Nakalembe Miriam, Mutyaba Twaha, Mirembe Florence
Department of Obstetrics and Gynecology, College of Health Sciences, Makerere University, Kampala, Uganda.
BMC Res Notes. 2016 Mar 16;9:170. doi: 10.1186/s13104-016-1984-8.
A cohort study was planned to evaluate vaccine immunogenicity and effect of malaria and helminth co-infections on the bivalent Human papilloma virus (HPV) vaccine. The study would involve self collected introital swabs, blood draws and stool sample collection. We therefore conducted a pilot study to assess the acceptability of these procedures among the students and their parents.
A cross-sectional study among forty four students from two purposively selected primary schools of Western Uganda. Exit interviews and two focus group discussions (FGD) (for parents) were conducted. Acceptability was measured by willingness to undergo the procedures again, recommending the procedures to others as well as proportion of introital swabs positive for β globulin. FGD determined acceptability of the parents and explored opinions and perceptions that would influence their decisions. HPV-16/18 and β globulin deoxyribonucleic acid (DNA) were analysed using a polymerase chain reaction (PCR) kit. All the students (100%) in the study were willing to provide a self- collected introital swab and a stool sample as well as recommending their friends while (86.3%) were willing for blood draws. There were 40/44 (90.1%) self collected introital swabs that had positive result for human β globulin though none of them was positive for HPV-16/18. In the FGD, it emerged that parents concerns were on the blood draws and introital swab collection which were addressed.
The study procedures were highly acceptable among this study population of students and their parents. Follow-up to assess HPV vaccine effectiveness and factors that may influence the vaccine in this age group is feasible.
计划开展一项队列研究,以评估疫苗免疫原性以及疟疾和蠕虫共感染对二价人乳头瘤病毒(HPV)疫苗的影响。该研究将涉及自行采集阴道拭子、采血和粪便样本采集。因此,我们开展了一项试点研究,以评估这些程序在学生及其家长中的可接受性。
对乌干达西部两所经目的抽样选取的小学的44名学生进行了一项横断面研究。进行了退出访谈和两次焦点小组讨论(针对家长)。可接受性通过再次接受这些程序的意愿、向他人推荐这些程序以及阴道拭子中β球蛋白呈阳性的比例来衡量。焦点小组讨论确定了家长的可接受性,并探讨了可能影响他们决策的意见和看法。使用聚合酶链反应(PCR)试剂盒分析HPV-16/18和β球蛋白脱氧核糖核酸(DNA)。研究中的所有学生(100%)都愿意自行采集阴道拭子和粪便样本,并推荐给朋友,而86.3%的学生愿意接受采血。44份自行采集的阴道拭子中有40份(90.1%)人β球蛋白检测呈阳性,不过HPV-16/18均为阴性。在焦点小组讨论中,家长们的担忧集中在采血和阴道拭子采集上,这些问题都得到了解决。
在该研究的学生及其家长群体中,研究程序具有很高的可接受性。开展后续研究以评估HPV疫苗效果以及可能影响该年龄组疫苗效果的因素是可行的。