Bibliografías temáticas / Critically ill children

Literatura académica sobre el tema "Critically ill children"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 3 de marzo de 2023

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Artículos de revistas sobre el tema "Critically ill children"

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Kamińska, Halla, Paweł Wieczorek, Eliza Skała-Zamorowska, Grażyna Deja y Przemysława Jarosz-Chobot. "Dysglycemia in critically ill children". Pediatric Endocrinology Diabetes and Metabolism 22, n.º 1 (2016): 21–25. http://dx.doi.org/10.18544/pedm-22.01.0046.

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Tyrrell, Cornelius T. y Scot T. Bateman. "Critically ill children". Pediatric Critical Care Medicine 13, n.º 2 (marzo de 2012): 204–9. http://dx.doi.org/10.1097/pcc.0b013e318219291c.

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Fortune, Peter-Marc y Stephen Playfor. "Transporting critically ill children". Anaesthesia & Intensive Care Medicine 10, n.º 10 (octubre de 2009): 510–13. http://dx.doi.org/10.1016/j.mpaic.2008.10.004.

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Fortune, Peter-Marc, Kate Parkins y Stephen Playfor. "Transporting critically ill children". Anaesthesia & Intensive Care Medicine 15, n.º 12 (diciembre de 2014): 577–80. http://dx.doi.org/10.1016/j.mpaic.2014.09.001.

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Fortune, Peter-Marc, Kate Parkins y Stephen Playfor. "Transporting critically ill children". Anaesthesia & Intensive Care Medicine 18, n.º 11 (noviembre de 2017): 562–66. http://dx.doi.org/10.1016/j.mpaic.2017.08.002.

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Harvey, Matthew, Sarah Edmunds y Arun Ghose. "Transporting critically ill children". Anaesthesia & Intensive Care Medicine 21, n.º 12 (diciembre de 2020): 641–48. http://dx.doi.org/10.1016/j.mpaic.2020.10.011.

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Foster, Jennifer. "Melatonin in Critically Ill Children". Journal of Pediatric Intensive Care 05, n.º 04 (28 de abril de 2016): 172–81. http://dx.doi.org/10.1055/s-0036-1583283.

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AbstractMelatonin, while best known for its chronobiologic functions, has multiple effects that may be relevant in critical illness. It has been used for circadian rhythm maintenance, analgesia, and sedation, and has antihypertensive, anti-inflammatory, antioxidant, antiapoptotic, and antiexcitatory effects. This review examines melatonin physiology in health, the current state of knowledge regarding endogenous melatonin production in pediatric critical illness, and the potential uses of exogenous melatonin in this population, including relevant information from basic sciences and other fields of medicine. Pineal melatonin production and secretion appears to be altered in critical illness, though understanding in pediatric critical illness is in early stages, with only 102 children reported in the current literature. Exogenous melatonin may be used for circadian rhythm disturbances and, within the critically ill population, holds promise for diseases involving oxidant stress. There are no studies of exogenous melatonin administration to critically ill children beyond the neonatal period.
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Yalcinkaya, Asli, Hakan Tekguc y Oguz Dursun. "Rhabdomyolysis in Critically ill Children". Turkish Journal of Pediatric Emergency and Intensive Care Medicine 1, n.º 2 (2014): 61–64. http://dx.doi.org/10.5505/cayb.2014.03522.

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Millichap, J. Gordon. "Myopathy in Critically Ill Children". Pediatric Neurology Briefs 18, n.º 2 (1 de febrero de 2004): 11. http://dx.doi.org/10.15844/pedneurbriefs-18-2-3.

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Menezes, Fernanda Souza de, Heitor Pons Leite, Juliana Fernandez, Silvana Gomes Benzecry y Werther Brunow de Carvalho. "Hypophosphatemia in critically ill children". Revista do Hospital das Clínicas 59, n.º 5 (2004): 306–11. http://dx.doi.org/10.1590/s0041-87812004000500015.

