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一种新型 22G 活检针的可行性和效率:一项前瞻性比较研究。

Feasibility and efficiency of a new 22G core needle: a prospective comparison study.

机构信息

Gastroenterology, Asian Institute of Gastroenterology, Hyderabad, India.

出版信息

Endoscopy. 2013 Oct;45(10):792-8. doi: 10.1055/s-0033-1344217. Epub 2013 Sep 25.

DOI:10.1055/s-0033-1344217
PMID:24068588
Abstract

BACKGROUND AND STUDY AIMS

Histological examination of core tissue samples may have advantages over cytology in endoscopic ultrasound (EUS)-guided sampling. We aimed to evaluate the feasibility and efficiency of a new 22G core biopsy needle.

PATIENTS AND METHODS

Consecutive patients with a pancreatic mass lesion or peri-intestinal lymphadenopathy sequentially underwent fine needle biopsy with both a newly developed 22G core needle (the FNB needle) and a standard 22G fine needle aspiration (FNA) needle, in randomized order.

RESULTS

In 144 patients, mean age 48 years (± standard deviation [SD] 14; range 18 - 82), with 145 lesions (mean lesion size 39 ± 15 mm, range 15 - 99), EUS-guided sampling was technically feasible with both needles in all patients. Mean number of passes to obtain sufficient tissue was 1.2 ± 0.5 with the core needle vs. 2.5 ± 0.9 with the standard needle (P < 0.001). FNB specimens were adequate for evaluation in 125 (86.2 %) vs. 127 (87.6 %) with FNA (P = 0.72). Among 139 patients available for follow-up, FNB provided a correct diagnosis in 110 (79.1 %) and FNA in 112 (80.6 %) (P = 0.73). Sensitivity, specificity, positive and negative predictive values, and accuracy for diagnosis of malignancy were 90 %, 100 %, 100 %, 93 %, 96 % for FNB and 77 %, 100 %, 100 %, 85 %, 92 % for FNA, respectively (P > 0.05).

CONCLUSION

FNB with the new 22G core needle was technically feasible, efficient and comparable to FNA with a standard needle. The core needle required fewer passes to provide an adequate sample, offering potentially shorter procedure time.

摘要

背景和研究目的

与内镜超声(EUS)引导下的取样相比,对核心组织样本进行组织学检查可能具有优势。我们旨在评估一种新型 22G 核心活检针的可行性和效率。

患者和方法

连续的胰腺肿块或肠周淋巴结病变患者,依次顺序使用新开发的 22G 核心针(FNB 针)和标准的 22G 细针抽吸(FNA)针进行细针活检,以随机顺序进行。

结果

在 144 例患者中,平均年龄为 48 岁(±标准偏差[SD] 14;范围 18-82),共有 145 个病变(平均病变大小为 39±15mm,范围 15-99),两种针均能在所有患者中进行技术上可行的 EUS 引导下取样。使用核心针获得足够组织的平均穿刺次数为 1.2±0.5 次,而标准针为 2.5±0.9 次(P<0.001)。FNB 标本可评估的比例为 125 例(86.2%)与 FNA 为 127 例(87.6%)(P=0.72)。在 139 例可随访的患者中,FNB 提供正确诊断的比例为 110 例(79.1%),FNA 为 112 例(80.6%)(P=0.73)。FNB 对恶性肿瘤的诊断的敏感性、特异性、阳性预测值、阴性预测值和准确性分别为 90%、100%、100%、93%、96%,而 FNA 分别为 77%、100%、100%、85%、92%(P>0.05)。

结论

新型 22G 核心针的 FNB 在技术上是可行的、高效的,与标准针的 FNA 相当。核心针需要更少的穿刺次数来提供足够的样本,可能会缩短手术时间。

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