Adverse Events Following Immunization AEFI AEFI WHAT IS

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Adverse Events Following Immunization, AEFI

Adverse Events Following Immunization, AEFI

AEFI WHAT IS AN AEFI? AEFI IS A MEDICAL INCIDENT AFTER AN IMMUNIZATION AND

AEFI WHAT IS AN AEFI? AEFI IS A MEDICAL INCIDENT AFTER AN IMMUNIZATION AND IS BELIEVED TO BE CAUSED BY THE IMMUNIZATION BASICALLY TWO TYPES AVOIDABLE AND UNAVOIDABLE

AEFI MODERN VACCINES § ARE GENERALLY SAFE § NOT ENTIRELY WITHOUT RISK § BENEFITS

AEFI MODERN VACCINES § ARE GENERALLY SAFE § NOT ENTIRELY WITHOUT RISK § BENEFITS FAR OUTWEIGH RISKS

AEFI WHY MONITORING OF AEFI ARE IMPORTANT ? § UPSETS PEOPLE § REFUSAL FOR

AEFI WHY MONITORING OF AEFI ARE IMPORTANT ? § UPSETS PEOPLE § REFUSAL FOR FURTHER IMMUNIZATION

AEFI CLASSIFICATION OF AEFI § VACCINE EFFECT § PROGRAMME ERROR § COINCIDENTAL § INJECTION

AEFI CLASSIFICATION OF AEFI § VACCINE EFFECT § PROGRAMME ERROR § COINCIDENTAL § INJECTION REACTION § UNKNOWN

AEFI THE USEFULLNESS OF MONITORING AEFI § TO IDENTIFY PROGRAMME ERRORS § IDENTIFY VACCINE

AEFI THE USEFULLNESS OF MONITORING AEFI § TO IDENTIFY PROGRAMME ERRORS § IDENTIFY VACCINE DEFECTS § TAKE CORRECTIVE MEASURES § INCREASE IMMUNIZATION ACCEPTANCE § IMPROVE THE QUALITY OF SERVICES

AEFI ARE DUE TO: 1 VACCINE EVENT CAUSED OR PRECIPITATED BY THE VACCINE WHEN

AEFI ARE DUE TO: 1 VACCINE EVENT CAUSED OR PRECIPITATED BY THE VACCINE WHEN GIVEN CORRECTLY, CAUSED BY THE INHERENT PROPERTIES OF THE VACCINE

AEFI 2 PROGRAMME ERROR EVENT CAUSED BY AN ERROR IN VACCINE: § PREPARATION §

AEFI 2 PROGRAMME ERROR EVENT CAUSED BY AN ERROR IN VACCINE: § PREPARATION § HANDLING § ADMINISTRATION

AEFI 3 COINCIDENTAL EVENT THAT HAPPENS AFTER IMMUNIZATION BUT NOT CAUSED BY THE VACCINE

AEFI 3 COINCIDENTAL EVENT THAT HAPPENS AFTER IMMUNIZATION BUT NOT CAUSED BY THE VACCINE – A CHANCE ASSOCIATION

AEFI 4 INJECTION REACTION EVENT FROM ANXIETY ABOUT, OR PAIN FROM THE INJECTION ITSELF

AEFI 4 INJECTION REACTION EVENT FROM ANXIETY ABOUT, OR PAIN FROM THE INJECTION ITSELF RATHER THAN THE VACCINE 5 UNKNOWN THE CAUSE OF THE EVENT CANNOT BE DETERMINED

AEFI SURVEILLANCE 1. DETECTION AND REPORTING 2. INVESTIGATION 3. DATA ANALYSIS 4. CORRECTIVE ACTION

AEFI SURVEILLANCE 1. DETECTION AND REPORTING 2. INVESTIGATION 3. DATA ANALYSIS 4. CORRECTIVE ACTION 5. EVALUATION

AEFI HOW CAN AEFI’S BE DETECTED? WHAT MECHANISMS ARE AVAILABLE?

