TY - JOUR
T1 - Relationship between the number of drugs used during percutaneous coronary intervention and adverse events in patients with chronic coronary syndrome
T2 - Analysis of CLIDAS database
AU - CLIDAS Research Group
AU - Hitomi, Yasuhiro
AU - Imai, Yasushi
AU - Kuwabara, Masanari
AU - Oba, Yusuke
AU - Kabutoya, Tomoyuki
AU - Kario, Kazuomi
AU - Makimoto, Hisaki
AU - Kohro, Takahide
AU - Shiraki, Eiichi
AU - Akashi, Naoyuki
AU - Fujita, Hideo
AU - Matoba, Tetsuya
AU - Miyamoto, Yoshihiro
AU - Kiyosue, Arihiro
AU - Tsujita, Kenichi
AU - Nakayama, Masaharu
AU - Nagai, Ryozo
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/10
Y1 - 2024/10
N2 - Background: Polypharmacy is associated with an increased risk of adverse events due to the higher number of drugs used. This is particularly notable in patients with chronic coronary syndrome (CCS), who are known to use a large number of drugs. Therefore, we investigated polypharmacy in patients with CCS, using CLIDAS, a multicenter database of patients who underwent percutaneous coronary intervention. Method and results: Between 2017 and 2020, 1411 CCS patients (71.5 ± 10.5 years old; 77.3 % male) were enrolled. The relationship between cardiovascular events occurring during the median follow-up of 514 days and the number of drugs at the time of PCI was investigated. The median number of drugs prescribed was nine. Major adverse cardiovascular events (MACE), defined as cardiovascular death, myocardial infarction, stroke, heart failure, transient ischemic attack, or unstable angina, occurred in 123 patients, and all-cause mortality occurred in 68 patients. For each additional drug, the adjusted hazard ratios for MACE and all-cause mortality increased by 2.069 (p = 0.003) and 1.102 (p = 0.010). The adjusted hazard ratios for MACE and all-cause mortality were significantly higher in the group using nine or more drugs compared to the group using eight or fewer drugs (1.646 and 2.253, both p < 0.001). Conclusion: This study showed that an increase in the number of drugs used for CCS may be associated with MACE and all-cause mortality. In patients with CCS, it might be beneficial to minimize the number of medications as much as possible, while managing comorbidities and using guideline-recommended drugs.
AB - Background: Polypharmacy is associated with an increased risk of adverse events due to the higher number of drugs used. This is particularly notable in patients with chronic coronary syndrome (CCS), who are known to use a large number of drugs. Therefore, we investigated polypharmacy in patients with CCS, using CLIDAS, a multicenter database of patients who underwent percutaneous coronary intervention. Method and results: Between 2017 and 2020, 1411 CCS patients (71.5 ± 10.5 years old; 77.3 % male) were enrolled. The relationship between cardiovascular events occurring during the median follow-up of 514 days and the number of drugs at the time of PCI was investigated. The median number of drugs prescribed was nine. Major adverse cardiovascular events (MACE), defined as cardiovascular death, myocardial infarction, stroke, heart failure, transient ischemic attack, or unstable angina, occurred in 123 patients, and all-cause mortality occurred in 68 patients. For each additional drug, the adjusted hazard ratios for MACE and all-cause mortality increased by 2.069 (p = 0.003) and 1.102 (p = 0.010). The adjusted hazard ratios for MACE and all-cause mortality were significantly higher in the group using nine or more drugs compared to the group using eight or fewer drugs (1.646 and 2.253, both p < 0.001). Conclusion: This study showed that an increase in the number of drugs used for CCS may be associated with MACE and all-cause mortality. In patients with CCS, it might be beneficial to minimize the number of medications as much as possible, while managing comorbidities and using guideline-recommended drugs.
KW - CCS
KW - Chronic coronary syndrome
KW - Number of prescriptions
KW - Polypharmacy
UR - http://www.scopus.com/inward/record.url?scp=85203646113&partnerID=8YFLogxK
U2 - 10.1016/j.ijcha.2024.101507
DO - 10.1016/j.ijcha.2024.101507
M3 - Article
AN - SCOPUS:85203646113
SN - 2352-9067
VL - 54
JO - IJC Heart and Vasculature
JF - IJC Heart and Vasculature
M1 - 101507
ER -