Drug Use and Type of Adverse Drug Events-Identified by a Trigger Tool in Different Units in a Swedish Pediatric Hospital.

adverse drug event inpatients patient safety pediatrics pharmaceutical preparation

Journal

Drug, healthcare and patient safety
ISSN: 1179-1365
Titre abrégé: Drug Healthc Patient Saf
Pays: New Zealand
ID NLM: 101544775

Informations de publication

Date de publication:
2020
Historique:
received: 26 09 2019
accepted: 13 12 2019
entrez: 27 2 2020
pubmed: 27 2 2020
medline: 27 2 2020
Statut: epublish

Résumé

The objectives of our study were to determine drug use, type and incidence of all adverse event associated with drug or drug-related processes (Adverse Drug Events, ADE) among pediatric inpatients in relation to hospital unit and length of stay. 600 pediatric (0-18 years) admissions at a Swedish university hospital during one year were included and stratified in blocks to 150 neonatal, surgical/orthopedic, medicine and emergency-medicine unit admissions, respectively. Adverse events were identified from medical records using a pediatric trigger tool. All triggers identifying an adverse event related to drugs and drug-related devices were included. Data on drug use were extracted from the hospital drug-data warehouse. In total, 17794 daily drug orders were administrated to 486 (81.0% exposed) admissions. Parental nutrition, potassium salts and morphine constituted half of all high-risk drugs prescribed. Two-thirds of intravenous irritating drug doses consisted of vancomycin, esomeprazole and meropenem. In 129 (21.5%) admissions, at least one ADE was identified, out of which 21 ADE were classified as more severe (National Coordinating Council Medication Error Reporting Prevention-Index, NCCMERP≥F). The ADE incidence was 47.4 (95% confidence interval: 39.4-57.3) per 1000 admission days and varied by unit category. In neonatal units, 56.9 (49.5-65.4) ADEs/1000 admission days were detected, in surgery/orthopedic 54.2 (40.3-72.8), in medicine 44.1 (33.1-58.7), and in emergency-medicine 14.3 (7.7-26.7) ADEs/1000 admission days were found. The most common types of ADEs were identified by triggers that were not directly aiming at drugs including insufficiently treated pain (incidence peaking already in the first days), skin, tissue or vascular harm (peaking at the end of the first week) and hospital-acquired infections (peaking in later admission days). Adverse drug events are common in pediatric patients. The incidence of ADEs and type of ADE varies by hospital unit and length of hospital stay.

Identifiants

pubmed: 32099481
doi: 10.2147/DHPS.S232604
pii: 232604
pmc: PMC6999776
doi:

Types de publication

Journal Article

Langues

eng

Pagination

31-40

Informations de copyright

© 2020 Nydert et al.

Déclaration de conflit d'intérêts

The authors declare that they have no other competing interests in this work.

Références

Med J Aust. 1995 Nov 6;163(9):458-71
pubmed: 7476634
Clin Pharmacol Ther. 1981 Aug;30(2):239-45
pubmed: 7249508
JAMA Pediatr. 2019 Aug 26;:
pubmed: 31449284
Am J Health Syst Pharm. 2011 Feb 1;68(3):227-40
pubmed: 21258028
J Clin Pharm Ther. 2016 Jun;41(3):246-55
pubmed: 27145467
JAMA. 2001 Apr 25;285(16):2114-20
pubmed: 11311101
Pediatrics. 2008 Apr;121(4):e927-35
pubmed: 18381521
Am J Infect Control. 2012 Dec;40(10):931-4
pubmed: 22575286
Pediatrics. 2018 Aug;142(2):
pubmed: 30006445
Int J Qual Health Care. 2016 Dec 1;28(6):640-649
pubmed: 27664822
Qual Saf Health Care. 2006 Jun;15(3):196-201
pubmed: 16751470
N Engl J Med. 1991 Feb 7;324(6):370-6
pubmed: 1987460
BMC Health Serv Res. 2014 Dec 21;14:655
pubmed: 25527905
J Gen Intern Med. 1995 Apr;10(4):199-205
pubmed: 7790981
Drug Saf. 2019 Nov;42(11):1329-1342
pubmed: 31290127
CMAJ. 2012 Sep 18;184(13):E709-18
pubmed: 22847964
BMJ Qual Saf. 2014 Aug;23(8):670-7
pubmed: 24764136
J Patient Saf. 2018 Jun;14(2):95-100
pubmed: 25853805
JAMA. 1997 Jan 22-29;277(4):307-11
pubmed: 9002493

Auteurs

Per Nydert (P)

Astrid Lindgren's Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Maria Unbeck (M)

Trauma and Reparative Medicine Theme, Karolinska University Hospital, Stockholm, Sweden.
Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.

Karin Pukk Härenstam (K)

Astrid Lindgren's Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Medical Management Centre, Department of Learning, Informatics, Management and Ethics, Karolinska Institutet, Stockholm, Sweden.

Mikael Norman (M)

Astrid Lindgren's Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Synnöve Lindemalm (S)

Astrid Lindgren's Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Classifications MeSH