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Mantoux Skin Testing: Sivagamy Kumaresan

The Mantoux test, also known as the tuberculin skin test, involves injecting a small amount of purified protein derivative (PPD) into the skin to test for exposure to tuberculosis (TB). It is used to diagnose TB infection or determine if preventive treatment is needed. To perform the test, 0.1ml of PPD is injected intradermally on the forearm and the size of induration is measured 48-72 hours later. An induration of 5mm or more indicates a positive result for high-risk groups and 15mm or more for others. Factors like BCG vaccination or infection with other mycobacteria can cause false positives, while anergy or recent exposure can cause

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0% found this document useful (0 votes)
121 views25 pages

Mantoux Skin Testing: Sivagamy Kumaresan

The Mantoux test, also known as the tuberculin skin test, involves injecting a small amount of purified protein derivative (PPD) into the skin to test for exposure to tuberculosis (TB). It is used to diagnose TB infection or determine if preventive treatment is needed. To perform the test, 0.1ml of PPD is injected intradermally on the forearm and the size of induration is measured 48-72 hours later. An induration of 5mm or more indicates a positive result for high-risk groups and 15mm or more for others. Factors like BCG vaccination or infection with other mycobacteria can cause false positives, while anergy or recent exposure can cause

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EvaNatasha
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPTX, PDF, TXT or read online on Scribd
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Mantoux Skin

Testing

Sivagamy Kumaresan

1
THE MANTOUX TEST
 The Mantoux test is the standard method of
determining whether a person is infected
with Mycobacterium tuberculosis.

 The local skin reaction to Tuberculin Purified


Protein Derivative (PPD) injected into the skin is
used to assess the individual’s sensitivity to
tuberculin protein.
MANTOUX TEST
 The mantoux test is given to :

 Children aged 3 months to 6 years living


at high risk environments.

 Infants and children under six years of age


with a history of residence or prolonged
stay (more than three months) in a country
of high endemic.
MANTOUX TEST

 There is a history of TB in a
household contact in the
last five years.

 Thosewho have had close


contact with a person with
known TB.
Administering the Mantoux
test
 Tuberculin PPD RT 23 SSI, 2 T.U./0.1
ml, solution for injection:
 1 dose = 0.1 ml contains 0.04
microgram Tuberculin PPD.
 Store at 2°C -8°C, protected from
light
 1ml graduated syringe fitted with a
short bevel 26G (0.45x10mm)
needle
1TU/0.1 5TU/0.1ml
ml
Injection site
 The test is usually applied on
the middle third of the flexor
surface of the forearm, as a
reaction may be weaker near the
wrist or the elbow joint.
 It is usually applied on the left
forearm.
 Ensure adequate lighting.
 Select an area of healthy skin
which is free of muscle
margins, heavy hair, veins,
sores, or scars.
 Only visibly dirty skin needs to
be washed with soap and water
Qualitas
Procedure
1)Use a 1mL syringe to
aspirate out 0.1 mL
of PPD RT 23.

2) Inject the PPD


intradermally on the volar
surface of the forearm.
Position the syringe at a 10-
15° to the forearm and
insert just below the
epidermis (about 2 mm).
3)Remove the needle
quickly. Do not massage
or use dressing. A well-
defined bleb of 6-10mm in
diameter should be formed
if injected correctly. If the
bleb is <6mm, repeat the
process 2.5cm from the
first site.

4) Mark down the site, date


and time of injection, both
on the forearm and in
patient’s record.
5)After 48 to 72 hours, read
the test result by marking
down the transverse
diameter of induration, not
erythema, by Sokal’s
ballpoint method.

6) Measure the largest


transverse diameter of
induration and note down in
millimeters
(mm).
READING THE MANTOUX TEST
 The reaction should be
evaluated 48-72 hours
after the injection
 Only the induration,
which is a hard, dense,
raised formation, is
measured.
 The area of erythema
is not included in the
measurement.
 Measure the diameter
of the induration
using a plastic
flexible millimetre
(mm) ruler.
POSITIVE PPD REACTION

5 or more millimeters 10 or more millimeters 15 or more millimeters

An induration of 5 or more millimeters is An induration of 10 or more millimeters is An induration of 15 or more millimeters is


considered positive for considered positive for considered positive for

People with HIV infection Foreign-born persons People with no risk factors
for TB

Close contacts HIV-negative persons who


inject illicit drugs

People who have had TB People with certain


disease before medical conditions

People who inject illicit Children younger than 4


drugs and whose HIV years old
status is unknown

Qualitas
A healthy person whose immune
system is normal, induration
greater than or equal to 15 mm is
considered a positive skin test.
 In most cases, people who have a
very small reaction or no reaction
probably do not have TB
infection.
 Induration of less than 2 mm,
without blistering, is considered a
negative skin test.
FALSE PPD
REACTION

FALSE POSITIVE FALSE NEGATIVE


PPD REACTION PPD REACTION
False-Positive PPD Reactions
 Sometimes people who are not infected
with M. tuberculosis will have a positive
reaction to the PPD tuberculin skin test.
This is called a false-positive reaction.

 two most common reasons for false


positive PPD reactions are:-
 infection with nontuberculous
mycobacteria (mycobacteria other than
M. tuberculosis)
 vaccination with BCG (bacillus Calmette-
Gurin).

Qualitas
False-Positive PPD Reactions

However, the reaction is more likely to be


truly caused by TB infection if any of the
following are true:
o The reaction is large
o The person was BCG-vaccinated a long
time ago
o The person comes from an area of the
world where TB is common
o The person has been exposed to
someone with infectious TB disease
o The person's family has a history of TB
Qualitas
disease
False-Negative Reactions

 Some people have a negative reaction to


the tuberculin skin test even though they
have TB infection. These are called false-
negative reactions.
 False-negative reactions may be caused by
 Anergy-absence of the normal immune
response to a particular antigen or
allergen.
 Recent TB infection (within the past 10
weeks)
 Very young age (younger than 6 months
Qualitas
old)
Type of Reaction Possible Cause People at Risk Action to Take*
False-positive *Nontuberculous *People infected *Evaluate for TB
mycobacteria with nontuberculous disease if person
mycobacteria has TB symptoms
*BCG vaccination
*People vaccinated *Assess likelihood of
with BCG true TB infection

False-negative Anergy *HIV-infected *May do anergy


people, other testing
people with
weakened immune
Recent TB infection systems *Retest 10 weeks
*People infected after exposure to
with M. TB ended
Very young age tuberculosis within
the past 10 weeks *Retest when child
*Children younger is 6 months old and
than 6 months old 10 weeks after
exposure to TB
ended
ADVERSE EFFECT

 Anaphylactic reaction and foreign body


reaction
 Slight risk of having a severe reaction to the
test including swelling and redness of the
arm, particularly in people who have had TB
or been infected previously and in those who
have previously had the BCG vaccine
 Local reactions such as regional lymphangitis
and adenitis may also occur on rare
occasions.
CONTRAINDICATION

 severe reaction (e.g:necrosis, blistering,


anaphylactic shock, or ulcerations) to a previous
TST.
Care of the PPD Testing Solution

 Liquid PPD is sensitive to light and temperature and may


become unstable if held in plastic syringes.

 Should be stored in cool environment between 35 and


46 degrees Fahrenheit

 PPD vial should be dated upon opening, and the


remainder discarded after 30 days, regardless of
expiration date

 Syringes should not be prefilled in anticipation of


demand, but filled at time of need.
24

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