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dc.contributor.author Meiring, Susan
dc.contributor.author Cohen, Cheryl
dc.contributor.author de Gouveia, Linda
dc.contributor.author du Plessis, Mignon
dc.contributor.author Kularatne, Ranmini
dc.contributor.author Hoosen, Anwar
dc.contributor.author Lekalakala, Ruth
dc.contributor.author Lengana, Sarona
dc.contributor.author Seetharam, Sharona
dc.contributor.author Naicke, Preneshni
dc.contributor.author Quan, Vanessa
dc.contributor.author Reubenson, Gary
dc.contributor.author Tempia, Stefano
dc.contributor.author von Mollendorf, Claire
dc.contributor.author von Gottberg, Anne
dc.date.accessioned 2020-07-14T09:32:51Z
dc.date.available 2020-07-14T09:32:51Z
dc.date.issued 2018
dc.identifier.issn 1058-4838
dc.identifier.issn 1537-6591
dc.identifier.uri http://hdl.handle.net/10386/3040
dc.description Article published in the Clinical Infectious Diseases vol 69(3):495–504 en_US
dc.description.abstract Background. Invasive meningococcal disease (IMD) is endemic to South Africa, where vaccine use is negligible. We describe the epidemiology of IMD in South Africa. Methods. IMD cases were identified through a national, laboratory-based surveillance program, GERMS-SA, from 2003–2016. Clinical data on outcomes and human immunodeficiency virus (HIV) statuses were available from 26 sentinel hospital sites. We conducted space-time analyses to detect clusters of serogroup-specific IMD cases. Results. Over 14 years, 5249 IMD cases were identified. The incidence was 0.97 cases per 100 000 persons in 2003, peaked at 1.4 cases per 100 000 persons in 2006, and declined to 0.23 cases per 100 000 persons in 2016. Serogroups were confirmed in 3917 (75%) cases: serogroup A was present in 4.7% of cases, B in 23.3%, C in 9.4%; W in 49.5%; Y in 12.3%, X in 0.3%; Z in 0.1% and 0.4% of cases were non-groupable. We identified 8 serogroup-specific, geo-temporal clusters of disease. Isolate susceptibility was 100% to ceftriaxone, 95% to penicillin, and 99.9% to ciprofloxacin. The in-hospital case-fatality rate was 17% (247/1479). Of those tested, 36% (337/947) of IMD cases were HIV-coinfected. The IMD incidence in HIV-infected persons was higher for all age categories, with an age-adjusted relative risk ratio (aRRR) of 2.5 (95% confidence interval [CI] 2.2–2.8; P < .001) from 2012–2016. No patients reported previous meningococcal vaccine exposure. Patients with serogroup W were 3 times more likely to present with severe disease than those with serogroup B (aRRR 2.7, 95% CI 1.1–6.3); HIV coinfection was twice as common with W and Y diseases (aRRR W = 1.8, 95% CI 1.1–2.9; aRRR Y = 1.9, 95% CI 1.0–3.4). Conclusions. In the absence of significant vaccine use, IMD in South Africa decreased by 76% from 2003–2016. HIV was associated with an increased risk of IMD, especially for serogroup W and Y diseases. en_US
dc.format.extent 11 pages en_US
dc.language.iso en en_US
dc.publisher Declining Infectious Medical Journal en_US
dc.relation.requires pdf en_US
dc.subject Meningococcus en_US
dc.subject Neisseria meningitidis en_US
dc.subject Epidemiology en_US
dc.subject South Africa en_US
dc.subject Invasive meningococcal disease en_US
dc.subject.lcsh Meningitis en_US
dc.subject.lcsh HIV (Disease) en_US
dc.subject.lcsh HIV infections en_US
dc.title Declining Incidence of Invasive Meningococcal Disease in South Africa: 2003–2016 en_US
dc.type Article en_US


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