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Bhutan 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 on 15 November 1979

TT for pregnant women introduced in 1983

HepB vaccine introduced in 1997

DTP-HepB vaccine introduced in 2003

AD syringes introduced in 2003

MR vaccine introduced in 2006

DTP-Hib-HepB vaccine introduced in 2009

HPV vaccine introduced in 2010

HepB birth dose introduced in 2012

TT vaccine replaced by Td vaccine in 2012

IPV vaccine introduced in 2015

tOPV to bOPV switched on 25 April 2016

MMR vaccine introduced in October 2016.

Source: cMYP 2014-2018 and VPDP/MOH

Table 1:

Basic information

1

2016

Total populaion 757,042

Live births 12,869

Children <1 year 11,227

Children <5 years 82,561

Children <15 years 229,796

Pregnant women 11,680

WCBA (15-49 years) 186,509

Neonatal mortality rate 18.3 (per 1,000 LB)

Infant mortality rate2 27.2 (per 1,000 LB)

Under-ive mortality rate 32.9 (per 1,000 LB)

Maternal mortality raio2 148 (per 100,000 LB)

1SEAR annual EPI reporing form, 2016 and WHO, World Health Staisics 2016 2VPDP/MOH

Division/Province/State/Region

-Dzongkhag/District 20

Gewog/Block 205

Sub-block/Ward 1,050

Village (approx.) 3,717

Populaion density (per sq. km) 18

Populaion living in urban areas 37%

Populaion using improved drinking-water sources2

97.7%

Populaion using improved sanitaion2 66.3%

Total expenditure on health as % of GDP 3.6%

Births atended by skilled health personnel2

74.6%

Neonates protected at birth against NT 83%

Table 2:

Immunization schedule, 2016

Vaccine Age of administraion

BCG Birth

HepB Birth

OPV Birth, 6 weeks, 10 weeks and 14 weeks

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

IPV 14 weeks

MMR 9 months and 24 months

DTP 24 months

HPV Females 12 years and grade VI girls

Td 6 and 12 years

Vitamin A 6 to 30 months (6 months interval) Source: WHO/UNICEF JRF,, 2016

(6)

Table 3:

Immunization system highlights

cMYP for immunizaion 2014-2018

NTAGI fully funcional

Spending on vaccines inanced by the government 41%

Spending on rouine immunizaion programme inanced by the government 24% Updated micro-plans that include aciviies to improve immunizaion coverage 20 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 Naional Health Survey 2012

>80% coverage for DTP-Hib-HepB3 20 districts (100%)

>90% coverage for MCV1 16 districts (80%)

>10% drop-out rate for DTP-Hib-HepB1 to DTP-Hib-HepB3 1 district (5%)

Source: WHO/UNICEF JRF, 2016

Figure 1:

National immunization coverage, 1980-2016

% Coverage

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

1980 1985 1990 1995 2000 2005 2010 2014 2015 2016

BCG 43 54 99 98 97 92 96 99 99 99

DTP3 6 41 96 87 92 95 91 99 99 98

OPV 4 41 96 86 98 95 92 98 98 97

MCV1 21 44 93 85 78 93 95 97 97 97

(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 0 0 10 3 262 3 ND

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

DTP-Hib-HepB3 coverage by district

(8)

Figure 5:

TT2+ coverage

1

and NT cases

2

, 1980-2016

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

Maternal and

neonatal tetanus elimination is sustained

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

%

NT Cases TT2+ Coverage

0.0

MNT eliminaion before 2000

(9)

Table 5:

AFP surveillance performance indicators, 2011-2016

Indicator 2011 2012 2013 2014 2015 2016

AFP cases 6 10 10 11 9 11

Wild poliovirus conirmed cases 0 0 0 0 0 0

Compaible cases 0 0 0 0 0 0

Non-polio AFP rate1 2.74 5.14 4.52 4.84 4.18 5.11

Adequate stool specimen collecion percentage2 83% 70% 80% 73% 67% 73%

Total stool samples collected 7 21 11 22 16 20

% NPEV isolaion 0 0 0 9 0 0

% Timeliness of primary result reported3 71 100 100 100 100 100

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

Last clinically-conirmed polio case was reported in 1986.

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

1995 OPV NID <5 years 80,336 99 100

1996-1997 OPV SNID <5 years 37,107 100 100

1997-1998 OPV SNID <5 years 37,465 100 100

1998-1999 OPV SNID <5 years 36,006 100 100

1999-2000 OPV SNID <5 years 36,541 100 100

2000-2001 OPV SNID <5 years 38,604 100 100

2001 OPV SNID <5 years 36,753 100 100

2002 OPV SNID <5 years 37,665 96 100

Source: WHO/UNICEF JRF, (muliple years)

Figure 9:

2016

Figure 8:

2015

Adequate stool specimen collection % by district

<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 %

1995 M naionwide 9 months to

15 years 69,285 100%

2000 M naionwide 9 months to

15 years 214,128 100%

2006 MR naionwide

9 months to 14 years children and

15 years to 44 years

women

338,040 98%

2016 MR subnaional 418 100%

(12)

0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19

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 0%

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 and no SIAs between 2009 & 2016.

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

Figure 12:

2016

Figure 13:

2015

Figure 14:

2016

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

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

Figure 11:

2015

Source: SEAR annual EPI reporing form,

2015 (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

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

Immunized Not immunized/ Unknown

0

(14)

Table 8:

Surveillance performance indicators for measles and rubella, 2012-2016

Year

No. of suspected measles

Case classiic

Discarded non-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 non-measles non-rubella incidence per

100,000 total populaion Proporion of districts reporing at least two

discarded non-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, 2011-2016

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

Public Health Laboratory

Naional measles/rubella laboratory

(16)

For contact or feedback:

Expanded Programme on Immunizaion Ministry of Health, Thimphu, Bhutan Tel: +975-2-332296, Fax: +975-2-332296 Email: [email protected]

www.health.gov.bt

Immunizaion and Vaccine Development (IVD)

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

Email: [email protected]

Gambar

Table 1: Basic information1 2016
Figure 1: National immunization coverage, 1980-2016
Figure 3: 2015
Figure 5: TT2+ coverage1 and NT cases2, 1980-2016
+7

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