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Tetanus

Tetanus is a neurological disease caused by Clostridium tetani, characterized by muscle rigidity, spasms, and autonomic dysfunction, primarily affecting unvaccinated individuals. The disease is preventable through vaccination, with higher incidence rates in developing countries and among agricultural workers. Treatment includes wound management, antibiotics, toxin neutralization, and muscle spasm control, while prevention relies on active immunization starting in infancy.

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0% found this document useful (0 votes)
2 views29 pages

Tetanus

Tetanus is a neurological disease caused by Clostridium tetani, characterized by muscle rigidity, spasms, and autonomic dysfunction, primarily affecting unvaccinated individuals. The disease is preventable through vaccination, with higher incidence rates in developing countries and among agricultural workers. Treatment includes wound management, antibiotics, toxin neutralization, and muscle spasm control, while prevention relies on active immunization starting in infancy.

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shivanisakthi143
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Tetanus

Introduction
• Tetanus is a neurological disease characterized by an acute onset of
hypertonia, painful muscular contractions (usually of the muscles of
the jaw and neck), and generalized muscle spasms without other
apparent medical causes.
• Only vaccine preventable disease that is infectious but not contagious.
CAUSATIVE AGENT
• Caused by CLOSTRIDIUM TETANI
• Anaerobic
• Motile
• Gram positive bacilli
• Oval, colourless, terminal spores - tennis racket or drumstick shape.
• It is found worldwide in soil, in inanimate environment, in animal
faeces & occasionally human faeces.
EPIDEMIOLOGY
• Tetanus is an international health problem, as spores are ubiquitous. The
disease occurs almost exclusively in persons who are unvaccinated or
inadequately immunized.
• Entirely preventable disease by immunization
• More common in developing and under developing countries.
• More prevalent in industrial establishment, where agricultural workers are
employed.
• Tetanus neonatorum is common due to lack of MCH care.
• Tetanus is important endemic infection in India.
• Causative factors
• Hand washing
• Delivery practices
TRANSMISSION
• Tetanus is not transmitted from person to person. Infection occurs
when C. tetani spores are introduced into acute wounds from trauma,
surgeries and injections, or chronic skin lesions and infections.
• The incubation period of tetanus is usually between 3 and 21 days
(median 7 days).
• Shorter incubation periods (<7 days) along with delays in seeking
treatment are associated with fatal outcomes.
• Outbreaks of tetanus related to injuries associated with natural
disasters such as earthquakes and tsunamis have been documented
Host Factors
• Age : It is the disease of active age (5-40 years), New born baby, female
during delivery or abortion
• Sex : Higher incidence in males than females
• Occupation: Agricultural workers are at higher risk
• Rural -Urban difference: Incidence of tetanus in urban areas is much
lower than in rural areas
• Immunity : Herd immunity does not protect the individual
• Environmental and social factors: Unhygienic custom habits,
Unhygienic delivery practices
ROUTE OF ENTRY
• Apparently trivial injuries
• Animal bites/human bites
• Open fractures
• Burns
• Gangrene
• In neonates usually via infected umbilical stumps
• Abscess
• Parenteral drug abuse
CLINICAL FEATURES:
• IP : Time from injury to the first symptom.The median incubation
period is 7 days, and, for most cases (73%), incubation ranges from 3-
21 days.
• Period of onset : It is the time from first symptoms to the reflex
spasm.
• In general the further the injury site is from the central nervous
system, the longer the incubation period.
• The shorter the incubation period, the higher the chance of death.
• Triad of muscle rigidity, spasms & autonomic dysfunction
• Early symptoms are neck stiffness, sore throat and poor mouth opening.
• Patients with generalized tetanus present with trismus (ie, lockjaw) in
75% of cases.
• Other presenting complaints include stiffness, neck rigidity, dysphagia,
restlessness, and reflex spasms. Spasms usually continue for 3-4 weeks.
• Subsequently, muscle rigidity becomes the major manifestation. Rigid
Abdomen.
• Muscle rigidity spreads in a descending pattern from the jaw and facial
muscles over the next 24-48 hours to the extensor muscles of the limbs -
stiff proximal limb muscles & relatively sparing hand & feet.
• Risus sardonicus: Sustained contraction of facial musculature produces
a sneering grin expression known as risus sardonicus.
• Contraction of the muscles at the angle of mouth and frontalis
• Trismus (Lock Jaw): Spasm of Masseter muscles.
• Opisthotonus: Spasm of extensor of the neck, back and legs to form a
backward curvature.
• Muscle spasticity
• Poor cough, inability to swallow, gastric stasis all increase the risk of
aspiration. Respiratory failure continues to be a major cause of
mortality in developing countries, whereas severe autonomic
dysfunction causes most deaths in the developed world.
NEONATAL TETANUS
• Neonatal tetanus is defined by the World Health Organization (WHO)
as “an illness occurring in a child who has the normal ability to suck
and cry in the first 2 days of life but who loses this ability between
days 3 and 28 of life and becomes rigid and has spasms.”
• Children born to inadequately immunized mothers, after unsterile
treatment of umbilical stump.
• During first 2 weeks of life.
• Poor feeding , rigidity and spasms
• It is easily preventable by 2 tetanus toxoid injections and '5 cleans'
while conducting deliveries.
LOCAL TETANUS
• Uncommon form
• Manifestations are restricted to muscles near the wound.
• Cramping and twisting in skeletal muscles surrounding the wound -
local rigidity
• Prognosis - excellent
Diagnosis
• Diagnosis is done clinically based on the presence of trismus,
dysphagia, generalized muscular rigidity, and/or spasm.
• An assay for antitetanus IgG levels is not readily available. However, a
level of 0.01 IU/mL or greater in serum is generally considered
protective, making the diagnosis of tetanus less likely.
DIFFERENTIAL DIAGNOSIS
• Drug induced Dystonic Reactions e.g. Phenothiazines
• Strychnine poisoning
• Neuroleptic Malignant Syndrome, Serotonin syndrome
• Trismus d/t Peritonsillar Abscess/Dental infection
• Dislocations, Mandible
• Encephalitis, Meningitis
• Hysteria
• Hypocalcemia
• Rabies
• Seizure disorder (partial or generalized)
• Stroke, Hemorrhagic
• Stroke, ischemic (cephalic tetanus)
• Subarachnoid Hemorrhage
Treatment
• 1.Wound Management:
• Debridement: Surgical removal of necrotic tissue to reduce bacterial load.

