Hypoparathyroidism Postprocedural
Conditions
Keywords
Hypoparathyroidism, PTH, Hypocalcemia
Brief summary
The purpose of the investigation is to study if the use of Fluobeam®-LX to identify parathyroid glands through autofluorescence during thyroid surgery, may reduce the risk of postoperative hypoparathyroidism, defined as low PTH in patients undergoing total thyroidectomy
Detailed description
Temporary and permanent hypoparathyroidism is probably the most important complication of total thyroidectomy. The rate of permanent hypoparathyroidism in quality registries are in the range of is 5-7 percent of patients undergoing surgery. Patients operated on benign disease with total thyroidectomy, and who suffer from permanent hypoparathyroidism (defined as medication with active Vitamin D analogue therapy for more than 6 months, are at increased risk of renal insufficiency. They also have, for unclear reasons, an increased risk of suffering from malignancy, compared to patients without this complication. Patients with known ischemic heart disease before surgery also have an increased risk of suffering a new episode of cardiovascular disease. Finally, patients with permanent hypoparathyroidism have an increased risk of mortality compared to patients without this complication. If, by using a technique for autofluorescence (Fluobeam® -LX), one can more accurately identify and avoid damage to the parathyroid glands during the surgical procedure, this would be of great importance for patients undergoing total thyroidectomy for thyroid disease. Patients undergoing total thyroidectomy are randomized to the use of Fluobeam® -LX to detect the parathyroid glands through autofluorescence during thyroid surgery, or clinical evaluation only (control). Outcome is evaluated by parathyroid hormon (PTH) levels the first postoperative day and the need for medication with calcium and Vitamin D up to 6 months postoperatively.
Interventions
Fluobeam®-LX is used to identify and evaluate parathyroid glands using auto-fluorescence during thyroid surgery.
Sponsors
Study design
Masking description
The participant is not informed of the assigned group, whereas the the care giver (surgeon) is informed due to the use (or not) of the Fluobeam®-LX. Randomization is performed 1: 1 in blocks of 10 via the Eurocrine quality register platform.
Intervention model description
Intervention group (intraoperative use of Fluobeam®-LX during thyroid surgery) Control group (clinical assessment and identification of parathyroid glands during thyroid surgery)
Eligibility
Inclusion criteria
Patients with thyroid disease planned for total thyroidectomy regardless of diagnosis
Exclusion criteria
* Previous thyroid surgery * Previous parathyroid surgery * Concurrent parathyroid surgery * Renal insufficiency * Pregnancy * Breast feeding * Allergy (contrast agent, iodine) * Inability to understand study information * Patient unable to participate in planned follow-up program
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative level of Parathyroid hormone (PTH) | First postoperative day | Low plasma parathyroid hormone (PTH) (below the normal reference range) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Autotransplantation of parathyroid tissue | Intraoperatively | Number of autotransplanted parathyroid glands |
| Postoperative medication with Active vitamin D | At discharge (up to 7 days), at 1 month and at 6 months | Medication with active Vitamin D; dihydrotachysterol (ATC A11CC02), alfacalcidol (ATC A11CC03), or calcitriol (ATC A11CC04) due to postoperative hypocalcaemia. Evaluated by standard questionaire in the database Eurocrine (yes/no) |
| Excised parathyroid glands | One week | Number of excised parathyroid glands found on the specimen at histopathology |
| Identification of parathyroid glands | Intraoperatively | Number of identified parathyroid glands |
| Time for operation | Intraoperatively | Time for surgery (skin to skin) in minutes |
| Hospital stay | One week | Hospital stay in days |
| Re-hospitalization due to hypocalcaemia | One month | Any subsequent hospitalization within 30 days for hypocalcaemia-related symptoms |
| Postoperative medication with oral calcium | At discharge (up to 7 days), at 1 month and at 6 months | Medication with oral calcium; calcium carbonate (A12AA04), and calcium lactate gluconate (A12AA06) Evaluated by standard questionaire in the database Eurocrine (yes/no) |
Countries
Austria, Norway, Poland, Sweden