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REVERSE COLD CHAIN
Presented by:
Palka Mittal
Sahdev Bishnoi
M.Voc. (Public Health)
CONTENT
 INTRODUCTION
 NEED OF REVERSE COLD CHAIN
 SURVEILLANCE STANDARDS
 CLASSIFICATION SCHEME
 STANDARDS FOR SAMPLE COLLECTION
 STORATGE AND TRANSPORT CONDITIONS
 REPORTING CRITERIA
 INNOVATIONS
Reverse Cold Chain
The process of maintaining the cold chain when heat sensitive items are stored
and transported in the reverse direction i.e. upward from the clinic to a depot
or laboratory.
Reverse Cold Chain-WHO
If a cold chain is what you call the transport chain that goes from a laboratory
to the field  where vaccines must be kept at a certain temperature from the
moment they are produced, until they are administered in order for them to
work  a reverse cold chain is the process of stool samples that need to be
tested getting back to the laboratory from the field at certain temperatures so
that the virus that might be in the sample will still be identifiable.
Why reverse cold chain?
 Poliomyelitis is targeted for eradication. Highly sensitive surveillance for
acute flaccid paralysis (AFP), including immediate case investigation, and
specimen collection are critical for documenting the absence of poliovirus
circulation for polio-free certification
 When any case of acute flaccid paralysis is found anywhere in the world,
stool samples from the affected child must be transported carefully to the
laboratory so that they can be tested to identify whether the poliovirus was
the cause.
Surveillance Standards of Poliomyelitis
As per WHO
Clinical case definition
 Any child under 15 years of age with AFP* or any person of any age with
paralytic illness if polio is suspected
Case classification
 Suspected case: A case that meets the clinical case definition
 Confirmed case
Final Classification Scheme for AFP
Cases
Standards for Sample collection
 Collect two samples 24-48 hours apart and within 14 days of the onset of
paralysis
 Volume of specimen must be adequate(approximately 8-10g)
 Appropriate documentation (i.e. laboratory request form)
 Sample must be in good condition, i.e. with no leakage or desiccation
 Evidence that the reverse cold chain has been maintained (presence of ice
or temperature indicator)
Specimen-Based Data
 Unique identifier
 Specimen number: 1 = first specimen; 2 = second specimen; 3 = other; 9 =
unknown
 Date of onset of paralysis
 Date of last OPV dose
 Date of collection of stool specimen
 Date stool specimen sent to laboratory
 Date stool specimen received in laboratory
 Condition of stool: 1 = good; 2 = poor; 9 = unknown
 Date final culture results sent from laboratory to EPI(Expanded Program on
Immunization)
Rules for Specimen Storage and
Transport
Poliovirus is sensitive to heat, therefore
 After collection, the specimens must be placed immediately in a refrigerator or, for
shipment, in a cold box at 08属C between frozen ice packs.
 Aim for the specimens to arrive at the laboratory within 72 hours of collection.
 If this is not possible, the specimens must be frozen (at -20属C) and then shipped
frozen, preferably with dry ice or with cold packs that have also been frozen at -
20属C.
 Try to limit repeated freezing and thawing to a minimum. This process of keeping
the specimen refrigerated or frozen is called a reverse cold chain.
Remember
 Avoid storing samples in refrigerators or cold boxes used for vaccines or
medicines.
 If separate storage is unavoidable, seal specimens in 2-3 layers of plastic
bags and separate them properly from vaccines.
Diagrammatic Representation
(a) 30-60 ml faeces container with
external screw cap.
(b) Sealed polyethylene bag to hold
faeces containers.
(c) Sealed polyethylene bag to hold
report form.
(d) Absorbent material (cotton wool
absorbs 8-10 times its own weight).
(e) Icepacks obtainable from national
EPI.
(f) High-density (30-35 kgs/m3)
polystyrene (small bubbles and firm
when squeezed).
(g) Infectious substance label.
(h) Outer carton of double-ply
corrugated cardboard or plastic.
Reporting Criteria
 Aggregated data on AFP cases should be included in routine monthly
surveillance reports
 Designated reporting sites at all levels should report at a specified
frequency (e.g. weekly or monthly) even if there are zero cases (often
referred to as "zero reporting")
 All outbreaks should be investigated immediately
 All AFP cases under 15 years of age or with paralytic illness at an age
where polio is suspected should be reported immediately and investigated
within 48 hours
 Active surveillance: Regular weekly visits should be made to selected
reporting sites that are most likely to admit acute flaccid paralysis patients
(e.g. major hospitals, physiotherapy centers) to look for unreported AFP
cases
Innovations in the reverse cold
chain
 Introduction of continual temperature recording probes known as Log
Tags to track specimens during their journey to the lab.
