Malya Sahu, Mashina Chomba, Dominique Mortel, Sarah Braun, Lorraine Chishimba, Frighton Mutete, Naluca Mwendaweli, Coolwe Namangala, Stanley Zimba, Deanna Saylor
{"title":"Factors associated with delay to diagnosis of multiple sclerosis in Zambia.","authors":"Malya Sahu, Mashina Chomba, Dominique Mortel, Sarah Braun, Lorraine Chishimba, Frighton Mutete, Naluca Mwendaweli, Coolwe Namangala, Stanley Zimba, Deanna Saylor","doi":"10.1177/13524585251344832","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/objectives: </strong>Delays to diagnosis of multiple sclerosis (MS) are largely unknown in sub-Saharan Africa. This study utilizes a quantitative approach to determine factors independently associated with delays to diagnosis among a cohort of Zambian people with MS.</p><p><strong>Methods: </strong>This cross-sectional study enrolled people with a confirmed diagnosis of MS at a public outpatient neurology clinic in Lusaka, Zambia. Standardized surveys were administered. Diagnostic delay was categorized into patient delay, health-system delay, and all delay. A multivariable linear regression model was used to determine factors independently associated with time to diagnosis.</p><p><strong>Results: </strong>A total of 22 participants had a confirmed diagnosis of MS. Median all delay from symptom onset to MS diagnosis was 11.4 months (interquartile range (IQR) = 4-35.5), with health-system delay accounting for the majority. Asian race correlated with a decrease in all delay, while evaluation outside of Zambia was associated with a decrease in patient delay and birthplace outside of Zambia correlated with decreased health-system delay.</p><p><strong>Conclusion: </strong>Black African people born in Zambia and evaluated in Zambia experienced prolonged diagnostic delays when compared to non-black Zambians born and/or evaluated outside Zambia, likely due to a combination of health system and patient factors, which necessitate further study to shorten time to diagnosis.</p>","PeriodicalId":520714,"journal":{"name":"Multiple sclerosis (Houndmills, Basingstoke, England)","volume":" ","pages":"13524585251344832"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Multiple sclerosis (Houndmills, Basingstoke, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/13524585251344832","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background/objectives: Delays to diagnosis of multiple sclerosis (MS) are largely unknown in sub-Saharan Africa. This study utilizes a quantitative approach to determine factors independently associated with delays to diagnosis among a cohort of Zambian people with MS.
Methods: This cross-sectional study enrolled people with a confirmed diagnosis of MS at a public outpatient neurology clinic in Lusaka, Zambia. Standardized surveys were administered. Diagnostic delay was categorized into patient delay, health-system delay, and all delay. A multivariable linear regression model was used to determine factors independently associated with time to diagnosis.
Results: A total of 22 participants had a confirmed diagnosis of MS. Median all delay from symptom onset to MS diagnosis was 11.4 months (interquartile range (IQR) = 4-35.5), with health-system delay accounting for the majority. Asian race correlated with a decrease in all delay, while evaluation outside of Zambia was associated with a decrease in patient delay and birthplace outside of Zambia correlated with decreased health-system delay.
Conclusion: Black African people born in Zambia and evaluated in Zambia experienced prolonged diagnostic delays when compared to non-black Zambians born and/or evaluated outside Zambia, likely due to a combination of health system and patient factors, which necessitate further study to shorten time to diagnosis.