Hayward Kelly L, Weersink Rianne A, Bernardes Christina M, McIvor Carolyn, Rahman Tony, Skoien Richard, Clark Paul J, Stuart Katherine A, Hartel Gunter, Valery Patricia C, Powell Elizabeth E
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Faculty of Medicine, The University of Queensland, Woolloongabba, QLD, Australia.
Drugs Real World Outcomes. 2023 Dec;10(4):605-618. doi: 10.1007/s40801-023-00390-2. Epub 2023 Oct 13.
Safe and appropriate use of medicines is essential to improve health outcomes in cirrhosis. However, little is known about the number and type of medicines dispensed to people with cirrhosis in Australia, as this predominantly occurs in the community. We aimed to characterise the prescriptions dispensed to people with cirrhosis and explore changes in the use of medication groups over time.
Pharmaceutical Benefits Scheme data between 1 January 2016 and 30 June 2020 was extracted for consenting CirCare participants (multi-site, prospective, observational study). Prescriptions dispensed from cirrhosis diagnosis until liver transplant or death were included. Safety classifications for dispensed medicines were defined using published evidence-based recommendations. The pattern of medication use was analysed in 6-monthly time intervals. Generalised estimating equations models were used to estimate the change in consumption of medicines over time.
Five hundred twenty-two patients (mean age 60 years, 70% male, 34% decompensated at recruitment) were dispensed 89,615 prescriptions during the follow-up period, representing a median of 136 [interquartile range (IQR) 62-237] prescriptions and a median of 16 (IQR 11-23) unique medicines per patient (total n = 9306 medicines). The most commonly used medicines were proton pump inhibitors (PPIs) (dispensed at least once to 73% of patients), opioids (68%) and antibiotics (89%). Polypharmacy was prevalent, with 59-69% of observed participants in each time period dispensed five or more unique medicines. Prescription medication use increased over time (p < 0.001) independently of age, comorbidity burden and liver disease aetiology. The likelihood of taking PPIs, opioids, antidepressants and inhaled medicines also increased with each successive time period. Use of angiotensin therapies, metformin and statins differed over time between patients with compensated versus decompensated cirrhosis. General practitioners prescribed 69% of dispensed medicines, including a higher proportion of 'unsafe' and 'safety unknown' medicines compared with consultants/specialists (p < 0.001).
Polypharmacy is common in people with cirrhosis and some medication groups may be overused. Pharmacovigilance is required and future medication safety efforts should target high-risk prescribing practices and promote medication rationalisation in the community.
安全、合理用药对于改善肝硬化患者的健康结局至关重要。然而,在澳大利亚,对于肝硬化患者所配药物的数量和种类知之甚少,因为这主要发生在社区。我们旨在描述肝硬化患者的处方特征,并探讨不同药物组的使用随时间的变化情况。
提取了2016年1月1日至2020年6月30日期间CirCare研究参与者(多中心、前瞻性、观察性研究)同意提供的药品福利计划数据。纳入从肝硬化诊断到肝移植或死亡期间所配的处方。根据已发表的循证推荐定义所配药物的安全性分类。以6个月为时间间隔分析用药模式。使用广义估计方程模型估计药物消费随时间的变化。
在随访期间,522名患者(平均年龄60岁,70%为男性,34%在招募时为失代偿期)共配得89,615张处方,每位患者的处方中位数为136张[四分位间距(IQR)62 - 237],每位患者的独特药物中位数为16种(IQR 11 - 23)(药物总数n = 9306种)。最常用的药物是质子泵抑制剂(PPI)(至少给73%的患者配过一次)、阿片类药物(68%)和抗生素(89%)。多重用药很普遍,在每个时间段中,59% - 69%的观察参与者配了五种或更多独特药物。处方用药量随时间增加(p < 0.001),与年龄、合并症负担和肝病病因无关。随着时间的推移,服用PPI、阿片类药物、抗抑郁药和吸入药物的可能性也增加。在代偿期与失代偿期肝硬化患者中,血管紧张素疗法、二甲双胍和他汀类药物的使用随时间有所不同。全科医生开出了69%的所配药物,与顾问医生/专科医生相比,他们开出的“不安全”和“安全性未知”药物比例更高(p < 0.001)。
多重用药在肝硬化患者中很常见,一些药物组可能存在过度使用的情况。需要进行药物警戒,未来的药物安全工作应针对高风险的处方行为,并促进社区用药的合理化。