[Influence of white blood cells count on parasite density in Malaria in children aged 6 to 59 months in Benin].

Tatiana Baglo, Alban Gildas Comlan Zohoun, Lutécia Zohoun, Antoine Sianou, Dorothée Kindé Gazard
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The gold standard technique for diagnosis is the thick drop combined with the calculation of parasite density (PD), which is determined on the basis of the number of parasites counted in a microscopic field against a proposed standard number of leukocytes. The number of leukocytes used to calculate the parasite density should ideally be the actual number of leukocytes in the patient per cubic millimetre of blood. However, in the absence of the availability of a blood count at the time of the thick drop, an average number of 8 000 leukocytes/mm<sup>3</sup> was used by the World Health Organisation (WHO) to estimate the parasite density. Nonetheless, in Benin the average number of leukocytes adopted by the National Malaria Control Programme (PNLP) is 6 000/mm<sup>3</sup>. 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Abstract

Background: For many years, the treatment of malaria was based on clinical presumptive diagnosis, making its differential diagnosis with other causes of hyperthermia difficult. This drug pressure has led to the emergence of Plasmodium strains resistant to the most commonly used antimalarial drugs. This is why in 2004, the health authorities decided to revise the policy of malaria management by adopting a new strategy based on the rational use of artemisininbased combination therapies after the biological confirmation of suspected malaria cases. The biological diagnosis is an essential part of malaria management. The gold standard technique for diagnosis is the thick drop combined with the calculation of parasite density (PD), which is determined on the basis of the number of parasites counted in a microscopic field against a proposed standard number of leukocytes. The number of leukocytes used to calculate the parasite density should ideally be the actual number of leukocytes in the patient per cubic millimetre of blood. However, in the absence of the availability of a blood count at the time of the thick drop, an average number of 8 000 leukocytes/mm3 was used by the World Health Organisation (WHO) to estimate the parasite density. Nonetheless, in Benin the average number of leukocytes adopted by the National Malaria Control Programme (PNLP) is 6 000/mm3. The aim of our study was to determine the impact of the leukocyte count on the calculation of the parasite density in cases of uncomplicated malaria.

Method: The study was a cross-sectional study with an analytical aim and took place in 2 hospitals in Benin, the Klouékanmey zone hospital in the south of Benin and the Djougou health centre in the north. It involved a population of 476 children aged between 6 and 59 months who were seen in consultation and in whom the clinical diagnosis of simple Plasmodium falciparum malaria was suspected. Children aged between 6 and 59 months, weighing at least 5 kg, with an axillary temperature ≥ 37.5°C at the time of consultation or a history of fever in the last 24 hours or other symptoms pointing to the diagnosis of malaria were included. Infestation was mono-specific for Plasmodium falciparum. Informed consent was required from the child's parents or guardian. The criteria for non-inclusion in our study were the presence of at least one sign of malaria severity, signs of severe malnutrition or a febrile state related to underlying infectious diseases other than malaria. Thick blood count and haemogram were systematically performed in all included children. Parasite density was calculated according to 3 methods, first using a weighted leukocyte count of 6 000/mm3 recommended by the Benin National Malaria Control Programme (PNLP), then a leukocyte count of 8 000/mm3 recommended by the World Health Organisation and finally the patient's actual leukocyte count obtained from the blood count. It should be noted that these different samples were respectively taken on the day of inclusion in compliance with the conditions of the pre-analytical phase in force in our medical biology laboratory.

Results: At the end of our study, 313 children, i.e. 65.76% of our study population had a positive white blood cell count with a positivity rate of 62.14% in Djougou, i.e. 174 children, and 70.9% in Klouékanmey, i.e. 139 children. The average leukocyte count in these children was 11,580/mm3. Among them, 205 children had an abnormal white blood cell count, i.e. 17 cases of leukopenia (5.43%) and 188 cases of hyperleukocytosis (60.06%). Using successively the average number of 6 000 leukocytes/mm3 proposed by the Benin PNLP and that of 8 000 leukocytes/mm3 proposed by the WHO, the average parasite densities were respectively 47,943 and 63,936 trophozoïtes/µl against 92,290 trophozoïtes/µl when the real number of leukocytes of the patients was used for the calculation of the PD. By using an average of 6 000 leukocytes/mm3 for PD calculation, 60% of the calculated PDs were underestimated and 6% were overestimated. Using an average of 8 000 leukocytes/mm3 resulted in 49% of PD being underestimated and 15% being overestimated. The difference between the three calculation methods was considered statistically significant (p value <0.05).

