Measles in Canada: 2013
Published by: The Public Health Agency of Canada
Issue: Volume 40-12: Measles in Canada
Date published: June 12, 2014
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Volume 40-12, June 12, 2014: Measles in Canada
Measles surveillance in Canada: Trends for 2013
Shane A1*, Hiebert J2, Sherrard L1 and Deehan H1
1 Centre for Immunization and Respiratory Infectious Diseases, Public Health Agency of Canada, Ottawa, ON
2 National Microbiology Laboratory, Public Health Agency of Canada
Objective: The objective of this report is to describe measles activity in Canada during 2013, in order to support the documentation and maintenance of measles elimination status.
Methods: A descriptive analysis of measles counts and incidence by age group, immunization history, hospitalization and province/territory, as well as a summary of 2013 outbreaks, was conducted using enhanced measles data captured through the Canadian Measles and Rubella Surveillance System. Genotype information and phylogenetic analysis for 2013 were summarized.
Results: In 2013, 83 confirmed measles cases were reported in seven provinces/territories for an incidence rate of 2.4 per 1,000,000 population. Incidence was highest in the youngest age groups (< 1 year, 1 to 4 years). Burden of disease was highest in the youngest age groups and children 10 to 14 years. Three-quarters of cases had been inadequately immunized, and 10% were hospitalized. There were nine measles outbreaks reported in 2013, one of which consisted of 42 cases in a non-immunizing community in Alberta.
Discussion: 2013 saw the fifth highest number of reported measles cases since 1998. While we continue to face challenges related to importation and heterogeneous immunization coverage, in 2013 Canada met or partially met all four criteria outlined by the Pan American Health Organization for measles elimination.
The last reported case of endemic measles in Canada occurred in November 1997; Canada's elimination status was achieved one year later in 1998 Footnote 1. The World Health Organization (WHO) Region of the Americas achieved elimination status in 2002, making it the first and only WHO Region to reach this goal. Elimination of measles is maintained as long as a single measles viral strain is not circulating continuously throughout Canada for a period of 12 months or more Footnote 2. Endemic measles activity persists across the European, African, Southeast Asian and Western Pacific regions Footnote 3. While endemic transmission has not been re-established in Canada, the possibility of importation of measles into the country remains, as a result of population exchange with endemic countries or countries experiencing measles outbreaks.
Subsequent outbreaks within Canada following a measles importation are often limited; however, there were large outbreaks of 94, 53, 82 and 678 cases in 2007, 2008, 2010 and 2011 Footnote 4 Footnote 5. Transmission within Canada is associated with those who are under- or unimmunized and areas with suboptimal immunization coverage. While 2-dose immunization coverage in Canada is generally high (the 2011-12 Childhood National Immunization Survey estimated 2-dose coverage by age 7 years to be 94.9% Footnote 6), it is not uniform across the country, within provinces and territories, or across sub-populations (e.g. religious communities that oppose vaccination). Given the lack of uniformity in coverage to achieve the ≥ 95% coverage recommended for measles herd immunity Footnote 7, the risk of domestic transmission following an importation of measles remains a reality.
As an ongoing component of Canada's commitment to the maintenance and documentation of measles elimination status, the Public Health Agency of Canada (the Agency) conducts enhanced measles surveillance. The post-elimination Canadian measles epidemiology has been previously reported for 1998-2001 Footnote 1 and 2002 to 2011 Footnote 4. There were only 10 confirmed measles cases reported in Canada in 2012, the majority (n = 6, 60.0%) of them importations without secondary spread. Information on these cases is available elsewhere Footnote 8. The objective of this report, therefore, is to describe measles activity in Canada during 2013, in order to support the documentation and maintenance of measles elimination status.
Enhanced measles surveillance is carried out in all provinces and territories through the Canadian Measles and Rubella Surveillance System. On a weekly reporting cycle, provinces and territories report cases of measles meeting the national case definition Footnote 9 to the Agency, including zero reporting, through a national case report form that is submitted by e-mail or fax. Three jurisdictions (British Columbia, Alberta, and Newfoundland and Labrador) are currently participating in the Measles and Rubella Surveillance pilot project, which provides real-time laboratory and epidemiological web-based reporting of suspect measles/rubella case investigations. Case details obtained from the national surveillance system case report forms and Measles and Rubella Surveillance web-based notifications were assessed against the national measles confirmed-case definition (laboratory confirmed or epidemiological link to a laboratory-confirmed case) before inclusion in the national database.
