Literature DB >> 36186239

Impact of Patient-Specific Aminoglycoside Monitoring for Treatment of Pediatric Cystic Fibrosis Pulmonary Exacerbations.

Brianna Hemmann1, Elizabeth Woods2, Tanya Makhlouf2, Chris Gillette3, Courtney Perry2,3, Mary Subramanian2, Holly Hanes4.   

Abstract

OBJECTIVE: Aminoglycosides are frequently used for empiric and definitive treatment of cystic fibrosis (CF) pulmonary exacerbations. Various methods have been described for aminoglycoside therapeutic drug monitoring. The objective of this study is to evaluate the effect of patient-specific pharmacokinetic calculations for aminoglycosides used to treat CF pulmonary exacerbations.
METHODS: Ambidirectional cohort study of patients admitted to a children's hospital from June 1, 2018, through February 28, 2019, and June 1, 2019, through February 8, 2021. The primary outcome was the occurrence of dosing changes after analysis of initial serum concentrations in either group. Secondary outcomes included occurrence of nephrotoxicity, duration of antibiotics, and length of stay.
RESULTS: Twenty-four patients (75%) in the intervention group versus zero in the control group required dosing adjustments after initial analysis of serum concentrations were completed (p < 0.001). There was not a statistically significant between-group difference for duration of antibiotics in days (median, 14 vs 13.5; Z, 1.07; p = 0.29) or length of stay (median, 11 vs 11; Z, -0.31; p = 0.76). There was also not a statistically significant between-group difference in forced expiratory volume in one second (FEV1) change from admission to discharge (11.4% vs 13.9%; t, 0.61; Degrees of Freedom, 39; p = 0.55). Two patients (6.25%) in the intervention group experienced nephrotoxicity compared with zero patients in the control group (risk difference, 6.25%; 95% CI, -2.14 to 14.64; number needed to harm, 16).
CONCLUSIONS: Patient-specific pharmacokinetic monitoring led to significantly more dosing changes and was associated with similar patient outcomes as trough-only monitoring. Further studies are needed to identify methods to optimize aminoglycoside dosing and monitoring for these patients with the goal of reducing toxicities while maximizing efficacy. Copyright. Pediatric Pharmacy Association. All rights reserved. For permissions, email: membership@pediatricpharmacy.org 2022.

Entities:  

Keywords:  aminoglycoside; cystic fibrosis; exacerbation; monitoring; pulmonary

Year:  2022        PMID: 36186239      PMCID: PMC9514759          DOI: 10.5863/1551-6776-27.7.655

Source DB:  PubMed          Journal:  J Pediatr Pharmacol Ther        ISSN: 1551-6776


  16 in total

Review 1.  Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis.

Authors:  Alan R Smyth; Jayesh Bhatt; Sarah J Nevitt
Journal:  Cochrane Database Syst Rev       Date:  2017-03-27

2.  Estimating drug-free period using a graphical method: an alternative way to monitor extended-interval dosing of gentamicin therapy.

Authors:  Ab Fatah Ab Rahman; Nursahjohana Md Sahak; Ahmad Maujad Ali
Journal:  Int J Pharm Pract       Date:  2017-02

3.  Once-daily tobramycin in cystic fibrosis: better for clinical outcome than thrice-daily tobramycin but more resistance development?

Authors:  Olaf Burkhardt; Christine Lehmann; Rajanikanth Madabushi; Vipul Kumar; Hartmut Derendorf; Tobias Welte
Journal:  J Antimicrob Chemother       Date:  2006-08-02       Impact factor: 5.790

4.  Therapeutic drug monitoring of once daily tobramycin in cystic fibrosis--caution with trough concentrations.

Authors:  Kingsley P Coulthard; Daniel G Peckham; Steven P Conway; Carol A Smith; Jan Bell; John Turnidge
Journal:  J Cyst Fibros       Date:  2006-07-07       Impact factor: 5.482

Review 5.  Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health.

Authors:  Peter J Mogayzel; Edward T Naureckas; Karen A Robinson; Gary Mueller; Denis Hadjiliadis; Jeffrey B Hoag; Lisa Lubsch; Leslie Hazle; Kathy Sabadosa; Bruce Marshall
Journal:  Am J Respir Crit Care Med       Date:  2013-04-01       Impact factor: 21.405

Review 6.  Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis.

Authors:  A R Smyth; K H Tan
Journal:  Cochrane Database Syst Rev       Date:  2006-07-19

7.  National survey of extended-interval aminoglycoside dosing in pediatric cystic fibrosis pulmonary exacerbations.

Authors:  William A Prescott
Journal:  J Pediatr Pharmacol Ther       Date:  2011-10

Review 8.  Developmental pharmacokinetics in pediatric populations.

Authors:  Hong Lu; Sara Rosenbaum
Journal:  J Pediatr Pharmacol Ther       Date:  2014 Oct-Dec

Review 9.  Management of Pseudomonas aeruginosa infection in cystic fibrosis patients using inhaled antibiotics with a focus on nebulized liposomal amikacin.

Authors:  Zarmina Ehsan; John P Clancy
Journal:  Future Microbiol       Date:  2015-11-17       Impact factor: 3.165

Review 10.  Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations.

Authors:  Patrick A Flume; Peter J Mogayzel; Karen A Robinson; Christopher H Goss; Randall L Rosenblatt; Robert J Kuhn; Bruce C Marshall
Journal:  Am J Respir Crit Care Med       Date:  2009-09-03       Impact factor: 21.405

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.