Conclusion: The use of 6 000 or 8 000 coefficients for the estimation of parasitaemia could lead to a significant underestimation of the parasite load.

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[白细胞计数对贝宁6 ~ 59月龄儿童疟疾寄生虫密度的影响]。
背景:多年来,疟疾的治疗是基于临床推定诊断,使其与其他热疗原因的鉴别诊断困难。这种药物压力导致出现了对最常用的抗疟疾药物具有耐药性的疟原虫菌株。正因为如此,卫生当局于2004年决定修订疟疾管理政策,在对疑似疟疾病例进行生物学确认后,采用一项基于合理使用青蒿素类复方疗法的新战略。生物学诊断是疟疾管理的重要组成部分。诊断的金标准技术是厚滴结合寄生虫密度(PD)的计算,这是根据在显微镜场中计算的寄生虫数量和建议的标准白细胞数量来确定的。理想情况下,用于计算寄生虫密度的白细胞数量应该是患者每立方毫米血液中白细胞的实际数量。然而,由于在厚滴时没有可用的血液计数,世界卫生组织(世卫组织)使用平均8000个白细胞/mm3来估计寄生虫密度。然而,在贝宁,国家疟疾控制规划采用的白细胞平均数量为6 000/立方毫米。我们研究的目的是确定白细胞计数对计算无并发症疟疾病例中寄生虫密度的影响。方法:本研究是一项具有分析目的的横断面研究,在贝宁的2家医院、贝宁南部的klou kanmey区医院和北部的Djougou保健中心进行。它涉及476名年龄在6至59个月之间的儿童,他们在咨询中被诊断为单纯恶性疟原虫疟疾。包括年龄在6至59个月之间、体重至少5公斤、会诊时腋窝温度≥37.5℃或过去24小时内有发热史或其他表明疟疾诊断的症状的儿童。恶性疟原虫的侵袭是单一特异性的。需要获得儿童父母或监护人的知情同意。不纳入我们研究的标准是存在至少一种疟疾严重程度的迹象,严重营养不良的迹象或与疟疾以外的潜在传染病相关的发热状态。对所有纳入的儿童进行了系统的血球计数和血象检查。根据3种方法计算寄生虫密度,首先使用贝宁国家疟疾控制规划(PNLP)推荐的加权白细胞计数6 000/mm3,然后使用世界卫生组织推荐的白细胞计数8 000/mm3,最后使用从血液计数中获得的患者实际白细胞计数。值得注意的是,这些不同的样品是在纳入当天分别按照我们医学生物学实验室现行的分析前阶段的条件进行的。结果:研究结束时,313名儿童白细胞计数阳性,占研究人群的65.76%,其中朱沟县174名儿童阳性率为62.14%,克鲁萨梅县139名儿童阳性率为70.9%。这些儿童的平均白细胞计数为11,580/mm3。其中白细胞计数异常205例,其中白细胞减少17例(5.43%),白细胞增多188例(60.06%)。依次采用贝宁PNLP提出的平均白细胞数6 000个/mm3和WHO提出的平均白细胞数8 000个/mm3计算PD时,平均寄生虫密度分别为47,943和63,936 trophozoïtes/µl,而采用患者实际白细胞数计算PD时,平均寄生虫密度为92,290 trophozoïtes/µl。通过使用平均6 000个白细胞/mm3计算PD, 60%的计算PD被低估,6%的计算PD被高估。使用平均8000个白细胞/mm3导致49%的PD被低估,15%被高估。结论:采用6 000或8 000系数估算寄生虫血症可能导致寄生虫负荷的严重低估。
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