9 research outputs found
Measles outbreak in South Africa: epidemiology of laboratory-confirmed measles cases and assessment of intervention, 2009-2011
BACKGROUND: Since 1995, measles vaccination at nine and 18 months has been routine in South Africa; however, coverage
seldom reached .95%. We describe the epidemiology of laboratory-confirmed measles case-patients and assess the impact
of the nationwide mass vaccination campaign during the 2009 to 2011 measles outbreak in South Africa.
METHODS: Serum specimens collected from patients with suspected-measles were tested for measles-specific IgM antibodies
using an enzyme-linked immunosorbent assay and genotypes of a subset were determined. To estimate the impact of the
nationwide mass vaccination campaign, we compared incidence in the seven months pre- (1 September 2009–11 April
2010) and seven months post-vaccination campaign (24 May 2010–31 December 2010) periods in seven provinces of South
Africa.
RESULTS: A total of 18,431 laboratory-confirmed measles case-patients were reported from all nine provinces of South Africa
(cumulative incidence 37 per 100,000 population). The highest cumulative incidence per 100,000 population was in children
aged ,1 year (603), distributed as follows: ,6 months (302/100,000), 6 to 8 months (1083/100,000) and 9 to 11 months
(724/100,000). Forty eight percent of case-patients were 40 years. A single strain of measles virus (genotype B3) circulated
throughout the outbreak. Prior to the vaccination campaign, cumulative incidence in the targeted vs. non-targeted age
group was 5.9-fold higher, decreasing to 1.7 fold following the campaign (P,0.001) and an estimated 1,380 laboratoryconfirmed
measles case-patients were prevented.
CONCLUSION: We observed a reduction in measles incidence following the nationwide mass vaccination campaign even
though it was conducted approximately one year after the outbreak started. A booster dose at school entry may be of value
given the high incidence in persons .5 years.Our acknowledgements go to the Department of Health South Africa,
National, provincial and districts, the South African Field Epidemiology
and Laboratory Training Programme (SAFELTP), for ongoing support in
surveillance and outbreak activities; Division of Epidemiology (Tsakani
Nkuna, Kelebogile Lebogang Motsepe) and Virology (Londiwe Mahlaba,
Mduduzi Buthelezi, Nomfundo Radebe, Muzi Hlanzi, Wayne Howard) at
the NICD-NHLS for data management and laboratory testing support
respectively and Private Laboratories for their support and referring
specimens to the NICD.www.plosone.orgam201
Warm mix asphalt vs. hot mix asphalt : flexural stiffness and fatigue life evaluation
Thesis (MScEng)--Stellenbosch University, 2014.ENGLISH ABSTRACT: The UNFCCC (United Nations Framework Convention on Climate Change), enabled
by the Kyoto Protocol, set enforced responsibilities on industrialised countries to
reduce the amount of emissions (greenhouse gases) produced. This global call for
the reduction of greenhouse gas emissions ensured that the manufacturing sector
commit to emission reduction.
The asphalt industry has embarked on a quest to find alternative methods of
producing and constructing asphalt mixes which will release less greenhouse gasses
into the atmosphere. These new methods include the reduction in production and
construction temperatures which in turn will reduce the amount of greenhouse
emissions produced. These new methods introduced the concept of warm mix
asphalt (WMA) to the alternative hot mix asphalt (HMA).
To produce a WMA mix at lower temperatures the binder needs to be in a workable
state so to effectively coat the aggregate and produce a good quality mix. WMA
technologies have been developed to enable production of mixes at lower
temperatures (effectively reducing emissions) whilst retaining the required binder
viscosity and properties needed to produce a quality mix. The question which needs
to be answered is whether the performance of these WMA mixes can compare with
that of HMA mixes.
In this study several WMA mixes (with different WMA technologies) are evaluated
against their equivalent HMA mixes in terms of fatigue life and flexural stiffness.
Phase angle results were also considered. Flexural stiffness is a mix property which
is dependent on loading time and temperature. It is used to measure the load spread
ability of a mix and also influences fatigue behaviour. Fatigue cracking occurs in the
material as a result of repeated cyclic loading. The evaluation and analysis conducted in this study show that WMA mixes can
compare favourably and even exceed that of HMA mixes in certain cases, although
some WMA mixes resulted in lower fatigue life or flexural stiffness than its
corresponding HMA mixes, which could be attributed to differences in mix
components and variables.
In this study a literature study, methodology, laboratory test results, a comparison of
mix results and conclusions and recommendations are made.AFRIKAANSE OPSOMMING: Die UNFCCC (United Nations Framework Convention on Climate Change) was in
staat gestel deur die Kyoto Protocol om verantwoordelikhede op geïndustrialiseerde
lande te forseer om die hoeveelheid van nadelige kweekhuisgasse wat geproduseer
word te verminder. Hierdie globale oproep tot die vermindering van kweekhuisgasse
verseker dat die vervaardigingsektor hulself verbind tot emissie vermindering.
Die asfalt industrie het begin met 'n soektog na alternatiewe metodes van
vervaardiging en die bou van asfaltmengsels wat minder kweekhuisgasse sal vrystel
in die atmosfeer. Hierdie nuwe metodes sluit die vermindering in produksie en
konstruksie temperature in wat op sy beurt die hoeveelheid kweekhuisgasse
geproduseer verminder. Hierdie nuwe metodes het die konsep van warm mengsel
asfalt (WMA) bekendgestel teenoor die alternatiewe ‘hot’ mengsel asfalt (HMA).
