|
Case 1 |
Case 2 |
Case 3 |
Age, known wheezer |
4 y, No |
1y, Yes |
10 y, No |
Asthma predictive index |
Negative |
Positive |
Negative |
Clinical features |
Fever, cough, breathing difficulty |
Breathing difficulty |
Fever, cough, breathing difficulty |
Dxygen saturation |
SpO2 89% |
SpO2 94% |
SpO2 94% |
Neutrophil-lymphocyte ratio |
7.08 |
0.44 |
1.05 |
C-reactive protein |
24 |
2.88 |
<2.8 |
Treatment |
Salbutamol metered dose inhaler |
Salbutamol metered dose inhaler |
Salbutamol metered dose inhaler
|
|
with spacer, IV MgSO4, |
with spacer |
with spacer |
Respiratory support |
HFNO (@ 2 L/kg flow and |
Oxygen by nasal cannula
|
HFNO (@ 2 L/kg flow and |
|
40% FiO2) |
@ 4 L/min |
40% FiO2) |
Steroids |
IV dexamethasone (@ 0.6 mg/kg/d) |
Oral prednisolone (@ 1 mg/kg/d) |
Oral prednisolone (@ 1mg/kg/d) |
Hospital stay (d) |
5 |
3 |
5 |
All children were RT-PCR positive, and had tachypnea, subcostal
retractions, and bilateral expiratory wheeze; Chest X-ray showed
bilateral lung hyper inflammation in all 3; None of the children
had any comorbidity; and HFNO: High-flow nasal oxygen; FiO2:
Fraction of inspired oxygen. |
COVID-19 associated asthma exacerbation [2] is rare;
although there is a theoretical risk of COVID-19 causing a virus
triggered asthma exacerbation. Previous epidemics of the coronavirus
also did not report significant numbers of asthma exacerbations [3].
Severe respiratory manifestations of COVID-19, though
uncommon in children have been reported and may be presumed to involve
clinical presentations related to small airways or alveolar involvement
or both. If small airways are predomi-nantly affected, treatment
modalities will include broncho-dilators, corticosteroids, oxygen
supplementation and respi-ratory support as required. However,
bronchodilators are potentially detrimental in a scenario of alveolar
disease due to pro-inflammatory effects on alveoli, worsening of
ventilation-perfusion mismatch and increased tachycardia [4]. There is
no clear-cut separation of these phenotypes and overlap may be expected.
Corticosteroids, typically in courses longer than that used in
exacerbations of asthma, are currently in use for treating severe
COVID-19 [4,5]. The role of antiviral treatment is not precisely known
especially in the pediatric context [4].
In our cases, we utilized C-reactive protein (CRP)
levels as an indicator of severity of inflammation. In one child CRP was
elevated but other markers of inflammation including D-dimer, S.
ferritin and serum fibrinogen were normal. More data is required to know
if inflammation and hypercoagulable states more commonly occur with
alveolar disease in contrast to small airways involvement as seen in
these three cases. The limitation of our workup lies in not testing for
viral co-infection which may have triggered the exacerbation as well.
Literature on pediatric asthma and COVID-19 is sparse
and limited to case reports highlighting mild disease mostly not
requiring hospitalizations and ICU care [1,6]. One of the mainstays of
aerosol therapy in acute wheezing episodes is nebulizations. However, it
also amplifies the risk of infection transmission by stimulating a cough
reflex, as well as generating a high volume of respiratory aerosols that
may be propelled over a longer distance thus infecting bystander hosts.
An added disadvantage being an increased risk of deposition of virus in
the lower lung [7], nebulizations in COVID-19 remains the least suitable
preference. Poor response to a metered dose inhaler/spacer, a child who
is uncooperative or unable to follow the directions required for metered
dose inhaler use and medication shortage remain the only possible
indications of using nebu-lizers in these children. The Global
initiative for asthma guidelines suggest that asthma exacerbations due
to COVID-19 should be treated with corticosteroids as appropriate [8].
However, there is no research on the choice of corticosteroid. No
adverse effects attributable to the use of steroids were noted in these
children.
Though rare, COVID-19 infection in children may
trigger a viral-induced wheeze that requires distinguishing from other
viral and asthma triggers. Severe illness requiring substantial
respiratory support may occur in these circumstances. Identifying
similar presentations and reporting may help also to resolve the
therapeutic dilemmas.
REFERENCES
1. Papadopoulos NG, Custovic A, Deschildre A, et
al. Impact of COVID-19 on Pediatric Asthma: Practice adjustments and
disease burden. J Allergy Clin Immunol Pract. 2020;8:2592-2599.e3.
2. Abrams EM, Szefler SJ. Managing Asthma during
Coronavirus Disease-2019: An example for other chronic conditions in
children and adolescents. J Pediatr. 2020; 222:221-26.
3. Van Bever HP, Chng SY, Goh DY. Childhood severe
acute respiratory syndrome, coronavirus infections and asthma. Pediatr
Allergy Immunol. 2004;15:206-9.
4. Raghunathan V, Dhaliwal MS. Pharmacological
manage-ment of COVID-19. J Pediatr Crit Care. 2020;7: S42-8.
5. Horby P, Lim WS, Emberson JR, et al.
Dexamethasone in hospitalized patients with Covid-19 - Preliminary
Report. N Engl J Med. 2020; NEJMoa2021436. [Epub ahead of print].
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by nebulizer: A serious, underappreciated risk. CMAJ. 2020; 192:E346.
8. COVID-19: GINA Answers to Frequently Asked
Questions on Asthma Management - Global Initiative for Asthma - GINA.
Global Initiative for Asthma - GINA. 2020. Accessed September 16, 2020.
Available from:
https://ginasthma.org/covid-19-gina-answers-to-frequently-askedquestions-on-asthma-management.