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Clinical Outcomes After Failed Endoscopic Detorsion for Sigmoid Volvulus: A Single-Center Retrospective Cohort Study
Hidehiro Kamezaki1,2, Arisa Kato1, Nana Yamada1,2
1Department of Gastroenterology Eastern Chiba Medical Center Chiba Japan.
Objectives:
Endoscopic detorsion is the first-line treatment for sigmoid volvulus (SV); however, detorsion is not always successful. We evaluated clinical outcomes after failed endoscopic detorsion and assessed recurrence in patients who achieved clinical success after decompression.
Methods:
This single-center retrospective cohort study included 47 patients with first-episode SV, of whom 43 underwent endoscopic management. Baseline characteristics and short-term outcomes were compared between successful and failed detorsion groups. Among patients with clinical success, the in-hospital course and 1-year cumulative recurrence were compared between the successful detorsion and successful decompression groups. Cumulative recurrence was evaluated using the Kaplan-Meier method.
Results:
Successful detorsion was achieved in 21 of 43 patients (48.8%). Among 22 patients with failed detorsion, 17 achieved clinical success after decompression, whereas five had clinical failure, including four who underwent emergency surgery and one who died the following day. The overall clinical success rate was 88.4% (38/43). Failed detorsion was associated with lower room-air oxygen saturation and higher lactate levels. Clinical success was less frequent in the failed detorsion group (77.3% vs. 100%, p = 0.065), and hospital stay was longer (median 13 vs. 7 days, p = 0.071). Among patients with clinical success, time to resumption of oral intake was shorter in the successful detorsion group (median 1.5 vs. 3 days, p = 0.004), whereas the 1-year cumulative recurrence rate was numerically higher but not statistically significant (79.6 vs. 51.3%, log-rank p = 0.087).
Conclusions:
After assessing the need for emergency surgery, decompression alone may not always require immediate repeat detorsion in selected patients who improve clinically.
Trial Registration:
N/A.
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