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January 25, 2026The Laryngoscope1 citations

Algorithmic Surgical Management of Primary Hyperparathyroidism and Its Variants: A Scoping Review

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FKFleur S. KabalaTFTodd E. FalconeKPKourosh Parham

Key Points

  • The aim is to explore and compare the management of different presentations of primary hyperparathyroidism, focusing on gaps in current approaches.
  • Conducted a comprehensive search in PubMed and Google Scholar using relevant terms.
  • Included peer-reviewed studies on surgical management of hyperparathyroidism published in English.
  • Reviewed and synthesized data using PRISMA ScR guidelines, involving two independent reviewers.
  • Imaging accuracy was greatest with 4DCT and PET scans, especially in multiglandular disease settings.
  • Lack of a ≥ 50% drop in intraoperative parathyroid hormone levels or levels below 40 pg/mL indicates high risk for persistence or recurrence.
  • Identified knowledge gaps that could improve management of variant primary hyperparathyroidism.

Abstract

ABSTRACT Objective Primary hyperparathyroidism (PHPT) has varied presentations whose successful surgical management demands integration of the expanding literature within a comprehensive decision‐making framework. Our objective is to compare the workup and management of variant (i.e., normocalcemic hyperparathyroidism (NCPHPT) and normohormonal hyperparathyroidism (NHPHPT)) to classic hyperparathyroidism (CPHPT), taking into account localization studies, surgical considerations, utility of intraoperative parathyroid hormone (IOPTH), and surveillance to identify gaps in knowledge that limit management outcomes of variant PHPT presentations. Data Sources A comprehensive search of PubMed and Google Scholar was conducted from June 11, 2024, to March 17, 2025, using MeSH terms and free‐text queries focused on imaging, surgery, and outcomes in PHPT and reported using PRISMA ScR guidelines. Review Methods Peer‐reviewed studies addressing surgical management of PHPT in adults, published in English, were included. Two reviewers independently screened all titles, abstracts, and full texts using previously developed inclusion criteria recorded in a shared spreadsheet. Twenty‐seven studies were included. Data were synthesized into a flow diagram to identify areas in need of further guidance. Results Imaging accuracy was highest with 4DCT and PET scans in both classic and variant PHPT, particularly in the setting of multiglandular disease. Not obtaining ≥ 50% IOPTH drop and/or levels below 40 pg/mL are risk factors for persistence or recurrence. Conclusions PHPT has varied presentations that demand nuanced approaches. Our review highlights knowledge gaps that, if addressed, will improve the care of patients with variant PHPT. Further prospective validation of this algorithmic summary is warranted to improve long‐term impact and patient outcomes.

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Cite This Study

Kabala et al. (2026) studied this question.

synapsesocial.com/papers/6975b306feba4585c2d6e755https://doi.org/10.1002/lary.70382
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