Surveillance for Lyme disease in Canada, 2009 to 2012 - CCDR: Volume 41-06, June 4, 2015
Canada Communicable Disease Report CCDR
ISSN 1481-8531 (On-line)
Surveillance for Lyme disease in Canada, 2009 to 2012
Ogden NHFootnote 1 Footnote *, Koffi JKFootnote 1, Lindsay LRFootnote 2, Fleming SFootnote 3, Mombourquette DCFootnote 3, Sanford CFootnote 4, Badcock JFootnote 5, Gad RRFootnote 5, Jain-Sheehan NFootnote 6, Moore SFootnote 6, Russell CFootnote 6, Hobbs LFootnote 6, Baydack RFootnote 7, Graham-Derham SFootnote 7, Lachance LFootnote 8, Simmonds KFootnote 8, Scott ANFootnote 8
Objectives: To summarize the first four years of national surveillance for Lyme disease in Canada from 2009 to 2012 and to conduct a preliminary comparison of presenting clinical manifestations in Canada and the United States.
Methods: The numbers and incidence of reported cases by province, month, year, age and sex were calculated. Logistic regression was used to examine trends over time. Acquisition locations were mapped and presenting clinical manifestations reported for jurisdictions where data was available. Variations by province, year, age and sex as well as presenting clinical symptoms were explored by logistic regression. An initial comparative analysis was made of presenting symptoms in Canada and the United States.
Results: The numbers of reported cases rose significantly from 144 in 2009 to 338 in 2012 (coefficient = 0.34, standard error = 0.07, P <0.05), mostly due to an increased incidence of infections acquired in Canada. More cases were classified as 'confirmed' (71.5%) than 'probable' (28.5%). Most cases occurred in locations where vector tick populations were known to be present. More men than women were affected (53.4% versus 46.6%), incidence was highest in adults aged 55 to 74 years and in children aged five to 14 years. Most cases (95%) were acquired from April to November. Of cases acquired in endemic areas, 39.7% presented with manifestations of early Lyme disease, while 60.3% had manifestations of disseminated Lyme disease. There were significant differences among age groups, sexes and provinces in the frequencies of reported clinical manifestations. The proportion of cases acquired in endemic areas presenting with early Lyme disease was lower than that reported in the US.
Conclusion: Lyme disease incidence is increasing in Canada. Most cases are acquired where vector tick populations are spreading and this varies geographically within and among provinces. There is also variation in the frequency of age, season and presenting manifestations. The lower proportion of cases presenting with early Lyme disease in Canada compared with the US suggests lower awareness of early Lyme disease in Canada, but this requires further study.
Lyme disease, caused by the bacterium Borrelia burgdorferi sensu stricto in North America is transmitted to humans from wild animal reservoir hosts by Ixodes spp. ticksFootnote 1 in their woodland habitatsFootnote 2. Lyme disease risk in Canada occurs where tick vectors are established in southern British Columbia (where the relatively inefficient tick vector Ixodes pacificus occurs) and in southern parts of central and eastern Canada into which the efficient tick vector I. scapularis is spreading from the United States, driving Lyme disease emergence in CanadaFootnote 3. Low-level Lyme disease risk occurs over a wider geographic area due to ticks dispersed from tick populations by migratory birdsFootnote 4 Footnote 5.
In light of the documented northern migration of ticks into Canada, Lyme disease became nationally notifiable in Canada in 2009 and basic information on human cases is submitted by all provinces and territories to the National Notifiable Disease Surveillance System (NNDSS) coordinated by the Public Health Agency of Canada (PHAC). A Lyme Disease Enhanced Surveillance (LDES) system was initiated by PHAC in 2010 with provincial public health organizations to obtain more detailed data on Lyme disease cases. Together, these surveillance systems aim to identify changing trends in Lyme disease incidence, the Canadian population at risk and the types of clinical disease in Canada to inform clinician-based Lyme disease diagnosis and reporting.
In this study, data from the first four years of national surveillance for Lyme disease (2009 to 2012) are presented and analyzed to describe the early patterns of Lyme disease emergence in Canada. As Lyme disease emergence in central and eastern Canada is likely an extension of the emergence of Lyme disease in the US, patterns of Lyme disease cases (age, season of acquisition and presenting manifestations) were compared against those reported in the United States.
