88 research outputs found
On the Case of Youth: Case Files, Case Studies, and the Social Construction of Adolescence
Case files and case studies occupy a significant place in histories of mental illness, sexuality, and "delinquency," and historians have considered the ways case files and case studies construct subjective categories and social problems. This paper foregrounds questions of age, and I ask how young people have been conceptualized within New Zealand case files and case studies between 1900 and 1960.1 suggest that, within the case record, the texts of adolescent subjectivity reveal wider concerns around work, discipline, respectability, and social order, along with changes in social science research and writing. At the same time, I argue that case files and case studies have played an active role in the social construction of adolescence in New Zealand's past.Peer Reviewe
Men Alone, Men Entwined: Reconsidering Colonial Masculinity
Two men pose together in an oval cut-out. The man on our right stands for the camera and lays his arm against the back of his seated companion. Both ignore the camera. They study a book instead, absorbed in the world portrayed by its pages. The pair shares a moment in time, a space, and also an intimate closeness; these are no men alone. What is their story, and what does it tell us about men's lives in late-nineteenth-century New Zealand
Unpublished Post-War Writing and Emergent Gay Cultures
The 1950s and â60s were pivotal decades in the emergence of modern gay life. New Zealandâs cities expanded rapidly after the end of the war, and the size of homosexual networks grew quickly. There were profound contradictions too. While many men partied, others were imprisoned for same-sex activity. A homemade queer literature accompanied these changes, and four examples illustrate the tensions of the time. The first, an essay called âDe Profundis for Today,â was the work of Dunedin businessman Ernie Webber, who wrote it in Mt Eden Prison in 1957. The second piece, an early 1960s novel titled âThe Rock Orchid,â is by Bert Pimley, a fellow inmate of Webber at Mt Eden. The third and fourth pieces, short essays by Auckland man Don Goodsell, are very different in their context and tone. The evocatively titled âDid You Ever See a Dream Limping?â and âThe Night is Young and Weâre So Beautifulâ tell not of imprisonment but of the social opportunities of New Zealandâs cities during the 1960
Queer trans-Tasman mobility, then and now
This article situates queer mobility within wider historical geographies of trans-Tasman flows of goods, people and ideas. Using case studies of womenâs and menâs experiences during the early twentieth century and the twenty-first century, it shows that same-sex desire is a constituent part of these flows. Conversely, antipodean mobility has fostered particular forms of desire, sexual identity, queer community and politics. Rural and urban landscapes in both New Zealand and Australia shape queer desire in a range of diverging and converging ways, and political and legal shifts in both countries have fostered changes in trans-Tasman travel over time. Our investigation of the circuits of queer mobility urges a wider examination of the significance of trans-Tasman crossings in queer lives, both historically and in contemporary society
Sociology Before Sociology at Otago University
A sociology minor appeared at Otago University in 2003 and a major in 2005, but these relatively late developments were preceded by a rich history of sociology-like research and teaching at our institution. This article presents a sociological prehistory which winds its way through aspects of the teaching and research of home science, preventive medicine, education, physical education, anthropology and several other disciplines, uncovering sociology-like approaches adopted in the university from the 1920s on. It then briefly considers the reasons behind the late establishment of a stand-alone sociology programme at the university.Peer Reviewe
Functional anonymisation: Personal data and the data environment
Anonymisation of personal data has a long history stemming from the expansion of the types of data products routinely provided by National Statistical Institutes. Variants on anonymisation have received serious criticism reinforced by much-publicised apparent failures. We argue that both the operators of such schemes and their critics have become confused by being overly focused on the properties of the data themselves. We claim that, far from being able to determine whether data are anonymous (and therefore non-personal) by looking at the data alone, any anonymisation technique worthy of the name must take account of not only the data but also their environment. This paper proposes an alternative formulation called functional anonymisation that focuses on the relationship between the data and the environment within which the data exist (their data environment). We provide a formulation for describing the relationship between the data and their environment that links the legal notion of personal data with the statistical notion of disclosure control. Anonymisation, properly conceived and effectively conducted, can be a critical part of the toolkit of the privacy-respecting data controller and the wider remit of providing accurate and usable data
Here Versus There: Creating British Sexual Politics Elsewhere
This reflection draws upon two recent âmomentsâ in British sexuality politicsâa series of Parliamentary debates on Global LGBT rights and Brighton Prideâs campaign to âHighlight Global LGBT Communitiesâ. It contrasts these two moments in order to demonstrate how, at a time when LGBT rights have ostensibly been âwonâ in the UK, there is an increasing tendency to shift focus to the persecution of SOGI minorities elsewhere in the world. This shift in focus sets up a binary of here versus there that is politically persuasive but ultimately limited and limiting. By reflecting on the way that this growing trend of creating sexual politics elsewhere occurs in two very different locations in British politics and activism, we seek to begin a conversation about the relational affects of placing sexual politics âelsewhereâ
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Effect of Hydrocortisone on Mortality and Organ Support in Patients With Severe COVID-19: The REMAP-CAP COVID-19 Corticosteroid Domain Randomized Clinical Trial.
