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Routine Administration of Vitamin K1 Prophylaxis to the Newborn
Routine Administration of Vitamin K1 Prophylaxis to the Newborn Practice Resource for Health Care Providers July 2016 Practice Resource Guide: ROUTINE ADMINISTRATION OF VITAMIN K1 PROPHYLAXIS TO THE NEWBORN The information attached is the summary of the position statement and the recommendations from the recent CPS evidence-based guideline for routine intramuscular administration of Vitamin K1 prophylaxis to the newborn*: www.cps.ca/documents/position/administration-vitamin-K-newborns Summary Vitamin K deficiency bleeding or VKDB (formerly known as hemorrhagic disease of the newborn or HDNB) is significant bleeding which results from the newborn’s inability to sufficiently activate vitamin K-dependent coagulation factors because of a relative endogenous and exogenous deficiency of vitamin K.1 There are three types of VKDB: 1. Early onset VKDB, which appears within the first 24 hours of life, is associated with maternal medications that interfere with vitamin K metabolism. These include some anticonvulsants, cephalosporins, tuberculostatics and anticoagulants. 2. Classic VKDB appears within the first week of life, but is rarely seen after the administration of vitamin K. 3. Late VKDB appears within three to eight weeks of age and is associated with inadequate intake of vitamin K (exclusive breastfeeding without vitamin K prophylaxis) or malabsorption. The incidence of late VKDB has increased in countries that implemented oral vitamin K rather than intramuscular administration. There are three methods of Vitamin K1 administration: intramuscular, oral and intravenous. The Canadian Paediatric Society (2016)2 and the American Academy of Pediatrics (2009)3 recommend the intramuscular route of vitamin K administration. The intramuscular route of Vitamin K1 has been the preferred method in North America due to its efficacy and high compliance rate. -
Vitamin K for the Prevention of Vitamin K Deficiency Bleeding (VKDB)
Title: Vitamin K for the Prevention of Vitamin K Deficiency Bleeding (VKDB) in Newborns Approval Date: Pages: NEONATAL CLINICAL February 2018 1 of 3 Approved by: Supercedes: PRACTICE GUIDELINE Neonatal Patient Care Teams, HSC & SBH SBH #98 Women’s Health Maternal/Newborn Committee Child Health Standards Committee 1.0 PURPOSE 1.1 To ensure all newborns are properly screened for the appropriate Vitamin K dose and route of administration and managed accordingly. Note: All recommendations are approximate guidelines only and practitioners must take in to account individual patient characteristics and situation. Concerns regarding appropriate treatment must be discussed with the attending neonatologist. 2.0 PRACTICE OUTCOME 2.1 To reduce the risk of Vitamin K deficiency bleeding. 3.0 DEFINITIONS 3.1 Vitamin K deficiency bleeding (VKDB) of the newborn: previously referred to as hemorrhagic disease of the newborn. It is unexpected and potentially severe bleeding occurring within the first week of life. Late onset VKDB can also occur in infants 2-12 weeks of age with severe vitamin k deficiency. Bleeding in both types is primarily gastro-intestinal and intracranial. 3.2 Vitamin K1: also known as phytonadione, an important cofactor in the synthesis of blood coagulation factors II, VII, IX and X. 4.0 GUIDELINES Infants greater than 1500 gm birthweight 4.1 Administer Vitamin K 1 mg IM as a single dose within 6 hours of birth. 4.1.1 The infant’s primary health care provider (PHCP): offer all parents the administration of vitamin K intramuscularly (IM) for their infant. 4.1.2 If parent(s) refuse any vitamin K administration to the infant, discuss the risks of no vitamin K administration, regardless of route, with the parent(s). -
Asthma Initiative Content
