The Journey and Barriers to Treatment of Patients With Renal Nutcracker Syndrome

Abstract

ObjectiveTo better understand renal nutcracker syndrome (NCS) from a patients’ perspective starting at presentation and followed through to diagnosis and management MethodsThis descriptive study was conducted on a national level via a self-selected online survey distributed via river sampling by a post on the Facebook Page ‘Renal Nutcracker Syndrome Support Group.’ ResultsOf the 22 responses collected, 95.5% were female and 91% self-identified as White. 43% experienced symptoms as teenagers and 62% were diagnosed as young adults. Prior to receiving a definitive diagnosis, over half of the respondents were worked up for kidney stones (57%) and ovarian cysts (48%) and saw at least 10-15 providers. Nearly 80% experienced constant pain throughout the day. Pain management included prescription oral pain relievers (38%), prescription patches (29%), and physical therapy (19%). Surgical procedures included nephrectomy with auto transplant (38%), left renal vein transposition (10%), and laparoscopic extravascular stent placement (10%). Respondents had high healthcare utilization for management of NCS. Nearly 30% were unable to work and had filed for disability. ConclusionAwareness of NCS should increase among healthcare providers of all specialties to improve quality of care to those living with NCS. It is crucial to keep NCS within the differential diagnosis in patients presenting with gross hematuria and unusual abdominal and/or flank pain.