The objective of national measles surveillance is to continuously monitor the presence of measles virus in Canada in a timely way. To meet this objective, the Canadian Measles and Rubella Surveillance System captures cases that were communicable in Canada, regardless of country of residence. This allows accurate international and national reporting of the presence of measles virus in Canada, which is an essential criterion for measles elimination. However, this might result in case count discrepancies between federal and provincial/territorial surveillance systems, since some provincial/territorial systems do not include measles cases among foreign nationals.
This report includes enhanced data of confirmed measles cases, reported by the provinces and territories through both the national surveillance system and the surveillance pilot project, with rash onset during epidemiological weeks 1 to 52 for the 2013 reporting year (i.e. from December 30, 2012, to December 28, 2013). Probable cases Footnote 9 are not nationally notifiable and therefore are not included in this report.
Case report form
The Canadian Measles and Rubella Surveillance System case report form is one page in length and designed to meet the objectives of national surveillance. The form facilitates collection of information on case identifiers (date of birth or age, gender, health unit, city, forward sortation area, date reported to health unit and date investigation was started); background, exposure and clinical information (date of rash onset, hospitalization, source of exposure, vaccination history [date of each dose] and whether the case was outbreak associated); and laboratory information (results of laboratory tests).
The data manager followed up with the reporting jurisdiction if information was missing on the form. At data entry, values coded as missing represented those that were blank on the form, and values coded as unknown represented those sought, but not available, from the reporting jurisdiction. A data validation process was conducted with provinces and territories in March 2014 for all measles cases reported nationally in 2013.
Measles virus genotyping was performed at the Public Health Agency of Canada's National Microbiology Laboratory. Appropriate clinical specimens (respiratory specimens and/or urines) collected from suspect or confirmed measles cases were submitted by provincial laboratories. The WHO's standardized genotyping regions of the 450 nucleotides encoding the carboxyl-terminus of the measles nucleoprotein, the N-450, and the full length hemagglutinin gene (H gene) Footnote 10 were amplified and sequenced from extracted nucleic acid. The sequences were aligned with WHO genotype reference sequences Footnote 11, and phylogenetic trees were generated using MEGA5 software Footnote 12.
Data management and statistical analysis
Data management was conducted with Microsoft Access 2010. Descriptive epidemiological analyses were conducted with SAS Enterprise Guide 5.1 Footnote 13. Distribution of confirmed measles cases by province and territory, age group, sex, immunization history and hospitalization were described. Case counts and proportions were calculated for categorical variables, and means/medians and ranges were calculated for continuous variables. Cases with missing or unknown responses were included in the denominators for proportions. Incidence rates were generated using population estimates from Statistics Canada for 2013 Footnote 14. Rates were calculated per 1,000,000 population for consistency with the PAHO recommended indicator Footnote 2.
The National Advisory Committee on Immunization's recommendations for measles immunization was used to determine whether cases' immunization status was up to date for age with measles-containing vaccine Footnote 15. Children aged < 1 year and adults born before 1970 were considered up to date for age with 0 or more doses of measles-containing vaccine. Cases aged 1 to 6 years were considered up to date for age with one or more doses of measles-containing vaccine and those aged 7 years and older (but born in 1970 or later) were up to date with two or more doses.
Essential criteria for measles elimination
In order to continue documentation and verification of measles elimination in the Region of the Americas, the Pan-American Health Organization (PAHO) has developed four criteria that it considers essential for each Member State to meet Footnote 2:
- Verify the interruption of endemic measles cases for a period of at least three years from the last known endemic case, in the presence of high-quality surveillance;
- Implement and maintain high-quality surveillance sensitive enough to detect imported and import-related cases;
- Verify the absence of endemic measles virus strains through viral surveillance; and
- Verify adequate immunization in the population.
Canada's performance towards maintenance of measles elimination was assessed against the four elimination criteria on the basis of the 2013 Canadian surveillance data.
