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The Work of Nurses in the Fever Unit at the Ontario Hospital Toronto: A Qualitative Descriptive Case StudyConnell, Mary 15 August 2019 (has links)
The aim of this study was to describe the process and practices that informed fever therapy treatment at the Ontario Hospital, Toronto, and to describe the work of mental health nurses providing fever therapy at the Ontario Hospital, Toronto from 1941 to 1950.
For almost a decade (1941 to 1950) the Ontario Hospital, Toronto operated a fever therapy unit for the treatment of neurosyphilis, an advanced stage of syphilis. This unit, the only one of its kind in Ontario, used specially designed cabinets to elevate patient temperatures in an attempt to kill the bacterium known to cause neurosyphilis. These treatments, lasting 8 to 10 hours, was taxing on patients, both mentally and physically, and often left the patient in a compromised medical state.
The fever unit at the Ontario Hospital, Toronto was managed entirely by mental health nurses with next to no oversight from physicians, even in times of adverse medical reaction. This image of the mental health nurse as a highly skilled and competent practitioner is not one that has been historically assigned to this area of nursing.
This thesis contributes to the history of mental health nursing in Ontario and nursing overall.
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Strains of African swine fever virus isolated from domestic pigs and from the tick Ornithodoros moubata in South AfricaPini, Attilio 08 August 2012 (has links)
Between 1973 and 1975, 21 outbreaks of ASF were confirmed in the endemic area of the northern Transvaal after an interval of 10 years in which the disease was silent. The new series of outbreaks coincided with the isolation, for the first time in South-Africa, of two HAd- strains of ASF virus. The first of these virus isolates, Lillie-148, was obtained from swine which, judging from circumstantial evidence, had been infected by a warthog carrier of virus. The pigs on the farm were affected by a form of disease with a lower pathogenicity than that observed in previous epidemics. The second HAd- strain 24823 was obtained from a case from which neither clinical nor pathological observations were available. From the results of the biological tests carried out at the laboratory, however, it was deduced that the disease in the field may have had a chronic course. When the carrier status of populations of the argasid tick Ornithodoros moubata collected from warthog burrows was investigated, it was found that the situation in South Africa is analogous to that in East Africa. Twenty five per cent of burrows were found to be infected; the mean infective titres of the tick suspensions varied between 104,5 and 105,2 BCHAd50 and the mean percentage of infected argasids varied between 1,62 and 3,45. Infected ticks were also found in the Marico district, which is adjacent to the endemic area, but ASF has never been recorded there. From tick suspension TS237, showing both delayed and reduced haemadsorbing effect in huffy coat cell cultures, a HAd population of ASF virus was segregated. From these observations it was inferred that ASF virus may mutate from the HAd+ to the HAd- form in the primary virus reservoir. Furthermore, the virus appears to be evolving towards less pathogenic forms irrespective of prior adaptation of the infectious agent to domestic stock under the epidemiological conditions prevailing in South Africa. During this investigation it was found that LLC-MK2 cell cultures were susceptible to ASF virus. Cytopathic effects were observed in primary isolation and peak infectivity coincided with complete destruction of the cell monolayers, attained after three to four serial passages. The sensitivity of LLC-MK2 cells for estimating the virus content of porcine tissues was in two instances comparable to that of huffy coat cells, but in another three cases it was 100 to 1000 times lower. It was concluded that LLC-MK2 cells were a suitable complement to huffy coat cultures for the cultivation of ASF virus, particularly for HAd- isolates. After 35 to 45 serial passages in LLC-MK2 cells the HAd+ strains of ASF virus lost their haemadsorbing characteristics. A similar mutation, but more gradual, was also observed in huffy coat cell cultures. The feasibility of plaque production was studied in LLC-MK2 cell monolayers. Plaques were obtained with all the strains studied, irrespective of their adaptation to LLC-MK2 or buffy coat cells when 0,4% Agarose was