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Presentor : Dr. kailash mittal
Moderator : Dr. M LTak sir
Dr. Neelam mam
HUMIDIFIER AND SCAVENGING
SYSTEM
Humidifiers
Humidification is a method to artificially condition the gas used
in respiration of a patient as a therapeutic modality.
Active method is by adding heat or water or both to the device &
passive which is recycling heat and humidity which is exhaled by
the patient.
Indications of Humidification
Primary:
Overcoming humidity deficit created when upper
airway is bypassed
To humidify dry medical gases
Secondary:
To manage hypothermia
To treat bronchospasm caused by cold air
Clinical signs and symptoms of
inadequate humidification
Dry and non-productive cough
Atelectasis
Increased airway resistance
Increased work of breathing
Increased incidence of infection
Thick and dehydrated secretions
Complaints of substernal pain and airway dryness
Physiology
Heat and moisture exchange is a primary function of the
upper respiratory tract, mainly the nose.
The nasal mucosal lining is kept moist by secretions from
mucous glands, goblet cells, transudation of fluid through
cell walls, and condensation of exhaled humidity.
As the inspired air enters the nose, it warms (convection) and
picks up water vapour from the moist mucosal lining
(evaporation).
Condensation occurs on the mucosal surfaces during
exhalation, and water is reabsorbed by the mucus .
The mouth is less effective at heat and moisture exchange
than the nose because of the low ratio of gas volume to moist
and warm surface area and the less vascular squamous
epithelium lining of oropharynx and hypopharynx.
As inspired gas moves into the lungs, it achieves BTPS conditions
(body temperature, 37° C; barometric pressure; saturated with
water vapor [100% relative humidity )
This point, normally approximately 5 cm below the carina, is
called the isothermic saturation boundary (ISB).
Above the ISB, temperature and humidity decrease during
inspiration and increase during exhalation.
Below the ISB, temperature and relative humidity remain
constant (BTPS).
The ISB shifts distally :- when a person breathes through the
mouth rather than the nose; when the person breathes cold, dry
air; when the upper airway is bypassed (breathing through an
artificial tracheal airway); or when the minute ventilation is
higher than normal.
When this shift of ISB occurs, additional surfaces of the airway
are recruited to meet the heat and humidity requirements of the
lung.
These shifts of the ISB can compromise the body’s normal heat
and moisture exchange mechanisms, and humidity therapy is
indicated.
Principles of humidifier
function
Temperature – As the temperature of a gas increases, its ability
to hold water vapour (capacity) increases .
Surface area – There is more opportunity for evaporation to
occur with greater surface area of contact between water and gas.
Time of contact – There is greater opportunity for evaporation
to occur, when a gas remains in contact with water for longer
duration .
Method of humidification
HumidifiersHumidifiers ––
a. Passive (Heat and Moisturea. Passive (Heat and Moisture
Exchangers/ HMEs) – hydrophobic/Exchangers/ HMEs) – hydrophobic/
hygroscopichygroscopic
b. Active – unheated/ heatedb. Active – unheated/ heated
NebulizersNebulizers
PASSIVE HUMIDIFIERS
Simplest designs are Heat and Moisture Exchangers
(HMEs)
Also called as condenser humidifier, artificial nose,
Swedish nose, nose humidifier, regenerative humidifier,
vapor condenser
Disposable devices that trap some exhaled water and
heat, and deliver them to patient on subsequent
inhalation (minimize water and heat loss)
When combined with a filter for bacteria and viruses 
called Heat and Moisture Exchanging Filter (HMEF)
particularly important when ventilating patients with
respiratory infections or compromised immune system
Exchanging medium enclosed
in plastic housing
Vary in size, shape, dead
space, pediatric and neonatal
HMEs with low dead space
available
May have a port to attach
gas sampling line for
respiratory gas monitor
Placed between ET tube and
breathing circuit
Hydrophobic HMEs –
1.1. Hydrophobic membrane with smallHydrophobic membrane with small
pores, pleated to increase surfacepores, pleated to increase surface
areaarea
2.2. Allow passage of water vapour but notAllow passage of water vapour but not
liquid water at usual ventilatoryliquid water at usual ventilatory
pressurespressures
3.3. Efficient bacterial and viral filtersEfficient bacterial and viral filters
4.4. Performance may be impaired by highPerformance may be impaired by high
ambient temperaturesambient temperatures
Hygroscopic HMEs
Contain low thermal conductivity wool ,foam or paper like material
coated with lithium chloride or calcium – to recollect the moisture
In exhaletion: some vapour will condense and the rest will absorbed by
hygroscopic salt
Inspiration: the low water pressure in the inspired air cause released the water
molecule direct from hygroscopic salt
high efficiency compare to hydrophobic HMEs
approximately 70% efficiency that is 40 mg/l on exhaled, 27 mg/L on return
TypeType HygroscopicHygroscopic HydrophobicHydrophobic
Heat and moistureHeat and moisture
exchanging efficiencyexchanging efficiency
ExcellentExcellent GoodGood
Effect of increased tidalEffect of increased tidal
volume on HMEvolume on HME
efficiencyefficiency
Slight decreaseSlight decrease Significant decreaseSignificant decrease
Filtration efficiencyFiltration efficiency
when drywhen dry
GoodGood ExcellentExcellent
Filtration efficiencyFiltration efficiency
when wetwhen wet
PoorPoor ExcellentExcellent
Resistance when wetResistance when wet SignificantlySignificantly
increasedincreased
Slightly increasedSlightly increased
Effect of nebulisedEffect of nebulised
medicationsmedications
Greatly increasedGreatly increased
resistanceresistance
Little effectLittle effect
 ideal HME should operate at 70% efficiency or better providing at least
30 mg/L water vapour.
