|
Indian Pediatr 2021;58: 686-687 |
 |
Clinical Profile and
Outcome of COVID-19 Among Immunocompromised Children
|
Sunil Kumar Rao,* Ashutosh Kumar, Rajniti Prasad,
Vineeta Gupta, Om Prakash Mishra
Department of Pediatrics, IMS-BHU, Varanasi, Uttar
Pradesh.
Email:
[email protected]
|
This retrospective study describes
the clinical profile, risk of infection and outcome of coronavirus
disease-19 in immuno-compromised children. It was found that children on
immuno-suppressant medication has 2.89 times increased risk of infection
(P=0.01). Disease manifestation was asymptomatic (P=0.01)
or mild with predominant gastrointestinal symptoms (P=0.02)
without alteration in immunosuppressive treatment regime.
Key words: COVID-19, Children,
Immunocompromised, Outcome.
|
Severe acute respiratory syndrome coronavirus 2
(SARS-CoV-2) infection in children manifests as mild to moderate disease
with low fatality [1]. There is limited information about susceptibility
to SARS-CoV-2 infection, clinical profile and outcome among
immunocompromised children in India. Published literature has revealed
milder disease and favorable outcome without discontinuation of
immunosuppressive medi-cation in these children [2-6]. We, herein
describe the clinical features and outcome of immunocompromised children
diagnosed with SARS-CoV-2 infection at our center.
This was a retrospective analysis of data from 1 June
to 31 October, 2020 at a tertiary care center of a teaching hospital.
The analysis was approved by institutional ethics committee. All
children admitted during the study period were screened for SARS-CoV-2
infection and those who were diagnosed with coronavirus disease 19
(COVID-19) were classified into immunocompromised and immunocompetent.
All immuno-compromised children in the present study were either on
anticancer drugs or immunosuppressive therapy for kidney diseases, and
fulfilling criteria for immunocompromised state [6]. The variables
extracted from the hospital records were age, gender, presenting
symptoms, complications, severity of illness, diagnosis, laboratory
investigations, imaging findings, treatment and outcome. The diagnosis
of COVID-19 was made by positive reverse transcription polymerase chain
reaction (RT-PCR) test for SARS-CoV-2. The severity of illness was
classified as per guidelines given by Ministry of Health and Family
Welfare, Government of India [7], and children were treated as per unit
protocol without alteration in immuno-suppressive treatment regime.
Proportions were compared using Fisher exact test.
Table I Clinical Profile and Outcome of Children with SARS-CoV-2 Infection
Variables |
Children with
COVID-19 |
|
Immuno- |
Immuno- |
|
competent |
compromised |
|
(n=9) |
(n=16) |
Comorbiditya |
5 |
16 |
Severity of illness |
|
|
Asymptomaticb |
0 |
8 (50) |
Mild |
0 |
3 (18.7) |
Moderate |
5 (55.5) |
3 (18.7) |
Severe (n=6) |
|
|
Septic shock |
4 (44.4) |
2 (12.5) |
ARDS |
2 (22.2) |
1 (5.9) |
Clinical features |
|
|
Fever |
9 (100) |
7 (43.7) |
Cough and difficulty in
breathing |
8 (88.8) |
3 (18.7) |
Diarrhea and vomiting |
0 |
7 (41.1) |
Convulsion and altered sensorium |
3 (33.3) |
0 |
Abdominal pain |
2 (22.2) |
5 (29.4) |
Treatmentd |
|
|
Hospitalization |
9 (100) |
8 (50) |
Oxygen |
4 |
2 |
Vasopressor requirement |
4 |
2 |
Died |
2 (20) |
2 (12.5) |
Data presented as no. or no. (%). aImmunocompetent:1
each with thalassemia, Wilson disease, diabetes,
epilepsy and congenital hydro-cephalous with shunt;
Immunodeficient: 8 children with nephritic syndrome, 2
with Non-Hodgkin lymphoma and 1 each of Hodgkin
lymphoma, acute lymphoblastic leukemia, acute myeloid
leukemia, myelodysplastic syndrome, aplastic anemia and
retinoblastoma, dOnly one immunocompetent patient
required ventilation. |
Data of 409 children were extracted during the study
period; 162 (396%) of these were immunocompromised. Of the 409 children,
26 (6.3%) were diagnosed with SARS-CoV-2. Data of one child was
incomplete and he was excluded from the analysis. The proportion of
SARS-CoV-2 positivity in immuno-compromised and immunocompetent children
was 16 (9.9%) and 9 (3.6%), respectively [OR (95% CI) 2.89 (1.24-6.73);
P=0.01]. Comorbidities were present in 184 (44.9%) children,
mainly malignancy in 78 (18.9%) and nephrotic syndrome (NS) in 67
(16.3%). The clinical profile and outcome of children with COVID-19 is
shown in Table I. All children with severe COVID-19 disease had
features of sepsis and shock; however, 3 children had acute respiratory
distress syndrome (ARDS). Only 12 children with COVID-19 underwent blood
biochemistry, and reports revealed anemia (n=6), leucopenia (n=5),
neutrophil-lymphocyte ratio>3 (n=5) and thrombocytopenia in 3
children. High resolution computed tomography of chest showed ground
glass opacities in two and air-bronchogram in three children. One child
presented with severe abdominal pain and computed tomography of abdomen
was suggestive of pancreatitis, he also had elevated amylase (217µ/L)
and lipase (365µ/L).
