尼日利亚拉各斯感染艾滋病毒的青少年的心理社会功能障碍和性发育迟缓。

Somtochukwu Rose Akunne, Elizabeth Eberechi Oyenusi, Adeseye Michael Akinsete, Abiola Olufunmilayo Oduwole
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引用次数: 0

摘要

随着使用抗逆转录病毒疗法后存活率的提高,感染人类免疫缺陷病毒(ALHIV)的青少年可能会出现青春期延迟和心理并发症等并发症。在尼日利亚,有关 ALHIV 性成熟延迟与心理社会功能障碍之间关系的数据十分有限。本研究的目的是确定 ALHIV 中性成熟延迟(DSD)和心理社会功能障碍(PSD)的发生率和相关性,并与未感染的青少年进行比较:这是一项在尼日利亚拉各斯大学教学医院(Lagos University Teaching Hospital,LUTH)进行的横断面研究,共有 144 名 ALHIV 感染者和同等数量的 HIV 阴性对照者参加,他们的年龄、性别和社会阶层均匹配。研究人员通过访谈者发放的调查问卷获得了参与者的信息,并分别使用坦纳分期标准和儿科症状清单工具对他们的性发育阶段和社会心理功能进行了评估。数据使用社会科学统计软件包第 23 版进行分析:ALHIV和HIV阴性对照组的平均年龄(±SD)分别为14.8(±3.0)岁和14.8(±2.9)岁。所有 ALHIV 均接受了 HAART 治疗,99.3% 处于临床 1 期。ALHIV(9.4%)和 HIV 阴性对照组(6.4%)的 DSD 患病率无明显差异(P= 0.402)。ALHIV 和 HIV 阴性对照组的 PSD 患病率分别为 4.9% 和 5.6% (P=0.791)。两组研究参与者的 PSD 和 DSD 之间无明显关联(p=0.459 和 p=0.301):结论:在感染和未感染艾滋病毒的青少年中,PSD 和 DSD 的发病率较低且相似,PSD 和 DSD 之间没有关联。然而,应该对青少年进行 PSD 常规筛查,以便及早发现并及时处理。
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Psychosocial dysfunction and delayed sexual development among adolescents living with HIV in Lagos, Nigeria.

With increasing survival following the use of antiretroviral therapy, adolescents living with Human Immunodeficiency Virus (ALHIV) could have complications such as delayed puberty and psychological complications. In Nigeria, there is limited data on the association between delayed sexual maturation and psychosocial dysfunction in ALHIV. The objective of this study was to determine the prevalence and the association between delayed sexual development (DSD) and psychosocial dysfunction (PSD) in ALHIV and compare it with uninfected adolescents.

Methodology: This was a cross-sectional study conducted at the Lagos University Teaching Hospital (LUTH), Nigeria and it involved 144 ALHIV and an equal number of HIV-negative controls who were matched for age, sex and social class. Information was obtained from participants using interviewer-administered questionnaires; their stages of sexual development and their psychosocial function were assessed using Tanner staging criteria and the Paediatric Symptom Checklist tool respectively. Data were analysed using the Statistical Package for Social Sciences software version 23.

Results: The mean (±SD) age of ALHIV and the HIV-negative controls was 14.8 (±3.0) and 14.8 (±2.9) years respectively. All the ALHIV were on HAART and 99.3% were in clinical stage 1. There was no significant difference between the prevalence of DSD among the ALHIV (9.4%) and the HIV-negative controls (6.4%) (p= 0.402). The prevalence of PSD in ALHIV and HIV-negative controls were 4.9% and 5.6% respectively (p=0.791). There was no significant association between PSD and DSD in both groups of study participants (p=0.459 and p=0.301).

Conclusion: The prevalence of PSD and DSD were low and similar among adolescents with and without HIV, and no association was found between PSD and DSD. However, routine screening of adolescents for PSD should be practised for early identification and prompt management where indicated.

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