2016
DOI: 10.1136/ejhpharm-2015-000766
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Antimicrobial consumption in a tertiary children’s hospital in Finland (2003–2013)

Abstract: Background Numbers of resistant pathogens are constantly increasing, and prudent use of antimicrobials is of paramount importance. In order to see whether any changes in the use of antimicrobials in recent years have occurred, we decided to monitor the consumption of these drugs at a single tertiary paediatric hospital. Materials and methods This single-centre retrospective study investigated the consumption of antimicrobials in defined daily doses (DDDs according to the Anatomical Therapeutical Chemical /DDD … Show more

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Cited by 5 publications
(6 citation statements)
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“…Our study indicated high use of quinolones, azoles, and penicillins, contrary to a hospital-based study in Finland from 2003 to 2013, which revealed an increase in penicillins, cephalosporins and carbapenems (31). Frequent use of cephalosporins was observed in Ethiopia (21).…”
Section: Resultscontrasting
confidence: 98%
“…Our study indicated high use of quinolones, azoles, and penicillins, contrary to a hospital-based study in Finland from 2003 to 2013, which revealed an increase in penicillins, cephalosporins and carbapenems (31). Frequent use of cephalosporins was observed in Ethiopia (21).…”
Section: Resultscontrasting
confidence: 98%
“…Laine et al [ 25 ] found a reduction in the consumption in penicillin G in their hospital in 2011–2012 which took place at the same time pneumococcal conjugate vaccine was introduced to the national immunization program in Finland (at 2010). We also had a reduction in the consumption of penicillin G at the same time.…”
Section: Discussionmentioning
confidence: 99%
“…The MMA is a 1200-bed tertiary healthcare centre with 27 departments. The Ethics Committee of the MMA approved the research protocol (Project MF/VMA/02/ [17][18][19].…”
Section: Methodsmentioning
confidence: 99%
“…The J01 antibacterials included in this study were the following: J01A tetracyclines (J01AAtigecycline), J01C beta-lactam antibacterials, penicillins (J01CA-ampicillin, J01CGampicillin/sulbactam, J01CE-benzilpenicillin sodium/procainbenzilpenicillin, J01CRamoxicillin/clavulanic acid, piperacillin/tazobactam), J01D other beta-lactam antibacterials (J01DBcefazolin, J01DC-cefuroxime, J01DD-cefotaxime, ceftazidime, ceftriaxone, J01DE-cefepime; J01DHcarbapenems), J01E sulfonamides and trimethoprim (J01EE-sulfametoxazol and trimethoprim), J01F macrolides, lincosamides and streptogramines (J01FAerythromicyn, azithromycin, J01FF-clindamycin), J01G aminoglycoside antibacterials (J01GBgentamicin, amikacin), J01M quinolone antibacterials (J01MA-ciprofloxacin, levofloxacin), J01X other antibacterials (J01XA-vancomycin, teicoplanin, J01XB-colistin, J01XD-metronidazole). The prescription of antifungal and antiviral drugs was excluded from the study [17]. According the patients' risk of developing CDI, antibiotics are grouped as: high risk-antibiotics (ATC codes: J01D, J01M and J01FF), medium-risk antibiotics (ATC codes: J01C, J01E, J01FA and J01G) and a low-risk antibiotics (ATC code: J01A) [5].…”
Section: Methodsmentioning
confidence: 99%
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