Summary of the mpox outbreak in Canada, April 28−December 31, 2022

CCDR

Volume 51-2/3, February/March 2025: Health Economics in Public Health

Outbreak Report

Summary of the mpox outbreak in Canada, April 28−December 31, 2022

Meera Bhulabhai1, Jeyasakthi Venugopal2, Mireille Plamondon2, Geneviève Bergeron3, Geneviève Cadieux3, Jesse Kancir4, Mayank Singal5, Katherine Twohig5, Austin Zygmunt6, Erin Schillberg2, Rukshanda Ahmad7, Julia Paul2

Affiliations

1 Emergency Management Branch, Public Health Agency of Canada, Toronto, ON

2 Infectious Diseases and Vaccination Programs Branch, Public Health Agency of Canada, Ottawa, ON

3 Direction régionale de santé publique de Montréal, Montréal, QC

4 Nova Scotia Health Authority, Halifax, NS

5 BC Centre for Disease Control, Vancouver, BC

6 Public Health Ontario, Toronto, ON

7 Data, Surveillance and Foresight Branch, Public Health Agency of Canada, Ottawa, ON

Correspondence

julia.paul@phac-aspc.gc.ca

Suggested citation

Bhulabhai M. Venugopal J, Plamondon M, Bergeron G, Cadieux G, Kancir J, Singal M, Twohig K, Zygmunt A, Schillberg E, Ahmad R, Paul J. Summary of the mpox outbreak in Canada, April 28−December 31, 2022. Can Commun Dis Rep 2025;51(2/3):93–101. https://doi.org/10.14745/ccdr.v51i23a04

Keywords: mpox, communicable diseases, zoonoses, orthopoxvirus, disease outbreaks, men who have sex with men

Abstract

Background: Mpox is an infectious disease caused by the monkeypox virus (MPXV), closely related to the virus that causes smallpox. In May 2022, cases of mpox were reported in previously non-endemic countries including Canada.

Objective: To summarize the epidemiology of the mpox outbreak in Canada, as well as key public health response activities, between April and December 2022.

Methods: The Public Health Agency of Canada (PHAC) worked closely with local, provincial and territorial public health authorities to develop national case investigation and reporting tools, including national case definitions for confirmed and probable mpox cases. Based on de-identified case data submitted to PHAC, patterns and trends were examined, including the distribution of cases by sociodemographic, clinical and transmission factors.

Results: Overall, 1,474 mpox cases (1,396 confirmed, 78 probable) were reported to PHAC. All reported cases were associated with MPXV clade IIb. Mpox disproportionately affected gay, bisexual and other men who have sex with men (80.0%) and those between 20−49 years of age (86.0%). Available data suggests that the most likely mode of disease acquisition was through sexual contact, with limited evidence on other possible modes of transmission. Some cases were hospitalized (3.0%); however, there were no mpox-related deaths in Canada.

Conclusion: Rapid coordination and surveillance activities supported the timely implementation of tailored interventions, including the procurement and distribution of vaccines. These actions, coupled with vaccination uptake and behavioural changes, contributed to reducing transmission and health impacts of mpox on the Canadian population.

Introduction

Mpox (formerly monkeypox) is a viral infectious disease caused by the monkeypox virus (MPXV), which is a species within the Orthopoxvirus genus. First discovered in non-human primates in 1958, human cases of this disease experience symptoms akin to those of smallpox but with a much lower case fatality rate Footnote 1. From the 1970s to the early 2000s, the epidemiological range of MPXV remained mostly limited to central and western Africa, given the proximity to its wildlife reservoir, including rodents and other small mammals Footnote 1. The occasional detection of cases outside the traditional endemic range of MPXV was mainly due to travel and exportation of reservoir animals Footnote 2Footnote 3Footnote 4Footnote 5Footnote 6. However, increased transmission among humans has been observed in the last two decades, likely relating to changes at the human-environment interface causing increased zoonotic spillovers; reduction in cross-protection from the smallpox vaccine following the end of global vaccination programs; and genetic evolution of MPXV Footnote 7.

On May 16, 2022, the United Kingdom reported a cluster of mpox cases among gay, bisexual and other men who have sex with men (GBMSM), without a history of travel to an endemic area Footnote 8. In Canada, the city of Montréal in Québec investigated the first cases of mpox between May 8−13, 2022 Footnote 9, and this cluster of cases was then confirmed by the Public Health Agency of Canada’s (PHAC) National Microbiology Laboratory on May 19, 2022 Footnote 10. The Public Health Agency of Canada conducted a preliminary risk assessment, escalated its Health Portfolio Operations Centre to a Level 2 (Increased Vigilance and Readiness) on May 21, 2022, and activated an Incident Management System to respond to the emergence of mpox and support the coordination of the outbreak investigation and response activities across the country, in collaboration with local, provincial and territorial (LPT) public health authorities. We conducted a descriptive analysis of mpox cases reported in Canada between April and December 2022, and examined differences in sociodemographic, clinical and transmission characteristics between GBMSM and non-GBMSM subgroups.