Importance: Evidence regarding corticosteroid use for severe coronavirus disease 2019 (COVID-19) is limited. Objective: To determine whether hydrocortisone improves outcome for patients with severe COVID-19. Design, Setting, and Participants: An ongoing adaptive platform trial testing multiple interventions within multiple therapeutic domains, for example, antiviral agents, corticosteroids, or immunoglobulin. Between March 9 and June 17, 2020, 614 adult patients with suspected or confirmed COVID-19 were enrolled and randomized within at least 1 domain following admission to an intensive care unit (ICU) for respiratory or cardiovascular organ support at 121 sites in 8 countries. Of these, 403 were randomized to open-label interventions within the corticosteroid domain. The domain was halted after results from another trial were released. Follow-up ended August 12, 2020. Interventions: The corticosteroid domain randomized participants to a fixed 7-day course of intravenous hydrocortisone (50 mg or 100 mg every 6 hours) (nâ=â143), a shock-dependent course (50 mg every 6 hours when shock was clinically evident) (nâ=â152), or no hydrocortisone (nâ=â108). Main Outcomes and Measures: The primary end point was organ support-free days (days alive and free of ICU-based respiratory or cardiovascular support) within 21 days, where patients who died were assigned -1 day. The primary analysis was a bayesian cumulative logistic model that included all patients enrolled with severe COVID-19, adjusting for age, sex, site, region, time, assignment to interventions within other domains, and domain and intervention eligibility. Superiority was defined as the posterior probability of an odds ratio greater than 1 (threshold for trial conclusion of superiority >99%). Results: After excluding 19 participants who withdrew consent, there were 384 patients (mean age, 60 years; 29% female) randomized to the fixed-dose (nâ=â137), shock-dependent (nâ=â146), and no (nâ=â101) hydrocortisone groups; 379 (99%) completed the study and were included in the analysis. The mean age for the 3 groups ranged between 59.5 and 60.4 years; most patients were male (range, 70.6%-71.5%); mean body mass index ranged between 29.7 and 30.9; and patients receiving mechanical ventilation ranged between 50.0% and 63.5%. For the fixed-dose, shock-dependent, and no hydrocortisone groups, respectively, the median organ support-free days were 0 (IQR, -1 to 15), 0 (IQR, -1 to 13), and 0 (-1 to 11) days (composed of 30%, 26%, and 33% mortality rates and 11.5, 9.5, and 6 median organ support-free days among survivors). The median adjusted odds ratio and bayesian probability of superiority were 1.43 (95% credible interval, 0.91-2.27) and 93% for fixed-dose hydrocortisone, respectively, and were 1.22 (95% credible interval, 0.76-1.94) and 80% for shock-dependent hydrocortisone compared with no hydrocortisone. Serious adverse events were reported in 4 (3%), 5 (3%), and 1 (1%) patients in the fixed-dose, shock-dependent, and no hydrocortisone groups, respectively. Conclusions and Relevance: Among patients with severe COVID-19, treatment with a 7-day fixed-dose course of hydrocortisone or shock-dependent dosing of hydrocortisone, compared with no hydrocortisone, resulted in 93% and 80% probabilities of superiority with regard to the odds of improvement in organ support-free days within 21 days. However, the trial was stopped early and no treatment strategy met prespecified criteria for statistical superiority, precluding definitive conclusions. Trial Registration: ClinicalTrials.gov Identifier: NCT02735707
Effect of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker initiation on organ support-free days in patients hospitalized with COVID-19
IMPORTANCE Overactivation of the renin-angiotensin system (RAS) may contribute to poor clinical outcomes in patients with COVID-19.
Objective To determine whether angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) initiation improves outcomes in patients hospitalized for COVID-19.
DESIGN, SETTING, AND PARTICIPANTS In an ongoing, adaptive platform randomized clinical trial, 721 critically ill and 58 nonâcritically ill hospitalized adults were randomized to receive an RAS inhibitor or control between March 16, 2021, and February 25, 2022, at 69 sites in 7 countries (final follow-up on June 1, 2022).
INTERVENTIONS Patients were randomized to receive open-label initiation of an ACE inhibitor (nâ=â257), ARB (nâ=â248), ARB in combination with DMX-200 (a chemokine receptor-2 inhibitor; nâ=â10), or no RAS inhibitor (control; nâ=â264) for up to 10 days.
MAIN OUTCOMES AND MEASURES The primary outcome was organ supportâfree days, a composite of hospital survival and days alive without cardiovascular or respiratory organ support through 21 days. The primary analysis was a bayesian cumulative logistic model. Odds ratios (ORs) greater than 1 represent improved outcomes.
RESULTS On February 25, 2022, enrollment was discontinued due to safety concerns. Among 679 critically ill patients with available primary outcome data, the median age was 56 years and 239 participants (35.2%) were women. Median (IQR) organ supportâfree days among critically ill patients was 10 (â1 to 16) in the ACE inhibitor group (nâ=â231), 8 (â1 to 17) in the ARB group (nâ=â217), and 12 (0 to 17) in the control group (nâ=â231) (median adjusted odds ratios of 0.77 [95% bayesian credible interval, 0.58-1.06] for improvement for ACE inhibitor and 0.76 [95% credible interval, 0.56-1.05] for ARB compared with control). The posterior probabilities that ACE inhibitors and ARBs worsened organ supportâfree days compared with control were 94.9% and 95.4%, respectively. Hospital survival occurred in 166 of 231 critically ill participants (71.9%) in the ACE inhibitor group, 152 of 217 (70.0%) in the ARB group, and 182 of 231 (78.8%) in the control group (posterior probabilities that ACE inhibitor and ARB worsened hospital survival compared with control were 95.3% and 98.1%, respectively).
CONCLUSIONS AND RELEVANCE In this trial, among critically ill adults with COVID-19, initiation of an ACE inhibitor or ARB did not improve, and likely worsened, clinical outcomes.
TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT0273570
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