Muhammad F. Mubarak
King Saud University, Saudi Arabia
Title: Proton Pump Inhibitor Use Following Esophageal Variceal Ligation and Its Impact on Clinical Outcomes: Real-World Data from the TriNetX Global Collaborative Network
Biography
Abstract
Background: Proton
pump inhibitors (PPIs) are frequently used after endoscopic variceal ligation
(EVL) to reduce post-procedural bleeding, though studies have shown mixed
results regarding their efficacy. While some suggest benefits, others report no
significant advantage and highlight potential risks, including infection,
kidney injury, and hepatic complications in cirrhotic patients. This study
utilizes the TriNetX global health research network to evaluate the outcomes of
PPI use following elective EVL for primary prophylaxis.
Methods: This retrospective cohort study was conducted using the
TriNetX database to evaluate adult patients with cirrhosis and esophageal
varices who underwent EVL for primary prophylaxis. Patients who received at
least two weeks of PPI therapy following EVL were compared to those who did not
receive PPI within one month post-procedure. Outcomes assessed included
esophageal bleeding, adverse events such as acute kidney injury (AKI),
pneumonia, spontaneous bacterial peritonitis (SBP), Clostridioides
difficile infection, hepatic encephalopathy, and all-cause mortality
at 4 weeks and 8 weeks.
Results: Of 6196 patients with cirrhosis and esophageal
varices who underwent EVL, 12% (n = 764) received adjuvant PPI
post-procedure, while 88% (n = 5432) did not receive PPI. After 1:1
propensity score matching, two well-balanced cohorts of 618 patients each were
analyzed. PPI use was not associated with a reduction in esophageal bleeding at
either 4 weeks (1.8% vs. 1.7%, p = 0.89) or 8 weeks (2.3% vs.
1.9%, p = 0.60). However, the composite adverse event
rate—including SBP, hepatic encephalopathy, pneumonia, C. difficile,
and acute kidney injury (AKI)—was significantly higher in the PPI group at both
4 weeks (7.9% vs. 3.0%, p < 0.01) and 8 weeks (13.2% vs.
3.0%, p < 0.01). Subgroup analysis showed no significant
differences in pneumonia, SBP, or C. difficile infection at
either time point. Hepatic encephalopathy was significantly more frequent in
the PPI group at 8 weeks (4.9% vs. 2.0%, p = 0.01), and AKI
occurred more often at both 4 weeks (5.7% vs. 2.0%, p <
0.01) and 8 weeks (9.6% vs. 2.1%, p < 0.01). Mortality was
similar at 4 weeks but significantly higher in the PPI group at 8 weeks (4.3%
vs. 1.7%, p < 0.01).
Conclusions: PPI
use after prophylactic EVL did not reduce bleeding risk and was linked to
higher rates of adverse events. These findings suggest routine use may not be
beneficial and should be reconsidered in cirrhotic patients who undergo EVL for
primary prophylaxis.