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The purpose of this paper is to review clinical studies on hypophosphatemia in pediatric intensive care unit patients with a view to verifying prevalence and risk factors associated with this disorder. We searched the computerized bibliographic databases Medline, Embase, Cochrane Library, and LILACS to identify eligible studies. Search terms included critically ill, pediatric intensive care, trauma, sepsis, infectious diseases, malnutrition, inflammatory response, surgery, starvation, respiratory failure, diuretic, steroid, antiacid therapy, mechanical ventilation. The search period covered those clinical trials published from January 1990 to January 2004. Studies concerning endocrinological disorders, genetic syndromes, rickets, renal diseases, anorexia nervosa, alcohol abuse, and prematurity were not included in this review. Out of 27 studies retrieved, only 8 involved pediatric patients, and most of these were case reports. One clinical trial and one retrospective study were identified. The prevalence of hypophosphatemia exceeded 50%. The commonly associated factors in most patients with hypophosphatemia were refeeding syndrome, malnutrition, sepsis, trauma, and diuretic and steroid therapy. Given the high prevalence, clinical manifestations, and multiple risk factors, the early identification of this disorder in critically ill children is crucial for adequate replacement therapy and also to avoid complications.
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Tesis sobre el tema "Critically ill children"

1

Branco, Ricardo Garcia. "Stress response in critically ill children". Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609718.

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Robertson, Gillian. "Hypernatraemic gastroenteritis in critically ill children". Master's thesis, University of Cape Town, 2005. http://hdl.handle.net/11427/9261.

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Ullman, Amanda. "The oral health of critically ill children". Thesis, Queensland University of Technology, 2009. https://eprints.qut.edu.au/31765/1/Amanda_Ullman_Thesis.pdf.

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Introduction. In adults, oral health has been shown to worsen during critical illness as well as influence systemic health. There is a paucity of paediatric critical care research in the area of oral health; hence the purpose of the Critically ill Children’s Oral Health (CCOH) study is to describe the status of oral health of critically ill children over time spent in the paediatric intensive care unit (PICU). The study will also examine the relationship between poor oral health and a variety of patient characteristics and PICU therapies and explore the relationship between dysfunctional oral health and PICU related Healthcare-Associated Infections (HAI). Method. An observational study was undertaken at a single tertiary-referral PICU. Oral health was measured using the Oral Assessment Scale (OAS) and culturing oropharyngeal flora. Information was also collected surrounding the use of supportive therapies, clinical characteristics of the children and the occurrence of PICU related HAI. Results. Forty-six participants were consecutively recruited to the CCOH study. Of the participants 63% (n=32) had oral dysfunction while 41% (n=19) demonstrated pathogenic oropharyngeal colonisation during their critical illness. The potential systemic pathogens isolated from the oropharynx and included Candida sp., Staphylococcus aureus, Haemophilus influenzae, Enterococcus sp. and Pseudomonas aeruginosa. The severity of critical illness had a significant positive relationship (p=0.046) with pathogenic and absent colonisation of the oropharynx. Sixty-three percent of PICU-related HAI involved the preceding or simultaneous colonisation of the oropharynx by the causative pathogen. Conclusion. Given the prevalence of poor oral health during childhood critical illness and the subsequent potential systemic consequences, evidence based oral hygiene practices should be developed and validated to guide clinicians when nursing critically ill children.
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Jones, P. R. "Haemodynamic instability during the intubation of critically-ill children". Thesis, University College London (University of London), 2012. http://discovery.ucl.ac.uk/1370569/.

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Haemodynamic instability is common during critical illness when homeostatic mechanisms are attenuated or already at the limit of their efficacy. Intubation is a crucial life-saving intervention which seeks to stabilize respiratory and cardiovascular function, but itself represents an additional, short-term haemodynamic challenge. This thesis aimed to investigate changes in heart rate during intubation of critically ill children. Heart rate was chosen as a crude measure of haemodynamic stability because it is most readily available even in time-critical pre-hospital settings. Focusing on heart rate also raised the question of the benefits of atropine pre-medication The first study was an international survey of Paediatric Intensivists using the Delphi methodology. There was agreement that there is a risk of death during intubation. There was no agreement about the capacity of atropine to reduce the incidence of bradycardia, hypotension or death. An observational study of 414 intubations in critically ill children was used to provide data for the thesis. Reductions in heart rate were common amongst first intubations in neonates, children between 28 days of age and eight years and further intubations in both groups. The limitations of using the minimum heart rate as a measure of haemodynamic disturbance were considered. An alternative measure of the change in heart rate, or ‘lost-beats’, was proposed and investigated. Atropine use was associated with less of a fall in heart rate and fewer lost heart beats during intubation. There was a strong association between a low heart rate and an increased incidence of arrhythmias and conduction abnormalities during intubation. Arrhythmias and conduction abnormalities were reduced, but not eliminated, by atropine pre-medication. Sinus tachycardia was not observed to convert to ventricular tachycardia or fibrillation when atropine was used. Mortality during critical care intubation was low (<0.5%). Atropine could not be statistically proven to have an effect on mortality during intubation although was associated with reduced intensive care mortality in children over 28 days of age but not in neonates. The association of atropine pre-medication with reduced PICU mortality in children over one month is unexpected and requires further investigation. A rabbit model of endotracheal intubation was used to investigate the consequences of vagal activation on blood pressure in hypovolaemia and endotoxaemia. Hypovolaemic rabbits observed a significantly smaller decrease in blood pressure after vagal stimulation than that in control rabbits. The relative change in blood pressure after vagal stimulation was similar between the endotoxaemic rabbits and controls. This finding suggests that different disease states may influence the haemodynamic function during intubation.
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Waardenburg, Dirk Adriaan van. "Protein metabolism and nutritional requirements in critically ill children". Maastricht : Maastricht : Maastricht University ; University Library, Universiteit Maastricht [host], 2008. http://arno.unimaas.nl/show.cgi?fid=15092.

