is clinical suspicion of a bacterial infection. Consider empiric antibiotic therapy as per local antibiogram. For COVID-19 patients with severe disease, also collect blood cultures, ideally prior to initiation of antimicrobial therapy.
Pathogenesis
Malaria is a potentially life-threatening parasitic disease caused by a protozoan having four types: Plasmodium vivax (P. vivax), Plasmodium falciparum (P. falciparum), Plasmodium malariae (P. malariae) and Plasmodium ovale (P. ovale). It is transmitted by the infective bite of Anopheles female mosquito. Man develops disease after 10 to 14 days of being bitten by an infective mosquito. Two types of parasites of human malaria, Plasmodium vivax (Pv), P. falciparum (Pf), are commonly reported from India. Inside the human host, the parasite undergoes a series of changes as part of its complex life cycle. The parasite completes life cycle in liver cells (pre-erythrocytic schizogony) and red blood cells (erythrocytic schizogony).
Infection with P. falciparum is the deadliest form of malaria.
Diagnosis
Diagnosis of malaria may be made by the use of RDT (bivalent) or microscopic examination of the blood smear. Early diagnosis and prompt initiation of treatment, as per national guidelines, is the key in preventing the progression of uncomplicated malaria to severe forms which can be fatal. In the current scenario, in endemic areas, all fever cases should be tested for malaria using RDT kits.
Clinical Features
Typically, malaria produces fever, headache, vomiting and other flu-like symptoms. The parasite infects and destroys red blood cells resulting in easy fatigue ability due to anemia, fits/convulsions and loss of consciousness. Parasites are carried by blood to the brain (cerebral malaria) and to other vital organs. Malaria in pregnancy poses a substantial risk to the mother, the fetus and the newborn infant. Pregnant women are less capable of coping with and clearing malaria infections, adversely affecting the unborn fetus.
Specific therapeutic considerations
Prompt malaria case management is very important for preventing serious cases and death due to malaria.
Plasmodium vivax (Pv) cases should be treated with Chloroquine for three days (25 mg/kg body weight divided over three days i.e. 10 mg/kg on day 1, 10 mg/kg on day 2 and 5 mg/kg on day 3) and Primaquine (0.25 mg/kg body weight daily for 14 days). Primaquine is used to prevent relapse but is contraindicated in pregnant women, infants and individuals with G6PD deficiency.
Plasmodium falciparum (Pf) cases should be treated with ACT (Artesunate 3 days + SulphadoxinePyrimethamine 1 day) @ Artesunate 4 mg/kg body weight daily for 3 days plus Sulfadoxine (25 mg/kg body weight) and Pyrimethamine (1.25 mg/kg body weight) on day 1. This is to be accompanied by single dose of Primaquine (0.75 mg/kg body weight) preferably on day 2. However, considering the reports of resistance to partner drug SP In North-Eastern States, the Technical Advisory Committee has recommended to use the co-formulated tablet of Artemether-Lumefantrine (ACT-AL) in North-Eastern States (Not recommended during the first trimester of pregnancy and in children weighing <5 kg).
For details of treatment of uncomplicated and complicated malaria in certain endemic areas, special population groups (pregnancy, children etc.) All healthcare providers should also follow the NVBDCP National Guidelines for treatment of malaria
Pathogenesis
Leptospirosis is primarily a contagious disease of animals, occasionally infects humans caused by pathogenic spirochete of the genus leptospira. Urinary shedding of organisms from infected animals (reservoir and carrier hosts like rodents, cattle, etc.) is the most important source of these bacterial pathogens. Contact with the organism via infected urine or urine-contaminated media results in human infection.
The most consistent pathologic finding in leptospirosis is vasculitis of capillaries, manifested by endothelial edema, necrosis, and lymphocytic infiltration. Capillary vasculitis is found in every affected organ system.
Diagnosis
The definitive diagnosis of leptospirosis depends on sero-conversion or four fold rise in antibody titer or isolation of leptospires from clinical specimen. Positive serology, preferably Microscopic Agglutination Test (MAT), using a range of Leptospira strains for antigens that should be representative of local strains.
Isolation (and typing) from blood or other clinical materials through culture of pathogenic leptospires. Culture and isolation can be very difficult requiring special media and longer incubation.
Clinical Features
Leptospirosis has a varied clinical manifestation. Like COVID, the severity of illness ranges from asymptomatic, mild self-limiting febrile illness to fulminant fatal disease. The disease typically presents as one of the following clinical categories.
Clinical illness lasts for a few days to 3 weeks or longer. Generally, there are two phases in the illness. The early phase illness is characterized by abrupt onset of high fever, myalgia (calves and lumbar region) and headache (retro-orbital/frontal). Other early phase manifestations include nausea, vomiting, abdominal pain, diarrhoea, cough and conjunctival suffusion (a pathognomonic finding of leptospirosis). Late phase illness occurs, 4-9 days after onset of symptoms, and is characterized by prolonged fever and systemic complications such as jaundice, renal failure, bleeding, respiratory failure etc.
