Heart Transplant Unit and Pharmacy Department, Hospital de la Santa Creu i Santa Pau, Barcelona, Spain.
UAB Medicine Department, Autonomous University of Barcelona (UAB), Barcelona, Spain.
Clin Transplant. 2019 Oct;33(10):e13682. doi: 10.1111/ctr.13682. Epub 2019 Aug 28.
Multimorbidity and therapeutic complexity are a recognized problem in the heart transplant (HTx) population. However, little is known about how best to quantify this complexity or the strategies that could reduce its burden.
This single-center, observational study included adult heart transplant recipients (HTxR) >1.5 years from transplant. We assessed multimorbidity (>2 comorbidities) and the patient-level Medication Regimen Complexity Index Spanish version (pMRCI-S) score. We also analyzed the independent predictors of pMRCI-S and the impact of the index score on specific clinical variables.
We included 135 chronic-stage HTxR. Comorbidities significantly increased after HTx (6 ± 3 vs 2 ± 2, P-value < .001). Patients took 12 ± 3 chronic drugs/d, 58% of them to treat comorbidities. The mean total pMRCI-S score was 42 ± 11, higher than in several other chronic diseases. The medication category drugs to treat comorbidities predicted a higher total pMRCI-S score (OR = 3.12, 95% CI 2.8-3.43, P-value < .001). Therapeutic complexity after HTx had an impact on solid malignancies (OR = 1.1, 95% CI 1.02-1.18, P-value = .02) and renal function (OR=-0.81, 95% CI -1.21-(-0.42), P-value < .001).
The multimorbidity and pMRCI-S scores obtained in HTx population were worrisomely high. The pMRCI score is a sensitive method that allows identification of the factors determining therapeutic complexity after HTx and selection of strategies to reduce pMRCI-S values.
多发病和治疗复杂性是心脏移植(HTx)人群中公认的问题。然而,对于如何最好地量化这种复杂性或降低其负担的策略知之甚少。
这是一项单中心、观察性研究,纳入了移植后超过 1.5 年的成年心脏移植受者(HTxR)。我们评估了多发病(>2 种合并症)和患者水平药物治疗方案复杂性指数西班牙语版(pMRCI-S)评分。我们还分析了 pMRCI-S 的独立预测因素及其对特定临床变量的影响。
我们纳入了 135 名慢性期 HTxR。合并症在 HTx 后显著增加(6 ± 3 与 2 ± 2,P 值<.001)。患者每天服用 12 ± 3 种慢性药物,其中 58%用于治疗合并症。平均总 pMRCI-S 评分为 42 ± 11,高于其他几种慢性疾病。治疗合并症的药物类别药物预测了更高的总 pMRCI-S 评分(OR = 3.12,95%CI 2.8-3.43,P 值<.001)。HTx 后的治疗复杂性对实体恶性肿瘤(OR = 1.1,95%CI 1.02-1.18,P 值=.02)和肾功能(OR = -0.81,95%CI -1.21-(-0.42),P 值<.001)有影响。
HTx 人群中获得的多发病和 pMRCI-S 评分高得令人担忧。pMRCI 评分是一种敏感的方法,可以确定确定 HTx 后治疗复杂性的决定因素,并选择降低 pMRCI-S 值的策略。