Literature DB >> 31595875

Risk factors for developing acute gastrointestinal, skin or respiratory infections following obstacle and mud run participation, the Netherlands, 2017.

Elisabeth M den Boogert1, Danielle M Oorsprong1, Ewout B Fanoy2,3, Alexander Cap Leenders4, Alma Tostmann5, Adriana Sg van Dam1.   

Abstract

BackgroundIn the Netherlands, obstacle, mud and survival runs are increasingly popular. Although outbreaks of gastroenteritis have been reported following these events, associated health risks have not been systematically assessed.AimTo investigate the incidence of acute gastrointestinal infections (AGI), skin infections (SI) and respiratory infections (RI) among obstacle run participants, as well as risk factors.MethodsBetween April and October 2017, we conducted a retrospective cohort study among 2,900 participants of 17 obstacle runs in the Netherlands. Demographic, symptomatic and behavioural data were collected from participants via an online questionnaire 1 week after participation in an obstacle run. Stool specimens were obtained from respondents for microbiological tests. Adjusted relative risks (aRR) and 95% confidence intervals (CI) using multilevel binomial regression analysis were calculated.ResultsOf 2,646 respondents (median age: 33 years; 53% male), 76 had AGI after the obstacle run; ingesting mud was associated with AGI (aRR: 1.7; 95% CI: 1.2-4.9) and 38 respondents had AGI during or in the week before the obstacle run. Overall, 103 respondents reported SI and 163 RI. Rinsing off in a hot tub was associated with SI (aRR: 2.2; 95% CI: 1.7-2.8). Of 111 stool specimens, 13 tested positive for six different pathogens. No clusters were found.ConclusionThe reported incidence of AGI, SI and RI was low. Risk of these infections could be decreased by informing participants on preventive measures, e.g. showering vs rinsing in the hot tub, avoiding ingesting mud and not participating with symptoms of AGI.

Entities:  

Keywords:  epidemiology; gastrointestinal disease; hygiene; infection control; mass gatherings; respiratory infections

Year:  2019        PMID: 31595875      PMCID: PMC6784448          DOI: 10.2807/1560-7917.ES.2019.24.40.1900088

Source DB:  PubMed          Journal:  Euro Surveill        ISSN: 1025-496X


Introduction

In the Netherlands, obstacle, mud and survival runs (for the purposes of this paper, collectively referred to as ‘obstacle runs’) are increasingly popular. Initially, trained or professional runners were the main participants in these races, but the sport has developed into a fun activity for friends and families. There is a growing number of participants each year (13,000 in 2012 to > 250,000 in 2017 [1]). The minimum age for participation varies between obstacle runs; it is usually based on the run’s distance and can be as young as 5 years old [2]. In 2017, over 150 obstacle runs were organised in the Netherlands [3]. Obstacle runs are races in which participants encounter different manufactured obstacles while running around a predefined course [4]. A mud run is basically the same, but intentionally features more mud [4]. Survival runs are a combination of an obstacle run and an endurance event; these require more technique and training than obstacle runs and are often non-commercial compared to obstacle races and mud runs [5,6]. As participants of obstacle runs are required to run, crawl or swim through untreated water and mud, risk of injury and infectious diseases such as acute gastrointestinal infection (AGI), respiratory infection (RI) and skin infection (SI) can be more prevalent in these races compared to more conventional running races. Since 2010, there have been multiple reports of AGI outbreaks following obstacle runs, open water swimming events and mountain biking events, and the ingestion of mud or water during these races was associated with the infections [7-14]. In Belgium and the Netherlands, several cases of leptospirosis were reported in 2015 after participation in an obstacle run and in the Netherlands, one case of tularaemia was linked to an obstacle run [15-17]. However, these reports do not provide information on the infectious disease risks and potential risk factors associated with obstacle run participation in general. Although there are publications about outbreaks following obstacle runs, a more systematic approach to identify the events’ potential risk factors is lacking. Research on the potential health risks of obstacle runs is therefore warranted, and outcomes could potentially support recommendations that may help to further improve safety and preventive measures at these events. This study investigated potential risk factors for developing AGI, RI or SI—such as accidentally swallowing mud/water, time between finish and rinsing off, or type of clothes worn—following participation in obstacle runs in the Netherlands. With the results, we aim to develop evidence-based preventative recommendations for organisers and participants of obstacle runs.

Methods

Study design

A retrospective cohort study was performed in four of 12 provinces in the Netherlands (Zuid-Holland, Noord-Brabant, Limburg and Gelderland) among participants of 17 obstacle runs that took place between April and October 2017. Obstacle runs were selected based on small (n < 1,000) and large (n > 1,000) numbers of participants to include both professional and voluntary organisations.

Study population

The study population was defined as all participants that took part in at least one of the 17 selected obstacle runs. Organisers of each obstacle run were contacted before the race and given information on the study. They were asked to send a message to all participants. The message contained a link to an online questionnaire and was sent via email or posted to social media or the obstacle run’s website 7–10 days after the event. For organisers, sending the message to participants was considered consent for participation in the study; for participants, starting the questionnaire was considered giving consent.