Human case data sources
NNDS data on annual numbers of cases reported to all provincial and territorial public health organizations by clinicians or via provincial laboratories were available for 2009 to 2012. Basic information reported included sex, age and episode date. The cases were classified as 'confirmed' or 'probable' by the provincial public health organizations submitting the data, except for British Columbia, Québec and New Brunswick who reported all cases without classifying them and did not report cases with erythema migrans rashes without laboratory support for the diagnosis.
The national surveillance case definition of Lyme diseaseFootnote 6
Clinical evidence of illness with laboratory confirmation by:
- Isolation of Borrelia burgdorferi from an appropriate clinical specimen, OR
- Detection of B. burgdorferi DNA by polymerase chain reaction, OR
- A positive serologic test result using the two-tier (ELISA and Western Blot) test with a history of residence in or visit to a Lyme disease-endemic area.*
P1 = Clinical evidence of illness with a positive serologic test result using the two-tier (ELISA and Western Blot) test, without a history of residence in, or visit to, a Lyme disease endemic area*
P2 = Clinician-observed erythema migrans without laboratory evidence but with history of residence in, or visit to, a Lyme disease endemic areaFootnote 1.
In 2010, the LDES was implemented in partnership with the provinces of Manitoba, Ontario, New Brunswick and Nova Scotia. In 2012, Alberta, Saskatchewan and Prince Edward Island joined. Data transferred in a standard form in the LDES included details of possible location of acquisition of infection within or outside Canada, details of clinical manifestations and methods of laboratory diagnosis. There were variations among provinces participating in the LDES in the data provided (Appendix 1).
Information on clinical features was provided by Manitoba, Ontario, New Brunswick and Nova Scotia, although Manitoba reported only two categories of symptoms: erythema migrans and 'other clinical evidence'; i.e., evidence of disseminated Lyme disease but without further details on symptoms. Categories of clinical manifestations were those of early Lyme disease (i.e., erythema migrans), early disseminated Lyme disease including manifestations of neuroborreliosis (Bell's palsy or other neurological manifestations of disseminated Lyme disease), cardiac manifestations and manifestations of late disseminated Lyme disease such as arthritis. (See text box below.) Note that it was assumed that all "P2" probable cases (i.e., cases with erythema migrans but no serological test result) were early Lyme disease having a single erythema migrans rather than multiple erythema migrans lesions (which occur in disseminated Lyme disease). Cases with multiple erythema migranswould be expected to have positive serological test results and be captured as confirmed or "P1" probable cases.
Main manifestations of Lyme diseaseFootnote 8
Early localized: erythema migrans +/- fever, arthralgias and headache
Early disseminated: Multiple erythema migrans +/- fever, arthralgias, headache and lymphadenopathy
Cardiac: AV block, tachyarrhythmias, myopericarditis, myocardial dysfunction
Neurologic: Aseptic meningitis, cranial neuropathy (e.g., Bell's palsy), motor or sensory radiculopathy
Late disseminated: Oligoarticular arthritis
Neurologic: Encephalopathy, axonal polyradiculoneuropathy, chronic encephalomyelitisFootnote 1
The data from both the LDES and NNDSS were summarized and, where possible, compared against similar data on Lyme disease case surveillance from the USFootnote 10) where similar data have been collected for over 20 years. Annual incidence in Canada, as well as province-, sex- and age group-specific incidence rates was calculated per 100,000 population. The denominators were census population estimates for July 1st for each year from 2009 to 2012Footnote 11. The proportion of cases reported by month and by case classification for each year was also calculated. Trends in the numbers of cases reported nationally for the period 2009 to 2012 ('confirmed' and 'probable' cases combined) were explored by logistic regression using weighted least squares estimation in Stata SE 11.0 for Windows (College Station, Tx), with year as the explanatory variable accounting for recent Canadian population estimatesFootnote 12. Analysis was conducted with case numbers and data reported at the time but these may change slightly due to retrospective identification of cases.
