CMAAO IMA HCFI CORONA MYTH BUSTER 10
Dr
K K Aggarwal
President
CMAAO, HCFI and Past National President CMAAO
COVID Virus behaves like any other virus
No. Most viral illnesses have
high lymphocyte counts but COVID 19 have low lymphocyte count.
Dengue taught us the value of platelet count interpreted
along with haematocrit and COVID 19 is now teaching us the value of lymphocytes
in blood test.
It has been a standard teaching that all viral fever
will have high lymphocytes counts. Low count will only occur with HIV, SARS
like illness, measles and hepatitis.
Now all studies have shown it to be an important marker
of COVID 19
In the latest study published in March 9, 2020, the
Lancet, the authors showed that baseline lymphocyte count was significantly
higher in survivors than non-survivors; in survivors, lymphocyte count was
lowest on day 7 after illness onset and improved during hospitalisation,
whereas severe lymphopenia was observed until death in non-survivors.
Clues for COVID-19 include leukopenia, seen in 30% to
45% of patients, and lymphocytopenia, seen in 85% of the patients in the case
series from China,
Other associated
lab findings are elevated alanine aminotransferase
and aspartate aminotransferase levels (37%).
High D-dimer levels and more severe lymphopenia have been
associated with mortality.
1. Chen N, Zhou M, Dong X, Qu J, Gong F. Epidemiological and clinical
characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan,
China: a descriptive study. Lancet. 2020 Jan 30. [Epub ahead of
print]
2. Li Q, Guan X, Wu P, Wang X, Zhou L, et al. Early Transmission Dynamics
in Wuhan, China, of Novel Coronavirus-Infected Pneumonia. N Engl J Med.
2020 Jan 29.
Most
fevers cannot be differentiated clinically
No, here are the tips
Fever with cough and cold- think of flu
Fever with retroorbital eye pain - think of dengue
Fever with joints pain which improves on bending -
think of Chikungunya
Fever with lymphocytosis – Think of Viral fever
Fever with lymphopenia: Think of Covid 19, acute
hepatitis, HIV
Fever with jaundice: Rules out viral hepatitis
Fever subsides capillary leakage appears in dengue
Low grade evening rise fever think of TB
Fever with chills and rigors: think of malaria,
Filaria, UTI, sepsis
Fever with cough and breathlessness: Think of COVID
like illness
Fever with ESR > 100: painful thyroiditis, sepsis,
Fever with SGOT > SGPT: dengue,
Fever with angry looking throat with no cough think of
streptococcal sore throat
Fever with red eyes: think of Zika illness
Fever with eschar think of scrub typhus
Fever with single chills: Think of pneumonia
Fever with Jaundice: Rule out leptospirosis,
Fever with involvement of skin, joint and or kidney
rule out auto immune disease
Fever with TLC > 15000 is sepsis
Fever with positive thump sign on live rule out liver
abscess
Its
unethical for doctors to create awareness about COVID 19
No, its as per MCI ethics regulations
MCI
ethics regulation
5.2
Public and Community Health: Physicians, especially those engaged in public
health work, should enlighten the public concerning quarantine regulations and
measures for the prevention of epidemic and communicable diseases. At all times
the physician should notify the constituted public health authorities of every
case of communicable disease under his care, in accordance with the laws, rules
and regulations of the health authorities. When an epidemic occurs a physician
should not abandon his duty for fear of contracting the disease himself.
7.11
A physician should not contribute to the lay press articles and give interviews
regarding diseases and treatments which may have the effect of advertising
himself or soliciting practices; but is open to write to the lay press under
his own name on matters of public health, hygienic 14 living or to deliver
public lectures, give talks on the radio/TV/internet chat for the same purpose
and send announcement of the same to lay press.
Loss of sense of smell is hallmark of COVID-19
No. Post-viral anosmia is one of the leading causes of
loss of sense of smell in adults, accounting for up to 40% cases of anosmia.
Viruses that give rise to the common cold are well known to cause
post-infectious loss, and over 200 different viruses are known to cause upper
respiratory tract infections. Previously described coronaviruses are thought to
account for 10-15% cases. It is therefore perhaps no surprise that the novel
COVID-19 virus would also cause anosmia in infected patients.
There is good evidence from South Korea, China and
Italy that significant numbers of patients with proven COVID-19 infection have
developed anosmia/hyposmia. In Germany it is reported that more than 2 in 3
confirmed cases have anosmia. In South Korea, where testing has been more
widespread, 30% of patients testing positive have had anosmia as their major
presenting symptom in otherwise mild cases. [ent.org]
Lopinavir-ritonavir
is the drug of choice
This combined protease inhibitor, which has primarily
been used for HIV infection, has in vitro activity against the SARS-CoV and appears to have some activity against
MERS-CoV in animal studies.
