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Article: Benefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients
Title | Benefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients |
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Authors | |
Issue Date | 13-May-2024 |
Publisher | Elsevier |
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 Identifier | http://hdl.handle.net/10722/344121 |
ISSN | 2023 Impact Factor: 11.6 2023 SCImago Journal Rankings: 3.091 |
DC Field | Value | Language |
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dc.contributor.author | Cheung, Ka Shing | - |
dc.contributor.author | Li, Bofei | - |
dc.contributor.author | Wong, Ian Yu-Hong | - |
dc.contributor.author | Law, Simon | - |
dc.contributor.author | Leung, Wai K | - |
dc.date.accessioned | 2024-07-03T08:40:49Z | - |
dc.date.available | 2024-07-03T08:40:49Z | - |
dc.date.issued | 2024-05-13 | - |
dc.identifier.citation | Clinical Gastroenterology and Hepatology, 2024 | - |
dc.identifier.issn | 1542-3565 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Clinical Gastroenterology and Hepatology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Benefit and Harm of Aspirin on Mortality From Gastrointestinal Cancers Vs Bleeding in Helicobacter pylori–Eradicated Patients | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.cgh.2024.05.003 | - |
dc.identifier.eissn | 1542-3565 | - |
dc.identifier.issnl | 1542-3565 | - |