Methods

Case definitions, data collection and investigation

Following the initial reporting of mpox cases in Canada, PHAC collaborated closely with affected local and provincial public health units and interim guidance issued by the World Health Organization Footnote 11 to develop national case definitions (see Table 1) Footnote 12 and investigation tools Footnote 13. This work relied on epidemiological and clinical observations made by public health units in the affected regions, as well as data shared by international partners. This rapid knowledge exchange from affected regions informed the development and harmonization of standardized tools for public health investigations across the country. Local, provincial and territorial public health authorities conducted case investigations and data were shared with PHAC on a weekly basis. Through case investigations, LPT public health authorities collected information on demographics, symptoms and clinical manifestations, as well as information on relevant risk factors, including recent sexual and travel history. Local, provincial and territorial public health authorities conducted their own molecular testing to screen or confirm cases whenever possible and were supported by National Microbiology Laboratory for confirmatory testing and genomic sequencing, as needed.

Table 1: National mpox case classifications in Canada, 2022
Case classification Definition
Confirmed A person who is laboratory-confirmed for mpox virus by detection of unique sequences of viral DNA either by real-time polymerase chain reaction and/or sequencing
Probable

A person of any age who presents with an unexplainedFootnote a acute rash or lesion(s)Footnote b

AND

Has one or more of the following:

  • An epidemiological linkFootnote c to a probable or confirmed mpox case in the 21 days before symptom onset, OR
  • Reported travel history to or place of residence in a location where mpox is reportedFootnote d in the 21 days before symptom onset
Suspected

A person of any age who presents with one or more of the following:

  • An unexplainedFootnote a acute rashFootnote b AND has at least one of the following signs or symptoms:
    • Headache
    • Acute onset of fever (higher than 38.5°C)
    • Lymphadenopathy (swollen lymph nodes)
    • Myalgia (muscle and body aches)
    • Back pain
    • Asthenia (profound weakness)
  • An unexplainedFootnote a acute genital, perianal or oral lesion(s)
Footnotes
Footnote a

Other common causes of acute rash can include varicella zoster, herpes zoster, measles, herpes simplex, syphilis, chancroid, lymphogranuloma venereum and hand-foot-and-mouth disease

Return to footnote a referrer

Footnote b

Acute rash: mpox illness includes a progressively developing rash that usually starts on the face and then spreads elsewhere on the body. The rash can affect the mucous membranes in the mouth, tongue and genitalia. The rash can also affect the palms of hands and soles of the feet. The rash can last for two to four weeks and progresses through the following stages: macules, papules, vesicles, pustules and scabs. Note: It is not necessary to obtain negative laboratory results for listed infectious causes of rash in order to classify a case as suspected

Return to footnote b referrer

Footnote c

An epidemiological link can be: face-to-face exposure, including health workers without appropriate personal protective equipment (PPE); direct physical contact, including sexual contact; or contact with contaminated materials, such as clothing or bedding

Return to footnote c referrer

Footnote d

Reported travel history includes regional, national or international travel in the 21 days before symptom onset to any area where mpox may be reported

Return to footnote d referrer

Interventions

The Public Health Agency of Canada coordinated various responses to the 2022 mpox outbreak in Canada. A critical component of PHAC’s response was the rapid deployment of medical countermeasures from existing stockpiles, primarily Imvamune® (Modified Vaccinia Ankara Bavarian Nordic), a vaccine originally approved for immunization against smallpox. The expansion of the vaccine’s indication to include immunization against all orthopoxviruses for adults considered at high risk for exposure had been granted by Health Canada in 2020, which allowed the rapid implementation of a vaccination program in response to the mpox outbreak. Local, provincial and territorial public health authorities initially offered one dose of the two-dose vaccine schedule to eligible individuals to strategically leverage the limited vaccine supply and maximize vaccination uptake. Following early recommendations issued by the Québec Immunization Committee, Montréal Public Health in Québec initiated the first post-exposure prophylaxis vaccination program for mpox on May 30, 2022, which was later expanded to include pre-exposure prophylaxis on June 14, 2022 Footnote 9. The National Advisory Committee on Immunization recommended the use of Imvamune for prophylaxis in the context of mpox outbreaks in Canada on June 8, 2022 Footnote 14, which supported the rapid implementation of vaccination programs against mpox in all other jurisdictions. The Public Health Agency of Canada continued to procure additional Imvamune vaccine doses to support program expansion of vaccination activities in all jurisdictions; worked closely with LPTs to establish harmonized, national guidance for health professionals Footnote 13 as well as case and contact management Footnote 15; issued travel health advisories; and disseminated tailored risk communication through official, press and social media platforms. The Public Health Agency of Canada’s activation was de-escalated to normal operations on December 15, 2022, following a sustained reduction in mpox case reports across Canada.

