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Progress Toward Measles Elimination — Western Pacific Region, 2009–2012

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Progress Toward Measles Elimination — Western Pacific Region, 2009–2012

HHS, CDC and MMWR Logos
MMWR Weekly
Volume 62, No. 22
June 7, 2013

Progress Toward Measles Elimination — Western Pacific Region, 2009–2012


Weekly

June 7, 2013 / 62(22);443-447

In 2005, the World Health Organization (WHO) Regional Committee for the Western Pacific Region (WPR) resolved that WPR should aim to eliminate measles* by 2012 (1). The recommended measles elimination strategies (2) in WPR include 1) achieving and maintaining high (≥95%) coverage with 2 doses of measles-containing vaccine (MCV) through routine immunization services and by implementing supplementary immunization activities (SIAs), when required; 2) conducting high-quality, case-based measles surveillance; 3) ensuring high-quality laboratory surveillance, with timely and accurate testing of specimens to confirm or discard suspected cases and detect measles virus for genotyping and molecular analysis; and 4) establishing and maintaining measles outbreak preparedness for rapid response and ensuring appropriate case management. This report updates the previous report (3) and describes progress toward eliminating measles in WPR during 2009–2012. During this period, measles incidence reached a historic low, decreasing by 83%, from 34.0 to 5.9 cases per million population. However, to achieve measles elimination in WPR, additional efforts are needed to strengthen routine immunization services in countries and areas with <95 2-dose="" a="" among="" and="" areas="" close="" countries="" coverage="" do="" dose="" first="" four="" gaps="" have="" immunity="" in="" introduce="" mcv2="" mcv="" measles-susceptible="" measles="" not="" of="" ongoing="" or="" p="" populations="" remaining="" routine="" schedule="" second="" sias="" that="" the="" to="" transmission.="" use="" virus="" with="" yet=""> Immunization Activities
Annual data on MCV coverage are reported from 36 of the 37 WPR countries and areas to WHO and the United Nations Children's Fund (UNICEF). MCV1 coverage in WPR increased from 96% in 2009 to 98% in 2012. The number of countries with ≥95% MCV1 coverage increased from 12 (33%) in 2009 to 15 (42%) in 2012. MCV1 was administered at 8 months in one (3%), at age 9 months in six (17%),§ at age 10 months in one (3%), at age 12 months in 24 (67%), and at age >12 months in four (11%) (Table 1).
The number of countries and areas that provide routine MCV2 increased from 32 (89%) in 2009 to 33 (92%) in 2012, and the number reporting ≥95% MCV2 coverage increased from 10 (28%) in 2009 to 11 (31%) in 2012. Among the 33 countries and areas reporting MCV2 coverage in 2012, the scheduled age of MCV2 administration ranged from 12 months to 7 years. During 2009–2012, approximately 226 million children were vaccinated during 16 measles SIAs (Table 2); of these, seven (44%) SIAs included rubella vaccine, and 10 (63%) added at least one other child health intervention.
Surveillance Activities
During 2009–2012, measles case-based surveillance was conducted in all 37 WPR countries and areas, including 14 countries and two areas that report data individually, and 21 countries and areas of the Pacific Islands that report data as one epidemiologic block. Measles surveillance data are reported monthly to WHO and supported by 385 laboratories participating in the WHO Global Measles and Rubella Laboratory Network** (4). Suspected measles cases were confirmed based on laboratory findings, an epidemiologic link, or clinical criteria.†† Key indicators of surveillance performance include 1) the number of suspected measles cases discarded as nonmeasles (target: ≥2 per 100,000 population); 2) the proportion of second-level administrative units with ≥1 nonmeasles discarded case per 100,000 population (target: ≥80%); 3) the percentage of suspected measles cases with adequate investigation that includes all essential data elements§§ (target: ≥80%); 4) the percentage of suspected measles cases with adequate specimens collected within 28 days of rash onset (target: ≥80%, excludes epidemiologically linked cases) (5); and 5) the percentage of specimens with laboratory results available within 7 days after receipt in the laboratory (target: ≥80%). The number of countries and areas with adequate data that met the target for suspected cases discarded as nonmeasles per 100,000 population increased from seven (50%) of 14 in 2009 to nine (64%) of 14 in 2012 (Table 3). From 2009 to 2012, suspected cases with adequate investigations increased from 38% to 89%, suspected cases with adequate specimens collected for laboratory testing increased from 79% to 93%, and the proportion of blood specimens received by the laboratory with results available within 7 days increased from 55% to 96% (Table 3).
Measles Disease Incidence and Measles Virus Genotypes
From 2009 to 2012, confirmed measles cases decreased 84%, from 54,291 to 8,524, and confirmed measles incidence per million population decreased 83%, from 34.0 to 5.9 (Table 1). In 2012, the highest confirmed measles incidence was reported from Malaysia (63.7 per million), the Philippines (15.9 per million), and New Zealand (12.3 per million) (Table 1). The highest number of confirmed cases was reported from China and decreased 88%, from 52,461 in 2009 to 6,183 in 2012 (Figure). During 2009–2012, the predominant measles virus genotypes detected in WPR were H1 in China, D9 in the Philippines, Malaysia, and Singapore; and D8 in Malaysia. Other measles virus genotypes that were identified and determined to have been related to measles virus importations from outside WPR included B3, D4, and G3.

