| Literature DB >> 32199709 |
Carl P Walther1, Vijay Nambi2, Nicola A Hanania3, Sankar D Navaneethan4.
Abstract
Pulmonary hypertension (PH) is a highly prevalent and important condition in adults with chronic kidney disease (CKD). In this review, we summarize the definition of PH, discuss its pathophysiology and classifications, and describe diagnostic and management strategies in patients with CKD, including those with kidney failure treated by kidney replacement therapy. In the general population, PH is classified into 5 groups based on clinical presentation, pathology, hemodynamics, and management strategies. In this classification system, PH in CKD is placed in a diverse group with unclear or multifactorial mechanisms, although underlying cardiovascular disease may account for most cases. CKD may itself directly incite pulmonary circulatory dysfunction and remodeling through uremic toxins, inflammation, endothelial dysfunction, and altered vasoregulation. Despite several studies describing the higher prevalence of PH in CKD and kidney failure, along with an association with poor outcomes, high-quality evidence is not available for its diagnostic and management strategies in those with CKD. In CKD not requiring kidney replacement therapy, volume management along with treatment of underlying risk factors for PH are critical. In those receiving hemodialysis, options are limited and transition to peritoneal dialysis may be considered if recurrent hypotension precludes optimal volume control.Entities:
Keywords: Chronic kidney disease (CKD); death; dialysis; end-stage renal disease (ESRD); heart failure; kidney failure; mean pulmonary arterial pressure (PAPm); pulmonary arterial hypertension (PAH); pulmonary circulatory dysfunction; pulmonary hypertension (PH); review; vascular remodeling; volume management
Mesh:
Year: 2020 PMID: 32199709 PMCID: PMC7247937 DOI: 10.1053/j.ajkd.2019.12.005
Source DB: PubMed Journal: Am J Kidney Dis ISSN: 0272-6386 Impact factor: 8.860