Data analyses

People with a confirmed or probable mpox infection with illness onset between April 28, 2022, and December 31, 2022, were included for the analysis. An epidemic curve was developed to visually summarize aggregate case numbers over time by epidemiological date, which was defined as the earliest available date from the following hierarchy: date of symptom onset, date of specimen collection for laboratory testing and date reported to the local public health unit. Descriptive statistics were computed to summarize case patterns by sociodemographic, clinical and transmission characteristics. Additionally, differences were examined across GBMSM and non-GBMSM subgroups. Statistically significant differences in case patterns between GBMSM and non-GBMSM were determined based on a t-test for continuous variables and a chi-square or Fisher’s exact test for categorical variables. Given the low number of probable cases, confirmed and probable mpox cases were examined together for all analyses. Information on sexual behaviours was not directly collected through case report forms but was derived based on available data from the following variables: sex, gender and gender(s) of sexual partner(s) in the 21 days before the date of symptom onset. Epidemiological link refers to a known case’s contact with another possible or known case or contact with contaminated material. Data are presented as counts and percentages (%). All analyses were conducted in R statistical software Footnote 16Footnote 17.

Results

A total of 1,474 mpox cases were reported to PHAC in 2022 (1,396 confirmed; 78 probable). The first two cases of mpox were confirmed on May 19, 2022, with the first reported case having a symptom onset date of April 28, 2022. Based on available information from laboratory testing and genomic sequencing, all mpox cases reported in 2022 were associated with MPXV clade IIb. As shown in Figure 1, there was a steady increase in cases, which included two peaks in the summer of 2022. The majority of cases were reported in Ontario, Québec and British Columbia, accounting for 96% of all cases (Table 2). No cases were reported in Prince Edward Island, Nunavut and the Northwest Territories. There was a notable decrease in cases starting in August 2022, and by October 2022, cases were more sporadic.

Figure 1: Distribution of confirmed or probable mpox cases in Canada by earliest date and province/territory, April–December 2022
Figure 1. Text version below.
Figure 1: Descriptive text

Figure 1 summarizes the number of confirmed or probable cases reported in a province or territory per day between April 28, 2022, and December 31, 2022. Cases are summarized by epidemiological date, which is the earliest known date from the following: date of symptom onset, date of specimen collection for laboratory testing or date reported to the local public health unit. Cases from provinces or territories with a cumulative case count less than five, which includes Manitoba, New Brunswick, Nova Scotia, Newfoundland and Labrador and Yukon, were aggregated and summarized together. Cases from Ontario are represented by dark blue bars, Québec in orange bars, British Columbia in dark green bars, Alberta in light blue bars and Saskatchewan in purple bars. Provinces or territories with a cumulative case count less than five are represented by light green bars. The start of the first mass vaccination program in Montréal, Québec is marked as May 30, 2022 in Figure 1.

Abbreviations: AB, Alberta; BC, British Columbia; ON, Ontario; PTs, provinces/territories in Canada; QC, Québec; SK, Saskatchewan


Table 2: Summary of mpox cases reported in Canada, 2022
Characteristic n (%) Unknown, n (%)
Total cases 1,474 (100%) N/A
Confirmed 1,396 (94.7%)
Probable 78 (5.3%)
Sex
Male 757 (98.7%) 707 (48.0%)
Female 9 (1.2%)
Gender
Woman 11 (0.8%) 152 (10.3%)
Man 1,296 (98.0%)
Transgender 4 (0.3%)
Non-binary 3 (0.2%)
Other 7 (0.5%)
Sexual orientation
GBMSM 1,184 (80.3%)

244 (16.6%)

Non-GBMSM 46 (3.1%)
Province
Ontario 700 (47.5%) 0 (0.0%)
Québec 525 (35.6%)
British Columbia 193 (13.1%)
Alberta 43 (2.9%)
Saskatchewan 6 (0.4%)
Newfoundland and Labrador 2 (0.1%)
Yukon 2 (0.1%)
Manitoba 1 (0.1%)
New Brunswick 1 (0.1%)
Nova Scotia 1 (0.1%)

Abbreviations: GBMSM, gay, bisexual and other men who have sex with men; non-GBMSM, all other sexual identities and behaviours, including those for whom we have no information on sex/gender and gender(s) of sexual partner(s); N/A, not applicable

Available data on sex and gender was as follows: 99.0% (n=757/767) of cases were of male sex (Table 2) and 98.0% (n=1,296/1,322) identified as men. Based on available information on sex, gender and gender(s) of sexual partner(s), 80.3% (n=1,184/1,474) were grouped as GBMSM, 3.1% (n=46/1,474) as non-GBMSM and information regarding the gender(s) of sexual partner(s) was unknown for 16.6% (n=244/1,474). The majority of cases were between 20−49 years old (86.1%, n=1,269/1,474), with a mean age of 37 years. There were no significant differences in the distribution of cases by age group between the GBMSM and non-GBMSM groups (Table 3). Nearly one-third of cases with available data (30.8%, n=299/972) reported living with HIV; a significantly higher proportion of people reported living with HIV in the GBMSM group (31.0%, n=246/793) compared to the non-GBMSM group (13.2%, n=5/38). Additionally, 7.0% (n=48/244) of cases for whom we have no information on the gender(s) of sexual partner(s) reported living with HIV. A diagnosis of a concurrent sexually transmitted or blood-borne infection was reported among 22.2% (n=209/941) of cases with information available, with 22.7% (n=173/763) in the GBMSM group and 20.6% (n=7/34) in the non-GBMSM group.

