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Plasmodium vevax and P. falciparum: Biological interactions and the possibility of cross-species immunity.间日疟原虫和恶性疟原虫:生物学相互作用及种间免疫的可能性。
Parasitol Today. 1997 Jun;13(6):227-31. doi: 10.1016/s0169-4758(97)01061-2.
2
Recovery from acute haemorrhage in normal men and women.正常男性和女性急性出血后的恢复情况。
J Physiol. 1955 Sep 28;129(3):583-93. doi: 10.1113/jphysiol.1955.sp005380.
3
Treatment of vivax malaria on the western border of Thailand.泰国西部边境间日疟的治疗
Trans R Soc Trop Med Hyg. 1999 Jul-Aug;93(4):433-8. doi: 10.1016/s0035-9203(99)90149-9.
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Red blood cell deformability as a predictor of anemia in severe falciparum malaria.红细胞变形性作为重症恶性疟贫血的预测指标。
Am J Trop Med Hyg. 1999 May;60(5):733-7. doi: 10.4269/ajtmh.1999.60.733.
5
Artesunate versus artemether for the treatment of recrudescent multidrug-resistant falciparum malaria.青蒿琥酯与蒿甲醚治疗复发性耐多药恶性疟的疗效比较
Am J Trop Med Hyg. 1998 Dec;59(6):883-8. doi: 10.4269/ajtmh.1998.59.883.
6
Chloroquine treatment for uncomplicated childhood malaria in an area with drug resistance: early treatment failure aggravates anaemia.在一个存在耐药性的地区,氯喹治疗儿童单纯性疟疾:早期治疗失败会加重贫血。
Trans R Soc Trop Med Hyg. 1998 Sep-Oct;92(5):556-60. doi: 10.1016/s0035-9203(98)90913-0.
7
Artesunate and mefloquine in the treatment of uncomplicated multidrug-resistant hyperparasitaemic falciparum malaria.青蒿琥酯和甲氟喹治疗非复杂性多重耐药高疟原虫血症恶性疟
Trans R Soc Trop Med Hyg. 1998 Mar-Apr;92(2):207-11. doi: 10.1016/s0035-9203(98)90750-7.
8
Artesunate/mefloquine treatment of multi-drug resistant falciparum malaria.青蒿琥酯/甲氟喹治疗多重耐药恶性疟
Trans R Soc Trop Med Hyg. 1997 Sep-Oct;91(5):574-7. doi: 10.1016/s0035-9203(97)90032-8.
9
In vivo removal of malaria parasites from red blood cells without their destruction in acute falciparum malaria.在急性恶性疟中,在不破坏疟原虫的情况下从红细胞中进行体内清除疟原虫。
Blood. 1997 Sep 1;90(5):2037-40.
10
The epidemiology of severe malaria in an area of low transmission in Thailand.泰国低传播地区重症疟疾的流行病学
Trans R Soc Trop Med Hyg. 1997 May-Jun;91(3):256-62. doi: 10.1016/s0035-9203(97)90066-3.

单纯性恶性疟后导致贫血的因素。

Factors contributing to anemia after uncomplicated falciparum malaria.

作者信息

Price R N, Simpson J A, Nosten F, Luxemburger C, Hkirjaroen L, ter Kuile F, Chongsuphajaisiddhi T, White N J

机构信息

Shoklo Malaria Research Unit, Mae Sod, Tak Province, Thailand.

出版信息

Am J Trop Med Hyg. 2001 Nov;65(5):614-22. doi: 10.4269/ajtmh.2001.65.614.

DOI:10.4269/ajtmh.2001.65.614
PMID:11716124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4337986/
Abstract

The factors contributing to anemia in falciparum malaria were characterized in 4,007 prospectively studied patients on the western border of Thailand. Of these, 727 patients (18%) presented with anemia (haematocrit < 30%), and 1% (55 of 5,253) required blood transfusion. The following were found to be independent risk factors for anemia at admission: age < 5 years, a palpable spleen, a palpable liver, recrudescent infections, being female, a prolonged history of illness (> 2 days) before admission, and pure Plasmodium falciparum infections rather than mixed P. falciparum and Plasmodium vivax infections. The mean maximum fractional fall in hematocrit after antimalarial treatment was 14.1% of the baseline value (95% confidence interval [CI], 13.6-14.6). This reduction was significantly greater in young children (aged < 5 years) and in patients with a prolonged illness, high parasitemia, or delayed parasite clearance. Loss of parasitized erythrocytes accounted for < 10% of overall red blood cell loss. Hematological recovery was usually complete within 6 weeks, but it was slower in patients who were anemic at admission (adjusted hazards ratio [AHR], 1.9, 95% CI, 1.5-2.3), and those whose infections recrudesced (AHR, 1.2, 95% CI, 1.01-1.5). Half the patients with treatment failure were anemic at 6 weeks compared with 19% of successfully treated patients (relative risk, 2.8, 95% CI, 2.0-3.8). Patients coinfected with P. vivax (16% of the total) were 1.8 (95% CI, 1.2-2.6) times less likely to become anemic and recovered 1.3 (95% CI, 1.0-1.5) times faster than those with P. falciparum only. Anemia is related to drug resistance and treatment failure in uncomplicated malaria. Children aged < 5 years of age were more likely than older children or adults to become anemic. Coinfection with P. vivax attenuates the anemia of falciparum malaria, presumably by modifying the severity of the infection.

摘要

在泰国西部边境对4007例患者进行前瞻性研究,以确定导致恶性疟贫血的因素。其中,727例患者(18%)出现贫血(血细胞比容<30%),1%(5253例中的55例)需要输血。以下因素被发现是入院时贫血的独立危险因素:年龄<5岁、可触及脾脏、可触及肝脏、复发感染、女性、入院前病程延长(>2天)以及单纯恶性疟原虫感染而非恶性疟原虫和间日疟原虫混合感染。抗疟治疗后血细胞比容的平均最大降幅为基线值的14.1%(95%置信区间[CI],13.6 - 14.6)。在幼儿(年龄<5岁)以及病程延长、寄生虫血症高或寄生虫清除延迟的患者中,这种降低更为显著。被寄生红细胞的损失占红细胞总损失量的<10%。血液学恢复通常在6周内完成,但入院时贫血的患者恢复较慢(调整后风险比[AHR],1.9,95%CI,1.5 - 2.3),感染复发的患者也是如此(AHR,1.2,95%CI,1.01 - 1.5)。治疗失败的患者中有一半在6周时贫血,而成功治疗的患者中这一比例为19%(相对风险,2.8,95%CI,2.0 - 3.8)。合并感染间日疟原虫的患者(占总数的16%)发生贫血的可能性比仅感染恶性疟原虫的患者低1.8倍(95%CI,1.2 - 2.6),恢复速度快1.3倍(95%CI,1.0 - 1.5)。贫血与非复杂性疟疾的耐药性和治疗失败有关。年龄<5岁的儿童比年龄较大的儿童或成人更易发生贫血。合并感染间日疟原虫可减轻恶性疟贫血,可能是通过改变感染的严重程度实现的。