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Indian Pediatr 2017;54: 163 |
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An Unusual Case of Neonatal Methemoglobinemia
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*Hasmukh Chapsi Gala and Amol Madave
Lilavati Hospital & Research Centre, Mumbai, India.
Email:
[email protected]
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A 26-day-old neonate weighing 3.4 kg, presented with an acute history of
loose motions, vomiting and drowsiness. At admission, patient was
dehydrated, acidotic and cyanosed. Blood gas was suggestive of severe
metabolic acidosis, which was corrected by intravenous hydration and
soda-bicarbonate therapy. There was purulent discharge from umbilicus
along with erythema; C-reactive protein (CRP) was 80 mg/L. Stool
microscopy showed 25-30 pus cells/high power field. A diagnosis of
sepsis was made, and he was started on intravenous antibiotics (Meropenem
and Vancomycin).
Despite oxygen therapy, pulse oximetry showed
saturation of 85% whereas arterial blood gas showed PaO 2
of 122 mmHg and saturation of 98%. In view of this discrepancy and
arterial blood being dark brown in color, diagnosis of methemoglobinemia
was strongly suspected. Blood level of methemoglobin was 31%, which
confirmed methemoglobinemia as a cause of cyanosis.
NADH b5 cytochrome reductase level was normal (11.5
IU/g Hb), ruling out hereditary causes of methemoglobinemia. On
enquiring about any drug intake, parents revealed history of topical
application of Silver sulfadiazine cream on umbilicus since 7th day of
age. Silver sulfadiazine application was immediately stopped. Patient
also had anemia with Hb of 9.4 g/dL; therefore, packed red blood cells
were transfused to improve oxygen carrying capacity.
He was treated with methylene blue (2 mg/kg
intravenously) after ruling out G-6 PD deficiency. Baby improved rapidly
after one dose of methylene blue. Cyanosis disappeared and sensorium
became normal. Repeat blood methemoglobin level was 3.9%. Umbilical pus
culture had growth of Staph. aureus, and baby received
antibiotics for 14 days. On follow up, child is now aged 6 years and is
doing well with normal growth and developmental parameters. He did not
suffer from any further episodes of methemoglobinemia.
Methemoglobinemia in a neonate can be congenital -
(due to hereditary deficiency of NADH cytochrome b5-reductase enzyme) or
acquired. Acquired methemo-globinemia in newborns and young infants
could be due to endogenous conditions, like diarrhea, sepsis and
acidosis or it can be due to exogenous drug or toxin [1-3]. Silver
sulfadiazine application, as a cause of neonatal methemoglobinemia is
rare. Systemic absorption of locally applied drugs is increased in
newborn babies as compared to older infants and children [4]. As such,
local application of silver sulfadiazine is generally contraindicated
in neonates and infants below 2 months of age [5]. Our patient developed
methemoglobinemia secondary to combination of exogenous (application of
silver sulfadiazine cream over umbilicus) and endogenous (sepsis,
diarrhea and acidosis) factors.
To conclude, a high index of suspicion is required
for early diagnosis of methemoglobinemia in neonates, and care should be
taken in choosing appropriate drug for local application in newborn
infants.
References
1. Nelson KA, Hosteler MA. An infant with
methoglobinemia. Hosp Phys. 2003; 39:31-38, 62.
2. Denshaw-Burke M. Methemoglobinemia. Available
from: http//www.emedicine.medscape.com/article/204178. Accessed
January 4, 2016.
3. DeBaun MR, Grimes A, Frei-Jones MJ, Vichinsky EP.
Hereditary methemoglobinemia. In: Berhman RE, Kleigman RM,
editors. Nelson Textbook of Pediatrics. 20th ed.
Philadelphia: Elsevier, 2016. p. 2347-8.
4. Rutter N. Percutaneous drug absorption in the
newborn: hazards and uses. Clin Perinatol. 1987;14:911-30.
5. Silver Sulfadiazine cream- FDA prescribing
information, side effects and uses. Available from:
http://www.drugs.com/pro/silver-sulfadiazine-cream.html Accessed
February 15, 2016.
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