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. 2026 Jul 3;16:1881347. doi: 10.3389/fcimb.2026.1881347

Table 6.

Analysis of adverse effects and medication adherence.

Adverse events VBQ
(n=178)
VA
(n=176)
VD
(n=175)
P-valuea P-valueb
Adverse effects
 Overall incidence 36 (20.2%) 32 (18.2%) 16 (9.1%) 0.626 0.003
 Diarrhea 4 (2.2%) 3 (1.7%) 2 (1.1%) 0.714 0.422
 Dizziness 2 (1.1%) 3 (1.7%) 3 (1.7%) 0.643 0.639
 Acid reflux/heartburn 10 (5.6%) 8 (4.5%) 2 (1.1%) 0.646 0.020
 Nausea/vomiting 7 (3.9%) 6 (3.4%) 6 (3.4%) 0.794 0.802
 Abdominal bloating 11 (6.2%) 10 (5.7%) 3 (1.7%) 0.843 0.032
 Abdominal pain 7 (3.9%) 2 (1.1%) 1 (0.6%) 0.095 0.034
 Rash 3 (1.7%) 1 (0.6%) 0 (0.0%) 0.320 0.085
 Bad breath 2 (1.1%) 2 (1.1%) 1 (0.6%) 1.000 0.572
 Other 2 (1.1%) 4 (2.3%) 0 (0.0%) 0.402 0.160
Good medication adherence 172 (96.6%) 169 (96.0%) 171 (97.7%) 0.762 0.539
a

VA group vs. VBQ group; bVD group vs. VBQ group.

VBQ, vonoprazan-bismuth-amoxicillin-doxycycline quadruple therapy; VA, vonoprazan-amoxicillin dual therapy; VD, vonoprazan-doxycycline dual therapy.