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Anticholinergic use is associated with lower mortality but not increased hip fracture risk in Parkinson's disease patients: a retrospective cohort study
被引:0
作者:
Ko, Po-Yen
[1
]
Wu, Po-Ting
[1
,2
,3
,4
]
Jou, I-Ming
[5
,6
,7
]
Chang, Renin
[8
,9
,10
]
Ma, Ching-Hou
[5
,6
]
机构:
[1] Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Orthoped, Tainan, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Dept Orthoped, Tainan, Taiwan
[3] Natl Cheng Kung Univ, Med Device Innovat Ctr, Tainan, Taiwan
[4] Natl Cheng Kung Univ, Dept Biomed Engn, Tainan, Taiwan
[5] Eda Hosp, Dept Orthoped, Kaohsiung, Taiwan
[6] I Shou Univ, Coll Med, Sch Med, Kaohsiung, Taiwan
[7] GEG Orthoped Clin, Tainan, Taiwan
[8] Kaohsiung Vet Gen Hosp, Dept Emergency Med, Kaohsiung, Taiwan
[9] Tajen Univ, Dept Recreat Sports Management, Pingtung, Taiwan
[10] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
关键词:
Antiparkisonism anticholinergic agent;
Parkinson's disease;
Hip fracture;
Survival rate;
Cohort study;
FALLS;
MEDICATIONS;
PREVALENCE;
MANAGEMENT;
NATIONWIDE;
D O I:
10.1186/s12877-024-05535-8
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
BackgroundIt is unclear whether antiparkinsonism anticholinergics (AAs) increase hip fracture (HFx) risk in Parkinson's disease (PD) patients. This study examined associations between AAs, HFx and mortality in PD using Taiwan's National Health Insurance Database.MethodsNewly diagnosed PD patients >= 50yrs were categorized by AAs exposure: PD with AAs (>= 90 days, n = 16,921), PD without AAs (never-exposed, n = 55,940), and demographically matched non-PD controls (n = 291,444). Competing risk of death was considered in Fine & Gray models analyzing HFx. Mortality was compared using Cox regression models.ResultsBoth PD groups were associated with higher HFx risk compared to non-PD controls (adjusted hazard ratio [HR] = 1.51 for PD with AAs; 1.53 without). No significant difference in HFx risk was observed between PD groups with and without AAs exposure. Both groups were associated with increased mortality compared to non-PD (adjusted HR = 2.24 with AAs; 2.44 without AAs). Among PD patients, those with AAs exposure were associated with lower mortality compared to those without AAs (adjusted HR = 0.93).ConclusionsPD was associated with increased HFx and mortality compared to non-PD, regardless of AAs exposure. AAs use was not associated with increased HFx risk and was associated with lower mortality. AAs use was not associated with increased fracture risk and was associated with lower mortality in PD, however further studies are needed to clarify these associations.
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