Analysis of numbers of endemic versus travel-related cases, location of acquisition and clinical features were performed on cases reported via the LDES by Manitoba, Ontario, New Brunswick and Nova Scotia. The likely locations of exposure of cases in Canada were mapped using ArcGIS Version 10.2 (ESRI) with point locations being the centroid of Forward Sortation Areas (Table 1) or endemic areas depending on reported location of acquisition. Known endemic areas and risk areasFootnote 3 were also mapped for visual comparison.
|Cases acquired in Canada with clinical dataFootnote 1|
|All probable cases||10||(18.5)||20||(31.7)||49||(38.3)||49||(34.5)||128||(33.1)|
|First probable case definition||8||(14.8)||15||(23.8)||40||(31.3)||24||(16.9)||87||(22.5)|
|Second probable case definition||2||(3.7)||5||(7.9)||9||(7.0)||25||(17.6)||41||(10.6)|
Variations among provinces, years, age groups and sex in the proportions reporting different clinical manifestations of disseminated Lyme disease were explored in logistic regression models in Stata SE 11.0. The outcome variables were presence/absence of erythema migrans, neurological manifestations, cardiac manifestations and arthritis/joint swelling in separate models. Explanatory variables of age, year, province and sex were first explored in bivariable analyses and those showing associations with the outcome at a level of significance of P <0.1 were included in multivariable models. Polynomial relationships of age with frequency of manifestations (using age and age squared as explanatory variables) were explored as suggested by visual inspection of Lowess smoothed graphs of these relationships. The most parsimonious multivariable models were sought by backward elimination of variables. The level of significance for the multivariable model was P <0.05.
Incidence and temporal trends
The numbers of reported cases rose significantly from 144 in 2009 to 338 in 2012 (coefficient = 0.34, standard error = 0.07, P <0.05; Table 1), with incidence rising from 0.4 to 1.0 per 100,000 population (Table 2).
|Prince Edward Island||0.0||0.0||0.7||1.4|
|Newfoundland and Labrador||0.0||0.2||0.0||0.0|
|Cases acquired in CanadaFootnote 1|
|Prince Edward Island||0.0||0.0||0.0||0.7|
Cases were reported from all provinces with most infections acquired in Canada occurring in British Columbia, Manitoba, Ontario, Québec, New Brunswick and Nova Scotia. All cases reported from Alberta and Newfoundland and Labrador were reported as acquired during travel outside Canada.
In 2012, incidence was >1.0 per 100,000 population in five provinces; Manitoba, Ontario, New Brunswick, Nova Scotia and Prince Edward Island (Table 2). Incidence increased primarily in Manitoba, Ontario, Québec, New Brunswick and Nova Scotia (Table 2). There was a slight decrease of the number of cases reported in British Columbia and Nova Scotia from 2011 to 2012.
The majority of cases were reported as 'confirmed' (Table 1). Of the cases without a reported history of travel outside Canada, 387 included data on clinical symptoms and likely location of infection. For these cases, (reported by Manitoba, Ontario, New Brunswick and Nova Scotia), the numbers of P1 and P2 'probable' cases could be estimated. For these provinces, most probable cases were of the P1 category (Table 1).
Incidence variation with age and sex
Incidence varied among age groups, being highest in older adults from 55 to 74 years and in children (those cases with reported ages less than 18) being highest in the five to 14 year age range (Figure 1). More cases were reported as males (476/891, 53.4%) than females (409/891, 46.6%), which was consistent for most (16/18) age groups (Figure 1).
Text Equivalent - Figure 1
|Incidence||Total Pop||Total Incidence|
Of 387 cases for which the type of episode date was recorded, the episode date was date of onset of illness for 328 (84.7%), date of specimen collection for diagnosis for 42 (10.8%), date of clinical or laboratory diagnosis for 13 (3.3%) and date of reporting for 3 (0.8%). Lyme disease cases had episode dates in all months of the year, but most (544/891, 61.1%) occurred from June to August (Figure 2). Cases in British Columbia tended to occur earlier and later in the year than in other provinces, while a greater proportion of cases occurred in October in Manitoba compared to other provinces (Figure 2).
Figure 2: The proportions of Lyme disease cases reported from 2009 to 2012 and acquired in Canada by episode dateFootnote 1
Text Equivalent - Figure 2
Geographic location of acquisition
Most cases acquired in Canada were acquired in areas where known endemic areas or risk areas occur, although cases were reported to occur outside these locations (Figure 3). The annual numbers of cases reported as acquired outside Canada from 2009 to 2012 was stable: between 38 to 48 cases per year from 2009 to 2012. For the 54 cases reported from 2009 to 2012 for which the location of travel out of Canada was provided, 38 (70.4%) were acquired in the US and 16 (29.6%) were acquired in Europe.