Case definitions

Case definitions were based on guidelines from the National Coordination for Communicable Diseases Control in the Netherlands [18,19] and were defined by a medical doctor and an infectious disease epidemiologist. AGI was defined as the development of any diarrhoea and/or vomiting within 14 days after the run. SI was defined as the development of red bumps on the skin or other skin abnormalities within 14 days after the run. RI was defined as the development of a cold, sore throat or cough within 14 days after the run. Injuries were defined as muscle or joint injuries contracted during the run. Wound was defined as a wound (cut or abrasion) contracted during the run. AGI: acute gastrointestinal infection; RI: respiratory infection; SI: skin infection.

Data collection

Epidemiological

Questionnaire data were collected via Collector innovative surveys [20]. The questionnaire included questions related to: (i) demographic characteristics; (ii) run-specific information including distance, time started and duration; (iii) health complaints experienced before, during and after the obstacle run, e.g. vomiting, diarrhoea, headache, injuries and wounds; and (iv) potential risk factors for infectious diseases, e.g. swallowing water/mud, type of clothing worn, food and drinks consumed, time between completion of the obstacle run and showering, chronic diseases (e.g. hay fever or other self-defined allergies, diabetes, immune disorders) and medications taken (e.g. antacids, antibiotics). Organisers could also add their own questions to get feedback regarding the organisation of the obstacle run. Participants had ca 1 week to complete the questionnaire. Organisers of 12 of the obstacle runs also sent a reminder email 3–8 days after the first invitation or posted a reminder on social media. An example of the questionnaire can be seen in Supplement S1.

Microbiological

Respondents with known contact details who indicated that they had symptoms of AGI before, during or after the run were asked if they would be willing to collect a stool specimen and send it to Jeroen Bosch Hospital’s microbiological laboratory for analysis. If they accepted, a stool sample taking kit was sent to their home address. Where possible, 10 respondents reporting AGI symptoms per obstacle run were included for stool testing within 3 weeks after the run; if less than 10 respondents reported symptoms of AGI, respondents who did not report symptoms of AGI were invited to provide a stool sample. This decision was made on the basis that an asymptomatic individual infected with a pathogen could still be a potential risk for onward transmission. Stool specimens were tested for Salmonella species, Shigella spp., Campylobacter spp., Shigatoxin producing Escherichia coli (STEC), noro- and sapovirus, Entamoeba histolytitica, Cryptosporidium parvum/hominis and Giardia lamblia, all by reverse transcriptase-PCR (RT-PCR). Specimens were also tested for rota- and adenovirus infections with a qualitative immunochromatographic test. STEC-positive specimens were further tested by RT-PCR to determine whether the strain belonged to the subgroup of enterohaemorrhagic Escherichia coli (EHEC).

Environmental

A checklist was developed to identify potential environmental health hazards at an obstacle run. During each of the 17 obstacle runs we visually inspected the trails for animal faeces and asked the organisers whether the water had been officially approved by local authorities for swimming, according to the items provided on the checklist. We assessed the hygienic standards of facilities—e.g. toilets, showers and food trucks—in the event area and also took water samples at two or three random points along the runs. These were collected so that samples would be rapidly available for analysis in the case of an outbreak. They were not collected for comparison between obstacle runs and were stored following collection.

Outbreak definition

An outbreak was defined as multiple participants of an obstacle run reporting the same clinical symptoms following participation and/or submitting stool specimens that tested positive for the same pathogen. The definition of an outbreak also depended on the specific pathogen found or the health complaints reported; these parameters were not specified beforehand for all possible infectious diseases. In general, we defined an outbreak as a higher incidence of an infectious disease in the study cohort than the expected incidence in the general Dutch population at the same time. This was assessed by a medical doctor with experience working in the field of infectious disease control.

Data analysis

The primary outcome of this study was the association between potential risk factors during obstacle runs, demographics and the development of AGI, RI and SI. Attack rates were calculated for subgroups of exposure. To determine the association between different potential risk factors and development of infections, a univariable multilevel analysis was conducted. Multilevel analysis was performed to take into account the potential clustering of effects among the 17 runs and relative risks (RR) were calculated accordingly. Following the univariable analysis, we included factors associated with infection with a p value < 0.05 in univariable analysis in a multivariable multilevel binomial regression. We considered a p value of < 0.05 to be statistically significant. Data were analysed using SPSS statistics 21 (IBM, New York, United States (US)) and STATA 14 (StataCorp, College Station, Texas, US).

Results

In total, 17 obstacle runs carried out over 14 weekends (between April and October 2017) in the Netherlands were included in this study. Of these runs, 12 were in the provinces of Noord-Brabant, two in Zuid-Holland, two in Gelderland and one in Limburg. The runs had ca 30,000 participants in total, ranging from 230–7,600 per run.

Questionnaire response

Of the 30,000 participants, 2,900 started the questionnaire and 2,646 (91%) completed it. Distribution of the questionnaire was not consistent between the obstacle runs, as contact information (specifically email addresses) was not available for all participants, e.g. when one participant signed up on behalf of a group. Therefore, for nine obstacle runs the link to the questionnaire was posted on social media or the obstacle run’s website. Because of this, it was not possible to determine precisely how many participants were reached via email, social media or the website in order to calculate the response rate.

