期刊论文详细信息
BMC Medicine
Incidence, characteristics and risk factors of adverse drug reactions in hospitalized children – a prospective observational cohort study of 6,601 admissions
Rosalind L Smyth1  Munir Pirmohamed4  Mark A Turner8  Anthony J Nunn2  Paula R Williamson3  Matthew Peak7  Jamie J Kirkham3  Lynne Cresswell6  Jennifer C Duncan7  Kim A Bird5  Helena L Mannix7  Louise E Bracken7  Jennifer R Bellis7  Elizabeth J Conroy3  Signe Thiesen2 
[1] Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK;Department of Women’s and Children’s Health, Institute of Translational Medicine (Child Health), University of Liverpool, Alder Hey Children's NHS Foundation Trust, Eaton Road, Liverpool L12 2AP, UK;Department of Biostatistics, University of Liverpool, Shelley’s Cottage, Brownlow Street, Liverpool L69 3GS, UK;The Wolfson Centre for Personalised Medicine, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Block A: Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3G, UK;Oncology Unit, Alder Hey Children’s NHS Foundation Trust, Eaton Road, Liverpool L12 2AP, UK;MRC Biostatistics Unit, Institute of Public Health, University Forvie Site, Robinson Way, Cambridge CB2 0SR, UK;Research and Development, Alder Hey Children’s NHS Foundation Trust, Eaton Road, Liverpool L12 2AP, UK;Department of Women’s and Children’s Health, University of Liverpool, First Floor, Liverpool Women’s Hospital, Crown Street, Liverpool L8 7SS, Uk
关键词: Peri- and post-operative pain management;    General anesthesia;    Risk factors;    Hospitalized children;    Drug safety;    Adverse drug reactions;   
Others  :  1132618
DOI  :  10.1186/1741-7015-11-237
 received in 2013-04-02, accepted in 2013-07-19,  发布年份 2013
PDF
【 摘 要 】

Background

Adverse drug reactions (ADRs) are an important cause of harm in children. Current data are incomplete due to methodological differences between studies: only half of all studies provide drug data, incidence rates vary (0.6% to 16.8%) and very few studies provide data on causality, severity and risk factors of pediatric ADRs. We aimed to determine the incidence of ADRs in hospitalized children, to characterize these ADRs in terms of type, drug etiology, causality and severity and to identify risk factors.

Methods

We undertook a year-long, prospective observational cohort study of admissions to a single UK pediatric medical and surgical secondary and tertiary referral center (Alder Hey, Liverpool, UK). Children between 0 and 16 years 11 months old and admitted for more than 48 hours were included. Observed outcomes were occurrence of ADR and time to first ADR for the risk factor analysis.

Results

A total of 5,118 children (6,601 admissions) were included, 17.7% of whom experienced at least one ADR. Opiate analgesics and drugs used in general anesthesia (GA) accounted for more than 50% of all drugs implicated in ADRs. Of these ADRs, 0.9% caused permanent harm or required admission to a higher level of care. Children who underwent GA were at more than six times the risk of developing an ADR than children without a GA (hazard ratio (HR) 6.40; 95% confidence interval (CI) 5.30 to 7.70). Other factors increasing the risk of an ADR were increasing age (HR 1.06 for each year; 95% CI 1.04 to 1.07), increasing number of drugs (HR 1.25 for each additional drug; 95% CI 1.22 to 1.28) and oncological treatment (HR 1.90; 95% CI 1.40 to 2.60).

Conclusions

ADRs are common in hospitalized children and children who had undergone a GA had more than six times the risk of developing an ADR. GA agents and opiate analgesics are a significant cause of ADRs and have been underrepresented in previous studies. This is a concern in view of the increasing number of pediatric short-stay surgeries.

