Optimal Number of Pleural Biopsies During Pleuroscopy (OPTIBIOP).

IF 2.3 Q2 RESPIRATORY SYSTEM
Jeeyune Bahk, Axel Duval, Sung Choi, Kimia Ganjaei, Mary B Beasley, Abhinav Agrawal, Udit Chaddha
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引用次数: 0

Abstract

Background: There is currently no evidence-based standard for the number of pleural biopsies required during pleuroscopy to achieve diagnostic adequacy. This study evaluated the cumulative diagnostic yield of sequential pleural biopsy aliquots obtained during rigid pleuroscopy.

Methods: We conducted a prospective, single-center observational pilot study of adult patients undergoing pleuroscopy. Biopsy specimens were obtained according to routine practice and submitted in sequential aliquots: aliquot 1 (biopsies 1 to 3), aliquot 2 (4 to 6), aliquot 3 (7 to 9), and aliquot 4 (≥10). Pathologic evaluation was performed sequentially to determine the earliest aliquot yielding a definitive diagnosis. Cumulative diagnostic yield, the need for additional aliquots for comprehensive biomarker testing, and complications were evaluated.

Results: A definitive diagnosis was achieved in all 104 patients. The median number of biopsies performed was 10 (IQR 6 to 14). The diagnostic yield for aliquot 1 (≤3 biopsies) was 93%. Among the 7% of cases requiring subsequent aliquots for diagnosis, 6 had diffuse parietal pleural abnormalities on pleuroscopy, while 1 had discrete lesions. Of the 17 patients who required comprehensive biomarker testing, 10 (59%) needed samples beyond the first aliquot. No major complications were reported.

Conclusion: While most diagnoses can be established with 3 or fewer biopsies, cases requiring additional biopsies were more frequently associated with diffuse pleural disease. These findings support tailoring the biopsy strategy to pleural morphology: lesion-directed sampling for focal disease and broader sampling for diffusely abnormal or benign-appearing pleura, especially when malignancy is suspected, or comprehensive biomarker testing is required.

胸膜镜检查中最佳胸膜活检次数(OPTIBIOP)。
背景:目前没有基于证据的标准,胸膜镜检查中需要胸膜活检的次数才能达到诊断的充分性。本研究评估了在刚性胸膜镜检查中获得的顺序胸膜活检结果的累积诊断率。方法:我们对接受胸膜镜检查的成年患者进行了一项前瞻性、单中心观察性先导研究。活检标本按常规采集,按顺序等分提交:等分1(活检1 ~ 3)、等分2(活检4 ~ 6)、等分3(活检7 ~ 9)、等分4(≥10)。随后进行病理评估,以确定最早的诊断结果。评估了累积诊断率、综合生物标志物检测的额外等价物需求以及并发症。结果:104例患者均获得明确诊断。活检的中位数为10例(IQR 6 ~ 14例)。aliquot 1(≤3次活检)的诊断率为93%。在7%需要后续检查诊断的病例中,6例胸膜壁层弥漫性异常,1例离散性病变。在17例需要综合生物标志物检测的患者中,10例(59%)需要的样本超过第一个同类。无重大并发症报道。结论:虽然大多数诊断可以通过3次或更少的活检来确定,但需要额外活检的病例更常与弥漫性胸膜疾病相关。这些发现支持根据胸膜形态调整活检策略:病灶性疾病的病灶定向取样和弥漫性异常或良性胸膜的更广泛取样,特别是当怀疑恶性肿瘤时,或需要进行全面的生物标志物检测。
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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来源期刊
CiteScore
4.40
自引率
6.10%
发文量
121
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