Reported by

W. William Schluter, MD, Wang Xiaojun, MD, Jorge Mendoza-Aldana, MD, Youngmee Jee, MD, PhD, Sergey Diorditsa, MD, PhD, Expanded Programme on Immunization, World Health Organization Western Pacific Regional Office, Manila, Philippines. Alya Dabbagh, PhD, Mick Mulders, PhD, Dept of Immunization, Vaccines, and Biologicals, World Health Organization, Geneva, Switzerland. Div of Viral Diseases, National Center for Immunization and Respiratory Diseases; Christopher Gregory, MD, James L. Goodson, MPH, Global Immunization Div, Center for Global Health, CDC. Corresponding contributor: James L. Goodson, jgoodson@cdc.gov, 404-639-8170.

Editorial Note

In 2012, the WPR Regional Committee reaffirmed its commitment to eliminate measles and urged member states to interrupt all residual endemic measles virus transmission as rapidly as possible (6). To achieve elimination, intensified efforts are needed to identify and close gaps in population immunity, by increasing coverage with MCV2 to ≥95% in all countries and areas and by conducting high-quality SIAs in countries with sustained measles virus transmission (e.g., China, Malaysia, and the Philippines). In countries and areas with <95 a="" action="" all="" and="" ao="" are="" areas="" birth="" childhood="" cohorts="" conduct="" countries="" coverage="" democratic="" do="" for="" four="" guinea="" identify="" immunization="" implement="" in="" increase="" introduction="" is="" islands="" mcv1="" mcv2.="" mcv2="" mcv="" measles-susceptible="" needed="" new="" not="" of="" opportunity="" or="" p="" papua="" people="" periodic="" populations.="" prepare="" provide="" receive="" remaining="" republic="" routine="" s="" schedule="" second="" services="" sias="" solomon="" strategies="" strengthen="" targeted="" that="" the="" to="" urgent="" vaccination="" vanuatu=""> The WPR Guidelines on Verification of Measles Elimination (7) were finalized in March 2013; progress toward measles elimination in WPR will be monitored by the Regional Verification Commission through annual progress reports from each country or area and from the Pacific Islands countries and areas reporting as one epidemiologic block. High-quality case-based measles surveillance is critical to the verification process. Despite overall improvement in measles surveillance performance, gaps persist, as reflected by the low proportion of second-level administrative units with one or more nonmeasles discarded case per 100,000 population. Additionally, incomplete investigations of suspected measles cases in some countries challenge efforts to rapidly identify and respond to outbreaks and to measure and document progress toward elimination. For example, in Vietnam, only six (0.8%) of the 771 suspected measles cases with specimens available for testing reported in 2012 were laboratory confirmed. However, 631 additional cases did not have specimens collected but were reported as clinically confirmed measles. The sensitivity of the measles surveillance system in other countries with discarded nonmeasles reporting rates of <2 100="" and="" be="" criteria.="" detect="" insufficient="" meet="" might="" or="" outbreaks="" p="" per="" population="" rapidly="" respond="" to="" verification=""> The WHO Global Vaccine Action Plan calls for the elimination of rubella and congenital rubella syndrome in five of the six WHO regions by 2020 (8). In April 2012, the Measles and Rubella Initiative launched the 2012–2020 Global Measles and Rubella Strategic Plan to integrate rubella with measles elimination efforts (9). Rubella-containing vaccine is not provided in six WPR countries and areas; five of these countries (Cambodia, Lao People's Democratic Republic, Papua New Guinea, Solomon Islands, and Vietnam) are eligible for financial support offered by the GAVI Alliance to conduct a wide-age-range SIA using combined measles-rubella vaccine followed by the introduction of rubella vaccine in their national routine immunization programs. In addition to contributing to rubella elimination, these SIAs would provide a unique opportunity to boost population immunity to measles and contribute momentum to achieve and sustain measles elimination in WPR.

