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Randomized Controlled Trial
Copyright: ©Author(s) 2026.
World J Hepatol. Apr 27, 2026; 18(4): 116153
Published online Apr 27, 2026. doi: 10.4254/wjh.v18.i4.116153
Table 3 Adverse events over 3 months follow-up, n (%)

Overall (n = 122)
FMT (n = 60)
Lactulose (n = 62)
P value
Any adverse events158 (47.5)32 (53.3)26 (41.9)0.21
Bloating18 (14.8)3 (5.0)15 (24.2)< 0.01
Abdominal pain16 (13.1)7 (11.7)9 (14.5)0.64
Diarrhoea11 (9.0)6 (10.0)5 (8.1)0.71
Vomiting4 (3.3)3 (5.0)1 (1.6)0.36
Malaise9 (7.4)7 (11.7)2 (3.2)0.09
Fever17 (13.9)12 (20.0)5 (8.1)0.06
Cough3 (2.5)3 (5.0)00.12
Constipation7 (5.7)7 (11.7)0< 0.01
Altered taste1 (0.8)1 (1.7)00.49
Death3 (2.5)2 (3.3)1 (1.6)0.62
Overt HE3 (2.5)2 (3.3)1 (1.6)1.00
Sepsis7 (5.7)5 (8.3)2 (3.2)0.13
Pneumonia2 (1.6)2 (3.3)0
Urosepsis2 (1.6)1 (1.7)1 (1.6)
Cellulitis1 (0.8)01 (1.6)
Gastrointestinal2 (1.6)2 (3.3)0


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