Specific therapeutic considerations
All clinically suspected leptospirosis patients in Leptospira endemic area during rainy season should be given presumptive treatment of leptospirosis i.e. Tab. Doxycycline 100 mg twice daily for 7 days.
Note: In children less than 6 years 30 to 50 mg/kg/day of Cap. Amoxycillin/Cap. Ampicillin should be given in divided doses 6 hourly for 7 days.
Diagnosis and clinical management of leptospirosis in community setting should be in accordance with National guidelines for prevention and control of leptospirosis
Pathogenesis
Scrub typhus is transmitted by the mite Leptotrombidium deliense. The vector mites inhabit sharply demarcated areas in the soil where the microecosystem is favourable (mite islands). Human beings are infected when they trespass into these mite islands and are bitten by the mite larvae (chiggers).
Scrub Typhus causes perivasculitis of the small blood vessels. O tsutsugamushi stimulates phagocytosis by the immune cells, and then escapes the phagosome. Scrub typhus may disseminate into multiple organs through endothelial cells and macrophages, resulting in the development of fatal complications.
Diagnosis
Scrub typhus may be diagnosed in the laboratory by:
Several serological tests are currently available for the diagnosis of rickettsial diseases like Weil-Felix Test (WFT), Indirect Immuno-flourescence (IIF), Enzyme linked Immunosorbent assay (ELISA) etc. Although many techniques have been used successfully for rickettsial sero diagnosis, rela-tively few are used regularly by most laboratories. BSL-3 Lab is not required for performing serological tests.
Enzyme linked Immunosorbent Assay (ELISA): ELISA techniques, particularly immunoglobulin M (IgM) capture assays, are probably the most sensitive tests available for rickettsial diagnosis, and the presence of IgM antibodies, indicate recent infection with rickettsial diseases. In cases of infecton with O. tsutsugamushi, a significant IgM antibody titer is observed at the end of the first week, whereas IgG antibodies appear at the end of the second week.
Molecular diagnosis (PCR) - For PCR, blood sample is collected in tubes containing EDTA or sodium citrate. However, blood clot, whole blood or serum can also be used for the detection of O. tsutsugamushi, R. rickettsii, R. typhi and R. prowazekii organisms by PCR test.
Clinical Features
Patients with scrub typhus may present early or later in the course of their disease. Inoculation through the chigger bite is often painless and unnoticed. A small painless papule initially appears at the site of infection and enlarges gradually. An area of central necrosis develops and is followed by eschar formation. The eschar (if present) is well developed at the initiation of the fevers, which may drive the patient to seek medical attention.
The incubation period lasts 6-20 days (average, 10 days). After incubation, persons may experience headaches, shaking chills, lymphadenopathy, conjunctival infection, fever, anorexia, and general apathy. The fever usually reaches 40-40.5°C (104-105°F).
Specific therapeutic considerations
If scrub typhus is suspected with COVID, treatment with Doxycycline (@ 200 mg/day in two divided doses for duration of 7 days) or Azithromycin (@ 500 mg in a single oral dose for 5 days) should be administered.
Management of the individual complications should be done as per the existing practices.
If the patient is in a primary care setup, the following criteria should be monitored to assess patients clinical progress. Early warning signs for referral to higher centre are:
Even though the basic preventive strategies of COVID-19 and seasonal influenza are different from diseases discussed in this document, it is desirable that there is synergy in the prevention of these diseases. The States must make use of their resources effectively as staff is also diverted to provide COVID-19 response. This can be achieved by combining prevention activities.
Integrated surveillance: It must be ensured that IDSP networks are strengthened to include surveillance of COVID-19 cases besides for dengue, malaria, chikungunya, leptospirosis, scrub typhus, seasonal influenza to maximize the use of resources.
Basic preventive measures for COVID-19 and seasonal influenza, like avoiding large gatherings, maintaining physical distance, hand hygiene and cough etiquette must be ensured at all times.
Vector control: Source reduction of mosquito breeding sites and adult control measures should be implemented in areas affected by or at risk of these diseases, especially in and around treatment facilities.
Use of approved insect repellents and ITN/LLINs is affective against vector borne diseases including scrub typhus.
Preventive measures against leptospirosis include wearing protective clothing for people at occupational risk (sanitation workers, rice-paddy and sugarcane workers etc.) and avoidance of swimming in water that may be contaminated.
Vaccination for seasonal influenza for healthcare workers and other high-risk groups to be implemented aggressively.
Community support must be garnered and community awareness drives on COVID-19 and other seasonal diseases must be ensured.
A concerted effort is required in prevention, surveillance, behaviour change communication and management of such cases. Alert vigil, a high index of suspicion and constant awareness of the possibility of co-infections can help physicians avert the adverse outcome of cases with coinfection and improve clinical outcomes.
Last Modified : 4/15/2021
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