Characteristics of the study population

The median age was 33 years (range: 5–71 years) and 1,435 (53%) were male. Following an obstacle run, 2.7% of respondents reported AGI, 3.7% reported SI and 5.8% reported RI (Table 1). The majority of respondents reported that they had no allergies or other chronic diseases (83.1% and 84.5%, respectively). A small number of respondents (8.1%) used medication at the time of the run.
Table 1

Characteristics of respondents from 17 obstacle runs, the Netherlands, 2017 (n = 2,900)

Characteristicsn%
Sex 2,693 100
Male1,43553.3
Female1,25846.7
Missing207NA
Age (years) 2,692 100
< 1831111.6
19–2536313.5
26–3586332.1
36–4578429.1
> 4537113.8
Missing208NA
Self-reported symptoms
Acute gastrointestinal infections 2,808 100
Yes762.7
No2,73297.3
Missing92NA
Skin infections 2,790 100
Yes1033.7
No2,68796.3
Missing110NA
Respiratory infections 2,790 100
Yes1635.8
No2,62794.2
Missing110NA
Current smoker 2,691 100
Yes1856.9
No2,50693.1
Missing209NA
Use of medicationa 2,658 100
Yes2168.1
No2,44291.9
Missing242NA
Allergiesb 2,658 100
Yes44916.9
No2,20983.1
Missing242NA
Other chronic diseasesc 2,658 100
Yes41115.5
No2,24784.5
Missing242NA
Exposure to open water or obstacle run (past 3 months) 2,864 100
Yes1,08037.7
No1,78462.3
Missing36NA

NA: not applicable.

a For example, antibiotics or antacids.

b For example, hay fever or other self-defined allergies.

c Other than allergies; for example, diabetes, immune disorders or gastrointestinal diseases.

Additional information on the questions asked in the questionnaire can be found in Supplement S1.

NA: not applicable. a For example, antibiotics or antacids. b For example, hay fever or other self-defined allergies. c Other than allergies; for example, diabetes, immune disorders or gastrointestinal diseases. Additional information on the questions asked in the questionnaire can be found in Supplement S1.

Characteristics of the obstacle runs

Table 2 describes the main characteristics assessed using the environmental checklist. Of 17 obstacle runs, 10 were single-day events, 13 took place on a day with no rain, 11 had running water for handwashing (but most did not have paper towels and soap), 16 had facilities for participants to rinse off afterwards and 14 handed out free food. At one obstacle run, fruit and packaged foods (i.e. granola bars) were distributed. At another, energy bars were handed out, but not fruit. Of the 13 obstacle runs where fruit was handed out, at six runs, volunteers peeled the fruit before distributing it to participants. Environmental samples were not tested, because there was no reported outbreak nor did respondents of the same run test positive for the same pathogen.
Table 2

Characteristics of the obstacle runs, the Netherlands, 2017 (n = 17)

Characteristicsn
Number of participants
< 1,0009
≥ 1,0008
Event duration (days)
110
27
Weather conditions
Heavy rain0
Light rain4
No rain13
Temperature (°C)
< 15.00
15.1–20.07
20.1–25.06
> 25.14
Swimming water
Only official2
Only non-official12
Both official and non-officiala 3
Hygiene facilities
Running water11
Paper towels4
Soap4
Rinse facilitiesb 16
Food and water distributed during obstacle run
Food14
Fruit without peelc 6
Free drinking water17
Animal faeces present on trail7

a Official swimming water was officially approved for swimming by local authorities and non-official swimming water was not checked by local authorities.

b For example, shower, garden hose or cold water tub.

c In 13 obstacle runs.

d Depending on the obstacle run this was either bottled water or tap water.

Additional information on the questions asked in the questionnaire can be found in Supplement S1.

a Official swimming water was officially approved for swimming by local authorities and non-official swimming water was not checked by local authorities. b For example, shower, garden hose or cold water tub. c In 13 obstacle runs. d Depending on the obstacle run this was either bottled water or tap water. Additional information on the questions asked in the questionnaire can be found in Supplement S1.

Epidemiological determinants

Reported health complaints

In total, 641 of 2,813 (22.8%) respondents reported health complaints (e.g. headache, stomach ache and vomiting) following participation in an obstacle run. Of those, five discovered a tick during or after the run, 156 (5.6%) reported receiving a wound, 131 (4.7%) reported an injury (mostly concerning the knee (n = 45) and ankle (n = 25)), two respondents broke a bone and six tore a muscle. In all three main health complaints reported, (AGI, RI and SI) females were more likely to report infections than males; AGI: 47 (68%) vs 22 (32%); SI: 68 (69%) vs 31 (31%); RI: 103 (69%) vs 47 (31%).

