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Autosomal Dominant Polycystic Kidney Disease: A Case Study
(Vol 36/No. 1. On-line test expires: 2/20/2011)
To receive continuing education credit, you must read the information in this article and take an on-line post test and fill out an on-line program evaluation form. The certificate will then be generated for you as a .pdf file which you can print out locally on your computer.

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  AUTHOR
Angela Phillips, MSN, RN, FNP-BC, CNN
Angela Phillips, MSN, RN, FNP-BC, CNN, is a Faculty Family Nurse Practitioner, West Texas A&M University College of Nursing and Health Science, Canyon, TX, and is the Clinic Director, Health Partners Clinic, Amarillo, TX.
  OUTLINE

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent genetic cause of chronic kidney disease (CKD) and renal failure in adults. CKD is increasingly managed within a primary care setting, and thus, it is important for primary care providers (PCPs) to be aware of ADPKD. Diagnosis of ADPKD is usually made based on kidney imaging studies and genetic testing. Treatment of ADPKD is a challenge for PCPs and should be managed collaboratively with a nephrologist. This article describes a case study of a patient with ADPKD who is managed by a family nurse practitioner (FNP) and a nephrologist. Through the examination of this complex case, a continuum of care can be arranged for the patient through the end of life.

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  CE RELATED INFORMATION
This offering for 1.2 contact hours is being provided by the American Nephrology Nurses’ Association (ANNA), This offering for 1.0 contact hours is being provided by the American Nephrology Nurses’ Association (ANNA). ANNA is accredited as a provider of continuing nursing education (CNE) by the American Nurses Credentialing Center’s Commission on Accreditation. ANNA is a provider approved by the California Board of Registered Nursing, provider number CEP 00910. This CNE article meets the Nephrology Nursing Certification Commission’s (NNCC’s) continuing nursing education requirements for certification and recertification.

  EDUCATIONAL OBJECTIVES

Goal: To provide an overview of autosomal dominant polycystic kidney disease.

Objectives:
1. Define autosomal dominant polycystic kidney disease.
2. Discuss how the FNP PCP should best treat and monitor a patient with autosomal dominant polycystic kidney disease.
3. Explain how the FNP PCP can educate and empower patients during their treatment of autosomal dominant polycystic kidney disease.

AUTHOR DISCLOSURE STATEMENT

Angela Phillips has no conflicts of interest to disclose.


 ANNA and HDCN CE POLICY STATEMENTS

The CE policy and disclosure statements of the American Nephrology Nurses' Association are given in detail on the Symposium Home Page. The CE policy statements of HDCN are listed on this page.