1.A decade's evidence review of sildenafil citrate.
National Journal of Andrology 2009;15(1):3-6
Erectile dysfunction (ED) is one of the most popular and disturbing sexual problems, which impairs patients' health and affects their quality of life. Sildenafil citrate, the first oral PDE-5 inhibitor in the world, has established its efficacy and safety credit in both doctors and ED patients. The authors reviewed the results of related studies in the last decade and made deeper insights into the use of sildenafil citrate in such aspects as the general drug tolerance and its influence on the cardiovascular system, potentiality of concomitant diseases with co-administration of other drugs, long-term safety, and ocular and genital safety.
Erectile Dysfunction
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drug therapy
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Evidence-Based Medicine
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Humans
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Male
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Phosphodiesterase Inhibitors
;
adverse effects
;
therapeutic use
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Piperazines
;
adverse effects
;
therapeutic use
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Purines
;
adverse effects
;
therapeutic use
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Retrospective Studies
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Sildenafil Citrate
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Sulfones
;
adverse effects
;
therapeutic use
2.Efficacy and safety of phosphodiesterase 5 inhibitors in the treatment of erectile dysfunction.
National Journal of Andrology 2005;11(8):631-634
Phosphodiesterase 5 inhibitors are recommended as first-line treatment of erectile dysfunction in many guidelines, because of their convenience, higher efficacy, and less side-effects. Since its first launch in 1998, sildenafil has been currently the best investigated phosphodiesterase 5 inhibitor with respect to long-term trails and quantity. Clinical trials showed the efficacy of sildenafil compared with placebo in many of the groups of patients who have ED, including those with cardiovascular disease, diabetes mellitus, depression, radical prostatectomy and dialysis. Typically the adverse effects reported in patients from clinical trials of sildenafil have been mild to moderate, and commonly include flushing and dyspepsia and transient visual disturbances. This article summarized recent reports on efficacy and safety of phosphodiesters 5 inhibitors in the treatment of erectile dysfunction.
Erectile Dysfunction
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drug therapy
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Humans
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Male
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Phosphodiesterase Inhibitors
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adverse effects
;
therapeutic use
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Piperazines
;
adverse effects
;
therapeutic use
;
Purines
;
adverse effects
;
therapeutic use
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Safety
;
Sildenafil Citrate
;
Sulfones
;
adverse effects
;
therapeutic use
3.Update of PDE5 inhibitors as treatment of ED.
National Journal of Andrology 2005;11(7):552-555
Erectile dysfunction is a common ailment in middle-aged and old men. The management of ED has entered a new stage since sildenafil was used to treat ED in 1998. Sildenafil became the first-line treatment for its efficacy and safety. In recent years, new PDE5 inhibitors--vardenafil and tadalafil came into market in succession, providing more options available for oral therapy. This review is about the development of preclinical and clinical medicine research on the three PDE5 inhibitors, and provide information for clinical choices.
Erectile Dysfunction
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drug therapy
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Humans
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Male
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Phosphodiesterase Inhibitors
;
adverse effects
;
therapeutic use
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Piperazines
;
adverse effects
;
therapeutic use
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Purines
;
adverse effects
;
therapeutic use
;
Sildenafil Citrate
;
Sulfones
;
adverse effects
;
therapeutic use
4.Efficacy and safety of sildenafil in the treatment of high altitude heart disease associated with severe pulmonary arterial hypertension in children: a preliminary evaluation.
Yan-Liang XIA ; Wei-Xiao YAN ; Hong CHEN
Chinese Journal of Contemporary Pediatrics 2014;16(7):745-748
OBJECTIVETo observe the clinical efficacy and safety of sildenafil in the treatment of high altitude heart disease associated with severe pulmonary arterial hypertension (PAH) in children.
METHODSFifty children (aged 2 months to 2 years) with high altitude heart disease associated with severe PAH, who were continuously transferred to the Intensive Care Unit between January 2011 and October 2013, were randomly assigned to observation and control groups. The control group was given conventional treatment, while the observation group received oral sildenafil [1 mg/(kg . d)] three times daily for 7-10 days in addition to the conventional treatment. Before and after treatment, hemodynamics, blood gas, routine blood parameters, and blood biochemical parameters were recorded.
RESULTSAfter treatment, the observation group had a significantly higher decrease in mean pulmonary artery pressure and significantly higher increases in arterial partial pressure of oxygen, cardiac output, cardiac index, and oxygenation index compared with the control group (P<0.05). In the observation group, there were no significant changes in mean arterial pressure, routine blood parameters and blood biochemical parameters (P>0.05), and no obvious adverse reactions were found.
CONCLUSIONSFor children with high altitude heart disease associated with severe PAH, sildenafil can effectively reduce pulmonary artery pressure and improve cardiac function and does not cause adverse reactions. This therapy has good safety according to the preliminary evaluation.
