|
Indian Pediatr 2012;49: 752-753
|
 |
Recurrent Neonatal Organophoshorus Poisoning
|
Yusuf Parvez, Aji Mathew and Satheesh Kalantra Kutti
From the Department of Pediatrics, Al-Jahra Hospital,
Kuwait.
Correspondence to: Dr Yusuf Parvez, Department of
Pediatrics, Al-Jahra Hospital, Kuwait.
Email: [email protected]
Received: October 04, 2011;
Initial review: November 15, 2011;
Accepted: April 26, 2012.
|
Organophosphorus poisoning in neonates is extremely rare and needs high
index of suspicion to diagnose it. The clinical presentation is often
confused with the features of sepsis like apnea, copious oral
secretions, diarrhea, letharginess, seizures. There may be recurrence of
manifestations due to chronic exposure. We report a classic case
admitted in the intensive care unit of our hospital.
Key words: Apnea, Seizures, Sepsis.
|
Organophosphorus poisoning
is rare in neonates. Transplacental route is the most common mode of
transmission, others being inhalation and ingestion; either
accidental or homicidal. The clinical manifestation often simulates
that of sepsis and leads to diagnostic dilemma. Careful clinical
examination and early intervention is needed to treat the patient.
Case Report
A 17-days-old Egyptian girl, a product of
non-consanguineous parents delivered by full term normal vaginal
delivery with no antenatal and perinatal complications was admitted
to our hospital with the history of poor feeding and poor activity
of one day duration. There was no history of fever or seizures. On
examination, child was found to be hypothermic, lethargic, and pale,
with mottled skin. She had recurrent apnea associated with
bradycardia. She had profuse salivation and frothy secretions from
mouth. CNS examination revealed pin-point pupils but other cranial
nerves were normal. Child was hypotonic but neonatal reflexes were
fairly elicitable. Her hemogram and electrolytes were normal and
blood gas analysis showed mild metabolic acidosis. The baby was put
on nasal CPAP along with other supportive therapy. Careful
interrogation of parents revealed the history of pesticide (Diazinon)
spray at home, two days prior to the development of symptoms in the
baby. With this history and physical examination findings, strong
possibility of organophosphorus toxicity was considered and child
was treated with multiple doses of Atropine and two doses of
pralidoxime. The patient’s activity improved after atropine and
pralidoxime doses. There were no further episodes of apnea,
bradycardia or miosis. The patient was weaned off from CPAP. Her
septic and metabolic screen came negative. Serum cholinesterase
level was very low 137U/L (Normal 5000-12000U/L).The patient was
discharged without sequale after two days. The patient remained
asymptomatic at home and was feeding (breast milk) well. She was
admitted again with similar clinical presentation within 48 hours
and was treated with atropine and pralidoxime till recovery. She had
a very low serum cholinesterase level at this admission (150 U/L).
In view of repeated poisoning in the child, breast milk was stopped
temporarily as it was suspected as one of the source of repeated
exposure and the mother’s serum cholinesterase level was also sent,
which turned out to be low too (1600 U/L). Child had complete
recovery after treatment. Cholinesterase levels came back to normal
value after few days. Parents were sent to social worker for
counseling but child abuse was ruled out. The baby is being followed
up regularly in pediatric neurology department and she is showing
normal developmental milestones according to her age.
Discussion
Organophosphorus poisoning in neonates is rare
and a very few cases have been reported so far. Most of the cases
reported are of babies born to mother who had organophosphorus
poisoning by insecticidal ingestion, either suicidal or homicidal,
just before delivery i.e. transplacentally acquired. Other modes of
poisoning can be either by inhalation, or ingestion, either
accidental or homicidal [1-3]. Few cases have been reported when
neonates were given herbal medicines contaminated with
organophosphorus compounds [3]. In our case, the house was sprayed
with very strong organophosphorus compound, diazinon and the baby
might have been exposed to poison either by inhalation or through
breast milk.
Diagnosis of organophosphorus poisoning in
children needs high index of suspicion as the clinical presentation
simulates sepsis. It can be proved by demonstrating low levels and
low activity of RBC Cholinesterase and pseudocholine esterase in the
baby. Mother’s serum or breast milk cholinesterase level could add
in confirming the diagnosis [4,5]. Treatment includes general
measures like airway support and ventilation, cardiovascular
support, pulse oximetry and ECG monitoring. The mainstay of medical
therapy in organophosphate poisoning include atropine, pralidoxime
(2-PAM), and benzodiazepines (eg, diazepam)
[4,5]..
Atropine reverses muscarnic effects and PAM reactivates the
phosphorylated choline esterase there by reverses muscle paralysis
(nicotinic effects). The patient should be followed up regularly as
the organophosphorus compounds may affect the development of an
infant, especially the social milestones [6,7].
Funding: None; Competing interests:
None stated.
References
1. Jajoo M, Saxena S, Pandey M. Transplacentally
acquired organophosphorus poisoning in a newborn. Ann Trop Paediatr.
2010;30:137-9.
2. Samarawickrema N, Pathmeswaran A,
Wickremasinghe R, Peiris-John R, Karunaratna M, Buckley N, et al.
Fetal effects of environmental exposure of pregnant women to
organophosphorus compounds in a rural farming community in Sri
Lanka. Clin Toxicol (Phila). 2008;46:489-95.
3. Abdullat EM, Hadidi MS, Alhadidi N, Al-Nsour
TS, Hadidi KA. Agricultural and horticultural pesticides fatal
poisoning; the Jordanian experience 1999-2002. J Clin Forensic Med.
2006;13:304-7.
4. Kaur I, Jayashree K, Hiranandani M, Singhi SC.
Severe organophosphate poisoning in a neonate. Indian Pediatr.
1996;33:517-9.
5. Choudhry VP, Jallali AJ, Haider G, Aram GN,
Ghani AR. Organophosphorus poisoning. Indian J Pediatr. 1987;54:
427-30.
6. Budhathoki S, Poudel P, Shah D. Clinical
profile and outcome of children presenting with poisoning or
intoxication: a hospital based study.Nepal Med Coll J.
2009;11:170-5.
7. Roegge CS, Timofeeva OA, Seidler FJ, Slotkin
TA, Levin ED. Developmental diazinon neurotoxicity in rats: later
effects on emotional response. Brain Res Bull. 2008;75:166-72.
|
|
 |
|