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Expanded programme on
immunisation (EPI)
Abdirisak Mohamed
IMMUNIZATION
•Immunization is defined as the procedure by which
the body is prepared to fight against a specific
disease.
•Immunization is of two types:
1. Passive immunization
2. Active immunization.
„ PASSIVE IMMUNIZATION
Passive immunization or immunity is produced without challenging the immune system of the
body.
done by administration of serum or gamma globulins from a person who is already immunized
(affected by the disease) to a non-immune person.
Passive immunization is acquired either naturally or artificially.
It is developed by injecting previously prepared antibodies using serum from humans or animals.
This type of immunity is useful for providing immediate protection against acute infections like
tetanus, measles, etc.
ACTIVE IMMUNIZATION
Active immunization or immunity is acquired by
activating immune system of the body.
Body develops resistance against disease by
producing antibodies following the exposure to
antigens.
 Active immunity is acquire
Naturally
Artificially
Active Natural Immunization
Naturally acquired active immunity involves activation of immune system in the
body to produce antibodies against microorganism.
 It is achieved in both clinical and subclinical infections
Active Artificial Immunization
It is achieved by the administration of vaccines or toxoids.
Herd Immunity
•It is a type of immunity that occurs when the vaccination of a
portion of population provides protection to unprotected individual.
•The higher the number of immune individuals, the lower the like
hood that a susceptible people will come in contact with an infectious
agent.
•Resistance to spread of infectious disease in a group because of few
susceptible members, making transmission unlikely.
Vaccine
8
Vaccine is a substance that is introduced into the
body to prevent the disease produced by certain
pathogens.
It consists of dead pathogens or live but attenuated
(artificially weakened) organisms.
The vaccine induces immunity against the pathogen,
either by production of antibodies or by activation of T
lymphocytes.
Types of vaccine
A. Live-attenuated (weakened) vaccines:
contain modified strains of a pathogen (bacteria or viruses) that have been
weakened but are able to multiply within the body and remain antigenic
enough to induce a strong immune response.
B.Killed-inactivated vaccines:
To produce this type of vaccines, bacteria or viruses are killed or inactivated
by a chemical treatment or heat.
C.Sub-unit vaccines
•Subunit vaccines include only the antigens that best
stimulate the immune system.
•In some cases, epitopes are used—the very specific
parts of the antigen that antibodies or T cells recognize
and bind to.
•Subunit vaccines contain only the essential antigens
and not all the other molecules that make up the
microbe, the chances of adverse reactions to the
vaccine are lower.
10
D. Combination
If more than one kind of immunizing agent is included in the vaccine it is
called a mixed or combined vaccine.
The advantage of combined vaccine is as below:
1.simplify administration
2.reduce cost
3.improving timeline of vaccination
4.reducing the storage
• Example of mixed vaccines are DPT,DT,DP,MMR,etc.
• POLYVALENT: It is prepared from 2 or more strain of the same species
11
vaccine Example
Live, attenuated
Measles, mumps, rubella (MMR combined
vaccine)
Varicella (chickenpox)
Influenza (nasal spray)
Rotavirus
Inactivated/Killed
Polio (IPV)
Hepatitis A 12
Combined DPT,TT
Subunit/conjugate
Hepatitis B
Influenza (injection)
Homophiles influenza type b (Hib)
Pertussis, Diphtheria, tetanus
Why Immunization ?
Key strategy to child survival
Protecting infants from diseases.
Lowers morbidity and mortality rates in children.
Indicator of a strong primary health care system.
What Is EPI?
• Expanded program on Immunization (EPI) is a world health organization
program, with the goal to make vaccines available to all children throughout the
world.
SCOPE OF EPI
Experience with smallpox eradication program showed the world that
immunization was the most powerful and cost-effective weapon against
vaccine preventable diseases.
In 1974, the WHO launched its “ Expanded program of immunization” (EPI)
against six most common preventable diseases (diphtheria, pertussis,
tetanus, polio, tuberculosis, measles and recently added
pneumococcal vaccine).
“Expanded” Means?
 Expanding the number of diseases to be covered
 Expanding the number of children and target population to be
covered
 Expanding coverage to all corners of the country and spreading
services to reach the less privileged sectors of the society.
