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Brief Summary

GUIDELINE TITLE

Case detection, diagnosis, and treatment of patients with primary aldosteronism: an Endocrine Society clinical practice guideline.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions for the quality of the evidence (+OOO, ++OO, +++O, and ++++); the strength of the recommendation (1 or 2); and for the difference between a "recommendation" and a "suggestion" are provided at the end of the "Major Recommendations" field.

Case Detection

The Task Force recommends the case detection of primary aldosteronism (PA) in patient groups with relatively high prevalence of PA. (1 | ++OO) These include patients with Joint National Commission (JNC) stage 2 (>160–179/100–109 mm Hg), stage 3 (>180/110 mm Hg), or drug resistant hypertension; hypertension and spontaneous or diuretic-induced hypokalemia; hypertension with adrenal incidentaloma; or hypertension and a family history of early onset hypertension or cerebrovascular accident at a young age (<40 years). The Task Force also recommends case detection for all hypertensive first-degree relatives of patients with PA. (1 | +OOO)

The Task Force recommends use of the plasma aldosterone-renin ratio (ARR) to detect cases of PA in these patient groups. (1 | ++OO)

Case Confirmation

Instead of proceeding directly to subtype classification, the Task Force recommends that patients with a positive aldosterone-renin ratio (ARR) undergo testing, by any of four confirmatory tests, to definitively confirm or exclude the diagnosis. (1 | ++OO)

Subtype Classification

The Task Force recommends that all patients with PA undergo an adrenal computed tomography (CT) scan as the initial study in subtype testing and to exclude large masses that may represent adrenocortical carcinoma. (1 | ++OO)

The Task Force recommends that, when surgical treatment is practicable and desired by the patient, the distinction between unilateral and bilateral adrenal disease be made by adrenal venous sampling (AVS) by an experienced radiologist. (1 | +++O)

In patients with onset of confirmed PA earlier than at 20 years of age and in those who have a family history of PA or of strokes at young age (<40 years), the Task Force suggests genetic testing for glucocorticoid-remediable aldosteronism (GRA). (2 | +OOO)

Treatment

The Task Force recommends that treatment by unilateral laparoscopic adrenalectomy be offered to patients with documented unilateral PA (i.e., aldosterone-producing adenoma [APA] or unilateral adrenal hyperplasia [UAH]). (1 | ++OO) If a patient is unable or unwilling to undergo surgery, the Task Force recommends medical treatment with a mineralocorticoid receptor (MR) antagonist. (1 | ++OO)

In patients with PA due to bilateral adrenal disease, the Task Force recommends medical treatment with an MR antagonist (1 | ++OO); the Task Force suggests spironolactone as the primary agent with eplerenone as an alternative. (2 | +OOO)

In patients with GRA, the Task Force recommends the use of the lowest dose of glucocorticoid that can normalize blood pressure and serum potassium levels rather than first-line treatment with a mineralocorticoid receptor (MR) antagonist. (1 | +OOO)

Definitions:

Strength of Recommendations

1 - Indicates a strong recommendation and is associated with the phrase "The Task Force recommends."

2 - Denotes a weak recommendation and is associated with the phrase "The Task Force suggests."

Quality of the Evidence

+OOO Denotes very low quality evidence

++OO Denotes low quality evidence

+++O Denotes moderate quality evidence

++++ Denotes high quality evidence

CLINICAL ALGORITHM(S)

An algorithm for the detection, confirmation, subtype testing, and treatment of primary aldosteronism is provided in the original guideline document under Figure 1.

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

In the original guideline document, each recommendation is linked to a description of the evidence, values that panelists considered in making the recommendation (when making these explicit was necessary), and remarks, a section in which panelists offer technical suggestions for testing conditions, dosing, and monitoring. These technical comments reflect the best available evidence applied to a typical patient. Often this evidence comes from the unsystematic observations of the panelists and should therefore be considered suggestions.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2008 Sep

GUIDELINE DEVELOPER(S)

The Endocrine Society - Disease Specific Society

SOURCE(S) OF FUNDING

The Endocrine Society

GUIDELINE COMMITTEE

Case Detection, Diagnosis, and Treatment of Patients with Primary Aldosteronism Task Force

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Task Force Members: John W. Funder; Robert M. Carey; Carlos Fardella; Celso E. Gomez-Sanchez; Franco Mantero; Michael Stowasser; William F. Young Jr; Victor M. Montori

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

John W. Funder, MD, PhD (Chair)—Financial or Business/Organizational Interests: Schering-Plough, Daiichi-Sankyo, Pfizer, Cancer Institute of N.S.W, Speedel, Garnett Passe and Rodney Williams Memorial Foundation, Merck, Eli Lilly, P3 Panel (Commonwealth of Australia); Significant Financial Interest or Leadership Position: Schering-Plough, Pfizer, Daiichi-Sankyo and Cancer Institute of N.S.W.

Robert M. Carey, MD—Financial or Business/Organizational Interests: Novartis, Pfizer, Daiichi-Sankyo; Significant Financial Interest or Leadership Position: none declared.

Carlos Fardella, MD—Financial or Business/Organizational Interests: National Fund for Scientific and Technological Development (Fondo Nacional de Desarrollo Científico y Tecnológico [FONDECYT]); Significant Financial Interest or Leadership Position: none declared.

Celso E. Gomez-Sanchez, MD—Financial or Business/Organizational Interests: American Heart Association; Significant Financial Interest or Leadership Position: Associate Editor for the journal Hypertension.

Franco Mantero, MD, PhD—Financial or Business/Organizational Interests: none declared; Significant Financial Interest or Leadership Position: Executive Committee of the International Society of Endocrinology.

Michael Stowasser, MBBS, FRACP, PhD—Financial or Business/Organizational Interests: none declared; Significant Financial Interest or Leadership Position: none declared.

William F. Young Jr., MSc, MD—Financial or Business/Organizational Interests: none declared; Significant Financial Interest or Leadership Position: Mayo Clinic, Clinical Endocrinology.

*Victor M. Montori, MD—Financial or Business/Organizational Interests: KER Unit (Mayo Clinic); Significant Financial Interest or Leadership Position: none declared.

*Evidence-based reviews for this guideline were prepared under contract with The Endocrine Society.

ENDORSER(S)

European Society of Endocrinology - Medical Specialty Society
European Society of Hypertension - Disease Specific Society
International Society of Endocrinology - Medical Specialty Society
International Society of Hypertension - Disease Specific Society
Japanese Society of Hypertension - Disease Specific Society

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

Electronic copies: Available in Portable Document Format (PDF) from The Endocrine Society.

Print copies: Available from The Endocrine Society, c/o Bank of America, P.O. Box 630721, Baltimore, MD 21263-0736; Phone: (301) 941.0210; Email: Societyservices@endo-society.org

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

The following are available:

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This NGC summary was completed by ECRI Institute on January 15, 2009. The information was verified by the guideline developer on February 4, 2009.

COPYRIGHT STATEMENT

DISCLAIMER

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Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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