used as a solidifying agent. The diameter of plaques ranged from 0,3 to 3,0 mm and this characteristic was unrelated to the haemadsorbing properties of the strains used. Plaque technique was successfully used to detect the presence of HAd- virus particles in HAd+ populations by subculturing selected virus-plaques into buffy coat cultures. The results of biological tests suggested that HAd strains have a reduced virulence which can vary within broad limits. The experience with strain Lillie-148 and 24823 showed that either acute or chronic or subclinical disease can follow infection of pigs with these isolates of virus. The results obtained with the two virus populations of strain TS237 emphasized the different degree of patho-genicity between HAd+ and HAd- virus. While the former was responsible for a peracute or acute form of disease, the latter produced chronic or subclinical infections. In pigs mild forms of ASF also developed following the inoculation of HAd+ strains obtained after serial passages in cell cultures. It was concluded that haemadsorption and pathogenicity are two characteristics that are not linked and can be modified independantly. AFRIKAANS : Gedurende die tydperk 1973-1975 het Afrikaansevarkpes (AVP), na 'n afwesigheid van 10 jaar, weer sy verskyning gemaak in die endemiese gebied van Noord Transvaal en altesaam 21 bevestigde geval1e is aangemeld. Die nuwe reeks uitbrake het sa.amgeval met die eerste isolasie in Suid-Afrika van twee HAd- stamme van AVP. Die eerste virusstam wat geisoleer is, was Lillie-148. Hierdie virusstam is geisoleer van 'n vark wat volgens omstandigheidsgetuienis deur 'n v1akvark besmet is. Die virus waarmee die varke op die plaas besmet is, het 'n laer patogenisiteit gehad as virusse van vorige uitbrake. Die tweede HAd- stam nl. 24823 is verkry van 'n geval waar geen kliniese of patologiese waarnemings beskikbaar was nieo Uit die resultate van laboratoriurntoetse is die gevolgtrekking gemaak dat die siekte wel moont1ik 'n kroniese verloop kon gehad het. Uit ondersoeke na die vektorstatus van populasies van die sagte bosluis Ornithodoros moubata, wat verkry is uit vlakvarkgate, is gevind dat die situasie in Suid-Afrika soortgelyk is aan die in Oos-Afrika. Daar is bevind dat 25 persent vlakvarkgate besmet is; dat die gemiddelde virus konsentrasies van bosluissuspensies varieer tussen 104,5 en 105,2 BCHAd50 en dat die gemiddelde persentasie van besmette bos1uise wissel tussen 1,62 en 3,45. Besmette bosluise is ook aangetref in die Marico-distrik wat aangrensend is aan die ensoötiese gebied en waar AVP nog nooit voorgekom het nie. 'n HAd- populasie van AVP virus is geisoleer van 'n bosluissuspensie, TS237, wat in wit selkulture 'n vertraagde en verminderde heem-adsorberende effek getoon het. Uit hierdie waarnemings is die gevolgtrekking gemaak dat AVP virus in die aanvanklike virus reservoir instaat is om van HAd+ na HAd- te muteer. Hieruit blyk dit dat onder die huidige epidemiese toestande, wat tans in Suid-Afrika heers, die virus skynbaar verander na 'n vorm van laer patogenisiteit. Dit geskied ongeag vroeëre aanpassing van die infektiewe agens by die plaaslike varkpopulasie onder heersende epidemiologiese toestande in Suid-Afrika. Gedurende hierdie ondersoek is dit aangetoon dat LLC-MK2 selkulture vatbaar is vir AVP virus. Primere virus isolasies toon sitopatogeniese effekte. Infektiwiteit bereik 'n piek na drie tot vier agtereenvolgende oorspuitings met algehele vernietiging van sellae. Die gevoelligheid van LLC-MK2 selle vir die bepaling van die virus inhoud van varkweefsel was in twee gevalle vergelykbaar met die van wit selle. In drie ander gevalle was dit 100 tot 1000 keer laer. Die gevolgtrekking is gemaak dat LLC-MK2 selle 'n geskikte aanvulling is vir wit selkulture vir die kweek van AVP virus, veral vir HAd- isolate. Die heem-adsorberende eienskappe van die HAd+ stam van AVP virus het verlore gegaan na 35 - 45 agtereenvolgende oorspuitings in LLC-MK2 selle. In wit selkulture is 'n soortgelyke mutasie waargeneem, hoewel dit meer geleidelik plaasgevind het. Die moontlikheid van plaket vorming in LLC-MK2 sellae is ondersoek. Wanneer 0,4% agarose as stollingsagens gebruik is, het alle stamme wat ondersoek is plakette opgelewer ongeag of hulle aangepas was vir LLC-MK2 selle of wit selle. Plakette se deursnee het gewissel tussen 0,3 en 3,0 mm. Hierdie eienskap is egter nie gekorreleerd met die betrokke stamme se heem-adsorberende eienskappe nie. Die teenwoordigheid van HAd- virus partikels in HAd+ populasies is aangetoon deur subkulture van geselekteerde plakette in