This study was exempt from research ethics board approval because the data set was the result of public health surveillance.
In 2013, a total of 83 confirmed measles cases were reported, for an overall incidence rate of 2.4 cases per 1,000,000 population. Of these cases, 53 (63.9%) were laboratory confirmed and 30 (36.1%) were epidemiologically linked to a laboratory-confirmed case.
Measles cases were reported in seven provinces and territories over 28 weeks in 2013. The maximum number of cases that occurred per week was 11, in weeks 45 and 46. These were outbreak-associated cases that occurred during the peak of a large outbreak in Alberta (Figure 1).
Figure 1. Number of reported measles cases by epidemiological week of rash onset and reporting province or territory, Canada, 2013
Text Equivalent - Figure 1
From January 1 to December 31 2013 there were 83 confirmed cases of measles reported in 7 provinces across Canada. The first case was reported on February 2, 2013 with cases being reported over a total of 28 weeks in 2013. The minimum number of cases reported was zero, in weeks 13 to 16, 18 to 22, 29, 31, 33, 37, 39 to 41, 49, 50 and 52. The maximum number of cases reported per week was 11 in weeks 45 and 46. These cases were part of a large outbreak in Alberta that included 42 cases and occurred from weeks 42 to 48.
Age, gender and geographic distribution
The majority of measles cases reported were male (n = 45, 54.2%). Children aged 1 to 4 years and 10 to 14 years each represented the highest proportion of cases (n = 17 and 20.5% each), followed by 15 to 19 and 20 to 24 year olds (n = 11 and 13.3% each). Of the four cases aged 40 years and older, three were born before 1970, the birth year cut-off for presumed natural immunity Footnote 15.
While the burden of disease extended from those aged 1 to 24 years, the incidence rate was highest among the youngest age groups (10.5 per 1,000,000 for those < 1 year; 11.0 per 1,000,000 for those 1 to 4 years) (Table 1).
|Age group (years)||M||F||CA||BC||AB||SK||MB||ON||QC||NB||NS||PE||NL||YT||NT||NU||Overall incidence rate|
|1 to 4||12||5||17||1||6||0||0||7||1||2||0||0||0||0||0||0||11.0|
|5 to 9||6||3||9||0||7||0||0||2||0||0||0||0||0||0||0||0||4.8|
|10 to 14||6||11||17||1||15||0||0||0||0||0||0||1||0||0||0||0||9.1|
|15 to 19||5||6||11||0||9||0||0||1||0||0||0||1||0||0||0||0||5.0|
|20 to 24||4||7||11||5||5||1||0||0||0||0||0||0||0||0||0||0||4.5|
|25 to 29||2||2||4||3||0||0||0||1||0||0||0||0||0||0||0||0||1.7|
|30 to 39||6||0||6||3||0||0||0||2||0||1||0||0||0||0||0||0||1.3|
|40 to 59||0||4||4||2||0||0||0||2||0||0||0||0||0||0||0||0||0.4|
Cases were reported in 7 of the 13 Canadian provinces and territories: Alberta (n = 43), British Columbia (n = 17), Ontario (n = 16), New Brunswick (n = 3), Prince Edward Island (n = 2), Quebec (n = 1) and Saskatchewan (n = 1). The incidence rate was highest in Prince Edward Island, given its small population, followed by Alberta, with 13.8 and 10.7 cases per 1,000,000 population respectively. The incidence for the each of the remaining provinces was less than 5.0 cases per 1,000,000 population (Table 1).
Of the 83 cases reported in 2013, 13.3% (n = 11) had an immunization status considered up to date for age (Table 2). These included four infants < 1 year who were too young to receive their first dose of measles-containing vaccine and one adult born before 1970. Conversely, 75.9% (n = 63) were not up to date for age at the time of infection and immunization status was unknown for 10.8% (n = 9); two of these were born before 1970 and are presumed to be immune regardless of immunization history.
|Age group (years)||Total||0 doses||Up To Date with
|One dose||Up To Date with
|1 to 4||17||14||0||2||2||1||0|
|5 to 9||9||9||0||0||-||0||0|
|10 to 14||17||17||0||0||-||0||0|
|15 to 19||11||10||0||0||-||1||0|
|20 to 24||11||7||0||0||-||2||2|
|25 to 29||4||3||0||1||0||0||0|
|30 to 39||6||1||0||0||-||0||5|
|40 to 59||4||2||1||0||-||0||2|
Mirroring the age group distribution of the cases, inadequate immunization status was most commonly reported in the 10 to 14 and 1 to 4 year age groups (27.0% and 22.2% respectively), followed by the 5 to 9 and 15 to 19 year olds (14.3 and 15.9% respectively).
