期刊文献+

577 nm激光光凝联合玻璃体内注射康柏西普治疗糖尿病性黄斑水肿的效果观察 被引量:23

Effect of 577 nm laser photocoagulation combined with intravitreal injection of conbercept on diabetic macular edema
下载PDF
导出
摘要 目的探讨577 nm激光光凝联合玻璃体内注射康柏西普治疗糖尿病性黄斑水肿的效果。方法选取2016年1月至2017年3月在我院治疗的糖尿病性黄斑水肿患者81例81眼,根据患者最终选取的治疗方案分为观察组43例43眼和对照组38例38眼,观察组给予577 nm激光光凝联合玻璃体内注射康柏西普治疗,对照组仅给予577 nm激光光凝,观察两组治疗前后最佳矫正视力(best corrected visual acuity,BCVA)和黄斑中心凹厚度(central fovea of macula thickness,CMT),分析观察组BCVA和CMT变化值与初始因素的相关性。结果随治疗时间延长,观察组和对照组BCVA、CMT相应改善(均为P<0.05);观察组治疗后1个月、3个月和6个月BCVA分别为0.37±0.09、0.44±0.10和0.52±0.13,均明显高于对照组(均为P<0.05);观察组治疗后1个月、3个月和6个月CMT分别为(351.03±41.43)μm、(270.32±40.03)μm和(220.01±32.91)μm,均明显低于对照组(均为P<0.05);BCVA变化值与糖尿病性黄斑水肿病程、治疗前BCVA呈负相关(r=-0.422、-0.410,均为P<0.05);CMT变化值与糖尿病性黄斑水肿病程、治疗前CMT呈负相关(r=-0.430、-0.415,均为P<0.05)。结论 577 nm激光光凝联合玻璃体内注射康柏西普治疗糖尿病性黄斑水肿效果较好,其效果与患者基线BCVA、糖尿病性黄斑水肿病程有一定相关性。 Objective To investigate the effect of 577 nm laser photocoagulation combined with intravitreal injection of conbercept in the treatment of diabetic macular edema. Methods Totally 81 patients (81 eyes) with diabetic macular edema were selected in our hospital from January 2016 to March 2017,and the patients were divided into the observation group (43 patients 43 eyes) and the control group (38 patients 38 eyes) according to the patients’ final selection.The patients in the observation group were treated with 577 nm laser photocoagulation combined with intravitreal injection of conbercept,and the control group was treated with 577 nm laser photocoagulation only,and the best corrected visual acuity (BCVA) and central fovea of macula thickness (CMT) in the two groups before and after treatment were observed,and the correlation of BCVA and CMT changes in the observation group and initial factors were analyzed. Results The BCVA and CMT in the observation group and the control group improved with the prolongation of treatment time (all P<0.05).The BCVA at 1 months,3 months and 6 months after treatment in the observation group were 0.37±0.09,0.44±0.10 and 0.52±0.13,respectively,which were significantly higher than those in the control group (all P<0.05).The CMT at 1 months,3 months and 6 months after treatment in the observation group were (351.03±41.43)μm,(270.32±40.03)μm and (220.01±32.91)μm,respectively,which were significantly lower than that of the control group (all P<0.05).The change of BCVA was negatively correlated with the duration of diabetic macular edema and BCVA before treatment (r=-0.422 and -0.410,both P<0.05).The change of CMT were negatively correlated with the duration of diabetic macular edema and BCVA before treatment (r=-0.430 and -0.415,both P<0.05). Conclusion The effect of 577 nm laser photocoagulation combined with intravitreal injection of conbercept on diabetic macular edema is better,and the effect is related to the baseline visual acuity of the patients and duration of diabetic macular edema.
作者 宋志刚 魏少华 SONG Zhi-Gang;WEI Shao-Hua(Department of Ophthalmology,Puyang Second People’s Hospital,Puyang 457000,Henan Province,China)
出处 《眼科新进展》 CAS 北大核心 2019年第4期373-375,共3页 Recent Advances in Ophthalmology
关键词 577nm激光 康柏西普 糖尿病性黄斑水肿 577nm laser conbercept diabeticmacular edema
  • 相关文献

参考文献10

二级参考文献63

  • 1Greeley SA, Tucker SE, Worrell HI, et al. Update in neonatal diabetes [ J]. Curt Opin Endocrinol Diabetes Obes ,2010,17 ( 1 ) : 13 - 19.
  • 2Flanagan SE, Patch AM, Mackay D J, et al. Mutations in ATP-sensitive K ^+ channel genes cause transient neonatal diabetes and permanent dia- betes in childhood or adulthood [ J ]. Diabetes, 2007,56 ( 7 ) : 1930 - 1937. D0I : 10. 2337/db07-0043.
  • 3Hamming KS, Soliman D, Matemisz LC, et al. Coexpressiort of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K ^+ channel [ J ]. Diabetes, 2009,58 ( 10 ) : 2419 - 2424. DOI : 10. 2337/ db09-0143.
  • 4Rubio-Cabezas O, Flanagan SE, Damhuis A, et al. K(ATP) channel mu- tations in infants with permanent diabetes diagnosed after 6 months of life[ J]. Pediatr Diabetes,2012,13 (4) :322 - 325.
  • 5Rubio-Cabezas O, Klupa T, Malecki MT, et al. CEED3 Consortium. Per- manent neonatal diabetes mellitus the importance of diabetes differential diagnosis in neonates and infants[ J]. Eur J Clin Invest,2011,41 (3) : 323 - 333. DOI : 10.1111/j. 1365-2362. 2010. 02409. x.
  • 6Murphy R, Ellard S, Hattersley AT. Clinical implications of a molecular genetic classification of monogenic beta-ceU diabetes[ J ]. Nat Clin Pract Endocrinol Metab,2008,4(4) :200 -213.
  • 7Edghill EL, Flanagan SE, Patch AM, et al. Neonatal Diabetes Interna- tional Collaborative Group, Hattersley AT, Ellard S: Insulin mutation screening in 1,044 patients with diabetes:mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diag- nosed in childhood or adulthood[ J]. Diabetes,2008,57:1034-1042.
  • 8Proks P, Antciff JF, Lippiat J, et al. Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal Diabetes plus neurological features[J]. PNAS,2004,101 (50):17539 - 17544. DOI: 10. 1073/ pnas. 0404756101.
  • 9Babenko AP, Polak M, Cava H, et al. Activating mutations in the ABCC8 gene in neonatal diabetes mellitus [ J ]. N Engl J Med, 2006,355 ( 5 ) : 456 - 466.
  • 10Porter JR, Barrett TG. Acquired non-type 1 diabetes in childhood : sub- types, diagnosis, and management [ J ]. Arch Dis Child, 2004,89 ( 12 ) : 1138 - 1144. DOI:10.1136/adc. 2003. 036608.

共引文献190

同被引文献167

引证文献23

二级引证文献56

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部