Topical Chlorhexidine 0.2% versus Topical Natamycin 5% for the Treatment of Fungal Keratitis in Nepal: A Randomized Controlled Noninferiority Trial.


Journal

Ophthalmology
ISSN: 1549-4713
Titre abrégé: Ophthalmology
Pays: United States
ID NLM: 7802443

Informations de publication

Date de publication:
05 2022
Historique:
received: 07 10 2021
revised: 02 12 2021
accepted: 02 12 2021
pubmed: 14 12 2021
medline: 27 4 2022
entrez: 13 12 2021
Statut: ppublish

Résumé

To investigate if topical chlorhexidine 0.2%, which is low cost and easy to formulate, is noninferior to topical natamycin 5% for the treatment of filamentous fungal keratitis. Randomized controlled, single-masked, noninferiority clinical trial. Adults attending a tertiary-level ophthalmic hospital in Nepal with filamentous fungal infection confirmed on smear or confocal microscopy. Participants were randomly allocated to receive topical chlorhexidine 0.2% or topical natamycin 5%. Primary analysis (intention-to-treat) was by linear regression, using baseline logarithm of the minimum angle of resolution (logMAR) best spectacle-corrected visual acuity (BSCVA) and treatment arm as prespecified covariates. Mixed fungal-bacterial infections were excluded from the primary analysis but included in secondary analyses and secondary safety-related outcomes. The noninferiority margin was 0.15 logMAR. This trial was registered with ISRCTN, number ISRCTN14332621. The primary outcome measure was BSCVA at 3 months. Secondary outcome measures included perforation or therapeutic penetrating keratoplasty by 90 days. Between June 3, 2019, and November 9, 2020, 354 eligible participants were enrolled and randomly assigned: 178 to chlorhexidine and 176 to natamycin. Primary outcome data were available for 153 and 151 of the chlorhexidine and natamycin groups, respectively. Of these, mixed bacterial-fungal infections were found in 20 cases (12/153 chlorhexidine, 8/151 natamycin) and excluded from the primary analysis. Therefore, 284 patients were assessed for the primary outcome (141 chlorhexidine, 143 natamycin). We did not find evidence to suggest chlorhexidine was noninferior to natamycin and in fact found strong evidence to suggest that natamycin-treated participants had significantly better 3-month BSCVA than chlorhexidine-treated participants, after adjusting for baseline BSCVA (regression coefficient, -0.30; 95% confidence interval [CI], -0.42 to -0.18; P < 0.001). There were more perforations and emergency corneal grafts in the chlorhexidine arm (24/175, 13.7%) than in the natamycin arm (10/173, 5.8%; P = 0.018, mixed infections included), whereas natamycin-treated cases were less likely to perforate or require an emergency corneal graft, after adjusting for baseline ulcer depth (odds ratio, 0.34; 95% CI, 0.15-0.79; P = 0.013). Treatment with natamycin is associated with significantly better visual acuity, with fewer adverse events, compared with treatment with chlorhexidine. Natamycin remains the preferred first-line monotherapy treatment for filamentous fungal keratitis.

Identifiants

pubmed: 34896126
pii: S0161-6420(21)00921-0
doi: 10.1016/j.ophtha.2021.12.004
pmc: PMC9037000
pii:
doi:

Substances chimiques

Antifungal Agents 0
Natamycin 8O0C852CPO
Voriconazole JFU09I87TR
Chlorhexidine R4KO0DY52L

Banques de données

ISRCTN
['ISRCTN14332621']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

530-541

Subventions

Organisme : Wellcome Trust
ID : 207472/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R010161/1
Pays : United Kingdom

Informations de copyright

Copyright © 2021 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jeremy J Hoffman (JJ)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom; Sagarmatha Choudhary Eye Hospital, Lahan, Nepal; Kilimanjaro Christian Medical Centre, Moshi, Tanzania. Electronic address: jeremy.hoffman@lshtm.ac.uk.

Reena Yadav (R)

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

Sandip D Sanyam (SD)

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

Pankaj Chaudhary (P)

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

Abhishek Roshan (A)

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

Sanjay K Singh (SK)

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

Sanjay K Singh (SK)

Eastern Region Eye Care Programme, Biratnagar, Nepal.

Sailesh K Mishra (SK)

Nepal Netra Jyoti Sangh, Kathmandu, Nepal.

Simon Arunga (S)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom; Mbarara University of Science and Technology, Mbarara, Uganda.

Victor H Hu (VH)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

David Macleod (D)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom; International Statistics & Epidemiology Group, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Astrid Leck (A)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Matthew J Burton (MJ)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom; National Institute for Health Research Biomedical Research Centre for Ophthalmology at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.

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Classifications MeSH