Of the 83 reported cases, 9.6% (n = 8) were hospitalized (Table 3). Half of the infants < 1 year and 30% of cases among adults 25 to 39 years were hospitalized. Hospitalization was infrequent among cases 1 to 24 years of age.
|Age group (years)||Total||Not hospitalized
|< 1||4||2 (50.0)||2 (50.0)||0 (-)|
|1 to 4||17||14 (82.4)||2 (11.8)||1 (5.9)|
|5 to 9||9||9 (100.0)||0 (-)||0 (-)|
|10 to 14||17||17 (100.0)||0 (-)||0 (-)|
|15 to 19||11||10 (90.9)||1 (9.1)||0 (-)|
|20 to 24||11||11 (100.0)||0 (-)||0 (-)|
|25 to 29||4||3 (75.0)||1 (25.0)||0 (-)|
|30 to 39||6||4 (66.7)||2 (33.3)||0 (-)|
|40 to 59||4||4 (100.0)||0 (-)||0 (-)|
|> 60||0||0 (-)||0 (-)||0 (-)|
|Unknown||0||0 (-)||0 (-)||0 (-)|
|Total||83||74 (89.2)||8 (9.6)||1 (1.2)|
During 2013, specimens were available to determine the genotype for 50 of 83 (60.2%) reported cases of measles. Measles genotypes were D8 (n = 34), B3 (n = 13), H1 (n = 2) and D4 (n = 1).
Measles genotype D8 was detected in 34 cases and seven outbreaks (Table 4). In general, this genotype has been associated with endemic transmission in the Eastern Mediterranean region, primarily in the Southeast Asian region Footnote 16. The genotype D8 sequences identified could be further subdivided as four sequence variants (Figure 2): those that were identical to MVs/Taunton.GBR/27.12 (GenBank accession number JX984461) (n = 18), MVs/Frankfurt Main.DEU/17.11 (GenBank accession number KF683445) (n = 10), MVs/Swansea.GBR/4.13 (GenBank accession number KF214761) (n = 4) and MVi/Villupuram.Ind/03.07 (GenBank accession number FJ765078) (n = 2). The two cases that had sequences identical to MVi/Villupuram.Ind/03.07 were part of an outbreak that began as a result of an importation from Thailand (Table 4), where the sequence was circulating (GenBank accession numbers KC631635, KC631637-41). Measles sequences identical to MVs/Swansea.GBR/4.13 were detected in four cases, of which the two primary cases (MVs/New Brunswick.CAN/7.13 and MVs/Ontario.CAN/8.13, Figure 2) had returned from Mexico (Table 4). At the time, this sequence variant had been reported to the WHO measles sequence database, MeaNS Footnote 16, only from the UK (Kevin Brown, Public Health, England: personal communication, March 7, 2013), supporting the identification of a UK tourist as the index case.
Each entry represents a sequence from an individual measles case. Phylogenetic trees demonstrate the relatedness of genetic sequences. Sequences on the same vertical line are identical. The length of horizontal lines separating sequences or branches of sequences is proportional to the number of differences (measured in single nucleotides) between the sequences (scale shown at the bottom left). WHO reference sequences Footnote 11 are shown in bold, italic font. Relevant sequence variants are shown in italics. These are identified within the WHO measles sequence database, MeaNS (accessible at http://www.who-measles.org/Public/Web_Front/sequence.php), and represent prevalent sequences within the database Footnote 11 Canadian sequences are shown in regular font and are identified by their WHO name, which indicates province and week of rash onset or specimen collection. Cases of imported virus are identified with "ex: < 3 letter country code >." Outbreaks are represented by colour fonts: sequences with the same colour, within the same genotype, are from the same outbreak.
