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Epidemiology of Vaccine Preventable diseases in Iran

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Presentation on theme: "Epidemiology of Vaccine Preventable diseases in Iran"— Presentation transcript:

1 Epidemiology of Vaccine Preventable diseases in Iran
Dr Seyed Mohsen Zahraei Center for Communicable Disease Control

2 Outline The mean and importance of surveillance
Surveillance system functionality Regional targets for Vaccine Preventable Diseases Progress towards achieving the targets in Polio, Measles and Rubella Challenges and opportunities

3 Definition of Surveillance
Disease surveillance is the ongoing systematic collection, analysis and interpretation of data and dissemination of INFORMATION to those who need to know FOR ACTION to be taken

4 Collection Analysis and Interpretation Surveillance Action
Dissemination

5 Importance of VPDs surveillance:
Demonstrate the real effectiveness of the vaccination programme in reaching its objective, reduction of VPDs: Measles control/elimination, MNTE, control of diphtheria and pertussis,….. Demonstrate the need for intervention: introduction of new vaccines Dangerous if not properly implemented: drawing incorrect conclusion: decreasing trend/low estimate of a disease, the programme is doing fine low burden of a disease, the new vaccine is not a priority

6 Process & Stages of Surveillance
Notification of suspect case Case investigation & specimen collection Reporting Laboratory testing Integration of field and laboratory data Final case classification Feedback

7 Core Surveillance Indicators
Timeliness of reporting Reporting rate Representativeness of reporting Adequacy of epidemiological investigation Timeliness of notification Laboratory confirmation Agent detection Specimen transport & lab reporting

8 Measles Surveillance in the Elimination Phase
Surveillance priorities: Confirm all cases Detect virus from all outbreaks (chains of transmission) Surveillance system attributes: Sensitive – identify all suspect cases of measles & rubella Timely – prompt notification, investigation and response Complete -- case investigations, laboratory confirmation & virus detection

9 Surveillance Indicators (1)
Timeliness (& completeness) of reporting Proportion of surveillance units reporting to the national level on time (Target: >80%) Used to identify poorly functioning units / districts / governorates / countries

10 Surveillance Indicators (2)
Reporting rate Reporting rate of discarded non-measles non-rubella cases at the national level Target: >2 cases per 100,000 population per year Representativeness of reporting Proportion of sub-national (province or governorate) units reporting >2 discarded cases/100,000 pop/yr Combine units, if needed, to achieve >100,000 pop Target: >80% Used to assess surveillance sensitivity at national & sub-national levels

11 Surveillance Indicators (3)
Adequacy of investigation Proportion of all suspected measles & rubella cases with adequate investigation initiated within 48 hours after notification An adequate investigation includes collection of all relevant data elements from each suspected case Data elements: Identifiers, residence, place of infection, age, sex rash onset date, specimen collection date, etc. Target: >80% Used to assess timeliness & completeness of case investigation (epidemiological component)

12 Surveillance Indicators (4)
Laboratory confirmation Proportion of suspected cases with adequate specimen for detecting acute measles or rubella infection collected and tested by a proficient laboratory. Adequate specimens include serum sample, DBS, or oral fluid, taken within 28 days after rash onset Cases not tested but confirmed by epi-linkage to a confirmed case of measles, rubella or other communicable disease excluded from denominator Target: >80% Used to assess completeness of case investigation (“serological” component)

13 Surveillance Indicators (5)
Virus detection Proportion of laboratory-confirmed outbreaks (chains of transmission) with adequate specimens for detecting measles or rubella virus collected and tested in an accredited laboratory. Adequate specimens include a) throat swabs or urine samples for virus isolation (collected <5 days after rash onset), or b) throat swabs or oral fluid samples for molecular detection (collected <14 days or <21 days, respectively, after rash onset) Target: >80% Used to assess completeness of case investigation (virological component)

14 Surveillance Indicators (6)
Timeliness of specimen transport Proportion of specimens received at the laboratory <5 days [Target: >80%] Timeliness of laboratory reporting Proportion of results reported by the laboratory <4 days of specimen receipt [Target: >80%] Used to assess timeliness of case investigation (epidemiological & laboratory components)

15 Summary Standardized definitions have been developed for case classification & elimination verification In the elimination phase, surveillance for measles & rubella needs to be Geographically representative Sensitive Timely Complete Current indicators are used to assess quality of case investigations & overall surveillance system Targets for indicators (>80%) are minimums

16 The Targets: for each country
Soonest possible (for countries that haven’t achieved yet) Achieve at least 90% DPT3 coverage at national level AND 80% in every district (target date 2010) Eliminate MNT soonest possible (target date 2007) By 2012 Eradicate polio By 2015, Eliminate measles (regional target) Reduce HBsAg prevalence to < 1% among <5 years children (Regional target) Reduce VPDs morbidity and mortality by 2/3 compared to 2000 (GIVS goal) Introduce new vaccines (Hib, PCV and Rota) to all countries as soon as possible (RC58, 2011)

17 Poliomyelitis Eradication Initiative The End Game

18 Poliomyelitis was selected for eradication because :
There is no animal reservoir. There is no chronic carrier state. Poliovirus survives poorly in the environment. Presence of effective vaccine against the disease

19 The Global Polio Eradication Emergency Action Plan aims to boost vaccination coverage in Nigeria, Pakistan and Afghanistan, the three remaining polio endemic countries, to levels needed to stop polio transmission.