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Agbeko, R. S. "Characterization of the acute phase response in critically ill children". Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1421089/.

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Humans come into contact and interact with potential infective agents. The innate immune system is the first line of response to ward off infection. Innate immunity is, in part, under genetic control. This genetic control may help us understand the differences between individuals in preventing infection or limiting infectious and inflammatory illness. Systemic inflammation is a complex disorder that is difficult to define. Current definitions are derived from consensus meetings. A need has been expressed for a more useful definition of systemic inflammation. The work presented here identifies some of the underlying hereditability in limiting or being more vulnerable to severe infectious and injurious insults. Individual differences in complement activation potential and endotoxin recognition underlie part of the observed differences in a systemic inflammatory response to severe infection and injury. An exploratory study using heart rate variability as a non-invasive method to distinguish infectious systemic inflammation from sterile systemic inflammation was inconclusive. Chapter 1 gives the background to this study and an introduction to the approaches taken in this thesis. Chapter 2 describes in detail the methods used in the genetic association study and physiological systems analysis. Chapter 3 goes into some detail about the potential pitfalls in genotyping association studies and how these were addressed in the current study. The areas of genotypi ng quality, linkage disequilibrium, ethnicity, sample size and validation of previously done work are discussed using MBL-2 and ACE as examples. Chapter 4 is a description of the work done on genetic variability in the endotoxin receptor complex and how in may result in the host response to severe infection and physical insults. TLR4 polymorphisms were associated with lower platelet counts in severe inflammation. The reasons for this are unclear but may point to a direct effect of the TLR4 pathways on platelets or indicate that platelet counts are a more sensitive marker of systemic inflammation than SIRS criteria. These data support the view that variation in TLR4 function influences the early inflammatory response. This phenomenon may be one aspect of reduced fitness in the capacity to respond appropriately to an insult. Chapter 5 reports the central role of complement in the acute phase response. Polymorphisms in two out of the three complement activation pathways were shown to have potential modifying effects in paediatric systemic inflammation. This chapter reports that polymorphisms in the CFH gene may modulate the acute inflammatory response and corroborates the previously reported finding that MBL-2 variant genotypes are a risk factor for the early occurrence of SIRS/sepsis in a large cohort of paediatric critical care patients, independent of other potentially important functional polymorphisms in the complement and innate immunity system. A better understanding of how these polymorphisms operate at the pathophysi ol ogi cal level is needed before these findings can be translated to clinically useful therapeutic modalities. This study demonstrates that genetic polymorphisms associated with reduced complement activation may be associated with early SIRS/sepsis. This is consistent with a view that appropriate complement activation occurring early following an infectious or inflammatory insult protects children from early SIRS/sepsis. Chapter 6 assesses the usefulness of full MBL-2 genotyping and compares the MBL-2 genotype and M BL serum levels between a cohort of healthy children and a cohort of critically ill paediatric patients. MBL2 genotyping did not render more information with regards to M BL serum level when all promoter and structural polymorphisms were identified over and above structural polymorphisms and the XY promoter polymorphism. The children admitted with infection did not have a surplus of M BL deficient genotypes as compared with healthy children. This suggests that M BL deficient genotypes do not predispose to severe infection. M BL serum levels in SIRS or sepsis were lower compared with critically ill children without systemic inflammation. M BL levels were most reduced in the acute phase response in those genotypes with intermediate serum levels, which may reflect a consumption of M BL in critical illness and an inability to maintain pre-insult M BL serum levels. Chapter 7 explores a novel way to discriminate SIRS from sepsis by means of heart rate variability analysis. In this small paired sample study no differences were seen in LF metrics to differentiate sterile SIRS from sepsis. Neither was there a difference in LF metrics between those children who went on to develop a nosocomial infection and those who did not. Normalised HF was significantly higher in sterile SIRS vs. sepsis. These preliminary finding require further validation and a longitudinal approach in a larger cohort. Finally, Chapter 8 discusses the findings of this thesis in the context of interpretation and of the findings and potential future approaches. This thesis supports the view that better metrics are required to discriminate systemic inflammation as well as the concept that in children control of an inflammatory threat is aided by a vigorous capacity to respond.
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Hatherill, Mark. "Transport of critically ill children in a resource-limited setting". Master's thesis, University of Cape Town, 2001. http://hdl.handle.net/11427/10987.

