Prevalence of Colorectal Neoplasms and Mortality in New Users of Low-Dose Aspirin With Lower Gastrointestinal Bleeding

2021 ◽  
Vol 28 (1) ◽  
pp. e19-e29 ◽  
Author(s):  
Frederikke S. Troelsen ◽  
Dóra K. Farkas ◽  
Anne G. Ording ◽  
Rune Erichsen ◽  
Susan Jick ◽  
...  
2019 ◽  
Vol 156 (6) ◽  
pp. S-472
Author(s):  
Frederikke S. Troelsen ◽  
Dóra K. Farkas ◽  
Anne Gulbech Ording ◽  
Rune Erichsen ◽  
Henrik Toft Sørensen

2020 ◽  
Vol 9 (4) ◽  
pp. 928
Author(s):  
Luis A. García Rodríguez ◽  
Angel Lanas ◽  
Montse Soriano-Gabarró ◽  
Pareen Vora ◽  
Lucía Cea Soriano

Estimates of the effect of proton pump inhibitors (PPIs) on risks of upper and lower gastrointestinal bleeding (UGIB and LGIB) among low-dose aspirin users in routine clinical practice are variable (UGIB) or lacking (LGIB). We aimed to establish these risks in the same observational study population. Using UK primary care data, we followed 199,049 new users of low-dose aspirin (75–300 mg/day) and matched non-users at start of follow-up to identify incident UGIB/LGIB cases. In nested case–control analyses, adjusted odds ratios (ORs) were calculated for concomitant PPI use vs. past (discontinued) PPI use among current low-dose aspirin users. For UGIB (n = 987), ORs (95% CIs) were 0.69 (0.54–0.88) for >1 month PPI use and 2.65 (1.62–4.3) for ≤1 month PPI use. Among the latter group, ORs (95% CIs) were 3.05 (1.75–5.33) for PPI initiation after start of aspirin therapy, and 1.66 (0.63–4.36) for PPI initiation on/before start of aspirin therapy. For LGIB (n = 1428), ORs (95% CIs) were 0.98 (0.81–1.17) for >1 month PPI use and 1.12 (0.73–1.71) for ≤1 month PPI use. Among low-dose aspirin users, maintaining PPI use (>1 month) was associated with a significantly reduced UGIB risk. Neither short nor long-term PPI use affected LGIB risk.


2017 ◽  
Vol 45 (12) ◽  
pp. 1542-1550 ◽  
Author(s):  
W.-C. Chen ◽  
K.-H. Lin ◽  
Y.-T. Huang ◽  
T.-J. Tsai ◽  
W.-C. Sun ◽  
...  

2019 ◽  
Vol 17 (5) ◽  
pp. 887-895.e6 ◽  
Author(s):  
Lucía Cea Soriano ◽  
Angel Lanas ◽  
Montse Soriano-Gabarró ◽  
Luis A. García Rodríguez

2020 ◽  
Vol 7 (1) ◽  
pp. e000453
Author(s):  
Frederikke Schønfeldt Troelsen ◽  
Dóra Körmendiné Farkas ◽  
Rune Erichsen ◽  
Henrik Toft Sørensen

ObjectiveAspirin may increase the risk of lower gastrointestinal bleeding (LGIB) from precursors of colorectal cancer (CRC). We investigated whether use of low-dose aspirin, through initiation of LGIB, may lead patients to undergo colonoscopy and polypectomy before manifest CRC.DesignWe conducted a historical cohort study (2005–2013) of all Danish residents who initiated low-dose aspirin treatment (n=412 202) in a setting without screening for CRC. Each new aspirin user was matched with three non-users (n=1 236 560) by age, sex and region of residence on the date of their matched new user’s first-time aspirin prescription (index date). We computed absolute risks (ARs), risk differences and relative risks (RRs) of LGIB, lower gastrointestinal endoscopy, colorectal polyps and CRC, comparing aspirin users with non-users.ResultsThe ARs were higher for new users than non-users for LGIB, lower gastrointestinal endoscopy, colorectal polyps and CRC within 3 months after index. Comparing new users with non-users, the RRs were 2.79 (95% CI 2.40 to 3.24) for LGIB, 1.73 (95% CI 1.63 to 1.84) for lower gastrointestinal endoscopy, 1.56 (95% CI 1.42 to 1.72) for colorectal polyps and 1.73 (95% CI 1.51 to 1.98) for CRC. The RRs remained elevated for more than 12 months after the index date, with the exception of CRC where the RRs were slightly decreased during the 3–5 years (RR 0.90, 95% CI 0.83 to 0.98) and more than 5 years (RR 0.91, 95% CI 0.82 to 1.00) following the index date.ConclusionThese findings indicate that aspirin may contribute to reduce CRC risk by causing premalignant polyps to bleed, thereby expediting colonoscopy and polypectomy before CRC development.


2018 ◽  
Vol 164 ◽  
pp. S239 ◽  
Author(s):  
F. Schønfeldt Troelsen ◽  
D. Körmendiné Farkas ◽  
A. Gulbech Ording ◽  
S. Friis ◽  
R. Erichsen ◽  
...  

2017 ◽  
Vol 46 (2) ◽  
pp. 200-201
Author(s):  
W.-C. Chen ◽  
K.-H. Lin ◽  
Y.-T. Huang ◽  
T.-J. Tsai ◽  
W.-C. Sun ◽  
...  

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