评估终末期肾功能不全血液透析患者的药物使用情况和潜在的用药不当:巴林一家三级医院的研究。

Pub Date : 2024-01-01 DOI:10.3233/JRS-230004
Kannan Sridharan
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引用次数: 0

摘要

背景:透析患者在使用多种药物、使用可能不适当的药物和具有潜在毒性风险的药物方面面临治疗挑战:本研究评估了血液透析患者的药物使用情况、潜在的不适当药物(PIM)、有发生 Torsades de Pointes(TdP)风险的药物以及处方方案的复杂性,并使用了药物方案复杂性指数量表:在接受血液透析的患者中开展了一项回顾性队列研究。药物分为四类:(i) 用于治疗肾脏并发症的药物;(ii) 心血管药物;(iii) 抗糖尿病药物;(iv) 对症治疗药物;(v) 其他。根据加拿大肾脏病医疗专业人员网络的 Can-SOLVE CKD 工作组的意见,药物被视为 PIM。该研究遵循 CredibleMeds 对已知、可能和有条件发生 TdP 风险的药物进行的分类,并根据预先验证的用药方案复杂性指数表对处方药的复杂性进行了评估,该指数表以形式/途径、用药频率和特殊说明要求为基础:研究共纳入 63 名参与者(49 名男性和 14 名女性),年龄中位数(范围)为 45(21-66)岁。最常见的用药类别是心血管药物,其次是治疗肾脏并发症的药物。值得注意的是,12 名患者(19.1%)服用了一种非甾体抗炎药,21 名患者(33.3%)服用了质子泵抑制剂,3 名患者(4.8%)服用了普瑞巴林,2 名患者(3.2%)服用了阿片类药物,1 名患者(1.6%)服用了塞来昔布。阿托伐他汀、呋塞米、奥美拉唑和别嘌醇是研究参与者最常服用的 PIM 药物,其次是其他药物。与其他类药物相比,用于对症治疗的药物的 PIM 值明显更高(P 结 论):血液透析患者的药物治疗负担沉重,PIM 比例较高,医疗方案复杂,处方药物有引发 TdP 的风险。因此,有必要使用临床决策支持工具来提高处方的合理性,并识别具有 TdP 风险的药物,引入抗菌药物管理,逐步停用效益风险比最低的药物。
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Assessment of drug utilization and potentially inappropriate medications in hemodialysis patients with end-stage renal dysfunction: A study in a tertiary care hospital in Bahrain.

Background: Patients undergoing dialysis pose therapeutic challenges in terms of polypharmacy, administration of potentially inappropriate drugs, and drugs with the potential risk of toxicity.

Objective: This study evaluated the use of drugs, potentially inappropriate medicines (PIM), drugs with risk of Torsades de Pointes (TdP), and the complexity of the prescribed regimen using the medication regimen complexity index scale in patients undergoing hemodialysis.

Methods: A retrospective cohort study was carried out amongst patients receiving hemodialysis. Drugs were classified into one of four classes: (i) drugs used in managing renal complications, (ii) cardiovascular drugs, (iii) anti-diabetic drugs, (iv) drugs for symptomatic management, and (v) others. Drugs were considered as PIM according to the Can-SOLVE CKD working group from a network of Canadian nephrology health professionals. The study adhered to the CredibleMeds classification of drugs with known, possible, and conditional risk of TdP and the complexity of prescribed medicines was evaluated based on the pre-validated medication regimen complexity index scale based on form/route, frequency of dosing, and requirement of special instructions.

Results: Sixty-three participants were included in the study (49 males and 14 females) with the median (range) age of 45 (21-66) years. Cardiovascular drugs followed by drugs used for managing renal complications were the most common classes administered. Notably, 12 (19.1%) patients received one of the non-steroidal anti-inflammatory drugs, 21 (33.3%) received a proton pump inhibitor, three (4.8%) received pregabalin, two (3.2%) received opioid drugs, and one (1.6%) was administered celecoxib. Atorvastatin, furosemide, omeprazole, and allopurinol were the most common PIM drugs administered to the study participants followed by others. Drugs used for symptomatic management had significantly more PIM compared to other classes (p < 0.0001). Six (9.5%) patients received drugs with known TdP risk, one with possible TdP risk, and 61 with conditional risk. Median (range) medical regimen complexity index score was 26.5 (2-62.5).

Conclusion: A huge burden of drug therapy was observed in the hemodialysis patients in terms of higher proportions of PIM, complex medical regimen, and prescription of drugs with risk of TdP. Implementation of clinical decision support tools enhancing rational prescription and identification of drugs with TdP risk, introducing antimicrobial stewardship, and stepwise deprescription of the drugs with the least benefit-risk ratio are warranted.

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