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Transportation of critically ill children by inexperienced personnel may be associated with increased risk of transfer-related adverse events and mortality. To audit paediatric intensive care unit (PICU) transfer activity and transfer-related adverse events in a resource-limited setting. Twenty-two bed regional PICU of a university children's hospital in Cape Town, South Africa. Prospective one-year audit of all children transferred directly to PICU from other hospitals. Data were collected for patient demographics and diagnostic category, referring hospital, transferring personnel, mode of transport, and the incidence of technical, clinical, and critical adverse events. Data are median (interquartile range, IQR). The transfers of 202 children, median age 2.8 months (1.1-14), median weight 3.5 kg (2.5-8.1) were analysed.
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Ista, Willem Gerrit. "Comfortably calm soothing sedation of critically ill children without withdrawal symptoms /". [S.l. : Rotterdam : The Author] ; Erasmus University [Host], 2008. http://hdl.handle.net/1765/13430.

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Ramelet, Anne-Sylvie. "The development of a multidimensional pain assessment scale for critically ill preverbal children". Thesis, Curtin University, 2006. http://hdl.handle.net/20.500.11937/1524.

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Adequate pain assessment is a pre-requisite for appropriate pain management. If pain remains untreated in critically ill young children, it can have dramatic short- and long-term consequences on their health and development. Apart from humanitarian reasons, the assessment of pain has been recognised in some parts of the world as the fifth vital sign and thus should be part of standard practice of pain management. The evaluation of pain in preverbal children is, nevertheless, challenging for health professionals, as they cannot rely on self-report when making their assessment. Observational pain instruments have been developed to facilitate this task, but none of these existing instruments are appropriate for the postoperative critically ill young child. The aim of this research was to provide a clinically valid pain instrument for health professionals to use in practice for the evaluation of the pain and the effectiveness of pain treatment in critically ill young children. This thesis presents research that was conducted in three phases to (a) describe pain, (b) develop, and (c) test the pain instrument. Conceptualisation of pain and psychometric theory informed the conceptual framework for this study. An observational design was used in Phase One of the study to define pain behaviour in critically ill infants. Correlational design was used in Phase Two and Three to determine the association between the newly developed pain scale and other pain assessment instruments. Phase One of the study was conducted in the paediatric intensive care units of two tertiary referral hospitals. Eight hundred and three recorded segments were generated from recordings of five critically ill infants, aged between 0 and 9 months, who had undergone major surgery.Results indicated significant physiological and behavioural changes in response to postoperative pain and when postoperative pain was exacerbated by painful procedures. Using the pain indicators observed in Phase One, in Phase Two the Multidimensional Assessment Pain Scale (MAPS) was developed and tested for reliability and validity in 43 postoperative preverbal children from the same settings. Internal consistency and interrater reliability were moderate and good, respectively. Concurrent and convergent validity was good. In Phase Three, the MAPS' response to analgesics and clinical utility was demonstrated in a convenience sample of 19 postoperative critically ill children aged between 0 and 3 1 months of age at a tertiary referral hospital in Western Australia. Development of a pain instrument is a complex and lengthy process. This study presents the preliminary psychometric properties that support the validity and clinical utility of the Multidimensional Assessment Pain Scale. The MAPS is a promising tool for assessing postoperative pain in critically ill young children, and its clinical validity will be strengthened with further testing and evaluation.
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Ramelet, Anne-Sylvie. "The development of a multidimensional pain assessment scale for critically ill preverbal children". Curtin University of Technology, School of Nursing and Midwifery, 2006. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=17177.

