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Outcomes of elective left colectomy in renal-transplanted patients: a single-center case-control study (LECoRT study)
Thomas Bardol1, Regis Souche2, Diane Genet2
1Digestive and Mini-invasive Surgery Unit, Department of Digestive Surgery and Transplantation, Montpellier University Hospital, University of Montpellier-Nimes, 641 Avenue du Doyen Gaston Giraud, 34090, Montpellier, France. t-bardol@chu-montpellier.fr.
Purpose:
Renal-transplanted patients are reported to have a high anastomotic leakage (AL) rate after colorectal surgery. We aimed to define AL-related morbidity and mortality rates after elective left colectomy in renal-transplanted patients.
Methods:
Data were prospectively collected between 2010 and 2015 from patients who underwent elective left colectomy with supra-peritoneal anastomosis in a single French referral hospital. We compared AL rate, and morbidity and mortality rates between renal-transplanted patients and controls.
Results:
We identified 120 patients who underwent elective left colectomy during the study period. We retrospectively divided this cohort into 20 (17%) kidney-transplanted recipients (KTR-group) and the remaining 100 patients comprised the control group (C-group). There were no significant differences in sex, age, ASA score, body mass index, history of abdominal surgery and benign/malignant disease ratio between the KTR-group and the C-group. The AL rate was approximately four times higher in the KTR-group versus the C-group (25% vs 7%, p = 0.028). Intra-abdominal septic complications (p = 0.0005) and reoperation rates (p = 0.025) were also higher in the KTR-group. The laparoscopic approach was performed less in the KTR-group (35% versus 93%, p < 0.0001).
Conclusion:
Renal transplantation was identified as a risk factor of AL following elective left colectomy, as well as increased intra-abdominal septic morbidity and higher reoperation rate. Further multicentric studies are required to identify potential independent risk factors of AL after colorectal surgery in these frail populations.
Trial Registration:
The present study was declared on ClinicalTrials.gov (ID: NCT04495023).
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