Medical Management of Vaccine Reactions in Adult Patients
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Differentiating Between Anxiety, Syncope & Anaphylaxis
Differentiating between anxiety, syncope & anaphylaxis Dr. Réka Gustafson Medical Health Officer Vancouver Coastal Health Introduction Anaphylaxis is a rare but much feared side-effect of vaccination. Most vaccine providers will never see a case of true anaphylaxis due to vaccination, but need to be prepared to diagnose and respond to this medical emergency. Since anaphylaxis is so rare, most of us rely on guidelines to assist us in assessment and response. Due to the highly variable presentation, and absence of clinical trials, guidelines are by necessity often vague and very conservative. Guidelines are no substitute for good clinical judgment. Anaphylaxis Guidelines • “Anaphylaxis is a potentially life-threatening IgE mediated allergic reaction” – How many people die or have died from anaphylaxis after immunization? Can we predict who is likely to die from anaphylaxis? • “Anaphylaxis is one of the rarer events reported in the post-marketing surveillance” – How rare? Will I or my colleagues ever see a case? • “Changes develop over several minutes” – What is “several”? 1, 2, 10, 20 minutes? • “Even when there are mild symptoms initially, there is a potential for progression to a severe and even irreversible outcome” – Do I park my clinical judgment at the door? What do I look for in my clinical assessment? • “Fatalities during anaphylaxis usually result from delayed administration of epinephrine and from severe cardiac and respiratory complications. “ – What is delayed? How much time do I have? What is anaphylaxis? •an acute, potentially -
Emerging Evidence for a Central Epinephrine-Innervated A1- Adrenergic System That Regulates Behavioral Activation and Is Impaired in Depression
Neuropsychopharmacology (2003) 28, 1387–1399 & 2003 Nature Publishing Group All rights reserved 0893-133X/03 $25.00 www.neuropsychopharmacology.org Perspective Emerging Evidence for a Central Epinephrine-Innervated a1- Adrenergic System that Regulates Behavioral Activation and is Impaired in Depression ,1 1 1 1 1 Eric A Stone* , Yan Lin , Helen Rosengarten , H Kenneth Kramer and David Quartermain 1Departments of Psychiatry and Neurology, New York University School of Medicine, New York, NY, USA Currently, most basic and clinical research on depression is focused on either central serotonergic, noradrenergic, or dopaminergic neurotransmission as affected by various etiological and predisposing factors. Recent evidence suggests that there is another system that consists of a subset of brain a1B-adrenoceptors innervated primarily by brain epinephrine (EPI) that potentially modulates the above three monoamine systems in parallel and plays a critical role in depression. The present review covers the evidence for this system and includes findings that brain a -adrenoceptors are instrumental in behavioral activation, are located near the major monoamine cell groups 1 or target areas, receive EPI as their neurotransmitter, are impaired or inhibited in depressed patients or after stress in animal models, and a are restored by a number of antidepressants. This ‘EPI- 1 system’ may therefore represent a new target system for this disorder. Neuropsychopharmacology (2003) 28, 1387–1399, advance online publication, 18 June 2003; doi:10.1038/sj.npp.1300222 Keywords: a1-adrenoceptors; epinephrine; motor activity; depression; inactivity INTRODUCTION monoaminergic systems. This new system appears to be impaired during stress and depression and thus may Depressive illness is currently believed to result from represent a new target for this disorder. -
Review Cutaneous Patterns Are Often the Only Clue to a a R T I C L E Complex Underlying Vascular Pathology