Table 3: Frequency and percent distribution of people with a confirmed or probable diagnosis of mpox by select demographic and clinical factors across subgroupsFootnote a
Case characteristics Overall
(N=1,474)
GBMSM
(n=1,184)
Non-GBMSM
(n=46)
p-value
n (%)
Age group (in years)
<15 2 (0.1%) N/A N/A 0.281Footnote b
15–19 8 (0.5%) 6 (0.5%) 0 (0.0%)
20–29 345 (23.4%) 271 (22.9%) 19 (41.3%)
30–39 579 (39.3%) 475 (40.1%) 12 (26.1%)
40–49 345 (23.4%) 276 (23.3%) 9 (19.6%)
50–59 136 (9.2%) 111 (9.4%) 3 (6.5%)
60–69 53 (3.6%) 41 (3.5%) 3 (6.5%)
≥70 5 (0.3%) 0 (0.0%) 0 (0.0%)
Hospitalized
Yes 46 (3.4%) 35 (3.1%) 2 (4.3%) 0.651Footnote c
No 1,319 (96.6%) 1,106 (96.9%) 44 (95.7%)
Admitted to an ICU
Yes 3 (1.1%) 3 (1.2%) 0 (0.0%) 1.000Footnote c
No 277 (98.9%) 244 (98.8%) 14 (100%)
HIV status
Positive 299 (30.8%) 246 (31.0%) 5 (13.2%) 0.019Footnote a
Negative 673 (69.2%) 547 (69.0%) 33 (86.8%)
Concurrent STBBI
Yes 209 (22.2%) 173 (22.7%) 7 (20.6%) 0.776
No 731 (77.8%) 590 (77.3%) 27 (79.4%)
Received vaccination
Yes 307 (45.2%) 276 (47.4%) 2 (11.8%) 0.004Footnote a
No 372 (54.8%) 306 (52.6%) 15 (88.2%)
Most common symptoms reported
Rash/lesion 1,245 (89.1%) 1,061 (91.5%) 41 (89.1%) 0.588Footnote c
Fever 744 (76.2%) 634 (75.5%) 24 (85.7%) 0.213
Chills 394 (75.2%) 331 (74.7%) 14 (82.4%) 0.580Footnote c
Lymphadenopathy 706 (73.2%) 610 (73.3%) 21 (65.6%) 0.336
Fatigue/exhaustion 699 (73.0%) 597 (72.0%) 23 (79.3%) 0.388
Site of lesion
Anogenital 483 (75.0%) 424 (76.4%) 14 (70.0%) 0.592Footnote c
Face 197 (30.6%) 172 (31.0%) 7 (35.0%) 0.704
Tongue/mouth/lip 89 (13.8%) 78 (14.1%) 4 (20.0%) 0.510Footnote c
Limbs 237 (36.8%) 199 (35.9%) 12 (60.0%) 0.028Footnote a
Hand 153 (23.8%) 126 (22.7%) 6 (30.0%) 0.425Footnote c
Feet 67 (10.4%) 52 (9.4%) 5 (25.0%) 0.039Footnote aFootnote b
Torso 186 (28.9%) 161 (29.0%) 8 (40.0%) 0.289
Number of lesions
≤1 33 (15.1%) 28 (15.0%) 1 (16.7%) 0.868Footnote b
2–9 126 (57.5%) 110 (58.8%) 3 (50.0%)
10–49 53 (24.2%) 45 (24.1%) 2 (33.3%)
50–99 5 (2.28%) 3 (1.6%) 0 (0.0%)
≥100 2 (0.9%) 1 (0.5%) 0 (0.0%)
Common exposures and likely mode of acquisition
Contact with a possible or known case/contaminated material 191 (59.1%) 162 (57.9%) 3 (50.0%) 0.700Footnote b
Person-to-person transmission via sexual contact 717 (96.2%) 642 (97.1%) 16 (80.0%) 0.003Footnote aFootnote b
Travel history in the 21 days prior to symptom onset 276 (22.1%) 241 (22.1%) 8 (17.8%) 0.489

