TY - JOUR
T1 - Does In Vitro Susceptibility Predict Clinical Outcome in Bacterial Keratitis?
AU - Chen, Aiyin
AU - Prajna, Lalitha
AU - Srinivasan, Muthiah
AU - Mahalakshmi, Rajendran
AU - Whitcher, John P.
AU - McLeod, Stephen
AU - Lietman, Thomas M.
AU - Acharya, Nisha R.
N1 - Funding Information:
This study was supported by That Man May See, San Francisco, California; the South Asia Research Fund, San Francisco, California, Grants U10-EY015114 (Dr Lietman) and K23EY017897 (Dr Acharya) from the National Eye Institute, Bethesda, Maryland, and a Research to Prevent Blindness Award (Dr Lietman) and a Research to Prevent Blindness Career Development Award (Dr Acharya), New York, New York. The authors indicate no financial conflict of interest. Involved in design of study (A.C., L.P., J.P.W., S.M., T.M.L., N.R.A.); conduct of study (A.C., L.P., M.S., T.M.L., N.R.A.); data collection and management (A.C., L.P., M.S., R.M., T.M.L., N.A.); data analysis and interpretation (A.C., R.M., M.S., T.M.L., N.R.A.); preparation of the manuscript (A.C., S.M., T.M.L., N.R.A.); and review and approval of the manuscript (A.C., L.P., M.S., R.M., J.P.W., S.M., T.M.L., N.R.A.). University of California, San Francisco Institutional Review Board approval was obtained for this study. The study and data collection were in conformity with the laws of India and informed consent was obtained from the patients.
PY - 2008/3
Y1 - 2008/3
N2 - Purpose: To determine whether clinical outcomes in bacterial keratitis are associated with antibiotic susceptibility. Design: Retrospective, ancillary study using data and samples from a completed randomized clinical trial. Methods: Forty-two patients were enrolled with culture-confirmed bacterial keratitis at Aravind Eye Hospital in South India. All patients received topical moxifloxacin and were randomized to receive either topical prednisolone phosphate or placebo. Outcomes included time to epithelialization, best spectacle-corrected visual acuity (BSCVA), and infiltrate/scar size at three months. Bacterial isolates were cultured, and minimum inhibitory concentration (MIC) to moxifloxacin was measured using Etests. Multiple linear regression was used to assess the effect of MIC on outcome, adjusting for enrollment characteristics. Results: MIC was associated with three-month infiltrate/scar size: each two-fold increase in MIC was associated with a 0.33-mm average diameter increase in scar size (P = .01). MIC was not associated with three-month BSCVA (P = .71) or time to epithelialization (P = .35). Conclusions: MIC was associated with infiltrate/scar size in bacterial keratitis. An ongoing larger, multicenter trial should provide further information on whether this association is maintained across subgroups of organisms.
AB - Purpose: To determine whether clinical outcomes in bacterial keratitis are associated with antibiotic susceptibility. Design: Retrospective, ancillary study using data and samples from a completed randomized clinical trial. Methods: Forty-two patients were enrolled with culture-confirmed bacterial keratitis at Aravind Eye Hospital in South India. All patients received topical moxifloxacin and were randomized to receive either topical prednisolone phosphate or placebo. Outcomes included time to epithelialization, best spectacle-corrected visual acuity (BSCVA), and infiltrate/scar size at three months. Bacterial isolates were cultured, and minimum inhibitory concentration (MIC) to moxifloxacin was measured using Etests. Multiple linear regression was used to assess the effect of MIC on outcome, adjusting for enrollment characteristics. Results: MIC was associated with three-month infiltrate/scar size: each two-fold increase in MIC was associated with a 0.33-mm average diameter increase in scar size (P = .01). MIC was not associated with three-month BSCVA (P = .71) or time to epithelialization (P = .35). Conclusions: MIC was associated with infiltrate/scar size in bacterial keratitis. An ongoing larger, multicenter trial should provide further information on whether this association is maintained across subgroups of organisms.
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U2 - 10.1016/j.ajo.2007.11.004
DO - 10.1016/j.ajo.2007.11.004
M3 - Article
C2 - 18207124
AN - SCOPUS:39149135531
SN - 0002-9394
VL - 145
SP - 409-412.e1
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 3
ER -