WAO Symposium Why Are Small Airways Important In Asthma? “Physiology Of Small Airways Disease” Thomas B Casale, MD Professor Of Medicine Chief, Allergy/Immunology Creighton University Omaha, NE USA Disease Process in Asthma is Located in All Parts of Bronchial Tree Including Small Airways and Alveoli Workgroep Inhalatie Technologie, Jun 1999. Relevant Questions On Small Airway Involvement In Asthma • How can „small airway disease‟ be defined? • What is the link between small airway abnormalities and clinical presentation in asthma ? • When does small airway involvement become relevant in the natural history of the disease? • Is it possible to reverse small airway abnormalities with pharmacological treatment? Contoli et al Allergy 2010; 65: 141–151 Pathophysiologic Changes in the Small Airways of Asthma Patients Transbronchial Biopsies 1 Lumen occlusion 2 Subepithelial fibrosis 3 Increase in smooth muscle mass 4 Inflammatory infiltrate 1 Immunostaining of eosinophils in small airway with major basic protein (in red) 2 Shows large number of eosinophils around the small airway Contoli M, et al. Allergy. 2010;65:141-151. Structural Alterations in Small Airways Associated With Fatal Asthma Small airway of a Small airway of a control subject subject with fatal asthma Mucus plugging Structural alterations in small airways have been implicated as an underlying reason for increased asthma severity and AHR….. Difficult to control asthma. Mauad T, et al. Am J Respir Crit Care Med. 2004;70:857-862. Differences In ECM Composition In Small Airways Between Fatal Asthma And Controls Dolhnikoff et al, JACI 2009; 123:1090-1097 Is There Differential Inflammation in Proximal and More Distal Airways? • Some studies suggest that the cellular infiltrate increases toward the periphery, but others show similar or decreased infiltration – May reflect heterogeneity of asthma as well as the different methods used in the studies . -
Epidemiology and Pulmonary Physiology of Severe Asthma
Epidemiology and Pulmonary Physiology of Severe Asthma a b Jacqueline O’Toole, DO , Lucas Mikulic, MD , c, David A. Kaminsky, MD * KEYWORDS Demographics Phenotype Health care utilization Pulmonary function Lung elastic recoil Ventilation heterogeneity Gas trapping Airway hyperresponsiveness KEY POINTS The definition of severe asthma is still a work in progress. The severity of asthma is predictive of higher health care utilization. Cluster analysis is useful in characterizing severe asthma phenotypes. Airway hyperresponsiveness in severe asthma is a result of abnormal airflow, lung recoil, ventilation, and gas trapping. Patients with severe asthma may have a reduced perception of dyspnea. INTRODUCTION Severe asthma is a characterized by a complex set of clinical, demographic, and physiologic features. In this article, we review both the epidemiology and pulmonary physiology associated with severe asthma. DEMOGRAPHICS OF SEVERE ASTHMA Asthma has long been recognized as a worldwide noncommunicable disease of importance. Within the population of individuals with asthma, there is a subgroup of individuals at high risk for complications, exacerbations, and a poor quality of life. The authors have nothing to disclose. a Department of Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Bur- lington, VT 05401, USA; b Division of Pulmonary and Critical Care Medicine, University of Ver- mont Medical Center, Given D208, 89 Beaumont Avenue, Burlington, VT 05405, USA; c Division of Pulmonary and Critical Care Medicine, University of Vermont College of Medicine, Given D213, 89 Beaumont Avenue, Burlington, VT 05405, USA * Corresponding author. E-mail address: [email protected] Immunol Allergy Clin N Am 36 (2016) 425–438 http://dx.doi.org/10.1016/j.iac.2016.03.001 immunology.theclinics.com 0889-8561/16/$ – see front matter Ó 2016 Elsevier Inc. -
Vitamin K Information for Parents-To-Be
Vitamin K Information for parents-to-be Maternity This leaflet has been written to help you decide whether your baby should receive a vitamin K supplement at birth. What is vitamin K? Vitamin K is needed for the normal clotting of blood and is naturally made in the bowel. page 2 Why is vitamin K given to newborn babies? All babies are born with low levels of vitamin K. Several days after birth, a baby will normally produce their own supply of vitamin K from natural bacteria found in their bowel. They can also get a small amount of vitamin K from their mother’s breast milk and it is added to formula milk. This can help the natural bacteria in the baby’s bowel to develop, which in turn improves their levels of vitamin K. However, babies are more at risk of developing vitamin K deficiency until they are feeding well. A deficiency in vitamin K is the main cause of vitamin K deficiency bleeding (VKDB). This can cause bleeding from the belly button, nose, surgical sites (i.e. following circumcision), and (rarely) in the brain. The risk of this happening is approximately 1 in 100,000 for full term babies. VKDB is a serious disorder, which may lead to internal bleeding. Signs of internal bleeding are: • blood in the nappy • oozing (bleeding) from the cord • nose bleeds • bleeding from scratches which doesn’t stop on its own • bruising • prolonged jaundice (yellowing of the skin) at three weeks if breast feeding and two weeks if formula feeding. VKDB can also lead to bleeding on the brain, which can cause brain damage and/or death. -
