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Volume 14 Issue 4
Jul.  2023
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Chinese Society of Rare Diseases, Rare Diseases Society of Chinese Research Hospital Association, National Rare Diseases Committee, Beijing Rare Disease Diagnosis, Treatment and Protection Society. Expert Consensus for the Diagnosis and Treatment of Bartter Syndrome in China(2023)[J]. Medical Journal of Peking Union Medical College Hospital, 2023, 14(4): 744-757. DOI: 10.12290/xhyxzz.2023-0207
Citation: Chinese Society of Rare Diseases, Rare Diseases Society of Chinese Research Hospital Association, National Rare Diseases Committee, Beijing Rare Disease Diagnosis, Treatment and Protection Society. Expert Consensus for the Diagnosis and Treatment of Bartter Syndrome in China(2023)[J]. Medical Journal of Peking Union Medical College Hospital, 2023, 14(4): 744-757. DOI: 10.12290/xhyxzz.2023-0207
shu

Expert Consensus for the Diagnosis and Treatment of Bartter Syndrome in China(2023)

Funds: 

National Key R & D Program of China 2022ZD0116003

National High Level Hospital Clinical Research Funding 2022-PUMCH-B-019

National High Level Hospital Clinical Research Funding 2022-PUMCH-D-002

Capital's Funds for Health Improvement and Research CFH 2020-2-4018

CAMS Innovation Fund for Medical Sciences 2021-I2M-1-003

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  • Corresponding authors: CHEN Limeng1, 2, E-mail: chenlimeng@pumch.cn
    CHEN Chaoying3, E-mail: chenchaoying484@aliyun.com
    ZHANG Shuyang2, E-mail: shuyangzhang103@163.com
    1. Department of Nephrology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
    2. State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
    3. Department of Nephrology, Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing 100020, China

  • Received Date: April 19, 2023
  • Accepted Date: May 14, 2023
  • Available Online: June 08, 2023
  • Issue Publish Date: July 29, 2023
    Graphical Abstract
    • Abstract
  • Bartter syndrome (BS) is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemia and hypochloremic metabolic alkalosis, and normal or low blood pressure. In severe cases, preterm delivery, hypovolemia, ventricular arrhythmia, rhabdomyolysis, renal failure, growth failure and sensorineural deafness may occur. In recent years, research on BS has made significant progress. The Bartter Syndrome Consensus Working Group has performed a systematic literature review, and based on evidence-based medicine, summarized aspects related to BS, including clinical manifestations and classification, diagnosis, treatment strategies, and management of complications. This consensus provides an important reference for the better diagnosis and treatment of BS.
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    • References (104)
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