Shortening Activated Partial Tromboplastin Time (APTT) Between Hypertension and Nonhypertension in Diabetic Mellitus Patients with Bevacizumab Intravitreal Injection

A. Winarni, Ni Luh Putu Widyasti, Natalia Christina Angsana, Rizto Wisuda Senuari, A. N. Agni, Agus Supartoto, M. B. Sasongko, Haryo Yudono
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Abstract

Introduction : Bevacizumab intravitreal injection could be detectable in plasma that might interfere  the coagulopathy and hemostasis condition. The purpose of this study was to investigate the difference of APTT between hypertensive and nonhypertensive diabetic mellitus patients with bevacizumab intravitreal injection. Methods : This was cohort study conducted at Sardjito General Hospital from March 2019 to June 2019. Thirty-two hypertension patients and 30 nonhypertension patients with diabetes mellitus who underwent bevacizumab intravitreal injection were included. Value of APTT was measured using ACLTOP300 machine prior and 1 week after IVB. The difference in mean APTT value prior and after IVB, range APTT value between two groups were assessed using independent t-test. The percentage of patients who had shortening of APTT in both groups was tested by two populations proportion test. Results : Mean APTT before IVB in hypertensive patients was 36.47 ± 2.92 seconds and in nonhypertensive patients was 36.33 ± 4.39 seconds with p value > 0.05. Mean value of APTT after IVB in hypertension patients was 35.42 ± 3.63 seconds and in nonhypertensive patients was 35.60 ± 3.13 seconds with p value > 0.05. APTT shortening in hypertensive patients was -1.03 ± 3.65 and nonhypertensive patients was -0.73 ± 2.55 with p value > 0.05. The risk of APTT shortening in hypertensive patients was 1.370 (0.831-2.258). The risk of APTT shortening in hypertensive patients who used antihypertensive drugs regularly was 0.538 (0.331- 0.874). Conclusion : There was no difference in shortening of APTT value 1 week after intravitreal bevacizumab injection between hypertensive and nonhypertensive groups in patients with diabetes mellitus. Hence, administration of IVB in hypertensive patients with regular antihypertensive therapy might be safe.  
贝伐单抗玻璃体内注射缩短高血压和非高血压糖尿病患者活化部分原活素时间(APTT
介绍:贝伐单抗玻璃体内注射可在血浆中检测到,可能会干扰凝血和止血状况。本研究的目的是探讨贝伐单抗在高血压和非高血压糖尿病患者玻璃体内注射后APTT的差异。方法:该队列研究于2019年3月至2019年6月在Sardjito总医院进行。32例高血压患者和30例合并糖尿病的非高血压患者接受了贝伐单抗玻璃体内注射。采用ACLTOP300仪测定静脉注射前和注射后1周APTT值。采用独立t检验评估两组间IVB前后平均APTT值、范围APTT值的差异。两组患者APTT缩短的比例采用两群体比例检验。结果:高血压患者IVB前平均APTT为36.47±2.92 s,非高血压患者平均APTT为36.33±4.39 s, p值> 0.05。高血压患者IVB后APTT平均值为35.42±3.63秒,非高血压患者为35.60±3.13秒,p值> 0.05。高血压患者APTT缩短为-1.03±3.65,非高血压患者APTT缩短为-0.73±2.55,p值均> 0.05。高血压患者APTT缩短风险为1.370(0.831-2.258)。定期使用降压药的高血压患者APTT缩短风险为0.538(0.331 ~ 0.874)。结论:高血压组与非高血压组糖尿病患者玻璃体内注射贝伐单抗后1周APTT值缩短无差异。因此,在常规降压治疗的高血压患者中使用IVB可能是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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