12 research outputs found

    Peri-operative red blood cell transfusion in neonates and infants: NEonate and Children audiT of Anaesthesia pRactice IN Europe: A prospective European multicentre observational study

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    BACKGROUND: Little is known about current clinical practice concerning peri-operative red blood cell transfusion in neonates and small infants. Guidelines suggest transfusions based on haemoglobin thresholds ranging from 8.5 to 12 g dl-1, distinguishing between children from birth to day 7 (week 1), from day 8 to day 14 (week 2) or from day 15 (≄week 3) onwards. OBJECTIVE: To observe peri-operative red blood cell transfusion practice according to guidelines in relation to patient outcome. DESIGN: A multicentre observational study. SETTING: The NEonate-Children sTudy of Anaesthesia pRactice IN Europe (NECTARINE) trial recruited patients up to 60 weeks' postmenstrual age undergoing anaesthesia for surgical or diagnostic procedures from 165 centres in 31 European countries between March 2016 and January 2017. PATIENTS: The data included 5609 patients undergoing 6542 procedures. Inclusion criteria was a peri-operative red blood cell transfusion. MAIN OUTCOME MEASURES: The primary endpoint was the haemoglobin level triggering a transfusion for neonates in week 1, week 2 and week 3. Secondary endpoints were transfusion volumes, 'delta haemoglobin' (preprocedure - transfusion-triggering) and 30-day and 90-day morbidity and mortality. RESULTS: Peri-operative red blood cell transfusions were recorded during 447 procedures (6.9%). The median haemoglobin levels triggering a transfusion were 9.6 [IQR 8.7 to 10.9] g dl-1 for neonates in week 1, 9.6 [7.7 to 10.4] g dl-1 in week 2 and 8.0 [7.3 to 9.0] g dl-1 in week 3. The median transfusion volume was 17.1 [11.1 to 26.4] ml kg-1 with a median delta haemoglobin of 1.8 [0.0 to 3.6] g dl-1. Thirty-day morbidity was 47.8% with an overall mortality of 11.3%. CONCLUSIONS: Results indicate lower transfusion-triggering haemoglobin thresholds in clinical practice than suggested by current guidelines. The high morbidity and mortality of this NECTARINE sub-cohort calls for investigative action and evidence-based guidelines addressing peri-operative red blood cell transfusions strategies. TRIAL REGISTRATION: ClinicalTrials.gov, identifier: NCT02350348

    New abolition, criminology and a critical carceral studies

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    Criminology has been slow to open up a conversation about decarceration and abolition in comparison with other disciplines, including history, geography, and gender, race, and critical ethnic studies. Scholars from these areas and actors on the ground—close up to confinement—have done most of the organizing against mass incarceration and theorizing of alternative possibilities. Why those experiences—and the theoretical traditions that inform their work—have been less recognized and developed in criminology is of pivotal concern as more criminologists move forward with the political project of decarceration. The extent to which criminology can sustain an alternative or abolitionist politics remains an open question. Amid growing conversations about decarceration and shifting rhetorics on punishment, we address some of the obstacles that limit criminology as a site from which to engage the abolitionist project, asking where criminologists might turn for interventionist models that move away from imprisonment and the violence of the carceral state. In this article, we advocate for and discuss the contours of critical carceral studies, a growing interdisciplinary movement for engaged scholarly and activist production against the carceral state. We discuss the imperatives for criminological engagement with critical carceral studies and sketch some of the terrain on which the discipline can contribute to the project, including important work to counter criminological discourses and knowledge production that reify and reproduce carceral logics and practices

    Perioperative critical events and morbidity associated with anesthesia in early life: subgroup analysis of United Kingdom participation in the neonate and children audit of anesthesia practice in Europe (NECTARINE) prospective multicenter observational study

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    BACKGROUND: The NEonate and Children audiT of Anaesthesia pRactice IN Europe (NECTARINE) prospective observational study reported critical events requiring intervention during 35.2% of 6542 anesthetic episodes in 5609 infants up to 60 weeks postmenstrual age. The United Kingdom (UK) was one of 31 participating countries. METHODS: Subgroup analysis of UK NECTARINE cases (12.8% of cohort) to identify perioperative critical events that triggered medical interventions. Secondary aims were to describe UK practice, identify factors more commonly associated with critical events, and compare 30-day morbidity and mortality between participating UK and non-UK centers. RESULTS: Seventeen UK centers recruited 722 patients (68.7% male, 36.1% born preterm, 48.1% congenital anomalies) undergoing anesthesia for 876 surgical or diagnostic procedures at 25-60 weeks postmenstrual age. Repeat anesthesia/surgery was common: 17.6% patients prior to and 14.4% during the recruitment period. Perioperative critical events triggered interventions in 300/876 (34.3%) cases. Cardiovascular instability (16.9% of cases) and/or reduced oxygenation (11.4%) were more common in younger patients and those with co-morbidities or requiring preoperative intensive support. A higher proportion of UK than non-UK cases were graded as ASA-Physical Status scores >2 or requiring urgent or emergency procedures, and 39% required postoperative intensive care. Thirty-day morbidity (complications in 17.2%) and mortality (8/715, 1.1%) did not differ from non-UK participants. CONCLUSIONS: Perioperative critical events and co-morbidities are common in neonates and young infants. Thirty-day morbidity and mortality data did not demonstrate national differences in outcome. Identifying factors associated with increased risk informs preoperative assessment, resource allocation, and discussions between clinicians and families

    Prodrugs available on the Brazilian pharmaceutical market and their corresponding bioactivation pathways

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    The aim of this paper was to emphasize the importance of prodrug design to therapy, by examining examples available on the Brazilian pharmaceutical market. The principles of prodrug design are briefly discussed herein. Examples of prodrugs from many important therapeutic classes are shown and their advantages relative to the drugs they are derived from are also discussed. Considering the importance of these therapeutic classes, from both therapy and economic standpoints, prodrug design is a very valuable aspect in the research of new drugs and for the pharmaceutical industry as a whole.<br>O objetivo do trabalho foi ressaltar a importĂąncia do planejamento de prĂł-fĂĄrmacos para a terapia, por meio de exemplos disponĂ­veis no mercado farmacĂȘutico brasileiro. Os princĂ­pios da latenciação sĂŁo sucintamente discutidos. Apresentam-se exemplos de prĂł-fĂĄrmacos de muitas classes terapĂȘuticas importantes e as vantagens relativas aos fĂĄrmacos dos quais derivam sĂŁo, tambĂ©m, discutidas. Considerando-se a importĂąncia dessas classes terapĂȘuticas, tanto do aspecto terapĂȘutico quanto do econĂŽmico, o planejamento de prĂł-fĂĄrmacos representa aspecto de grande valor na busca de novos fĂĄrmacos e na indĂșstria farmacĂȘutica como um todo
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