, Volume 41, Issue 1, pp 15–20 | Cite as

The efficacy of voriconazole in 24 ocular Fusarium infections

  • P. Troke
  • G. Obenga
  • T. Gaujoux
  • P. Goldschmidt
  • A.-L. Bienvenu
  • M. Cornet
  • F. Grenouillet
  • D. Pons
  • S. Ranque
  • K. Sitbon
  • C. Chaumeil
  • V. Borderie
  • O. Lortholary
Clinical and Epidemiological Study



We examined, retrospectively, the efficacy of voriconazole in Fusarium eye infections.


Voriconazole-treated patients with proven or probable keratitis or endophthalmitis from the voriconazole database (9 patients) and six French ophthalmology departments (15 patients) were included. Sociodemographic features, predisposing factors, history of corneal trauma, associated ocular conditions, other diseases and prior therapies were analysed. Investigator-determined success was defined as infection resolution with medical treatment. Failure was no response or persistent infection and required surgery.


Most patients were Caucasian (83 %) and male (71 %). The infection was keratitis (63 %) or endophthalmitis (37 %) and proven in 23 (96 %). Prior therapy included topical and/or systemic amphotericin (46 %), fluconazole (17 %) or others (33 %), often in combination. Causative fungi were Fusarium solani (14, 58 %), Fusarium moniliforme (1), Fusarium oxysporum (1) and Fusarium spp. (8). Voriconazole was administered systemically, topically and/or by intraocular injection, and 16 patients (67 %) received salvage and eight primary therapy. The overall response was 67 % (73 % keratitis and 56 % endophthalmitis) but seven patients required adjunctive surgery. However, response was 63 % for eight primary therapy patients and 69 % for 16 salvage therapy patients. Response by species was Fusarium solani 64 % (9/14) and all others 80 % (8/10). In 13 patients (77 %), voriconazole was used in combination (response 69 vs. 64 % alone) with topical [amphotericin B 10/24 (42 %), caspofungin 5 (21 %), natamycin 1 (4 %)] and systemic agents [caspofungin 3 (13 %), amphotericin 2 (8 %)].


Topical and systemic voriconazole appears to be effective alone or in combination with other agents for treating severe Fusarium keratitis or endophthalmitis.


Voriconazole Ophthalmology Fusariosis Keratitis Endophthalmitis 



P.T. received an honorarium from Pfizer in connection with the data finalisation, analysis and writing of this manuscript. G. O. was paid consultant to Pfizer for the collection of the French Mycosis Group data for this manuscript.

Conflict of interest

P. T. was previously an employee of and then a consultant to Pfizer; G.O. none to declare; T.G. none to declare; P.G. none to declare; A.-L.B. none to declare; M. C. none to declare; F. G. has received speaker fees from Schering and MSD; D. P. none to declare; S. R. none to declare; K. S. none to declare; V. B. none to declare; O. L. is a member of the speaker bureaus of Pfizer, MSD, Astellas and Gilead Sciences. Pfizer had no decision-making role in the design, execution, analysis or reporting of this research.


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Copyright information

© Springer-Verlag 2012

Authors and Affiliations

  • P. Troke
    • 1
  • G. Obenga
    • 2
  • T. Gaujoux
    • 3
  • P. Goldschmidt
    • 3
  • A.-L. Bienvenu
    • 4
  • M. Cornet
    • 5
  • F. Grenouillet
    • 6
  • D. Pons
    • 7
  • S. Ranque
    • 8
  • K. Sitbon
    • 9
  • C. Chaumeil
    • 3
  • V. Borderie
    • 3
  • O. Lortholary
    • 2
    • 9
    • 10
  1. 1.The Old CourtBroadstairs, KingsgateUK
  2. 2.Service des Maladies Infectieuses et Tropicales, Centre d’Infectiologie Necker Pasteur, Hôpital Necker Enfants MaladesUniversité Paris-DescartesParisFrance
  3. 3.Centre Hospitalier National d’Ophtalmologie des XV–XXParisFrance
  4. 4.Faculté de MédecineUniversité Lyon 1LyonFrance
  5. 5.Hôtel DieuParisFrance
  6. 6.Hôpital Jean MinjozBesançonFrance
  7. 7.Gabriel MontPiedClermont-FerrandFrance
  8. 8.La TimoneMarseilleFrance
  9. 9.Institut Pasteur, Centre National de Référence Mycoses Invasives et Antifongiques, Unité de Mycologie MoléculaireParisFrance
  10. 10.CNRS URA3012ParisFrance

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