AEFI HOW CAN AEFI’S BE DETECTED? WHAT MECHANISMS ARE AVAILABLE?

AEFI LIST OF AEFI 1. LOCAL ADVERSE EVENTS 2. CNS ADVERSE EVENTS 3. OTHER

AEFI LIST OF AEFI 1. LOCAL ADVERSE EVENTS 2. CNS ADVERSE EVENTS 3. OTHER ADVERSE EVENTS

AEFI LOCAL ADVERSE EVENTS 1. INJECTION SITE ABSCESS STERILE BACTERIAL

AEFI LOCAL ADVERSE EVENTS 1. INJECTION SITE ABSCESS STERILE BACTERIAL

AEFI FORMATION OF A STERILE ABSCESS 1. WRONG ROUTE (SC INSTEAD OF DEEP IM)

AEFI FORMATION OF A STERILE ABSCESS 1. WRONG ROUTE (SC INSTEAD OF DEEP IM) 2. NOT SHAKING THE VACCINE BOTTLE BEFORE DRAWING IN TO THE SYRINGE 3. WRONG DOSE (LARGER DOSE)

AEFI 2. LYMPHADENITIS AT LEAST ONE LYMPH NODE 1. 5 CM IN SIZE OR

AEFI 2. LYMPHADENITIS AT LEAST ONE LYMPH NODE 1. 5 CM IN SIZE OR DRAINING SINUS OVER LYMPH NODE 2 – 6 MONTHS AFTER BCG ON THE SAME SIDE AS INOCULATION

AEFI 3. SEVERE LOCAL REACTION REDNESS AND/OR SWELLING AT THE SITE WITH ONE OR

AEFI 3. SEVERE LOCAL REACTION REDNESS AND/OR SWELLING AT THE SITE WITH ONE OR MORE OF THE FOLOWWING 1. SWELLING BEYOND JOINT 2. LASTING MORE THAN 3 DAYS OR 3. REQUIRES HOSPITALIZATION

AEFI CNS ADVERSE EVENTS 1. ACUTE PARALYTIC POLIOMYELITIS • WITHIN 4 -75 DAYS §

AEFI CNS ADVERSE EVENTS 1. ACUTE PARALYTIC POLIOMYELITIS • WITHIN 4 -75 DAYS § RESIDUAL PARALYSIS AFTER 60 DAYS OR DEATH

AEFI 2. GBS OCCURING WITHIN 30 DAYS 3. ENCEPHALOPATHY CASES OCCURING WITHIN 72 HOURS

AEFI 2. GBS OCCURING WITHIN 30 DAYS 3. ENCEPHALOPATHY CASES OCCURING WITHIN 72 HOURS AFTER VACCINATION

AEFI 4. ENCEPHALITIS CASES OCCURING WITHIN 72 HOURS 5. MENINGITIS WITHIN 1 - 6

AEFI 4. ENCEPHALITIS CASES OCCURING WITHIN 72 HOURS 5. MENINGITIS WITHIN 1 - 6 WEEKS SEIZURES – AFEBRILE - FEBRILE

AEFI OTHER ADVERSE EVENTS 1. ALLERGIC REACTION 2. ANAPHYLACTIC SHOCK 3. ARTHRALGIA 4. DISSEMINATED

AEFI OTHER ADVERSE EVENTS 1. ALLERGIC REACTION 2. ANAPHYLACTIC SHOCK 3. ARTHRALGIA 4. DISSEMINATED BCG-IT IS 5. HIGH FEVER

AEFI OTHER ADVERSE EVENTS(CONT) 6. HYPOTENSIVE EPISODE (SHOCK/COLLAPSE) 7. OSTEITIS/OSTEOMYELITIS 8. PERSISTENT SCREAMING 9.