References

  1. World Health Organization, Regional Committee for the Western Pacific. Resolution WPR/RC56.R8: measles elimination, hepatitis B control, and poliomyelitis eradication. Manila, Philippines: World Health Organization; 2005. Available at http://www2.wpro.who.int/rcm/en/archives/rc56/rc_resolutions/wpr_rc56_r08.htmExternal Web Site Icon.
  2. World Health Organization, Regional Office for the Western Pacific. Western Pacific Region measles elimination field guide (2013 version). Manila, Philippines: World Health Organization; 2013 (in press).
  3. World Health Organization. Progress towards the 2012 measles elimination goal in the WHO's Western Pacific Region, 1990–2008, Wkly Epidemiol Rec 2009;84:271–9.
  4. Featherstone DA, Rota PA, Icenogle J, et al. Expansion of the global measles and rubella laboratory network 2005-09. J Infect Dis 2011;204(Suppl 1):S491–8.
  5. World Health Organization. Framework for verifying elimination of measles and rubella. Wkly Epidemiol Rec 2013;88:89–99.
  6. World Health Organization, Regional Committee for the Western Pacific. Resolution WPR/RC63.5: elimination of measles and acceleration of rubella control. Hanoi, Vietnam: World Health Organization; 2012. Available at http://www.wpro.who.int/about/regional_committee/63/resolutions/wpr_rc63_r5_measles_elimination_03oct.pdf Adobe PDF fileExternal Web Site Icon.
  7. World Health Organization, Regional Office for the Western Pacific. Western Pacific Region guidelines on verification of measles elimination (2013 version). Manila, Philippines: World Health Organization; 2013 (in press).
  8. World Health Organization. Global vaccine action plan: report by the Secretariat. Geneva, Switzerland: World Health Organization; 2012. Available at http://apps.who.int/gb/ebwha/pdf_files/wha65/a65_22-en.pdf Adobe PDF fileExternal Web Site Icon.
  9. World Health Organization. Global measles and rubella strategic plan: 2012–2020. Geneva, Switzerland: World Health Organization; 2012. Available at http://www.who.int/immunization/newsroom/Measles_Rubella_StrategicPlan_2012_2020.pdf Adobe PDF fileExternal Web Site Icon.

* Measles elimination is defined as the absence of endemic measles virus transmission in a defined geographic area (e.g., region or country) for ≥12 months in the presence of a well-performing surveillance system.
The Pitcairn Islands, with a population of approximately 50 persons, does not report immunization coverage data to WHO/UNICEF.
§ Papua New Guinea also provides a supplementary dose of MCV at age 6 months.
The epidemiologic block of the Pacific Islands countries and areas includes American Samoa, Cook Islands, Fiji, French Polynesia, Guam, Kiribati, the Marshall Islands, the Federated States of Micronesia, Nauru, New Caledonia, Niue, the Commonwealth of the Northern Mariana Islands, Palau, the Pitcairn Islands, Samoa, Solomon Islands, Tokelau, Tonga, Tuvalu, Vanuatu, and Wallis and Futuna.
** This network includes one WHO global specialized laboratory in Japan, three regional reference laboratories (in Melbourne, Australia; Beijing, China; and Hong Kong, China), 19 national or subnational laboratories, and 31 provincial and 331 prefecture-level laboratories in China.
†† Cases that meet the WHO clinical case definition of measles for which no adequate specimen was collected and cannot be epidemiologically linked to a laboratory-confirmed case of measles.
§§ Essential data elements include name or identifier, date of birth or age, sex, place of residence, vaccination status or date of last vaccination, date of rash onset, date of notification, date of investigation, date of specimen collection, and place of infection or travel history.

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