TY - JOUR
T1 - Long-term use of aspirin and the risk of gastrointestinal bleeding
AU - Huang, Edward S.
AU - Strate, Lisa L.
AU - Ho, Wendy W.
AU - Lee, Salina S.
AU - Chan, Andrew T.
N1 - Funding Information:
Funding: Supported by grants ( CA 87969 , CA 55075 , CA 107412 , CA 137178 ) from the National Cancer Institute , National Institutes of Health . Dr. Chan was a recipient of the American Gastroenterological Association/Foundation for Digestive Health and Nutrition Pilot Research Award for this work. Dr. Chan is a Damon Runyon Clinical Investigator. Dr. Huang is supported by American Gastroenterological Association Fellow to Faculty Transition Award . No pharmaceutical industry funds were received for preparation of this manuscript. The National Cancer Institute, the National Institutes of Health, the American Gastroenterological Association, the Foundation for Digestive Health and Nutrition, and the Damon Runyon Cancer Research Foundation had no role in the collection, management, analysis, or interpretation of the data, and had no role in the preparation, review, or approval of the manuscript.
PY - 2011/5
Y1 - 2011/5
N2 - Background: In short-term trials, aspirin is associated with gastrointestinal bleeding. However, the effect of dose and duration of aspirin use on risk remains unclear. Methods: We conducted a prospective study of 87,680 women enrolled in the Nurses' Health Study in 1990 who provided biennial data on aspirin use. We examined the relative risk (RR) of major gastrointestinal bleeding requiring hospitalization or blood transfusion. Results: During a 24-year follow-up, 1537 women reported a major gastrointestinal bleeding. Among women who used aspirin regularly (<2 standard [325 mg] tablets/week), the multivariate RR of gastrointestinal bleeding was 1.43 (95% confidence interval [CI], 1.29-1.59) when compared with nonregular users. Compared with women who denied any aspirin use, the multivariate RRs of gastrointestinal bleeding were 1.03 (95% CI, 0.85-1.24) for women who used 0.5 to 1.5 standard aspirin tablets/week, 1.30 (95% CI, 1.07-1.58) for women who used 2 to 5 tablets/week, 1.77 (95% CI, 1.44-2.18) for women who used 6 to 14 tablets/week, and 2.24 (95% CI, 1.66-3.03) for women who used more than 14 tablets/week (Ptrend < .001). Similar dose-response relationships were observed among short-term users (≤5 years; Ptrend <.001) and long-term users (>5 years; Ptrend <.001). In contrast, after adjustments were made for dose, increasing duration of use did not confer a greater risk of bleeding (Ptrend = .28). Conclusion: Regular aspirin use is associated with gastrointestinal bleeding. Risk seems more strongly related to dose than duration of aspirin use. Efforts to minimize adverse effects of aspirin therapy should emphasize using the lowest effective dose among both short- and long-term users.
AB - Background: In short-term trials, aspirin is associated with gastrointestinal bleeding. However, the effect of dose and duration of aspirin use on risk remains unclear. Methods: We conducted a prospective study of 87,680 women enrolled in the Nurses' Health Study in 1990 who provided biennial data on aspirin use. We examined the relative risk (RR) of major gastrointestinal bleeding requiring hospitalization or blood transfusion. Results: During a 24-year follow-up, 1537 women reported a major gastrointestinal bleeding. Among women who used aspirin regularly (<2 standard [325 mg] tablets/week), the multivariate RR of gastrointestinal bleeding was 1.43 (95% confidence interval [CI], 1.29-1.59) when compared with nonregular users. Compared with women who denied any aspirin use, the multivariate RRs of gastrointestinal bleeding were 1.03 (95% CI, 0.85-1.24) for women who used 0.5 to 1.5 standard aspirin tablets/week, 1.30 (95% CI, 1.07-1.58) for women who used 2 to 5 tablets/week, 1.77 (95% CI, 1.44-2.18) for women who used 6 to 14 tablets/week, and 2.24 (95% CI, 1.66-3.03) for women who used more than 14 tablets/week (Ptrend < .001). Similar dose-response relationships were observed among short-term users (≤5 years; Ptrend <.001) and long-term users (>5 years; Ptrend <.001). In contrast, after adjustments were made for dose, increasing duration of use did not confer a greater risk of bleeding (Ptrend = .28). Conclusion: Regular aspirin use is associated with gastrointestinal bleeding. Risk seems more strongly related to dose than duration of aspirin use. Efforts to minimize adverse effects of aspirin therapy should emphasize using the lowest effective dose among both short- and long-term users.
KW - Aspirin
KW - Dose
KW - Duration
KW - Gastrointestinal bleeding
KW - Long-term
UR - http://www.scopus.com/inward/record.url?scp=79955641250&partnerID=8YFLogxK
U2 - 10.1016/j.amjmed.2010.12.022
DO - 10.1016/j.amjmed.2010.12.022
M3 - Article
C2 - 21531232
AN - SCOPUS:79955641250
SN - 0002-9343
VL - 124
SP - 426
EP - 433
JO - American Journal of Medicine
JF - American Journal of Medicine
IS - 5
ER -