Department of Ophthalmology, Strategic Support Force Medical Center, Anxiang Bei 9#, Beijing, China.
BMC Ophthalmol. 2022 Dec 22;22(1):509. doi: 10.1186/s12886-022-02666-7.
To evaluate the possibilty of preventing recurrent vitreous hemorrhage (RVH) after vitrectomy in proliferative diabetic retinopathy (PDR) patients with unabsorbed vitreous hemorrhage (VH) by intravitreal injection of viscoelastic agent (VA) at the end of the surgery and compared its effect with triamcinolone acetonide (TA).
This was a pilot prospective, observational study. PDR patients with VH who underwent vitrectomy were assigned to 3 groups according to the tamponade applicated at the end of the surgery, including VA group (intravitreally injected 1 ml VA if the retina was prone to bleed during the operation), TA group (intravitreally injected 2 mg TA when there was much exudates), or balanced salt solution (BSS) group (no tamponade). Then postoperative follow-up was performed routinely until 6 months after surgery. The primary outcome was the incidence of RVH, secondary outcome were the best-corrected visual acuity (BCVA) and introcular pressure (IOP). Cataract formation and other complication were also assessed.
A total of 68 eyes, from 68 patients, were included. 18,18,32 eyes were enrolled in the VA group, TA group and BSS group, respectively. The integral incidence of RVH after vitrectomy was 5.6%, 5.6% and 12.5% respectively (P = 0.602). There was no early RVH in VA or TA group, whereas 3 early RVHs were identified in BSS group, however there was no significant difference (P = 0.171). Every group had one late RVH case. In all groups, final BCVA showed significant improvement compared to baseline. BCVA at any postoperative visit showed no significant differences among 3 groups. Mean IOP was higher 1 week after surgery in VA group compared with the other groups; however, in other times the differences were not significant. No cataract formation and other complication was noted in 3 groups.
Intravitreal injection of VA or TA at the end of vitrectomy for PDR patients with unabsorbed VH tend to reduce the incidence of early RVH after vitrectomy similarly. As VA was preferred to applicate in the eyes that were prone to bleed, intravitreal injection of VA at the end of vitrectomy might be a promising method for preventing RVH in PDR patients.
为评估在增生性糖尿病视网膜病变(PDR)患者玻璃体积血(VH)未吸收的情况下,通过手术结束时玻璃体内注射黏弹性剂(VA)预防玻璃体切除术后再发性玻璃体积血(RVH)的可能性,并与曲安奈德(TA)进行比较。
这是一项前瞻性、观察性的初步研究。接受玻璃体切除术的 VH 的 PDR 患者根据手术结束时的填塞物分为 3 组,包括 VA 组(如果术中视网膜容易出血,则玻璃体内注射 1ml VA)、TA 组(如果有大量渗出物,则玻璃体内注射 2mg TA)或平衡盐溶液(BSS)组(无填塞物)。然后常规进行术后随访,直至术后 6 个月。主要结局是 RVH 的发生率,次要结局是最佳矫正视力(BCVA)和眼内压(IOP)。还评估了白内障形成和其他并发症。
共纳入 68 只眼,68 例患者。VA 组、TA 组和 BSS 组分别纳入 18、18 和 32 只眼。玻璃体切除术后 RVH 的总发生率分别为 5.6%、5.6%和 12.5%(P=0.602)。VA 或 TA 组均无早期 RVH,BSS 组有 3 例早期 RVH,但无显著差异(P=0.171)。各组均有 1 例晚期 RVH。所有组的最终 BCVA 均较基线显著提高。3 组在任何术后访视的 BCVA 均无显著差异。VA 组术后 1 周的平均 IOP 高于其他组;然而,在其他时间差异无统计学意义。3 组均未发生白内障形成和其他并发症。
对于 VH 未吸收的 PDR 患者,在玻璃体切除术中结束时玻璃体内注射 VA 或 TA 可能会降低玻璃体切除术后早期 RVH 的发生率。由于 VA 更适合应用于容易出血的眼睛,因此玻璃体切除术中结束时玻璃体内注射 VA 可能是预防 PDR 患者 RVH 的一种有前途的方法。