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Sri Lanka 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 launched in 1978

Inacivated JE vaccine introduced in 1988 and live JE vaccine naionwide in 2011

Rubella vaccine introduced in 1996

Vitamin A supplementaion added in 2000

MR vaccine and aTd vaccine introduced in 2001

HepB vaccine introduced in 2003

DTP-Hib-HepB vaccine introduced in 2008

MMR vaccine introduced in 2011

IPV introduced in 2015

Naionwide fIPV introduced in 2016

tOPV to bOPV switched on 30 April 2016.

Source: cMYP 2017-2021 and EPI/MOH

Table 1:

Basic information

1

2016

Total populaion 21,164,458

Live births 331,073

Children <1 year 330,461

Children <5 years 1,820,143

Children <15 years 5,333,443

Pregnant women 331,073

WCBA (15-49 years) 4,939,621

Neonatal mortality rate 5.4 (per 1,000 LB)

Infant mortality rate 8.4 (per 1,000 LB)

Under-ive mortality rate 9.8 (per 1,000 LB)

Maternal mortality raio 30 (per 100,000 LB)

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

Division/Province/State/Region 9

District 26

Medical oicer of health (MOH) areas 337

Populaion density (per sq. km) 324

Populaion living in urban areas 18%

Populaion using improved drinking-water

sources 94%

Populaion using improved sanitaion 92%

Total expenditure on health as % of GDP 3.1%

Births atended by skilled health personnel 99%

Neonates protected at birth against NT 95%

Table 2:

Immunization schedule, 2016

Vaccine Age of administraion

BCG Birth

DTP-Hib-HepB 2 months, 4 months and 6 months

OPV 2 months, 4 months, 6 months, 18 months and 5 years

IPV (fIPV) 2 months and 4 months

JE_LiveAtd 1 year

MMR 9 months and 3 years

DTP 18 months

DT 5 years

aTd 12 years

TT Pregnant women (2 doses in 1st pregnancy and 1 dose in subsequent 3 pregnancies)

Vitamin A 6 to 36 months 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 2017-2021

NTAGI fully funcional

Spending on vaccines inanced by the government no data

Spending on rouine immunizaion programme inanced by the government 74%

Updated micro-plans that include aciviies to improve immunizaion coverage 26 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 coverage survey Nuwara Eliya district 2016

>80% coverage for DTP-Hib-HepB3 26 districts (100%)

>90% coverage for MCV1 26 districts (100%)

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

Source: WHO/UNICEF JRF, 2016

1980 1985 1990 1995 2000 2005 2010 2014 2015 2016

BCG 61 71 84 90 98 99 99 99 99 99

DTP3 46 70 86 93 99 99 99 99 99 99

OPV 46 71 86 92 99 99 99 99 99 99

MCV1 20 80 87 99 99 99 99 99 99

(7)

<70% 70% - 79% 80% - 89% >90%

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 23 0 60 416 1,129 30 3

Source: WHO/UNICEF JRF, (muliple years) ND=No data

(8)

1980 1985 1990 1995 2000 2005 2010 2011 2012 2013 2014 2015 2016

NT Cases TT2+ Coverage 0

1 WHO/UNICEF JRF, Country oicial esimates, 1980-2015

2WHO vaccine-preventable diseases: monitoring system 2015 & JRF 2015

Maternal and neonatal tetanus elimination is sustained

MNT eliminaion before 2000

© WHO/Sri Lanka/K Reidey

(9)

Table 5:

AFP surveillance performance indicators, 2011-2016

Indicator 2011 2012 2013 2014 2015 2016

AFP cases 88 75 103 84 70 65

Wild poliovirus conirmed cases 0 0 0 0 0 0

Compaible cases 0 0 0 0 0 0

Non-polio AFP rate1 1.42 1.54 1.66 1.59 1.35 1.20

Adequate stool specimen collecion percentage2 86% 80% 82% 75% 77% 85%

Total stool samples collected 175 156 168 134 137 104

% NPEV isolaion 1 4 6 5.3 10 3.8

% Timeliness of primary result reported3 99 89 98 98 89 81

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

The last laboratory conirmed polio case due to WPV was reported in November 1993.

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

1997 OPV NID <5 years 1,838,465 97 95

1998 OPV NID <5 years 1,856,850 92 88

1999 OPV NID <5 years 2,320,556 93 93

2000 OPV NID <5 years 634,999 93 93

2001 OPV SNID <5 years 514,821 96 91

2002 OPV SNID <5 years 272,559 98 97

2003 OPV SNID <5 years 536,269 97 98

Source: NCCPE reports and 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

2016

No. of cases

Year

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 2 districts 10 to 15

years 1,987,847 95

2004 MR naionwide 16 to 20

years 1,890,326 72

2013 M naionwide 6 to 12

months 176,587 96

(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

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

> 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

< 1 year

2011 2012 2013 2014 2015 2016

0

(14)

Table 8:

Surveillance performance indicators for measles and rubella, 2012-2016

Year

No. of suspect

ed measles

Case classiicaion (number) Indicators

Measles Rubella

Disc

ar

ded non-measles

non-rubella c

ases

Annual incidence of con

irmed measles c

ases per

million t

ot

al popula

ion

Annual incidence of con

irmed rubella c

ases per

oporion of all suspect

ed

measles and rubella c

ases

tha

t ha

ve had an adequa

te

in

ves

ig

aion iniia

ted within

48 hour

s of noiic

aion

Disc

ar

ded non-measles

non-rubella incidence per 100,000 t

ot

al popula

ion

Pr

oporion of subna

ional

measles non-rubella c

ases

per 100,000 t

ot

al popula

ion

Pr

oporion of sub-na

ional

sur

veillance units r

eporing

Source: SEAR annual EPI reporing form (2012-2016) ND=No data

Year

Serum specimen collect

ed fr

Serum specimen receiv

ed in

labor

a

tor

y

within 5 da

ys of

collecion Specimen posiiv

e f

or

measles IgM Specimen posiiv

e f

or

rubella IgM

% R

esults within

4 da

tecion Genotypes de

tect

*this includes 5 rubella Igm posiive samples that were subsequently excluded as they are post vaccinaion and one sample that was a repeat sample Source: SEAR annual EPI reporing form (2012-2016) ND=No data

(15)

Figure 19:

WHO supported laboratory network for VPD surveillance

Medical Research Insitute, Colombo • Naional polio laboratory

• Naional measles and rubella laboratory • Naional Japanese encephaliis laboratory • Rotavirus laboratory

(16)

For contact or feedback:

Expanded Programme on Immunizaion Ministry of Health, Colombo, Sri Lanka

Tel: +94 11 2695112; Fax: +94-11-2696583 Email: samithag@hotmail.com

www.health.gov.lk

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
Table 3: Immunization system highlights
Table 4: Reported cases of vaccine preventable diseases, 2011-2016
Figure 5: TT2+ coverage1 and NT cases2, 1980-2016
+7

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