Text Equivalent - Figure 3
Four regions are identified on the map as areas with human cases of Lyme disease. These regions cover five provinces: Manitoba, Ontario, Quebec, New Brunswick, and Nova Scotia. Sites where human cases have been reported are identified by 5 different sizes of blue dots, with the smallest dot representing 1-4 cases and the largest dot representing 17-21 cases. In addition to this indicator of the number of human cases in a geographic area, risk areas are identified by outlining an area that is then filled in with red diagonal lines. Two inset maps are provided for the Windsor Montreal corridor, and Nova Scotia where the predominant number of human cases have been found with the outlined risk areas typically surrounding one or more of the blue dots.
Of the 353 cases for which information on all five categories of clinical manifestations were available, 157 (44.4%) reported erythema migrans alone (and were therefore early Lyme disease) and a further 92 reported EM with manifestations of disseminated Lyme disease. Manifestations of early disseminated Lyme disease were reported for 98 cases (27.8%) for which the following symptoms were reported: 92 cases (26.1%) reported neurological manifestations (Bell's palsy was reported for 30 cases [8.5%] and other neurological manifestations for 74 cases [21.0%]) and cardiac manifestations for 17 cases (4.8%) (Figure 4). Manifestations of late disseminated Lyme disease, e.g., arthritis, were reported for 133 cases (37.8%) (Figure 4). Multiple manifestations were reported for 131 cases (37.2%). Of all the reported cases with disseminated Lyme disease, the proportion of cases reporting neurological, cardiac and arthritis manifestations were respectively 38%, 7% and 55%.
Figure 4: Percentage of cases reported in the Lyme Disease Enhanced Surveillance with different clinical manifestations of Lyme disease compared against those reported in surveillance in the US (10)Footnote a
Text Equivalent - Figure 4
|All neurological manifestations||26.06232295||12|
According to the surveillance case definitions, cases of early Lyme disease (the "P2" case definition: erythema migrans without laboratory test support for the diagnosis) can only be reported from patients having contact with known Lyme disease-endemic areas. Therefore, to determine the proportions of cases being diagnosed with early Lyme disease versus disseminated Lyme disease (early and/or late), the denominator must be the number of cases with information on clinical manifestations that were reported as having been acquired in known endemic areas. There were 302 cases, with information on clinical manifestations reported as acquired in endemic areas in Manitoba, Ontario, New Brunswick and Nova Scotia. Of these 220 (72.8%) reported erythema migrans, but erythema migrans was the sole manifestation for 120 cases (39.7%), so only 39.7% of cases were reported in early Lyme disease, while the rest (60.3%) had symptoms of disseminated Lyme disease (Figure 5). In New Brunswick, cases of erythema migrans without serological support for the diagnosis are not reported, but for four of the nine cases (44.4%) with data on clinical manifestations, erythema migrans was the only clinical manifestation. Therefore possible under-reporting of "P2" probable cases (erythema migrans acquired in an endemic area) in all the provinces was not simply attributable to lack of reporting in New Brunswick. The number of cases during the period 2009 to 2012 from the three provinces reporting information on all five clinical features (Ontario, New Brunswick & Nova Scotia) was 275.
Text Equivalent - Figure 5
|Lyme disease type||percentage||United States|
|All disseminated LD||56.4||43.6|
|Late disseminated LD||37.8||32|
|Early disseminated LD||18.5||11.6|
Of the cases acquired in endemic areas, 199 (72%) reported erythema migrans (of which 120 [43.6%] had erythema migrans as the only clinical manifestation), 25 (9.1%) had Bell's palsy, 60 (21.8%) had other neurological symptoms (a total of 74 [26.9%] had neurological symptoms of any kind), 14 (5.1%) had cardiac symptoms and 104 (37.8%) had arthritis or joint swelling. More than one clinical manifestation was reported for 107 (38.9%) cases. Overall, of cases acquired in endemic areas 120 (43.6%) were early Lyme disease (reported to have erythema migrans as the only manifestation) and 155 (56.4%) were disseminated Lyme disease. Of the disseminated Lyme disease cases 51 (18.5%) were early disseminated Lyme disease (reported to have neurological or cardiac manifestations but not arthritis) and 104 (37.8%) were late disseminated Lyme disease (reported to have arthritis).
The frequency of reported erythema migrans was highest for children and adults >50 years compared to other age groups, although after adjusting for year, the frequency of reporting of erythema migrans increased linearly with age (Table 3, Figure 6). The frequency of neurological manifestations and cardiac symptom reports varied significantly among age groups. Neurological manifestations were most frequently reported for 20 to 59 year-olds and relatively rarely reported for younger children and adults over 60, while cardiac symptoms were only seen in cases aged 20 to 69, particularly in cases aged 30 to 49 (Figure 6). The proportion of cases reporting neurological symptoms was also significantly higher in Ontario than in Nova Scotia and New Brunswick combined and was lower in women than men (Table 3). There were no significant differences among ages, sexes, provinces and years in the proportion of cases that reported arthritis (data not shown).
