Pharmacy Services, Mayo Clinic, Rochester, Minnesota.
Division of Pediatric Hematology/Oncology, St Louis Children's Hospital, St Louis, Missouri.
Pediatr Blood Cancer. 2021 Mar;68(3):e28872. doi: 10.1002/pbc.28872. Epub 2021 Jan 5.
To evaluate the correlation between an uncapped, actual body weight-based unfractionated heparin dosing strategy, we performed a body mass index-based subanalysis of a previously reported pediatric cohort. Nearly half (45%) of obese patients were supra-therapeutic on initial anti-FXa assessment. Obese patients achieved therapeutic anti-FXa significantly faster than nonobese patients (median 4 vs 12 hours, P = .0192) and were more likely to have any supra-therapeutic anti-FXa levels (77% vs 35%; P = .0021). There was no statistically significant difference in major or clinically relevant nonmajor bleeding rates between weight categories (P = .69). Prospective pediatric studies are warranted to confirm our findings.
为了评估无上限、实际基于体重的未分级肝素给药策略的相关性,我们对先前报道的儿科队列进行了基于体重指数的亚组分析。近一半(45%)肥胖患者在初始抗 FXa 评估时处于超治疗范围。与非肥胖患者相比,肥胖患者达到治疗性抗 FXa 的速度明显更快(中位数 4 小时 vs 12 小时,P=0.0192),并且更有可能出现任何超治疗范围的抗 FXa 水平(77% vs 35%;P=0.0021)。在体重类别之间,主要或临床上显著非主要出血率没有统计学上的显著差异(P=0.69)。需要进行前瞻性儿科研究来证实我们的发现。