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Indian Pediatr 2013;50: 695-696
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Locked-in Syndrome as a Presentation of
Snakebite
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Chandrika Azad, Vidushi Mahajan and Kana Ram Jat
From the Department of Pediatrics, Government Medical
College and Hospital, Chandigarh, India.
Correspondence to: Dr Chandrika Azad, Assistant
Professor, Department of Pediatrics, Govt. Medical College and Hospital,
Sector 32, Chandigarh 160 030, India.
Email:
[email protected]
Received: August 31, 2012;
Initial review: October 25, 2012;
Accepted: February 14, 2013.
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Snake bite is a common condition in tropical countries. Neurotoxic
features of snake bite vary from early morning neuroparalytic syndrome
to various cranial nerve palsies. Locked in syndrome (LIS) is a rare
presentation. We present four children that had LIS; three patients had
total and one had incomplete LIS. All patients made successful recovery
with polyvalent anti-snake venom and supportive management. This case
series highlights the importance of early diagnosis of LIS in snake
bite.
Key words: Children, Locked in syndrome, Snakebite.
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Snake envenomation is a major cause of
mortality and morbidity all over the world but more so in
developing countries because of lack of advanced life support
equipment [1]. Various presentations of snake bite may include
neuromuscular paralysis, bleeding disorder, renal failure and so
on. Neurological manifestations are caused by elapidae group
(Cobras, kraits). The common krait is nocturnally active snake
with painless bite; so many patients with neurological
manifestations present to emergency without history of snake
bite [2]. In 60%-70% of cases, snakebite occurs when the
patients were asleep and site of bite is undetectable in 17%
cases [3]. Thus,
high degree of suspicion is required in such cases to reach at a
diagnosis.
Locked in syndrome (LIS) is a neurological
syndrome in which despite being conscious patient is unable to
communicate [4]. It is rarely reported in snake bite [5,7]. We
report 4 children with LIS following snake bite.
Case-Reports
Case 1: A 2-year-old child presented with
bleeding from ear, followed by altered sensorium and respiratory
failure within two hours of initial complaints. At admission,
child had respiratory arrest with severe bradycardia, absent
peripheral and central pulses, and Glasgow coma scale (GCS)
score of 3; pupils were fixed and dilated and doll’s eye
movements were absent. After initial resuscitation, he was noted
to have some movement of right toe. Seven hours later, snake
bite was suspected and polyvalent anti-snake venom (ASV) was
administered. Thirty hours later, after receiving 25 vials,
child had spontaneous respiration, movements of lower limbs and
eye opening but pupils were still fixed and dilated. Pupillary
reactions became normal on day three, doll’s eye movement
appeared a day later, and the child was discharged in premorbid
condition on day ten.
Case 2: A-ten-year-old boy presented with
history of anxiety, pain abdomen and vomiting appearing acutely
early morning, while sleeping on the floor of his cottage. His
sister had died an hour back with similar complaints. Parents
did not report any venomous bite. At admission, he had
bradycardia, gasping respiration and GCS of 3. Pupils were fixed
and dilated and doll’s eye movement were absent. He was put on
respiratory support. There was no improvement over next 48
hours. Detailed examination revealed fang marks on one foot so
ASV was given. On day six, parents noted fluttering of eyelids
and next day he had spontaneous respiration and limb movements.
After one week, doll’s eye movements appeared but internal
ophthalmoplegia persisted. CT head was normal and fundus
examination did not show features of optic neuritis. At
discharge, five weeks later, internal ophthalmoplegia was
persisting.
Case 3: A One-and- half-year old child
with history of snake bite presented to the emergency department
with breathing difficulty. At admission, she had gasping
respiration, bradycardia, GCS of 3, fixed dilated pupils and
absent Doll’s eye movement. There was no response to ASV. After
36 hours, she started having spontaneous respiration and
occasional movement of limbs. She used to cry on looking at
parents. On day four, pupillary size and reaction became normal.
She was discharged on day 10 in premorbid condition.
Case 4: A Seven-year-old boy presented
with history of sudden onset of pain abdomen and vomiting, while
in the playground. At admission, he had gasping respiration. Two
hours later, he was atonic, areflexic; pupils were fixed and
dilated with absent doll’s eye movements. After ruling out other
causes (normal cerebrospinal fluid examination, CT head, and
liver function tests); possibility of snake bite was entertained
and ASV was given. After 10 vials of ASV, ptosis resolved and
child started responding using eye movements; 25 vials later,
spontaneous limb movements appeared but internal ophthalmoplegia
persisted. Three weeks later, at discharge, internal
ophthalmoplegia was persisting.
Discussion
Neurotoxic manifestations of snake bite vary
in severity but pediatric case reports of LIS due to snake bite
are rare [7].
In LIS, patient is conscious yet unable to
communicate. It can be of three types: classic, in which patient
has quadriplegia and anarthria with preservation of
consciousness and vertical eye movements. Incomplete LIS is
similar to classic except remnants of voluntary movement other
than vertical eye movement are present. In total LIS, there is
total immobility and inability to communicate, with preserved
consciousness [4]. Usual causes of LIS are stroke, trauma or
encephalitis of ventral pontine area but it can also be caused
by extensive bilateral destruction of corticobulbar and
corticospinal tracts in the cerebral peduncles [8]. LIS can also
be caused by peripheral causes such as severe Guillan-Barre’s
syndrome, neuromuscular junction blockade (myasthenia gravis,
toxins, snake bite), etc.
LIS in snake bite occurs due to neuromuscular
paralysis of voluntary muscles which in turn is caused by
neuromuscular transmission blockade (krait venom acts pre-synaptically
while cobra venom acts post-synaptically) [2]. Irreversible
binding of toxin to presynaptic portion makes clinical recovery
slow in krait envenomation as recovery occurs only with the
formation of new neuromuscular junctions [9], as was seem it our
cases, especially case 2. Such long duration of LIS in snake
bite is not reported previously. Duration of LIS varied from 30
hours to six days. In about 50% cases of LIS, it has been seen
that family members are the first one to note that patient is
able to communicate [10], as was seen in case 2.
Snake bite documentation was done only in one
case by the caregivers, in the rest of the cases, clinical
scenario was typical of painless krait bite [3]. Since
differential diagnoses of unresponsive patient are exhaustive,
high degree of suspicion is required in such cases, especially
during rainy season. Fixed dilated pupils and absent doll’s eye
movement can easily be interpreted as brain death, if
possibility of LIS is not considered. Physicians need to be
aware of likelihood of snakebite presenting as LIS, especially
in the appropriate clinical setting.
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