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      Risk of complications after core needle biopsy in pheochromocytoma/paraganglioma

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          Abstract

          Core needle biopsy (CNB) has been used with caution in pheochromocytoma and paraganglioma (PPGL) due to concerns about catecholamine-related complications. While it is unclear what scientific evidence supports this claim, it has limited the acquisition of biological samples for diagnostic purposes and research, especially in metastatic PPGL. We performed a systematic review and individual patient meta-analysis to evaluate the risk of complications after CNB in PPGL patients. The primary and secondary objectives were to investigate the risk of death and the occurrence of complications requiring intervention or hospitalization, respectively. Fifty-six articles describing 86 PPGL patients undergoing CNB were included. Of the patients (24/71), 34% had metastases and 53.4% (31/58) had catecholamine-related symptoms before CNB. Of the patients (14/41), 34.1% had catecholamine excess testing prior to the biopsy. No CNB-related deaths were reported. Four patients (14.8%, 4/27) experienced CNB-related complications requiring hospitalization or intervention. One case had a temporary duodenal obstruction caused by hematoma, two cases had myocardial infarction, and one case had Takotsubo cardiomyopathy. Eight patients (32%, 8/25) had CNB-related catecholamine symptoms, mainly transient hypertension, excessive diaphoresis, tachycardia, or hypertensive crisis. The scientific literature does not allow us to make any firm conclusion on the safety of CNB in PPGL. However, it is reasonable to argue that CNB could be conducted after thorough consideration, preparation, and with close follow-up for PPGL patients with a strong clinical indication for such investigation.

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          Most cited references35

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          The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: checklist and explanations.

          The PRISMA statement is a reporting guideline designed to improve the completeness of reporting of systematic reviews and meta-analyses. Authors have used this guideline worldwide to prepare their reviews for publication. In the past, these reports typically compared 2 treatment alternatives. With the evolution of systematic reviews that compare multiple treatments, some of them only indirectly, authors face novel challenges for conducting and reporting their reviews. This extension of the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses) statement was developed specifically to improve the reporting of systematic reviews incorporating network meta-analyses. A group of experts participated in a systematic review, Delphi survey, and face-to-face discussion and consensus meeting to establish new checklist items for this extension statement. Current PRISMA items were also clarified. A modified, 32-item PRISMA extension checklist was developed to address what the group considered to be immediately relevant to the reporting of network meta-analyses. This document presents the extension and provides examples of good reporting, as well as elaborations regarding the rationale for new checklist items and the modification of previously existing items from the PRISMA statement. It also highlights educational information related to key considerations in the practice of network meta-analysis. The target audience includes authors and readers of network meta-analyses, as well as journal editors and peer reviewers.
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            Liver biopsy.

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              Pheochromocytoma and Paraganglioma

                Author and article information

                Journal
                Endocr Relat Cancer
                Endocr Relat Cancer
                ERC
                Endocrine-Related Cancer
                Bioscientifica Ltd (Bristol )
                1351-0088
                1479-6821
                26 April 2023
                26 April 2023
                01 July 2023
                : 30
                : 7
                : e220354
                Affiliations
                [1 ]Department of Medical Sciences , Uppsala University, Uppsala, Sweden
                [2 ]Department of Surgical Sciences , Uppsala University, Uppsala, Sweden
                [3 ]Klinik für Endokrinologie , Diabetologie und Klinische Ernährung, Universitätsspital Zürich (USZ) and Univeristät Zürich (UZH), Zurich, Switzerland
                [4 ]Medizinische Klinik und Poliklinik IV , Klinikum der Universität München, Munich, Germany
                [5 ]Section on Medical Neuroendocrinology , Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
                Author notes
                Correspondence should be addressed to L Zhang: Liang.Zhang@ 123456medsci.uu.se

                This paper is part of a themed collection on Advances and Future Directions in Pheochromocytoma and Paraganglioma. The Collection Editors for this collection were Karel Pacak (NICHHD, USA) and Roderick Clifton-Bligh (University of Sydney, Australia).

                Author information
                http://orcid.org/0000-0001-8448-6754
                http://orcid.org/0000-0002-9423-8970
                http://orcid.org/0000-0002-3541-3767
                Article
                ERC-22-0354
                10.1530/ERC-22-0354
                10304911
                37185155
                00302594-ae29-438b-b785-ee88f7a44af0
                © the author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 31 March 2023
                : 26 April 2023
                Categories
                Thematic Research

                Oncology & Radiotherapy
                pheochromocytoma,paraganglioma,core needle biopsy,diagnosis,risk
                Oncology & Radiotherapy
                pheochromocytoma, paraganglioma, core needle biopsy, diagnosis, risk

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