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Timor-Leste 2017

(2)

Acronyms

AD Auto disable

AEFI Adverse events following immunization

AFP Acute flaccid paralysis

BCG Bacillus Calmette-Guérin vaccine

CES Coverage evaluation survey

cMYP Comprehensive multi-year plan

CRS Congenital rubella syndrome

DHS Demographic health survey

DT Diphtheria tetanus toxoid, pediatric

DTP Diphtheria – tetanus – pertussis vaccine

DTP-Hib-HepB Pentavalent vaccine

DTP-Hib-HepB3 3rd dose pentavalent vaccine

EPI Expanded programme on immunization

GDP Gross domestic product

HCW Health care worker

HepB Hepatitis B vaccine

Hib Haemophilus influenzae type b

HPV Human papilloma virus

IgM Immunoglobulin M

IPV Inactivated poliovirus vaccine

JE Japanese encephalitis

JE_Live-Atd JE live attenuated vaccine

JRF WHO UNICEF joint reporting form

LB Live birth

M Measles

MCV1 First dose measles containing vaccine

MCV2 Second dose measles containing vaccine

MICS Multiple indicator cluster survey

MMR Measles mumps rubella vaccine

MNT Maternal and neonatal tetanus

MR Measles rubella vaccine

NCIP National committee on immunization practices

NID National immunization day

NTAGI National technical advisory group on immunization

NPEV Non-polio enterovirus

NT Neonatal tetanus

OPV Oral poliovirus vaccine

bOPV Bivalent OPV

tOPV Trivalent OPV

PCV Pneumococcal conjugate vaccine

SEAR WHO South-East Asia Region

SIA Supplementary immunization activities

SNID Subnational immunization day

Td Tetanus diphtheria toxoid; older children, adults

TT Tetanus toxoid

TT2+ 2 or more doses TT

VDPV Vaccine derived poliovirus

VPD Vaccine preventable diseases

WCBA Women of child bearing age

(3)

Contents

Impact of rouine immunizaion

Page

No.

EPI history 5

Basic informaion 2016 Table 1 5

Immunizaion schedule 2016 Table 2 5

Naional immunizaion coverage 1980 - 2016 Figure 1 6

Immunizaion system highlights Table 3 6

DTP3 coverage, diphtheria and pertussis cases 1980 - 2016 Figure 2 7

Reported cases of vaccine preventable diseases 2011 - 2016 Table 4 7

DTP-Hib-HepB3 coverage by district 2015 Figure 3 7

DTP-Hib-HepB3 coverage by district 2016 Figure 4 7

Towards measles eliminaion and rubella/congenital rubella

syndrome control

Page

No.

MCV1 and MCV2 coverage, measles and rubella cases, 1980-2016 Figure 10 11

MCV supplementary immunizaion aciviies Table 7 11

MCV1 coverage by district 2015 Figure 11 12

MCV1 coverage by district 2016 Figure 12 12

MCV2 coverage by district 2015 Figure 13 12

MCV1 coverage by district 2016 Figure 14 12

Immunity against measles – immunity proile by age in 2016 Figure 15 12

Subnaional risk assessment for measles and rubella Figure 16 12

Sporadic and outbreak associated measles cases by month 2011 - 2016 Figure 17 13

Immunizaion status of conirmed (laboratory and Epi linked) measles outbreak

associated cases by age 2011 – 2016 Figure 18 13

Quality of ield and laboratory surveillance for measles and rubella 2012 - 2016 Table 8 14

Performance of laboratory surveillance 2012 - 2016 Table 9 14

WHO supported laboratory network for VPD surveillance Figure 19 15

Maternal and neonatal tetanus eliminaion is sustained

Page

No.

TT2+ coverage and NT cases 1980 - 2016 Figure 5 8

Polio-free status is maintained

Page

No.

AFP surveillance indicators 2011 - 2016 Table 5 9

Non-polio AFP rate by district 2015 Figure 6 9

Non-polio AFP rate by district 2016 Figure 7 9

Adequate stool specimen collecion percentage by district 2015 Figure 8 10

Adequate stool specimen collecion percentage by district 2016 Figure 9 10

(4)

WHO South-East Asia Region

(5)

EPI history

EPI started in 1978

EPI re-structured in March 2000 DTP-HepB vaccine introduced

in 2007

DTP-Hib-HepB) vaccine

introduced in 2012

MR vaccine introduced in

Feb 2016

Second dose of MR introduced

in Feb 2016

HepB birth dose introduced in

Feb 2016

DPT/DT vaccine (booster dose)

introduced in Feb 2016

IPV introduced in Feb 2016 tOPV to bOPV switched on

18 April 2016 .

Source: cMYP 2016-2020 and EPI/MOH

Table 1:

Basic information

1

2016

Total populaion 1,231,262

Live births 35,426

Children <1 year 33,548

Children <5 years 176,377

Children <15 years 493,795

Pregnant women 38,969

WCBA (15-49 years) 154,605

Neonatal mortality rate 22.3 (per 1,000 LB)

Infant mortality rate 44.7 (per 1,000 LB)

