Outpatient parenteral antifungal therapy (OPAT) for invasive fungal infections with intermittent dosing of liposomal amphotericin B.
Adolescent
Adult
Aged
Aged, 80 and over
Ambulatory Care
/ methods
Amphotericin B
/ administration & dosage
Antifungal Agents
/ administration & dosage
Aspergillosis
/ drug therapy
Drug Resistance, Fungal
Female
Humans
Invasive Fungal Infections
/ drug therapy
Male
Middle Aged
Mucormycosis
/ drug therapy
Netherlands
Young Adult
Invasive fungal infection
antifungal stewardship
liposomal amphotericin B
outpatient parenteral antibiotic treatment
triazole resistance
Journal
Medical mycology
ISSN: 1460-2709
Titre abrégé: Med Mycol
Pays: England
ID NLM: 9815835
Informations de publication
Date de publication:
01 Oct 2020
01 Oct 2020
Historique:
received:
16
10
2019
revised:
10
12
2019
accepted:
20
12
2019
pubmed:
23
1
2020
medline:
27
5
2021
entrez:
23
1
2020
Statut:
ppublish
Résumé
Triazole resistant A. fumigatus has been documented in many parts of the world. In the Netherlands, incidence is now above 10% and results in the need for long-term parenteral therapy with liposomal amphotericin B (LAmB). The long terminal half-life of LAmB suggests that intermittent dosing could be effective, making the application of outpatient antifungal therapy (OPAT) possible. Here, we report our experience with the use of OPAT for Invasive Fungal Infections (IFI). All adult patients treated with LAmB with a 2 or 3 times weekly administration via the outpatient departments in four academic tertiary care centers in the Netherlands and Belgium since January 2010 were included in our analysis. Patient characteristics were collected, as well as information about diagnostics, therapy dose and duration, toxicity, treatment history and outcome of the IFI. In total, 18 patients were included. The most frequently used regimen (67%) was 5 mg/kg 3 times weekly. A partial response to the daily treatment prior to discharge was confirmed by CT-scan in 17 (94%) of patients. A favorable outcome was achieved in 13 (72%) patients. Decrease in renal function occurred in 10 (56%) cases but was reversible in all and was treatment limiting in one patient only. The 100-day mortality and 1-year mortality after initiation of OPAT were 0% and 6%, respectively. In a selected population, and after confirmation of initial response to treatment, our data support the use of OPAT with LAmB for treatment of IFI in an intermittent dosing regimen.
Identifiants
pubmed: 31965178
pii: 5713420
doi: 10.1093/mmy/myz134
pmc: PMC7527269
doi:
Substances chimiques
Antifungal Agents
0
Amphotericin B
7XU7A7DROE
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
874-880Informations de copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology.
Références
Mycoses. 2017 Mar;60(3):146-154
pubmed: 27878878
J Pharm Pharmacol. 2017 Dec;69(12):1672-1683
pubmed: 28815602
Clin Microbiol Infect. 2016 Jun;22(6):570.e1-9
pubmed: 27091095
Int J Antimicrob Agents. 2019 Mar;53(3):284-293
pubmed: 30395989
Lancet Infect Dis. 2009 Dec;9(12):789-95
pubmed: 19926038
Clin Infect Dis. 2019 May 2;68(Suppl 4):S244-S259
pubmed: 31222254
Clin Infect Dis. 2019 Jan 1;68(1):1-4
pubmed: 30551156
Clin Infect Dis. 2016 Aug 15;63(4):e1-e60
pubmed: 27365388
Clin Infect Dis. 2019 May 2;68(Suppl 4):S260-S274
pubmed: 31222253
BMJ. 1998 Aug 8;317(7155):379-84
pubmed: 9694753
J Infect Chemother. 2018 Sep;24(9):725-728
pubmed: 29773439
Pharmacotherapy. 2005 May;25(5):690-7
pubmed: 15899731
Clin Microbiol Infect. 2019 Jul;25(7):799-806
pubmed: 30580035
Emerg Infect Dis. 2013 May;19(5):832-4
pubmed: 23697829
N Engl J Med. 2002 Aug 8;347(6):408-15
pubmed: 12167683
Cancer. 2003 Jul 15;98(2):315-9
pubmed: 12872351
Front Microbiol. 2015 May 08;6:428
pubmed: 26005442
Transplantation. 2015 Apr;99(4):848-54
pubmed: 25531982
Curr Treat Options Infect Dis. 2014 Sep;6(3):309-325
pubmed: 25328449
Drug Resist Updat. 2015 Jul-Aug;21-22:30-40
pubmed: 26282594
Emerg Infect Dis. 2015 Jun;21(6):1041-4
pubmed: 25988348
J Clin Pharm Ther. 2001 Dec;26(6):445-51
pubmed: 11722682
Clin Infect Dis. 2015 Mar 1;60(5):713-20
pubmed: 25414266
Int J Antimicrob Agents. 2008 Feb;31(2):135-41
pubmed: 18162375
J Antimicrob Chemother. 2007 May;59(5):941-51
pubmed: 17400589
J Antimicrob Chemother. 1992 Oct;30(4):535-41
pubmed: 1490923
J Antimicrob Chemother. 2004 Dec;54(6):1096-102
pubmed: 15509617
Clin Infect Dis. 2019 May 2;68(Suppl 4):S241-S243
pubmed: 31222252
Int J Antimicrob Agents. 2009 Dec;34(6):570-4
pubmed: 19744837
Infect Dis (Lond). 2015 Jan;47(1):39-45
pubmed: 25415655
Clin Microbiol Rev. 2019 May 15;32(3):
pubmed: 31092507
Expert Opin Drug Saf. 2017 Mar;16(3):329-339
pubmed: 28004589
J Antimicrob Chemother. 2015 May;70(5):1522-6
pubmed: 25630644
Curr Opin Infect Dis. 2013 Dec;26(6):493-500
pubmed: 24126719
Crit Care Med. 1996 Aug;24(8):1311-5
pubmed: 8706484
J Antimicrob Chemother. 2014 Mar;69(3):805-8
pubmed: 24107387
Clin Infect Dis. 2018 Jan 6;66(1):11-19
pubmed: 29020202
Drugs. 2016 Mar;76(4):485-500
pubmed: 26818726
Clin Infect Dis. 2008 Jun 15;46(12):1813-21
pubmed: 18462102
Clin Infect Dis. 2009 Jun 15;48(12):1743-51
pubmed: 19435437
Int J Nephrol. 2019 Jan 28;2019:8629891
pubmed: 30809394