pp11 - 46 ABstract Review Cutaneous patterns are often the only clue to a A R T I C L E complex underlying vascular pathology. Reticulate pattern is probably one of the most important DERMATOLOGICAL dermatological signs of venous or arterial pathology involving the cutaneous microvasculature and its MANIFESTATIONS OF VENOUS presence may be the only sign of an important underlying pathology. Vascular malformations such DISEASE. PART II: Reticulate as cutis marmorata congenita telangiectasia, benign forms of livedo reticularis, and sinister conditions eruptions such as Sneddon’s syndrome can all present with a reticulate eruption. The literature dealing with this KUROSH PARSI MBBS, MSc (Med), FACP, FACD subject is confusing and full of inaccuracies. Terms Departments of Dermatology, St. Vincent’s Hospital & such as livedo reticularis, livedo racemosa, cutis Sydney Children’s Hospital, Sydney, Australia marmorata and retiform purpura have all been used to describe the same or entirely different conditions. To our knowledge, there are no published systematic reviews of reticulate eruptions in the medical Introduction literature. he reticulate pattern is probably one of the most This article is the second in a series of papers important dermatological signs that signifies the describing the dermatological manifestations of involvement of the underlying vascular networks venous disease. Given the wide scope of phlebology T and its overlap with many other specialties, this review and the cutaneous vasculature. It is seen in benign forms was divided into multiple instalments. We dedicated of livedo reticularis and in more sinister conditions such this instalment to demystifying the reticulate as Sneddon’s syndrome. There is considerable confusion pattern. -
Skin Manifestations of Illicit Drug Use Manifestações Cutâneas
RevABDV81N4.qxd 12.08.06 13:10 Page 307 307 Educação Médica Continuada Manifestações cutâneas decorrentes do uso de drogas ilícitas Skin manifestations of illicit drug use Bernardo Gontijo 1 Flávia Vasques Bittencourt 2 Lívia Flávia Sebe Lourenço 3 Resumo: O uso e abuso de drogas ilícitas é um problema significativo e de abrangência mun- dial. A Organização das Nações Unidas estima que 5% da população mundial entre os 15 e 64 anos fazem uso de drogas pelo menos uma vez por ano (prevalência anual), sendo que meta- de destes usam regularmente, isto é, pelo menos uma vez por mês. Muitos dos eventos adver- sos das drogas ilícitas surgem na pele, o que torna fundamental que o dermatologista esteja familiarizado com essas alterações. Palavras-chave: Drogas ilícitas; Drogas ilícitas/história; Drogas ilícitas/efeitos adversos; Pele; Revisão Abstract: Illicit drug use and abuse is a major problem all over the world. The United Nations estimates that 5% of world population (aged 15-64 years) use illicit drugs at least once a year (annual prevalence) and half of them use drugs regularly, that is, at least once a month. Many adverse events of illicit drugs arise on the skin and therefore dermatologists should be aware of these changes. Keywords: Street drugs; Street drugs/history; Street drugs/adverse effects; Skin; Review HISTÓRICO Há mais de cinco mil anos na Mesopotâmia, minorar o sofrimento dos condenados. região onde hoje se situa o Iraque, os poderes cal- Provavelmente seja o ópio a droga nephente à qual mantes, soníferos e anestésicos do ópio (do latim Homero se referia como “o mais poderoso destrui- opium, através do grego opion, ‘seiva, suco’) já eram dor de mágoas”.1,2 conhecidos pelos sumérios. -
Cocaine Intoxication and Hypertension
THE EMCREG-INTERNATIONAL CONSENSUS PANEL RECOMMENDATIONS Cocaine Intoxication and Hypertension Judd E. Hollander, MD From the Department of Emergency Medicine, University of Pennsylvania, Philadelphia, PA. 0196-0644/$-see front matter Copyright © 2008 by the American College of Emergency Physicians. doi:10.1016/j.annemergmed.2007.11.008 [Ann Emerg Med. 2008;51:S18-S20.] with cocaine intoxication is analogous to that of the patient with hypertension: the treatment should be geared toward the Cocaine toxicity has been reported in virtually all organ patient’s presenting complaint. systems. Many of the adverse effects of cocaine are similar to When the medical history is clear and symptoms are mild, adverse events that can result from either acute hypertensive laboratory evaluation is usually unnecessary. In contrast, if the crisis or chronic effects of hypertension. Recognizing when the patient has severe toxicity, evaluation should be geared toward specific disease requires treatment separate from cocaine toxicity the presenting complaint. Laboratory evaluation may include a is paramount to the treatment of patients with cocaine CBC count; determination of electrolyte, glucose, blood urea intoxication. nitrogen, creatine