Abbreviations: GBMSM, gay, bisexual and other men who have sex with men; ICU, intensive care unit; non-GBMSM, all other sexual identities and behaviours, including those for whom we have no information on sex/gender and gender(s) of sexual partner(s); N/A, not applicable; STBBI, sexually transmitted and blood-borne infection

Footnotes
Footnote a

Statistically significant (p<0.05) difference between GBMSM and non-GBMSM mpox cases. The p-value was determined based on a χ2 test of homogeneity at α=0.05

Return to footnote a referrer

Footnote b

The p-value determined based on an independent t-test to compare mean age (in years) between GBMSM and non-GBMSM mpox cases

Return to footnote b referrer

Footnote c

The p-value determined based on Fisher’s exact test instead of a χ2 test given that expected cell values are less than five

Return to footnote c referrer

Among the GBMSM group, sexual contact was the most likely mode of acquisition for 97.1% (n=642/661) of cases, and 57.9% (n=162/280) of cases were epidemiologically linked. Among the non-GBMSM group with available data, sexual contact was the most likely mode of acquisition for 80.0% (n=16/20) of cases, whilst 50.0% (n=3/6) had a known epidemiological link.

The majority of cases provided information on recent travel history during the 21 days before symptom onset (84.8%, n=1,250/1,474), with 22.1% (n=276/1,250) reporting travel outside their province of residence. Among those with travel outside their province of residence, 37.7% (n=104/276) reported international travel, 36.6% (n=101/276) reported domestic travel and 5.1% (n=14/276) reported both international and domestic travel.

Of all cases with information available, 45.2% (n=307/679) reported receiving a vaccination for one or more of the following: previous smallpox vaccination unrelated to the current outbreak; pre-exposure prophylaxis for the current outbreak; or post-exposure prophylaxis for the current outbreak. The proportion of people who received a vaccination was significantly higher among GBMSM (47.4%, n=276/582) compared to the non-GBMSM group (11.8%, n=2/17), reflecting vaccination eligibility criteria, which were based on the epidemiology within the context of the outbreak in Canada.

The five most common symptoms reported among cases with available data were rash/lesions (89.1%, n=1,245/1,398), fever (76.2%, n=744/977), chills (75.2%, n=394/524), lymphadenopathy (73.2%, n=706/964) and fatigue/exhaustion (73.0%, n=699/958). There were no significant differences in common symptom presentation between the GBMSM and non-GBMSM groups. The most common site for a rash was the anogenital/perianal area (75.0%, n=483/1,474). A significantly higher proportion of cases in the non-GBMSM group reported a rash on their limbs (60.0%, n=12/20) and feet (25.0%, n=5/20) compared to the GBMSM group (35.9% and 9.4%, respectively). Among those with information on the number of lesions, the majority of cases reported two to nine lesions (57.5%, n=126/219).

Of all cases for whom information was available, 3.4% (n=46/1,365) were hospitalized, and 1.0% (n=3/300) were admitted to an intensive care unit. Among the GBMSM group, 3.1% of cases (n=35/1,141) were hospitalized, and 4.3% (n=2/46) of non-GBMSM cases were hospitalized; no statistically significant difference in hospitalization between GBMSM and non-GBMSM groups was observed.

Discussion

This paper describes the epidemiology of the multi-jurisdictional mpox outbreak in Canada between April and December 2022. The 2022 mpox outbreak in Canada predominantly affected GBMSM in large metropolitan cities (Toronto, Montréal and Vancouver) and sexual contact was the likely route of transmission for most cases Footnote 9Footnote 18Footnote 19. Similar to other affected countries during the 2022 global mpox outbreak Footnote 20, initial transmission within high-contact sexual networks likely drove the rapid increase in cases in June 2022. Across both the GBMSM and non-GBMSM groups, the most common symptoms were rash/lesions, fever, chills, lymphadenopathy and fatigue/exhaustion. A higher proportion of cases among GBMSM were living with HIV, compared to non-GBMSM, which is similar to findings from the 2022 global mpox outbreak Footnote 20. However, there was no statistically significant difference in hospitalization status between the two groups, and the majority of overall cases did not require hospitalization, suggesting low disease severity within the Canadian context. No mpox-related deaths were reported in Canada throughout the outbreak.

Our data also show that the non-GBMSM group had a relatively lower percentage of cases associated with sexual transmission than the GBMSM group. Additionally, presentation of a rash on limbs and feet were significantly more common among non-GBMSM compared to GBMSM, which may suggest variable sites of inoculation and lesion patterns by subgroup. A global case series examining transmission in women and non-binary individuals across 15 countries during the 2022 mpox outbreak reported that acquisition through close household and occupational contacts were more common among this group, compared to sexual contact Footnote 21. In Canada, there were no reported cases of occupational transmission and a limited number of cases among household contacts, including children younger than 15 years. Given the limited number of non-GBMSM cases in Canada, it is difficult to draw conclusions about other possible modes of transmission.

