Home Medicine Surgical treatment of secondary hyperparathyroidism in children with chronic kidney disease. Experience in 19 patients
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Surgical treatment of secondary hyperparathyroidism in children with chronic kidney disease. Experience in 19 patients

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Published/Copyright: March 25, 2024

Abstract

Objectives

Secondary hyperparathyroidism (sHPT) is an important contributor to bone disease and cardiovascular calcifications in children with chronic kidney disease (CKD). When conservative measures are ineffective, parathyroidectomy is indicated. The aim of our study was to evaluate the efficacy and safety of subtotal parathyroidectomy (sPTX) in pediatric and adolescent patients, and to provide a rationale for considering this aggressive treatment in CKD patients with uncontrolled sHPT.

Methods

We retrospectively analyzed the medical records of 19 pediatric CKD patients on dialysis with refractory sHPT who underwent sPTX at our institution between 2010 and 2020. All patients had clinical, radiological, and biochemical signs of renal osteodystrophy.

Results

One year after sPTX, parathyroid hormone (PTH) levels (median and interquartile range (IQR)) dropped from 2073 (1339–2484) to 164 (93–252) pg/mL (p=0.0001), alkaline phosphatase (ALP) levels from 1166 (764–2373) to 410 (126–421) IU/L (p=0.002), and the mean (±SDS) calcium-phosphate (Ca*P) product from 51±11 to 41±13 mg2/dL2 (p=0.07). Postoperatively, all patients presented with severe hungry bone syndrome (HBS) and required intravenous and oral calcium and calcitriol supplementation. None of them had other postoperative complication. Histological findings had a good correlation with preoperative parathyroid ultrasound imaging (n: 15) in 100 % and with technetium-99m (99mTc) sestamibi scintigraphy (n: 15) in 86.6 %. Clinical and radiological signs of bone disease improved in all patients.

Conclusions

Pediatric sPTX is effective and safe to control sHPT and calcium-phosphate metabolism in children with CKD on dialysis and may mitigate irreversible bone deformities and progression of cardiovascular disease.


Corresponding author: Silvia Mercedes Gil, 36947 Endocrinology Department, Hospital Nacional de Pediatria “Juan P. Garrahan”, Buenos Aires, Argentina, E-mail:

  1. Research ethics: Not applicable.

  2. Informed consent: The informed consent for surgery for all patients includes authorization for potential publications.

  3. Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: Authors state no conflict of interest.

  5. Research funding: None declared.

  6. Data availability: The raw data can be obtained on request from the corresponding author.

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/jpem-2023-0492).


Received: 2023-11-03
Accepted: 2024-02-23
Published Online: 2024-03-25
Published in Print: 2024-04-25

© 2024 Walter de Gruyter GmbH, Berlin/Boston

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