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Submitted on January 16, 2008
Accepted on June 10, 2008
Prince Henry's Institute of Medical Research (J.W.F.), Clayton, Australia; University of Virginia Health System (R.M.C.), Charlottesville, Virginia; Facultad de Medicina Pontificia Universidad Católica de Chile (C.F.), Santiago, Chile; G.V. (Sonny) Montgomery VA Medical Center (C.E.G-S.), Jackson, Mississippi; University of Padova (F.M.), Padua, Italy; University of Queensland (M.S.), Brisbane, Australia; Mayo Clinic (W.F.Y.), Rochester, Minnesota; and Mayo Clinic (V.M.M.), Rochester, Minnesota
* To whom correspondence should be addressed. E-mail: govt-prof{at}endo-society.org.
Objective: To develop clinical practice guidelines for the diagnosis and treatment of patients with primary aldosteronism.
Participants: The Task Force comprised a chair, selected by the Clinical Guidelines Subcommittee (CGS) of The Endocrine Society, six additional experts, one methodologist, and a medical writer. The Task Force received no corporate funding or remuneration.
Evidence: Systematic reviews of available evidence were used to formulate the key treatment and prevention recommendations. We used the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) group criteria to describe both the quality of evidence and the strength of recommendations. We used recommend for strong recommendations and suggest for weak recommendations.
Consensus Process: Consensus was guided by systematic reviews of evidence and discussions during one group meeting, several conference calls, and multiple e-mail communications. The drafts prepared by the task force with the help of a medical writer were reviewed successively by The Endocrine Society's CGS, Clinical Affairs Committee (CAC), and Council. The version approved by the CGS and CAC was placed on The Endocrine Society's Web site for comments by members. At each stage of review, the Task Force received written comments and incorporated needed changes.
Conclusions: We recommend case detection of primary aldosteronism be sought in higher risk groups of hypertensive patients and those with hypokalemia by determining the aldosterone-renin ratio under standard conditions, and that the condition be confirmed/excluded by one of four commonly used confirmatory tests. We recommend that all patients with primary aldosteronism undergo adrenal computed tomography (CT) as the initial study in subtype testing and to exclude adrenocortical carcinoma. We recommend the presence of a unilateral form of primary aldosteronism should be established/excluded by bilateral adrenal venous sampling by an experienced radiologist and, where present, optimally treated by laparoscopic adrenalectomy. We recommend that patients with bilateral adrenal hyperplasia, or those unsuitable for surgery, optimally be treated medically by mineralocorticoid receptor antagonists.
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