Advantage:
 inexpensive
 easy to use
 Small and lightweight
 silent in operations
 do not required water, temperature monitor, alarms
 No burns, no danger of over hydrations and electric shock.
Disadvantages:
 less effective than active humidifiers
 can deliver only limited humidity
 increased in dead space (Boots et al 2006)
 Need change the HME every 24(Boots et al 1993) or 48(Djedaini et al
1995)
Contraindications
For patients with thick, copious, or bloody secretions
For patients with an expired tidal volume less than 70%
of the delivered tidal volume (e.g., patients with large
bronchopleural fistulas or incompetent or absent
endotracheal tube cuffs)
 For patients whose body temperature is less than 32° C
For patients with high spontaneous minute volumes
(>10 L/min)
ACTIVE HUMIDIFIERS
Add water to gas by passing the gas over a water
chamber (passover humidifier) or through a
saturated wick (wick humidifier), bubbling it
through water (bubble-through humidifier), or
mixing it with vaporized water (vapour-phase
humidifier)
Unlike passive humidifiers, they do not filter
respiratory gases
2 types –
1. Unheated
2. Heated
UNHEATED HUMIDIFIERS
 bubble-through devices used to increase humidity
in oxygen supplied to patients via facemask or
nasal canula
Simple containers containing distilled water through
which oxygen is passed and it gets humidified
Maximum humidity that can be achieved is 9mg
H2O/L
HEATED HUMIDIFIERS
Incorporate a device to warm water in the
humidifier, some also heat inspiratory tube
content -
Humidification chamber – transparent (easy to
check water level) contains liquid water,
disposable/ reusable
Heat source – heated rods immersed in water or
plate at bottom of humidification chamber
Inspiratory tube – conveys humidified gas from
humidifier outlet to patient
 If unheated  gas will cool and lose some of its
moisture as it travels to the patient, water trap necessary to
collect condensed water
 Heated or insulated  more precise control of
temperature and humidity delivered to patient, avoids
moisture rainout
Temperature monitor – to measure gasto measure gas
temperature at patient end of breathing systemtemperature at patient end of breathing system
Thermostat device
1.1.Servo-controlled unitsServo-controlled units – automatically regulates– automatically regulates
power to heating element in response topower to heating element in response to
temperature sensed by a probe near patienttemperature sensed by a probe near patient
connection/ humidifier outlet, these deviceconnection/ humidifier outlet, these device
equipped with alarmequipped with alarm
2.2.Nonservo-controlled unitsNonservo-controlled units – provides power to– provides power to
heating element according to setting of a control,heating element according to setting of a control,
irrespective of delivered temperatureirrespective of delivered temperature
Controls – most humidifier allow temperature selection at end ofmost humidifier allow temperature selection at end of
delivery tube or at humidification chamber outletdelivery tube or at humidification chamber outlet
AlarmsAlarms alarm may warn when temp. at patient end of the circuitalarm may warn when temp. at patient end of the circuit
deviates from set temp , when displacement of temperature probe,deviates from set temp , when displacement of temperature probe,
disconnection of heater wire, low water level in humidificationdisconnection of heater wire, low water level in humidification
chamber, faulty airway temperature probe , lack of gas flow in thechamber, faulty airway temperature probe , lack of gas flow in the
circuitcircuit
In circle system, heated humidifier is placed in the
inspiratory limb downstream of unidirectional valve
by using an accessory breathing tube
Must not be placed in the expiratory limb
Filter, if used, must be placed upstream of
humidifier to prevent it from becoming clogged
In Mapleson systems, humidifier is usually placed in
fresh gas supply tube
Humidifier must be lower than patient to avoid risk
of water running down the tubing into the patient
Condensate must be drained periodically & a water
trap inserted in the most dependent part of the
tubing to prevent blockage or aspiration
Heater wire in delivery tube should not be bunched,
but strung evenly along length of tube
Delivery tube should not rest on other surfaces or
be covered with sheets, blankets, or other
materials; a boom arm or tube tree may be used
for support
AdvantagesAdvantages ––
1.Capable of delivering saturated gas at body
temperature or above, even with high flow rates
2.More effective humidification than an HME
DisadvantagesDisadvantages ––
1.Bulky and somewhat complex
2.Involve high maintenance costs, electrical hazards,
and increased work (temperature control, refilling
the reservoir, draining condensate, cleaning, and
sterilization)
3.Offers relatively little protection against heat loss
during anesthesia as compared to circulating water
and forced-air warming
Assessment of need
Either an HME or an HH can be used to condition inspired
gases:
HMEs are better suited for short-term use (≤96 hours) and
during transport.
HHs should be used for patients requiring long-term
mechanical ventilation (>96 hours) or for patients for whom
HME use is contraindicated.
