National Institute for Medical Research, Dodoma Medical Research Centre, Dodoma, Tanzania.
National Institute for Medical Research, Health Systems, Policy and Translational Research Section, Dar es Salaam, Tanzania.
BMJ Open. 2024 Feb 12;14(2):e077741. doi: 10.1136/bmjopen-2023-077741.
To determine the community's perception on the magnitude of Xeroderma pigmentosum (XP) disease and healthcare-seeking practices in Micheweni, Pemba in response to the public widespread information on the increased burden of the disease.
Mixed-methods cross-sectional study.
Micheweni district, Pemba.
211 male and female adults in the household survey, three caretakers/parents of patients with XP in the case study, 20 key community leaders/influential people and health workers in in-depth interviews and 50 community members and other leaders in six focus groups.
This study has revealed that XP disease exists in few families of which some of them have more than one child affected. The record review showed that there were a total of 17 patients who were diagnosed with the disease for the past 3 years, however only 10 were alive during the time of the survey. Findings from the community members revealed that several patients were believed to have XP disease and perceived causes include inheritance, food types, beliefs and other sociocultural practices. Stigma and discrimination were reported by caretakers and religious leaders. However, some cases believed to be XP were identified as other skin conditions when clinical examination was performed by the team of our researchers. There is a great confusion about XP and other skin diseases.
The study has shown that XP affects only few families, hence termed as concentrated rather than a generalised disease. Due to the rareness of the disease, majority of people in the district are unaware of the disease, hence confusing it with other skin conditions. There is a need for the government in collaboration with other stakeholders to provide educational programme to community members about the disease to address the misconception about the magnitude of the disease.
确定米切维尼(Micheweni)、奔巴(Pemba)社区对着色性干皮病(XP)疾病严重程度的认知,以及该疾病负担加重后人们的就医行为,因为公众对此类信息已有广泛了解。
混合方法的横断面研究。
奔巴米切维尼区。
家庭调查中 211 名男女成年人,病例研究中 3 名 XP 患者的照顾者/父母,深入访谈中 20 名关键社区领导/有影响力的人和卫生工作者,6 个焦点小组中 50 名社区成员和其他领导。
本研究表明,XP 疾病存在于少数家庭中,其中一些家庭有多个患病子女。记录审查显示,过去 3 年来共有 17 名患者被诊断出患有该疾病,但在调查时只有 10 名患者仍在世。社区成员的调查结果显示,一些患者被认为患有 XP 疾病,其病因包括遗传、食物类型、信仰和其他社会文化习俗。照顾者和宗教领袖报告了耻辱和歧视。然而,当我们的研究人员小组进行临床检查时,一些被认为是 XP 的病例被确定为其他皮肤疾病。XP 和其他皮肤疾病之间存在很大的混淆。
该研究表明,XP 仅影响少数家庭,因此称为集中性疾病,而非普遍性疾病。由于该疾病罕见,区大多数人对此病并不了解,因此将其与其他皮肤疾病混淆。政府需要与其他利益攸关方合作,为社区成员提供有关该疾病的教育计划,以解决对疾病严重程度的误解。