Price R N, Simpson J A, Nosten F, Luxemburger C, Hkirjaroen L, ter Kuile F, Chongsuphajaisiddhi T, White N J
Shoklo Malaria Research Unit, Mae Sod, Tak Province, Thailand.
Am J Trop Med Hyg. 2001 Nov;65(5):614-22. doi: 10.4269/ajtmh.2001.65.614.
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.
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。