TY - JOUR
T1 - Diabetes association with self-reported health, resource utilization, and prognosis post-myocardial infarction
AU - Nicolau, José C.
AU - Brieger, David
AU - Owen, Ruth
AU - Furtado, Remo H.M.
AU - Goodman, Shaun G.
AU - Cohen, Mauricio G.
AU - Simon, Tabassome
AU - Westermann, Dirk
AU - Granger, Christopher B.
AU - Grieve, Richard
AU - Yasuda, Satoshi
AU - Chen, Jiyan
AU - Hedman, Katarina
AU - Mellström, Carl
AU - Brandrup-Wognsen, Gunnar
AU - Pocock, Stuart J.
N1 - Funding Information:
Editorial support was provided by Cactus Life Sciences (part of Cactus Communications) and funded by AstraZeneca. The long-Term rIsk, clinical manaGement, and healthcare Resource utilization of stable coronary artery dISease (TIGRIS) study is sponsored by AstraZeneca AB, Södertälje, Sweden. The sponsor contributed to the study conception and design and commented on the analyses. José C. Nicolau has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, BMS, Boehringer Ingelheim, GlaxoSmithKline, Merck, Novartis, Pfizer, and Sanofi. David Brieger has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Eli Lilly, Merck, and Sanofi. Ruth Owen and Stuart J. Pocock have received research grant support from AstraZeneca. Remo H.M. Furtado reports grants and personal fees from AstraZeneca, personal fees from Servier, and grants from EMS, Pfizer, Novo Nordisk, DalCor, Novartis, and Jansen, all of these were outside of the submitted work. Shaun G. Goodman has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, CSL Behring, Daiichi Sankyo, Eli Lilly, Fenix Group International, Ferring Pharmaceuticals, GlaxoSmithKline, HLS Therapeutics, Janssen/Johnson & Johnson, Luitpold Pharmaceuticals, Matrizyme, Merck, Novartis, Novo Nordisk, Pfizer, Regeneron, Sanofi, Servier, and Tenax Pharmaceuticals. Mauricio G. Cohen has received speaker/consulting honoraria and/or research grant support from AstraZeneca, Medtronic, Abiomed, and Merit Medical. Tabassome Simon has received speaker/consulting honoraria and/or research grant support from Astellas, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Eli Lilly, GlaxoSmithKline, Merck, Novartis, Pfizer, and Sanofi. Dirk Westermann has received speaker/consulting honoraria and/or research grant support from AstraZeneca, Bayer, Berlin-Chemie, Biotronik, and Novartis. Christopher B.Granger has received consulting honoraria and/or research grant support from Armetheon, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Daiichi Sankyo, Eli Lilly, Gilead, GlaxoSmithKline, Hoffmann-La Roche, Janssen, Metronic, Pfizer, Salix Pharmaceuticals, Sanofi, Takeda, and The Medicines Company. Richard Grieve has nothing to disclose. Satoshi Yasuda has received speaker/consulting honoraria and/or research grant support from Takeda, Daiichi Sankyo, AstraZeneca, Boehringer Ingelheim, and BMS. Jiyan Chen has received research grant support from AstraZeneca and consulting honoraria from MicroPort, APT Medical, and JW Medical. Katarina Hedman, Carl Mellström, and Gunnar Brandrup-Wognsen are employees of AstraZeneca.
Funding Information:
José C. Nicolau has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, BMS, Boehringer Ingelheim, GlaxoSmithKline, Merck, Novartis, Pfizer, and Sanofi. David Brieger has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Eli Lilly, Merck, and Sanofi. Ruth Owen and Stuart J. Pocock have received research grant support from AstraZeneca. Remo H.M. Furtado reports grants and personal fees from AstraZeneca, personal fees from Servier, and grants from EMS, Pfizer, Novo Nordisk, DalCor, Novartis, and Jansen, all of these were outside of the submitted work. Shaun G. Goodman has received speaker/consulting honoraria and/or research grant support from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, CSL Behring, Daiichi Sankyo, Eli Lilly, Fenix Group International, Ferring Pharmaceuticals, GlaxoSmithKline, HLS Therapeutics, Janssen/Johnson & Johnson, Luitpold Pharmaceuticals, Matrizyme, Merck, Novartis, Novo Nordisk, Pfizer, Regeneron, Sanofi, Servier, and Tenax Pharmaceuticals. Mauricio G. Cohen has received speaker/consulting honoraria and/or research grant support from AstraZeneca, Medtronic, Abiomed, and Merit Medical. Tabassome Simon has received speaker/consulting honoraria and/or research grant support from Astellas, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Eli Lilly, GlaxoSmithKline, Merck, Novartis, Pfizer, and Sanofi. Dirk Westermann has received speaker/consulting honoraria and/or research grant support from AstraZeneca, Bayer, Berlin‐Chemie, Biotronik, and Novartis. Christopher B.Granger has received consulting honoraria and/or research grant support from Armetheon, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Daiichi Sankyo, Eli Lilly, Gilead, GlaxoSmithKline, Hoffmann‐La Roche, Janssen, Metronic, Pfizer, Salix Pharmaceuticals, Sanofi, Takeda, and The Medicines Company. Richard Grieve has nothing to disclose. Satoshi Yasuda has received speaker/consulting honoraria and/or research grant support from Takeda, Daiichi Sankyo, AstraZeneca, Boehringer Ingelheim, and BMS. Jiyan Chen has received research grant support from AstraZeneca and consulting honoraria from MicroPort, APT Medical, and JW Medical. Katarina Hedman, Carl Mellström, and Gunnar Brandrup‐Wognsen are employees of AstraZeneca.