Determinants associated with acute gastrointestinal infections

Of 2,831 respondents, 38 had AGI during or in the week before the obstacle run. The multilevel univariable analysis showed that 10 determinants were associated with the development of AGI following an obstacle run. In the multivariable model, five remained statistically significant, including swallowing mud (RR: 2.4; 95% CI: 1.2–4.9), having allergies (RR: 1.7; 95% CI: 1.2–2.5) and being female (RR: 1.9; 95% CI: 1.2–2.8). Drinking alcohol on the day of an obstacle run and having chronic diseases other than allergies decreased the risk for AGI following an obstacle run (RR: 0.34; 95% CI: 0.16–0.71 and RR: 0.51; 95% CI: 0.33–0.79, respectively) (Table 3).
Table 3

Determinants for developing acute gastrointestinal infections in obstacle run participants, the Netherlands, 2017 (n = 2,808)

VariablesTotalna Cases of AGIb Attack rate (%)Univariable analysisMultivariable analysis
RR(95% CI)p valueRR(95% CI)c p value
Respondent characteristics
Age (years)
0–1831161.90.69 (0.22–2.2)0.5300.63 (0.21–1.9)0.412
19–25363154.11.5 (0.71–3.1)0.2931.2 (0.55–2.6)0.661
26–35863242.8Ref Ref
36–45784222.81.01 (0.64–1.6)0.9691.01 (0.59–1.7)0.964
> 4537120.540.19 (0.04–0.87) 0.032 0.23 (0.05–1.1)0.067
Sex
Male1,435221.5Ref Ref
Female1,258473.72.4 (1.8–3.3) 0.000 1.9 (1.2–2.8) 0.003
Current smoker
No2,506652.6Ref NA
Yes18542.20.8 (0.35–2.0)0.681NA
Exposure to open water or obstacle run (past 3 months)
No1,746563.2Ref Ref
Yes1,062201.90.59 (0.40–0.86) 0.006 0.71 (0.47–1.1)0.118
Use of medication (incl. antacids)d
No2,442622.5Ref NA
Yes21662.81.09 (0.45–2.7)0.843NA
Use of antacids
No2,637672.5Ref NA
Yes2114.81.9 (0.37–9.4)0.444NA
Allergiese
No2,209492.2Ref Ref
Yes449194.21.9 (1.3–2.8) 0.001 1.7 (1.2–2.5) 0.004
Chronic diseases other than allergiesf
No2,247612.7Ref Ref
Yes41171.70.63 (0.43–0.91) 0.014 0.51 (0.33–0.79) 0.003
Run characteristics
Distance (km)
0–4.919031.60.54 (0.11–2.6)0.446NA
5–7.91,093322.9Ref NA
8–10469122.60.87 (0.38–2.0)0.750NA
10.1–15786212.70.91 (0.44–1.9)0.808NA
> 15.127083.01.01 (0.48–2.2)0.975NA
Outside temperature (°C)
≤ 15.000NANANA
15.1–20.01,149403.5Ref NA
20.1–25.0802172.10.61 (0.26–1.4)0.255NA
≥ 25.1 °C857192.20.64 (0.30–1.4)0.245NA
Official swimming waterg
Non-official1,945502.6Ref NA
Official411112.71.04 (0.49–2.2)0.918NA
Both452153.31.3 (0.70–2.4)0.419NA
Number of event days
11,201221.8Ref NA
21,607543.41.8 (0.97–3.5)0.064NA
Animal faeces present on trail
No1,856583.1Ref NA
Yes952181.90.61 (0.32–1.1)0.122NA
Specific exposure
Type of shower water used
Tap water2,364592.5Ref NA
Open water23673.01.2 (0.65–2.2)0.573NA
Hot tub8022.51.002 (0.43–2.4)0.997NA
Other3512.91.1 (0.37–3.5)0.813NA
Shower time (hours after run)
< 11,840522.8RefNA
1–3706152.10.75 (0.43–1.3)0.313NA
> 317421.20.41 (0.17–0.95) 0.037 NA
Toilet used
No862182.1RefNA
Yes1,856512.81.3 (0.80–2.2)0.276NA
Water in mouth
No1,092161.5RefRef
Yes, not swallowed1,200352.92.0 (1.1–3.8) 0.036 2.0 (0.94–4.1)0.071
Yes, swallowed440194.32.9 (1.4–6.2) 0.004 2.2 (0.97–5.2)0.061
Mud in mouth
No1,762392.2RefRef
Yes, not swallowed882242.71.2 (0.8–1.9)0.3501.02 (0.61–1.7)0.946
Yes, swallowed8578.23.7 (1.8–7.7) 0.000 2.4 (1.2–4.9) 0.015
Consumed beverages
Drinking water from organisation
No45971.5 RefNA
Yes2,229622.81.8 (0.79–4.2)0.162NA
Soda
No2,130602.8 RefNA
Yes55891.60.57 (0.29–1.1)0.105NA
Energy drink
No2,165532.5 RefNA
Yes523163.11.2 (0.73–2.1)0.419NA
Alcoholic beverage
No2,031623.1 RefRef
Yes65771.10.35 (0.18–0.67) 0.002 0.34 (0.16–0.71) 0.004
Coffee/tea
No2,196552.5RefNA
Yes492142.91.1 (0.62–2.1)0.682NA
Juice
No1,791392.2 RefNA
Yes5823.51.6 (0.27–9.4)0.613NA

AGI: acute gastrointestinal infections; CI: confidence interval; incl.: including; NA: not applicable; Ref: reference; RR: relative risk.

a Number of respondents who were exposed to the exposure variable.

b Number of respondents with gastrointestinal infections in the week after the event and exposure to the exposure variable.

c Adjusted for any exposure with p value < 0.05 in the univariable analysis.

d For example, antibiotics or antacids.

e For example, hay fever or other self-defined allergies.

f Other than allergies; for example, diabetes, immune disorders and gastrointestinal diseases.

g Official swimming water was officially approved for swimming by local authorities and non-official swimming water was not checked by local authorities.

