Management of Premature Ejaculation and Erectile Dysfunction
When both premature ejaculation and erectile dysfunction coexist, treat the erectile dysfunction first with PDE5 inhibitors, as many men will experience resolution of premature ejaculation once erectile function improves. 1, 2
Initial Diagnostic Approach
The sexual history must distinguish whether ejaculation occurs prematurely due to lack of control versus loss of erection after normal ejaculation, as this determines the treatment sequence. 1, 2 Key diagnostic elements include:
- Intravaginal ejaculatory latency time (IELT): Self-estimated timing after penetration, with <2 minutes indicating PE 1
- Presence of masturbatory and morning erections: Their presence suggests preserved erectile capacity and points toward psychogenic ED 3
- Temporal relationship: Determine whether PE developed secondary to ED from anxiety about maintaining erections or from requiring intense stimulation 1
- Perceived control, distress, and interpersonal difficulty related to both dysfunctions 1
Physical examination should identify anatomical abnormalities associated with either condition, but routine laboratory testing is not required unless specific findings from history or examination warrant it. 1
Treatment Algorithm
Step 1: Initiate PDE5 Inhibitor Therapy for Erectile Dysfunction
Start with phosphodiesterase-5 inhibitors as first-line therapy for ED, with options including sildenafil, tadalafil, or vardenafil. 1, 2 These agents demonstrate high efficacy and safety even in difficult-to-treat populations like diabetic patients. 1, 4
Critical safety screening before prescribing PDE5 inhibitors: 5
- Absolute contraindications: Concurrent nitrate use (nitroglycerin, isosorbide dinitrate/mononitrate) or guanylate cyclase stimulators (riociguat) 5
- Cardiovascular risk assessment: High-risk cardiac profiles contraindicate both sexual activity and PDE5-I use 2
- Active ingredient persistence: Tadalafil remains in the body for more than 2 days after a single dose, longer with kidney/liver problems 5
Tadalafil demonstrates sustained efficacy at 24 hours (61% successful intercourse vs 37% placebo) and 36 hours (64% vs 37% placebo) after dosing. 5 Daily tadalafil 2.5-10 mg provides continuous treatment without timing restrictions relative to sexual activity. 5
Step 2: Reassess Premature Ejaculation After ED Treatment
Many patients experience resolution of PE once erectile function improves, eliminating the need for additional PE-specific therapy. 1, 2 If PE persists after successful ED treatment, proceed to Step 3.
Step 3: Add SSRI Therapy for Persistent Premature Ejaculation
If premature ejaculation persists after ED treatment, add selective serotonin reuptake inhibitors as the primary pharmacologic intervention. 2 All SSRI use for PE is off-label in the United States. 1, 2
Daily dosing SSRIs provide the most robust evidence: 1, 2
- Paroxetine: Most effective SSRI for PE 1
- Sertraline, fluoxetine, or clomipramine: Alternative options 1
- Expected outcomes: 2.5- to 4.3-fold increases in IELT, with greater improvements in patients with baseline IELT <30 seconds 1
On-demand dapoxetine (30-60 mg taken 1-3 hours before sexual activity) is approved for PE in Europe but not FDA-approved in the US. 1, 2 Side effects include nausea, diarrhea, and dizziness, with treatment discontinuation rates reaching 90% at 2 years due to cost and disappointment with on-demand nature. 1
Critical SSRI counseling points: 1
- Avoid sudden cessation or rapid dose reduction to prevent SSRI withdrawal syndrome 1
- Caution in adolescents and men with comorbid depression, particularly with suicidal ideation 1
- 40% of patients refuse to begin or discontinue within 12 months due to concerns about taking an antidepressant 1
PDE5 inhibitors and dapoxetine can be safely combined for patients with both conditions. 1
Step 4: Consider Topical Anesthetics as Alternative or Adjunct
Topical anesthetics (lidocaine/prilocaine creams or sprays) are moderately effective in delaying ejaculation. 1 The EMA-approved spray formulation provides standardized dosing. 1
Common pitfalls: 1
- Significant penile hypoesthesia may occur 1
- Partner absorption can cause discomfort or numbness 1
- Prevention strategy: Use condoms or thoroughly wash penis prior to penetration 1
Step 5: Incorporate Behavioral Therapy
Combining behavioral and pharmacological approaches produces superior outcomes compared to either modality alone. 1, 2 Behavioral therapy leads to significantly greater IELT increases and improved satisfaction scores on validated PE instruments when added to pharmacotherapy. 1
Involve the sexual partner in treatment decisions when possible, as shared decision-making optimizes outcomes. 1, 6 Consider referral to mental health professionals with sexual health expertise, particularly for lifelong PE. 2, 6
Second-Line and Experimental Options
For patients failing first-line therapy, α1-adrenoreceptor antagonists may be considered, though efficacy data remains very limited. 1
Surgical management (dorsal nerve neurotomy, radiofrequency ablation, hyaluronic acid augmentation) should be considered experimental and only performed in ethical board-approved clinical trials due to risk of permanent penile sensation loss. 1, 6
Treatment Targets and Monitoring
The primary treatment outcome is patient and partner satisfaction, not arbitrary physiological measures. 1, 2 Treatment goals include:
- Regaining sense of control over ejaculation timing 2, 6
- Achieving satisfaction with sexual intercourse for both partners 2, 6
- Reducing distress and interpersonal difficulties 2, 6
Assess therapeutic outcomes in terms of patient self-perceived treatment invasiveness, treatment-associated improvement of erectile function, treatment-related side effects, and treatment-associated satisfaction. 1
Critical Safety Reminder
No medications have FDA approval specifically for premature ejaculation—all pharmacotherapy is off-label use. 1, 2, 6 Patients require comprehensive counseling about the off-label nature of treatment, potential for known and unknown side effects, and the weak evidence base for some interventions. 2