The outbreak was contained using multi-level approaches with efforts across various levels of government, relying heavily on existing liaisons with local public health units that were most affected by the outbreak, as well as community engagement and advocacy. At the federal level, PHAC: 1) activated an Incident Management System aimed at coordinating and responding to the emerging mpox outbreak, 2) conducted risk assessments to evaluate the domestic situation, 3) recommended actions grounded in evidence and 4) coordinated national meetings to share data and information, collaborate on products and disseminate best practices to respond effectively to the outbreak. At the local and provincial/territorial level, successful strategies included mass pre-exposure prophylaxis vaccination clinics, case and contact management, guidance to health care providers and use of antivirals for clinically severe cases Footnote 9. Local, provincial and territorial public health authorities engaged with community organizations (e.g., Gay Men’s Sexual Health Alliance in Ontario) to help mobilize affected communities with mpox-related knowledge (e.g., signs and symptoms, mpox vaccination, testing resources, safer sex messaging, etc.) and encourage testing in the presence of compatible symptoms through social media and popular dating applications.

While targeted vaccination played an important role in curbing the mpox outbreak Footnote 22Footnote 23, evidence from mathematical models calibrated to both Canadian case and vaccination data from 2022 highlighted the importance of changes to sexual practices as a major driver in decreasing transmission and the duration of the outbreak Footnote 24.

Sporadic detection of mpox cases continue to occur globally with small, localized increases in activity occurring in many jurisdictions, including Canada, since 2022 Footnote 25Footnote 26. It is, therefore, important that jurisdictions continue their surveillance efforts for mpox to ensure early detection of a resurgence in cases, including new outbreaks linked to different MPXV lineages, and to continue to offer vaccination against mpox for those who are eligible to minimize transmission and severity of disease Footnote 22Footnote 23. Mpox is a notifiable disease in most provinces and territories across Canada, and in August 2024, it became a nationally notifiable disease, which facilitates ongoing surveillance work. Public Health Agency of Canada, along with federal/LPT partners, are continuing to collaborate and conduct surveillance activities, including laboratory-based and wastewater surveillance of MPXV Footnote 27.

Limitations

Due to the complexity of rapidly establishing enhanced surveillance to characterize an emerging infection, there are several considerations regarding the quality and consistency of reported data. First, the development of the national case report form was iterative, with initial cases potentially missing some information that was later prioritized (e.g., expanded data capture for gender). Second, due to the diversity of public health systems across LPTs, some information could not be collected or was incomplete. While a history of vaccination against mpox may have mitigated the extent and severity of the overall clinical presentation of cases Footnote 23, a high level of missing data for vaccination history (54%) in the national mpox dataset precluded an assessment of this variable in this report. Some data, such as risk factors and likely source of acquisition, were also self-reported, which could have been impacted by recall bias as well as stigma. Lastly, it is likely that the number of mpox cases reported is an underestimate of the true burden of disease as those with mild symptoms who did not seek health care would not have been tested for MPXV.

Conclusion

The patterns and characteristics of the mpox outbreak in Canada were similar to other countries implicated in the 2022 global mpox outbreak, whereby GBMSM were disproportionately impacted. Changes in sexual practices and uptake of vaccinations helped to rapidly reduce transmission of mpox during the 2022 outbreak in Canada. Alongside partners, PHAC will continue to vigilantly monitor for cases and use evidence-informed practices to support the timely implementation of public health interventions to reduce transmission.

Authors' statement

  • MB — Conceptualization, investigation, methodology, formal analysis, data interpretation, writing−original draft, writing−review & editing
    JV — Conceptualization, investigation, methodology, formal analysis, data interpretation, writing−original draft, writing−review & editing
    MP — Investigation, methodology, data interpretation, writing−original draft, writing−review & editing
    GB — Investigation, methodology, data interpretation, writing−review & editing
    GC — Investigation, methodology, data interpretation, writing−review & editing
    JK — Investigation, methodology, data interpretation, writing−review & editing
    MS — Investigation, methodology, data interpretation, writing−review & editing
    KT — Investigation, methodology, data interpretation, writing−review & editing
    AZ — Investigation, methodology, data interpretation, writing−review & editing
    ES — Investigation, methodology, data interpretation, writing−review & editing
    RA — Investigation, methodology, data interpretation, writing−review & editing
    JP — Conceptualization, investigation, methodology, data interpretation, writing−review & editing

Competing interests

None.

ORCID numbers

Acknowledgements

We thank local, provincial and territorial public health authorities for leading public health investigations, and for reporting and sharing case data with PHAC. We would also like to acknowledge the work of federal partners, including PHAC’s Mpox Incident Management System team for leading national response activities and the Centre for Data Management, Innovation and Analytics for their role in managing the national mpox database.

Funding

This work was supported the Public Health Agency of Canada, Public Health Ontario and the BC Centre for Disease Control.

