Incident Stroke in Pediatric Sickle Cell Anemia Despite Overall Improved Transcranial Doppler Velocity in a Ugandan Hydroxyurea Trial: Antecedent and Ongoing Risks.

IF 2.4 3区 医学 Q2 HEMATOLOGY
Bill Wambaka, Amiirah Mpungu, Vincent Mboizi, Dennis Kalibbala, Grace Nambatya, Susan Murungi, Maxencia Kabatabaazi, Maria Nakafeero, Phillip Kasirye, Deogratias Munube, Ruth Namazzi, Richard Idro, Nancy S Green
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Abstract

Introduction: Transcranial Doppler ultrasound (TCD) screening for primary stroke prevention in children with sickle cell anemia (SCA) was established in higher-resource regions, targeting interventions for highest velocity ("abnormal"). We sought to identify additional stroke risk factors in Uganda.

Methods: We conducted a 30-month open-label single-arm Ugandan hydroxyurea trial, dose-escalated to maximum-tolerated dose, aimed to test brain protection for children aged 3-9 years with SCA. Study procedures included history, clinical stroke examination, and prospective TCD and laboratory assessments.

Results: Overall, 264 children received study HU, mean age 5.6 ± 1.7, hemoglobin 7.8 ± 1.2 g/dL, fetal hemoglobin (HbF) 11.9% ± 8.1%, enrolment TCD mean TAMV 148.4 ± 29.3 cm/sec; 15 (5.7%) had abnormal TCD. The mean TAMV at trial completion was 131.9 ± SD 25.7 cm/sec. Four participants without abnormal enrolment TCD developed acute stroke within the initial 16 months (incidence 0.62 per 100 person-years): two had enrolment HbF ≤3.1%, two had low oxygen saturation (90%), and one had recurring severe anemia necessitating multiple transfusions. Apparent stroke precipitants were severe malaria, acute chest syndrome, recent pain crisis, or uncertain cause. At trial completion, eight additional participants had a higher risk TCD category than at enrolment.

Conclusion: The effectiveness of TCD screening for stroke prevention may vary by region, as no participant with an incident stroke was at the highest risk. Antecedent and/or ongoing SCA-related risks of anemia, low HbF, hypoxemia, infections, and/or disease complications likely contributed to stroke despite trial HU. Results suggest that TCD alone may not fully identify the highest stroke risk in the region, and there is a need for primary stroke prevention from early childhood and continuous hydroxyurea therapy.

在乌干达的一项羟脲试验中,尽管经颅多普勒速度总体改善,儿童镰状细胞性贫血的卒中事件:先前和正在进行的风险。
简介:经颅多普勒超声(TCD)筛查用于镰状细胞性贫血(SCA)儿童初级卒中预防在资源较高的地区建立,针对最高速度(“异常”)的干预措施。我们试图确定乌干达的其他中风危险因素。方法:我们进行了一项为期30个月的乌干达开放标签单臂羟脲试验,剂量递增至最大耐受剂量,旨在测试3-9岁SCA患儿的脑保护作用。研究程序包括病史、临床卒中检查、前瞻性TCD和实验室评估。结果:总体而言,264名儿童接受了研究HU,平均年龄5.6±1.7岁,血红蛋白7.8±1.2 g/dL,胎儿血红蛋白(HbF) 11.9%±8.1%,入组TCD平均TAMV 148.4±29.3 cm/sec;TCD异常15例(5.7%)。试验结束时的平均TAMV为131.9±SD 25.7 cm/sec。4名未出现异常入组TCD的参与者在最初16个月内发生急性卒中(发病率0.62 / 100人年):2名入组HbF≤3.1%,2名低氧饱和度(90%),1名复发性严重贫血需要多次输血。明显的中风前兆是严重疟疾、急性胸综合征、近期疼痛危象或不明原因。在试验结束时,另外8名参与者的TCD类别风险高于入组时。结论:TCD筛查预防脑卒中的有效性可能因地区而异,因为没有参与者的卒中发生率最高。尽管试验HU,但先前和/或持续的sca相关贫血、低HbF、低氧血症、感染和/或疾病并发症可能导致卒中。结果表明,仅TCD可能无法完全识别该地区最高卒中风险,需要从儿童早期开始进行初级卒中预防并持续进行羟基脲治疗。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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