
doi: 10.1345/aph.1e487
pmid: 15941818
OBJECTIVETo review the pharmacologic and clinical trial data of the Food and Drug Administration–approved phosphodiesterase 5 (PDE5) inhibitors for the treatment of erectile dysfunction (ED).DATA SOURCESPrimary research and review articles were identified through a search of ScienceDirect, PubMed/MEDLINE, and International Pharmaceutical Abstracts (1990–August 2004). The following search terms were used in the Medicine Dentistry and Pharmacology, Toxicology, and Pharmaceutical Sciences subcategories: phosphodiesterase 5 inhibitor, PDE5 inhibitor, erectile dysfunction, sildenafil, vardenafil, tadalafil, prostatectomy, and diabetes. Web of Science (1990–August 2004) was used to search for additional abstracts using the same search terms as above. The package inserts for sildenafil, vardenafil, and tadalafil were also consulted.STUDY SELECTION AND DATA EXTRACTIONAll identified research, review articles, and abstracts were assessed for relevance, and all relevant information was included. Priority was given to the primary medical literature and clinical trial reports.DATA SYNTHESISED is a common disorder in males with increased prevalence associated with age and presence of cardiovascular disease, prostatectomy, or diabetes mellitus. Sildenafil, vardenafil, and tadalafil are selective PDE5 inhibitors currently available for treatment of ED. Their pharmacology and pharmacokinetics vary slightly, but with potentially important clinical differences in duration of activity; all have similar clinical efficacy and adverse effect profiles in patients with ED of various causes.CONCLUSIONSSildenafil, vardenafil, and tadalafil are safe and effective PDE5 inhibitors for the treatment of ED.
Cyclic Nucleotide Phosphodiesterases, Type 5, Male, Prostatectomy, Clinical Trials as Topic, Phosphodiesterase Inhibitors, Phosphoric Diester Hydrolases, Triazines, Imidazoles, Piperazines, Sildenafil Citrate, Tadalafil, Diabetes Complications, Postoperative Complications, Erectile Dysfunction, 3',5'-Cyclic-GMP Phosphodiesterases, Purines, Humans, Drug Interactions, Sulfones, Carbolines
Cyclic Nucleotide Phosphodiesterases, Type 5, Male, Prostatectomy, Clinical Trials as Topic, Phosphodiesterase Inhibitors, Phosphoric Diester Hydrolases, Triazines, Imidazoles, Piperazines, Sildenafil Citrate, Tadalafil, Diabetes Complications, Postoperative Complications, Erectile Dysfunction, 3',5'-Cyclic-GMP Phosphodiesterases, Purines, Humans, Drug Interactions, Sulfones, Carbolines
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 67 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