kinase, and creatinine levels; arterial blood The initial physiologic effect of cocaine on the cardiovascular gas analysis; urinalysis; and cardiac marker determinations. system is a transient bradycardia as a result of stimulation of the Increased creatine kinase level occurs with rhabdomyolysis. vagal nuclei. Tachycardia typically ensues, predominantly from Cardiac markers are increased in myocardial infarction. Cardiac increased central sympathetic stimulation. Cocaine has a troponin I is preferred to identify acute myocardial13 infarction. cardiostimulatory effect through sensitization to epinephrine A chest radiograph should be obtained in patients with and norepinephrine. -
Atopic Children and Use of Prescribed Medication: a Comprehensive Study in General Practice
RESEARCH ARTICLE Atopic children and use of prescribed medication: A comprehensive study in general practice David H. J. Pols1*, Mark M. J. Nielen2, Arthur M. Bohnen1, Joke C. Korevaar2, Patrick J. E. Bindels1 1 Department of General Practice, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands, 2 NIVEL, Netherlands Institute for Health Services Research, Utrecht, The Netherlands a1111111111 * [email protected] a1111111111 a1111111111 a1111111111 Abstract a1111111111 Purpose A comprehensive and representative nationwide general practice database was explored to study associations between atopic disorders and prescribed medication in children. OPEN ACCESS Citation: Pols DHJ, Nielen MMJ, Bohnen AM, Korevaar JC, Bindels PJE (2017) Atopic children Method and use of prescribed medication: A All children aged 0±18 years listed in the NIVEL Primary Care Database in 2014 were comprehensive study in general practice. PLoS ONE 12(8): e0182664. https://doi.org/10.1371/ selected. Atopic children with atopic eczema, asthma and allergic rhinitis (AR) were journal.pone.0182664 matched with controls (not diagnosed with any of these disorders) within the same general Editor: Anthony Peter Sampson, University of practice on age and gender. Logistic regression analyses were performed to study the differ- Southampton School of Medicine, UNITED ences in prescribed medication between both groups by calculating odds ratios (OR); 93 dif- KINGDOM ferent medication groups were studied. Received: March 24, 2017 Accepted: July 13, 2017 Results Published: August 24, 2017 A total of 45,964 children with at least one atopic disorder were identified and matched with Copyright: © 2017 Pols et al. This is an open controls. Disorder-specific prescriptions seem to reflect evidence-based medicine guide- access article distributed under the terms of the lines for atopic eczema, asthma and AR. -
Quick Tips on Recognizing Cutaneous Manifestations of Systemic Disease
FEATURE ARTICLE 2.0 Quick Tips on Recognizing Contact Hours Cutaneous Manifestations of Systemic Disease Jennifer Cittadino ABSTRACT: Although many skin manifestations are isolated This article will concentrate on nonmalignant cutaneous to a dermatological disorder, some skin manifestations can manifestations of systemic disease. The body systems will berelatedtoadeeper,moresystemicissue.Theskinis be reviewed, and their associated skin manifestations will be related to other body systems and functions. The impor- discussed. Some of the skin manifestations can be seen in tance of being able to recognize these dermatological multiple systemic disorders, such as erythema nodosum, manifestations and associate them with potential systemic which can be seen in pulmonary disorders, collagen and disease can be a critical diagnostic tool for the practitioner. vascular disorders, and gastrointestinal disorders. Pictures Sometimes, these skin manifestations can be the first sign will be provided when possible. of an internal disease. Although challenging, recognition, prompt diagnosis, and treatment can alter the course of a CARDIOVASCULAR AND PULMONARY SYSTEM life-threatening illness. There are several general cutaneous signs of cardiovascular Key words: Cutaneous, Dermatology, Systemic, Skin disease that may commonly be seen. These findings may include edema, cyanosis, clubbing of the nails, and corneal he skin is the largest organ in the body and one arcus. The corneal arcus appears as a gray-white ring around of the most visible body systems. The skin has the cornea and correlates with age and cholesterol levels. a reciprocal relationship between what is visu- A diagonal earlobe crease is also reported to be a marker for alized on the surface and what is occurring coronary artery disease (Uliasz & Lebwohl, 2008). -