Figure 2. Phylogenetic tree of measles N-450 sequences detected in Canada in 2013 (n = 50)
Text Equivalent - Figure 2
The phylogenetic tree of measles N-450 sequences detected in Canada in 2013 (n=50) is shown in figure 2. Measles genotype D8 was detected in 34 cases in 7 outbreaks. The genotype D8 sequences identified could be subdivided as four sequence variants: those that were identical to MVs/Taunton.GBR/27.12 (n=18), MVs/Frankfurt Main.DEU/17.11 (n=10), MVs/Swansea.GBR/4.13 (n=4) and MVi/Villupuram.Ind/03.07 (n=2). The majority of the D8 sequences in 2013 were identical to the MVs/Taunton.GBR/27.12 sequence variant (n=18) and all 18 were linked to the Netherlands where the same sequence variant was associated with an ongoing outbreak. Fifteen were associated with the Alberta outbreak while the remaining three were unrelated importations. Measles genotype B3 was detected in 13 cases and was associated with two outbreaks where the origin could not be determined. All Canadian B3 viruses sequenced were identical to the MVi/Harare.ZWE/38.09 sequence variant. All genotype B3 cases were identical at the primary genotyping region, the N-450. Genotypes H1 (n=2) and D4 (n=1) were detected in three sporadic cases in 2013.
In the months of June and July, four outbreaks occurred simultaneously in three provinces: Ontario, Prince Edward Island and British Columbia (n = 2), and sequences identical to MVs/Frankfurt Main.DEU/17.11 was identified from all four outbreaks (Figure 2). At the time of the outbreaks, the MVs/Frankfurt Main.DEU/17.11 sequence variant was circulating in the European region (GenBank accession numbers KF269094, KJ690815, KF290740, KF715463, KF269089) and detected in the United States (GenBank accession number KF385861). Sequencing of the secondary WHO genotyping region, the H gene, did not differentiate the four outbreaks (Figure 3).
WHO reference sequences Footnote 11 are shown in bold, italic font. Canadian sequences are shown in regular font and are identified by their WHO name, which indicates province and week of rash onset or specimen collection. Cases of imported virus are identified with "ex:< 3 letter country code>." Outbreaks are represented by colour fonts: sequences with the same colour, within the same genotype, are from the same outbreak.
Figure 3. Phylogenetic tree of measles H gene sequences detected in Canada in 2013 (n = 43)
Text Equivalent - Figure 3
The phylogenetic tree of measles H gene sequences detected in Canada in 2013 (n=43) is shown in figure 3. Two of the separate importations of D8 sequence identical to the MVs/Taunton.GBR/27.12 sequence variant had distinct H gene sequences (MVs/Ontario.CAN/30.13 and MVs/British Columbia.CAN/31.13). Although all genotype B3 cases were identical at the primary genotyping region, the N-450, the outbreaks and sporadic cases of genotype B3 were distinguished by H gene sequencing.
The majority of the D8 sequences in 2013 were identical to the MVs/Taunton.GBR/27.12 sequence variant (n = 18), and all 18 were linked to the Netherlands (Figure 2), where the same sequence variant was associated with an ongoing outbreak (Susan Hahné, RIVM - Centre for Infectious Disease Control, the Netherlands: personal communication, June 12, 2013). Fifteen were associated with the Alberta outbreak, and the remaining three were unrelated importations. Two of the separate importations had distinct H gene sequences (MVs/Ontario.CAN/30.13 and MVs/British Columbia.CAN/31.13, Figure 3).
Measles genotype B3 was detected in 13 cases and was associated with two outbreaks whose origin could not be determined (Table 4, Figure 2). Genotype B3 has been associated with endemic transmission throughout the African region as well as a number of countries in the Eastern Mediterranean region Footnote 16. All Canadian B3 viruses sequenced were identical to the MVi/Harare.ZWE/38.09 sequence variant (GenBank accession number JF973033). At the time of the first outbreak in Ontario, this sequence variant was circulating in the Eastern Mediterranean region (GenBank accession numbers KC737549 and KF145165). Two sporadic cases were imported from Pakistan between outbreaks. At the time of the fourth outbreak in British Columbia, in the fall of 2013, this sequence variant was being reported from the Western Pacific and European regions in addition to the Eastern Mediterranean region (GenBank accession numbers KJ690812-4, KF468720, AB854746-7 and KF740427). At the end of the year, this sequence variant was also imported from the Philippines. Although all genotype B3 cases were identical at the primary genotyping region, the N-450 (Figure 2), the outbreaks and sporadic cases were distinguished by H gene sequencing (Figure 3).