NebulizerNebulizer
 Produces and disperses liquid particles in a gas stream or
aerosol mist
 Use - produce humidification & deliver drug such as
bronchodilator, mucolytic agent and decongestant
 Size of the water droplet is between 0.5 to 5µm
 Particles more than 5µm unable to reach the peripheral
airways
 Particles less 0.5µm is very light, and will come back with
expired gases without being deposited in airways
 2 types of nebulizer
 pneumatic Nebulizers
 Ultrasonic nebulizers.
 pneumatic nebulizers
 Works: by forced a jet of high-pressure
gas into a liquid - inducing shearing
forces - breaking the water up into fine
water particles
 produces particles of size 5 to 30 µm
 only 30 to 40% of particles produced
are in optimal range
 Most of the particles get deposited in
wall of main airways
Ultrasonic nebulizer
 used piezoeeletric crystal
 Works:
Crystal transducer converts: radio waves
into high-frequency mechanical
vibrations
vibration is transmitted to the water
surface
The high mechanical energy creates
cavitation in the fluid
it formed a standing wave which will
disperses liquid particles
 Frequency of oscillation determines the
size of the water particles
 Aerosol size of 1 to 10 µm
 95% of particles produced are in optimal range
 Particles deposited directly in airway
 Very effective for deliver bronchodilator
Hazards from nebulizer:
cause over hydrations
Hypothermia
Infection can be transmitted
edema of the airway wall
Advantages and disadvantages
of nebulizer
Advantages
It can carry air that fully saturated with water vapor without
heat.
We can increase the amount of the water vapor in the inhaled
air.
Disadvantage
The pneumatic nebulizer needs high air flow to operate.
The ultrasonic nebulizer need electric supply to operate thus it
may cause electric shock
SCAVENGING SYSTEM
INTRODUCTION :
 scavenging is the collection and subsequent removal of waste
anesthetic gases from both the anesthesia machine and the
anesthetising location.
Trace level of an anesthetic gas is a conc. far below that
needed for clinical anesthesia or can be detected by smell
Trace gases conc. depending on FGF, ventilation system , the
length of time of anesthesia, anesthetic technique and other
variables
Trace gas level expressed in parts per million (ppm)
Problems attributed to trace gases
Spontaneous abortions :
Higher rates of spontaneous abortion in OR personnel than
in women in other settings.
Infertility : Studies found higher than expected rates of
involuntary infertility among exposed
Impaired Skilled performance : one study showed that
neuropsychological symptoms and tiredness were reported
more by individuals in OR that are less scavenged
Birth Defects : Studies in human found increase in congenital
abnormalities in children of exposed personnel
Carcinogenicity : A large study found higher risk of cancer in
females than males who are exposed, but data has been
questioned.
Liver disease : recurrent hepatitis – halothane reported in
few individuals
Renal Disease
Hematological : higher rate of leukamia.
Cardiac Disease : higher Freq of HTN and
dysrrthythmias
In 1977 National Institute for
Occupational Safety and Health
(NIOSH) –
recommended exposure limits for
trace gas level (nitrous oxide and
halogenated agent )
anesthetic
gas
Max. TWA
conc.[ppm]
Halogenated
agent alone
2
Nitrous
oxide alone
25
Halogenated
gas +nitrous
oxide
0.5 + 25
Dental
facilities[nitr
ous oxide
alone]
50
The 2 major causes of waste gas contamination in the
O.R :
 Equipment failure or lack of understanding of proper
equipment
 The anesthetic technique used -
 Failure to turn off gas flow control valve and vaporizers when
the circuit is disconnected from the patient.
 use poorly fitting masks.
 Flushing of circuit in room.
 Using uncuffed endotracheal tubes that do not create a
completely sealed airway or using cuffed tubes without
inflating the cuff
Spilling liquid anesthetic during the filling of vaporizers.
Use of breathing circuits other than circle system
The use of scavenging devices with anesthesia delivery systems
is the most effective way to decrease waste anesthetic gases.
An efficient scavenging system is capable of reducing ambient
concentrations of waste gases by up to 90%.
Components of the scavenger system:
Gas collection assembly.
Transfer tubing.
Scavenging interface .
Gas disposal tubing .
Gas disposal assembly.
1.Gas collecting assembly
Captures excess anesthetic gases and delivers it to the transfer
tubing.
WAG are vented from anesthesia system through either
adjustable pressure limiting valve or ventilator relief valve.
Conventional machine have seprate outlet port for these valve
however newer have only one
 some anesthetic workstations may also exhaust the ventilator
drive gas in to scavenging system
2.Transfer tubing
The transfer tubes carries excess gas from gas collecting assembly to
scavenging interface.
The tubes must have 30 mm connectors on either end, sometimes yellow
color-coded .
The tubes should be sufficiently rigid to prevent kinking and as short as
possible to minimize the chance of occlusion.
Separate tubes from the APL valve and ventilator relief valve merge into a
single hose before they enter scavenging interface.
If the transfer tube is occluded, baseline breathing circuit pressure will
increase and barotrauma can occur.
3.Scavenging interface
The scavenger interface is the most important component because it
protects the breathing circuit or ventilator from excess positive or
negative pressure.
 the interface should limit pressure between -.5 and 3.5 cm of h2o under
normal working condition.
Positive-pressure relief is mandatory, irrespective of the type of disposable
system (active or passive) used, to vent excess gas in case of occlusion
distal to interface.
 negative pressure relief will be necessary in active disposable system to
protect breathing circuit or ventilator from subatmospheric pressure .
scavenger interfaces may be open
closed
OPEN INTERFACE:
It contains no valves and is open to
the atmosphere, allowing positive
and negative pressure relief.
Open interfaces should be used
only with active disposable systems
that have a central evacuation
system.
 open interfaces require a
reservoir because waste gases are
intermittently discharged in surges
whereas flow from the evacuation
system is continuous.
