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(1)

Snake Bite

Dr Ahmed Wayez MD Medicine Deptt. of Medicine

(2)

INTRODUCTION

Snake bite is one of the major public health problems in the tropics.

It is also emerging as an occupational disease of agricultural workers.

In view of their strong beliefs and many associated myths, people resort to

magico –religious treatment for snake bite thus, causing delay in seeking

proper treatment.

(3)

SNAKE BITE INCIDENCES

Papua New Guinea has some of the highest snakebite rates in the world, with the

country’s rural central province recording an annual incidence of 561.9 cases per 100

000 population

Snakebites are concentrated in mainly rural areas and vary considerably by season, with the peak incidence seen in the rainy and

harvesting seasons

(4)

Snake bite deaths worldwide

(5)

Epidemiology

India is estimated to have the

highest snakebite mortality in the world.

Accoding to WHO: in India 50,000 deaths/yr

Males:Female- 2:1.

Majority of the bites being on the

lower extremities.

(6)

1.

2.

3.

4.

Causes of mortality:

Not reaching health facility in time

Lack of awareness and knowledge

Harmful first aid practices

Lack of training among primary

care health workers

(7)

Snakes of India

– – – –

236 species

Only 13 are poisonous Of these four, namely

Common cobra ( Naja naja ),

Russell’s viper ( Dabiola russelii ),

Saw-scaled viper ( Echis carinatus ) and

Common krait ( Bungarus caeruleus ) Are believed to be responsible for

most of the poisonous bites in India.

(8)

Venomous v/s Non-venomous

(9)

Fang marks

(10)

Snakes of India

Common krait (Bungarus caeruleus): black or bluish black, with white crossbars

(11)

Snakes of India

Cobra ( Naja ): Hood, spectacle mark

(12)

RUSSELL’S VIPER ( Dabiola russelii )

Key identification feature is the black edged almond or chain shaped marks on the back

(13)

Saw-scaled viper (

Echis

carinatus

)

(14)

PIT VIPER

wider head than neck and stocky body

rough scaled snake with large eyes,

(15)

DIAGNOSIS OF SNAKE BITE

History

Fang Marks: classically, two puncture

wounds separated by a distance varying from 8mm to 4cm, depending on the

species involved.

However a side swipe may produce only a single puncture,while multiple bites could result in numerous fang marks.

20 whole blood clotting test (20WBCT)

(16)

20 Minute Whole Biood Clotting Test (20 WBCT)

Bedside, most reliable test of coagulation.

A few mililiter venous blood in a glass vessel

Left at room temperature for 20 minutes.

After 20 minutes tilt vessel gently, do not shake it.

If the blood is still liquid then the patient has incoagulable blood (clot test +).

Clot test +: repeat 6 hourly, to test for the requirement of repeat doses of ASV.

(17)

Clinical features

Local features :

fang marks ,

severe pain/burning

swelling and discolouration,

discharge/ bleeding from bite site blister formation,

(18)

Species: Signs and Symptoms

Signs/Symptoms and Potential Treatments

Cobra Krait Russell’s

Viper Saw Scaled Viper

Other Vipers Local pain/ Tissue

Damage Yes No Yes Yes Yes

Ptosis/Neurotoxicity Yes Yes Yes! NO No

Coagulation No No Yes Yes Yes

Renal Problems No No Yes NO Yes

Neostigmine &

Atropine Yes No? No? NO No

(19)

Fang marks Persistent bleeding from fang marks 40min after bite of pit viper

Blistering at site of bite

(20)

Systemic features

Krait,Cobra: Neurotoxicity

Pre-paralytic stage : Vomiting ,

Headache,

Paralytic stage :

Drooping eyelids

Difficulty in speaking/swallowing Difficulty in breathing

(21)
(22)

Systemic features

• – –

Viper : Haemotoxic

Generalised bleeding manifestations.

Epistaxis,

Hemoptysis,

Bleeding gums Hematuria

Purpuric spots Renal failure

Shock

(23)

Systemic features

Sea snake : Myotoxic

Muscle pain,

Muscle stiffness, Myoglobinuria

Urine output (Renal failure)

(24)

Management: First aid

Mnemonic “CARRY NO R.I.G.H.T.”

CARRY = just carry the victim. Do not allow to walk even for a short distance

No - Tourniquate

No - Electrotherapy

No – Cutting, suctioning

No - Pressure immobilization

No- Nitric oxide donor (Nitrogesic ointment/

Nitrate Spray)

No- washing the bite site with soap or any other solution

(25)

Management: First aid

R = Reassure the patient..

