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碘化卵磷脂片与螺内酯治疗中国未控制糖尿病患者中心性浆液性视网膜病变的疗效和安全性。

Efficacy and safety of iodized lecithin tablets versus spironolactone in alleviating central serous retinopathy among Chinese patients with uncontrolled diabetes.

机构信息

Department of Ophthalmology, Affiliated Zhangjiagang Hospital of Soochow University, Zhangjiagang, China.

Department of Ophthalmology, First Affiliated Hospital of Shanghai Jiaotong University, Shanghai, China.

出版信息

Pak J Pharm Sci. 2023 Mar;36(2(Special)):595-599.


DOI:
PMID:37548195
Abstract

To compare the effectiveness and safety of spironolactone versus lecithin-bound iodine in patients with central serous retinopathy (CSR). Chinese diabetes patients aged>18 years with CSR with persistent increased level of subretinal fluid (SRF) were enrolled. Subjects were randomized to receive either oral lecithin-bound iodine (390µg/kg/day) or oral spironolactone (50mg/day) for 6 months. A total of 200 patients were randomized and completed the study. Compared to spironolactone group, patients treated with lecithin-bound iodine had greater proportion of eye with complete resolution (87% vs 81%, p>0.005). Higher improvement in height of SRF was observed in lecithin-bound iodine-treated patients as compared with Spironolactone-treated patients (91.2[87.5] vs 142.5 [121.1]; p>0.005). However, no statistically significant difference was observed on none of comparisons. Compared to Spironolactone, the patients treated with lecithin-bound iodine had greater improvement in lesion size, central macular thickness and best-corrected visual acuity. However, no statistically significant difference was observed in any of parameter assessed. (p>0.005). The results of the present study suggested that the lecithin-bound iodine was found more effective (nnumerically) than spironolactone in Chinese diabetes patients with CSR.

摘要

比较螺内酯与卵磷脂结合碘治疗中心性浆液性脉络膜视网膜病变(CSR)的有效性和安全性。

入选中国年龄>18 岁的糖尿病 CSR 患者,伴有持续增加的视网膜下液(SRF)水平。将受试者随机分为口服卵磷脂结合碘(390μg/kg/天)或口服螺内酯(50mg/天)组,治疗 6 个月。共 200 例患者随机分组并完成研究。与螺内酯组相比,接受卵磷脂结合碘治疗的患者中完全缓解的眼比例更高(87% vs 81%,p>0.005)。与螺内酯治疗组相比,接受卵磷脂结合碘治疗的患者的 SRF 高度改善更明显(91.2[87.5] vs 142.5 [121.1];p>0.005)。然而,在任何比较中均未观察到统计学差异。与螺内酯相比,接受卵磷脂结合碘治疗的患者在病变大小、黄斑中心厚度和最佳矫正视力方面有更大的改善。然而,在评估的任何参数中均未观察到统计学差异。(p>0.005)。本研究结果表明,在伴有 CSR 的中国糖尿病患者中,与螺内酯相比,卵磷脂结合碘更有效(数值上)。

相似文献

[1]
Efficacy and safety of iodized lecithin tablets versus spironolactone in alleviating central serous retinopathy among Chinese patients with uncontrolled diabetes.

Pak J Pharm Sci. 2023-3

[2]
SPIRONOLACTONE FOR NONRESOLVING CENTRAL SEROUS CHORIORETINOPATHY: A RANDOMIZED CONTROLLED CROSSOVER STUDY.

Retina. 2015-12

[3]
Spironolactone versus observation in the treatment of acute central serous chorioretinopathy.

Br J Ophthalmol. 2017-10-31

[4]
Mineralocorticoid receptor antagonism in the treatment of chronic central serous chorioretinopathy: a pilot study.

Retina. 2013

[5]
Investigating the efficacy and safety of oral spironolactone in patients with central serous chorioretinopathy.

J Fr Ophtalmol. 2021-1

[6]
COMPARISON OF SHORT-TERM EFFICACY BETWEEN ORAL SPIRONOLACTONE TREATMENT AND PHOTODYNAMIC THERAPY FOR THE TREATMENT OF NONRESOLVING CENTRAL SEROUS CHORIORETINOPATHY.

Retina. 2019-1

[7]
CENTRAL SEROUS CHORIORETINOPATHY TREATED WITH MINERALOCORTICOID ANTAGONISTS: A ONE-YEAR PILOT STUDY.

Retina. 2016-3

[8]
Eplerenone for chronic central serous chorioretinopathy-a randomized controlled prospective study.

Acta Ophthalmol. 2017-11

[9]
Comparison of two mineralcorticosteroids receptor antagonists for the treatment of central serous chorioretinopathy.

Int Ophthalmol. 2017-10

[10]
Long-term results and recurrence rates after spironolactone treatment in non-resolving central serous chorio-retinopathy (CSCR).

Graefes Arch Clin Exp Ophthalmol. 2017-2

引用本文的文献

[1]
Interventions for central serous chorioretinopathy: a network meta-analysis.

Cochrane Database Syst Rev. 2025-6-16

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