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Adequate pain assessment is a pre-requisite for appropriate pain management. If pain remains untreated in critically ill young children, it can have dramatic short- and long-term consequences on their health and development. Apart from humanitarian reasons, the assessment of pain has been recognised in some parts of the world as the fifth vital sign and thus should be part of standard practice of pain management. The evaluation of pain in preverbal children is, nevertheless, challenging for health professionals, as they cannot rely on self-report when making their assessment. Observational pain instruments have been developed to facilitate this task, but none of these existing instruments are appropriate for the postoperative critically ill young child. The aim of this research was to provide a clinically valid pain instrument for health professionals to use in practice for the evaluation of the pain and the effectiveness of pain treatment in critically ill young children. This thesis presents research that was conducted in three phases to (a) describe pain, (b) develop, and (c) test the pain instrument. Conceptualisation of pain and psychometric theory informed the conceptual framework for this study. An observational design was used in Phase One of the study to define pain behaviour in critically ill infants. Correlational design was used in Phase Two and Three to determine the association between the newly developed pain scale and other pain assessment instruments. Phase One of the study was conducted in the paediatric intensive care units of two tertiary referral hospitals. Eight hundred and three recorded segments were generated from recordings of five critically ill infants, aged between 0 and 9 months, who had undergone major surgery.
Results indicated significant physiological and behavioural changes in response to postoperative pain and when postoperative pain was exacerbated by painful procedures. Using the pain indicators observed in Phase One, in Phase Two the Multidimensional Assessment Pain Scale (MAPS) was developed and tested for reliability and validity in 43 postoperative preverbal children from the same settings. Internal consistency and interrater reliability were moderate and good, respectively. Concurrent and convergent validity was good. In Phase Three, the MAPS' response to analgesics and clinical utility was demonstrated in a convenience sample of 19 postoperative critically ill children aged between 0 and 3 1 months of age at a tertiary referral hospital in Western Australia. Development of a pain instrument is a complex and lengthy process. This study presents the preliminary psychometric properties that support the validity and clinical utility of the Multidimensional Assessment Pain Scale. The MAPS is a promising tool for assessing postoperative pain in critically ill young children, and its clinical validity will be strengthened with further testing and evaluation.
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Libros sobre el tema "Critically ill children"

1

Diakogiannaki, Eleftheria. Neopterin secretion in critically ill septic infants and children. Roehampton: University of Surrey Roehampton, 2004.

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R, Wong Hector, Shanley Thomas P y SpringerLink (Online service), eds. Resuscitation and Stabilization of the Critically Ill Child. London: Springer-Verlag London, 2009.

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Karin, McCloskey, ed. Evaluation, stabilization, and transport of the critically ill child. St. Louis: Mosby Year Book, 1992.

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Great Britain. National Assembly for Wales., ed. Gofalu am blant difrifol wael: Safonau = Caring for critically ill children : standards. Caerdydd: Llywodraeth Cynulliad Cymru = Welsh Assembly Government, 2003.

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D, Dickerman Joseph y Lucey Jerold F, eds. Smith's The critically ill child: Diagnosis and medical management. 3a ed. Philadelphia: Saunders, 1985.

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Philo, Jolene. A different dream for my child: Meditations for parents of critically and chronically ill children. Grand Rapids, Mich: Discovery House Publishers, 2009.

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Philo, Jolene. A different dream for my child: Meditations for parents of critically and chronically ill children. Grand Rapids, Mich: Discovery House Publishers, 2009.

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Philo, Jolene. A different dream for my child: Meditations for parents of critically and chronically ill children. Grand Rapids, Mich: Discovery House Publishers, 2009.

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Philo, Jolene. A different dream for my child: Meditations for parents of critically and chronically ill children. Grand Rapids, Mich: Discovery House Publishers, 2009.

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A different dream for my child: Meditations for parents of critically and chronically ill children. Grand Rapids, Mich: Discovery House Publishers, 2009.

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Capítulos de libros sobre el tema "Critically ill children"

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Meyer, Rosan y Luise Marino. "Nutrition in Critically Ill Children". En Clinical Paediatric Dietetics, 66–80. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118915349.ch5.

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Schepens, T. y H. Mtaweh. "Muscle Dysfunction in Critically Ill Children". En Annual Update in Intensive Care and Emergency Medicine, 583–94. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-37323-8_44.