References

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Footnote 2

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Footnote 3

Formenty P, Muntasir MO, Damon I, Chowdhary V, Opoka ML, Monimart C, Mutasim EM, Manuguerra JC, Davidson WB, Karem KL, Cabeza J, Wang S, Malik MR, Durand T, Khalid A, Rioton T, Kuong-Ruay A, Babiker AA, Karsani ME, Abdalla MS. Human monkeypox outbreak caused by novel virus belonging to Congo Basin clade, Sudan, 2005. Emerg Infect Dis 2010;16(10):1539–45. https://doi.org/10.3201/eid1610.100713

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Footnote 4

Yong SE, Ng OT, Ho ZJ, Mak TM, Marimuthu K, Vasoo S, Yeo TW, Ng YK, Cui L, Ferdous Z, Chia PY, Aw BJ, Manauis CM, Low CK, Chan G, Peh X, Lim PL, Chow LP, Chan M, Lee VJ, Lin RT, Heng MK, Leo YS. Imported Monkeypox, Singapore. Emerg Infect Dis 2020;26(8):1826–30. https://doi.org/10.3201/eid2608.191387

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Footnote 5

Vaughan A, Aarons E, Astbury J, Balasegaram S, Beadsworth M, Beck CR, Chand M, O’Connor C, Dunning J, Ghebrehewet S, Harper N, Howlett-Shipley R, Ihekweazu C, Jacobs M, Kaindama L, Katwa P, Khoo S, Lamb L, Mawdsley S, Morgan D, Palmer R, Phin N, Russell K, Said B, Simpson A, Vivancos R, Wade M, Walsh A, Wilburn J. Two cases of monkeypox imported to the United Kingdom, September 2018. Euro Surveill 2018;23(38):1800509. https://doi.org/10.2807/1560-7917.ES.2018.23.38.1800509

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Footnote 6

Centers for Disease Control and Prevention. Update: multistate outbreak of monkeypox--Illinois, Indiana, Kansas, Missouri, Ohio, and Wisconsin, 2003. MMWR Morbid Mortal Wkly Rep 2003;52(27):642–6. https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5227a5.htm

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Footnote 7

Zebardast A, Latifi T, Shafiei-Jandaghi NZ, Gholami Barzoki M, Shatizadeh Malekshahi S. Plausible reasons for the resurgence of Mpox (formerly Monkeypox): an overview. Trop Dis Travel Med Vaccines 2023;9(1):23. https://doi.org/10.1186/s40794-023-00209-6

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Footnote 8

UK Health Security Agency. News story: Monkeypox cases confirmed in England – latest updates. London, UK: Government of the UK; 2022. [Accessed 2024 Mar 15]. https://www.gov.uk/government/news/monkeypox-cases-confirmed-in-england-latest-updates

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Footnote 9

Harrison LB, Bergeron G, Cadieux G, Charest H, Fafard J, Levade I, Blais AC, Huchet E, Trottier B, Vlad D, Szabo J, Thomas R, Poulin S, Greenaway C, Zaharatos GJ, Oughton M, Chakravarti A, Pilarski R, Bui-Nguyen A, Benomar K, Libman MD, Vinh DC, Duggan AT, Graham M, Klein MB, Barkati S. Monkeypox in Montréal: Epidemiology, Phylogenomics, and Public Health Response to a Large North American Outbreak. Ann Intern Med 2023;176(1):67–76. https://doi.org/10.7326/M22-2699

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Footnote 10

Public Health Agency of Canada. Monkeypox brief, June 2022. Can Commun Dis Rep 2022;48(6):291. https://www.canada.ca/en/public-health/services/reports-publications/canada-communicable-disease-report-ccdr/monthly-issue/2022-48/issue-6-june-2022/monkeypox-virus-canada-2022.html

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Footnote 11

World Health Organization. Multi-country monkeypox outbreak in non-endemic countries 2022. Geneva, CH: WHO; 2022. [Accessed 2024 April 4]. https://www.who.int/emergencies/disease-outbreak-news/item/2022-DON385

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Footnote 12

Public Health Agency of Canada. National case definition: Mpox (monkeypox). Ottawa, ON: PHAC; 2022. https://www.canada.ca/en/public-health/services/diseases/mpox/health-professionals/national-case-definition.html

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Footnote 13

Public Health Agency of Canada. Mpox (monkeypox): For health professionals. Ottawa, ON: PHAC; 2024. [Accessed 2024 April 4]. https://www.canada.ca/en/public-health/services/diseases/mpox/health-professionals.html

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Footnote 14

Public Health Agency of Canada. NACI Rapid Response: Interim guidance on the use of Imvamune in the context of monkeypox outbreaks in Canada. Ottawa, ON: PHAC; 2024. https://www.canada.ca/en/public-health/services/immunization/national-advisory-committee-on-immunization-naci/guidance-imvamune-monkeypox.html

