Adenoma detection rate and tolerability of 2 ultra-low-volume bowel preparations in screening: a noninferiority randomized controlled trial

被引:0
|
作者
Serradesanferm, Anna [1 ,2 ,3 ]
Tora-Rocamora, Isabel [1 ,3 ,4 ]
Pozo, Angels [1 ,2 ,3 ]
Ocana, Teresa [2 ,3 ]
Diaz, Mireia [6 ]
Moreira, Rebeca [5 ]
Rivero-Sanchez, Liseth [2 ,4 ,5 ,6 ]
Ortiz, Oswaldo [2 ,5 ,6 ]
Carballal, Sabela [2 ,4 ,5 ,6 ]
Moreira, Leticia [2 ,4 ,5 ,6 ]
Vaquero, Eva C. [2 ,5 ,6 ]
Ordas, Ingrid [2 ,5 ,6 ]
Bayarri, Carolina [4 ,5 ]
Daca-Alvarez, Maria [5 ,6 ]
Torres, Sonia [5 ]
Grau, Jaume [3 ,4 ]
Balaguer, Francesc [2 ,4 ,5 ,6 ]
Castells, Antoni [2 ,4 ,5 ,6 ]
Pellise, Maria [2 ,4 ,5 ,6 ]
机构
[1] Hosp Clin Barcelona, Dept Prevent Med & Epidemiol, Barcelona, Spain
[2] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
[3] ISGlobal, Barcelona, Spain
[4] Univ Barcelona, Barcelona, Spain
[5] Hosp Clin Barcelona, Dept Gastroenterol, Barcelona, Spain
[6] Inst Invest Biomed August Pi i Sunyer IDIBAPS, Barcelona, Spain
关键词
GASTROINTESTINAL ENDOSCOPY; COLONOSCOPY; QUALITY; IMPACT;
D O I
10.1016/j.gie.2024.07.007
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aims: The adenoma detection rate (ADR), recognized as a surrogate marker for colorectal cancer (CRC) incidence and mortality reduction, is closely linked to the efficacy of bowel cleansing. However, there is a dearth of evidence examining the impact on ADR when using 2 distinct very-low-dose bowel cleansing products. This study sought to compare ADR in an immunochemical fecal occult blood test (iFOBT)-based organized screening program by using 1 L of polyethylene glycol plus ascorbate (1L-PEGA) versus sodium picosulfate with magnesium citrate (SPMC), both administered in a split-dose regimen. Methods: We conducted a comparative, parallel, randomized, noninferiority, and low-intervention clinical trial targeting individuals from a population CRC screening program aged 50 to 69 years with a positive iFOBT result scheduled for a workup colonoscopy in the morning. Participants were randomized to either 1L-PEGA or SPMC for bowel cleansing. The main outcome was ADR, whereas secondary outcomes were bowel preparation quality, safety, tolerability, and satisfaction. Results: A total of 1002 subjects, 501 were included in each group. There were no differences between groups with respect to pooled ADR (SPMC, 56.5% [95% CI, 52.1-60.8]; 1L-PEGA, 53.7% [95% CI, 49.3-58.0]; relative risk, .95 [95% CI, .85-1.06]); therefore, SPMC demonstrated noninferiority in ADR compared with 1L-PEGA (difference, 2.8%; 2-sided 95% lower confidence limit, -3.4). In addition, there were no significant differences in mean lesions regardless of size and location between arms. Bowel preparation favored 1L-PEGA (96.2% vs 89.2%, P < .001), whereas SPMC exhibited significantly higher safety and tolerability, as shown by fewer nonserious treatment-emergent adverse events. Conclusions: SPMC emerged as a noninferior laxative compared with 1L-PEGA concerning ADR. Despite the superior bowel preparation quality associated with 1L-PEGA, the safety, tolerability, and overall satisfaction of participants were higher with SPMC.
引用
收藏
页码:158 / 167.e7
页数:17
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