Component Of EPI:
Routine Immunization:
 Children 0-23 months – immunization with 8 EPI antigens
 Pregnant ladies by TT.
Supplemental Immunization Activities:
 Routine immunization does not ensure 100% coverage of the mobile population i.e. nomads, NAs, hard to reach areas /
missed areas. So SIAs are scheduled to ensure coverage of this population / areas.
 NIDs / SNIDs: children < 5 years receive polio drops (3-days campaign)
Disease Surveillance:
 To detect every case of target diseases, the suspected cases of seven VPDs are reported by health facilities to the
district health authorities for immediate launching of the control measures.
Mopping up:
 Special campaigns 5-8 km around the infected locality to localize the disease and stop its transmission.
The objectives of EPI:
1. To achieve 100% coverage with all EPI vaccines.
2. Eradication of polio to maintain polio free status.
3. Elimination of measles.
4. To Reduce Seroprevalence Of HBsAg to < 1%
among under five.
5.Elimination of Neonatal Tetanus .
6. To maintain zero level of diphtheria.
7-Prevention of severe forms of TB ( TB meningitis &military
TB).
8- To reduce the incidence of whooping cough
9- To Reduce the incidence of Bacteria Meningitis due to
haemophelus influenza.
10- To Maintain Immunization Safety.
11-To prepare for introduction of new vaccines
Somalia EPI
• EPI Vaccines
• All vaccines used in Somalia by EPI program are safe, procured
through UNICEF from manufactures pre-qualified and accredited by
WHO.
• The national EPI Programme provides the following vaccines:
• BCG: It contains live attenuated Mycobacterium bovis (M. bovis), and comes
in powder form. It must be reconstituted with a diluent before use. It is
essential that only the diluent supplied with the vaccine be used. BCG vaccine
should be kept at 2°C–8°C after reconstitution. Any remaining reconstituted
vaccine must be discarded after six hours or at the end of the immunization
session, whichever comes first.
Somalia EPI
• Oral Polio Vaccine (OPV): It is prepared from attenuated live polio virus, and is
presented as a liquid vaccine that is provided in glass vials with droppers in a
separate plastic bag. In consultation with global partners, the country will make an
informed decision on the introduction of IPV and phasing-out of OPV.
• Pentavalent DTP-HepB+Hib vaccine: It contains diphtheria toxoid, tetanus toxoid,
pertussis, Hepatitis B and Haemophilus type b vaccine; and is provided as liquid form
in vials of ten doses.
• Measles vaccine is provided as a powder, with a diluent in a separate vial. Before it
can be used, it must be reconstituted. It is essential that only the diluent supplied
with the vaccine be used. After reconstitution measles vaccine should be kept at
2°C–8°C. Any remaining reconstituted vaccine must be discarded after six hours or at
the end of the immunization session, whichever comes first.
• Tetanus Toxoid (TT) is provided as a liquid in vials and also in prefilled auto-disable
injection devices.
EPI SCHEDULE
Immunization schedule
• According to the recommended schedule all children will receive one
dose of BCG vaccine, 3 doses of DTP-HepB+Hib, 4 doses of OPV, and
one dose of measles vaccine before their first birthday/First year.
• Table 1: Routine immunization schedule for infants, 0 -11 months
Age Vaccines
Birth (up to 1 week) BCG OPV0
6 weeks DTP-HepB+Hib1 OPV1
10 weeks DTP-HepB+Hib2 OPV2
14 weeks DTP-HepB+Hib3 OPV3
9 months MCV1
18 months MCV2
Immunization schedule for pregnant women and
WBCA (15- 45 years)
Dose Time for administration Duration of protection
TT 1 at first contact OR as early as possible during pregnancy None
TT 2 at least 4 weeks after TT1 1-3 years
TT 3 at least 6 months after TT2 5 years
TT 4 at least 1 year after TT3 10 years
TT 5 at least 1 year after TT4 For all child bearing
years
Summary of routes of administration and
injection sites
Vaccine Route of administration Injection site
BCG Intradermal Upper Left Arm
DTP-HepB+Hib Intramuscular Outer mid-thigh (Right)
OPV Oral Mouth
Measles Subcutaneous Upper Right arm
Tetanus toxoid Intramuscular Outer, upper arm (Left)
Cold Chain
•The ‘cold chain’ is the system of
transporting and storing vaccines at
recommended temperature from the
point of manufacture to the point of
use.
