Health journey of Nigerian patients with systemic lupus erythematosus.

IF 1.9 4区 医学 Q3 RHEUMATOLOGY Lupus Pub Date : 2025-04-01 Epub Date: 2025-03-04 DOI:10.1177/09612033251324482
Hakeem Babatunde Olaosebikan, Abubakar Yerima, Gbenga Joshua Odunlami, Courage Ukponmwan Uhunmwangho, Henry Madu Nwankwo, Musa Bello Kofar Na'isa, Mary Agun-Ebreme, Ibrahim Daiyabu, Ilo Azizat Bamisebi, Etseoghena Igebu, Henry Ekpenyong, Hassana Hindatu Aliyu, Olufemi Oladipo Adelowo
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Abstract

BackgroundAlthough there is an increase in prevalence and incidence of lupus worldwide, the journey to diagnosis is unduly delayed. This delay is associated with worse outcomes. Sub-Saharan Africa has witnessed an increase in lupus diagnosis in recent decades with no specific data on the time to diagnosis of lupus.ObjectivesWe measured and documented lupus diagnostic delays, patients' experiences, and factors associated with delayed diagnosis and provided recommendations for early diagnosis.MethodsThis is a three-month cross-sectional study of 245 patients diagnosed with lupus who are members of a Nigerian lupus support group. Included participants fill out patients' administered questionnaire in a Google doc. The questionnaire captured all aspects of the study objectives. Four diagnostic journey intervals were defined. Delayed diagnosis was defined as a time interval from first symptoms to lupus diagnosis greater than or equal to 6 months.ResultsThe majority of participants were under 40 years of age (n-187, 76.3%) and predominantly female (n-226, 92.9%). About 53.9% of participants were diagnosed between 6 months and 2 years after their first symptoms, while 42% visited the first doctor within 6 months of symptom onset. Roughly half of the participants were referred to rheumatologists within 6 months of their visit to the last doctor, while 50.2% of the participants were diagnosed within 4 weeks of the rheumatologist's evaluation. Delayed diagnosis and delayed referral were documented in 80% and 66.9% of participants respectively. Low income (OR-7.4), internal organ manifestations (OR-4.5), and multiple doctors' visits (OR-11.6) were independently associated with delayed diagnosis.ConclusionsDiagnostic delay is observed in the majority of our patients. This delay is associated with multiple hospital visits, low income, and internal organ manifestations. There should be concerted efforts in SSA to improve the rheumatology workforce and incorporate non-specialists in clinical service delivery.

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尼日利亚系统性红斑狼疮患者的健康历程。
背景:虽然狼疮的患病率和发病率在世界范围内有所增加,但诊断的过程却被过度地推迟了。这种延迟与更糟糕的结果有关。近几十年来,撒哈拉以南非洲的狼疮诊断有所增加,但没有关于狼疮诊断时间的具体数据。目的:我们测量并记录狼疮诊断延迟、患者经历和延迟诊断相关因素,并为早期诊断提供建议。方法:这是一项为期三个月的横断面研究,245名被诊断为狼疮的患者是尼日利亚狼疮支持小组的成员。参与者在谷歌文档中填写患者管理的问卷。调查问卷涵盖了研究目标的所有方面。定义了四个诊断行程间隔。延迟诊断定义为从首次症状到狼疮诊断的时间间隔大于或等于6个月。结果:参与者以40岁以下为主(n-187, 76.3%),以女性为主(n-226, 92.9%)。约53.9%的参与者在首次出现症状后6个月至2年内被诊断出来,而42%的参与者在症状出现后6个月内首次就诊。大约一半的参与者在他们最后一次看医生后的6个月内被转介给风湿病学家,而50.2%的参与者在风湿病学家评估后的4周内被诊断出来。延迟诊断和延迟转诊分别为80%和66.9%的参与者。低收入(OR-7.4)、内脏器官表现(OR-4.5)和多次就诊(OR-11.6)与延迟诊断独立相关。结论:在我们的大多数患者中观察到诊断延迟。这种延迟与多次医院就诊、低收入和内脏器官表现有关。在SSA应该有协调一致的努力,以改善风湿病的劳动力和纳入非专家在临床服务提供。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus
Lupus 医学-风湿病学
CiteScore
4.20
自引率
11.50%
发文量
225
审稿时长
1 months
期刊介绍: The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…
期刊最新文献
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