| Literature DB >> 28727678 |
Sudhir Khanal, Rajendra Bohara, Stephen Chacko, Mohammad Sharifuzzaman, Mohammad Shamsuzzaman, James L Goodson, Alya Dabbagh, Katrina Kretsinger, Deepak Dhongde, Jayantha Liyanage, Sunil Bahl, Arun Thapa.
Abstract
In 2013, at the 66th session of the Regional Committee of the World Health Organization (WHO) South-East Asia Region (SEAR), a regional goal was established to eliminate measles and control rubella and congenital rubella syndrome* by 2020 (1). WHO-recommended measles elimination strategies in SEAR countries include 1) achieving and maintaining ≥95% coverage with 2 doses of measles-containing vaccine (MCV) in every district, delivered through the routine immunization program or through supplementary immunization activities (SIAs)†; 2) developing and sustaining a sensitive and timely measles case-based surveillance system that meets targets for recommended performance indicators; and 3) developing and maintaining an accredited measles laboratory network (2). In 2014, Bangladesh, one of 11 countries in SEAR, adopted a national goal for measles elimination by 2018 (2,3). This report describes progress and challenges toward measles elimination in Bangladesh during 2000-2016. Estimated coverage with the first MCV dose (MCV1) increased from 74% in 2000 to 94% in 2016. The second MCV dose (MCV2) was introduced in 2012, and MCV2 coverage increased from 35% in 2013 to 93% in 2016. During 2000-2016, approximately 108.9 million children received MCV during three nationwide SIAs conducted in phases. During 2000-2016, reported confirmed measles incidence decreased 82%, from 34.2 to 6.1 per million population. However, in 2016, 56% of districts did not meet the surveillance performance target of ≥2 discarded nonmeasles, nonrubella cases§ per 100,000 population. Additional measures that include increasing MCV1 and MCV2 coverage to ≥95% in all districts with additional strategies for hard-to-reach populations, increasing sensitivity of measles case-based surveillance, and ensuring timely transport of specimens to the national laboratory will help achieve measles elimination.Entities:
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Year: 2017 PMID: 28727678 PMCID: PMC5657944 DOI: 10.15585/mmwr.mm6628a3
Source DB: PubMed Journal: MMWR Morb Mortal Wkly Rep ISSN: 0149-2195 Impact factor: 17.586
FIGUREAggregated measles cases,* estimated coverage with the first and second dose of measles-containing vaccine (MCV1 and MCV2), and supplementary immunization activities (SIAs)**,†† — Vaccine Preventable Disease Surveillance Report, Bangladesh, 1980–2016
* Laboratory-confirmed, epidemiologically linked and clinically compatible cases with fever; rash; and cough, coryza or conjunctivitis; reported as of Dec 2015 to World Health Organization (WHO) South-East Asia Region (2016 Joint Reporting Form [JRF]).
† 1990–2015 coverage data from WHO/UNICEF estimates of national immunization coverage as published in July 2016; for 2016, coverage data are from country official estimates (submitted through 2016 JRF).
§ National measles catch-up SIA targeted children aged 9 mos–10 yrs, implemented in two phases: 1) Sep 2005, targeting 1,481,321 children; 2) Feb 2006, targeting 34,199,590 children. Overall administrative coverage >100%.
¶ National measles follow-up SIA targeted children aged 9–59 mos, conducted Feb 14–28, 2010, targeting 18,136,066 children.
** National measles-rubella catch-up SIA targeted children aged 9 mos–14 yrs, conducted during Jan 25–Feb 13, 2014 targeting 51,745,231 children.
†† Specific SIA dates are as follows: Sep 3–22, 2005; Feb 25–Mar 16, 2006; Feb 14–28, 2010; Feb 13–Mar 25, 2014.
Measles incidence,* number of reported measles cases by case classification, age group, and vaccination status — Vaccine Preventable Disease Surveillance Report, Bangladesh, 2001–2016
| Year | WHO/UNICEF JRF aggregate reporting† | Measles case-based reporting§ | ||||||||||||||
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| No. of measles cases by classification | Age of confirmed measles cases, No. (%) | MCV doses received by confirmed measles cases, No. (%) | ||||||||||||||
| No. of reported measles cases | Incidence (cases/ million population) | Suspected¶ | Confirmed** | Laboratory-confirmed | Epi-linked | Clinically compatible | <9 mos | 9 mos–4 yrs | 5–9 yrs | 10–14 yrs | ≥15 yrs | ≥2 | 1 | Zero | Unknown | |
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| 2001 | 4,414 | 34.2 | — | — | — | — | — | — | — | — | — | — | — | — | — | — |
| 2002 | 3,484 | 26.6 | — | — | — | — | — | — | — | — | — | — | — | — | — | — |
