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Clinical problems in hemodialysis patients with autosomal dominant polycystic kidney disease

Ismail Kocyigit1, Eray Eroglu1, Ozkan Gungor2

  • 1Department of Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.

Seminars in Dialysis
|April 18, 2018
PubMed

Insights

Autosomal dominant polycystic kidney disease (ADPKD) is a genetic kidney disorder causing large cysts. This review focuses on managing ADPKD complications in hemodialysis patients.

Area of Science:

  • Nephrology
  • Genetics
  • Internal Medicine

Background:

  • Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited kidney disorder.
  • It leads to massive kidney cyst enlargement and is a leading cause of chronic kidney disease (CKD).
  • ADPKD is a multi-system disorder associated with hypertension and cardiovascular/cerebrovascular events.

Purpose of the Study:

  • To review specific clinical problems encountered in ADPKD patients undergoing hemodialysis.
  • To discuss current management strategies for these clinical issues.

Main Methods:

  • Literature review of clinical problems and management in ADPKD patients on hemodialysis.
  • Synthesis of information on disease-specific complications and therapeutic approaches.

Main Results:

  • ADPKD presents unique clinical challenges in hemodialysis patients.
  • Management requires addressing systemic complications alongside kidney disease progression.

Conclusions:

  • Effective management of ADPKD in hemodialysis patients necessitates a comprehensive approach.
  • Addressing hypertension, cardiovascular, and cerebrovascular complications is crucial for patient outcomes.

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