ADHD medications and cardiovascular adverse events in children and adolescents: cross-national comparison of risk communication in drug labeling

被引:5
|
作者
Sieluk, Jan [1 ]
Palasik, Brittany [2 ]
dosReis, Susan [1 ]
Doshi, Peter [1 ]
机构
[1] Univ Maryland, Sch Pharm, Pharmaceut Hlth Serv Res Dept, 220 Arch St,12th Floor,Room 01-228, Baltimore, MD 21201 USA
[2] Univ Utah Hosp & Clin, Salt Lake City, UT USA
关键词
ADHD; stimulants; atomoxetine; cardiovascular safety; risk; labeling; pharmacoepidemiology; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; DEFICIT HYPERACTIVITY DISORDER; AMBULATORY BLOOD-PRESSURE; ONCE-DAILY ATOMOXETINE; CARDIAC SAFETY; METHYLPHENIDATE; INFORMATION; STIMULANTS; YOUNG; CHILDHOOD;
D O I
10.1002/pds.4164
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose Regulators approve written medical information for healthcare professionals and consumers, but the consistency of these sources has not been studied. We investigated the consistency of information regarding four cardiovascular risks of attention-deficit/hyperactivity disorder (ADHD) medications approved in four countries. Methods Professional and consumer product labeling for five ADHD medications approved in Australia, Canada, the UK, and the USA were obtained in March/April 2016. Language describing the relationship between medication and elevated blood pressure and/or heart rate, myocardial infarction, stroke, and sudden death was extracted verbatim and classified into one of four categories based on the described relationship between medication and adverse event: "confirmed," "unconfirmed," "mixed," and "not mentioned." We judged the consistency of messages delivered to healthcare professionals and consumers as either "consistent" or "inconsistent." Results We obtained 20 healthcare professional labels and 20 corresponding consumer labels for the five ADHD medications registered in all four countries. Not all professional and consumer labeling contained language regarding all four adverse events. Of the 80 theoretically evaluable drug-risk pairs, 38 (48%) were not evaluable because of absence of mention of the adverse event in the consumer label. For the remaining 42, the potential causal relationship was expressed consistently in professional and consumer labeling in 25 (60%) cases. The cardiovascular risk profile was not described consistently across all four countries for any of the five drugs. Conclusions Product labeling provides healthcare professionals and consumers with inconsistent messages regarding the potential causal relationship between stimulant use and specific cardiovascular risks in children and adolescents. Copyright (C) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:274 / 284
页数:11
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  • [1] Practitioner Review: Current best practice in the management of adverse events during treatment with ADHD medications in children and adolescents
    Cortese, Samuele
    Holtmann, Martin
    Banaschewski, Tobias
    Buitelaar, Jan
    Coghill, David
    Danckaerts, Marina
    Dittmann, Ralf W.
    Graham, John
    Taylor, Eric
    Sergeant, Joseph
    [J]. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 2013, 54 (03) : 227 - 246
  • [2] IMPACT OF A RESTRICTIVE DRUG ACCESS PROGRAM ON THE RISK OF CARDIOVASCULAR ENCOUNTERS IN CHILDREN EXPOSED TO ADHD MEDICATIONS
    Guertin, Jason
    LeLorier, Jacques
    Durand, Madeleine
    Gow, Robert
    Holbrook, Anne
    Levine, Mitchell
    [J]. JOURNAL OF POPULATION THERAPEUTICS AND CLINICAL PHARMACOLOGY, 2014, 21 (03): : E357 - E369
  • [3] National surveillance of emergency department visits for outpatient adverse drug events in children and adolescents
    Cohen, Adam L.
    Budnitz, Daniel S.
    Weidenbach, Kelly N.
    Jernigan, Daniel B.
    Schroeder, Thomas J.
    Shehab, Nadine
    Pollock, Daniel A.
    [J]. JOURNAL OF PEDIATRICS, 2008, 152 (03): : 416 - 421
  • [4] A STANDARD INTERNATIONAL VERSION OF THE DRUG BURDEN INDEX FOR CROSS-NATIONAL COMPARISON OF THE FUNCTIONAL BURDEN OF MEDICATIONS IN OLDER PEOPLE
    Faure, Remi
    Dauphinot, Virginie
    Krolak-Salmon, Pierre
    Mouchoux, Christelle
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2013, 61 (07) : 1227 - 1228
  • [5] STIMULANT USE AND CARDIOVASCULAR RISK AMONG CHILDREN AND ADOLESCENTS WITH ADHD: WHAT PRODUCT LABELING DOES, OR DOES NOT, TELL US
    Palasik, B.
    Sieluk, J.
    dosReis, S.
    Doshi, P.
    [J]. VALUE IN HEALTH, 2015, 18 (07) : A747 - A747
  • [6] A Cross-National Comparison of Risk and Protective Factors for Adolescent Drug Use and Delinquency in the United States and the Netherlands
    Oesterle, Sabrina
    Hawkins, J. David
    Steketee, Majone
    Jonkman, Harrie
    Brown, Eric C.
    Moll, Marit
    Haggerty, Kevin P.
    [J]. JOURNAL OF DRUG ISSUES, 2012, 42 (04) : 337 - 357
  • [7] Obstructive Sleep Apnea in Children and Adolescents and the Risk of Major Adverse Cardiovascular Events: A Nationwide Cohort Study in Taiwan
    Tzeng, Nian-Sheng
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    Lu, Ru-Band
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    Chiang, Wei-Shan
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    Chang, Shan-Yueh
    Chien, Wu-Chien
    [J]. JOURNAL OF CLINICAL SLEEP MEDICINE, 2019, 15 (02): : 275 - 283
  • [8] Use of ADHD drugs in children and young adults does not increase risk of serious cardiovascular adverse events compared with non-use
    Winterstein, Almut G.
    [J]. EVIDENCE-BASED MENTAL HEALTH, 2012, 15 (02) : 43 - 43
  • [9] National surveillance of emergency department visits for outpatient adverse drug events in children and adolescents (vol 152, pg 416, 2008)
    Cohen
    [J]. JOURNAL OF PEDIATRICS, 2008, 152 (06): : 893 - 893
  • [10] Cross-National Comparison of Breastfeeding, Malnutrition and Associated Risk Factors among Mexican-Origin Children Living in Mexico and the US
    Campos, Ana Paola
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    Hawkins, Summer Sherburne
    [J]. CROSS-CULTURAL RESEARCH, 2021, 55 (04) : 287 - 318