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1.
Medicine (Baltimore) ; 98(21): e15515, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-31124931

RESUMEN

PURPOSE: To evaluate the efficacy and safety of orally administered grape seed proanthocyanidin extract (GSPE) in patients with non-proliferative diabetic retinopathy (NPDR). METHODS: In this randomized (1:2:2), multicentre, double-blind trial, patients (n = 124; age: 40-78 years) were administered placebo, calcium dobesilate (CD; 750 mg/d), or GSPE (150 mg/d) orally for up to 12 months. All patients had retinal thickening with hard exudates (HEs) that met predefined criteria; the median best-corrected visual acuity was 0.8, as assessed using the Snellen visual acuity card. The main outcome measure was an improvement in HEs by at least 1 grade on a 10-grade severity scale. This was evaluated using fundus photography over 1 year. RESULTS: The rate of improvement in the HE severity was higher in the GSPE group than in the CD group. No statistically significant difference existed among the study groups in optical coherence tomography parameters, such as central subfield macular thickness and total macular volume (TMV). However, in the GSPE group, TMV after 9 months of treatment was significantly decreased compared with that at baseline. The GSPE group showed a significantly greater improvement in HE severity than did the placebo or CD group. Four cases in the GSPE group and 2 in the CD group were determined to have developed potential treatment-related adverse reactions, which were all gastrointestinal in nature. CONCLUSIONS: Oral GSPE therapy for 1 year improved HEs in patients with NPDR. The efficacy of GSPE for HEs was higher than that of oral CD in the study patients.


Asunto(s)
Dobesilato de Calcio/administración & dosificación , Retinopatía Diabética/tratamiento farmacológico , Exudados y Transudados/efectos de los fármacos , Extracto de Semillas de Uva/administración & dosificación , Hemostáticos/administración & dosificación , Proantocianidinas/administración & dosificación , Administración Oral , Anciano , Retinopatía Diabética/patología , Método Doble Ciego , Femenino , Humanos , Masculino , Persona de Mediana Edad , Índice de Severidad de la Enfermedad , Tomografía de Coherencia Óptica , Resultado del Tratamiento , Agudeza Visual/efectos de los fármacos
2.
Medicine (Baltimore) ; 96(50): e9257, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29390365

RESUMEN

RATIONALE: Cases of bilateral acute angle closure have been reported after use of various drugs. PATIENT CONCERNS: A 52-year-old woman visited the emergency room and complained of acute bilateral ocular pain and decreased vision accompanied by headache, nausea, and vomiting. One day before, she had started a herbal medicine containing Ma-huang for weight loss. On examinations, myopic shift, edematous cornea, increased intraocular pressure, shallow anterior chamber, and thickened choroid on both eyes were observed. DIAGNOSES: Angle closure glaucoma induced by drug (Ma-huang). INTERVENTIONS: To promptly quit the offending drug and apply ocular hypotensives and cycloplegics. OUTCOMES: Her symptoms and signs were relieved after antiglaucoma medications and no significant recurrence has been occurred. LESSONS: Physicians prescribing weight loss medications containing Ma-huang must be aware of the potentially sight-threatening adverse effect of bilateral acute angle closure.


Asunto(s)
Ephedra sinica/efectos adversos , Glaucoma de Ángulo Cerrado/inducido químicamente , Miopía/inducido químicamente , Enfermedad Aguda , Diagnóstico Diferencial , Femenino , Glaucoma de Ángulo Cerrado/tratamiento farmacológico , Humanos , Persona de Mediana Edad , Miopía/tratamiento farmacológico , República de Corea
3.
Am J Chin Med ; 32(2): 291-301, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15315266

RESUMEN

The efficacy and safety of SKI306X, an herbal anti-arthritic agent, was compared with that of diclofenac sodium for the treatment of osteoarthritis of the knee. In a randomized, double-blind, active comparator-controlled trial, a total of 249 patients were randomly assigned to receive either 200 mg of SKI306X three times daily or 100 mg of diclofenac sustained release (SR) once daily. Clinical efficacy variables (visual analog scale, Lesquesne index and global satisfaction score) and adverse events were monitored at baseline and 2nd and 4th weeks of treatment. SKI306X demonstrated efficacy statistically comparable to that of diclofenac, as assessed by the VAS and patients' and investigators' global satisfaction score. Both treatments were well tolerated, however, the SKI306X treatment group experienced less heartburn (4.0% versus 13.7%, p = 0.015, chi-square test). In this four-week trial, SKI306X was well tolerated and demonstrated clinical efficacy comparable to that of diclofenac SR.


Asunto(s)
Antiinflamatorios no Esteroideos/farmacología , Diclofenaco/farmacología , Medicamentos Herbarios Chinos/farmacología , Osteoartritis/tratamiento farmacológico , Administración Oral , Adulto , Anciano , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/efectos adversos , Preparaciones de Acción Retardada , Diclofenaco/administración & dosificación , Diclofenaco/efectos adversos , Método Doble Ciego , Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos Herbarios Chinos/efectos adversos , Femenino , Humanos , Articulación de la Rodilla/patología , Masculino , Persona de Mediana Edad , Osteoartritis/patología , Satisfacción del Paciente , Resultado del Tratamiento
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