Drittel Darren, Schreiber-Stainthorp William, Delau Olivia, Gurunathan Sakteesh V, Chodosh Joshua, Segev Dorry L, McAdams-DeMarco Mara, Katz Seymour, Dodson John, Shaukat Aasma, Faye Adam S
Thomas Jefferson University-Sidney Kimmel Medical College, Philadelphia, Pennsylvania, USA.
Department of Medicine at New York University Langone Health, New York, New York, USA.
Am J Gastroenterol. 2025 Apr 1;120(4):844-855. doi: 10.14309/ajg.0000000000003036. Epub 2024 Aug 20.
As the inflammatory bowel disease (IBD) patient population is aging, the prevalence of polypharmacy is rising. However, data exploring the prevalence, risk factors, and clinical outcomes associated with polypharmacy among older adults with IBD are limited. The aim of the study is to determine (i) prevalence of polypharmacy (≥5 medications) and potentially inappropriate medication (PIM) utilization in older adults with IBD, (ii) changes in medications over time, (iii) predictors of polypharmacy, and (iv) the impact of polypharmacy/PIMs on 1-year hospitalization rates.
We conducted a retrospective single-center study of older adults with IBD from September 1, 2011, to December 31, 2022. Wilcoxon-signed rank and McNemar tests were used to assess changes in polypharmacy between visits, with ordinal logistic regression and Cox proportional hazards models used to determine risk factors for polypharmacy and time to hospitalization, respectively.
Among 512 older adults with IBD, 74.0% experienced polypharmacy at the initial visit, with 42.6% receiving at least one PIM. In addition, severe polypharmacy (≥10 medications) was present among 28.6% individuals at the index visit and increased to 38.6% by the last visit ( P < 0.01). Multivariable analysis revealed that age ≥70 years, body mass index ≥30.0 kg/m 2 , previous IBD-related surgery, and the presence of comorbidities were associated with polypharmacy. Moreover, severe polypharmacy ( adj hazard ratio 1.95, 95% confidence interval 1.29-2.92), as well as PIM use ( adj hazard ratio 2.16, 95% confidence interval 1.37-3.43) among those with polypharmacy, was significantly associated with all-cause hospitalization within a year of the index visit.
Severe polypharmacy was initially present in more than 25% of older adults with IBD and increased to 34% within 4 years of the index visit. Severe polypharmacy, as well as PIM utilization among those with polypharmacy, were also associated with an increased risk of hospitalization at 1 year, highlighting the need for deprescribing efforts in this population.
随着炎症性肠病(IBD)患者群体的老龄化,联合用药的患病率正在上升。然而,探索IBD老年患者中联合用药的患病率、风险因素和临床结局的数据有限。本研究的目的是确定:(i)IBD老年患者联合用药(≥5种药物)和潜在不适当用药(PIM)的使用率;(ii)药物随时间的变化;(iii)联合用药的预测因素;以及(iv)联合用药/PIM对1年住院率的影响。
我们对2011年9月1日至2022年12月31日期间的IBD老年患者进行了一项回顾性单中心研究。采用Wilcoxon符号秩检验和McNemar检验评估各次就诊之间联合用药的变化,分别采用有序逻辑回归和Cox比例风险模型确定联合用药的风险因素和住院时间。
在512名IBD老年患者中,74.0%在初次就诊时存在联合用药情况,42.6%的患者接受了至少一种PIM。此外,28.6%的患者在首次就诊时存在严重联合用药(≥10种药物),到最后一次就诊时增加到38.6%(P<0.01)。多变量分析显示,年龄≥70岁、体重指数≥30.0kg/m²、既往IBD相关手术以及合并症的存在与联合用药有关。此外,严重联合用药(调整后风险比1.95,95%置信区间1.29-2.92)以及联合用药患者中的PIM使用(调整后风险比2.16,95%置信区间1.37-3.43)与首次就诊后一年内的全因住院显著相关。
超过25%的IBD老年患者最初存在严重联合用药情况,在首次就诊后4年内增加到34%。严重联合用药以及联合用药患者中的PIM使用也与1年住院风险增加相关,突出了该人群中减少用药的必要性。