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一项在澳大利亚接受心血管药物治疗的人群中进行的多药物使用的全国性研究。

A nationwide study of multimedicine use in people treated with cardiovascular medicines in Australia.

机构信息

Centre for Big Data Research in Health, UNSW Sydney, Sydney, New South Wales, Australia.

St Vincent's Clinical School, UNSW Sydney, Sydney, New South Wales, Australia.

出版信息

Pharmacotherapy. 2022 Nov;42(11):828-836. doi: 10.1002/phar.2735. Epub 2022 Oct 27.

Abstract

STUDY OBJECTIVE

Multimorbidity and multimedicine use are common in people with cardiovascular disease and can lead to harms, such as prescribing errors and drug interactions. We quantified multimedicine use in people treated with cardiovascular medicines in a national sample of Australians.

DESIGN

Cross-sectional study.

DATA SOURCE

Pharmaceutical dispensing claims for a 10% random sample of Australians.

PATIENTS

Australian adults dispensed any cardiovascular medicine between June and August 2019.

INTERVENTION

None.

MEASUREMENTS

We quantified the number and type of cardiovascular and non-cardiovascular medicines dispensed during the study period, and the number of unique prescribers, by age and sex.

MAIN RESULTS

We identified 493,081 people dispensed any cardiovascular medicine (median age = 67 years, 50.2% women). The population prevalence of cardiovascular medicine dispensing increased from 1.7% (n = 10,503) in people 18-34 years to 80.1% (n = 99,271) in people 75-84 years. Cardiovascular medicine dispensing varied by sex; women 18-34 years were more likely to be dispensed any cardiovascular medicine than men (male:female prevalence ratio [PR] = 0.84, 95% confidence interval [CI] = 0.81-0.87), whereas the prevalence of cardiovascular medicine dispensing was higher in men 35-44 years (PR = 1.27, 95% CI 1.24-1.30) and 45-54 years (PR = 1.24, 95% CI 1.22-1.26) and was similar between sexes in people ≥65 years. Overall, both women and men were dispensed a median of 2.0 (interquartile range [IQR] = 1.0-3.0) cardiovascular medicines. Two-thirds of people ≥65 years (73.5%; n = 208,524) were dispensed ≥2 cardiovascular medicines, with 16.6% (n = 6736) of people ≥85 years dispensed five or more. Women and men were dispensed a median of 2.0 (IQR = 1.0-5.0) and 2.0 (IQR = 0.0-4.0) non-cardiovascular medicines, respectively, to treat comorbid conditions, commonly gastroesophageal reflux disease medicines (32.2% of women and 26.6% of men), antibiotics (28.7% of women and 22.4% of men), and antidepressants (26.3% of women and 15.9% of men). One quarter of both sexes had multiple prescribers for their cardiovascular medicines alone, whereas 54.5% (n = 134,939) of women and 49.9% (n = 122,706) of men had multiple prescribers for all medicines.

CONCLUSION

Multimedicine use is common in people treated with cardiovascular medicines and presents a risk for inappropriate prescribing. Understanding the comorbid conditions commonly treated concurrently with cardiovascular disease can help improve co-prescribing guidelines and develop a person-centered approach to multimorbidity treatment.

摘要

研究目的

心血管疾病患者常同时患有多种疾病并使用多种药物,这可能导致用药错误和药物相互作用等不良后果。本研究旨在量化澳大利亚心血管疾病患者心血管药物治疗中的多重用药情况。

设计

横断面研究。

数据来源

澳大利亚随机抽取的 10%的成年人的药品配药记录。

患者

2019 年 6 月至 8 月期间使用任何心血管药物的澳大利亚成年人。

干预措施

无。

测量指标

根据年龄和性别,我们量化了研究期间开具的心血管药物和非心血管药物的种类和数量,以及开具药物的独特医生数量。

主要结果

我们确定了 493081 名使用任何心血管药物的患者(中位数年龄为 67 岁,50.2%为女性)。心血管药物的人群患病率从 18-34 岁人群的 1.7%(n=10503)增加到 75-84 岁人群的 80.1%(n=99271)。心血管药物的使用因性别而异;18-34 岁女性使用任何心血管药物的可能性高于男性(女性:男性患病率比 [PR]为 0.84,95%置信区间 [CI]为 0.81-0.87),而 35-44 岁和 45-54 岁男性使用心血管药物的患病率更高(PR 分别为 1.27 和 1.24,95% CI 分别为 1.24-1.26),≥65 岁人群中男女使用心血管药物的患病率相似。总体而言,女性和男性分别使用了中位数为 2.0(四分位距 [IQR]为 1.0-3.0)和 2.0(IQR 为 0.0-4.0)种心血管药物。≥65 岁的人群中有三分之二(73.5%;n=208524)同时使用≥2 种心血管药物,≥85 岁的人群中有 16.6%(n=6736)同时使用 5 种或更多种药物。女性和男性分别使用中位数为 2.0(IQR 为 1.0-5.0)和 2.0(IQR 为 0.0-4.0)种非心血管药物来治疗合并症,最常见的是胃食管反流病药物(女性占 32.2%,男性占 26.6%)、抗生素(女性占 28.7%,男性占 22.4%)和抗抑郁药(女性占 26.3%,男性占 15.9%)。四分之一的男女患者仅因心血管疾病就有多个开处方的医生,而 54.5%(n=134939)的女性和 49.9%(n=122706)的男性因所有药物都有多个开处方的医生。

结论

心血管药物治疗患者的多重用药情况较为常见,这可能会导致不适当的用药。了解同时治疗心血管疾病的常见合并症有助于改善共病治疗的联合处方指南,并制定以患者为中心的多重疾病治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ba7/9828398/369166d5f2c2/PHAR-42-828-g003.jpg

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