尼日利亚联邦首都地区HAART诊所贫血和疟疾合并感染艾滋病毒的状况:一项横断面研究。

Microbiology insights Pub Date : 2020-10-19 eCollection Date: 2020-01-01 DOI:10.1177/1178636120947680
Nneoma Confidence JeanStephanie Anyanwu, David Jesutobi Oluwatimileyin, Peace Temitope Sunmonu
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引用次数: 1

摘要

背景:疟疾和艾滋病毒是全球公共卫生关注的两种重大感染。疟疾感染是流行发展中国家发病和死亡的主要原因之一,艾滋病患者的合并感染使预后恶化;贫血是感染最常见的血液学结果。研究背景和目的:本研究旨在确定2019年2月至7月期间在阿布贾选定医院就诊的艾滋病毒感染患者中贫血和疟疾合并感染的患病率。方法:对420例12 ~ 67岁艾滋病病毒阳性患者采用酶免疫分析法和显微镜法进行疟疾检测。使用结构化问卷来获取社会人口统计学和危险因素(使用疟疾预防措施的频率、贫血史、血型、疟疾病史和CD4+计数),同时使用微红细胞压积仪检查包装细胞体积以确定贫血状态。采用IBM SPSS v25对数据进行分析。结果:研究参与者的平均年龄为37.5岁(±12.48岁)。共有142份(33.8%)样本呈疟疾阳性,68名艾滋病毒感染者(16.2%)贫血;420例患者中4.8%同时存在疟疾合并感染和贫血。男性合并感染疟疾者较多(36.0%,P = 0.617),女性合并感染贫血者较多(22.7%,P = 0.058)。61至70岁的患者疟疾发病率最高,51至60岁的患者贫血率最高。除CD4+计数正常的患者外,暴露于评估危险因素较多的患者合并感染和贫血较多。疟疾合并感染对贫血的发病没有显著影响。镜检对酶免疫分析(EIA)的有效性检测灵敏度为83.1%,特异性为98.6%。这些变量与患者的寄生虫病密度无相关性。结论:该研究强调,与该地区以前的报告相比,艾滋病毒患者中疟疾合并感染和贫血的发生率更高,尽管合并感染并未显著影响贫血状况。鉴于这一趋势,必须制定策略来遏制这些疾病。还提倡进行人口研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Status of Anaemia and Malaria Co-infection With HIV From HAART Clinics in Federal Capital Territory, Nigeria: A Cross-Sectional Study.

Status of Anaemia and Malaria Co-infection With HIV From HAART Clinics in Federal Capital Territory, Nigeria: A Cross-Sectional Study.

Status of Anaemia and Malaria Co-infection With HIV From HAART Clinics in Federal Capital Territory, Nigeria: A Cross-Sectional Study.

Status of Anaemia and Malaria Co-infection With HIV From HAART Clinics in Federal Capital Territory, Nigeria: A Cross-Sectional Study.

Background: Malaria and HIV are 2 significant infections of critical public health concern globally. Malaria infection is one of the preceding causes of morbidity and mortality in endemic developing countries, and its co-infections in HIV patients worsen prognosis; with anaemia being the most common haematologic outcome of the infections.

Context and purpose of study: This study was aimed at determining the prevalence of anaemia and malaria co-infection among HIV-infected patients attending selected hospitals in Abuja between February and July 2019.

Methods: A cross-sectional study was carried out to detect malaria in 420 HIV-positive patients who were 12 to 67 years old, using enzyme immunoassay and microscopy. A structured questionnaire was used to capture socio-demographic and risk factors ([Frequency of] Use of Malaria preventive Measures, History of anaemia, Blood type, malaria antecedents, and CD4+ Count) while packed cell volume was checked using micro haematocrit reader to determine anaemia status. Data were analysed using IBM SPSS v25.

Results: The mean age of the study participants was 37.5 (±12.48). A total of 142 (33.8%) samples were positive for malaria, and 68 of the HIV-infected patients (16.2%) were anaemic; 4.8% of the 420 patients had malaria co-infection and anaemia simultaneously. More male participants had malaria co-infection (36.0%, P = .617) while more female participants had anaemia (22.7%, P = .058). Patients aged 61 to 70 years had the highest rates of malaria and those aged 51 to 60 years were most anaemic. Except for patients with normal CD4+ count, those who were more exposed to the evaluated risk factors were more co-infected and anaemic. Malaria co-infection did not significantly affect the onset of anaemia. Test for the validity of Microscopy against Enzyme Immunoassay (EIA) showed 83.1% sensitivity and 98.6% specificity. No association was observed between the variables and the parasitaemia density of the patients.

Conclusions: This study highlighted higher rates of malaria co-infection and anaemia among HIV patients when compared with previous reports in the region although co-infection did not significantly affect anaemia status. Given this trend, strategies must be put in place to checkmate these ailments. Population studies are also advocated.

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