Beyond Loss of Kidney Function: Patient Care in Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Marie C HoganKathryn E SimmonsLawrence UllmanMaryam GondalNeera K DahlPublished in: Kidney360 (2023)
ADPKD patients benefit from specialized care over their lifetimes, starting with diagnosis of the condition with ongoing discussion of both the renal course and extra-renal issues. Both renal and extra-renal issues may continue to cause major morbidity even after successful kidney transplant or initiation of renal replacement therapy and extra-renal disease aspects should always be considered as part of routine management. In this review we will focus on updates in pain/depression screening, cardiac manifestations, liver and pancreatic cysts, kidney stone management and genetic counseling. In some instances, we have shared our current clinical practice rather than an evidence-based guideline. We anticipate more standardization of care following the release of the KDIGO guidelines for management in ADPKD later this year.
Keyphrases
- polycystic kidney disease
- clinical practice
- palliative care
- healthcare
- pain management
- ejection fraction
- newly diagnosed
- acute kidney injury
- chronic pain
- heart failure
- genome wide
- neuropathic pain
- spinal cord injury
- prognostic factors
- spinal cord
- hiv infected
- human immunodeficiency virus
- patient reported outcomes
- atrial fibrillation
- copy number
- hiv testing
- antiretroviral therapy