Although the use
of this agent for treatment of COVID-19 has been described in case reports,
there was no difference in time to clinical improvement or mortality at 28 days
in a randomized trial of 199 patients with severe COVID-19 given
lopinavir-ritonavir (400/100 mg) twice daily for 14 days in addition to
standard care versus those who received standard of care alone [
Cao B, Wang Y, Wen D, et al. A Trial of Lopinavir-Ritonavir in Adults Hospitalized with Severe Covid-19. N Engl J Med 2020.]
Cao B, Wang Y, Wen D, et al. A Trial of Lopinavir-Ritonavir in Adults Hospitalized with Severe Covid-19. N Engl J Med 2020.]
Virus can be transmitted through
breast milk
The only report of
testing found no virus in the maternal milk of six patients [111]. However, droplet transmission could
occur through close contact during breastfeeding. Thus, mothers with confirmed
COVID-19 or symptomatic mothers with suspected COVID-19 should take precautions
to prevent transmission to the infant during breastfeeding (including assiduous
hand hygiene and use of a facemask).
Alternatively, to
minimize direct contact, the infant can be fed expressed breastmilk by another
caregiver until the mother has recovered, provided that the other caregiver is
healthy and follows hygiene precautions.
Women who choose
not to breastfeed must take similar precautions to prevent transmission through
close contact when formula is used. [Chen H, Guo J, Wang C, et al. Clinical characteristics and
intrauterine vertical transmission potential of COVID-19 infection in nine
pregnant women: a retrospective review of medical records. Lancet 2020;
395:809.]
There are no guidelines
for discontinuation of home isolation
The US CDC has issued recommendations on
discontinuation of home isolation, which include both test-based and
non-test-based strategies.
The choice of strategy depends upon the patient
population (eg, immunocompromised versus nonimmunocompromised), the availability
of testing supplies, and access to testing.
When a test-based strategy is used,
patients may discontinue home isolation when there is:
Resolution of fever without the use of fever-reducing
medications AND
Improvement in respiratory symptoms (eg, cough,
shortness of breath) AND
Negative results of a US FDA Emergency Use Authorized
molecular assay for COVID-19 from at least two consecutive nasopharyngeal swab
specimens collected ≥24 hours apart (total of two negative specimens)
When a non-test-based strategy is used,
patients may discontinue home isolation when the following criteria are met:
At least seven days have passed since symptoms first
appeared AND
At least three days (72 hours) have passed since
recovery of symptoms (defined as resolution of fever without the use of
fever-reducing medications and improvement in respiratory symptoms [eg, cough,
shortness of breath])
In some cases, patients may have had
laboratory-confirmed COVID-19, but they did not have any symptoms when they
were tested. In such patients, home isolation may be discontinued when at least
seven days have passed since the date of their first positive COVID-19 test so
long as there was no evidence of subsequent illness.
The use of non-test-based strategies that use time
since illness onset and time since recovery as the criteria for discontinuing
precautions is based upon findings that transmission is most likely to occur in
the early stage of infection. However, data are limited, particularly in
immunocompromised patients, and this strategy may not prevent all instances of
secondary spread. [uptrodate dot com]
You
require two tests to declare recovery?
Ideally 4. Factors include
resolution of clinical signs and symptoms and negative results of
reverse-transcription polymerase chain reaction (RT-PCR) testing for severe
acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on two sequential
paired nasopharyngeal and throat specimens (four specimens total, each
handled separately), with each pair collected ≥24 hours apart [Centers
for Disease Control and Prevention. Interim Considerations for Disposition of
Hospitalized Patients with 2019-nCoV Infection. https://www.cdc.gov/coronavirus/2019-ncov/hcp/disposition-hospitalized-patients.html
(Accessed on February 11, 2020).]
You can not diagnose COVID 19 without tests
In some cases,
testing for COVID-19 may not be accessible, particularly for individuals who
have a compatible but mild illness that does not warrant hospitalization.
If the clinician
has sufficient concern for possible COVID-19 (eg, there is community
transmission), it is reasonable to advise the patient to self-isolate at home
(if hospitalization is not warranted) and alert the clinician about worsening
symptoms. The optimal duration of home isolation in such cases is uncertain.
Continuing steroids
in COVI 19 patients will harm
For individuals
with underlying conditions who require treatment with these agents and
are without evidence of COVID-19, there is no evidence that
routinely discontinuing treatment is of any benefit. In addition, discontinuing
these medications may result in loss of response when the agent is
reintroduced. This approach is supported by statements from American and other
dermatology, rheumatology, and gastroenterology societies.
Normally immunocompromised patients with COVID-19 are at
increased risk for severe disease, and the decision to discontinue prednisolone,
biologics, or other immunosuppressive drugs in the
setting of infection must be determined on a case-by-case basis.
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