Ali Hatem, Murtaza Asam, Anderton John, Ahmed Aimun
Renal Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.
Renal Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK ; Renal Department, Royal Preston Hospital, Lancashire Teaching Hospitals NHS Foundation Trust, Sharoe Green, Fulwood, Preston, PR2 9HT UK.
Springerplus. 2015 Sep 12;4(1):491. doi: 10.1186/s40064-015-1292-0. eCollection 2015.
Real time ultrasound guided percutaneous kidney biopsy has become the standard procedure to assess the pathology of native kidneys and renal transplants. No specific technique has shown to be totally free of post biopsy bleeding complications. Few Studies have looked at the rates of post biopsy bleeding complications comparing different needle size, post biopsy haematoma size, or clinical predictors of the complication rates. In this study we aim to assess safety and adequacy of the real time ultrasound guided biopsy using free hands (ultrasound-assisted) and ultrasound-guided technique.
The results of 527 elective native and kidney transplant biopsy performed as a day case procedure at Lancashire Teaching Hospitals were retrospectively reviewed (499 native and 28 allograft biopsies). Biopsies were grouped into 4 groups according to the technique and the needle size; group 1 (n = 119; performed by free hands-ultrasound assisted- technique using 14G needle) Group 2 (n = 59; performed by free hands-ultrasound-assisted technique using 16G needle), group 3 (n = 195; performed by ultrasound-guided technique using 14G), and group 4 (n = 154; performed by ultrasound-guided technique using 16G). The 4 groups were matched in age, sex, weight, haemoglobin, serum creatinine, INR, PT, and PTT time.
The overall tissue specimen was adequate in 80.45 % of the cases, with no difference between group 1 and 3 (81.5 and 80.52 % respectively, p = 0.82) or between group 2 and 4 (86.44 and 77.3 % respectively, p = 0.13). The overall major complications rate was 2.84 %, with no difference between group 1 and 3 (2.5 and 1 % respectively, p = 0.30) or group 2 and 4 (5 and 4.5 % respectively, p = 0.86). The overall minor complications was 3.7 % with no difference between group 2 and 4 (3.3 and 5.84 % respectively, p = 0.46), however, minor complications were higher in group 1 compared to group 3 (5.8 and 1 % respectively, p = 0.01).There was no difference between using 14G and 16G needle size in terms of tissue adequacy(p = 0.7), major complications (p = 0.2 for drop in Hb >10 g/l, p = 0.08 for blood transfusion, p = 0.35 for embolization) or minor complication items(p = 0.4 for drop in Hb, 10 g/l,p = 0.1 for haematuria, p = 0.7 for hematoma).
When using a 14G needle, there is higher risk of minor complications in the free hands-(ultrasound-assisted) technique compared to the ultrasound-guided technique. There is no difference in the rates of major or minor complications between free hand and needle-guided technique using 16G needles. Both techniques showed adequate tissue sampling.
实时超声引导下经皮肾活检已成为评估自体肾和肾移植病理的标准方法。尚无特定技术能完全避免活检后出血并发症。很少有研究比较不同针径、活检后血肿大小或并发症发生率的临床预测因素与活检后出血并发症的发生率。在本研究中,我们旨在评估徒手(超声辅助)和超声引导技术进行实时超声引导活检的安全性和充分性。
回顾性分析了在兰开夏郡教学医院作为日间手术进行的527例择期自体肾和肾移植活检的结果(499例自体肾活检和28例同种异体移植活检)。活检根据技术和针径分为4组;第1组(n = 119;采用徒手超声辅助技术,使用14G针),第2组(n = 59;采用徒手超声辅助技术,使用16G针),第3组(n = 195;采用超声引导技术,使用14G针),第4组(n = 154;采用超声引导技术,使用16G针)。4组在年龄、性别、体重、血红蛋白、血清肌酐、国际标准化比值(INR)、凝血酶原时间(PT)和部分凝血活酶时间(PTT)方面相匹配。
80.45%的病例总体组织标本足够,第1组和第3组之间(分别为81.5%和80.52%,p = 0.82)或第2组和第4组之间(分别为86.44%和77.3%,p = 0.13)无差异。总体主要并发症发生率为2.84%,第1组和第3组之间(分别为2.5%和1%,p = 0.30)或第2组和第4组之间(分别为5%和4.5%,p = 0.86)无差异。总体轻微并发症发生率为3.7%,第2组和第4组之间无差异(分别为3.3%和5.84%,p = 0.46),然而,第1组的轻微并发症发生率高于第3组(分别为5.8%和1%,p = 0.01)。在组织充分性(p = 0.7)、主要并发症(血红蛋白下降>10 g/l时p = 0.2,输血时p = 0.08,栓塞时p = 0.35)或轻微并发症项目(血红蛋白下降10 g/l时p = 0.4,血尿时p = 0.1,血肿时p = 0.7)方面,使用14G和16G针径没有差异。
与超声引导技术相比,使用14G针时,徒手(超声辅助)技术发生轻微并发症的风险更高。使用16G针时,徒手和针引导技术在主要或轻微并发症发生率方面没有差异。两种技术均显示组织取样充分。