If 1 is not included in the 95% confidence interval of a ratio, the ratio was considered statistically significant. When the incidence of a symptom in a group was zero, the approach as described in Firth was used,18 by means of the brglm package in R.19,20 During the study period, 99 ISA and 114 IBD, planning to travel with a non-immunocompromised travel companion, were eligible PLX3397 for inclusion. Of the ISA pairs, 16 (16%) did not want to participate and 8 (8%) were lost to follow-up after inclusion. Of the IBD pairs, 31 (27%) did not want to participate and 12 (11%) were lost to follow-up. The remaining participants all provided

a completed diary. The study sample comprised 75 ISA and their 75 controls, and 71 IBD and their 71 controls. Of these

146 pairs, 124 (85%) were included at the Public Health Service Amsterdam and 22 (15%) at the University Medical Centre Leiden. Table 1 shows their characteristics. Sixty-five ISA (86%) and 58 IBD pairs (82%) matched for country of birth. Only 10 ISA (13%) and 18 IBD pairs (25%) matched for gender. The median travel duration was 16 days in both groups. Of the ISA, 68% had a rheumatic disease. Of IBD, 52% had Crohn’s disease and 48% had ulcerative colitis. CX-4945 chemical structure Of the ISA, 40 (53%) used one immunosuppressive agent, 24 (32%) two immunosuppressive agents, and 11 (15%) three immunosuppressive agents. Of IBD, 22 (31%) had not used any immunosuppressive agent, 30 (42%) used one immunosuppressive agent, 16 (23%) two immunosuppressive agents, and 3 (4%) three immunosuppressive agents. Table 2 shows ID-8 the travel-related symptoms by prevalence, IR, mean duration among symptomatics, and the number of symptomatic days per symptom for ISA and their travel companions. The figure in Table 2 shows the accompanying IRR and OR on a logarithmic scale. Likewise, Table 3 shows the results for IBD and their controls. Data concerning the occurrence of pre-travel-related symptoms are described in the text whenever relevant, and are not presented in the tables. The prevalence of travel-related diarrhea was 47% among ISA and 40% among controls. The IR of travel-related diarrhea was 0.76 versus 0.66 per person-month; the IRR showed no significant

difference. The number of days with diarrhea was 1.32 per month among ISA, comparable to controls. Also before travel, diarrhea outcome measures showed no significant differences between ISA and controls. For both ISA and controls, diarrhea outcome measures were significantly higher during travel than before travel. The IR and the number of days for signs of skin infection were significantly higher among ISA than among controls, both before and during travel. Only among ISA, the outcome measures for signs of skin infection increased after departure. The travel-related IR and number of days for fatigue and arthralgia were higher among ISA than among controls. However, these measures also differed before travel and showed no significant increase after departure.