Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange.
Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange.
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DOI:
10.1111/trf.16807
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发表时间:
2022-03
期刊:
影响因子:
2.9
通讯作者:
Fasano RM
中科院分区:
文献类型:
--
作者:
Wade J;Yee MEM;Easley KA;Pahz S;Butler H;Zerra PE;Josephson CD;Fasano RM
Chronic automated red cell exchange (RCE) is increasingly employed for sickle cell disease (SCD). There is a paucity of data on the incidence of RCE adverse events (AEs) and potential patient and procedural risk factors for AEs. A retrospective review of pediatric SCD patients receiving chronic RCE over 3 years was performed to determine the frequency of AEs and identify procedural and patient AE risk factors. AE incidence, AE rate, incidence rate ratios (IRRs), and relative risks (RR) were calculated based on various procedural and patient characteristics by univariable (UV) and multivariable (MV) analyses. In 38 patients receiving 760 procedures, there were 150 (19.7%) AEs, of which 36 (4.7%) were symptomatic AEs. The rate of AEs was 20.2 per 100 person-months [95% CI 17.2, 23.6]. and the rate of symptomatic AEs was 4.8 per 100 person-months [95% CI 3.49, 6.70]. AE incidences were: hypocalcemia (117; 15.4%), dizziness (22; 3.0%), hypotension (15; 2.0%), and nausea (14; 1.8%). Patients with a baseline Hct ≥30% experienced more total AEs and symptomatic AEs. Pre-procedure initial systolic BP < 50th percentile and patients with severe CNS vasculopathy and non SCA phenotype (i.e. HbSC or Sβ+ thalassemia) were associated with an increase in total AEs. IHD depletion was not associated with an increased incidence of AEs or symptomatic AEs. SCD patients with Hct ≥30%, systolic BP <50th percentile, severe CNS vasculopathy and possibly non-SCA genotype may be at higher risk for RCE-related AEs. The effect of IHD on AE risk is likely minimal. Individualized AE risk assessment should be performed in all SCD patients undergoing chronic automated RCE.
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