Khan Muhammad Saim, Sameen Murtaza, Lodhi Arshad Ali, Ahmed Munawar, Ahmed Noman, Kamal Mustafa, Junejo Sameen Afzal
Muhammad Saim Khan, Department of Ophthalmology, Armed Forces Institute of Ophthalmology (AFIO), Rawalpindi, Pakistan.
Murtaza Sameen, Department of Ophthalmology, Armed Forces Institute of Ophthalmology (AFIO), Rawalpindi, Pakistan.
Pak J Med Sci. 2016 Sep-Oct;32(5):1158-1163. doi: 10.12669/pjms.325.10755.
To evaluate the effect of half adult dose of oral Rifampicin on mean change in best corrected visual acuity and central macular thickness in patients with central serous chorioretinopathy.
Thirty-eight eyes of 31 patients with idiopathic central serous chorioretinopathy (CSCR) were registered. Unaided Visual acuity, best corrected visual acuity was documented and detailed slit lamp examination along with dilated ophthalmoscopy was performed. All subjects were treated with oral Rifampicin 300 mg (half adult dose) daily for 03 months. Patients underwent a complete ocular and systemic examination as well as central macular thickness (CMT) measurement by optical coherence tomography (OCT) every month after starting treatment until four months. Fundus fluorescein angiography (FFA) was performed in recurrent cases. Liver function tests were carried out prior to the treatment and during follow up period.
A total of 38 eyes of 31 patients (24 males, 07 females) were included in the study. Mean age of patients was 36.16±3.19 years (range 30-44). Mean best corrected visual acuity (BCVA) before treatment was 0.56±0.11 and improved to 0.47±0.14 at 04 weeks (P<0.001) of treatment. The mean CMT at the time of presentation was 494.39±96.29 um and was decreased to 306.90±50.71 um after 04 weeks of treatment (P<0.001). The mean induced reduction in CMT was 187.48±122 um (P<0.001) while that in BCVA 0.41±0.16 at 04 weeks of treatment (P<0.001). Liver function tests were within normal range before and after the treatment.
Half adult dose rifampicin (300mg) is effective and safe in treatment of central serous chorioretinopathy without causing any systemic imbalance.
评估口服半量成人剂量利福平对中心性浆液性脉络膜视网膜病变患者最佳矫正视力和中心黄斑厚度平均变化的影响。
登记31例特发性中心性浆液性脉络膜视网膜病变(CSCR)患者的38只眼。记录裸眼视力、最佳矫正视力,并进行详细的裂隙灯检查及散瞳眼底检查。所有受试者每日口服利福平300mg(半量成人剂量),持续3个月。治疗开始后直至4个月,每月对患者进行一次全面的眼部和全身检查以及通过光学相干断层扫描(OCT)测量中心黄斑厚度(CMT)。复发病例进行眼底荧光血管造影(FFA)检查。治疗前及随访期间进行肝功能检查。
本研究共纳入31例患者(24例男性,7例女性)的38只眼。患者平均年龄为36.16±3.19岁(范围30 - 44岁)。治疗前平均最佳矫正视力(BCVA)为0.56±0.11,治疗4周时提高至0.47±0.14(P<0.001)。就诊时平均CMT为494.39±96.29μm,治疗4周后降至306.90±50.71μm(P<0.001)。治疗4周时CMT平均降低187.48±122μm(P<0.001),而BCVA平均降低0.41±0.16(P<0.001)。治疗前后肝功能检查均在正常范围内。
半量成人剂量利福平(300mg)治疗中心性浆液性脉络膜视网膜病变有效且安全,不会引起任何全身失衡。