The efficiency of it depends on several factors:
A.The vacuum flow rate per min must equal or exceed the
minute volume of excess gases to prevent spillage.
B.Spillage will occur if the volume of a single exhaled
breath exceeds the capacity of reservoir.
Open interfaces
are safer for the patients.
CLOSED INTERFACE:
It communicates with the atmosphere through valves.
Two types of closed interfaces are commercially available:
 positive pressure relief only
 positive and negative pressure relief
POSITIVE PRESSURE RELIEF ONLY:
 It has a single positive pressure relief valve and is designated to be used
only with passive disposable systems.
Transfer of the waste gas from the interface to the disposable system
relies on the slight positive pressure of the waste gases leaving the patient’s
breathing system, because a negative pressure evacuation system is not
used.
In this system reservoir bag is not required.
POSITIVE AND NEGATIVE PRESSURE RELIEF:
 It has positive and negative pressure relief valve in addition to a reservoir
bag.
It is used with active disposable systems.
The effectiveness of a closed system in preventing spillage depends on:
the rate of waste gas inflow
the evacuation flow rate
the size of the reservoir
Leakage occurs only when the reservoir bag becomes fully inflated and
pressure increases sufficiently to open the positive pressure relief valve .
4.Gas disposal tubing
The gas disposable tubing conducts waste gas from the Scavenging
interface to the gas disposable assembly.
It should be collapse proof and should run overhead, if possible to
minimize the chance of accidental occlusion.
Connection to an active gas disposable system should be DISS type
connector
5.Gas disposal assembly
It ultimately eliminates excess waste gas.
It is of two types:
 Active
 Passive
Active assembly:
most commonly used. It uses central evacuation system.
A vacuum pump serves as mechanical flow inducing device that removes
the waste gases.
An interface with a negative pressure relief valve is mandatory because
the pressure within the system is negative.
Central evacuations are
- Piped Vacuum - central vaccum system
- Active duct system - employs flow inducing devices (fans ,
pumps , blowers etc..) to move large volume of gas at low
pressures
Advantages
 Convenient in large hospitals, where many machines are in use in
different locations
More effective at keeping pollution low level because most leaks will
be inward
Disadvantages
  Vacuum system and pipe work is a major expense 
 not a automatic must be turn ON and OFF
Passive disposable system:
 does not use a mechanical flow inducing device.
 anesthetic gases flow through the system by the pressure raised
above atmospheric by the patient exhaling, by manually
squeezing the reservoir beg , or by ventilator
Positive pressure relief is mandatory, but a negative pressure
relief and reservoir are not.
types
- Room ventilation system
- Recirculating or nonrecirculating
- Piping direct to atmosphere
- Adsorption devices
- Catalyst decomposition
 use activated charcoal or zeolite
connected to the outlet of the
scavenging system
removes halogenated anesthetics but
not nitrous oxide
These are simple and portable
Halogenated gases not release to
atmosphere (decrease green house
effect)
Adsorption device
Disadvantages
They are fairly expensive and are effective for short period of
time
  replaced regularly and pose to storage and disposal
problem
  Does not remove nitrous oxid
Catalytic Decomposition :
Catalytic decomposition can be used to convert nitrous oxide
to nitrogen and oxygen, reducing its contribution to the
greenhouse effect
Evaluation of Anesthetic Equipment
Each piece of equipment involved in the delivery of inhalant
anesthetics should be evaluated regularly to assure its function and
integrity.
Procedures for checkout of anesthesia equipment, depending
on the equipment to be used, should include the following:
Status of the high-pressure system, including the oxygen
supply and nitrous oxide supply - The nitrous oxide supply
should not leak when the cylinder valve is on and the nitrous oxide
flowmeter is off.
 Status of the low-pressure system (flowmeter function) - A
negative-pressure leak test should be performed at the common gas
outlet or the outlet of the vaporizer immediately upstream from the
breathing system.
Status of the breathing system - An appropriate leak test for a
circle system and Noncircle systems should be done. The quantity
of leakage can be measured by determining the flow rate of oxygen
necessary to maintain a constant pressure in the system, and the
leak rate should be less than 300 ml/min at 30 cm of h2O.
Status of the scavenging system - The scavenging system should
be properly attached at all connectors, and the appropriate vacuum
should be assured for active systems. If charcoal canisters are
employed for scavenging, they should be changed at appropriate
intervals.
Monitoring of the Effectiveness of
Antipollution Techniques
Monitoring trace-gas concentrations in the workplace provides a
quantitative assessment of the effectiveness of a waste-gas control
program.
An air-monitoring program is most appropriately started after anesthesia
delivery systems have been equipped with scavenging systems and after
other techniques for minimizing waste gas pollution are in place.
 An ideal approach would include frequent air monitoring, at least
semiannual evaluations.
Equipment for determining trace gas conc.
infrared analyzer , dosimeter . Ionizing leak detector
Effectiveness
Unscavenged operating rooms show 10-70 ppm halothane, and
400-3000 ppm N2O.
 scavenging brings these levels down to 1 and 60 ppm
respectively.
 Adding careful attention to leaks and technique can yield levels
as low as 0.005 and 1 ppm.
HAZARDS
Scavenging system functionally extends the anesthesia circuit all the way
from the anesthesia machine to the disposable site.
Obstruction of scavenging pathway can cause excessive positive pressure in
the breathing circuit and barotrauma can occur.
 excessive vacuum applied can result in undesirable negative pressures
within breathing system.
