Hospital Pharmacy, University Hospital, LMU Munich, Munich, Germany.
Doctoral Program Clinical Pharmacy, University Hospital, LMU Munich, Munich, Germany.
J Clin Pharm Ther. 2022 May;47(5):676-684. doi: 10.1111/jcpt.13597. Epub 2022 Jan 10.
Hepatic impairment (HI) is a known risk factor for drug safety. The MELD score (Model-for-endstage-liver-disease), calculated from serum creatinine, bilirubin and International Normalized Ratio (INR), is a promising screening tool corresponding to Child-Pugh Score (CPS) for drug adjustment. We tested the feasibility of MELD as an automatic screening tool accounting for correct calculation, interfering factors (IF) and detection of patients corresponding to CPS-B/C potentially requiring drug adjustment.
We retrospectively calculated MELD for a 3-month cohort of surgical patients and assessed need for adjustment of MELD parameters to standard values. IF for INR (oral anticoagulants) and serum creatinine (renal insufficiency (RI; eGFR<60 ml/min/1.73m²); as well as drugs elevating creatinine levels (DECL)) and the number of patients with MELD scores corresponding to CPS-B/C were analysed. For MELD ≥7.5, liver and bile diagnoses were recorded.
Of 1183 patients, MELD was calculable for 761 (64%; median 7.5, range 6.4-36.8). Parameters had to be adjusted for 690 (91%) patients. IF of parameters were RI in 172 (23%), INR-elevating drugs in 105 (14%) and DECL in 33 (4%) patients. Of 335 (44%) patients with MELD ≥7.5, 122 (36%) had documented liver or bile diagnoses. MELD 10-<15 (corresponding to CPS-B) was found for 105 (14%), MELD ≥15 (corresponding to CPS-C) for 66 (9%) of the 761 patients with a calculated MELD. Referred to all patients, drug adjustments due to possible HI were recommendable for 14% of patients with suspected CPS-B/C.
MELD is a feasible screening tool for HI as a risk factor for drug safety at hospital admission when appropriately considering correct parameter adjustment and RI and INR-elevating drugs as IF. Further evaluation of sensitivity and specificity is needed.
肝损伤(HI)是药物安全性的已知风险因素。MELD 评分(终末期肝病模型)由血清肌酐、胆红素和国际标准化比值(INR)计算得出,是一种有前途的药物调整筛选工具,与 Child-Pugh 评分(CPS)相对应。我们测试了 MELD 作为一种自动筛选工具的可行性,该工具可以考虑正确计算、干扰因素(IF)和检测对应于 CPS-B/C 可能需要药物调整的患者。
我们回顾性地计算了 3 个月手术患者队列的 MELD,并评估了调整 MELD 参数以符合标准值的必要性。分析了 INR(口服抗凝剂)和血清肌酐(肾功能不全(eGFR<60ml/min/1.73m²);以及升高肌酐水平的药物(DECL)的 IF)和 MELD 评分对应于 CPS-B/C 的患者数量。对于 MELD≥7.5,记录了肝脏和胆汁的诊断。
在 1183 名患者中,761 名(64%;中位数 7.5,范围 6.4-36.8)可计算 MELD。需要调整参数的患者为 690 名(91%)。参数的 IF 为肾功能不全的患者 172 名(23%),INR 升高药物的患者 105 名(14%)和 DECL 的患者 33 名(4%)。在 335 名(44%)MELD≥7.5 的患者中,有 122 名(36%)有记录的肝脏或胆汁诊断。发现 105 名(14%)患者的 MELD 为 10-<15(对应于 CPS-B),66 名(9%)患者的 MELD≥15(对应于 CPS-C)。在所有患者中,由于可能的 HI 而推荐调整药物的患者比例为疑似 CPS-B/C 患者的 14%。
当适当考虑正确的参数调整和 RI 以及 INR 升高的药物作为 IF 时,MELD 是入院时药物安全性的 HI 风险因素的一种可行的筛选工具。需要进一步评估其敏感性和特异性。