The Effect of Continuous Positive Airway Pressures on Lung Volumes
Paraplegia (1996) 34, 54- 58 © 1996 International Medical Society of Paraplegia All rights reserved 0031-1758/96 $12.00 The effect of continuous positive airway pressures on lung volumes in tetraplegic patients 2 LA Harveyl and ER Ellis 2 1 Physiotherapy Department, The Prince Henry Hospital, Sydney; School of Physiotherapy, Faculty of Health Sciences, The University of Sydney, Sydney, Australia Continuous positive airway pressure (CPAP) is widely advocated for the treatment of respiratory complications. However the effects of CPAP on the respiratory function of tetraplegic patients have not yet been investigated. The purpose of this study was to examine the effects of breathing with different levels of CPAP on the relationship between closing volume (CV) and functional residual capacity (FRC) in ten recently injured, but otherwise healthy tetraplegic patients with lesions between the fourth and eighth cervical segments. Lung volumes were measured before, during and after 32 min of zero end-expiratory pressure and 5 and 10 cm H20 of CPAP. FRC was measured by the open-circuit nitrogen washout method and CV was measured by the single breath nitrogen washout method. FRC was unaffected by zero end-expiratory pressure, but both 5 cm H20 and 10 cm H20 of CPAP caused significant increases in FRC. FRC returned to pre-CPAP values by the first minute after removal of 5 and 10 cm H20 of CPAP. We were unable to measure CVs in any subjects. It was concluded that 5 and 10 cm H20 of CPAP increase FRC in healthy tetraplegic individuals, but that these increases are rapidly lost with the subsequent removal of CPAP. -
Vitamin K for Newborn Babies: Information for Parents
Vitamin K for Newborn Babies Information for parents This leaflet explains what vitamin K is, and its importance in preventing bleeding problems in newborn babies. We hope it gives you enough information to help you make an informed choice about this part of your baby’s care. What is vitamin K? Vitamin K occurs naturally in food (especially red meat and some green vegetables). It is also produced by friendly bacteria in our gut. We all need it as it helps to make our blood clot and to prevent bleeding problems. Newborn babies and young infants have very little vitamin K. How do low levels of Vitamin K affect a newborn baby? A very small number of babies suffer bleeding problems due to a shortage of vitamin K. This is called Vitamin K Deficiency Bleeding (or VKDB for short). The classical form usually happens in the first week of life. The baby may bleed from the mouth or nose or from the stump of the umbilical cord. Late onset VKDB is a more serious problem which happens after the baby is about three weeks old. The bleeding is sometimes into the gut or the brain and in some cases it can cause brain damage or even death. How can Vitamin K Deficient Bleeding be prevented? The Scottish Government recommends that all newborn babies are given vitamin K to reduce the chances of dangerous internal bleeding. The most effective treatment is a single dose of vitamin K injected into the thigh muscle shortly after birth. Vitamin K by mouth is also effective in most cases but your baby will need to have a number of doses through the first 1-3 months of life. -
Hyperemesis Gravidarum: Strategies to Improve Outcomes
