Patient-Reported Outcome Measures Used in Primary Hyperparathyroidism: A Scoping Review.

Journal: Annals of surgical oncology

This scoping review evaluated how patient-reported outcome measures (PROMs) have been used in primary hyperparathyroidism (PHPT) research.

Across 243 primary PHPT studies:

  • 147 studies (49.7%) described symptoms or quality-of-life (QoL) concepts that could have been quantified with PROMs but did not use them.
  • 96 studies (50.3%) incorporated at least one PROM (median 1 per study; IQR 1–2), with 36 distinct PROMs identified.

Most commonly used tools:

  • 36-item Short Form Health Survey (SF-36): 42 studies
  • Parathyroidectomy Assessment of Symptoms (PAS): 20 studies
  • Beck Depression Inventory (BDI): 12 studies

PROMs most often targeted symptom burden and mental health (e.g., anxiety, depression).

Disease-specific validity in PHPT was documented for only three instruments:

  • SF-36
  • PAS
  • Primary Hyperparathyroidism Quality of Life Questionnaire

All other tools had been validated only in non-PHPT populations.

The authors conclude that PHPT research underutilizes rigorously validated PROMs, leading to missed opportunities to accurately assess health-related quality of life. They recommend more systematic and appropriate use of validated PROMs in future PHPT clinical studies to support reliable, patient-centered outcome assessment.

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