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Walleigh, Diana J., Douglas M. Smith, Emily L. McGinnis y Nicholas S. Abend. "Status Epilepticus in Critically Ill Children". En Status Epilepticus, 353–69. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-58200-9_28.

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Perry, Mallory A. y Sapna R. Kudchadkar. "Sleep Considerations in Critically Ill Children". En Sleep in Critical Illness, 273–89. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-06447-0_16.

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Paganelli, Massimiliano. "Liver Transplantation in Critically Ill Children". En Liver Diseases in the Pediatric Intensive Care Unit, 143–60. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-79132-2_10.

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Sharma, Alok. "Fungal Infection in Critically Ill Children". En Infectious Diseases in the Pediatric Intensive Care Unit, 97–112. London: Springer London, 2008. http://dx.doi.org/10.1007/978-1-84628-917-0_3.

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Yap, Hui-Kim y Lourdes Paula R. Resontoc. "Peritoneal Dialysis in Critically Ill Children". En Critical Care Nephrology and Renal Replacement Therapy in Children, 307–23. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-90281-4_20.

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Todres, I. D. "Critical Airway Obstruction in Children". En Care of the Critically Ill Patient, 1309–33. London: Springer London, 1992. http://dx.doi.org/10.1007/978-1-4471-3400-8_78.

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Stormorken, Anne. "Tolerance and Withdrawal in Critically Ill Children". En Sedation and Analgesia for the Pediatric Intensivist, 143–51. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-52555-2_11.

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Bruce, D. A. "Treatment of Severe Head Injury in Children". En Care of the Critically Ill Patient, 1399–413. London: Springer London, 1992. http://dx.doi.org/10.1007/978-1-4471-3400-8_83.

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Actas de conferencias sobre el tema "Critically ill children"

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Yanni, Gema Nazri y Rina Amalia C. Saragih. "Platelet Profile Distribution in Critically Ill Children". En International Conference of Science, Technology, Engineering, Environmental and Ramification Researches. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0010098808870890.

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Carlton, E., S. Gorga, J. Close, A. Dews, K. Paice, J. Struza, R. Barbaro, H. C. Prescott y T. Cornell. "Clinician Prediction of Organ Failure in Critically Ill Children". En American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a4805.

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Verbeeten, P., S. Ray y M. Peters. "G450(P) The distribution of heart rate in critically ill children". En Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 24–26 May 2017, ICC, Birmingham. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313087.443.

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Laird, A., S. Lawson, M. Morrow y M. Terris. "P35 Improving team competencies in the management of critically ill children". En Abstracts of the Association for Simulation Practice in Healthcare Annual Conference, 6th to 7th November 2017, Telford, UK. The Association for Simulated Practice in Healthcare, 2017. http://dx.doi.org/10.1136/bmjstel-2017-aspihconf.119.

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Cronin, M., L. Dervan y S. Watson. "Use of Quetiapine in Treatment of Delirium in Critically Ill Children". En American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a1876.

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Stroup, Emily Kunce, Yuan Luo y L. Nelson Sanchez-Pinto. "Phenotyping Multiple Organ Dysfunction Syndrome Using Temporal Trends in Critically Ill Children". En 2019 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2019. http://dx.doi.org/10.1109/bibm47256.2019.8983126.

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Hui, Wun Fung y Kam Lun Hon. "417 The application of extracorporeal blood purification (EBP) in critically ill children". En RCPCH Conference Singapore. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/bmjpo-2021-rcpch.234.

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Choi, Daniel H., Sonali Basu y David Steinhorn. "Ascorbic Acid Levels in Critically-Ill Children and the Impact of Nutrition". En AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.421-a.

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Murphy, Sinead, Chaitanya Undavalli, Amy Weaver y Sheri Crow. "Developmental Outcomes in Critically Ill Children: A Population Based Birth Cohort Report". En Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.315.

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Hui, Wun Fung, Vivian Pui Ying Chan, Kam Lun Hon y Man Hong Poon. "414 Risk factor and outcome of acute kidney injury among critically ill children". En RCPCH Conference Singapore. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/bmjpo-2021-rcpch.232.

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Informes sobre el tema "Critically ill children"

1

Very strict blood sugar control in critically ill children provides no benefit. National Institute for Health Research, mayo de 2017. http://dx.doi.org/10.3310/signal-000416.

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Age of stored blood used for transfusions in critically ill children doesn’t affect outcomes. National Institute for Health Research, febrero de 2020. http://dx.doi.org/10.3310/signal-000883.

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