Under-ive mortality rate 52.6 (per 1,000 LB)

Maternal mortality raio 215 (per 100,000 LB)

1SEAR annual EPI reporing form, 2016 and WHO, World Health Staisics 2016

Division/Province/State/Region

-Municipaliies 13

Postos/Sub-district 65

Sucos/Village 442

Populaion density (per sq. km) 71

Populaion living in urban areas 32%

Populaion using improved

drinking-water sources 70%

Populaion using improved sanitaion 39%

Total expenditure on health as % of GDP 1.4%

Births atended by skilled health personnel 21%

Neonates protected at birth against NT 81%

Table 2:

Immunization schedule, 2016

Vaccine Age of administraion

BCG Birth

OPV Birth, 6 weeks, 10 weeks and 14 weeks

DTP-Hib-HepB 6 weeks, 10 weeks and 14 weeks

MR 9 months and 18 months

TT Females 15 to 49 years (1st pregnancy contact, +1 month, +6 months, +1 year, +1 year)

Vitamin A 6 to 36 months (with 6 months interval)

IPV 14 weeks

DT 6 years

Source: WHO/UNICEF JRF, 2016

(6)

Figure 1:

National immunization coverage, 1980-2016

Source: WHO/UNICEF esimates of naional immunizaion coverage, July 2017 revision

Table 3:

Immunization system highlights

cMYP for immunizaion 2016-2020

NTAGI fully funcional

Spending on vaccines inanced by the government 76%

Spending on rouine immunizaion programme inanced by the government 39%

Updated micro-plans that include aciviies to improve immunizaion coverage 13 districts (100%)

Naional policy for health care waste management including waste from immunizaion aciviies in place

Naional system to monitor AEFI in place

Most recent EPI CES EPI CES Dili municipality and 12 other

municipaliies 2015

>80% coverage for DTP-Hib-HepB3 13 districts (100%)

>90% coverage for MCV1 7 districts (54%)

>10% drop-out rate for DTP-Hib-HepB1 to DTP-Hib-HepB3 no district

Source: WHO/UNICEF JRF, 2016

2002 2004 2006 2008 2010 2014 2015 2016

BCG 75 72 74 85 79 84 84 85

DTP3 54 57 63 79 72 77 76 85

OPV 38 57 62 79 72 76 75 83

MCV1 56 55 61 73 66 74 70 78

(7)

Figure 3:

2015

Figure 4:

2016

Source: SEAR annual EPI reporing form, 2016 (administraive data) Source: SEAR annual EPI reporing form, 2015 (administraive data)

Figure 2:

DTP3 coverage

1

, diphtheria and pertussis cases

2

, 1980-2016

Year

Diphtheria Cases Pertussis Cases DTP3 Coverage

%

1WHO/UNICEF esimates of naional immunizaion coverage, July 2017 revision 2WHO vaccine-preventable diseases: monitoring system 2016

Table 4:

Reported cases of vaccine preventable diseases, 2011-2016

Year Polio Diphtheria Pertussis NT

(% of all tetanus) Measles Rubella Mumps JE CRS

2011 0 0 4 2 (67%) 802 0 0 0 0

Source: WHO/UNICEF JRF (2011-2016) ND=No data

DTP-Hib-HepB3 coverage by district

(8)

%

NT Cases TT2+ Coverage

0

2002 2004 2006 2008 2010 2011 2012 2013 2014 2015 2016

Figure 5:

TT2+ coverage

1

and NT cases

2

, 1980-2016

1 WHO/UNICEF JRF, Country oicial esimates, 1980-2016 2WHO vaccine-preventable diseases: monitoring system 2016

Maternal and

neonatal tetanus elimination is sustained

MNT eliminaion in 2012

© WHO/Timor-Leste/S Singh

(9)

Table 5:

AFP surveillance performance indicators, 2011-2016

Indicator 2011 2012 2013 2014 2015 2016

AFP cases 0 5 5 3 0 10

Wild poliovirus conirmed cases 0 0 0 0 0 0

Compaible cases 0 0 0 0 0 0

Non-polio AFP rate1 0 1.00 1.61 0.59 0.00 1.87

Adequate stool specimen collecion percentage2 0 40% 20% 67% 0 50

Total stool samples collected 0 5 5 4 0

-% NPEV isolaion 0 0 0 0 0

-% Timeliness of primary result reported3 0 100 68 100 0

-1Number of discarded AFP cases per 100,000 children under 15 years of age.

2Percent with 2 specimens, at least 24 hours apart and within 14 days of paralysis onset. 3Results reported within 14 days of sample received at laboratory.