wit selkulture te maak. Uit die resultate van biologiese toetse is die gevolgtrekking gemaak dat die HAd- stamme 'n verlaagde virulensie het wat kan wissel tussen wye grense. Die ondervinding met stam Lillie-148 en stam 24823 het aangetoon dat varke wat met hierdie virus stamme besmet raak akute, kroniese of subkliniese siekte toestande ontwikkel. Die graad van verskil tussen die patogenisiteit tussen HAd+ en HAd- virus is beklemtoon deur die resultate wat verkry is met die twee virus populasies van starn TS237. Die HAd+ stam veroorsaak perakute of akute vorms van die siekte terwyl HAd- starn kroniese of subkliniese infeksie tot gevolg het. Matige vorme van AVP is ook verkry nadat varke geinokuleer is met 'n HAd<sup+ starn wat 'n aantal oorspuitings in selkulture ondergaan het. Die afleiding is gemaak dat heem- adsorpsie en patogenisiteit twee eienskappe is wat nie verbonde is nie en dus onafhanklik van mekaar gemodifiseer kan word. Copyright / Gedurende die tydperk 1973-1975 het Afrikaansevarkpes (AVP), na 'n afwesigheid van 10 jaar, weer sy verskyning gemaak in die endemiese gebied van Noord Transvaal en altesaam 21 bevestigde geval1e is aangemeld. Die nuwe reeks uitbrake het sa.amgeval met die eerste isolasie in Suid-Afrika van twee HAd- stamme van AVP. Die eerste virusstam wat geisoleer is, was Lillie-148. Hierdie virusstam is geisoleer van 'n vark wat volgens omstandigheidsgetuienis deur 'n v1akvark besmet is. Die virus waarmee die varke op die plaas besmet is, het 'n laer patogenisiteit gehad as virusse van vorige uitbrake. Die tweede HAd- stam nl. 24823 is verkry van 'n geval waar geen kliniese of patologiese waarnemings beskikbaar was nieo Uit die resultate van laboratoriurntoetse is die gevolgtrekking gemaak dat die siekte wel moont1ik 'n kroniese verloop kon gehad het. Uit ondersoeke na die vektorstatus van populasies van die sagte bosluis Ornithodoros moubata, wat verkry is uit vlakvarkgate, is gevind dat die situasie in Suid-Afrika soortgelyk is aan die in Oos-Afrika. Daar is bevind dat 25 persent vlakvarkgate besmet is; dat die gemiddelde virus konsentrasies van bosluissuspensies varieer tussen 104,5 en 105,2 BCHAd50 en dat die gemiddelde persentasie van besmette bos1uise wissel tussen 1,62 en 3,45. Besmette bosluise is ook aangetref in die Marico-distrik wat aangrensend is aan die ensoötiese gebied en waar AVP nog nooit voorgekom het nie. 'n HAd- populasie van AVP virus is geisoleer van 'n bosluissuspensie, TS237, wat in wit selkulture 'n vertraagde en verminderde heem-adsorberende effek getoon het. Uit hierdie waarnemings is die gevolgtrekking gemaak dat AVP virus in die aanvanklike virus reservoir instaat is om van HAd+ na HAd- te muteer. Hieruit blyk dit dat onder die huidige epidemiese toestande, wat tans in Suid-Afrika heers, die virus skynbaar verander na 'n vorm van laer patogenisiteit. Dit geskied ongeag vroeëre aanpassing van die infektiewe agens by die plaaslike varkpopulasie onder heersende epidemiologiese toestande in Suid-Afrika. Gedurende hierdie ondersoek is dit aangetoon dat LLC-MK2 selkulture vatbaar is vir AVP virus. Primere virus isolasies toon sitopatogeniese effekte. Infektiwiteit bereik 'n piek na drie tot vier agtereenvolgende oorspuitings met algehele vernietiging van sellae. Die gevoelligheid van LLC-MK2 selle vir die bepaling van die virus inhoud van varkweefsel was in twee gevalle vergelykbaar met die van wit selle. In drie ander gevalle was dit 100 tot 1000 keer laer. Die gevolgtrekking is gemaak dat LLC-MK2 selle 'n geskikte aanvulling is vir wit selkulture vir die kweek van AVP virus, veral vir HAd- isolate. Die heem-adsorberende eienskappe van die HAd+ stam van AVP virus het verlore gegaan na 35 - 45 agtereenvolgende oorspuitings in LLC-MK2 selle. In wit selkulture is 'n soortgelyke mutasie waargeneem, hoewel dit meer geleidelik plaasgevind het. Die moontlikheid van plaket vorming in LLC-MK2 sellae is ondersoek. Wanneer 0,4% agarose as stollingsagens gebruik is, het alle stamme wat ondersoek is plakette opgelewer ongeag of hulle aangepas was vir LLC-MK2 selle of wit selle. Plakette se deursnee het gewissel tussen 0,3 en 3,0 mm. Hierdie eienskap is egter nie gekorreleerd met die betrokke stamme se heem-adsorberende eienskappe nie. Die teenwoordigheid van HAd- virus partikels in HAd+ populasies is aangetoon deur subkulture van geselekteerde plakette in wit selkulture te maak. Uit die resultate van biologiese toetse is die gevolgtrekking gemaak dat die HAd- stamme 'n verlaagde virulensie het wat kan wissel tussen wye grense. Die ondervinding met stam Lillie-148 en stam 