Manufacturer
Distributor
Vaccine
Depots
Provider
office
Client
Why is the cold chain important ?
1. Vaccines are:
 Biological products
 lose potency with time
 Process irreversible and accelerated if
proper storage conditions are not
adhered to.
2. Assurance in potent product
and vaccine programmes
 Professional responsibility
 Confident the vaccines you give
will be effective
 Public Health responsibility
 Public confidence in immunisation
programmes
3. Ensuring maximum benefit
from immunisations
Responsibility not to waste scarce NHS
resources
Reduce wastage from errors
4.Compliance with
SPC/Manufacturer
Any vaccine that has not been stored at
a temperature of 2-8ºC as per its
licensing conditions is no longer a
licensed product
Cold chain storage equipment
Walk in cold
rooms
Deep freezers Ice lined
refrigerators
A. Walk in cold rooms(WIC)
At regional level
Storage up to 3 months
Serve 4-5 districts
B. Deep freezers
At district & PHC levels
Temp :- -15oc to -25oc
At PHC, used only for the preparation of
ice packs
In case of power failure these freezers
can maintain the cabinet temp. for 18-22
hours
20-25 icepack can be prepared by a 140L
in deep freezers with continuous electric
supply of 8 hours.
C. Ice Lined Refrigerators(ILR)
Both at district and PHC levels
Temp :- +2oc to +8oc
ILR’s are top opening, can hold
cold air inside better than front
opening refrigerators
It can keep vaccine safe with 8
hours of continuous electric
supply in a 24 hours period.
• Arrangement of vaccine order top to bottom:
Hepatitis B
DPT & TT
BCG
Measles
OPV
• Discard any frozen hep.b, DPT, & TT.
• Keep spaces between boxes
• Measles & OPV can be kept over 2 rows of empty ice-packs on the
floor of the ILR.
Vaccine Stability
• Sensitivity to
HEAT
OPV
Measles
BCG
MMR
Hepatitis B
DT
• Sensitivity to
COLD
HepB and
combination
Influenza
*BCG
(*Freeze dried)
MOST SENSITIVE
Temperature must be
recorded twice in a day
with dial thermometer
LEAST SENSITIVE
Light Sensitive
Sensitive to strong light, sunlight, ultraviolet,
fluorescents (neon)
OPV
Measles
MMR
Varicella
Meningococcal C Conjugate
Most DTaP containing vaccines
Vaccines should always
be stored in their
original packaging until
point of use to protect
them from light
Vaccine Storage
Use a dedicated vaccine
fridge
Safeguard electricity supply
No more than 50% full
Place vaccines in clearly
labelled plastic mesh baskets
 Group vaccines by type
(Paediatric, Adult,
Adolescent)
X No food or medical
specimens
X Do not place fridge in
direct sunlight or near heat
source
X Do not store vaccines for
more than 1 month at PHC.
X Do not store vaccines in
fridge doors or in solid
plastic trays/containers
within the fridge
X Keep vaccines away from
fridge walls and cold air
vents
Picture taken from www.medisave.co.uk
DO’sDON’T’s
Transporting Equipment
Cold
boxes
Vaccine
carriers
Day
carriers
Used for transport of vaccines
Fully frozen ice packs placed at the
bottom and sides
DPT, TT, DT should not be kept in
direct contact
1.Cold boxes
Used to carry small quantity of
vaccines(16 to 20 vials)
For out of reach sessions
4 icepacks are used
2.Vaccine
carriers
3.Day carriers
Used to carry very small quantities of
vaccines(6 to 8 vials)
For a near by session
2 icepacks are used
For only 2 hours period
ICE PACKS
•It contains water & no salt should be added to it.
•The water should be filled up to the level marked on
the side.
•If there is leakage such icepack should be discarded.