Additional information on the questions asked in the questionnaire can be found in Supplement S1.

The questions on diarrhoea and vomiting were asked later on in the questionnaire and some respondents stopped before answering these questions. Only responses from those who answered these questions were included.

AGI: acute gastrointestinal infections; CI: confidence interval; incl.: including; NA: not applicable; Ref: reference; RR: relative risk. a Number of respondents who were exposed to the exposure variable. b Number of respondents with gastrointestinal infections in the week after the event and exposure to the exposure variable. c Adjusted for any exposure with p value < 0.05 in the univariable analysis. d For example, antibiotics or antacids. e For example, hay fever or other self-defined allergies. f Other than allergies; for example, diabetes, immune disorders and gastrointestinal diseases. g Official swimming water was officially approved for swimming by local authorities and non-official swimming water was not checked by local authorities. Additional information on the questions asked in the questionnaire can be found in Supplement S1. The questions on diarrhoea and vomiting were asked later on in the questionnaire and some respondents stopped before answering these questions. Only responses from those who answered these questions were included.

Determinants associated with skin infections

Five determinants were associated with the development of SI following an obstacle run in the univariable analysis and three remained statistically significant in the multivariable model. These included rinsing off after the run in a hot tub compared to running tap water and being female (RR: 2.2; 95% CI: 1.7–2.8 and RR: 2.3; 95% CI: 1.3–3.9, respectively). An outside temperature of > 25 °C decreased the risk for SI (RR: 0.53; 95% CI: 0.31–0.91) (Table 4).
Table 4

Determinants for developing skin infections in obstacle run participants, the Netherlands, 2017 (n = 2,790)

VariablesTotalna Cases of SIb Attack rate(%)UnivariableMultivariable
RR(95% CI)p valueRR(95% CI)c p value
Respondent characteristics
Age (years)
0–18311113.50.92 (0.48–1.8)0.8191.2 (0.58–2.5)0.607
19–25363215.81.5 (0.94–2.4)0.0891.4 (0.84–2.3)0.202
26–35863333.8RefRef
36–45784253.20.83 (0.46–1.5)0.5550.92 (0.50–1.7)0.797
> 4537192.40.63 (0.38–1.1)0.0810.76 (0.42–1.4)0.360
Sex
Male1,435312.2RefRef
Female1,258685.42.5 (1.4–4.6) 0.003 2.3 (1.3–3.9) 0.004
Exposure to open water or obstacle run (past 3 months)
No1,733734.2RefNA
Yes1,057302.80.67 (0.39–1.2)0.166NA
Allergiesd
No2,209763.4RefNA
Yes449224.91.4 (0.95–2.1)0.087NA
Chronic diseases other than allergiese
No2,247743.3RefRef
Yes411245.81.8 (1.03–3.1) 0.040 1.7 (0.97–2.8)0.065
Run characteristics
Outside temperature (°C)
≤ 15.000NANANA
15.1–20.01,137625.5RefRef
20.1–25.080202.50.46 (0.23–0.89) 0.022 0.56 (0.31–1.005)0.052
≥ 25.1 °C853212.50.45 (0.23–0.90) 0.023 0.53 (0.31–0.91) 0.022
Number of event days
11,193544.5RefNA
21,597493.10.68 (0.30–1.5)0.341NA
Animal faeces present on trail
No1,841613.3RefNA
Yes949424.41.3 (0.64–2.8)0.436NA
Specific exposures
Type of shower water used
Tap water2,364763.2RefRef
Open water236166.82.1 (0.80–5.6)0.1331.5 (0.67–3.4)0.319
Hot tub8067.52.3 (1.6–3.4) 0.000 2.2 (1.7–2.8) 0.000
Other3512.90.89 (0.10–8.1)0.9160.66 (0.08–5.4)0.696
Shower time (hours after run)
< 11,840613.3RefNA
1–3706324.51.4 (0.96–2.0)0.086NA
> 317463.51.04 (0.50–2.1)0.915NA
Clothes worn
Long pants, long sleeves333144.2RefNA
Long pants, short sleeves/short pants, long sleeves combined1,420523.70.87 (0.49–1.6)0.642NA
Short pants, short sleeves889303.40.80 (0.35–1.8)0.603NA
Other7833.90.91 (0.29–2.9)0.880NA

CI: confidence interval; NA: not applicable; Ref: reference; RR: relative risk; SI: skin infections.

a Number of respondents who were exposed to the exposure variable.

b Number of respondents with skin infections in the week after the event and exposure to the exposure variable.

c Adjusted for any exposure with p value < 0.05 in the univariable analysis.

d For example, hay fever or other self-defined allergies.

e Other than allergies; for example, diabetes, immune disorders and gastrointestinal diseases.

