Retrospective Cohort Study
Copyright ©The Author(s) 2019.
World J Gastroenterol. Dec 14, 2019; 25(46): 6743-6751
Published online Dec 14, 2019. doi: 10.3748/wjg.v25.i46.6743
Table 1 Baseline characteristics of the study population
Tailored therapy using DPO-PCR (n = 50)Empirical bismuth-based quadruple therapy (n = 104)P value
Age, mean ± SD (yr)58.3 ± 13.957.4 ± 11.60.3
Men, n (%)30 (60.0)56 (53.8)0.5
Smoking, n (%)13 (26.0)17 (16.3)0.2
Drinking, n (%)16 (32.0)34 (32.7)0.8
Comorbidity
Hypertension, n (%)11 (22.0)31 (29.8)0.4
Diabetes mellitus, n (%)11 (22.0)17 (16.3)0.5
Cardiovascular disease, n (%)2 (4.0)6 (5.8)0.6
Reasons for eradication, n (%)
Peptic ulcer disease37 (64.0)28 (26.9)0.002
Post ESD due to EGC8 (16.0)3 (2.9)0.003
Post ESD due to adenoma5 (10.0)2 (1.9)0.024
MALToma2 (4.0)0 (0.0)0.04
Chronic atrophic gastritis with intestinal metaplasia2 (4.0)71 (68.3)< 0.001
Nodular gastritis3 (6.0)0 (0.0)
Clarithromycin resistance diagnosed by DPO-PCR, n (%)Non available
No37 (74.0)
A2142G positive1 (2.0)
A2143G positive12 (24.0)
Table 2  Helicobacter pylori eradication success rates and complication rates, n (%)
Eradication rateTailored therapy using DPO-PCR (n = 50)Empirical bismuth-based quadruple therapy (n = 104)P value
Intention-to-treat analysis48 (96.0)98 (94.2)0.6
Per-protocol analysis48/50 (96.0)95/100 (95.0)0.8
Table 3 Eradication-related adverse events, n (%)
Tailored therapy using DPO-PCR (n = 50)Empirical bismuth-based quadruple therapy (n = 104)P value
Eradication-related side effects< 0.001
No44 (88.0)59 (56.7)
Yes6 (12.0)45 (43.7)
Abdominal discomfort0 (0.0)1 (1.0)
Nausea/vomiting3 (6.0)12 (11.5)
Diarrhea/loose stool0 (0.0)12 (11.5)
Dyspepsia2 (4.0)10 (9.6)
General weakness1 (2.0)6 (5.8)
Taste disturbance0 (0.0)4 (3.8)
Treatment compliances
50 (100.0)100 (96.2)0.2