Vaccine Vial Monitor(VVM)
VVM is a label containing heat sensitive
material that is placed on a vaccine vial to
register heat exposure over time
Vaccine vial
monitor
Stage 1
• Inner square
lighter than
outer circle
Stage 2
• Inner square still
lighter than
outer circle
Stage 3
• Color of inner
square matches
the outer circle
Stage 4
• Color of inner
square darker
than outer circle
Combined effects of time and temperature
cause the inner square to darken gradually and
irreversibly
VVM does not directly measure the vaccine
potency but gives info about the main factor that
affects potency
Epi seminar

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Epi seminar

  • 1. Expanded programme on immunisation (EPI) Abdirisak Mohamed
  • 2. IMMUNIZATION •Immunization is defined as the procedure by which the body is prepared to fight against a specific disease. •Immunization is of two types: 1. Passive immunization 2. Active immunization.
  • 3. „ PASSIVE IMMUNIZATION Passive immunization or immunity is produced without challenging the immune system of the body. done by administration of serum or gamma globulins from a person who is already immunized (affected by the disease) to a non-immune person. Passive immunization is acquired either naturally or artificially. It is developed by injecting previously prepared antibodies using serum from humans or animals. This type of immunity is useful for providing immediate protection against acute infections like tetanus, measles, etc.
  • 4. ACTIVE IMMUNIZATION Active immunization or immunity is acquired by activating immune system of the body. Body develops resistance against disease by producing antibodies following the exposure to antigens.  Active immunity is acquire Naturally Artificially
  • 5. Active Natural Immunization Naturally acquired active immunity involves activation of immune system in the body to produce antibodies against microorganism.  It is achieved in both clinical and subclinical infections Active Artificial Immunization It is achieved by the administration of vaccines or toxoids.
  • 6. Herd Immunity •It is a type of immunity that occurs when the vaccination of a portion of population provides protection to unprotected individual. •The higher the number of immune individuals, the lower the like hood that a susceptible people will come in contact with an infectious agent. •Resistance to spread of infectious disease in a group because of few susceptible members, making transmission unlikely.
  • 7.
  • 8. Vaccine 8 Vaccine is a substance that is introduced into the body to prevent the disease produced by certain pathogens. It consists of dead pathogens or live but attenuated (artificially weakened) organisms. The vaccine induces immunity against the pathogen, either by production of antibodies or by activation of T lymphocytes.
  • 9. Types of vaccine A. Live-attenuated (weakened) vaccines: contain modified strains of a pathogen (bacteria or viruses) that have been weakened but are able to multiply within the body and remain antigenic enough to induce a strong immune response. B.Killed-inactivated vaccines: To produce this type of vaccines, bacteria or viruses are killed or inactivated by a chemical treatment or heat.
  • 10. C.Sub-unit vaccines •Subunit vaccines include only the antigens that best stimulate the immune system. •In some cases, epitopes are used—the very specific parts of the antigen that antibodies or T cells recognize and bind to. •Subunit vaccines contain only the essential antigens and not all the other molecules that make up the microbe, the chances of adverse reactions to the vaccine are lower. 10
  • 11. D. Combination If more than one kind of immunizing agent is included in the vaccine it is called a mixed or combined vaccine. The advantage of combined vaccine is as below: 1.simplify administration 2.reduce cost 3.improving timeline of vaccination 4.reducing the storage • Example of mixed vaccines are DPT,DT,DP,MMR,etc. • POLYVALENT: It is prepared from 2 or more strain of the same species 11
  • 12. vaccine Example Live, attenuated Measles, mumps, rubella (MMR combined vaccine) Varicella (chickenpox) Influenza (nasal spray) Rotavirus Inactivated/Killed Polio (IPV) Hepatitis A 12
  • 13. Combined DPT,TT Subunit/conjugate Hepatitis B Influenza (injection) Homophiles influenza type b (Hib) Pertussis, Diphtheria, tetanus
  • 14. Why Immunization ? Key strategy to child survival Protecting infants from diseases. Lowers morbidity and mortality rates in children. Indicator of a strong primary health care system.
  • 15. What Is EPI? • Expanded program on Immunization (EPI) is a world health organization program, with the goal to make vaccines available to all children throughout the world.
  • 16. SCOPE OF EPI Experience with smallpox eradication program showed the world that immunization was the most powerful and cost-effective weapon against vaccine preventable diseases. In 1974, the WHO launched its “ Expanded program of immunization” (EPI) against six most common preventable diseases (diphtheria, pertussis, tetanus, polio, tuberculosis, measles and recently added pneumococcal vaccine).
  • 17. “Expanded” Means?  Expanding the number of diseases to be covered  Expanding the number of children and target population to be covered  Expanding coverage to all corners of the country and spreading services to reach the less privileged sectors of the society.
