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Dig Liver Dis ; 53(9): 1171-1177, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-33994129

RESUMEN

INTRODUCTION: The effectiveness of bowel cleansing is a key element for high-quality colonoscopy. Recently, a 1 L polyethylene glycol plus ascorbate (PEG-ASC) solution has been introduced, but effectiveness and safety of this preparation have not been assessed in IBD patients. This study aims to evaluate effectiveness and safety of 1 L PEG-ASC solution in patients with IBD compared to controls. METHODS: We retrospectively analysed prospectively collected data on a cohort of 411 patients performing a colonoscopy after preparation with 1 L PEG-ASC, consecutively enrolled in 5 Italian centres. RESULTS: Overall, 185/411 (45%) were patients with IBD and 226/411 (55%) served as controls. A significantly higher cleansing success was achieved in IBD patients (92.9% vs 85.4%, p = 0.02). The multiple regression model showed that presence of IBD (OR=2.514, 95%CI=1.165-5.426; P = 0.019), lower age (OR=0.981, 95%CI=0.967-0.996; P = 0.014), split preparation (OR=2.430, 95%CI=1.076-5.492; P = 0.033), absence of diabetes (OR=2.848, 95%CI=1.228-6.605; P = 0.015), and of chronic constipation (OR=3.350, 95%CI=1.429-7.852; P = 0.005), were independently associated with cleansing success. The number of treatment-emergent adverse events (TEAEs) (51 vs 62%, p = 0.821), and of patients with TEAEs (22.2% vs 21.2%, p = 0.821), were similar in IBD patients and in controls, respectively. CONCLUSIONS: Results from this study support the effectiveness and safety of 1 L PEG-ASC solution in IBD patients, which may improve the definition of endoscopic outcomes both in Crohn's disease and ulcerative colitis.


Asunto(s)
Ácido Ascórbico/análogos & derivados , Catárticos/administración & dosificación , Colitis Ulcerosa/complicaciones , Colonoscopía/métodos , Enfermedad de Crohn/complicaciones , Fosfatidiletanolaminas/administración & dosificación , Adulto , Ácido Ascórbico/administración & dosificación , Ácido Ascórbico/efectos adversos , Catárticos/efectos adversos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Fosfatidiletanolaminas/efectos adversos , Estudios Retrospectivos
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