(MPN) Symptoms
RECOGNIZING SYMPTOMS RECOGNIZING YOUR MPN SYMPTOMS The MPN LANDMARK SURVEY* is a large-scale analysis of patients with myeloproliferative neoplasms (MPNs) and Healthcare Professionals (HCPs) who treat these rare, chronic blood cancers (813 patients; 457 hematologists/oncologists). The results from LANDMARK provide new information that validates previous findings about the effect of MPN symptoms and their impact on the lives of patients, even those with low-risk MPNs. Fatigue is a symptom of particular note. Across diseases it was reported as the most common and severe symptom, and the one that patients most wanted to resolve. Symptoms such as fatigue can be vague and challenging to quantify. It is difficult to measure tiredness and its impact on daily life. In addition to physical symptoms, patients in the survey reported emotional difficulties—feeling irritable, angry or depressed. Many patients surveyed suffered with their MPN symptoms for a year or more before diagnosis. LANDMARK helps to confirm that MPN symptoms have a significant, negative impact on daily activities and quality of life, often resulting in limited or canceled family and/or social activities. For some, it means having to miss days from work, reduce hours, or even leave their job. These issues create stress, anxiety, and financial hardship for MPN patients. This information is intended to help patients validate the impact of MPN symptoms and know that they are not alone. SYMPTOM RECOGNITION Patients in the survey often did not recognize the connection between certain symptoms they were experiencing and their MPN. For example, patients with MPNs often have difficulty sleeping; however, some patients who reported this symptom did not realize it was related to their MPN. -
Epipen Injection Label
EPIPEN®- epinephrine injection EPIPEN Jr®- epinephrine injection Mylan Specialty L.P. ---------- EpiPen® (epinephrine) Auto-Injector 0.3 mg EpiPen® = one dose of 0.30 mg epinephrine (USP, 1:1000, 0.3 mL) EpiPen Jr® (epinephrine) Auto-Injector 0.15 mg EpiPenJr® = one dose of 0.15 mg epinephrine (USP, 1:2000, 0.3 mL) DESCRIPTION Each EpiPen® Auto-Injector delivers a single dose of 0.3 mg epinephrine injection, USP, 1:1000 (0.3 mL) in a sterile solution. Each EpiPen Jr® Auto-Injector delivers a single dose of 0.15 mg epinephrine injection, USP, 1:2000 (0.3 mL) in a sterile solution. The EpiPen and EpiPen Jr Auto-Injectors each contain 2 mL epinephrine solution. Approximately 1.7 mL remains in the auto- injector after activation and cannot be used. Each 0.3 mL in the EpiPen Auto-Injector contains 0.3 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0. Each 0.3 mL in the EpiPen Jr Auto-Injector contains 0.15 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is B-(3, 4-dihydroxyphenyl)-a-methyl-aminoethanol, with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the Reference ID: 3176782 formation of melanin. -
Patients on Beta-Blockers
Systemic Allergic & Immunoglobulin Disorders Bryan L. Martin, DO, MMAS, FACAAI, FAAAAI, FACP, FACOI Emeritus Professor of Medicine and Pediatrics President, American College of Allergy, Asthma & Immunology Disclosures . None 2 Objectives . Pass the boards! . Recognize anaphylaxis and understand the new guidelines for the treatment of anaphylaxis . Compare and contrast anaphylactic and anaphylactoid reactions 3 The Patient . 45 year old woman goes to lunch with her friends . While eating she develops GI upset, dizziness, shortness of breath and hives . Her friends drive her to your nearby clinic Initial Evaluation . Your nurse gets the history of sudden onset of GI upset, dizziness, shortness of breath and hives while eating a shrimp salad. The patient now has audible wheezing, tachycardia, and a blood pressure of 110/60 . Your initial response . Take a detailed history of everything the patient had to eat for lunch . Ask if she has a history of any medical issues such as asthma, diabetes or heart disease . Give nebulized beta agonist . Give 50 mg of oral diphenhydramine . Give 0.3 ml of IM epinephrine Anaphylaxis presentation . Your nurse gets the history of sudden onset of GI upset, dizziness, shortness of breath and hives while eating lunch. The patient now has audible wheezing, tachycardia, and a blood pressure of 110/60 . Your initial response . Take a detailed history of everything the patient had to eat for lunch . Ask if she has a history of any medical issues such as asthma, diabetes or heart disease . Give nebulized beta agonist . Give 50 mg of oral diphenhydramine . Give 0.3 ml of IM epinephrine Initial Response to anaphylaxis . -