20 Polio-free Status of 21 Countries of EMRO is Maintained
- cVDPV in Yemen 2011 last case Oct 2011 - Continuous cVDPV in Somalia from with last case in 23/07/2012 Polio Cases 2011 September 2012 Country P1 P3 P1P3 Pakistan 196 2 32 1 Afghanistan 80 17 EMRO 09/09/2012

21 % of NP AFP cases 6-< 59 months with 3 or more OPV doses
by province in EMR countries, 2012 Routine OPV3 coverage, 2011 Source: WHO/UNICEF Estimates of National Immunization Coverage EMRO 09/09/2012

22 Immunity profile of NP AFP cases 6-59 months in
EMR countries, 2012 up to 09/09/12

23 VDPVs isolated in EMR 2005 2006 2007 2008 2009 2010 2011 2012 AFG EGY
Country 2005 2006 2007 2008 2009 2010 2011 2012 AFG cVDPV2 (01) cVDPV2 (05) cVDPV 2 (01) EGY aVDPV2 (Sewage Behira) iVDPV3 (01) aVDPV 2 (Sewage Behira) aVDPV 1 Helwan-Cairo iVDPV1 (01) iVDPV2 (01) IRAN iVDPV1 + iVDPV2 (01) iVDPV2 (02) KWT IRAQ MOR iVDPV2 Detected in Spain SAA SOM VDPV2 (02) cVDPV2 (03) cVDPV2 (07) cVDPV 2 (02) cVDPV2 (09) SYR VDPV2 (01) aVDPV 2(01) Sudan aVDPV2 (01) South Sudan TUN iVDPV2 (1) iVDPV1 (a) P1 iVDPV (a) P3 iVDPV? (b) YEM cVDPV 2 (09) aVDPV3 (01) 23

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28 Measles and Rubella Elimination in EMR Countries

29 Measles cases down by 62% Measles deaths down by 74%
Reported cases of measles Measles cases down by 62% Measles deaths down by 74% measles cases show a declining trend over the past 10 years, as countries in all regions accelerated activities to control measles. But resurgence of outbreaks particularly in Africa (blue part of bars and europe (red part of bars) account for increasing number seen from 2010. But overall trends for mortality are on the low side… amazing progress overall Progress in global measles control, 2000–2010. WER 3 Feb 2012, vol. 87, 5 (pp 45–52) Lancet in press; 2012 IVB model by Simons, Ferrari et al.

30 Source: Country reports Inadequate surveillance
2,052 Source: Country reports Inadequate surveillance

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32 Measles Cases, Incidence and Virus Genotypes, 2009- 2012*
Year Measles Suspected Cases Confirmed Measles cases Measles Incidence/Million Detected Genotype Lab Epi-Linked Clinical/ Compatible Total 2009 1282 118 7 132 257 3.4 D4 , H1 2010 2489 259 275 534 7.15 D4 , D1 2011 2641 18 114 135 1.8 D4 2012 2394 154 4 49 201 2.6 B3, H1, D4 * Up to August

33 Measles Confirmed Cases, 2009 – 2012*
* Display in line graph the distribution of confirmed measles cases by month for 2009 – 2012 up to August

34 Geographical Distribution Of Confirmed Measles Cases By Province, 2009 - 2012
Map 2009 Map 2010 Map 2012 Map 2011

35 Confirmed measles Cases ( Lab+Epi-linked ) by age group 2009 - 2012

36 Source: Country reports
Inadequate/No surveillance

37 Rubella detected cases based on fever and rash surveillance system, Iran, 2005-2011
Suspected cases Number of Tested Rubella Positive Measles positive 2005  536 410 11 6 2006  943 771 15 45 2007  900 796 5 21 2008  972 868 10 2009  1282 1159 9 118 2010  2489 2212 22 258 2011  2476 2232 18 Total 9598 8448 87 460

38 CRS Surveillance in Iran
Established in 2004, after MR mass campaign. Accelerated passive surveillance, comprehensive All hospitals which may admit suspected cases are covered

39 CRS suspected Case Definition
An infant (0-11 months) whose mother had suspected or confirmed history of rubella in pregnancy An infant (0-11 months) with heart disease and or ophthalmic disease and or deafness

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42 CRS suspected cases by sign

43 Summary Progress Challenges Well developed PHC network
High immunity level Robust surveillance system Challenges New reporting sites Training Private sector partnership Need to performance indicators


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