  • 18. Component Of EPI: Routine Immunization:  Children 0-23 months – immunization with 8 EPI antigens  Pregnant ladies by TT. Supplemental Immunization Activities:  Routine immunization does not ensure 100% coverage of the mobile population i.e. nomads, NAs, hard to reach areas / missed areas. So SIAs are scheduled to ensure coverage of this population / areas.  NIDs / SNIDs: children < 5 years receive polio drops (3-days campaign) Disease Surveillance:  To detect every case of target diseases, the suspected cases of seven VPDs are reported by health facilities to the district health authorities for immediate launching of the control measures. Mopping up:  Special campaigns 5-8 km around the infected locality to localize the disease and stop its transmission.
  • 19. The objectives of EPI: 1. To achieve 100% coverage with all EPI vaccines.
  • 20. 2. Eradication of polio to maintain polio free status.
  • 21. 3. Elimination of measles.
  • 22. 4. To Reduce Seroprevalence Of HBsAg to < 1% among under five.
  • 24. 6. To maintain zero level of diphtheria.
  • 25. 7-Prevention of severe forms of TB ( TB meningitis &military TB).
  • 26. 8- To reduce the incidence of whooping cough
  • 27. 9- To Reduce the incidence of Bacteria Meningitis due to haemophelus influenza.
  • 28. 10- To Maintain Immunization Safety.
  • 29. 11-To prepare for introduction of new vaccines
  • 30. Somalia EPI • EPI Vaccines • All vaccines used in Somalia by EPI program are safe, procured through UNICEF from manufactures pre-qualified and accredited by WHO. • The national EPI Programme provides the following vaccines: • BCG: It contains live attenuated Mycobacterium bovis (M. bovis), and comes in powder form. It must be reconstituted with a diluent before use. It is essential that only the diluent supplied with the vaccine be used. BCG vaccine should be kept at 2°C–8°C after reconstitution. Any remaining reconstituted vaccine must be discarded after six hours or at the end of the immunization session, whichever comes first.
  • 31. Somalia EPI • Oral Polio Vaccine (OPV): It is prepared from attenuated live polio virus, and is presented as a liquid vaccine that is provided in glass vials with droppers in a separate plastic bag. In consultation with global partners, the country will make an informed decision on the introduction of IPV and phasing-out of OPV. • Pentavalent DTP-HepB+Hib vaccine: It contains diphtheria toxoid, tetanus toxoid, pertussis, Hepatitis B and Haemophilus type b vaccine; and is provided as liquid form in vials of ten doses. • Measles vaccine is provided as a powder, with a diluent in a separate vial. Before it can be used, it must be reconstituted. It is essential that only the diluent supplied with the vaccine be used. After reconstitution measles vaccine should be kept at 2°C–8°C. Any remaining reconstituted vaccine must be discarded after six hours or at the end of the immunization session, whichever comes first. • Tetanus Toxoid (TT) is provided as a liquid in vials and also in prefilled auto-disable injection devices.
  • 33. Immunization schedule • According to the recommended schedule all children will receive one dose of BCG vaccine, 3 doses of DTP-HepB+Hib, 4 doses of OPV, and one dose of measles vaccine before their first birthday/First year. • Table 1: Routine immunization schedule for infants, 0 -11 months Age Vaccines Birth (up to 1 week) BCG OPV0 6 weeks DTP-HepB+Hib1 OPV1 10 weeks DTP-HepB+Hib2 OPV2 14 weeks DTP-HepB+Hib3 OPV3 9 months MCV1 18 months MCV2
  • 34. Immunization schedule for pregnant women and WBCA (15- 45 years) Dose Time for administration Duration of protection TT 1 at first contact OR as early as possible during pregnancy None TT 2 at least 4 weeks after TT1 1-3 years TT 3 at least 6 months after TT2 5 years TT 4 at least 1 year after TT3 10 years TT 5 at least 1 year after TT4 For all child bearing years
  • 35. Summary of routes of administration and injection sites Vaccine Route of administration Injection site BCG Intradermal Upper Left Arm DTP-HepB+Hib Intramuscular Outer mid-thigh (Right) OPV Oral Mouth Measles Subcutaneous Upper Right arm Tetanus toxoid Intramuscular Outer, upper arm (Left)
  • 36.
