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心脏移植受者中合并用药与免疫抑制剂相比药物不依从的流行率:来自国际横断面 BRIGHT 研究的结果。

Prevalence of Medication Nonadherence to Co-medication Compared to Immunosuppressants in Heart Transplant Recipients: Findings From the International Cross-sectional BRIGHT Study.

机构信息

Institute of Nursing Science, Department Public Health, Faculty of Medicine, University of Basel, Basel, Switzerland.

Hospital Municipal Vila Santa Catarina - Ministério da Saúde PROADI-SUS, São Paulo, Brazil; School of Nursing, Federal University of São Paulo, São Paolo, Brazil.

出版信息

Clin Ther. 2019 Jan;41(1):130-136. doi: 10.1016/j.clinthera.2018.11.007. Epub 2018 Dec 24.

Abstract

PURPOSE

To assess and compare the prevalence of medication nonadherence (MNA) (implementation and persistence) to immunosuppressants and co-medications in heart transplant recipients.

METHODS

MNA prevalence was assessed using the Basel Assessment of Adherence to Immunosuppressive Medications Scale (self-report) and compared using logistic regression in a 4-continent sample of 1397 heart transplant recipients from 36 heart transplant centers in 11 countries.

FINDINGS

MNA was significantly (α = 0.05) higher to co-medications than to immunosuppressants (taking nonadherence: 23.9% vs 17.3%; odds ratio [OR] = 1.5; 95% CI, 1.30-1.73; drug holiday: 5.7% vs 1.9%; OR = 3.17; 95% CI, 2.13-4.73; dose alteration: 3.8% vs 1.6%; OR = 2.46; 95% CI, 1.49-4.06; and discontinuation: 2.6% vs 0.5%; OR = 5.15; 95% CI, 2.36-11.20).

IMPLICATIONS

The observed MNA necessitates adherence-enhancing interventions encompassing the entire post-heart transplant medication regimen. ClinicalTrials.gov identifier: NCT01608477.

摘要

目的

评估和比较心脏移植受者免疫抑制剂和合并用药的用药不依从(MNA)(执行和坚持)的发生率。

方法

使用巴塞尔评估免疫抑制药物依从性量表(自我报告)评估 MNA 的发生率,并在来自 11 个国家的 36 个心脏移植中心的 1397 名心脏移植受者的 4 大洲样本中使用逻辑回归进行比较。

发现

与免疫抑制剂相比,合并用药的 MNA 显著更高(不依从:23.9%比 17.3%;比值比[OR]为 1.5;95%可信区间,1.30-1.73;药物假期:5.7%比 1.9%;OR 为 3.17;95%可信区间,2.13-4.73;剂量调整:3.8%比 1.6%;OR 为 2.46;95%可信区间,1.49-4.06;停药:2.6%比 0.5%;OR 为 5.15;95%可信区间,2.36-11.20)。

意义

观察到的 MNA 需要包含整个心脏移植后药物治疗方案的增强依从性干预措施。临床试验注册号:NCT01608477。

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