Elsevier

Mayo Clinic Proceedings

Volume 87, Issue 8, August 2012, Pages 766-778
Mayo Clinic Proceedings

Diagnosis and treatment guidelines
The Princeton III Consensus Recommendations for the Management of Erectile Dysfunction and Cardiovascular Disease

https://doi.org/10.1016/j.mayocp.2012.06.015Get rights and content

Abstract

The Princeton Consensus (Expert Panel) Conference is a multispecialty collaborative tradition dedicated to optimizing sexual function and preserving cardiovascular health. The third Princeton Consensus met November 8 to 10, 2010, and had 2 primary objectives. The first objective focused on the evaluation and management of cardiovascular risk in men with erectile dysfunction (ED) and no known cardiovascular disease (CVD), with particular emphasis on identification of men with ED who may require additional cardiologic work-up. The second objective focused on reevaluation and modification of previous recommendations for evaluation of cardiac risk associated with sexual activity in men with known CVD. The Panel's recommendations build on those developed during the first and second Princeton Consensus Conferences, first emphasizing the use of exercise ability and stress testing to ensure that each man's cardiovascular health is consistent with the physical demands of sexual activity before prescribing treatment for ED, and second highlighting the link between ED and CVD, which may be asymptomatic and may benefit from cardiovascular risk reduction.

Section snippets

Recommendations

The recommendations of the third Princeton Consensus Conference focus on (1) evaluation and management of cardiovascular risk in men with ED and no known CVD, (2) reevaluation and modification of the second conference recommendations for evaluation of cardiac risk associated with sexual activity in men with known CVD, and (3) the role of TRT in ED and CVD management.

Evaluation and Management of Cardiovascular Risk in the Patient With ED With No Known CVD

The consensus panel defines cardiovascular risk as the risk of morbid events over a 3- to 5-year interval from the onset of ED (American College of Cardiology Foundation/American Heart Association [ACCF/AHA] class Ib)3, 4 and provides recommendations for the evaluation and management of cardiovascular risk in men with ED and no known CVD. The panel's approach broadens the use of the 2010 ACCF/AHA guideline for assessment of cardiovascular risk in asymptomatic adults to address an at-risk

Management of ED in the Patient With Known CVD

The objective of this algorithm is to estimate the cardiovascular risk associated with sexual activity in patients with ED and known CVD (Figure). Herein, risk refers to the likelihood of mortal or morbid events during or shortly after sexual activity. The panel's recommendations are similar to those developed during the first and second Princeton Consensus Conferences.1, 2 However, the current recommendations classify patients with New York Heart Association (NYHA) class II as low risk rather

Recommendations

Consistent with other guidelines, the recommendations of the third Princeton Consensus Panel emphasize an approach to risk assessment that integrates multiple aspects of cardiometabolic health. Sexual function should be incorporated into CVD risk assessment for all men, and ED may allow identification of at-risk men who require further cardiovascular evaluation. The scientific evidence suggests that a comprehensive approach to cardiovascular risk reduction will improve overall vascular health,

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    Dr Nehra is now with the Department of Urology, Rush University Medical Center, Chicago, IL. Dr Billups is now with the James Buchanan Brady Urological Institute, Johns Hopkins Medical Institutions, Baltimore, MD.

    Potential Competing Interests: Dr Jackson is a speaker for Pfizer, New York, NY, Eli Lilly & Co, Indianapolis, IN, and Bayer, Leverkusen, Germany. Dr Miner is a consultant to Eli Lilly & Co, Abbott Laboratories, Chicago, IL, Auxilium Pharmaceuticals Inc, Malvern, PA, Boehringer Ingelheim, Ingelheim, Germany, and Endo Pharmaceuticals, Chadds Ford, PA, and conducts personal research for GlaxoSmithKline, London, UK, and Auxilium Pharmaceuticals Inc.

    Dr Billups is a consultant to Endo Pharmaceuticals and Abbott Laboratories.

    Dr Burnett is a consultant to Endo Pharmaceuticals, Abbott Laboratories, Timm Medical Technologies, Eden Prairie, MN, VIVUS Inc, Mountain View, CA, Auxilium Pharmaceuticals Inc, and Shionogi Inc, Florham Park, NJ; has received grant support from Pfizer; and has participated in clinical trials for VIVUS Inc and Auxilium Pharmaceuticals Inc.

    Dr Buvat is a consultant to Eli Lilly & Co and Nextmed, Tucson, AZ.

    Dr Carson is a consultant to and a speaker for GlaxoSmithKline, Eli Lilly & Co, Pfizer, and Auxilium Pharmaceuticals Inc.

    Dr Cunningham is a consultant to Abbott Laboratories, Endo Pharmaceuticals, and GlaxoSmithKline and is a speaker for Abbott Laboratories, Endo Pharmaceuticals, and Merck, Whitehouse Station, NJ.

    Dr Ganz is a consultant to Pfizer, Gilead, Forest City, CA, and Roche, Basel, Switzerland.

    Dr Goldstein is a consultant to Coloplast, Humlebæk, Denmark, Medtronic Vascular, Fridley, MN, Slate, and VIVUS Inc; a speaker for Abbott Laboratories, Auxilium Pharmaceuticals Inc, Coloplast, Eli Lilly & Co, Endo Pharmaceuticals, Medtronic Vascular, and Slate Pharmaceuticals, Lake Forest, IL, performs personal research for Auxilium Pharmaceuticals Inc, BioSante Pharmaceuticals, Lincolnshire, IL, Medtronic Vascular, Slate, and Target Health, New York, NY; and is an expert witness for Pfizer and Bayer.

    Dr Guay is a consultant to Auxilium Pharmaceuticals Inc, Abbott Laboratories, Endo Pharmaceuticals, and Repros Therapeutics, The Woodlands, TX.

    Dr Hackett is a speaker and conducts personal research for Bayer and Eli Lilly & Co.

    Dr Kloner is a speaker for Pfizer.

    Dr Kostis is a consultant to Merck/Schering and Palatin Technologies Inc, Cranbury, NJ; a speaker for Forest Laboratories, New York, NY, Merck, and Sanofi-Aventis; and has received research support from Medtronic and Novartis, Basel, Switzerland.

    Dr Rosen is a consultant to Eli Lilly & Co, Boehringer Ingelheim, Palatin Technologies Inc, and Auxilium Pharmaceuticals Inc.

    Dr Sadovsky is a consultant to Pfizer, Boehringer Ingelheim, and Eli Lilly & Co.

    Dr Seftel is a consultant to Auxilium Pharmaceuticals Inc, Endo Pharmaceuticals, Actient, Abbott Laboratories, Eli Lilly & Co, and Pfizer.

    Dr Vlachopoulos is a consultant to Eli Lilly & Co and has received research support from Pfizer.

    Dr Wu is a consultant to Eli Lilly & Co, is a speaker for Galapagos NV, Mechelen, Belgiu, and conducts personal research for Bayer.

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