• 2.Antibiotics:
• First-line: Metronidazole 500 mg IV q6–8h for 7–10 days
• Alternative: Penicillin G 2–4 million units IV q4–6h
• (Metronidazole preferred now because Penicillin may potentiate GABA antagonism
and worsen spasms).

• 3.Neutralization of Toxin:
• Human Tetanus Immunoglobulin (TIG):
• Dose: 3000–6000 units IM as a single dose (infiltrate part of the dose around the
wound if possible).
• If TIG unavailable → Equine antitoxin (20,000–100,000 units IV after test dose).
• 4. Control of Muscle Spasms:
• Benzodiazepines (drug of choice):
• Diazepam 10–40 mg IV every 1–4 hours or continuous infusion (0.1–0.3 mg/kg/hr).
• Alternative: Midazolam infusion (0.1–0.2 mg/kg/hr).
• Severe spasms or rigidity:
• Neuromuscular blockade with agents like vecuronium or pancuronium + mechanical ventilation.

• 5.Supportive Care:
• ICU care: Required for most moderate-to-severe cases.
• Airway management: Endotracheal intubation or tracheostomy may be necessary in severe
cases.
• Nutrition: High caloric requirements (40–50 kcal/kg/day) due to hypermetabolic state. Enteral
feeding preferred.
• Autonomic dysfunction management:
• Labetalol or magnesium sulfate infusion for sympathetic overactivity.
Prevention
• Tetanus is completely preventable by active tetanus immunization.
• Immunization is thought to provide protection for 10 years.

• Begins in infancy with the DTP series of shots. The DTP vaccine is a "3-
in-1" vaccine that protects against diphtheria, pertussis, and tetanus.
Active Immunization
A - has had a complete course of toxoid or booster dose with in
the past 5 year
B - has had a complete course of toxoid or booster dose more
then 5 years ago & less then 10 years ago
C - has had a complete course of toxoid or a booster dose more
then 10 year ago
D - has not had a complete course of toxoid or immunity status
unknown

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