Table 3: Final multivariable models, following backward elimination of non-significant (P >0.05) variables, for which the outcome variables were the proportion of cases showing erythema migrans, neurological manifestations and cardiac manifestations
|Variable||Odds ratio||95% Confidence interval||Wald z||P value|
|Outcome = erythema migrans|
|Year 2010 versus 2009||1.364||0.616-3.018||0.77||>0.1|
|Year 2011 versus 2009||2.232||1.109-4.489||2.25||<0.05|
|Year 2012 versus 2009||2.860||1.416-5.778||2.93||<0.01|
|Outcome = neurological manifestations|
|Women versus men||0.561||0.345-0.940||-2.19||<0.05|
|Ontario versus New Brunswick and Nova Scotia||3.781||1.849-7.772||3.62||<0.001|
|Outcome = cardiac manifestations|
Figure 6: Percentage of cases by age group that showed erythema migrans, neurological manifestations, cardiac manifestations or arthritis/joint swellingFootnote b
Text Equivalent - Figure 6
The annual number of Lyme disease cases reported in Canada more than doubled from 2009 to 2012. Most of this increase was associated with Lyme disease that was acquired in provinces from Manitoba eastward. This trend and the pattern of change in incidence among provinces is consistent with the geographic spread of I. scapularis and Lyme disease risk in eastern and central Canada, although increasing awareness among the public and health practitioners may be resulting in a greater proportion of reported cases. The reported number of Lyme disease cases is likely an underestimate due to expected under-reporting of Lyme disease in emerging areasFootnote 13 and because early Lyme disease cases can be reported only if acquired in Lyme disease-endemic areas unless supported by laboratory evidence. Cases acquired outside these areas are not reported to public health.
Two thirds of Lyme disease cases were 'confirmed' which is consistent with the risk of acquiring Lyme disease being particularly high in Lyme disease-endemic areas. Tick surveillanceFootnote 3 Footnote 14 Footnote 15 shows that the I. scapularis population is expanding its geographic range in Canada and nearly a quarter of reported disseminated Lyme disease cases were acquired in areas not known as endemic areas (and were P1 probable cases). However, most of these cases occurred in 'risk' areas where populations of I. scapularis are emerging (Figure 3). In risk and endemic areas, incidence may be much higher (over 25/100,000) than province-level incidence values (16). A small number of Lyme disease cases occurred where I. scapularis populations are not yet known but where little field surveillance has occurred to date to verify their presence or absence.
The incidence of reported cases among adults was highest in those over 54 years of age, in men and in children under 15 years old. This pattern is consistent with US surveillanceFootnote 10. These age groups and men may be particularly at risk of acquiring Lyme disease. However, children and older adults reported early Lyme disease manifestations more frequently and manifestations of disseminated Lyme disease less frequently, so high incidence in these groups may reflect greater awareness and earlier presentation for diagnosis compared to younger adults.
The seasonality of cases in Canada was similar to that observed in the USFootnote 10 and was consistent with tick-borne transmission. I. scapularis and I. pacificus are active from April to November and human outdoor recreational activities in woodlands are also most likely to occur at this time. Nymphal ticks transmit most cases of Lyme diseaseFootnote 17, but cases were acquired in early spring and autumn when adult ticks are most active. Consistent with longer season activity of I. pacificus compared to I. scapularisFootnote 18, more cases occurred earlier and later in the year in British Columbia where I. pacificus is the vector. Delays between infection and onset or diagnosis of disseminated Lyme disease could explain reporting of some cases in winterFootnote 9, although some early Lyme disease cases had a reported date of onset in winter. Why more Lyme disease cases were reported in autumn in Manitoba compared to other provinces in unclear, as ticks would also be active in other provinces at this time.