Loss of Monitoring Input – it may mask the strong odor of a volatile
anesthetic agent, delaying recognition of an overdose
Alarm failure – neg. pressure from the scavenging system interface prevent
the bellows from collapsing when breathing system is disconnected & Low
airway pressure alarm not activated.
THANK U….THANK U….

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Humidifier & scavenging system

  • 1. Presentor : Dr. kailash mittal Moderator : Dr. M LTak sir Dr. Neelam mam HUMIDIFIER AND SCAVENGING SYSTEM
  • 2. Humidifiers Humidification is a method to artificially condition the gas used in respiration of a patient as a therapeutic modality. Active method is by adding heat or water or both to the device & passive which is recycling heat and humidity which is exhaled by the patient.
  • 3. Indications of Humidification Primary: Overcoming humidity deficit created when upper airway is bypassed To humidify dry medical gases Secondary: To manage hypothermia To treat bronchospasm caused by cold air
  • 4. Clinical signs and symptoms of inadequate humidification Dry and non-productive cough Atelectasis Increased airway resistance Increased work of breathing Increased incidence of infection Thick and dehydrated secretions Complaints of substernal pain and airway dryness
  • 5. Physiology Heat and moisture exchange is a primary function of the upper respiratory tract, mainly the nose. The nasal mucosal lining is kept moist by secretions from mucous glands, goblet cells, transudation of fluid through cell walls, and condensation of exhaled humidity. As the inspired air enters the nose, it warms (convection) and picks up water vapour from the moist mucosal lining (evaporation).
  • 6. Condensation occurs on the mucosal surfaces during exhalation, and water is reabsorbed by the mucus . The mouth is less effective at heat and moisture exchange than the nose because of the low ratio of gas volume to moist and warm surface area and the less vascular squamous epithelium lining of oropharynx and hypopharynx.
  • 7. As inspired gas moves into the lungs, it achieves BTPS conditions (body temperature, 37° C; barometric pressure; saturated with water vapor [100% relative humidity ) This point, normally approximately 5 cm below the carina, is called the isothermic saturation boundary (ISB). Above the ISB, temperature and humidity decrease during inspiration and increase during exhalation. Below the ISB, temperature and relative humidity remain constant (BTPS).
  • 8. The ISB shifts distally :- when a person breathes through the mouth rather than the nose; when the person breathes cold, dry air; when the upper airway is bypassed (breathing through an artificial tracheal airway); or when the minute ventilation is higher than normal. When this shift of ISB occurs, additional surfaces of the airway are recruited to meet the heat and humidity requirements of the lung. These shifts of the ISB can compromise the body’s normal heat and moisture exchange mechanisms, and humidity therapy is indicated.
  • 9.
  • 10.
  • 11. Principles of humidifier function Temperature – As the temperature of a gas increases, its ability to hold water vapour (capacity) increases . Surface area – There is more opportunity for evaporation to occur with greater surface area of contact between water and gas. Time of contact – There is greater opportunity for evaporation to occur, when a gas remains in contact with water for longer duration .
  • 12. Method of humidification HumidifiersHumidifiers –– a. Passive (Heat and Moisturea. Passive (Heat and Moisture Exchangers/ HMEs) – hydrophobic/Exchangers/ HMEs) – hydrophobic/ hygroscopichygroscopic b. Active – unheated/ heatedb. Active – unheated/ heated NebulizersNebulizers
  • 13. PASSIVE HUMIDIFIERS Simplest designs are Heat and Moisture Exchangers (HMEs) Also called as condenser humidifier, artificial nose, Swedish nose, nose humidifier, regenerative humidifier, vapor condenser Disposable devices that trap some exhaled water and heat, and deliver them to patient on subsequent inhalation (minimize water and heat loss) When combined with a filter for bacteria and viruses  called Heat and Moisture Exchanging Filter (HMEF) particularly important when ventilating patients with respiratory infections or compromised immune system
  • 14. Exchanging medium enclosed in plastic housing Vary in size, shape, dead space, pediatric and neonatal HMEs with low dead space available May have a port to attach gas sampling line for respiratory gas monitor Placed between ET tube and breathing circuit
  • 15. Hydrophobic HMEs – 1.1. Hydrophobic membrane with smallHydrophobic membrane with small pores, pleated to increase surfacepores, pleated to increase surface areaarea 2.2. Allow passage of water vapour but notAllow passage of water vapour but not liquid water at usual ventilatoryliquid water at usual ventilatory pressurespressures 3.3. Efficient bacterial and viral filtersEfficient bacterial and viral filters 4.4. Performance may be impaired by highPerformance may be impaired by high ambient temperaturesambient temperatures
  • 16. Hygroscopic HMEs Contain low thermal conductivity wool ,foam or paper like material coated with lithium chloride or calcium – to recollect the moisture In exhaletion: some vapour will condense and the rest will absorbed by hygroscopic salt Inspiration: the low water pressure in the inspired air cause released the water molecule direct from hygroscopic salt high efficiency compare to hydrophobic HMEs approximately 70% efficiency that is 40 mg/l on exhaled, 27 mg/L on return
  • 17. TypeType HygroscopicHygroscopic HydrophobicHydrophobic Heat and moistureHeat and moisture exchanging efficiencyexchanging efficiency ExcellentExcellent GoodGood Effect of increased tidalEffect of increased tidal volume on HMEvolume on HME efficiencyefficiency Slight decreaseSlight decrease Significant decreaseSignificant decrease Filtration efficiencyFiltration efficiency when drywhen dry GoodGood ExcellentExcellent Filtration efficiencyFiltration efficiency when wetwhen wet PoorPoor ExcellentExcellent Resistance when wetResistance when wet SignificantlySignificantly increasedincreased Slightly increasedSlightly increased Effect of nebulisedEffect of nebulised medicationsmedications Greatly increasedGreatly increased resistanceresistance Little effectLittle effect
  • 18.  ideal HME should operate at 70% efficiency or better providing at least 30 mg/L water vapour. Advantage:  inexpensive  easy to use  Small and lightweight  silent in operations  do not required water, temperature monitor, alarms  No burns, no danger of over hydrations and electric shock.