24823 het aangetoon dat varke wat met hierdie virus stamme besmet raak akute, kroniese of subkliniese siekte toestande ontwikkel. Die graad van verskil tussen die patogenisiteit tussen HAd+ en HAd- virus is beklemtoon deur die resultate wat verkry is met die twee virus populasies van starn TS237. Die HAd+ stam veroorsaak perakute of akute vorms van die siekte terwyl HAd- starn kroniese of subkliniese infeksie tot gevolg het. Matige vorme van AVP is ook verkry nadat varke geinokuleer is met 'n HAd<sup+ starn wat 'n aantal oorspuitings in selkulture ondergaan het. Die afleiding is gemaak dat heem- adsorpsie en patogenisiteit twee eienskappe is wat nie verbonde is nie en dus onafhanklik van mekaar gemodifiseer kan word. Copyright / Thesis (DVSc)--University of Pretoria, 1977. / Companion Animal Clinical Studies / unrestricted
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Variation in Diagnostic Testing and Empiric Acyclovir Use for HSV Infection in Febrile InfantsTreasure, Jennifer 25 May 2022 (has links)
No description available.
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Immunogenicity and toxicity of yellow fever vaccines : a systematic reviewMakhunga-Ramfolo, Nondumiso Siphosakhe 08 July 2011 (has links)
BACKGROUND Yellow fever (YF) is a non-contagious, mosquito borne haemorrhagic fever caused by a single-strand RNA flaviviruses. YF is endemic in the tropics primarily in South America and Africa although the vectors are present in Asia, Europe, Pacific and Middle East. Human beings serve as viraemic hosts for mosquito infection. YF carries a high burden of disease, particularly in developing countries with up to 200 000 cases reported annually and a case fatality rate of 20-50%.The pathogenesis is poorly understood and little research has been conducted .There is no known cure or specific treatment for YF and prevention remains the mainstay the public health approach in terms of effectiveness and cost. The World Health Organisation (WHO) conventions have made vaccination mandatory for travel to endemic countries to prevent outbreaks and transmission to susceptible individuals. YF vaccine is one of the oldest vaccines known and in use and is derived from an attenuated virus strain 17D originally produced in the 1930s. The vaccine has historically been considered effective and safe. However, severe life-threatening side effects to the vaccine have been reported in the past 20 years. Acute vaccinerelated viscerotropic (AVD) and neurotropic (AND) side effects have been reported globally particularly in the elderly. The adverse reactions typically present as YF- like illness resulting in multi-organ failure with death as a possible outcome. OBJECTIVES To estimate the immunogenicity and toxicity of 17D and 17DD YF vaccines by summarizing the available data from randomised controlled trials. STUDY DESIGN A summary of randomized controlled trials (RCT) of YF vaccine immunogenicity and safety and tolerability was obtained using standard meta-analysis methodologies. METHODS A comprehensive literature search was conducted in order to identify trial that met with predetermined inclusion and exclusion criteria. Features of each study were noted taking into account the type of vaccine used, the duration of follow up, assignment to intervention, blinding and randomization methods. Three studies were eventually pooled and effect size estimates reported in each study were noted and analysed using meta-analysis software, MIX. Reports on the side effects post vaccination were summarized and analysed. RESULTS The difference in outcomes between the standard 17DD YF vaccines intervention, traded as Arilvax ® and the 17D YF vaccines traded as YF-Vax ® and Stamaril ® was negligible in terms of effect size. Effect sizes that considered the means between the treatment and control groups demonstrated a difference that favoured the control group viz. Arilvax ®. The pooled results also showed significant publication bias most likely attributable to the small number of studies considered. The pooled and annotated forest plot supported the available literature in confirming the effectiveness of YF vaccines in conferring immunity. A summary of tolerability events CONCLUSIONS This study has confirmed the effectiveness of YF vaccines in terms of immunogenicity and also demonstrated that YF vaccines are well tolerated and safe The small number of study units considered in this study presented challenges for analysis and for interpretation but highlighted the need for more research to be conducted in this area. The results are in keeping with the existing body of evidence supporting the robustness of the immunological response to YF vaccination. The safety and tolerability of the vaccine established in this study was also consistent with known literature. There are important implications for further research and implementation that became evident such as the need for further studies to be conducted in African populations where the burden of disease is highest. / Dissertation (MSc)--University of Pretoria, 2010. / Clinical Epidemiology / unrestricted
