This protocol is for patients with hypoparathyroidism in whom the standard first-line approach has not adequately controlled calcium levels. When conventional management fails to meet its treatment targets, a structured next-step approach is required.
Conventional treatment — activated vitamin D analogues (alfacalcidol or calcitriol) together with dietary calcium, calcium supplementation, and vitamin D supplementation — did not achieve the required targets: calcium within the target range, freedom from symptomatic hypocalcaemia, phosphate and magnesium within the reference range, normal 24-hour urinary calcium excretion, and an adequate 25-hydroxyvitamin D level. Failure to reach these goals is the trigger for escalation.
Sustained calcium levels in the target range without ongoing reliance on activated vitamin D or calcium supplements; normalisation of phosphate levels; reduced 24-hour urinary calcium excretion; improved eGFR. Treatment effects are evaluated 6–12 months after initiation.
DOI: 10.1093/ejendo/lvaf222
Doses of palopegteriparatide are adjusted according to calcium levels with up or down titration once a week (with a maximum change of ±3 μg/day each week).
We suggest to titrate the dose of PTH replacement therapy to achieve sustained calcium levels in the target range without the need for concurrent activated vitamin D treatment or calcium supplements.
If PTH replacement therapy is initiated, we suggest evaluating the treatment effects after 6–12 months, depending on treatment goals.
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