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红细胞葡萄糖-6-磷酸脱氢酶缺乏对登革出血热患者的影响。

Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic fever.

作者信息

Tanphaichitr Voravarn S, Chonlasin Rachaneekorn, Suwantol Lerlugsn, Pung-Amritt Parichat, Tachavanich Kalaya, Yogsan Suthee, Viprakasit Vip

机构信息

Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 2002 Aug;85 Suppl 2:S522-9.

Abstract

Eighty nine males aged 1-13 years diagnosed with dengue haemorrhagic fever (DHF) and admitted to the Department of Pediatrics Siriraj Hospital from March 1998 to April 2000 were included in this study. 17 cases (19.1%) had red blood cell glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and 72 cases (80.9%) had normal G-6-PD enzyme activities. Most of the patients were classified as DHF grade II in severity. 3 of 17 G-6-PD deficient cases had serious complications and all of them had acute intravascular hemolysis requiring blood transfusions. One of these also had hematemesis, one had azothemia and the other one had renal failure and severe liver failure with hepatic encephalopathy. In the cases without obvious hemolytic or hepatic complications, G-6-PD deficient cases had mildly but significantly higher total birirubin and indirect bilirubin, as well as a lower hematocrit than those who had normal G-6-PD. Reticulocyte count was low during the acute phase, however, during recovery, the levels were significantly increased in both groups. In the non G-6-PD deficient group, G-6-PD enzyme levels were significantly decreased during the acute phase compared to the normal controls but rose significantly to normal levels during the recovery phase. There were no statistically significant differences in other laboratory data. All patients recovered fully from DHF. The prevalence of G-6-PD deficiency in male patients who had DHF in this study was 19.1 per cent which was higher than the prevalence in a previous study of 12 per cent in Bangkok. This may imply that G-6-PD deficient males suffer more from DHF compared to normal G-6-PD subjects.

摘要

1998年3月至2000年4月期间,89名年龄在1至13岁、被诊断为登革出血热(DHF)并入住诗里拉吉医院儿科的男性患者被纳入本研究。17例(19.1%)有红细胞葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症,72例(80.9%)G-6-PD酶活性正常。大多数患者的严重程度被归类为DHF二级。17例G-6-PD缺乏症患者中有3例出现严重并发症,均有急性血管内溶血,需要输血。其中1例还出现呕血,1例出现氮血症,另1例出现肾衰竭和严重肝功能衰竭伴肝性脑病。在无明显溶血或肝脏并发症的病例中,G-6-PD缺乏症患者的总胆红素和间接胆红素略高但显著高于G-6-PD正常的患者,血细胞比容也较低。急性期网织红细胞计数较低,但恢复期两组的网织红细胞计数均显著增加。在非G-6-PD缺乏组中,急性期G-6-PD酶水平与正常对照组相比显著降低,但恢复期显著上升至正常水平。其他实验室数据无统计学显著差异。所有患者均从DHF中完全康复。本研究中患DHF的男性患者中G-6-PD缺乏症的患病率为19.1%,高于之前在曼谷进行的一项研究中的12%患病率。这可能意味着与G-6-PD正常的受试者相比,G-6-PD缺乏的男性患DHF的情况更严重。

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