  • 19. Disadvantages:  less effective than active humidifiers  can deliver only limited humidity  increased in dead space (Boots et al 2006)  Need change the HME every 24(Boots et al 1993) or 48(Djedaini et al 1995)
  • 20. Contraindications For patients with thick, copious, or bloody secretions For patients with an expired tidal volume less than 70% of the delivered tidal volume (e.g., patients with large bronchopleural fistulas or incompetent or absent endotracheal tube cuffs)  For patients whose body temperature is less than 32° C For patients with high spontaneous minute volumes (>10 L/min)
  • 21. ACTIVE HUMIDIFIERS Add water to gas by passing the gas over a water chamber (passover humidifier) or through a saturated wick (wick humidifier), bubbling it through water (bubble-through humidifier), or mixing it with vaporized water (vapour-phase humidifier) Unlike passive humidifiers, they do not filter respiratory gases 2 types – 1. Unheated 2. Heated
  • 22. UNHEATED HUMIDIFIERS  bubble-through devices used to increase humidity in oxygen supplied to patients via facemask or nasal canula Simple containers containing distilled water through which oxygen is passed and it gets humidified Maximum humidity that can be achieved is 9mg H2O/L
  • 23.
  • 24. HEATED HUMIDIFIERS Incorporate a device to warm water in the humidifier, some also heat inspiratory tube content - Humidification chamber – transparent (easy to check water level) contains liquid water, disposable/ reusable Heat source – heated rods immersed in water or plate at bottom of humidification chamber
  • 25. Inspiratory tube – conveys humidified gas from humidifier outlet to patient  If unheated  gas will cool and lose some of its moisture as it travels to the patient, water trap necessary to collect condensed water  Heated or insulated  more precise control of temperature and humidity delivered to patient, avoids moisture rainout
  • 26. Temperature monitor – to measure gasto measure gas temperature at patient end of breathing systemtemperature at patient end of breathing system Thermostat device 1.1.Servo-controlled unitsServo-controlled units – automatically regulates– automatically regulates power to heating element in response topower to heating element in response to temperature sensed by a probe near patienttemperature sensed by a probe near patient connection/ humidifier outlet, these deviceconnection/ humidifier outlet, these device equipped with alarmequipped with alarm 2.2.Nonservo-controlled unitsNonservo-controlled units – provides power to– provides power to heating element according to setting of a control,heating element according to setting of a control, irrespective of delivered temperatureirrespective of delivered temperature
  • 27. Controls – most humidifier allow temperature selection at end ofmost humidifier allow temperature selection at end of delivery tube or at humidification chamber outletdelivery tube or at humidification chamber outlet AlarmsAlarms alarm may warn when temp. at patient end of the circuitalarm may warn when temp. at patient end of the circuit deviates from set temp , when displacement of temperature probe,deviates from set temp , when displacement of temperature probe, disconnection of heater wire, low water level in humidificationdisconnection of heater wire, low water level in humidification chamber, faulty airway temperature probe , lack of gas flow in thechamber, faulty airway temperature probe , lack of gas flow in the circuitcircuit
  • 28.
  • 29.
  • 30. In circle system, heated humidifier is placed in the inspiratory limb downstream of unidirectional valve by using an accessory breathing tube Must not be placed in the expiratory limb Filter, if used, must be placed upstream of humidifier to prevent it from becoming clogged In Mapleson systems, humidifier is usually placed in fresh gas supply tube
  • 31. Humidifier must be lower than patient to avoid risk of water running down the tubing into the patient Condensate must be drained periodically & a water trap inserted in the most dependent part of the tubing to prevent blockage or aspiration Heater wire in delivery tube should not be bunched, but strung evenly along length of tube Delivery tube should not rest on other surfaces or be covered with sheets, blankets, or other materials; a boom arm or tube tree may be used for support
  • 32. AdvantagesAdvantages –– 1.Capable of delivering saturated gas at body temperature or above, even with high flow rates 2.More effective humidification than an HME
  • 33. DisadvantagesDisadvantages –– 1.Bulky and somewhat complex 2.Involve high maintenance costs, electrical hazards, and increased work (temperature control, refilling the reservoir, draining condensate, cleaning, and sterilization) 3.Offers relatively little protection against heat loss during anesthesia as compared to circulating water and forced-air warming
  • 34. Assessment of need Either an HME or an HH can be used to condition inspired gases: HMEs are better suited for short-term use (≤96 hours) and during transport. HHs should be used for patients requiring long-term mechanical ventilation (>96 hours) or for patients for whom HME use is contraindicated.
  • 35.
  • 36. NebulizerNebulizer  Produces and disperses liquid particles in a gas stream or aerosol mist  Use - produce humidification & deliver drug such as bronchodilator, mucolytic agent and decongestant  Size of the water droplet is between 0.5 to 5µm  Particles more than 5µm unable to reach the peripheral airways  Particles less 0.5µm is very light, and will come back with expired gases without being deposited in airways  2 types of nebulizer  pneumatic Nebulizers  Ultrasonic nebulizers.
