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Cyanosis and “mass SpO2 screening” in pandemic times

Published online by Cambridge University Press:  20 October 2021

Ravindra S. Pawar*
Affiliation:
Department of Pediatrics, Dr D Y Patil Medical College Hospital and Research Institute, Kolhapur, Maharashtra, India
Anil B. Kurane
Affiliation:
Department of Pediatrics, Dr D Y Patil Medical College Hospital and Research Institute, Kolhapur, Maharashtra, India
*
Author for correspondence: Dr R. S. Pawar, Kids Heart Clinic, Above Bank of Baroda, Opposite Irwin Christian High School, Parvati Multiplex Square, Kolhapur, Maharashtra 416001, India. Tel: +91 9545507284. E-mail: drravipawar@gmail.com
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Abstract

Type
Letter to the Editor
Copyright
© The Author(s), 2021. Published by Cambridge University Press

To the Editors,

Ever since World Health Organisation has declared the Coronavirus disease-19 pandemic, Reference Cucinotta and Vanelli1 it has been affecting millions worldwide. Preventive measures and especially checking saturations have become the norm. In a span of just 4 months, two cases of methaemoglobinemia were diagnosed, only due to the increased awareness among layman about saturation checks.

First was a 10-month-old asymptomatic boy evaluated on detecting saturation of 88% by his parents. An otherwise healthy infant weighing 9 kg, and not on any medications, had no clubbing and normal physical and cardiovascular system examination. Chest X-ray, echocardiography and saline contrast echocardiography were normal and not suggestive of any intra-cardiac or intra-pulmonary shunting. Arterial blood gases showed normal PO2 values and hence serum methaemoglobin levels were done, which were 12.3% (normal < 1.5%). Parents were reassured and no further management was required. Second was a 10-year-old boy, hitherto unevaluated, investigated because parents were symptomatic for Coronavirus disease-19, was having saturations of 90%, no clubbing, widely split and fixed second heart sound and an ejection systolic murmur. Echocardiogram showed large atrial septal defect with left to right shunt and normal pulmonary venous drainage. Arterial blood gases showed normal PO2 and hence again, methaemoglobinemia was suspected and his serum methaemoglobin levels were 36.3%. He underwent successful surgical atrial septal defect closure.

Congenital methaemoglobinemia is a very rare disease, with real incidence unknown. Reference Benz, Ebert, Hoffman, Benz, Silberstein, Anastasi, Heslop and Weitz2 Diagnosis is difficult because of asymptomatic status and clinically unrecognisable cyanosis. In Coronavirus disease-19, “happy hypoxaemia” has been a danger sign, Reference Dhont, Derom, Van Braeckel, Depuydt and Lambrecht3 and hence public health systems across the world have been stressing on detecting decreasing saturation levels even for asymptomatic individuals. An indirect by-product of this “mass SpO2 screening” has been the increased incidence and diagnosis of methaemoglobinemia. Increased health awareness, mandatory preventive measures and early detection of certain diseases can be considered as a silver lining in this otherwise dark cloud

Financial support

None.

Conflicts of interest

None.

Ethical standards

Not applicable.

References

Cucinotta, D, Vanelli, M. WHO declares COVID-19 a pandemic. Acta Biomed 2020; 91: 157160. DOI 10.23750/abm.v91i1.9397.Google ScholarPubMed
Benz, EJ, Ebert, B. Hemoglobin variants associated with hemolytic anemia, altered oxygen affinity, and methemoglobinemias. In: Hoffman, R, Benz, EJ, Silberstein, LE, Anastasi, J, Heslop, H, Weitz, J (eds). Hematology: Basic Principles and Practice. Elsevier Science, Amsterdam, 2018: 608615.CrossRefGoogle Scholar
Dhont, S, Derom, E, Van Braeckel, E, Depuydt, P, Lambrecht, BN. The pathophysiology of ‘happy’ hypoxemia in COVID-19. Respir Res 2020; 21: 198. DOI 10.1186/s12931-020-01462-5.CrossRefGoogle ScholarPubMed