Survival in primary hyperparathyroidism over five decades (1965-2010) a population-based retrospective study.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 34245931.
- Also identified by DOI 10.1016/j.bone.2021.116099 and PMC identifier 10495014.
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Abstract
Survival in patients with primary hyperparathyroidism (PHPT) remains uncertain. To update survival in patients with PHPT in a United States community population. Retrospective cohort study. Community population in Rochester, Minnesota. Residents who met criteria for PHPT from 1965 to 2010. Survival was estimated using the Kaplan Meier product-limit method. The Cox proportional hazards model was used to determine associations, as relative hazards (RR) with 95% confidence intervals (CI), of various risk factors with time to death. The overall age and gender-adjusted survival compared to white Minnesota residents. We identified 1139 PHPT individuals, 76% female, with a median age of 58 years. Most were observed without parathyroidectomy (69%). The relative risk of death among the entire cohort was 0.996 (95% CI: 0.91-1.09, P = 0.935) which was not different compared to Minnesota residents. Those with maximum serum calcium level ≥ 10.8 mg/dL (0.7 mg/dL above the reference range) had an increase in mortality (RR 1.32, 95% CI: 1.10-1.58, P = 0.002). Survival among all PHPT individuals after parathyroidectomy was no different from expected (RR = 1.06, 95% CI 0.89-1.28; P = 0.508). Mortality was significantly decreased after parathyroidectomy in those with serum calcium levels ≥10.8 mg/dL (HR 0.47, 95% CI: 0.36-0.61, P < 0.001). Mortality in the entire cohort was not different from expected. PHPT patients with a maximum serum calcium level ≥ 10.8 mg/dL had increased mortality. Survival was improved after parathyroidectomy in those with this degree of hypercalcemia.
Medical subject headings
- Hypercalcemia
- Hyperparathyroidism, Primary