Figure 6:

2015

Figure 7:

2016

Polio-free

status is maintained

Non-polio AFP rate by district

<1 1 – 1.99

>2 No non-polio AFP case

(10)

Table 6:

OPV SIAs

Year Vaccine Geographic

coverage Target age

Target populaion Coverage (%)

Round 1 Round 2 Round 1 Round 2

2005 OPV NID <5 years 177,713 93 102

2015* OPV NID <5 years 522,943 - 96

-* During MR vaccinaion campaign. Source: WHO/UNICEF JRF

Adequate stool specimen collection % by district

Figure 9:

2016

Figure 8:

2015

<60% 60% - 79%

>80% No AFP

(11)

Towards

measles elimination and rubella/CRS control

Figure 10:

MCV1 and MCV2 coverage

1

, measles and rubella cases

2

, 1980-2016

Measles Cases Rubella MCV1 Coverage MCV2 Coverage

763

% Coverage

No. of cases

Year

2002 2004 2006 2008 2010 2011 2012 2013 2014 2015 2016 No

data

1WHO/UNICEF esimates of naional immunizaion coverage, July 2017 revision 2WHO vaccine-preventable diseases: monitoring system 2016

Table 7:

MCV SIAs

Year Anigen Geographic

coverage Target group Target

Coverage %

2003 M naionwide 9 to 59

months 128,318 99

2006 M naionwide 6 months to

14 years 390,687 40

2009 M naionwide 9 to 59

months 167,136 76

2011 M naionwide 6 months to

14 years 494,427 92

2015 MR naionwide 6 months to

14 years 501,832 97

(12)

0%

Percent of population

Age (in years)

Protected by maternal antibodies Protected by routine vaccination with 1st dose

Protected by routine vaccination with 2nd dose Protected by SIAs

Immune due to past infection Susceptible

Figure 15:

Immunity against measles - immunity profile by age in 2016*

* Modeled using MSP tool ver 2 assuming the schedule and MCV coverage remain unchanged in 2016.

<80% 80% - 89% 90% - 94% >95%

Source: SEAR annual EPI reporing form, 2016 (administraive data)

Figure 12:

2016

Figure 11:

2015

Source: SEAR annual EPI reporing form, 2015 (administraive data)

Figure 14 :

2016

Figure 13:

2015

Source: SEAR annual EPI reporing form, 2016 (administraive data)

Source: SEAR annual EPI reporing form, 2015 (administraive data)

Figure 16:

Sub-national risk assessment -measles and rubella

MCV1 coverage by district

MCV2 coverage by district

Source: developed using WHO risk assessment tool based on JRF & ARF data base

(13)

Figure 17:

Sporadic and outbreak associated measles cases* by month 2011-2016

Sporadic measles

Outbreak associated measles

No of cases

0

*Includes laboratory conirmed and epidemiologically linked cases Source: SEAR Monthly VPD reports

Figure 18:

Immunization status of confirmed (laboratory and EPI linked) measles

outbreak associated cases, by age, 2011-2016

2011 2012 2013 2014 2015 2016

0

> 15 years

10-14 years

5-9 years

1-4 years

< 1 year

> 15 years

10-14 years

5-9 years

1-4 years

< 1 year

> 15 years

10-14 years

5-9 years

1-4 years

< 1 year

> 15 years

10-14 years

5-9 years

1-4 years

< 1 year

> 15 years

10-14 years

5-9 years

1-4 years

< 1 year

> 15 years

10-14 years

5-9 years

1-4 years

(14)

Table 8:

Surveillance performance indicators for measles and rubella, 2012-2016

Year

No. of suspected measles

Case classiic

Discarded measles non-rubella cases

Annual incidence of

conirmed measles cases per million total populaion

Annual incidence of

conirmed rubella cases per million total populaion Proporion of all suspected

measles and rubella cases that have had an adequate

invesigaion iniiated within 48 hours of noiicaion

Discarded measles

non-rubella incidence per 100,000 total populaion

Proporion of districts reporing at least two

discarded measles

non-rubella cases per 100,000 total populaion

Proporion of sub-naional surveillance units reporing to the naional level on ime Lab-conirmed

AR annual EPI reporing f

orm (2012-2016)

ND=No dat

a

Year

Serum specimen collected from suspected measles cases

Serum specimen received in laboratory

within 5 days of collecion

Specimen

posiive for

measles IgM

Specimen

posiive for

rubella IgM

% Results within 4 days of receipt

% Posiive cases

tested for viral

detecion

AR annual EPI reporing f

orm (2012-2016)

ND=No dat

a

Table 9:

Performance of laboratory surveillance, 2012-2016

(15)

Figure 19:

WHO supported laboratory network for VPD surveillance

Naional Health Laboratory, Dili

(16)

For contact or feedback:

Expanded Programme on Immunizaion Ministry of Health, Dilli, Timor-Leste Tel: +670-77351964, Fax: +670-7250097 Email: mmausiry@gmail.com

www.moh.gov.tl

Immunizaion and Vaccine Development (IVD)

WHO-SEARO, IP Estate, MG Marg, New Delhi 110002, India Tel: +91 11 23370804, Fax: +91 11 23370251

Email: SearEpidata@who.int

Gambar

Table 1: Basic information1 2016
Figure 1: National immunization coverage, 1980-2016
Figure 2: DTP3 coverage1, diphtheria and pertussis cases2, 1980-2016
Figure 5: TT2+ coverage1 and NT cases2, 1980-2016
+7

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