Immunocompromised children had a significantly higher
risk of SARS CoV-2 infection which may be due to the need of frequent
hospital visits for their medications (chemotherapy), which exposed them
to get infection. However, they had a lower hospitalization rate [8
(50%) vs 9 (100%), P=0.01] as compared to immunocompetent
children possibly because of day care treatment protocol. The occurrence
of disease was lesser in immunocompromised children, with most being
either asymptomatic or with mild disease, and with complete recovery. It
is possibly due to weaker immune response under the influence of
immunosuppressants. Similar observations were reported in a survey
conducted in 25 countries (>200 children tested and 10000 at risk) among
children on anticancer treatment [8] and in a systematic review of 16
articles (100 adults, 10 children) by Minotti, et al. [5], which
concluded that these children had asymptomatic or mild disease, and had
a favorable outcome. Severe disease manifestations and require-ment of
intensive care, respiratory support, and inotropes were comparable
between the two groups. Overall mortality was 16% and this might be a
reflection of high incidence of non-COVID sepsis and associated
complications in these patients. In a study on 113 children with kidney
diseases receiving immunosuppressive medications from 30 countries;
authors found that only 9.7% had severe grade of disease [3]. Features
of relapse, or new organ involvement (pancreas) or new onset
glomerulonephritis have been seen in children with nephrotic syndrome in
present study and this might be like other viruses, SARS Co-V-2
infection may also precipitate relapses or infect new organ [9,10].
The present study has few limitations, one being
retrospective analysis and small sample size, and short term follow-up.
Additionally, admitting policy kept on changing during the study period
depending on government guidelines. We conclude that children with
immunosuppressant medication are at an increased risk of SARS Co-V-2
infection, and disease manifestations may be asymptomatic or mild with
predominantly gastrointestinal symptoms.
Contributors: SKR, RP, VG, OPM: concept,
design, drafting of the manuscript, critical analysis; AK: acquisition
of data, analysis and interpretation. All authors approved the final
version of manuscript, and are accountable for all aspects related to
the study.
Funding: None; Competing interests: None
stated.
REFERENCES
1. Meena J, Yadav J, Saini L, et al. Clinical
features and outcome of SARS-CoV-2 infection in children: A systematic
review and meta-analysis. Indian Pediatr. 2020;57:820-26.
2. Marlais M, Wlodkowski T, Vivarelli M, et al. The
severity of COVID-19 in children on immunosuppressive medication. Lancet
Child Adolesc Health. 2020;4:e17-18.
3. Marlais M, Wlodkowski T, Al-Akash S, et al.
COVID-19 in children treated with immunosuppressive medication for
kidney disease. Arch Dis Child. 2020 Dec 21;archdischild-2020-320616
(Online ahead of print).
4. El Dannan H, Al Hassani M, Ramsi M. Clinical
course of COVID-19 among immunocompromised children: A clinical
case series BMJ. Case Rep. 2020;13:e237804.
5. Minotti C, Tirelli F, Barbieri E, et al. How is
immunosuppressive status affecting children and adults in SARS-CoV-2
infection? A systematic review. J Infection. 2020;81: e61-66.
6. Vasudevan A, Mantan M, Krishnamurthy S, et al.
Managing children with renal diseases during the COVID-19 pandemic.
Indian Pediatr. 2020;57:641-51.
7. Government of India, Ministry of Health and Family
Welfare Guidelines on clinical management of COVID-19. Directorate
General of Health Services (EMR Division); p. 3-5. Accessed December 23,
2020. Available from: https://www.mohfw.gov.in/pdf/ Guidelines on
Clinical Management of COVID 1912020.pdf
8. Hrusak O, Kalina T, Wolf J, et al. Flash survey on
severe acute respiratory syndrome coronavirus-2 infections in paediatric
patients on anticancer treatment. Euro J Cancer. 2020;132:11-16.
9. Alvarado A, Franceschi G, Resplandor E, et al.
COVID-19 associated with onset nephrotic syndrome in a pediatric
patient: Coincidence or related conditions? Pediatr Nephrol.
2021;36:205-07.
10. Harambat J, Allard L, Godron-Dubrasquet A.
Relapse rate of nephrotic syndrome in the time of COVID-19. Pediatr
Nephrol. 2021; 36:211-12.
|
|
 |
|