Sikma Maaike A, Hunault Claudine C, Kirkels Johannes H, Verhaar Marianne C, Kesecioglu Jozef, de Lange Dylan W
Intensive Care and Dutch Poisons Information Center, University Medical Center Utrecht, University Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Dutch Poisons Information Center, University Medical Center Utrecht, University Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Eur J Drug Metab Pharmacokinet. 2018 Jun;43(3):311-320. doi: 10.1007/s13318-017-0453-7.
Acute kidney injury (AKI) is frequently observed after heart transplantation and is associated with morbidity and mortality. However, many confounding factors also contribute to the development of AKI in heart transplants. We hypothesized that supratherapeutic whole-blood tacrolimus trough concentrations are associated with AKI.
In a retrospective observational cohort from April 2005 to December 2012, all adult heart transplantation patients were included. AKI was assessed in the first 2 weeks after transplantation as classified by the Kidney Disease Improving Global Outcomes Network (KDIGO). Whole-blood tacrolimus trough concentrations were determined from day 1 to day 14 and at 1, 3, 6 and 12 months post-transplantation. The therapeutic range was 9 to 15 ng/ml in the first 2 months and tapered to 5-8 ng/ml thereafter. The relationship between supratherapeutic tacrolimus trough concentrations and AKI was evaluated. The impact of various potentially confounding factors on tacrolimus concentrations and AKI was considered.
We included 110 patients. AKI occurred in 57% of patients in the first week. Recovery from AKI was seen in 24%. The occurrence of chronic kidney disease (CKD) was 19% at 1 year. Whole-blood tacrolimus trough concentrations were often supratherapeutic and, despite correction for confounding factors, independently associated with AKI (OR 1.66; 95% CI 1.20-2.31).
Supratherapeutic whole-blood tacrolimus trough concentrations are independently associated with the development of AKI in adult heart transplantation patients. More stringent dosing of tacrolimus early after transplantation may be critical in preserving the kidney function.
心脏移植术后常出现急性肾损伤(AKI),且与发病率和死亡率相关。然而,许多混杂因素也会导致心脏移植患者发生AKI。我们推测,全血他克莫司谷浓度高于治疗水平与AKI有关。
在一项对2005年4月至2012年12月的回顾性观察队列研究中,纳入了所有成年心脏移植患者。根据改善全球肾脏病预后组织(KDIGO)的分类标准,在移植后的前2周评估AKI情况。在移植后第1天至第14天以及移植后1、3、6和12个月测定全血他克莫司谷浓度。治疗范围在最初2个月为9至15 ng/ml,此后逐渐降至5 - 8 ng/ml。评估高于治疗水平的他克莫司谷浓度与AKI之间的关系。考虑了各种潜在混杂因素对他克莫司浓度和AKI的影响。
我们纳入了110例患者。57%的患者在第一周发生AKI。24%的患者AKI得以恢复。1年时慢性肾脏病(CKD)的发生率为19%。全血他克莫司谷浓度常常高于治疗水平,并且尽管对混杂因素进行了校正,但仍与AKI独立相关(比值比1.66;95%置信区间1.20 - 2.31)。
全血他克莫司谷浓度高于治疗水平与成年心脏移植患者AKI的发生独立相关。移植后早期更严格地调整他克莫司剂量对于保护肾功能可能至关重要。