I = Immobilize in the same way as a fractured limb. Do not apply any

compression

G H = Get to Hospital Immediately. NO Traditional remedies

T = Tell the Doctor of any systemic

symptoms that manifest on the way of hospital.

(26)

PRESSURE IMMOBILISATION

Its purpose is to retard the movement of venom from bite site into circulation, thus buying time for the patient to reach

medical care.

(27)

Cont.

Be prepared to treat the shock and provide cardiopulmonary resuscitation (CPR).

Get the victim to the nearest secondary or tertiary care hospital where antivenom can be provided

(28)

DO NOTS IN FIRST AID

Do not apply a tourniquet.

Do not wash the bite site with soap or any other solution to remove the venom.

Do not make cuts or incisions on or near the bitten area.

Do not use electrical shock.

Do not freeze or apply extreme cold to the area of bite.

Do not apply any kind of potentially harmful herbal or folk remedy. .

(29)

Cont.

Do not attempt to suck out venom with your mouth.

Do not give the victim drink, alcohol or other drugs.

Do not attempt to capture, handle or kill the snake and patients should not be taken to quacks.

(30)
(31)

Management: specific measures

1.

2.

3.

Anti snake venom (ASV):

Indications:

Neurotoxicity Haemotoxicity Shock

Total required dose will be between 10 vials to 30 vials usually.

Any hypersensitivity reaction should be dealt with adrenaline, steroids and anti histaminics

Ventilatory support if respiratory distress Hemodialysis- may be required

(32)

Anti-snake venom (ASV)

Anti-snake venom (ASV)is the mainstay of treatment.

Antivenom is immunoglobulin [usually pepsin- refined F(ab’)2 fragment of whole IgG] purified

from the plasma of a horse, donkey or sheep that has been immunized with the venoms of one or more species of snake.

In India, polyvalent ASV, i.e. effective against all the four common species; Russell’s viper,

common cobra, common Krait and saw-scaled Viper and no monovalent ASVs are available

(33)

Antivenom treatment should be given as soon as it is indicated.

It may reverse systemic envenoming even when this has persisted for several days or, in the case of haemostatic abnormalities, for two or more weeks.

20WBCT done 6 hourly

It is, therefore, appropriate to give

antivenom for as long as evidence of the coagulopathy persists.

HOW LONG ASV CAN BE GIVEN?

(34)

ROUTE?

Freeze-dried (lyophilized) antivenoms are reconstituted,

usually with 10ml of sterile water for injection per ampoule.

Two methods of administration are recommended:

(1) Intravenous “push” injection: Reconstituted freeze-dried antivenom is given by slow intravenous injection(not more than 2 ml/minute).

(2) Intravenous infusion: Reconstituted freeze-dried

antivenom is diluted in approximately 5-10 ml of isotonic fluid per kg body weight) and is infused at a constant rate over a period of about one hour

Patients must be closely observed for at least one hour after starting intravenous antivenom administration, so that early anaphylactic antivenom reactions can be

detected and treated early with epinephrine(adrenaline)

(35)

Cont.

Local administration of ASV is not

recommended as it is extremely painful and can raise the intracompartmental pressure.

Intramuscular inj are not recommended because

Slow absorption by I/M route.

Bioavailability is poor, adequate plasma concentration not achieved

Pain at injection site and

Risk of haematoma formation

(36)

Anti-snake Venom Administration

INDICATIONS

Evidence of systemic toxicity.

Hemodynamic or respiratory instability

Hypotension, respiratory distress Hemotoxicity

Clinically significant bleeding or abnormal coagulation studies Neurotoxicity

Any evidence of toxicity usually beginning with CN abnormalities and progressing to descending

paralysis including diaphragm Evidence of local toxicity

Progressive soft tissue swelling

(37)

TEST DOSE

Anti-snake Venom Test Dose NOT recommended

Test doses have not been shown to be

predictive of anaphylactic reaction or late serum sickness.

(38)

DOSE of ASV

Total required dose will be between 10 vials to 30

vials usually, as each vial neutralizes 6mg of Russells Viper venom.

Starting with 10 vials ensures that there is sufficient ASV to neutralize the average amount of venom

injected and any remaining free flowing venom during the next 12 hours.

Even in the large study from south India, the amount of ASV exceeded 50 vials in some patients.

So decision of the treating physician is of utmost importance, because the guidelines may not be useful for all patients.

(39)

Response to initial dose of ASV

: If an adequate dose of appropriate antivenom has been administered, the following responses may be observed.

(a) General: The patient feels better. Nausea, headache and generalised

aches and pains may disappear very quickly. .

(b) Spontaneous systemic bleeding (e.g. from the gums): This usually stops within 15-30 minutes.

(c) Blood coagulability (as measured by 20WBCT): This is usually restored in 3-9 hours.