The Art and Science of Infusion Nursing Hyperemesis Gravidarum Strategies to Improve Outcomes 03/11/2020 on //7dIgeiLuhMkL9kWvKwgfAPGFMPj02nltGDDFVobkWqncHWQRlSg9yjBWU9jBuwQSAQCN6yy/R8eEgzReezmPfm5ALSU3NvEsywdL7iOhefmPs35WVNSjdaQz7H5GI7 by http://journals.lww.com/journalofinfusionnursing from Downloaded Downloaded Kimber Wakefield MacGibbon, BSN, RN from http://journals.lww.com/journalofinfusionnursing ABSTRACT Hyperemesis gravidarum (HG) is a debilitating and potentially life-threatening pregnancy disease marked by weight loss, malnutrition, and dehydration attributed to unrelenting nausea and/or vomiting; HG increases the risk of adverse outcomes for the mother and child(ren). The complexity of HG affects every aspect of a woman’s life during and after pregnancy. Without methodical intervention by knowledgeable and proactive clinicians, life-threatening complications may develop. Effectively managing HG requires an understanding of both physical and psychosocial by //7dIgeiLuhMkL9kWvKwgfAPGFMPj02nltGDDFVobkWqncHWQRlSg9yjBWU9jBuwQSAQCN6yy/R8eEgzReezmPfm5ALSU3NvEsywdL7iOhefmPs35WVNSjdaQz7H5GI7 stressors, recognition of potential risks and complications, and proactive assessment and treatment strategies using innovative clinical tools. Key words: antiemetic, enteral nutrition, genetics, granisetron, HELP score, hyperemesis gravidarum, intravenous, malnutrition, nausea, neurodevelopmental disorder, ondansetron, parenteral nutrition, pregnancy, premature delivery, total parenteral nutrition, vomiting, vomiting center, Wernicke’s encephalopathy, -
Vitamin K1 (Phytomenadione) 2021 Newborn Use Only
Vitamin K1 (Phytomenadione) 2021 Newborn use only Alert Check ampoule carefully as an adult 10 mg ampoule (Konakion MM Adult) is also available. USE ONLY Konakion MM Paediatric. Vitamin K Deficiency Bleeding is also known as Haemorrhagic Disease of Newborn (HDN) Indication Prophylaxis and treatment of vitamin K deficiency bleeding (VKDB) Action Fat soluble vitamin. Promotes the activation of blood coagulation Factors II, VII, IX and X in the liver. Drug type Vitamin. Trade name Konakion MM Paediatric. Presentation 2 mg/0.2 mL ampoule. Dose IM prophylaxis (Recommended route)(1) Birthweight ≥ 1500 g - 1 mg (0.1 mL of Konakion® MM) as a single dose at birth. Birthweight <1500 g - 0.5 mg (0.05 mL of Konakion® MM) as a single dose at birth. Oral prophylaxis(1) 2 mg (0.2 mL of Konakion® MM) for 3 doses: • First dose: At birth. • Second dose: 3–5 days of age (at time of newborn screening) • Third dose: During 4th week (day 22-28 of life). • It is imperative that the third dose is given no later than 4 weeks after birth as the effect of earlier doses decreases after this time. • Repeat the oral dose if infant vomits within an hour of an oral dose or if diarrhoea occurs within 24 hours of administration. IV Prophylaxis (5) May be given in sick infants if unable to give IM or oral injection. 0.3 mg/kg (0.2-0.4 mg/kg) as a single dose as a slow bolus (maximum 1 mg/minute). Dose can be repeated weekly. IV treatment of Vitamin K deficiency bleeding (VKDB) 1 mg IV as a slow bolus (maximum 1 mg/minute). -
Hyperemesis Gravidarum
YPEREMESIS GRAVIDARUM WILLIAMS 2020/RCOG GUIDLINE DR. ROYA FARAJI Hyperemesis Gravidarum: Severe unrelenting nausea and vomiting —hyperemesis gravidarum—is defined variably as being sufficiently severe to produce weight loss, dehydration, ketosis, alkalosis from loss of hydrochloric acid, and hypokalemia. it is severe and unresponsive to simple dietary modification and antiemetics. Other causes should be considered because ultimately hyperemesis gravidarum is a diagnosis of exclusion Incidence Reports of population incidences vary. It is appear to be an ethnic or familial predilection. In population-based studies from California, Nova Scotia, and Norway, the hospitalization rate for hyperemesis gravidarum was 0.5 to 1 percent. Up to 20 percent of those hospitalized in a previous pregnancy for hyperemesis will again require hospitalization . In general, obese women are less likely to be hospitalized for this. Etiopathogenesis The Etiopathogenesis of hyperemesis gravidarum is unknown and is likely multifactorial. It apparently is related to high or rapidly rising serum levels of pregnancy-related hormones. Putative culprits include human chorionic gonadotropin (hCG), estrogen, progesterone, leptin, placental growth hormone, prolactin, thyroxine, and adrenocortical hormone . More recently implicated are other hormones that include ghrelins, leptin, nesfatin-1, and peptide YY. Superimposed on this hormonal cornucopia are an imposing number of biological and environmental factors. Moreover, in some but not all severe cases, interrelated psychological components play a major role . Other factors that increase the risk for admission include hyperthyroidism, previous molar pregnancy, diabetes, gastrointestinal illnesses, some restrictive diets, and asthma and other allergic disorders . An association of Helicobacter pylori infection has been proposed, but evidence is not conclusive Chronic marijuana use may cause the similar cannabinoid hyperemesis syndrom. -