AEFI OTHER ADVERSE EVENTS(CONT) 6. HYPOTENSIVE EPISODE (SHOCK/COLLAPSE) 7. OSTEITIS/OSTEOMYELITIS 8. PERSISTENT SCREAMING 9. SEPSIS (SEVERE GENERALIZED ILLNESS CONFIRMED BY BLOOD CULTURE)

AEFI OTHER ADVERSE EVENTS(CONT) 10. TOXIC SHOCK SYNDROME FEVER, VOMITTING AND WATERY DIARRHOEA- FEW

AEFI OTHER ADVERSE EVENTS(CONT) 10. TOXIC SHOCK SYNDROME FEVER, VOMITTING AND WATERY DIARRHOEA- FEW HOURS AFTER IMMUNIZATION – OFTEN LEADING TO DEATH

Examples of types & frequency of AEFIs (in some common vaccines)

Examples of types & frequency of AEFIs (in some common vaccines)

AEFI • Avoiding Programme Errors – – Use sterile needle & syringe for every

AEFI • Avoiding Programme Errors – – Use sterile needle & syringe for every injection Reconstitute only with specific diluent Discard reconstituted vaccines after six hours Do not store drugs & other medicines in the same fridge as the vaccines and diluents – Train & supervise health workers to ensure safe injection practices – Monitor, Investigate and Act when AEFIs occur

AEFI • Why monitor AEFI? – No vaccines are 100% safe and without any

AEFI • Why monitor AEFI? – No vaccines are 100% safe and without any risks – It is important to know the risks and how to handle such an event when it occurs – Informing people correctly on AEFI helps keep public’s confidence in the immunization programmes – Monitoring AEFI also helps improve the quality of service

AEFI • Steps in AEFI surveillance – Detection and reporting – Investigation – Data

AEFI • Steps in AEFI surveillance – Detection and reporting – Investigation – Data analysis – Corrective and other actions – Evaluation

AEFI • Detection and reporting – Every individual that administers an immunization injection should

AEFI • Detection and reporting – Every individual that administers an immunization injection should know about AEFI – There should be a national system for detecting and reporting of AEFI – At least the following should be included in the national AEFI monitoring system- “trigger events” • All injection site abscesses • All cases of BCG lymphadenitis • All deaths suspected to be related to immunization • All hospitalisation suspected to be related to immunization

AEFI • Detection and reporting – The above basic categories act as “trigger” mechanisms

AEFI • Detection and reporting – The above basic categories act as “trigger” mechanisms for further course of action – The national monitoring system should define the flow of information and mechanisms for taking actions – While minor events may be recorded and reported as a routine activity to be analysed only at periodic times, sudden, unexplained deaths or large scale hospitalisation or a cluster of events reported following immunisation warrants immediate investigation

AEFI • Investigation – AEFI investigation will attempt to • confirm or propose alternative

AEFI • Investigation – AEFI investigation will attempt to • confirm or propose alternative diagnosis of the reported event • identify the specifications of the vaccine incriminated • examine the operational aspects of the programme • identify whether it was an isolated event or a cluster of events and, if a cluster, where the immunization was given and what vaccines were used – Preliminary investigation may be carried out by the local health worker, but serious AEFIs or clusters of AEFIs should be investigated by special teams from district or central level

AEFI • Investigation – Data on the patient(s); vaccine (lot number, expiry, manufacturer, lab

AEFI • Investigation – Data on the patient(s); vaccine (lot number, expiry, manufacturer, lab results if any), storage, reconstitution practice, diluent used, general disease information in the area, similar disease episodes in unimnunized persons in the same locality, etc. should be collected – Collect samples of vaccines and diluents used (make sure vaccine sample collected are kept in the cold chain)

AEFI: An example of an AEFI investigation • Background – It is reported that

AEFI: An example of an AEFI investigation • Background – It is reported that following a measles campaign in a primary school in District X, several children had convulsions. It was widely rumoured that the measles injection was responsible for it • Hypothesis – that the reported health event (convulsion) was an AEFI following measles vaccination • Define the case – You define your ‘case’ as any child in that primary school who received measles injection on that particular day and had convulsions.