Additional information on the questions asked in the questionnaire can be found in Supplement S1.

The question on skin infections was asked later on in the questionnaire and some respondents stopped before answering this question. Only responses from those who answered this question were included.

CI: confidence interval; NA: not applicable; Ref: reference; RR: relative risk; SI: skin infections. a Number of respondents who were exposed to the exposure variable. b Number of respondents with skin infections in the week after the event and exposure to the exposure variable. c Adjusted for any exposure with p value < 0.05 in the univariable analysis. d For example, hay fever or other self-defined allergies. e Other than allergies; for example, diabetes, immune disorders and gastrointestinal diseases. Additional information on the questions asked in the questionnaire can be found in Supplement S1. The question on skin infections was asked later on in the questionnaire and some respondents stopped before answering this question. Only responses from those who answered this question were included.

Determinants associated with respiratory infections

Five determinants were associated with the development of RI following an obstacle run in the univariable analysis and three remained statistically significant in the multivariable model. These included being aged 19–25 years (compared to 26–35 years) and being female (RR: 1.8; 95% CI: 1.2–2.9 and RR: 2.1; 95% CI: 1.6–3.0, respectively). Being aged ≥ 45 years (compared to 26–35 years) decreased the risk for developing RI (RR: 0.31; 95% CI: 0.16–0.60) (Table 5).
Table 5

Determinants for developing respiratory infections in obstacle run participants, the Netherlands, 2017 (n = 2,790)

VariablesTotalna Cases of RIb Attack rate(%)UnivariableMultivariable
RR(95% CI)p valueRR(95% CI)c p value
Respondent characteristics
Age (years)
0–18311206.41.2 (0.88–1.7)0.2451.4 (0.98–2.0)0.061
19–2536338102.0 (1.2–3.1) 0.003 1.8 (1.2–2.9) 0.011
26–35863465.3RefRef
36–45784415.20.98 (0.59–1.6)0.9411.1 (0.64–1.7)0.842
> 4537151.40.25 (0.13–0.48) 0.000 0.31 (0.16–0.60) 0.000
Sex
Male1,435473.3RefRef
Female1,2581038.22.5 (1.9–3.4) 0.000 2.1 (1.6–3.0) 0.000
Current smoker
No2,5061355.4RefNA
Yes185158.11.5 (0.92–2.5)0.107NA
Exposure to open water or obstacle run (past 3 months)
No17331096.3RefNA
Yes1057545.10.81 (0.56–1.2)0.268NA
Use of medication (incl. antacids)d
No2,4421375.6RefNA
Yes216115.10.91 (0.52–1.6)0.733NA
Use of medication for allergies
No2,6041425.5RefNA
Yes546112.0 (0.90–4.6)0.087NA
Use of medication for respiratory diseases
No2,6111455.6RefNA
Yes4736.41.1 (0.42–3.1)0.784NA
Allergiese
No2,2091094.9RefRef
Yes449398.71.8 (1.1–2.8) 0.014 1.6 (0.99–2.6)0.054
Chronic diseases other than allergiesf
No2,2471165.2RefNA
Yes411327.81.5 (0.99–2.3)0.054NA
Run characteristics
Outside temperature (°C)
≤ 15.000NANANA
15.1–20.01,137786.9RefNA
20.1–25.0800506.30.91 (0.60–1.4)0.667NA
≥ 25.1853354.10.60 (0.26–1.4)0.235NA
Rain on event day
Heavy rain00NANANA
Light rain663416.2Ref NA
No rain2,1271225.70.93 (0.58–1.5)0.750NA
Number of event days
11,193776.5RefNA
21,597865.40.83 (0.51–1.4)0.462NA
Specific exposures
Type of shower water used
Tap water2,3641295.5RefRef
Open water236187.61.4 (1.1–1.8) 0.016 1.3 (0.84–2.0)0.246
Hot tub8045.00.92 (0.54–1.6)0.7491.2 (0.64–2.1)0.626
Other3512.90.52 (0.05–5.2)0.5790.51 (0.06–4.3)0.536
Water in mouth
No1,092534.9RefNA
Yes, not swallowed1,200756.31.3 (0.84–2.0)0.240NA
Yes, swallowed440255.71.2 (0.78–1.8)0.451NA
Mud in mouth
No1,762965.5RefNA
Yes, not swallowed882525.91.1 (0.74–1.6)0.683NA
Yes, swallowed8555.91.1 (0.45–2.6)0.863NA

CI: confidence interval; incl.: including; NA: not applicable; Ref: reference; RI: respiratory infections; RR: relative risk.

a Number of respondents who were exposed to the exposure variable.

b Number of respondents with respiratory infections in the week after the event and exposure to the exposure variable.

c Adjusted for any exposure with p value < 0.05 in the univariable analysis.

d For example, antibiotics or antacids.

e For example, hay fever or other self-defined allergies.

f Other than allergies; for example, diabetes, immune disorders or gastrointestinal diseases.