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Footnote 15

Public Health Agency of Canada. Mpox: Public health management of human cases and associated human contacts in Canada. Ottawa, ON: PHAC; 2024. [Accessed 2024 Mar 15]. https://www.canada.ca/en/public-health/services/diseases/mpox/health-professionals/management-cases-contacts.html

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Footnote 16

R Core Team. R: A language and environment for statistical computing. R Core Team: Vienna, AT: GBIF; 2022. https://www.gbif.org/tool/81287/r-a-language-and-environment-for-statistical-computing

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Footnote 17

RStudio Team. RStudio: Integrated Development for R. Boston, MA: RStudio; 2022. https://www.r-project.org/conferences/useR-2011/abstracts/180111-allairejj.pdf

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Footnote 18

BC Centre for Disease Control. Mpox. Vancouver, BC: BCCDC. [Accessed 2024 Mar 15]. http://www.bccdc.ca/health-info/diseases-conditions/mpox#summary

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Footnote 19

Public Health Ontario. Enhanced Epidemiological Summary: Mpox in Ontario: May 1, 2022 to July 31, 2023. Toronto, ON: PHO; 2023. https://www.publichealthontario.ca/-/media/Documents/M/2022/monkeypox-episummary.pdf

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Footnote 20

World Health Organization. 2022-24 Mpox (Monkeypox) Outbreak: Global Trends. Geneva, CH: WHO; 2024. https://worldhealthorg.shinyapps.io/mpx_global/

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Footnote 21

Thornhill JP, Palich R, Ghosn J, Walmsley S, Moschese D, Cortes CP, Galliez RM, Garlin AB, Nozza S, Mitja O, Radix AE, Blanco JL, Crabtree-Ramirez B, Thompson M, Wiese L, Schulbin H, Levcovich A, Falcone M, Lucchini A, Sendagorta E, Treutiger CJ, Byrne R, Coyne K, Meyerowitz EA, Grahn AM, Hansen AE, Pourcher V, DellaPiazza M, Lee R, Stoeckle M, Hazra A, Apea V, Rubenstein E, Jones J, Wilkin A, Ganesan A, Henao-Martínez AF, Chow EJ, Titanji BK, Zucker JE, Ogoina D, Orkin CM; Share-Net writing group. Human monkeypox virus infection in women and non-binary individuals during the 2022 outbreaks: a global case series. Lancet 2022;400(10367):1953–65. https://doi.org/10.1016/S0140-6736(22)02187-0

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Footnote 22

Brousseau N, Carazo S, Febriani Y, Padet L, Hegg-Deloye S, Cadieux G, Bergeron G, Fafard J, Charest H, Lambert G, Talbot D, Longtin J, Dumont-Blais A, Bastien S, Dalpé V, Minot PH, De Serres G, Skowronski DM. Single-dose Effectiveness of Mpox Vaccine in Quebec, Canada: Test-negative Design With and Without Adjustment for Self-reported Exposure Risk. Clin Infect Dis 2024;78(2):461–9. https://doi.org/10.1093/cid/ciad584

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Footnote 23

Allard R, Leclerc P, Bergeron G, Cadieux G. Breakthrough cases of mpox: one-dose vaccination is associated with milder clinical manifestations. J Infect Public Health 2024;17(4):676–80. https://doi.org/10.1016/j.jiph.2024.02.015

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Footnote 24

Milwid RM, Li M, Fazil A, Maheu-Giroux M, Doyle CM, Xia Y, Cox J, Grace D, Dvorakova M, Walker SC, Mishra S, Ogden NH. Exploring the dynamics of the 2022 mpox outbreak in Canada. J Med Virol 2023;95(12):e29256. https://doi.org/10.1002/jmv.29256

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Footnote 25

Leonard CM, Poortinga K, Nguyen E, Karan A, Kulkarni S, Cohen R, Garrigues JM, Marutani AN, Green NM, Kim AA, Sey K, Pérez MJ. Mpox Outbreak - Los Angeles County, California, May 4–August 17, 2023. MMWR Morb Mortal Wkly Rep 2024;73(2):44–8. https://doi.org/10.15585/mmwr.mm7302a4

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Footnote 26

Pisano L, Magliulo M, Turco M, Farini J, Rapaccini AL, Lagi F, Bartoloni A, Pimpinelli N. The never-ending story of mpox epidemic: tracing a new cluster in Florence, Italy. Travel Med Infect Dis 2024;59:102704. https://doi.org/10.1016/j.tmaid.2024.102704

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Footnote 27

Sachdeva H, Shahin R, Ota S, Isabel S, Mangat CS, Stuart R, Padhi S, Chris A, Mishra S, Tan DH, Braukmann TW, Eshaghi A, Mejia EM, Hizon NA, Finkelstein M. Preparing for Mpox Resurgence: Surveillance Lessons From Outbreaks in Toronto, Canada. J Infect Dis 2024;229 Supplement_2:S305–12. https://doi.org/10.1093/infdis/jiad533

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