  • 37.  pneumatic nebulizers  Works: by forced a jet of high-pressure gas into a liquid - inducing shearing forces - breaking the water up into fine water particles  produces particles of size 5 to 30 µm  only 30 to 40% of particles produced are in optimal range  Most of the particles get deposited in wall of main airways
  • 38. Ultrasonic nebulizer  used piezoeeletric crystal  Works: Crystal transducer converts: radio waves into high-frequency mechanical vibrations vibration is transmitted to the water surface The high mechanical energy creates cavitation in the fluid it formed a standing wave which will disperses liquid particles  Frequency of oscillation determines the size of the water particles
  • 39.  Aerosol size of 1 to 10 µm  95% of particles produced are in optimal range  Particles deposited directly in airway  Very effective for deliver bronchodilator Hazards from nebulizer: cause over hydrations Hypothermia Infection can be transmitted edema of the airway wall
  • 40. Advantages and disadvantages of nebulizer Advantages It can carry air that fully saturated with water vapor without heat. We can increase the amount of the water vapor in the inhaled air. Disadvantage The pneumatic nebulizer needs high air flow to operate. The ultrasonic nebulizer need electric supply to operate thus it may cause electric shock
  • 42. INTRODUCTION :  scavenging is the collection and subsequent removal of waste anesthetic gases from both the anesthesia machine and the anesthetising location. Trace level of an anesthetic gas is a conc. far below that needed for clinical anesthesia or can be detected by smell Trace gases conc. depending on FGF, ventilation system , the length of time of anesthesia, anesthetic technique and other variables Trace gas level expressed in parts per million (ppm)
  • 43. Problems attributed to trace gases Spontaneous abortions : Higher rates of spontaneous abortion in OR personnel than in women in other settings. Infertility : Studies found higher than expected rates of involuntary infertility among exposed Impaired Skilled performance : one study showed that neuropsychological symptoms and tiredness were reported more by individuals in OR that are less scavenged
  • 44. Birth Defects : Studies in human found increase in congenital abnormalities in children of exposed personnel Carcinogenicity : A large study found higher risk of cancer in females than males who are exposed, but data has been questioned. Liver disease : recurrent hepatitis – halothane reported in few individuals Renal Disease Hematological : higher rate of leukamia. Cardiac Disease : higher Freq of HTN and dysrrthythmias
  • 45. In 1977 National Institute for Occupational Safety and Health (NIOSH) – recommended exposure limits for trace gas level (nitrous oxide and halogenated agent ) anesthetic gas Max. TWA conc.[ppm] Halogenated agent alone 2 Nitrous oxide alone 25 Halogenated gas +nitrous oxide 0.5 + 25 Dental facilities[nitr ous oxide alone] 50
  • 46. The 2 major causes of waste gas contamination in the O.R :  Equipment failure or lack of understanding of proper equipment  The anesthetic technique used -  Failure to turn off gas flow control valve and vaporizers when the circuit is disconnected from the patient.  use poorly fitting masks.  Flushing of circuit in room.  Using uncuffed endotracheal tubes that do not create a completely sealed airway or using cuffed tubes without inflating the cuff
  • 47. Spilling liquid anesthetic during the filling of vaporizers. Use of breathing circuits other than circle system The use of scavenging devices with anesthesia delivery systems is the most effective way to decrease waste anesthetic gases. An efficient scavenging system is capable of reducing ambient concentrations of waste gases by up to 90%.
  • 48. Components of the scavenger system: Gas collection assembly. Transfer tubing. Scavenging interface . Gas disposal tubing . Gas disposal assembly.
  • 49. 1.Gas collecting assembly Captures excess anesthetic gases and delivers it to the transfer tubing. WAG are vented from anesthesia system through either adjustable pressure limiting valve or ventilator relief valve. Conventional machine have seprate outlet port for these valve however newer have only one  some anesthetic workstations may also exhaust the ventilator drive gas in to scavenging system
  • 50. 2.Transfer tubing The transfer tubes carries excess gas from gas collecting assembly to scavenging interface. The tubes must have 30 mm connectors on either end, sometimes yellow color-coded . The tubes should be sufficiently rigid to prevent kinking and as short as possible to minimize the chance of occlusion. Separate tubes from the APL valve and ventilator relief valve merge into a single hose before they enter scavenging interface. If the transfer tube is occluded, baseline breathing circuit pressure will increase and barotrauma can occur.
  • 51. 3.Scavenging interface The scavenger interface is the most important component because it protects the breathing circuit or ventilator from excess positive or negative pressure.  the interface should limit pressure between -.5 and 3.5 cm of h2o under normal working condition. Positive-pressure relief is mandatory, irrespective of the type of disposable system (active or passive) used, to vent excess gas in case of occlusion distal to interface.  negative pressure relief will be necessary in active disposable system to protect breathing circuit or ventilator from subatmospheric pressure . scavenger interfaces may be open closed
  • 52. OPEN INTERFACE: It contains no valves and is open to the atmosphere, allowing positive and negative pressure relief. Open interfaces should be used only with active disposable systems that have a central evacuation system.  open interfaces require a reservoir because waste gases are intermittently discharged in surges whereas flow from the evacuation system is continuous.