Additional information on the questions asked in the questionnaire can be found in Supplement S1.

The question on respiratory infections was asked later on in the questionnaire and some respondents stopped before answering this question. Only responses from those who answered this question were included.

CI: confidence interval; incl.: including; NA: not applicable; Ref: reference; RI: respiratory infections; RR: relative risk. a Number of respondents who were exposed to the exposure variable. b Number of respondents with respiratory infections in the week after the event and exposure to the exposure variable. c Adjusted for any exposure with p value < 0.05 in the univariable analysis. d For example, antibiotics or antacids. e For example, hay fever or other self-defined allergies. f Other than allergies; for example, diabetes, immune disorders or gastrointestinal diseases. Additional information on the questions asked in the questionnaire can be found in Supplement S1. The question on respiratory infections was asked later on in the questionnaire and some respondents stopped before answering this question. Only responses from those who answered this question were included.

Clinical microbiological results

The laboratory received stool specimens from 111 respondents from 17 obstacle runs, of which 13 tested positive for six different pathogens (no participant tested positive for the same pathogen as another participant in the same run). These pathogens were sapovirus (n = 5), norovirus (n = 4), Shigella spp. (n = 1), enterohaemorrhagic Escherichia coli (EHEC) (n = 1), Campylobacter jejuni (n = 1) and Giardia lamblia (n = 2). Four of these pathogens (norovirus, sapovirus, G. lamblia and C. jejuni) explained the acute gastrointestinal complaints of seven respondents, with two reporting gastrointestinal symptoms before the obstacle run and five after. The EHEC-positive respondent reported headache and red bumps on the skin. The other six positive respondents (G. lamblia, norovirus, sapovirus, Shigella spp.) did not report any health complaints.

Discussion

To our knowledge, this is the first study investigating the incidence of AGI, SI and RI following participation in an obstacle run, as well as risk factors. Not many infectious diseases were reported by respondents in the questionnaire of this study (in 2.7%–5.8% of respondents), which suggests a low risk for infection after participation in an obstacle run. The primary care continuous morbidity surveillance system estimated that from April to October 2017, 2% of the Dutch adult population had consulted a general practitioner (GP) for an AGI and 4% for an RI [21]; no primary care data was available for SI. Although the incidences of AGI and RI from our study are seemingly comparable to those obtained from primary care in the Netherlands, the latter only reflects diseases in people who attended a GP and, therefore, may not be generalisable to the general population. In this study, the ingestion of mud was associated with AGI, supporting current advice offered to participants, i.e. to avoid ingesting water/mud by trying to keep their mouths closed during obstacle runs. This advice arose due to similar findings regarding the risk for infectious diseases observed in other (outbreak) investigations related to events that include water or mud, e.g. mountain bike events and city swims [7-14]. We acknowledge this is not always feasible due to the high oxygen demand during intense activity. Previous studies have also found a protective effect of alcohol on the risk of developing AGI [22-25]. This effect could be attributed to the ethanol and antioxidants or other substances in the alcoholic beverages [25]. However, as we did not collect information on the number of alcoholic beverages consumed by participants, nor when they consumed it (i.e. before, during or after the obstacle run), the protective association we found should be interpreted with caution. We found that respondents with allergies were more at risk for AGI in multivariable analysis and those with a chronic disease other than allergies were more at risk for SI and RI in univariable analysis. We also found that having one or more chronic diseases had a protective effect on AGI. This could partially be explained by the non-specific definition of chronic diseases in our study. Several chronic diseases (e.g. eczema and diabetes) were grouped together since the number of each reported disease was too low to analyse separately. Proper handwashing is a very effective measure for the prevention of infectious disease [26]. In our study, we found that 13 obstacle runs did not have adequate handwashing facilities, e.g. with running water, soap and paper towels. Food was distributed at 14 obstacle runs and, as it is not practical for participants to wash their hands during an obstacle run (and they are likely covered in mud when the food is distributed), unpeeled fruits and packaged foods may be better options.

Strengths and limitations

Due to the large study population and inclusion of several different obstacle runs, we believe the results could be relevant to other events with similar environmental conditions. Further, as several obstacle runs were investigated, the identified risk factors may be more generalisable. There are several limitations with this study. First, it is likely that there was self-selection bias, wherein participants who developed symptoms after an obstacle run were more likely to take part in the study than those who remained healthy. This may have resulted in an overestimation of the attack rate for AGI, SI and RI. Second, recall bias may have occurred, as participants received the questionnaire 1 week after participating in the run and exposure to potential risk factors may have been recalled better by respondents who developed symptoms. Although this bias is expected to be minimal, the RR and risk factors identified may have been overestimated. Third, it is known that women tend to report poorer health than men on self-reported health indicators [27], which may explain the high incidence on AGI, SI and RI reported among women. Fourth, the incidence of infectious diseases reported in this study may have been overestimated, as not all symptoms reported are exclusive to AGI, RI and SI. For example, respiratory disease can occur due to allergies. It was not possible, however, to differentiate between the underlying causes of certain symptoms, which could have resulted in an overestimation of the incidence of AGI, RI and SI in this study. Further, respondents were asked about infectious disease symptoms that occurred following the obstacle run, so the symptoms reported may not have been caused by the event. Fifth, due to the design of the study, the results of the microbiological analysis were not compared with a control group. In future studies, however, stool sample testing should be done directly after onset of symptoms and a control group should be included so the results can be compared and used as part of an outbreak investigation, should the need arise. Finally, we investigated frequencies of disease in this study, but diseases such as tularaemia and leptospirosis—which have longer incubation periods than the time given to complete the questionnaire—might have been missed. However, as these are rare diseases in the Netherlands and the symptoms are not widely recognised, it is unlikely that these diseases would have been identified even with a longer time period allocated to the questionnaire.