 Incentives are paid for informants who report a case.
THANK YOU!!!
ANY QUESTIONS?

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Reverse cold chain

  • 1. REVERSE COLD CHAIN Presented by: Palka Mittal Sahdev Bishnoi M.Voc. (Public Health)
  • 2. CONTENT INTRODUCTION NEED OF REVERSE COLD CHAIN SURVEILLANCE STANDARDS CLASSIFICATION SCHEME STANDARDS FOR SAMPLE COLLECTION STORATGE AND TRANSPORT CONDITIONS REPORTING CRITERIA INNOVATIONS
  • 3. Reverse Cold Chain The process of maintaining the cold chain when heat sensitive items are stored and transported in the reverse direction i.e. upward from the clinic to a depot or laboratory.
  • 4. Reverse Cold Chain-WHO If a cold chain is what you call the transport chain that goes from a laboratory to the field where vaccines must be kept at a certain temperature from the moment they are produced, until they are administered in order for them to work a reverse cold chain is the process of stool samples that need to be tested getting back to the laboratory from the field at certain temperatures so that the virus that might be in the sample will still be identifiable.
  • 5. Why reverse cold chain? Poliomyelitis is targeted for eradication. Highly sensitive surveillance for acute flaccid paralysis (AFP), including immediate case investigation, and specimen collection are critical for documenting the absence of poliovirus circulation for polio-free certification When any case of acute flaccid paralysis is found anywhere in the world, stool samples from the affected child must be transported carefully to the laboratory so that they can be tested to identify whether the poliovirus was the cause.
  • 6. Surveillance Standards of Poliomyelitis As per WHO Clinical case definition Any child under 15 years of age with AFP* or any person of any age with paralytic illness if polio is suspected Case classification Suspected case: A case that meets the clinical case definition Confirmed case
  • 8. Standards for Sample collection Collect two samples 24-48 hours apart and within 14 days of the onset of paralysis Volume of specimen must be adequate(approximately 8-10g) Appropriate documentation (i.e. laboratory request form) Sample must be in good condition, i.e. with no leakage or desiccation Evidence that the reverse cold chain has been maintained (presence of ice or temperature indicator)
  • 9. Specimen-Based Data Unique identifier Specimen number: 1 = first specimen; 2 = second specimen; 3 = other; 9 = unknown Date of onset of paralysis Date of last OPV dose Date of collection of stool specimen Date stool specimen sent to laboratory Date stool specimen received in laboratory Condition of stool: 1 = good; 2 = poor; 9 = unknown Date final culture results sent from laboratory to EPI(Expanded Program on Immunization)
  • 10. Rules for Specimen Storage and Transport Poliovirus is sensitive to heat, therefore After collection, the specimens must be placed immediately in a refrigerator or, for shipment, in a cold box at 08属C between frozen ice packs. Aim for the specimens to arrive at the laboratory within 72 hours of collection. If this is not possible, the specimens must be frozen (at -20属C) and then shipped frozen, preferably with dry ice or with cold packs that have also been frozen at - 20属C. Try to limit repeated freezing and thawing to a minimum. This process of keeping the specimen refrigerated or frozen is called a reverse cold chain.
  • 11. Remember Avoid storing samples in refrigerators or cold boxes used for vaccines or medicines. If separate storage is unavoidable, seal specimens in 2-3 layers of plastic bags and separate them properly from vaccines.
  • 12. Diagrammatic Representation (a) 30-60 ml faeces container with external screw cap. (b) Sealed polyethylene bag to hold faeces containers. (c) Sealed polyethylene bag to hold report form. (d) Absorbent material (cotton wool absorbs 8-10 times its own weight). (e) Icepacks obtainable from national EPI. (f) High-density (30-35 kgs/m3) polystyrene (small bubbles and firm when squeezed). (g) Infectious substance label. (h) Outer carton of double-ply corrugated cardboard or plastic.
  • 13. Reporting Criteria Aggregated data on AFP cases should be included in routine monthly surveillance reports Designated reporting sites at all levels should report at a specified frequency (e.g. weekly or monthly) even if there are zero cases (often referred to as "zero reporting") All outbreaks should be investigated immediately All AFP cases under 15 years of age or with paralytic illness at an age where polio is suspected should be reported immediately and investigated within 48 hours Active surveillance: Regular weekly visits should be made to selected reporting sites that are most likely to admit acute flaccid paralysis patients (e.g. major hospitals, physiotherapy centers) to look for unreported AFP cases
  • 14. Innovations in the reverse cold chain Introduction of continual temperature recording probes known as Log Tags to track specimens during their journey to the lab. Incentives are paid for informants who report a case.