KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.

نویسندگان

  • Gopala K Rangan
  • Stephen I Alexander
  • Katrina L Campbell
  • Mark Aj Dexter
  • Vincent W Lee
  • Pamela Lopez-Vargas
  • Jun Mai
  • Andrew Mallett
  • Chirag Patel
  • Manish Patel
  • Michel C Tchan
  • Allison Tong
  • David J Tunnicliffe
  • Philip Vladica
  • Judy Savige
چکیده

KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease GOPALA K RANGAN, STEPHEN I ALEXANDER, KATRINA L CAMPBELL, MARK AJ DEXTER, VINCENT W LEE, PAMELA LOPEZ-VARGAS, JUN MAI, ANDREW MALLETT, CHIRAG PATEL, MANISH PATEL, MICHEL C TCHAN, ALLISON TONG, DAVID J TUNNICLIFFE, PHILIP VLADICA and JUDY SAVIGE Centre for Transplant and Renal Research, Westmead Millennium Institute, The University of Sydney, Sydney, Department of Renal Medicine, Westmead Hospital, Western Sydney Local Health District, Centre for Kidney Research, The Children’s Hospital at Westmead, Department of Nephrology, The Children’s Hospital at Westmead, Department of Neurological Surgery, Westmead Private Hospital, Sydney School of Public Health, The University of Sydney, Department of Nephrology, Liverpool Hospital and Bankstown Hospital, Discipline of Surgery, Western Clinical School, The University of Sydney, Department of Urology, Westmead Hospital, Department of Genetic Medicine, Westmead Hospital, Sydney Medical School, The University of Sydney, Department of Radiology, Westmead Hospital, Western Sydney Local Health District, New South Wales, Department of Nutrition and Dietetics, The Princess Alexandra Hospital, Faculty of Health Sciences and Medicine, Bond University, Kidney Health Service and Conjoint Kidney Research Laboratory, Royal Brisbane and Women’s Hospital, Centre for Kidney Disease Research, Centre for Chronic Disease and CKD, QLD, School of Medicine, The University of Queensland, Centre for Rare Diseases Research, Institute for Molecular Bioscience, The University of Queensland, Genetic Health Queensland, Royal Brisbane and Women’s Hospital, Brisbane, Queensland, Department of Nephrology, The Royal Melbourne Hospital, Parkville, and Department of Medicine, The University of Melbourne, Victoria, Australia

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KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone Disease.

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KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of End-Stage Kidney Disease.

those that are being considered as potential kidney donors, need to be carefully screened and excluded from having ADPKD (KHA-CARI ADPKD Guidelines: Genetics, Imaging, and Screening subtopics), prior to living donor transplantation. Nephrectomy of a polycystic kidney prior to the time of transplantation may be required due to insufficient intra-abdominal space for the new allograft. Nephrectomy...

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KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Screening for Polycystic Kidney Disease.

a. We recommend prior to screening at-risk individuals should receive appropriate counseling regarding the potential benefits and risks of making the diagnosis of autosomal dominant polycystic kidney disease from their general practitioner in consultation with a clinical geneticist or nephrologist (2A). b. We recommend that screening of individuals who are at-risk (50% chance) be performed by r...

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KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis.

a. We recommend that the standard methodology for genetic diagnosis of autosomal dominant polycystic kidney disease is polymerase chain reaction (PCR) amplification (including long-range PCR for the first 33 exons of PKD1) followed by Sanger sequencing (1A) or next-generation sequencing where available (1D). b. We suggest that individuals with a clinical diagnosis of autosomal dominant polycyst...

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KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease.

a. We recommend screening for polycystic liver disease in all patients diagnosed with autosomal dominant polycystic kidney disease using abdominal ultrasound (1C). b. We recommend that all female patients with autosomal dominant polycystic kidney disease and liver cysts undergo counseling regarding the risks of pregnancy and exogenous estrogen exposure in worsening liver cyst growth (1C). c. We...

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عنوان ژورنال:
  • Nephrology

دوره 21 8  شماره 

صفحات  -

تاریخ انتشار 2016