Aravind Eye Hospital, Pondicherry, India.
Francis I. Proctor Foundation, University of California, San Francisco, San Francisco, California.
Ophthalmology. 2019 Aug;126(8):1084-1089. doi: 10.1016/j.ophtha.2019.03.020. Epub 2019 Mar 20.
To determine if there is a benefit to adjuvant intrastromal voriconazole (ISV) injections for primary treatment of filamentous fungal keratitis.
Outcome-masked, randomized controlled clinical trial.
Patients with moderate vision loss resulting from a smear-positive fungal ulcer.
Study eyes were randomized to topical natamycin plus ISV injection versus topical natamycin alone.
The primary outcome of the trial was microbiological cure on 3-day repeat culture analysis. Secondary outcomes included microbiological cure on 7-day repeat culture analysis; 3-week and 3-month best spectacle-corrected visual acuity; infiltrate or scar size or both; rate of perforation; therapeutic penetrating keratoplasty (TPK); and other adverse events.
A total of 151 patients with smear-positive ulcers were screened and 70 were enrolled at Aravind Eye Hospital, Pondicherry, India. Baseline cultures grew Fusarium in 19 samples (27%), Aspergillus in 17 samples (24%), and other filamentous fungi in 19 samples (27%) and showed negative results in 13 samples (19%). Those randomized to ISV injection had 1.82 times the odds of 3-day culture positivity after controlling for baseline culture status (95% confidence interval [CI], 0.65-5.23; P = 0.26, bias-corrected logistic regression) and 1.98 times the odds of positive 7-day culture results, after controlling for baseline culture status (95% CI, 0.69-5.91; P = 0.20, bias-corrected logistic regression). Those randomized to ISV injection showed 0.5 logMAR lines (approximately 0.5 Snellen lines) of decreased visual acuity (95% CI, -2.6 to 3.6 lines; P = 0.75) and 0.55 mm worse infiltrate or scar size or both at 3 months after controlling for baseline values (95% CI, -0.13 to 1.25; P = 0.11). Intrastromal voriconazole injections showed a 2.85-fold increased hazard of perforation after controlling for baseline infiltrate depth (95% CI, 0.76-10.75; P = 0.12) but no difference in the rate of TPK (hazard ratio, 0.95; 95% CI, 0.44-2.04; P = 0.90).
There seems to be no benefit to adding ISV injections to topical natamycin in the primary treatment of moderate to severe filamentous fungal ulcers. Studies consistently suggest that voriconazole has a limited role in the treatment of filamentous fungal ulcers.
确定辅助应用角膜内伏立康唑(ISV)注射是否有益于丝状真菌角膜炎的初始治疗。
结果盲法、随机对照临床试验。
因真菌性溃疡而出现中度视力丧失的患者。
研究眼随机分为局部那他霉素联合 ISV 注射与局部那他霉素单独治疗。
试验的主要结局是 3 天重复培养分析的微生物学治愈率。次要结局包括 7 天重复培养分析的微生物学治愈率;3 周和 3 个月最佳矫正视力;浸润或瘢痕大小或两者兼而有之;穿孔率;治疗性穿透性角膜移植术(TPK);以及其他不良事件。
共筛选了 151 例涂片阳性溃疡患者,其中 70 例在印度 Pondicherry 的 Aravind 眼科医院入组。基线培养物中,19 例(27%)为镰刀菌,17 例(24%)为曲霉菌,19 例(27%)为其他丝状真菌,13 例(19%)结果为阴性。在控制基线培养状态后,随机分配到 ISV 注射组的患者 3 天培养阳性的可能性增加 1.82 倍(95%置信区间[CI],0.65-5.23;P=0.26,偏倚校正逻辑回归),控制基线培养状态后 7 天培养阳性的可能性增加 1.98 倍(95%CI,0.69-5.91;P=0.20,偏倚校正逻辑回归)。随机分配到 ISV 注射组的患者在控制基线值后 3 个月时视力下降 0.5 logMAR 行(约 0.5 Snellen 行)(95%CI,-2.6 至 3.6 行;P=0.75),浸润或瘢痕大小增加 0.55 mm 或两者兼而有之(95%CI,-0.13 至 1.25;P=0.11)。在控制基线浸润深度后,ISV 注射组穿孔的风险增加了 2.85 倍(95%CI,0.76-10.75;P=0.12),但穿透性角膜移植术的发生率无差异(风险比,0.95;95%CI,0.44-2.04;P=0.90)。
在中度至重度丝状真菌性溃疡的初始治疗中,似乎没有必要在局部那他霉素中添加 ISV 注射。研究一致表明,伏立康唑在丝状真菌性溃疡的治疗中作用有限。