Genotypes H1 (n = 2) and D4 (n = 1) were detected in three sporadic cases in 2013 (Figure 2). Genotype H1 was twice imported from the Western Pacific region, where it is endemic Footnote 16. Genotype D4 has been associated with endemic transmission in the Eastern Mediterranean, Southeast Asian and European regions Footnote 16. The source of the D4 case was unknown, although it was identical to a sequence variant circulating in the European region, MVs/Manchester.GBR/10.09 (GenBank accession numbers GQ370461, KC709569 and KF831037).
Summary of 2013 Canadian measles outbreaks
Nationally, an outbreak is defined as two or more cases of measles linked by person, place and time Footnote 17. In 2013, there were nine outbreaks composed of 71 cases. Of the remaining 12 non-outbreak-associated cases, seven were importations, and there was insufficient information to associate five cases with an existing outbreak.
Key characteristics of the reported outbreaks are included in Table 4. Outbreaks are presented in chronological order of rash onset of the index case. When the nature of the epidemiological links between outbreak-associated cases was not clearly described on the national case report form, this is specified in the table.
More than half (n = 42) of the outbreak-associated cases in 2013 was the result of a large outbreak in Alberta from October 16 to November 25 (duration: 40 days). This outbreak occurred in a non-immunizing community as a result of an importation from the Netherlands. The majority of the cases were male, median age was 13 years, and all cases were unimmunized. Additional details regarding this outbreak are provided elsewhere Footnote 18.
The following outbreak summary excludes the Alberta outbreak cases so as to not skew the results. The median number of cases per outbreak was 3.5 (the mean was similar at 3.6). The median duration from onset dates of the index case and last outbreak-associated cases was 14.5 days (or one incubation period from infection to rash onset) Footnote 19. The majority of the outbreaks (75.0%, n = 6) were limited to two generations of spread (median: 2). While outbreaks 3 and 4 (Ontario) were more extensive temporally, they were restricted to only five and six cases respectively. The origin of three outbreaks could not be determined.
Canadian measles in the global context
Of the 83 reported cases in 2013, 14.5% (n = 12) were classified as imported and 54.2% (n = 45) were epidemiologically linked to an imported case. Source of exposure could not be identified for 8.4% (n = 7), and 22.9% (n = 19) were epidemiologically linked to a case whose source of exposure was unknown.
The suspected country of exposure was identified for all importations. The 12 importations were acquired from the European Region (Austria/Italy/France [n = 1] and the Netherlands [n = 3]), the Western Pacific Region (China [n = 1], the Philippines [n = 1], and Taiwan [n = 1]), the Eastern Mediterranean Region (Pakistan [n = 2]), the Southeast Asian Region (Thailand [n = 1]) and the Region of the Americas (Mexico [n = 2]).
All importations were the result of a Canadian travelling to a measles-endemic country or being exposed to other travellers from measles-endemic countries (e.g.exposure to UK resident in Mexico). One importation was the result of a foreign national traveling to Canada while the infection was communicable.
|#||Prov.||No. of cases||Onset date range (duration in days; number of generations)||Strain and sequence designation||Description|
January 31 to February 12
(13; 2 generations)
|2||NB and ON||4||
February 19 to March 4
(14; 2 generations)
February 24 to March 21
(26; 3 generations)
June 8 to July 24
(47; 4 generations)
June 10 to June 22
(13; 2 generations)
June 10 to June 26
(17; 2 generations)
June 24 to July 6
(13; 2 generations)
September 2 to September 16
(15; 2 generations)
October 16 to November 25
(41; 4 generations)
Maintenance of measles elimination
PAHO's four essential criteria for measles elimination are listed in Table 5 with a description of the indicator used to measure them and a summary of how the measles surveillance data support Canada's ongoing efforts to sustain its elimination status.
|Criterion Footnote 17||Indicator||Description|
Verify the interruption of endemic measles cases for a period of at least 3 years from the last known endemic case, in the presence of high-quality surveillance
Zero cases of endemic transmission
Documentation and verification of interruption of endemic measles in Canada from 1998 to 2011 are provided elsewhere Footnote 1 Footnote 4.