Funding Information:
Editorial support was provided by Cactus Life Sciences (part of Cactus Communications) and funded by AstraZeneca. The long‐Term rIsk, clinical manaGement, and healthcare Resource utilization of stable coronary artery dISease (TIGRIS) study is sponsored by AstraZeneca AB, Södertälje, Sweden. The sponsor contributed to the study conception and design and commented on the analyses.
Publisher Copyright:
© 2020 The Authors. Clinical Cardiology published by Wiley Periodicals LLC.
PY - 2020/12
Y1 - 2020/12
N2 - Background: Diabetes mellitus (DM) is associated with increased cardiovascular (CV) risk. We compared health-related quality of life (HRQoL), healthcare resource utilization (HRU), and clinical outcomes of stable post-myocardial infarction (MI) patients with and without DM. Hypothesis: In post-MI patients, DM is associated with worse HRQoL, increased HRU, and worse clinical outcomes. Methods: The prospective, observational long-term risk, clinical management, and healthcare Resource utilization of stable coronary artery disease study obtained data from 8968 patients aged ≥50 years 1 to 3 years post-MI (369 centers; 25 countries). Patients with ≥1 of the following risk factors were included: age ≥65 years, history of a second MI >1 year before enrollment, multivessel coronary artery disease, creatinine clearance ≥15 and <60 mL/min, and DM treated with medication. Self-reported health status was assessed at baseline, 1 and 2 years and converted to EQ-5D scores. The main outcome measures were baseline HRQoL and HRU during follow-up. Results: DM at enrollment was 33% (2959 patients, 869 insulin treated). Mean baseline EQ-5D score (0.86 vs 0.82; P <.0001) was higher; mean number of hospitalizations (0.38 vs 0.50, P <.0001) and mean length of stay (LoS; 9.3 vs 11.5; P =.001) were lower in patients without vs with DM. All-cause death and the composite of CV death, MI, and stroke were significantly higher in DM patients, with adjusted 2-year rate ratios of 1.43 (P <.01) and 1.55 (P <.001), respectively. Conclusions: Stable post-MI patients with DM (especially insulin treated) had poorer EQ-5D scores, higher hospitalization rates and LoS, and worse clinical outcomes vs those without DM. Strategies focusing specifically on this high-risk population should be developed to improve outcomes. Trial registration: ClinicalTrials.gov: NCT01866904 (https://clinicaltrials.gov).
AB - Background: Diabetes mellitus (DM) is associated with increased cardiovascular (CV) risk. We compared health-related quality of life (HRQoL), healthcare resource utilization (HRU), and clinical outcomes of stable post-myocardial infarction (MI) patients with and without DM. Hypothesis: In post-MI patients, DM is associated with worse HRQoL, increased HRU, and worse clinical outcomes. Methods: The prospective, observational long-term risk, clinical management, and healthcare Resource utilization of stable coronary artery disease study obtained data from 8968 patients aged ≥50 years 1 to 3 years post-MI (369 centers; 25 countries). Patients with ≥1 of the following risk factors were included: age ≥65 years, history of a second MI >1 year before enrollment, multivessel coronary artery disease, creatinine clearance ≥15 and <60 mL/min, and DM treated with medication. Self-reported health status was assessed at baseline, 1 and 2 years and converted to EQ-5D scores. The main outcome measures were baseline HRQoL and HRU during follow-up. Results: DM at enrollment was 33% (2959 patients, 869 insulin treated). Mean baseline EQ-5D score (0.86 vs 0.82; P <.0001) was higher; mean number of hospitalizations (0.38 vs 0.50, P <.0001) and mean length of stay (LoS; 9.3 vs 11.5; P =.001) were lower in patients without vs with DM. All-cause death and the composite of CV death, MI, and stroke were significantly higher in DM patients, with adjusted 2-year rate ratios of 1.43 (P <.01) and 1.55 (P <.001), respectively. Conclusions: Stable post-MI patients with DM (especially insulin treated) had poorer EQ-5D scores, higher hospitalization rates and LoS, and worse clinical outcomes vs those without DM. Strategies focusing specifically on this high-risk population should be developed to improve outcomes. Trial registration: ClinicalTrials.gov: NCT01866904 (https://clinicaltrials.gov).
KW - cardiovascular events
KW - diabetes
KW - healthcare resource utilization
KW - myocardial infarction
KW - quality of life
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U2 - 10.1002/clc.23476
DO - 10.1002/clc.23476
M3 - Article
C2 - 33146924
AN - SCOPUS:85096699953
SN - 0160-9289
VL - 43
SP - 1352
EP - 1361
JO - Clinical Cardiology
JF - Clinical Cardiology
IS - 12
ER -