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Article: Benefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients

TitleBenefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients
Authors
Issue Date13-May-2024
PublisherElsevier
Citation
Clinical Gastroenterology and Hepatology, 2024 How to Cite?
Abstract

Background: We investigated benefit-risk profile of aspirin on mortality reduction from chemoprevention of gastrointestinal (GI) cancer versus excess mortality from bleeding among Helicobacter pylori (HP)-eradicated patients, and its interaction with proton pump inhibitors (PPIs).

Methods: HP-eradicated patients (between 2003 and 2016), identified from a territory-wide database, were observed from date of HP therapy till death or end of study (July 2020). Primary exposure was aspirin use as time-varying variable. Primary outcome was GI cancer-related (gastrointestinal, hepatobiliary or pancreatic cancer) death and secondary outcome was bleeding-related (GIB or intracranial bleeding) death. Adjusted hazard ratio (aHR) of outcomes was calculated by multivariable Cox model after adjusting for age, sex, comorbidities and concomitant medications. Benefit-risk profile was expressed as adjusted absolute risk difference of cancer-related deaths and bleeding-related deaths between aspirin users and non-users.

Results: 87,967 subjects were followed for a median of 10.1years, with 1,294 (1.5%) GI cancer-related deaths and 304 (0.3%) bleeding-related deaths. Aspirin was associated with lower GI cancer-related mortality (aHR:0.51;95%CI:0.42-0.61), but higher bleeding-related mortality (aHR:1.52;95%CI:1.11-2.08). Among PPI users, aHR of bleeding-related mortality with aspirin was 1.06 (95%CI:0.70-1.63). For whole cohort, adjusted absolute risk difference between aspirin users and non-users was 7 (95%CI: 5-8) fewer cancer-related and 1 (95%CI: 0.3-3) more bleeding-related death per 10,000 person-years. Among concomitant PPI-aspirin use, there were 9 (95%CI:8-10) fewer cancer-related deaths per 10,000 person-years without increase in bleeding-related deaths.

Conclusions: GI-cancer mortality benefit from aspirin outweighs bleeding-related mortality in HP-eradicated subjects, which is further enhanced by PPI use.


Persistent Identifierhttp://hdl.handle.net/10722/344121
ISSN
2023 Impact Factor: 11.6
2023 SCImago Journal Rankings: 3.091

 

DC FieldValueLanguage
dc.contributor.authorCheung, Ka Shing-
dc.contributor.authorLi, Bofei-
dc.contributor.authorWong, Ian Yu-Hong-
dc.contributor.authorLaw, Simon-
dc.contributor.authorLeung, Wai K-
dc.date.accessioned2024-07-03T08:40:49Z-
dc.date.available2024-07-03T08:40:49Z-
dc.date.issued2024-05-13-
dc.identifier.citationClinical Gastroenterology and Hepatology, 2024-
dc.identifier.issn1542-3565-
dc.identifier.urihttp://hdl.handle.net/10722/344121-
dc.description.abstract<div><p><strong>Background: </strong>We investigated benefit-risk profile of aspirin on mortality reduction from chemoprevention of gastrointestinal (GI) cancer versus excess mortality from bleeding among Helicobacter pylori (HP)-eradicated patients, and its interaction with proton pump inhibitors (PPIs).</p><p><strong>Methods: </strong>HP-eradicated patients (between 2003 and 2016), identified from a territory-wide database, were observed from date of HP therapy till death or end of study (July 2020). Primary exposure was aspirin use as time-varying variable. Primary outcome was GI cancer-related (gastrointestinal, hepatobiliary or pancreatic cancer) death and secondary outcome was bleeding-related (GIB or intracranial bleeding) death. Adjusted hazard ratio (aHR) of outcomes was calculated by multivariable Cox model after adjusting for age, sex, comorbidities and concomitant medications. Benefit-risk profile was expressed as adjusted absolute risk difference of cancer-related deaths and bleeding-related deaths between aspirin users and non-users.</p><p><strong>Results: </strong>87,967 subjects were followed for a median of 10.1years, with 1,294 (1.5%) GI cancer-related deaths and 304 (0.3%) bleeding-related deaths. Aspirin was associated with lower GI cancer-related mortality (aHR:0.51;95%CI:0.42-0.61), but higher bleeding-related mortality (aHR:1.52;95%CI:1.11-2.08). Among PPI users, aHR of bleeding-related mortality with aspirin was 1.06 (95%CI:0.70-1.63). For whole cohort, adjusted absolute risk difference between aspirin users and non-users was 7 (95%CI: 5-8) fewer cancer-related and 1 (95%CI: 0.3-3) more bleeding-related death per 10,000 person-years. Among concomitant PPI-aspirin use, there were 9 (95%CI:8-10) fewer cancer-related deaths per 10,000 person-years without increase in bleeding-related deaths.</p><p><strong>Conclusions: </strong>GI-cancer mortality benefit from aspirin outweighs bleeding-related mortality in HP-eradicated subjects, which is further enhanced by PPI use.<br></p></div>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofClinical Gastroenterology and Hepatology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleBenefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients-
dc.typeArticle-
dc.identifier.doi10.1016/j.cgh.2024.05.003-
dc.identifier.eissn1542-3565-
dc.identifier.issnl1542-3565-

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