Conclusion

Our study suggests that the risk of contracting AGI, SI or RI following participation in an obstacle run is low. However, the potential for disease outbreaks related to such events can be high, as seen in previous studies [7-14]. To limit the occurrence of outbreaks and sporadic infections, we recommend that organisers of obstacle runs inform participants of infectious disease risks and potential preventive measures they could take, e.g. practicing good hand hygiene, not participating if they are ill, not swallowing mud and showering directly after the run. In addition, we recommend that organisers adequately facilitate these preventive measures, e.g. by installing proper handwashing and shower facilities and only distributing foods that are unpeeled/packaged during the obstacle run. Based on visual inspections, we also recommend that organisers fulfil the national hygiene guidelines regarding the toilets and showers around the obstacle run course.
  13 in total

1.  Using the internet for rapid investigation of an outbreak of diarrhoeal illness in mountain bikers.

Authors:  S L Griffiths; R L Salmon; B W Mason; C Elliott; D Rh Thomas; C Davies
Journal:  Epidemiol Infect       Date:  2010-06-29       Impact factor: 2.451

2.  Campylobacteriosis outbreak associated with ingestion of mud during a mountain bike race.

Authors:  T L Stuart; J Sandhu; R Stirling; J Corder; A Ellis; P Misa; S Goh; B Wong; P Martiquet; L Hoang; E Galanis
Journal:  Epidemiol Infect       Date:  2010-03-25       Impact factor: 2.451

Review 3.  Moderate alcohol consumption and the immune system: a review.

Authors:  Javier Romeo; Julia Wärnberg; Esther Nova; Ligia E Díaz; Sonia Gómez-Martinez; Ascensión Marcos
Journal:  Br J Nutr       Date:  2007-10       Impact factor: 3.718

4.  The protective effect of alcoholic beverages on the occurrence of a Salmonella food-borne outbreak.

Authors:  Juan B Bellido-Blasco; Alberto Arnedo-Pena; Enrique Cordero-Cutillas; Manuel Canós-Cabedo; Concha Herrero-Carot; Lourdes Safont-Adsuara
Journal:  Epidemiology       Date:  2002-03       Impact factor: 4.822

5.  The protective effect of alcohol on the occurrence of epidemic oyster-borne hepatitis A.

Authors:  J A Desenclos; K C Klontz; M H Wilder; R A Gunn
Journal:  Epidemiology       Date:  1992-07       Impact factor: 4.822

6.  [Tularaemia in a boy following participation in a mud race].

Authors:  M Zijlstra; C C C Hulsker; E B Fanoy; R Pijnacker; A Kraaijeveld; M G J Koene; T F W Wolfs
Journal:  Ned Tijdschr Geneeskd       Date:  2017

7.  A large outbreak of gastrointestinal illness at an open-water swimming event in the River Thames, London.

Authors:  V Hall; A Taye; B Walsh; H Maguire; J Dave; A Wright; C Anderson; P Crook
Journal:  Epidemiol Infect       Date:  2017-02-06       Impact factor: 4.434

8.  Gastrointestinal disease outbreaks in cycling events: are preventive measures effective?

Authors:  R Mexia; L Vold; B T Heier; K Nygård
Journal:  Epidemiol Infect       Date:  2012-05-16       Impact factor: 4.434

9.  Outbreak of campylobacteriosis associated with a long-distance obstacle adventure race--Nevada, October 2012.

Authors:  Mariah Zeigler; Chad Claar; Daviesha Rice; Jack Davis; Tammy Frazier; Alex Turner; Corinna Kelley; Jonathan Capps; Andrea Kent; Valerie Hubbard; Christiana Ritenour; Cristina Tuscano; Zuwen Qiu-Shultz; Collette Fitzgerald Leaumont
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2014-05-02       Impact factor: 17.586

10.  Risk factors for gastroenteritis associated with canal swimming in two cities in the Netherlands during the summer of 2015: A prospective study.

Authors:  Rosa Joosten; Gerard Sonder; Saara Parkkali; Diederik Brandwagt; Ewout Fanoy; Lapo Mughini-Gras; Willemijn Lodder; Erik Ruland; Evelien Siedenburg; Suzanne Kliffen; Wilfrid van Pelt
Journal:  PLoS One       Date:  2017-04-03       Impact factor: 3.240

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