Simal Ine, Somers Annemie, Amrouch Cheima, Capiau Andreas, Cherubini Antonio, Cruz-Jentoft Alfonso J, Gudmundsson Adalsteinn, Soiza Roy L, O 'Mahony Denis, Petrovic Mirko
Department of Pharmacy, Ghent University Hospital, Ghent, Belgium.
Department of Internal Medicine and Paediatrics, Ghent University, Ghent, Belgium.
Eur Geriatr Med. 2024 Oct;15(5):1357-1367. doi: 10.1007/s41999-024-01025-7. Epub 2024 Aug 2.
Drug-drug interactions (DDIs) are prevalent among multimorbid and polymedicated older adults and can increase the risk of adverse drug reactions (ADRs), hospital admissions, and mortality. This study describes the incidence and prevalence of 66 clinically relevant DDIs and analyses the occurrence of 12 corresponding predefined ADRs in older inpatients enrolled in the SENATOR trial.
The sub-study of the SENATOR trial that involved 1537 multimorbid older inpatients, recruited from 2016 to 2018 in six academic teaching hospitals in Belgium, Iceland, Ireland, Italy, Scotland, and Spain respectively, and analysed 66 potentially clinically significant DDIs. Descriptive analysis determined DDI and corresponding ADR prevalence/incidence.
At baseline (median age: 78 [72, 84], 52.8% male), the prevalence of patients with DDIs was high (50.9%), increased during hospitalisation (55.2%) and reduced to 49.7% after 12 weeks. The most common DDIs were: ≥ 2 potassium reducing drugs (17.1%), ≥ 3 centrally acting drugs (9.0%), and SSRI + loop/thiazide diuretic (7.2%). Of all participants, one-third experienced a prevalent (36.6%)/incident (35.8%) ADR. Major serum electrolyte disturbance had the highest incidence (10.7%)/prevalence (11.5%). Incident ADRs were more common in patients with DDIs (p = 0.013). A higher prevalence of new onset falls (p = 0.013), major constipation (p = 0.004), and major serum electrolyte disturbances (p = 0.006) was observed in patients with related and thus potentially causal DDIs.
Clinicians should, be aware of DDIs and the involved drug classes that can lead to an increased rate of ADRs in older multimorbid inpatients. Regularly reevaluating the appropriateness of the frequently prescribed drug classes and initiating judicious deprescribing is recommended.
药物相互作用(DDIs)在患有多种疾病且使用多种药物的老年人中普遍存在,可增加药物不良反应(ADRs)、住院率和死亡率的风险。本研究描述了66种临床相关药物相互作用的发生率和患病率,并分析了参与SENATOR试验的老年住院患者中12种相应预定义药物不良反应的发生情况。
SENATOR试验的子研究纳入了1537名患有多种疾病的老年住院患者,分别于2016年至2018年在比利时、冰岛、爱尔兰、意大利、苏格兰和西班牙的六家学术教学医院招募,并分析了66种潜在具有临床意义的药物相互作用。描述性分析确定了药物相互作用及相应药物不良反应的患病率/发生率。
基线时(中位年龄:78岁[72, 84],男性占52.8%),存在药物相互作用的患者患病率较高(50.9%),住院期间有所增加(55.2%),12周后降至49.7%。最常见的药物相互作用为:≥2种降钾药物(17.1%)、≥3种中枢作用药物(9.0%)以及选择性5-羟色胺再摄取抑制剂(SSRI)+袢利尿剂/噻嗪类利尿剂(7.2%)。在所有参与者中,三分之一经历了常见(36.6%)/新发(35.8%)的药物不良反应。严重血清电解质紊乱的发生率(10.7%)/患病率(11.5%)最高。新发药物不良反应在存在药物相互作用的患者中更为常见(p = 0.013)。在存在相关且因此可能有因果关系的药物相互作用的患者中,新发跌倒(p = 0.013)、严重便秘(p = 0.004)和严重血清电解质紊乱(p = 0.006)的患病率更高。
临床医生应意识到药物相互作用以及可能导致老年多病住院患者药物不良反应发生率增加的相关药物类别。建议定期重新评估常用药物类别的合理性,并谨慎启动减药。