  • 53. The efficiency of it depends on several factors: A.The vacuum flow rate per min must equal or exceed the minute volume of excess gases to prevent spillage. B.Spillage will occur if the volume of a single exhaled breath exceeds the capacity of reservoir. Open interfaces are safer for the patients.
  • 54. CLOSED INTERFACE: It communicates with the atmosphere through valves. Two types of closed interfaces are commercially available:  positive pressure relief only  positive and negative pressure relief
  • 55.
  • 56. POSITIVE PRESSURE RELIEF ONLY:  It has a single positive pressure relief valve and is designated to be used only with passive disposable systems. Transfer of the waste gas from the interface to the disposable system relies on the slight positive pressure of the waste gases leaving the patient’s breathing system, because a negative pressure evacuation system is not used. In this system reservoir bag is not required.
  • 57. POSITIVE AND NEGATIVE PRESSURE RELIEF:  It has positive and negative pressure relief valve in addition to a reservoir bag. It is used with active disposable systems. The effectiveness of a closed system in preventing spillage depends on: the rate of waste gas inflow the evacuation flow rate the size of the reservoir Leakage occurs only when the reservoir bag becomes fully inflated and pressure increases sufficiently to open the positive pressure relief valve .
  • 58. 4.Gas disposal tubing The gas disposable tubing conducts waste gas from the Scavenging interface to the gas disposable assembly. It should be collapse proof and should run overhead, if possible to minimize the chance of accidental occlusion. Connection to an active gas disposable system should be DISS type connector
  • 59. 5.Gas disposal assembly It ultimately eliminates excess waste gas. It is of two types:  Active  Passive Active assembly: most commonly used. It uses central evacuation system. A vacuum pump serves as mechanical flow inducing device that removes the waste gases. An interface with a negative pressure relief valve is mandatory because the pressure within the system is negative.
  • 60. Central evacuations are - Piped Vacuum - central vaccum system - Active duct system - employs flow inducing devices (fans , pumps , blowers etc..) to move large volume of gas at low pressures Advantages  Convenient in large hospitals, where many machines are in use in different locations More effective at keeping pollution low level because most leaks will be inward Disadvantages   Vacuum system and pipe work is a major expense   not a automatic must be turn ON and OFF
  • 61. Passive disposable system:  does not use a mechanical flow inducing device.  anesthetic gases flow through the system by the pressure raised above atmospheric by the patient exhaling, by manually squeezing the reservoir beg , or by ventilator Positive pressure relief is mandatory, but a negative pressure relief and reservoir are not. types - Room ventilation system - Recirculating or nonrecirculating - Piping direct to atmosphere - Adsorption devices - Catalyst decomposition
  • 62.  use activated charcoal or zeolite connected to the outlet of the scavenging system removes halogenated anesthetics but not nitrous oxide These are simple and portable Halogenated gases not release to atmosphere (decrease green house effect) Adsorption device
  • 63. Disadvantages They are fairly expensive and are effective for short period of time   replaced regularly and pose to storage and disposal problem   Does not remove nitrous oxid Catalytic Decomposition : Catalytic decomposition can be used to convert nitrous oxide to nitrogen and oxygen, reducing its contribution to the greenhouse effect
  • 64. Evaluation of Anesthetic Equipment Each piece of equipment involved in the delivery of inhalant anesthetics should be evaluated regularly to assure its function and integrity. Procedures for checkout of anesthesia equipment, depending on the equipment to be used, should include the following: Status of the high-pressure system, including the oxygen supply and nitrous oxide supply - The nitrous oxide supply should not leak when the cylinder valve is on and the nitrous oxide flowmeter is off.  Status of the low-pressure system (flowmeter function) - A negative-pressure leak test should be performed at the common gas outlet or the outlet of the vaporizer immediately upstream from the breathing system.
  • 65. Status of the breathing system - An appropriate leak test for a circle system and Noncircle systems should be done. The quantity of leakage can be measured by determining the flow rate of oxygen necessary to maintain a constant pressure in the system, and the leak rate should be less than 300 ml/min at 30 cm of h2O. Status of the scavenging system - The scavenging system should be properly attached at all connectors, and the appropriate vacuum should be assured for active systems. If charcoal canisters are employed for scavenging, they should be changed at appropriate intervals.
  • 66. Monitoring of the Effectiveness of Antipollution Techniques Monitoring trace-gas concentrations in the workplace provides a quantitative assessment of the effectiveness of a waste-gas control program. An air-monitoring program is most appropriately started after anesthesia delivery systems have been equipped with scavenging systems and after other techniques for minimizing waste gas pollution are in place.  An ideal approach would include frequent air monitoring, at least semiannual evaluations. Equipment for determining trace gas conc. infrared analyzer , dosimeter . Ionizing leak detector
  • 67. Effectiveness Unscavenged operating rooms show 10-70 ppm halothane, and 400-3000 ppm N2O.  scavenging brings these levels down to 1 and 60 ppm respectively.  Adding careful attention to leaks and technique can yield levels as low as 0.005 and 1 ppm.
  • 68. HAZARDS Scavenging system functionally extends the anesthesia circuit all the way from the anesthesia machine to the disposable site. Obstruction of scavenging pathway can cause excessive positive pressure in the breathing circuit and barotrauma can occur.  excessive vacuum applied can result in undesirable negative pressures within breathing system. Loss of Monitoring Input – it may mask the strong odor of a volatile anesthetic agent, delaying recognition of an overdose Alarm failure – neg. pressure from the scavenging system interface prevent the bellows from collapsing when breathing system is disconnected & Low airway pressure alarm not activated.