Pain Assessment and Treatment in Children with Significant Impairment of the Central Nervous System Julie Hauer, Amy J
CLINICAL REPORT Guidance for the Clinician in Rendering Pediatric Care Pain Assessment and Treatment in Julie Hauer, MD, FAAP, a, b Amy J. Houtrow, MD, PhD, MPH, FAAP, c SECTION ON HOSPICE ChildrenAND PALLIATIVE MEDICINE, COUNCIL With ON CHILDREN Significant WITH DISABILITIES Impairment of the Central Nervous System Pain is a frequent and significant problem for children with impairment abstract of the central nervous system, with the highest frequency and severity occurring in children with the greatest impairment. Despite the significance of the problem, this population remains vulnerable to underrecognition and undertreatment of pain. Barriers to treatment may include uncertainty in identifying pain along with limited experience and fear with the use of aComplex Care Service, Division of General Pediatrics, Boston medications for pain treatment. Behavioral pain-assessment tools are Children’s Hospital, Assistant Professor, Harvard Medical School, Boston Massachusetts; bSeven Hills Pediatric Center, Groton, reviewed in this clinical report, along with other strategies for monitoring Massachusetts; and cDepartment of Physical Medicine and Rehabilitation, University of Pittsburgh, Pediatric Rehabilitation pain after an intervention. Sources of pain in this population include Medicine, Rehabilitation Institute, Children’s Hospital of Pittsburgh of acute-onset pain attributable to tissue injury or inflammation resulting UPMC, Pittsburgh, Pennsylvania in nociceptive pain, with pain then expected to resolve after treatment Dr Hauer conceptualized and drafted the initial manuscript, reviewed and responded to questions and comments from all reviewers, and directed at the source. Other sources can result in chronic intermittent pain contributed to writing the final manuscript; Dr Houtrow contributed that, for many, occurs on a weekly to daily basis, commonly attributed to to the initial drafting and editing at all stages, including the final manuscript; and all authors approved the final manuscript as gastroesophageal reflux, spasticity, and hip subluxation. -
Diphenhydramine (Systemic) Epinephrine (Systemic)
DIPHENHYDRAMINE (SYSTEMIC) ^ Diphenhist [OTC] see DiphenhydrAMINE (Systemic) on page 34 Insomnia, occasional: Oral: Children 2 to 12 years, weighing 10 to 50 kg (off-label use): DiphenhydrAMINE (Systemic) Limited data available: 1 mg/kg administered 30 minutes before bedtime; maximum single dose: 50 mg (Russo, 1976) Brand Names: US Aler-Dryl [OTC]; Allergy Relief Childrens Children ≥12 years and Adolescents: Refer to adult dosing. [OTC]; Allergy Relief [OTC]; Altaryl [OTC]; Anti-Hist Allergy [OTC]; Motion sickness: Banophen [OTC]; Benadryl Allergy Childrens [OTC]; Benadryl Prophylaxis: Oral: Allergy [OTC]; Benadryl Dye-Free Allergy [OTC]; Benadryl [OTC]; Manufacturer's labeling: Infants, Children, and Adolescents: Complete Allergy Medication [OTC]; Complete Allergy Relief [OTC]; Note: Administer 30 minutes before motion Dicopanol FusePaq; Dicopanol RapidPaq; Diphen [OTC]; Diphenh- Weight-directed dosing: 5 mg/kg/day divided into 3 to 4 doses; ist [OTC]; Genahist [OTC]; Geri-Dryl [OTC]; GoodSense Allergy maximum: 300 mg daily Relief [OTC]; Naramin [OTC]; Nighttime Sleep Aid [OTC]; Nytol Fixed dosing: 12.5 to 25 mg 3 to 4 times daily Maximum Strength [OTC]; Nytol [OTC]; Ormir [OTC]; PediaCare Alternate dosing: Children 2 to 12 years: Limited data available: Childrens Allergy [OTC]; Pharbedryl; Pharbedryl [OTC]; Q-Dryl 0.5 to 1 mg/kg/dose every 6 hours; maximum single dose: [OTC]; QlearQuil Nighttime Allergy [OTC]; Quenalin [OTC] [DSC]; 25 mg. First dose should be administered 1 hour before travel Scot-Tussin Allergy Relief [OTC]; Siladryl