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. 2014 Apr;20(4):649–657. doi: 10.3201/eid2004.131718

Table 3. Associations between travel-associated risk factors and rates of blaCTX-M, qnrB, and qnrS acquisition among 122 healthy travelers from the Netherlands, 2010–2012*.

Traveler characteristic
No. travelers
Antimicrobial drug resistance genes acquired by travelers
bla CTX-M
qnrB
qnrS
No. (%)
OR (95% CI)‡

No. (%)
OR (95% CI)‡

No. (%)
OR (95% CI)‡
Region visited
Europe and America§¶ 16† 1 (6.3) 1.00 6 (37.5) 1.00 3 (18.8) 1.00
Southeast Asia 28† 5 (17.9) 3.34 
(0.34–33.14) 7 (25.0) 0.47 (0.12–1.90) 21 (75.0) 15.74 
(3.13–79.24)
Indian subcontinent 31† 18 (58.1) 26.22 
(2.86–240.18) 10 (32.3) 0.71 (0.18–2.71) 19 (61.3) 9.23 
(1.94–43.87)
Northern Africa 16† 5 (31.3) 7.28 
(0.70–75.92) 5 (31.3) 0.64 (0.14–2.98) 7 (43.8) 2.90 (0.54–15.57)
Southern Africa
17†
5 (29.4)
5.57 
(0.56–55.77)

5 (29.4)
0.65 (0.15–2.84)

6 (35.3)
2.41 (0.46–12.66)
Sex
71 25 (35.2) 1.00 25 (35.2) 1.00 41 (57.7) 1.00
M
51
13 (25.5)
0.62 (0.23–1.67)

15 (29.4)
1.06 (0.44–2.57)

21 (41.2)
0.39 (0.15–1.00)
Antimicrobial drug use
No§ 107 32 (29.9) 1.00 35 (32.7) 1.00 52 (48.6) 1.00
Yes
15
6 (40.0)
1.44 (0.40–5.25)

5 (33.3)
1.28 (0.36–4.51)

10 (66.7)
1.64 (0.43–6.22)
Traveler’s diarrhea
No§ 77 20 (26.0) 1.00 25 (32.5) 1.00 40 (51.9) 1.00
Yes
45
18 (40.0)
1.84 (0.70–4.82)

15 (33.3)
0.97 (0.40–2.37)

22 (48.9)
0.65 (0.26–1.63)
*OR, odds ratio. Boldface indicates statistical significance (p<0.05).
†Numbers do not total 122 because the 14 travelers who visited multiple or unknown regions were added to a remainder category not included in this table.
‡ORs and 95% CIs of the associations between risk factor and acquisition of resistance gene (negative before travel and positive after travel) by multivariable logistic regression analysis. Models included the following variables: travel destination, age, travel duration, sex, and antimicrobial drug use within 3 mo. preceding the travel, and traveler’s diarrhea.
§Reference category.
¶Southern Europe, Central and South America, previously reported non–high-risk regions, were pooled to establish an adequately sized reference category.