| 2003 | 4,067 | 30.6 | 721 | 640 | 56 | 584 | — | 46 (7.2) | 303 (47.3) | 212 (33.1) | 59 (9.2) | 20 (3.1) | — | 169 (26.4) | 436 (68.1) | 35 (5.5) |
| 2004 | 9,743 | 71.3 | 6,612 | 5,517 | 318 | 5,199 | — | 524 (9.5) | 2662 (48.3) | 1653 (30.0) | 448 (8.1) | 230 (4.2) | — | 2,189 (39.7) | 2,554 (46.3) | 774 (14.0) |
| 2005 | 25,934 | 186.4 | 27,539 | 14,877 | 739 | 14,138 | — | 1358 (9.1) | 5670 (38.1) | 4889 (32.9) | 1763 (11.9) | 1197 (8.1) | 5 (0.0) | 8,103 (54.5) | 4,973 (33.4) | 1,796 (12.1) |
| 2006 | 6,192 | 43.7 | 7,820 | 3,058 | 169 | 2,889 | — | 306 (10.0) | 1069 (34.9) | 1076 (35.2) | 392 (12.8) | 215 (7.0) | 1,085 (35.5) | 1,146 (37.5) | 773 (25.3) | 54 (1.8) |
| 2007 | 2,924 | 20.3 | 14,482 | 6 | 6 | — | — | — | 3 (50.0) | 2 (33.3) | 1 (16.7) | — | 2 (33.3) | 4 (66.7) | — | — |
| 2008 | 2,660 | 18.1 | 8,308 | 139 | 16 | 123 | 5 | 12 (8.6) | 77 (55.4) | 33 (23.7) | 7 (5.0) | 10 (7.2) | 2 (1.4) | 68 (48.9) | 69 (49.6) | — |
| 2009 | 718 | 4.9 | 14,896 | 78 | 35 | 43 | 212 | 8 (10.3) | 47 (60.3) | 9 (11.5) | 9 (11.5) | 5 (6.4) | 1 (1.3) | 27 (34.6) | 50 (64.1) | — |
| 2010 | 788 | 5.3 | 14,745 | 66 | 51 | 15 | 440 | 7 (10.6) | 24 (36.4) | 19 (28.8) | 3 (4.5) | 13 (19.7) | 27 (40.9) | 17 (25.8) | 22 (33.3) | — |
| 2011 | 5,625 | 37.4 | 14,696 | 5,329 | 1,930 | 3,399 | 741 | 359 (6.7) | 1820 (34.2) | 1426 (26.8) | 460 (8.6) | 1264 (23.7) | 1427 (26.8) | 1,559 (29.3) | 2343 (43.9) | — |
| 2012 | 1,986 | 13.1 | 8,291 | 1,793 | 715 | 1,078 | 599 | 211 (11.8) | 551 (30.7) | 361 (20.1) | 176 (9.8) | 494 (27.6) | 381 (21.2) | 601 (33.5) | 656 (36.6) | 155 (8.6) |
| 2013 | 237 | 1.5 | 5,229 | 200 | 77 | 123 | 325 | 32 (16.0) | 70 (35.0) | 45 (22.5) | 14 (7.0) | 39 (19.5) | 28 (14.0) | 88 (44.0) | 63 (31.5) | 21 (10.5) |
| 2014 | 289 | 1.9 | 3,041 | 288 | 145 | 143 | 175 | 41 (14.2) | 145 (50.3) | 58 (20.1) | 15 (5.2) | 29 (10.1) | 56 (19.4) | 100 (34.7) | 131 (45.5) | 1 (0.3) |
| 2015 | 240 | 1.5 | 3,435 | 250 | 158 | 92 | 64 | 32 (12.8) | 125 (50.0) | 42 (16.8) | 22 (8.8) | 29 (11.6) | 87 (34.8) | 81 (32.4) | 75 (30.0) | 7 (2.8) |
| 2016 | 972 | 6.0 | 4,291 | 972 | 618 | 354 | 81 | 149 (15.3) | 543 (55.9) | 161 (16.6) | 27 (2.8) | 92 (9.5) | 123 (12.7) | 262 (27.0) | 559 (57.5) | 28 (2.9) |
Abbreviations: epi = epidemiologically; JRF = Joint Reporting Form; MCV = measles-containing vaccine; WHO = World Health Organization.
* Measles incidence calculated based on reported confirmed measles cases and population by countries through WHO/UNICEF JRF.
† National measles case data as reported to WHO South-East Asia Region Office (SEARO) as of December 2015 through the WHO/UNICEF JRF. Bangladesh uses administrative data reported through the national Health Management Information system (HMIS) to report in the JRF. The HMIS receives aggregated data from all the health facilities in the country, including private and public clinics and hospitals.
§ Data from case-based measles surveillance through the Vaccine Preventable Diseases surveillance network reported to WHO SEARO as of December 2016.
¶ An illness in any person a clinician suspects of having measles infection or in any person with fever and maculopapular rash and cough, coryza, or conjunctivitis.
** Includes laboratory-confirmed and epidemiologically linked cases. An epidemiologically linked case is one that meets the clinical case definition and is linked epidemiologically to a laboratory-confirmed or another epidemiologically confirmed case.
National measles case-based surveillance performance indicator targets and progress toward meeting them — Vaccine Preventable Disease Surveillance Report, Bangladesh, 2013–2016
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* An illness in any person a clinician suspects of having measles infection, or in any person with fever and maculopapular rash and cough, coryza, or conjunctivitis.
† Includes collection of all the following data elements about each suspected case of measles or rubella: patient name or identifiers, place of residence, place of infection (at least to district level), age (or date of birth), sex, date of rash onset, date of specimen collection, measles-rubella vaccination status, date of last measles-rubella or measles-mumps-rubella vaccination, date of notification, date of investigation, and travel history.
§ A blood specimen collected within 28 days of the onset of rash.
¶ A World Health Organization (WHO)-accredited laboratory that has an established quality assurance program or one with oversight by a WHO-accredited laboratory.
** Changed to 4 days from 7 day in 2015.