Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
World Neurosurg. 2023 Aug;176:e254-e264. doi: 10.1016/j.wneu.2023.05.046. Epub 2023 May 18.
Brain tumor biopsies are essential for pathologic diagnosis. However, hemorrhagic complications after biopsies may occur, leading to suboptimal outcomes. This study aimed to evaluate the associated factors of hemorrhagic complications after brain tumor biopsies and propose countermeasures.
We retrospectively collected data on 208 consecutive patients with brain tumors (malignant lymphoma or glioma) who underwent a biopsy from 2011-2020. We evaluated factors and microbleeds (MBs) in the tumor plus relative cerebral/tumoral blood flow (rCBF) at the biopsy site on preoperative magnetic resonance imaging (MRI).
Postoperative all and symptomatic hemorrhage occurred in 21.6% and 9.6% of patients. In univariate analysis, a needle biopsy was significantly associated with the risk of all and symptomatic hemorrhages compared to techniques that allow adequate hemostatic manipulation (i.e., open and endoscopic biopsies). Multivariate analyses revealed that a needle biopsy and gliomas of World Health Organization (WHO) grade III/IV were significantly associated with postoperative all and symptomatic hemorrhages. Multiple lesions were also an independent risk factor for symptomatic hemorrhages. On preoperative MRI, abundant MBs in the tumor and MBs at the biopsy sites, in addition to high rCBF, were significantly associated with postoperative all and symptomatic hemorrhages.
We recommend the following measures to prevent hemorrhagic complications: consider biopsy techniques that allow adequate hemostatic manipulation preferentially; perform more careful hemostasis in cases of suspected gliomas of WHO grade III/IV, multiple lesions, and abundant MBs in the tumors; and, if there are multiple candidate biopsy sites, select areas with lower rCBF and no MBs as a biopsy target.
脑肿瘤活检对于病理诊断至关重要。然而,活检后可能会发生出血并发症,导致预后不佳。本研究旨在评估脑肿瘤活检后出血并发症的相关因素并提出对策。
我们回顾性收集了 2011 年至 2020 年间 208 例连续接受脑肿瘤(恶性淋巴瘤或神经胶质瘤)活检的患者数据。我们评估了术前磁共振成像(MRI)上肿瘤内的相关因素和微出血(MB)以及活检部位的相对脑/肿瘤血流(rCBF)。
术后所有和症状性出血分别发生在 21.6%和 9.6%的患者中。在单因素分析中,与允许充分止血操作的技术(即开放和内镜活检)相比,针吸活检显著增加了所有和症状性出血的风险。多因素分析显示,针吸活检和世界卫生组织(WHO)分级 III/IV 的神经胶质瘤与术后所有和症状性出血显著相关。多发病灶也是症状性出血的独立危险因素。在术前 MRI 上,肿瘤内大量 MB 和活检部位的 MB 以及高 rCBF 与术后所有和症状性出血显著相关。
我们建议采取以下措施预防出血并发症:优先考虑允许充分止血操作的活检技术;在疑似 WHO 分级 III/IV 的神经胶质瘤、多发病灶和肿瘤内大量 MB 的情况下,更加小心地止血;如果有多个候选活检部位,选择 rCBF 较低且无 MB 的区域作为活检目标。