Molecular and epidemiological surveillance will continue through 2014 to ensure that there is no persistent circulation of the viral strains identified in 2013 for a period equal to or greater than 12 months.
Implement and maintain high-quality surveillance sensitive enough to detect imported and import-related cases
> 2 suspect cases per 100,000 population adequately investigated
Criterion partially met
Data to support this indicator not available nationally. However, a national estimate was determined from the Measles and Rubella Surveillance pilot project data for the 2011 reporting year. The national measles-like illness investigation rate was 19 per 100,000 population. Note: this indicator was estimated during an outbreak year (Quebec 2011). Comparatively, the national estimate during the 2006 non-outbreak year was 12 per 100,000 population.
Verify the absence of endemic measles virus strains through viral surveillance
Measles genotype assessed in 80% of outbreaks
The measles genotype was identified in 100% of the outbreaks in 2013.
Verify adequate immunization in the population
95% of population cohorts aged 1 to 40 years have received a measles-containing vaccine
Criterion partially met
Data to support this indicator not available nationally for all age groups. The most recent national immunization coverage survey estimated first dose measles-containing vaccine coverage among 2 year olds to be 95.2% and second dose measles-containing vaccine coverage among 7 year olds to be 94.9% in 2011 Footnote 6. However, according to epidemiological investigation of recent outbreaks and communication with provinces and territories we know that immunization coverage is heterogeneous across Canada, and there are areas with lower (and higher) coverage.
This report summarizes the epidemiology of measles in Canada in 2013. Although measles has been eliminated in Canada, we continue to see cases of disease. While the 83 reported cases in 2013 represent the fifth highest number annually since 1998, eight of the nine outbreaks were highly restricted in their case distribution by either person or time (i.e. small number of cases or short outbreak duration). These findings suggest a possible combination of prompt and effective public health intervention and/or high immunization coverage among contacts. However, the large outbreak in the non-immunizing community in Alberta highlights the ongoing challenges in maintaining measles elimination in a country with heterogeneous immunization coverage.
In 2013, Canada had a number of importations, all from countries with endemic measles or outbreaks. All but one of these importations were by Canadians who acquired the disease while travelling abroad (the other was a foreign resident who travelled to Canada while communicable), emphasizing the continued importance of ensuring that all Canadians are adequately immunized, particularly before travelling.
Four measles genotypes were observed in 2013, D8 being the most prevalent and geographically represented (five provinces reported cases associated with this genotype).
Canada met or partially met all four criteria for measles elimination in 2013. Epidemiological and molecular measles surveillance was able to confirm the absence of circulation of any one dominant viral strain, although ongoing surveillance is required to ensure that this is sustained. While suspect case investigations are not captured at the national level, the proxy indicator measured through the Measles and Rubella Surveillance pilot project indicates an investigation rate in excess of the minimum required. Finally, despite national coverage estimates of 95%, pockets of people and groups within the population remain susceptible.
Outcome information (e.g. duration of hospitalization, complications or death) on measles cases is not captured through national surveillance. Therefore, characterization of measles cases by severity of disease is not possible. Immunization status was unknown for 11% of cases, which limits our ability to fully understand the distribution of disease by immunization history.
The ability to collect detailed immunization histories of cases may be a challenge at the local level, where information is primarily gathered and submitted to provincial and then federal authorities for surveillance purposes. Improving the collection of immunization history in case reports should be explored.
We gratefully acknowledge the contribution of our provincial and territorial measles partners for providing data to the Canadian Measles and Rubella Surveillance System, for their input towards the format of this report and for their content review.
Conflicts of interest
There are no conflicts of interest to declare.
This work was supported by the Public Health Agency of Canada.
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