Altitude ; Familial Primary Pulmonary Hypertension ; Female ; Heart Diseases ; drug therapy ; Humans ; Hypertension, Pulmonary ; complications ; physiopathology ; Infant ; Male ; Piperazines ; adverse effects ; therapeutic use ; Purines ; adverse effects ; therapeutic use ; Sildenafil Citrate ; Sulfones ; adverse effects ; therapeutic use ; Vasodilator Agents ; adverse effects ; therapeutic use
5.Advances in application of sildenafil to erectile dysfunction.
Zheng LI ; Zheng-Mu WU ; Yi-Xin WANG
National Journal of Andrology 2005;11(6):473-476
Since the worldwide introduction of sildenafil in 1998, 23 million patients with ED have been treated with the drug, and the accumulated experiences have proved its safety and efficacy. This article presents a review about the action mechanism and metabolic process of sildenafil, with a particular focus on the application of sildenafil to ED diagnosis, the curative effect of its daily use on ED, the standard treatment, combined therapy and progressive protocol with sildenafil for ED and its complications, along with such safety aspect as its effect on the sight.
Drug Therapy, Combination
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Erectile Dysfunction
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drug therapy
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Humans
;
Male
;
Phosphodiesterase Inhibitors
;
adverse effects
;
therapeutic use
;
Piperazines
;
adverse effects
;
therapeutic use
;
Purines
;
adverse effects
;
therapeutic use
;
Sildenafil Citrate
;
Sulfones
;
adverse effects
;
therapeutic use
6.Safety of Sildenafil in men with cardiovascular diseases.
National Journal of Andrology 2005;11(3):223-225
Sildenafil is widely used to treat erectile dysfunction (ED). Because many patients with ED have cardiovascular diseases, doctors and patients are concerned over the safety of Sildenafil in patients with cardiovascular diseases. The review focuses on the safety of sildenafil for ED patients with cardiovascular diseases.
Cardiovascular Diseases
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complications
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Erectile Dysfunction
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complications
;
drug therapy
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Humans
;
Male
;
Piperazines
;
adverse effects
;
therapeutic use
;
Purines
;
Sildenafil Citrate
;
Sulfones
;
Vasodilator Agents
;
adverse effects
;
therapeutic use
7.Treatment of erectile dysfunction after radical retropubic prostatectomy with PDE5 inhibitor.
National Journal of Andrology 2005;11(9):708-712
The rate of erectile dysfunction after radical retropubic prostatectomy is from 10% to 100%. The prevalence of erectile dysfunction after nerve-sparing radical prostatectomy is more than one third. In the patients who had undergone bilateral NS, 72% responded to sildenafil, 71.7% and 59.7% responded to 20 mg and 10 mg of vardenafil respectively. For all randomized patients who received tadalafil, the mean percentage of successful penetration attempts was 54% and the mean percentage of successful intercourse attempts was 41%. For the subgroup with evidence of postoperative tumescence these values were 69% and 52%, respectively. No head-to-head trials have been performed with sildenafil, vardenafil and tadalafil in treatment of erectile dysfunction after radical prostatectomy.
Carbolines
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therapeutic use
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Erectile Dysfunction
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drug therapy
;
etiology
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Humans
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Imidazoles
;
therapeutic use
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Male
;
Phosphodiesterase Inhibitors
;
therapeutic use
;
Piperazines
;
therapeutic use
;
Prostatectomy
;
adverse effects
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Purines
;
therapeutic use
;
Sildenafil Citrate
;
Sulfones
;
therapeutic use
;
Tadalafil
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Triazines
;
therapeutic use
;
Vardenafil Dihydrochloride
8.Sildenafil citrate for erectile dysfunction in male kidney transplant recipients.
Feng LIU ; Genfu ZHANG ; Xining JI ; Chibing HUANG ; Pingxian WANG ; Mingqi FAN
National Journal of Andrology 2004;10(6):455-457
OBJECTIVETo evaluate the efficacy and safety of sildenafil citrate in man kidney transplant recipients with erectile dysfunction.
METHODSOne hundred and seventy married males, aged 26 approximately 50 years, who had received kidney transplantations at least half a year before and whose serum creatinine was under 133 umol/l, were selected randomly in the study. Their sexual function was investigated according to the International Index of Erectile Function-5 (IIEF-5), and those with erectile dysfunction (ED) were treated with oral sildenafil citrate for 6 months. The efficacy was assessed by IIEF-5.
RESULTSFifty-three men with ED received oral sildenafil citrate for 6 months. At the end of the treatment, each index in IIEF-5 increased significantly. There were no interactions between sildenafil and cyclosporine and there was no significant adverse effect of sildenafil on the graft function.
CONCLUSIONSildenafil is an effective and safe agent for the treatment of ED in kidney transplant recipients.