Lung Elastic Recoil and Ventilation Heterogeneity of Diffusion-Dependent Airways in Older People with Asthma and Fixed Airflow Obstruction
AGORA | RESEARCH LETTER Lung elastic recoil and ventilation heterogeneity of diffusion-dependent airways in older people with asthma and fixed airflow obstruction To the Editor: Small airways are abnormal in asthma [1]. One measurement of small airway function is Sacin, derived from the multiple-breath nitrogen washout (MBNW) test. Sacin reflects ventilation heterogeneity in diffusion-dependent airways, and is correlated with airway hyperresponsiveness [2] and asthma control [3]. Theoretically, heterogeneity of diffusion-dependent ventilation can arise due to the heterogeneity of cross-sectional areas of airway openings in terminal airways and the acini [4]. Therefore, Sacin may be affected by structural changes in those airways. The elastic properties of the lung may also affect Sacin,as the phase III slope, a marker of ventilation heterogeneity derived from the single-breath nitrogen washout, correlates with lung compliance in explanted lungs of smokers and in healthy lungs [5]. Reduced lung elastic recoil makes a large contribution to airflow obstruction in asthma [6], particularly in older individuals who may develop fixed airflow obstruction (FAO). FAO typifies chronic obstructive pulmonary disease (COPD) but can occur in older asthmatics who have never smoked and despite adequate treatment [7, 8]. Since FAO is associated with age and Sacin is more abnormal in older asthmatics compared to younger [2], we hypothesised that the increase in Sacin in older people with asthma was due to loss of lung elastic recoil. Therefore, the aim of this study was to examine the relationships between Sacin and elastic recoil pressure and compliance. We enrolled subjects from tertiary hospital clinics who were >40 years old, had ⩽5-pack-year smoking history and a physician diagnosis of asthma. -
“Children Are Not Small Adults!” Derek S
4 The Open Inflammation Journal, 2011, 4, (Suppl 1-M2) 4-15 Open Access “Children are not Small Adults!” Derek S. Wheeler*1,2, Hector R. Wong1,2 and Basilia Zingarelli1,2 1Division of Critical Care Medicine, Cincinnati Children’s Hospital Medical Center, The Kindervelt Laboratory for Critical Care Medicine Research, Cincinnati Children’s Research Foundation, USA 2Department of Pediatrics, University of Cincinnati College of Medicine, USA Abstract: The recognition, diagnosis, and management of sepsis remain among the greatest challenges in pediatric critical care medicine. Sepsis remains among the leading causes of death in both developed and underdeveloped countries and has an incidence that is predicted to increase each year. Unfortunately, promising therapies derived from preclinical models have universally failed to significantly reduce the substantial mortality and morbidity associated with sepsis. There are several key developmental differences in the host response to infection and therapy that clearly delineate pediatric sepsis as a separate, albeit related, entity from adult sepsis. Thus, there remains a critical need for well-designed epidemiologic and mechanistic studies of pediatric sepsis in order to gain a better understanding of these unique developmental differences so that we may provide the appropriate treatment. Herein, we will review the important differences in the pediatric host response to sepsis, highlighting key differences at the whole-organism level, organ system level, and cellular and molecular level. Keywords: Pediatrics, sepsis, shock, severe sepsis, septic shock, SIRS, systemic inflammatory response syndrome, critical care. THE PEDIATRIC HOST RESPONSE TO SEPSIS Sepsis is exceedingly more common in children less than 1 year of age, with rates 10-fold higher during infancy Key Differences at the Whole-organism Level compared to childhood and adolescence [2].