Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.

<h4>Objectives</h4>This post-trial data linkage analysis was to utilize the data of Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) participants linked with their Medicare data to examine the risk of hospitalized and non-hospitalized gastrointestinal...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Xianglin L Du, Lara M Simpson, Brian C Tandy, Judith L Bettencourt, Barry R Davis
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/8c13057ef2a94c0191147151a426d094
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8c13057ef2a94c0191147151a426d094
record_format dspace
spelling oai:doaj.org-article:8c13057ef2a94c0191147151a426d0942021-12-02T20:12:44ZRisk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.1932-620310.1371/journal.pone.0260107https://doaj.org/article/8c13057ef2a94c0191147151a426d0942021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0260107https://doaj.org/toc/1932-6203<h4>Objectives</h4>This post-trial data linkage analysis was to utilize the data of Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) participants linked with their Medicare data to examine the risk of hospitalized and non-hospitalized gastrointestinal (GI) bleeding associated with antihypertensives.<h4>Settings</h4>ALLHAT was a multicenter, randomized, double-blind, active-controlled trial conducted in a total of 42,418 participants aged ≥55 years with hypertension in 623 North American centers. Data for ALLHAT participants who were aged at ≥65 have been linked with their Medicare claims data.<h4>Participants</h4>A total of 16,676 patients (4,480 for lisinopril, 4,537 for amlodipine, and 7,659 for chlorthalidone) with complete Medicare claims data were available for the final analysis.<h4>Results</h4>The cumulative incidences through March 31, 2002 of hospitalized GI bleeding were 5.4%, 5.8% and 5.4% for amlodipine, lisinopril, and chlorthalidone arms, respectively, but were not statistically significant among the 3 arms after adjusting for confounders in Cox regression models. The cumulative incidences of non-hospitalized GI bleeding were also similar across the 3 arms (12.0%, 12.2% and 12.0% for amlodipine, lisinopril, and chlorthalidone, respectively). The increased risk of GI bleeding by age was statistically significant after adjusting for confounders (HR = 1.04 per year, 95% CI: 1.03-1.05). Smokers also had a significantly higher risk of having hospitalized GI bleeding (1.45, 1.19-1.76). Hispanics, those who used aspirin or atenolol in-trial, had diabetes, more education, and a history of stroke had a significantly lower risk of having GI bleeding than their counterparts. Other factors such as gender, history of CHD, prior antihypertensive use, use of estrogen in women, and obesity did not have significant effects on the risk of GI bleeding.<h4>Conclusion</h4>There were no statistically significant differences on the risk of hospitalized or non-hospitalized GI bleeding among the 3 ALLHAT trial arms (amlodipine, lisinopril, and chlorthalidone) during the entire in-trial follow-up.Xianglin L DuLara M SimpsonBrian C TandyJudith L BettencourtBarry R DavisPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11, p e0260107 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xianglin L Du
Lara M Simpson
Brian C Tandy
Judith L Bettencourt
Barry R Davis
Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
description <h4>Objectives</h4>This post-trial data linkage analysis was to utilize the data of Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) participants linked with their Medicare data to examine the risk of hospitalized and non-hospitalized gastrointestinal (GI) bleeding associated with antihypertensives.<h4>Settings</h4>ALLHAT was a multicenter, randomized, double-blind, active-controlled trial conducted in a total of 42,418 participants aged ≥55 years with hypertension in 623 North American centers. Data for ALLHAT participants who were aged at ≥65 have been linked with their Medicare claims data.<h4>Participants</h4>A total of 16,676 patients (4,480 for lisinopril, 4,537 for amlodipine, and 7,659 for chlorthalidone) with complete Medicare claims data were available for the final analysis.<h4>Results</h4>The cumulative incidences through March 31, 2002 of hospitalized GI bleeding were 5.4%, 5.8% and 5.4% for amlodipine, lisinopril, and chlorthalidone arms, respectively, but were not statistically significant among the 3 arms after adjusting for confounders in Cox regression models. The cumulative incidences of non-hospitalized GI bleeding were also similar across the 3 arms (12.0%, 12.2% and 12.0% for amlodipine, lisinopril, and chlorthalidone, respectively). The increased risk of GI bleeding by age was statistically significant after adjusting for confounders (HR = 1.04 per year, 95% CI: 1.03-1.05). Smokers also had a significantly higher risk of having hospitalized GI bleeding (1.45, 1.19-1.76). Hispanics, those who used aspirin or atenolol in-trial, had diabetes, more education, and a history of stroke had a significantly lower risk of having GI bleeding than their counterparts. Other factors such as gender, history of CHD, prior antihypertensive use, use of estrogen in women, and obesity did not have significant effects on the risk of GI bleeding.<h4>Conclusion</h4>There were no statistically significant differences on the risk of hospitalized or non-hospitalized GI bleeding among the 3 ALLHAT trial arms (amlodipine, lisinopril, and chlorthalidone) during the entire in-trial follow-up.
format article
author Xianglin L Du
Lara M Simpson
Brian C Tandy
Judith L Bettencourt
Barry R Davis
author_facet Xianglin L Du
Lara M Simpson
Brian C Tandy
Judith L Bettencourt
Barry R Davis
author_sort Xianglin L Du
title Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
title_short Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
title_full Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
title_fullStr Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
title_full_unstemmed Risk of hospitalized and non-hospitalized gastrointestinal bleeding in ALLHAT trial participants receiving diuretic, ACE-inhibitor, or calcium-channel blocker.
title_sort risk of hospitalized and non-hospitalized gastrointestinal bleeding in allhat trial participants receiving diuretic, ace-inhibitor, or calcium-channel blocker.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/8c13057ef2a94c0191147151a426d094
work_keys_str_mv AT xianglinldu riskofhospitalizedandnonhospitalizedgastrointestinalbleedinginallhattrialparticipantsreceivingdiureticaceinhibitororcalciumchannelblocker
AT laramsimpson riskofhospitalizedandnonhospitalizedgastrointestinalbleedinginallhattrialparticipantsreceivingdiureticaceinhibitororcalciumchannelblocker
AT brianctandy riskofhospitalizedandnonhospitalizedgastrointestinalbleedinginallhattrialparticipantsreceivingdiureticaceinhibitororcalciumchannelblocker
AT judithlbettencourt riskofhospitalizedandnonhospitalizedgastrointestinalbleedinginallhattrialparticipantsreceivingdiureticaceinhibitororcalciumchannelblocker
AT barryrdavis riskofhospitalizedandnonhospitalizedgastrointestinalbleedinginallhattrialparticipantsreceivingdiureticaceinhibitororcalciumchannelblocker
_version_ 1718374836868218880