  • 37.
  • 38. Cold Chain •The ‘cold chain’ is the system of transporting and storing vaccines at recommended temperature from the point of manufacture to the point of use. Manufacturer Distributor Vaccine Depots Provider office Client
  • 39. Why is the cold chain important ? 1. Vaccines are:  Biological products  lose potency with time  Process irreversible and accelerated if proper storage conditions are not adhered to. 2. Assurance in potent product and vaccine programmes  Professional responsibility  Confident the vaccines you give will be effective  Public Health responsibility  Public confidence in immunisation programmes 3. Ensuring maximum benefit from immunisations Responsibility not to waste scarce NHS resources Reduce wastage from errors 4.Compliance with SPC/Manufacturer Any vaccine that has not been stored at a temperature of 2-8ºC as per its licensing conditions is no longer a licensed product
  • 40. Cold chain storage equipment Walk in cold rooms Deep freezers Ice lined refrigerators
  • 41. A. Walk in cold rooms(WIC) At regional level Storage up to 3 months Serve 4-5 districts
  • 42. B. Deep freezers At district & PHC levels Temp :- -15oc to -25oc At PHC, used only for the preparation of ice packs In case of power failure these freezers can maintain the cabinet temp. for 18-22 hours 20-25 icepack can be prepared by a 140L in deep freezers with continuous electric supply of 8 hours.
  • 43. C. Ice Lined Refrigerators(ILR) Both at district and PHC levels Temp :- +2oc to +8oc ILR’s are top opening, can hold cold air inside better than front opening refrigerators It can keep vaccine safe with 8 hours of continuous electric supply in a 24 hours period.
  • 44. • Arrangement of vaccine order top to bottom: Hepatitis B DPT & TT BCG Measles OPV • Discard any frozen hep.b, DPT, & TT. • Keep spaces between boxes • Measles & OPV can be kept over 2 rows of empty ice-packs on the floor of the ILR.
  • 45. Vaccine Stability • Sensitivity to HEAT OPV Measles BCG MMR Hepatitis B DT • Sensitivity to COLD HepB and combination Influenza *BCG (*Freeze dried) MOST SENSITIVE Temperature must be recorded twice in a day with dial thermometer LEAST SENSITIVE
  • 46. Light Sensitive Sensitive to strong light, sunlight, ultraviolet, fluorescents (neon) OPV Measles MMR Varicella Meningococcal C Conjugate Most DTaP containing vaccines Vaccines should always be stored in their original packaging until point of use to protect them from light
  • 47. Vaccine Storage Use a dedicated vaccine fridge Safeguard electricity supply No more than 50% full Place vaccines in clearly labelled plastic mesh baskets  Group vaccines by type (Paediatric, Adult, Adolescent) X No food or medical specimens X Do not place fridge in direct sunlight or near heat source X Do not store vaccines for more than 1 month at PHC. X Do not store vaccines in fridge doors or in solid plastic trays/containers within the fridge X Keep vaccines away from fridge walls and cold air vents Picture taken from www.medisave.co.uk DO’sDON’T’s
  • 49. Used for transport of vaccines Fully frozen ice packs placed at the bottom and sides DPT, TT, DT should not be kept in direct contact 1.Cold boxes Used to carry small quantity of vaccines(16 to 20 vials) For out of reach sessions 4 icepacks are used 2.Vaccine carriers
  • 50. 3.Day carriers Used to carry very small quantities of vaccines(6 to 8 vials) For a near by session 2 icepacks are used For only 2 hours period
  • 51. ICE PACKS •It contains water & no salt should be added to it. •The water should be filled up to the level marked on the side. •If there is leakage such icepack should be discarded.
  • 52. Vaccine Vial Monitor(VVM) VVM is a label containing heat sensitive material that is placed on a vaccine vial to register heat exposure over time Vaccine vial monitor
  • 53. Stage 1 • Inner square lighter than outer circle Stage 2 • Inner square still lighter than outer circle Stage 3 • Color of inner square matches the outer circle Stage 4 • Color of inner square darker than outer circle Combined effects of time and temperature cause the inner square to darken gradually and irreversibly VVM does not directly measure the vaccine potency but gives info about the main factor that affects potency