AEFI: example contd. . • Case investigation – Line list all children, with age

AEFI: example contd. . • Case investigation – Line list all children, with age & sex, who had received measles injection on that day – Find those that reported to have had convulsions – Find out all the details regarding the convulsionsonset time after immunization, manner of convulsion, recovery following the convulsion, concomitant medications, fever, any other health problems. Determine the quality of the vaccine (expiry, storage), reconstitution, diluent, injection process, etc. – Take samples of the vaccine vials used for lab testing – Scrutinise the stock entries, stock balance, etc.

AEFI: example contd. . – One child had an attack of fit half an

AEFI: example contd. . – One child had an attack of fit half an hour after the immunization. Following this three other children had fainting spells in the same class. All recovered spontaneously although the child who had the first convulsion took longer to recover. Also, the first child sustained a minor cut on the forehead from the fall – Next day, five more children called in sick on grounds that they had also attacks of fits after the school

AEFI • Data analysis – Once the data is collected, it should be analysed

AEFI • Data analysis – Once the data is collected, it should be analysed as quickly as possible to determine whether the AEFI is • Programme related (incorrect dose of vaccine, wrong site, wrong diluent, improper storage & handling, use of other medicines as diluent, etc. ) • Vaccine induced AEFI • Coincidental AEFIs (caused by something other than vaccine or programme errors) • Unknown – Laboratory support • If patient hospitalised, tests may confirm diagnosis • Testing vaccines often yield doubtful answers • Send case investigation report with vaccine for test

AEFI: example contd. . • Data Analysis – You find that the vaccine used

AEFI: example contd. . • Data Analysis – You find that the vaccine used has not expired, was well maintained in the cold chain, correct diluent was used, – There was no evidence of contamination, the health workers always discarded reconstituted vaccine at the end of the session. – The medical history showed that the fits which the other children had were mere fainting spells, lasting only for a few moment, with spontaneous recovery. No subsequent attacks occurred – The index child had a true convulsion. No fever or other illnesses at that time.

AEFI: example contd. . – However, going over the medical history of the child,

AEFI: example contd. . – However, going over the medical history of the child, the health worker recalled that last year the same child had an episode of convulsion for which he had provided treatment. He had advised that the parents should consult a medical or a neurological expert for further management. On questioning, it was found that the parents did not have the time or the money to do that and it was felt that it would resolve naturally

AEFI • Corrective and other actions – Action must not wait for investigation to

AEFI • Corrective and other actions – Action must not wait for investigation to be completed – Treat the patient(s) as the first response – Communicate, inform the public, parents, media people on the event, actions being taken & next steps – Once the investigation is completed, publicise the results – Take corrective actions, where necessary – Training of health workers & supervision to prevent avoidable AEFIs in future

AEFI: example contd. . • Conclusion – From the available information, and based on

AEFI: example contd. . • Conclusion – From the available information, and based on the data analysis, you conclude that event was not an AEFI, but Coincidental. – Following this, you will take time to explain to the parents, teachers and the community about the event, your investigation and your final conclusions.

AEFI • Evaluation – Like any other surveillance systems, AEFI surveillance must also be

AEFI • Evaluation – Like any other surveillance systems, AEFI surveillance must also be evaluated periodically to examine its usefulness and to modify it if necessary – Issues to consider when evaluating a surveillance system are • timeliness, completeness, accuracy of the system • swiftness with which response was effected when a trigger event was reported • appropriateness of actions taken • potential for strengthening of immunization system

AEFI An ounce of prevention is always better than a pound of cure. Good

AEFI An ounce of prevention is always better than a pound of cure. Good training & close supervision of health workers, coupled with a functioning surveillance system for monitoring & reporting are the best guarantee against the likelihood of an event occurring at all