Data on the types of Lyme disease cases reported from endemic areas suggests there is suboptimal awareness of Lyme disease among the public and front line medical practitioners. A history of erythema migrans was reported for >80% of cases acquired in known endemic areas. However only 40% of cases were reported during early Lyme disease and 60% were likely disseminated Lyme disease, even though erythema migrans was recorded as a manifestation in many disseminated Lyme disease cases. This suggests that many reported cases of disseminated Lyme disease could have been diagnosed and treated earlier, but either the affected patients did not know what the erythema migrans rash was (and didn't present themselves for diagnosis at this stage) or medical practitioners did not diagnose and treat the cases at this stage. In the US, where awareness among the public and medical practitioners is expected to be greater, >56% of reported cases were early Lyme diseaseFootnote 10.
Overall proportions of clinical manifestations of disseminated Lyme disease cases in Canada were similar to those in the United States. When the proportions of disseminated Lyme disease cases showing neurological manifestations, cardiac manifestations and arthritis (i.e., late Lyme disease) were compared against similar data from the USFootnote 10, there were some differences. The proportions that were late disseminated Lyme disease were similar (55% and 50% for Canada and the US respectively), but the proportion of cases reporting neurological symptoms was lower in Canada (38% versus 47% in the US) and the proportion reporting cardiac manifestations was higher in Canada (7% versus 3% in the US). Additional Canadian surveillance data is required to determine whether this is a consistent difference and if it changes over time. Tracking occurrence of Lyme carditis is also important because it has been associated with sudden deathsFootnote 19.
Neurological and cardiac manifestations were more likely to be reported for younger adults whereas there was no evidence of age-associated variations in the frequency of reporting arthritis. Neurological manifestations were less likely to be reported for males than females. The reasons for these observations are not clear and require further exploration. Reporting of neurological symptoms was more common in Ontario than the Maritimes possibly due to different methods of reporting symptoms among provinces or due to geographic variation in B. burgdorferi strainsFootnote 20.
The observations and results of this study represent a first view of Lyme disease surveillance data in Canada and it is too early to make firm conclusions regarding these preliminary trends. It is possible that data on location of acquisition and manifestation of infection in Canada is affected by issues of recall and other inaccuracies. The findings here require further study to be corroborated and to assess causality.
These data suggest that Lyme disease is emerging in Canada, with most cases occurring in seasons when and locations where Lyme disease risk in the environment is known to occur. Incidence was higher in men, in adults over 54 years old and children under 15 years old. The proportion of cases reported in early Lyme disease was lower than expected suggesting suboptimal awareness of Lyme disease during the surveillance period. Variations among provinces and age groups in the proportions of cases reporting erythema migrans and neurological and cardiac manifestations of disseminated Lyme disease were found, although are at present unexplained.
The authors thank Yann Pelcat of PHAC for preparing Figure 3.
Conflict of interest
|Data description||Data type||Provinces supplying data|
|Case classification||Confirmed/Probable||AB, SK, MB, ON, PEI, NS, NL|
|Episode date||Day, Month, Year||All|
|Type of episode dateFootnote i||Category: Onset/Sample collection/Diagnosis/Report||MB, ON, NB, NS, PEIFootnote v|
|Travel outside Canada||Yes/No||AB, SK, MB, ON, NB, PEI, NS, NL|
|Exposure to known endemic area in Canada within last 30 daysFootnote i||Yes/No||MB, ON, NB, NS|
|Name/identifier of endemic area in CanadaFootnote i||Geolocator|
|Exposure to known endemic area outside Canada within last 30 daysFootnote i||Yes/No||MB, ON, NB, NS|
|Name/identifier of endemic area outside CanadaFootnote i||Geolocator||MB, ON, NB, NS|
|Forward sortation area of residence (FSA: the first three digits off postal code)Footnote iFootnote ii||Geolocator||MB, ON, NB, NS|
|Symptoms of early Lyme disease (erythema migrans)Footnote i||Yes/No||MB, ON, NB, NS|
|Symptoms of disseminated Lyme diseaseFootnote i||Yes/No||MB, ON, NB, NS|
|Symptoms of disseminated Lyme disease: Bell's palsyFootnote i||Yes/No||ON, NB, NSFootnote i|
|Symptoms of disseminated Lyme disease: other neurological symptomsFootnote iFootnote iii||Yes/No||ON, NB, NSFootnote i|
|Symptoms of disseminated Lyme disease: cardiac symptomsFootnote iFootnote iv||Yes/No||ON, NB, NSFootnote i|
|Symptoms of late Lyme disease: Recurrent arthritis/joint swellingFootnote i||Yes/No||ON, NB, NSFootnote i|
|Method of diagnosisFootnote i||Category: Serology/PCR/Culture||MB, ON, NB, NS*|
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