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Some preliminary studies of Rocky Mountain spotted fever vectors in UtahCoffey, Marvin Dale 01 August 1953 (has links)
That the tick, Dermacentor andersoni Stiles, was the vehicle of transmission for the disease Rocky Mountain spotted fever was first suggested by Wilson and Chowning (1902). The disease itself has been recognized since 1873, being first known from the Bitter Root Valley of Montana. The first medical record, however, was reported from Idaho by Wood (1896).
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Evaluation of a recombinant rift valley fever virus nucleocapsid protein as a vaccine and an immunodiagnostic reagentVan Vuren, Petrus Jansen 17 January 2012 (has links)
The serodiagnosis of Rift Valley fever (RVF) relies on the use of inactivated whole virus based reagents
which present biosafety, financial and operational constraints. There are no vaccines for humans, the
availability of animal vaccines is limited and they have several drawbacks. The aim of this study was to
evaluate a bacterially expressed recombinant RVF virus (RVFV) nucleocapsid protein (recNP) as a safe
immunodiagnostic reagent, and an immunogen in a mouse and host animal model. Several enzyme-linked
immunosorbent assays (ELISAs) were developed in this study, enabling sensitive and specific detection
of antibodies and RVFV antigen in human and animal specimens. The recNP was combined with
different adjuvants and used to immunize mice and sheep subsequently challenged with a virulent wild
type RVFV strain. Depending on the recNP/adjuvant combination, protection against disease in mice
ranged between 17 and 100%, with sterilizing immunity elicited in some experimental groups, compared
to 100% morbidity/mortality and excessive viral replication in adjuvant and PBS control mice.
Immunization with recNP combined with Alhydrogel, an adjuvant that biases immunity towards Th2
humoral immunity, that yielded 100% protection, induced an earlier and stronger type I interferon
response in mice after challenge, compared to repression of the same gene in adjuvant and PBS control
mice. There was massive activation of pro-inflammatory responses and genes with pro-apoptotic effects
in the livers of control mice at the acute phase of infection, accompanied by high viral replication,
possibly contributing to the pathology of the liver. There was also evidence of activation and repression
of several genes involved in activation of B- and T-cell immunity in control mice, some indicating
possible immune evasion by the challenge virus. Immunization of sheep with the same recNP/adjuvant
combinations were, however, not able to decrease replication of challenge virus. The recNP based
ELISAs are an important addition to and improvement of the currently available serodiagnostic tests for
RVF. The mechanism by which recNP immunization protects mice from developing severe disease
during the acute phase of infection is now better understood, but the mechanism for earlier clearance of
the virus needs further investigation.
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Three separate investigations into the possible teratogenicity of maternal hyperthermia in humansSpraggett, Kitty. January 1982 (has links)
No description available.
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A Meta-Analysis of the Diagnostic Performance of Procalcitonin in the Diagnosis of Serious Bacterial Infection in Pediatric Febrile NeutropeniaFitzgerald, Sarah E., M.D. 08 October 2012 (has links)
No description available.
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Salmonella spp. Interactions with the Gallbladder during Chronic CarriageGonzalez-Escobedo, Geoffrey 27 September 2013 (has links)
No description available.
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The cytopathogenic effect of hog cholera virus and pseudorables virus in tissue culture /Christensen, John Alfred January 1955 (has links)
No description available.
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