(d) In shocked patients: Blood pressure may increase within the first 30-60 minutes and arrhythmias such as sinus bradycardia may

resolve.

(e) Neurotoxic envenoming (cobra bites)

may begin to improve as early as 30 minutes after antivenom, but usually takes several hours.

(f) Active haemolysis may cease within a few hours and the urine returns to its normal colour

(40)

REPEAT DOSES

Criteria for giving more antivenom

Persistence or recurrence of blood incoagulability after 6 hours(measured by 20WBCT) or of bleeding after 1-2 hours.

Deteriorating neurotoxic or cardiovascular signs after 1-2 hours of administering intial dose of ASV Maximum dose of ASV is around 50 vials.

ASV should be administered over a period of 1hour.

(41)

In hemotoxic envenomation;

Once initial dose has been administered over one hour,

In patients who continue to bleed briskly, the dose of antivenom should be repeated within 1-2 hours.

20WBCT test every 6 hours

If positive, repeat dose of ASV.

This is based on the observation that, if a large dose of antivenom (more than enough to neutralize the venom procoagulant enzymes) is given initially, the time taken for the liver to restore coagulable levels of fibrinogen and other clotting factors is 3-9 hours This reflects the period the liver requires to restore clotting factors.

(42)

In Neurotoxic envenomation

Antivenom treatment alone cannot be relied

upon to save the life of a patient with bulbar and respiratory paralysis

Death may result from Aspiration,

Airway obstruction or Respiratory failure.

A clear airway must be maintained.

Once there is loss of gag reflex and pooling of secretions in the pharynx, failure of the cough reflex or respiratory distress, a cuffed

endotracheal tube or laryngeal mask airway should be inserted

(43)

Neostigmine test.

Should be performed in every patient with neurotoxic envenoming

Atropine sulphate (0.6 mg for adults; 50 μg/kg for children) or glycopyrronium is given by intravenous injection followed by neostigmine bromide by

intramuscular injection (0.5-2.5 mg for adults, 0.04 mg/kg for Children.)

The patient is observed over the next 30-60 minutes

(neostigmine) or 10-20 minutes (edrophonium) for signs of improved neuromuscular transmission.

Ptosis may disappear and ventilatory capacity (peak flow, FEV-1 or maximum expiratory pressure) may

improve.

If positive institute regular atropine & neostigmine.

(44)

Treatment of hypotension and shock

Snake bite causes of hypotension and shock.

Anaphylaxis Vasodilatation Cardiotoxicity Hypovolaemia

Antivenom reaction Respiratory failure

Acute pituitary and adrenal insufficiency Septicaemia

Treatment- a selective vasoconstrictor such as dopamine may be given by intravenous infusion, preferably into a

central vein (starting dose 2.5-5mcg/kg/minute).

(45)

Adverse reactions to anti-snake venom

Fear of potentially life threatening adverse

reactions causes reluctance amongst some to treat snakebite.

However, if handled early and with the primary drug of choice, these reactions are easily managed.

Patients should be monitored closely as there is evidence that many anaphylactoid reactions go unnoticed

(46)

Adverse reactions to anti-snake venom

At the first sign of any of the following:

Urticaria, itching, fever, shaking chills, nausea, vomiting, diarrhea,

abdominal cramps, tachycardia, hypotension, bronchospasm and angio- oedema:

1. ASV should be discontinued

2. 0.5 mg. of 1:1000 adrenaline should be given IM

The pediatric dose is 0.01 mg/kg body weight of adrenaline IM.

Evidence shows that adrenaline reaches necessary blood plasma levels in 8 minutes via the IM route, but up to 34 minutes in the subcutaneous route.

(47)

Treatment of adverse reactions to anti-snake venom

100 mg of hydrocortisone and 10 mg of H1 antihistamine will be administered IV.

The dose for children is 0.2 mg/kg of antihistamine IV and 2 mg/kg.

If after 10 to 15 minutes the patient’s condition has not improved or is worsening, second dose of 0.5 mg of adrenaline 1:1000 IM is given.

This can be repeated for a third and final occasion but in the vast majority of reactions, 2 doses of adrenaline will be sufficient.

(48)

Once the patient has recovered ASV can be restarted

Given slowly for 10-15 minutes (under close monitoring) Then the normal drip rate should be resumed

(49)

FOLLOW-UP

After discharge from hospital, victim should be followed.

If discharged within 24 hours, patient should be advised to return if there is any worsening of

symptoms such as bleeding, pain or swelling at the site of bite, difficulty in breathing, altered

sensorium, etc.

The patients should also be explained about

serum sickness which may manifest after 5–10 days

References

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