Adult ; Erectile Dysfunction ; drug therapy ; Humans ; Kidney Transplantation ; Male ; Middle Aged ; Piperazines ; adverse effects ; therapeutic use ; Purines ; Sildenafil Citrate ; Sulfones
9.Systematic Review and Meta-Analysis of Pulmonary Hypertension Specific Therapy for Exercise Capacity in Chronic Obstructive Pulmonary Disease.
Jinkyeong PARK ; Ju Hee SONG ; Dong Ah PARK ; Jae Seoung LEE ; Sang Do LEE ; Yeon Mok OH
Journal of Korean Medical Science 2013;28(8):1200-1206
Some patients with chronic obstructive pulmonary disease (COPD) have pulmonary hypertension (PH) that adversely affects survival. We performed a systematic review and meta-analysis to assess whether PH-specific therapies have an effect for stable COPD. Data sources were Medline, EMBASE, Cochrane Central Register of Controlled Trials, Korea med and references from relevant publications. Randomized prospective trials that compared PH specific therapy in COPD for more than 6 weeks with placebo were included. The outcomes were the exercise capacity and adverse events. Four randomized controlled trials involving 109 subjects were included in the analysis. Two trials involved bosentan, one sildenafil and one beraprost. The studies varied in duration of treatment from 3 to 18 months. In a pooled analysis of four trials, exercise-capacity was not significantly improved with PH-specific treatment for COPD (risk ratio, -5.1; 95% CI, -13.0 to 2.8). COPD with overt PH significantly improved the exercise capacity (mean difference, 111.6; 95% CI, 63.3 to 159.9) but COPD with PH unknown did not (mean difference, 26.6; 95% CI, -24.3 to 77.5). There was no significant difference in hypoxemia (mean difference, 2.6; 95% CI, -3.7 to 8.8). PH specific treatments have a significant effect in improving exercise capacity in COPD with overt PH.
Anoxia
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Antihypertensive Agents/adverse effects/*therapeutic use
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Clinical Trials as Topic
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Databases, Factual
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Epoprostenol/adverse effects/analogs & derivatives/therapeutic use
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Humans
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Hypertension, Pulmonary/complications/*drug therapy
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Piperazines/adverse effects/therapeutic use
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Pulmonary Disease, Chronic Obstructive/*etiology
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Purines/adverse effects/therapeutic use
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Questionnaires
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Risk Factors
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Sulfonamides/adverse effects/therapeutic use
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Sulfones/adverse effects/therapeutic use
10.Selective serotonin reuptake inhibitors in the treatment of premature ejaculation.
Wei-fu WANG ; Le CHANG ; Suks MINHAS ; David J RALPH
Chinese Medical Journal 2007;120(11):1000-1006
OBJECTIVETo review and assess the update studies regarding selective serotonin reuptake inhibitors (SSRIs) in the treatment of premature ejaculation (PE) and then provide practical recommendations and possible mechanisms concerning state of the art knowledge for the use of SSRIs in alleviating PE.
DATA SOURCESUsing the Medline, 48 articles published from January 1st, 1996 to August 1st, 2006 concerning the use of SSRIs and their possible mechanisms in alleviating PE were found and reviewed.
STUDY SELECTIONPE, rapid ejaculation, early ejaculation and SSRIs were employed as the keywords, and relevant articles about the use of SSRIs and their possible mechanisms in the treatment of PE were selected.
RESULTSMany kinds of SSRIs, such as fluoxetine, sertraline, paroxetine and citalopram, have widely been employed to treat PE. However, their effects are moderate and there is no a universal agreement about the kind, dose, protocol and duration. Dapoxetine, as the first prescription treatment of PE, may change this bottle-neck situation. SSRIs are suggested to be used in young men with lifelong PE, and acquired PE when etiological factors are removed but PE still exists. Phosphodiesterase 5 inhibitors (PDE(5)-Is) are suggested to be employed alone or combined with SSRIs when SSRIs fail to treat PE or sexual dysfunction associated with SSRIs occurs. The protocol of taking drugs on demand based on taking them daily for a suitable period is proposed to be chosen firstly. The possible mechanisms include increasing serotonergic neurotransmission and activating 5-hydroxytryptamine 2C (5-HT(2C)) receptors, then switching the ejaculatory threshold to a higher level, decreasing the penile sensitivity and their own effect of antidepression.
CONCLUSIONThe efficacies of the current SSRIs are moderate in the treatment of PE and they have not been approved by the FDA, therefore new SSRI like dapoxetine needs to be further evaluated.
Clinical Trials as Topic ; Ejaculation ; drug effects ; Humans ; Male ; Piperazines ; therapeutic use ; Purines ; therapeutic use ; Serotonin Uptake Inhibitors ; adverse effects ; pharmacology ; therapeutic use ; Sexual Dysfunction, Physiological ; drug therapy ; Sildenafil Citrate ; Sulfones ; therapeutic use