37 research outputs found
Participial perception verb complements in Old English
In this paper, I shall examine the complements of perception verbs in Old English involving a
noun phrase and a present participle. What kind of perception is described by these structures? Do
they evoke the perception of an event, or that of an entity? It will be shown here that there are
good reasons to believe that an NP + present participle sequence could function as the equivalent
of the traditional âAcIâ construction when used with perception verbs. I shall also attempt to
determine to what extent the syntax of this construction matches the semantics: is the internal
argument of the perception verb the NP alone, or some kind of combination of the NP and the
participle? This question is particularly interesting in the light of Declerckâs (1982) remarks on
participle perception verb complements in modern English. Finally, I shall take a look at morphological
parametres: sometimes the participle inflects to agree with the NP, whereas on other occasions
it does not. What might the implications of this kind of variation be
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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
Sur la distribution et les origines de do périphrastique
Lowrey Brian. Sur la distribution et les origines de do pĂ©riphrastique. In: Bulletin des anglicistes mĂ©diĂ©vistes, N°75, ĂtĂ© 2009. pp. 23-60
La directionnalitĂ© et la nature non-tĂ©lĂ©ologique de lâĂ©volution linguistique
This paper deals with the nature of linguistic change, and, taking examples from the history of English, seeks to show that, contrary to what appears to be a widely held assumption, there is no reason to suppose that because one language undergoes a certain type of change, a similar change will necessarily take place in other, related languages. On the contrary, purely local factors may, and indeed often do decide which potential innovations will succeed, and which will fail. We look at two areas of English grammar in particular, the so-called ânarrative perfectâ and infinitival complements of causative verbs, and compare the changes which have taken place within these fields in English to those which have occurred in French. The comparison shows not only that French and English have evolved in completely different directions, but also that assuming language change to be teleological in nature can lead to the wrong predictions being made as to which developments are likely to take place in the futur
Les causatifs du moyen-anglais et leurs compléments
1. Introduction : les causatifs et les types de complĂ©ment LâĂ©tude des causatifs analytiques du moyen-anglais met en Ă©vidence de nombreuses diffĂ©rences par rapport Ă la langue contemporaine. Certains verbes faisant partie intĂ©grante du systĂšme causatif de lâanglais contemporain ne sâemploient que rarement dans ce sens, voire pas du tout, Ă lâĂ©poque du moyen-anglais (GET, HAVE), alors que dâautres (DO, LET) ont reçu dâautres fonctions ou bien ont tout simplement dispara de la langue (GAR). 1.1..
A propos de la grammaticalisation de l'impératif périphrastique en let*
Lowrey Brian. A propos de la grammaticalisation de l'impératif périphrastique en let*. In: Bulletin des anglicistes médiévistes, N°70, Hiver 2006. pp. 1-29
Causative verbs in West Saxon Old English
Lowrey Brian. Causative verbs in West Saxon Old English. In: Bulletin des anglicistes médiévistes, N°78, Hiver 2010. pp. 57-88
L'invariant Ă l'Ă©preuve de la diachronie
In this paper, we take a critical look at the notion of the semantic invariant, still widely accepted among French linguists working on English. We examine the invariant in the light of data from the history of English, in an attempt to show that such a framework is simply too rigid to take account of attested, dynamic phenomena such as variation and grammaticalisation in natural languages, and that the distribution of linguistic items, synchronically or diachronically, cannot be explained by a static approach based exclusively on the surface form. We argue instead for a flexible approach, compatible with current models of language change and taking the influence of pragmatic factors into account