【 授权许可】

   
2013 Thiesen et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150304021832444.pdf 867KB PDF download
Figure 2. 54KB Image download
Figure 1. 97KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Powell-Jackson PR, Tredger JM, Williams R: Hepatotoxicity to sodium valproate: a review. Gut 1984, 25:673-681.
  • [2]Rashed AN, Wong IC, Cranswick N, Tomlin S, Rascher W, Neubert A: Risk factors associated with adverse drug reactions in hospitalised children: international multicentre study. Eur J Clin Pharmacol 2011, 68:801-810.
  • [3]Sharfstein JM, North M, Serwint JR: Over the counter but no longer under the radar - pediatric cough and cold medications. New Engl J Med 2007, 357:2321-2324.
  • [4]Srinivasan A, Budnitz D, Shehab N, Cohen A: Infant deaths associated with cough and cold medications - two states, 2005. Morb Mortal Wkly Rep 2007, 56:1-4.
  • [5]Davies EC, Green CF, Taylor S, Williamson PR, Mottram DR, Pirmohamed M: Adverse drug reactions in hospital in-patients: a prospective analysis of 3695 patient-episodes. PLoS One 2009, 4:e4439.
  • [6]Demers P, Fraser D, Goldbloom RB, Haworth JC, LaRochelle J, MacLean R, Murray TK: Effects of tetracyclines on skeletal growth and dentition. A report by the Nutrition Committee of the Canadian Paediatric Society. Can Med Assoc J 1968, 99:849-854.
  • [7]Bateman DN, Rawlins MD, Simpson JM: Extrapyramidal reactions with metoclopramide. Br Med J (Clin Res Ed) 1985, 291:930-932.
  • [8]Smyth RMD, Gargon E, Kirkham J, Cresswell L, Golder S, Smyth R, Williamson P: Adverse drug reactions in children-a systematic review. PLoS One 2012, 7:e24061.
  • [9]Simmons C, Georgeson EM, Hill RC: Adverse drug reactions: can we reduce the risk? Hosp Pharm 1998, 33:1568-1576.
  • [10]Van Kraaij DJW, Haagsma CJ, Go IH, Gribnau FWJ: Drug use and adverse drug reactions in 105 elderly patients admitted to a general medical ward. Neth J Med 1994, 44:166-173.
  • [11]Edwards IR, Aronson JK: Adverse drug reactions: definitions, diagnosis, and management. Lancet 2000, 356:1255-1259.
  • [12]Gallagher RM, Kirkham JJ, Mason JR, Bird KA, Williamson PR, Nunn AJ, Turner MA, Smyth RL, Pirmohamed M: Development and inter-rater reliability of the Liverpool adverse drug reaction causality assessment tool. PLoS One 2011, 6:e28096.
  • [13]Hartwig SC, Siegel J, Schneider PJ: Preventability and severity assessment in reporting adverse drug reactions. Am J Hosp Pharm 1992, 49:2229-2232.
  • [14]Von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP: The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Rev Esp Salud Publica 2008, 82:251-259.
  • [15]Ferner RE, Aronson JK: Preventability of drug-related harms - part I: a systematic review. Drug Saf 2010, 33:985-994.
  • [16]Schumock GT, Thornton JP: Focusing on the preventability of adverse drug reactions. Hosp Pharm 1992, 27:538.
  • [17]Hallas J, Harvard B, Gram LF, Grodum E, Brosen K, Haghfelt T, Damsbo N: Drug related hospital admissions: the role of definitions and intensity of data collection, and the possibility of prevention. J Intern Med 1990, 228:83-90.
  • [18]Naranjo CA, Busto U, Sellers EM: A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther 1981, 30:239-245.
  • [19]Farrokhi S, Pourpak Z, Fattahi F, Ashrafi MR, Majdinasab P, Gholami K, Moin M: Adverse drug and medical instrument reactions in a pediatric intensive care unit. Pharmacoepidemiol Drug Saf 2009, 18:761-762.
  • [20]Turner S, Nunn AJ, Fielding K, Choonara I: Adverse drug reactions to unlicensed and off-label drugs on paediatric wards: a prospective study. Acta Paediatr 1999, 88:965-968.
  • [21]Gallagher RM, Mason JR, Bird KA, Kirkham JJ, Peak M, Williamson PR, Nunn AJ, Turner MA, Pirmohamed M, Smyth RL: Adverse drug reactions causing admission to a paediatric hospital. PLoS ONE 2012, 7:e50127.
  • [22]Koenig L, Gu Q: Growth of ambulatory surgical centers, surgery volume, and savings to medicare. Am J Gastroenterol 2013, 108:10-15.
  • [23]NHS Modernisation Agency: 10 High Impact Changes for Service Delivery and Improvement. London: Department of Health Publications; 2004.
  • [24]Diez L: Assessing the willingness of parents to pay for reducing postoperative emesis in children. Pharmacoeconomics 1998, 13:589-595.
  • [25]Arnott J, Hesselgreaves H, Nunn AJ, Peak M, Pirmohamed M, Smyth RL, Turner MA, Young B: Enhancing communication about paediatric medicines: lessons from a qualitative study of parents’ experiences of their child’s suspected adverse drug reaction. PLoS ONE 2012, 7:e46022.
  文献评价指标  
  下载次数:33次 浏览次数:18次