Om ‘n WMA mengsel te produseer by laer temperature, moet die bindmiddel in 'n
werkbare toestand wees om die aggregaat heeltemal te bedek en 'n goeie gehalte
mengsel te produseer. WMA tegnologie is ontwikkel om die produksie van mengsels
teen laer temperature te realiseer (vermindering die uitlaatgasse), terwyl die vereiste
bindmiddel viskositeit en eienskappe wat nodig is om 'n kwaliteit mengsel te
produseer behou word. Die vraag wat beantwoord moet word, is of die prestasie van
hierdie WMA mengsel kan vergelyk word met dié van HMA mengsel.
In hierdie studie is 'n paar WMA mengsels (met verskillende WMA tegnologie)
geëvalueer teen hul ekwivalent HMA mengsels in terme van vermoeiing en buig
styfheid. Fase hoek resultate is ook in ag geneem. Buig styfheid is 'n mengsel
eienskap wat afhanklik is van die laai tyd en temperatuur. Dit word gebruik om die las
verspreiding vermoë van 'n mengsel te meet en beïnvloed ook vermoeiing gedrag.
Vermoeidheid krake kom voor in die materiaal as gevolg van herhaalde sikliese laai. Die evaluering en ontleding in hierdie studie toon dat WMA mengsels goed vergelyk
en selfs in sekere gevalle meer as dié van HMA mengsels, hoewel sommige WMA
mengsels laer vermoeidheid lewe of buig styfheid as die ooreenstemmende HMA
mengsels gewys het, wat toegeskryf kan word tot verskille in mengsel komponente
en veranderlikes.
In hierdie studie word 'n literatuurstudie, metodiek, laboratorium toets resultate, 'n
vergelyking van die mengsel resultate en gevolgtrekkings en aanbevelings gemaak
Measles outbreak in South Africa, 2003 - 2005
OBJECTIVES: Measles was virtually eliminated in South Africa following control activities in 1996 / 7. However, from July 2003 to November 2005, 1 676 laboratory-confirmed measles cases were reported in South Africa. We investigated the outbreak's cause and the role of HIV.
DESIGN: We traced laboratory-confirmed case-patients residing in the Johannesburg metropolitan (JBM) and O R Tambo districts. We interviewed laboratory- or epidemiologically confirmed case-patients or their caregivers to determine vaccination status and, in JBM, HIV status. We calculated vaccine effectiveness using the screening method.
SETTING: Household survey in JBM and O R Tambo districts.
OUTCOME MEASURES: Vaccine effectiveness, case-fatality rate, and hospitalisations.
RESULTS: In JBM, 109 case-patients were investigated. Of the 57 case-patients eligible for immunisation, 27 (47.4%) were vaccinated. Fourteen (12.8%) case-patients were HIV infected, 46 (42.2%) were HIV uninfected, and 49 (45.0%) had unknown HIV status. Among children aged 12 - 59 months, vaccine effectiveness was 85% (95% confidence interval (CI) : 63, 94) for all children, 63% for HIV infected, 75% for HIV uninfected, and 96% for children with unknown HIV status. (Confidence intervals were not calculated for sub-groups owing to small sample size.) In O R Tambo district, 157 case-patients were investigated. Among the 138 case-patients eligible for immunisation, 41 (29.7%) were vaccinated. Vaccine effectiveness was 89% (95% CI 77, 95).
CONCLUSIONS: The outbreak's primary cause was failure to vaccinate enough of the population to prevent endemic measles transmission. Although vaccine effectiveness might have been lower in HIV-infected than in uninfected children, population vaccine effectiveness remained high
Characteristics of laboratory-confirmed measles cases before and after the vaccination campaign in seven South African provinces, 2009–2010.
*<p>Age and sex known in 6,729 and 6,866 cases respectively; <b>#</b> Age and sex known in 1,291 and 1,319 cases respectively; mo = months; yr = years.</p><p>Please note: population for the <1 year unavailable per month; as a result, the population was estimated by dividing the population of <1 year by 12.</p
Weekly* number of measles IgM positive cases: South Africa, 2009–2011.
<p>* Week calculated from date of specimen collection (n = 17 351), date received (n = 1 067) or date tested (n = 13).</p
Age-specific incidence of laboratory-confirmed measles cases, South Africa, 2009–2011.
<p>Age-specific incidence of laboratory-confirmed measles cases, South Africa, 2009–2011.</p
Reported administrative vaccination coverage<sup>*</sup> by province during the nationwide mass vaccination campaign, South Africa, May/April 2010.
*<p>Administrative method: number of doses delivered divided by the target population which is determined from the census projections.</p><p>mo = months; yr = years.</p>**<p>8 of 9 provinces of South Africa included, Gauteng Province excluded as widespread vaccination was conducted in this province in 2009.</p><p>Source: Personal Communication: National Department of Health, South Africa.</p
Map showing nine South African provinces and overall cumulative incidence per 100 000 population by province, 2009–2011.
<p>Map showing nine South African provinces and overall cumulative incidence per 100 000 population by province, 2009–2011.</p