Thirumalai Balaji, Blamires Trudi L, Brooker Lucenne, Deeks Jon
Department of Ophthalmology, Kettering General Hospital, Rothwell Road, Kettering, NN16 8UZ, UK.
BMC Ophthalmol. 2007 Feb 9;7:2. doi: 10.1186/1471-2415-7-2.
To assess the safety of abandoning the next day post-operative review in preference for assessment only 2 hours post-surgery for both phacoemulsification and extracapsular surgery with heavier molecular weight ocular viscoelastic devices (OVD).
475 patients who underwent uncomplicated cataract surgery using heavier molecular weight ocular viscoelastic device (Healon GV) were studied. Of these 415 were phacoemulsification and 60 extracapsular and none received Intraocular pressure (IOP) lowering prophylaxis at the end of surgery. All were examined at 2 hours post-surgery and on the following day. Results were tabulated and analysed assessing wound stability, corneal clarity, anterior chamber reaction and IOP.
In the time between the two assessments 44 (10.6%) patients developed a total of 53 new problems, with a majority being increases in IOP. Based on the lower threshold of IOP of 30 mmHg, the incidence of new problems at the next-day assessment was 9.8% (95% CI: 7.0 to 13.6) in the phacoemulsification group and 16.3% (7.3 to 29.7)in the extracapsular surgery group. At the higher threshold of IOP of 35 mmHg the corresponding figures were 6.6% and 16.3%.
There is a higher incidence of new problems at the next-day assessment than previous studies with conventional OVD. Therefore results from previous studies using standard OVDs cannot be simply extrapolated to heavier molecular weight OVDs. When these agents are used, routine use of an ocular hypotensive agent may be necessary to increase the safety of abandoning the review on the first post-operative day for phacoemulsification patients. This is to be studied.
评估对于白内障超声乳化术和使用更高分子量眼用粘弹性装置(OVD)的囊外摘除术,放弃术后次日复查而仅在术后2小时进行评估的安全性。
对475例行使用更高分子量眼用粘弹性装置(Healon GV)的无并发症白内障手术的患者进行研究。其中415例行超声乳化术,60例行囊外摘除术,且所有患者在手术结束时均未接受降低眼压的预防性治疗。所有患者均在术后2小时及次日接受检查。将结果列表并分析,评估伤口稳定性、角膜清晰度、前房反应和眼压。
在两次评估之间,44例(10.6%)患者共出现53个新问题,大多数是眼压升高。基于30 mmHg的较低眼压阈值,超声乳化术组次日评估时新问题的发生率为9.8%(95%可信区间:7.0至13.6),囊外摘除术组为16.3%(7.3至29.7)。在35 mmHg的较高眼压阈值时,相应数字分别为6.6%和16.3%。
与以往使用传统OVD的研究相比,次日评估时新问题的发生率更高。因此,以往使用标准OVD的研究结果不能简单地外推至更高分子量的OVD。当使用这些药物时,对于白内障超声乳化术患者,可能有必要常规使用降眼压药物以提高放弃术后第一天复查的安全性。这有待进一步研究。