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红细胞增多性高黏滞血症无症状综合征:部分血浆置换输血的效果

Asymptomatic syndrome of polycythemic hyperviscosity: effect of partial plasma exchange transfusion.

作者信息

Bada H S, Korones S B, Pourcyrous M, Wong S P, Wilson W M, Kolni H W, Ford D L

机构信息

Department of Pediatrics, Boling Center for Developmental Disabilities, University of Tennessee, Memphis.

出版信息

J Pediatr. 1992 Apr;120(4 Pt 1):579-85. doi: 10.1016/s0022-3476(05)82487-4.

Abstract

We determined the cerebral hemodynamic changes in infants with asymptomatic polycythemic hyperviscosity syndrome and whether treatment with partial plasma exchange transfusion (PPET) would affect hemodynamics as well as outcome. From a routine cord blood hematocrit screening, 71 babies were identified as needing to be tested for polycythemic hyperviscosity. In addition to clinical evaluation, each infant had radial artery hematocrit and viscosity determinations, blood gas determinations, cerebral blood flow velocity studies, cranial ultrasonography, and noninvasive intracranial pressure determination. Babies with symptomatic hyperviscosity (n = 17) were treated by PPET, whereas those with asymptomatic hyperviscosity (n = 28) were randomly selected to have PPET (n = 14) or to be observed (n = 14). The remaining babies (n = 26) with normal viscosity served as control subjects. Both hematocrit and viscosity decreased after PPET but remained unchanged in babies with hyperviscosity who were merely observed. Reversal of cerebral blood flow velocity abnormalities was observed after PPET in the infants with symptomatic hyperviscosity, whereas those who had no symptoms had normal results on Doppler studies at the outset, and no significant changes occurred with either PPET or observation. There were two deaths in the group with symptoms. A total of 46 babies returned for follow-up evaluation at a mean age of 30 +/- 7.7 months. Outcome of the control group was no better than that of those who had hyperviscosity, and outcomes did not differ between the babies with symptomatic and those with asymptomatic hyperviscosity, nor between those treated with PPET and those who were only observed. Multivariate analysis revealed that other perinatal risk factors and race rather than polycythemia or PPET, significantly influenced long-term outcome.

摘要

我们确定了无症状性红细胞增多症高黏滞综合征婴儿的脑血流动力学变化,以及部分血浆置换输血(PPET)治疗是否会影响血流动力学及预后。通过常规脐血血细胞比容筛查,确定71例婴儿需要进行红细胞增多症高黏滞血症检测。除临床评估外,每个婴儿均进行了桡动脉血细胞比容和黏度测定、血气测定、脑血流速度研究、头颅超声检查以及无创颅内压测定。有症状性高黏滞血症的婴儿(n = 17)接受PPET治疗,而无症状性高黏滞血症的婴儿(n = 28)被随机分为接受PPET治疗组(n = 14)或观察组(n = 14)。其余黏度正常的婴儿(n = 26)作为对照组。PPET治疗后血细胞比容和黏度均下降,但仅接受观察的高黏滞血症婴儿的这些指标未发生变化。有症状性高黏滞血症的婴儿接受PPET治疗后,脑血流速度异常得到逆转,而无症状的婴儿最初多普勒检查结果正常,PPET治疗或观察均未使其发生显著变化。有症状组有2例死亡。共有46例婴儿在平均年龄30±7.7个月时返回进行随访评估。对照组的预后并不优于高黏滞血症婴儿,有症状和无症状高黏滞血症婴儿的预后无差异,接受PPET治疗和仅接受观察的婴儿预后也无差异。多因素分析显示,其他围产期危险因素和种族而非红细胞增多症或PPET,对长期预后有显著影响。

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