Rechallenging nonresponders to tadalafil and vardenafil: a reallife study - PowerPoint PPT Presentation

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Rechallenging nonresponders to tadalafil and vardenafil: a reallife study

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Hatzimouratidis K, Moysidis K, Bekos A, Tsimtsiou Z, Ioannidis E, Hatzichristou D. 2nd Department of Urology, 'Papageorgiou' General Hospital and ... – PowerPoint PPT presentation

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Title: Rechallenging nonresponders to tadalafil and vardenafil: a reallife study


1
Rechallenging non-responders to tadalafil and
vardenafil a real-life study
  • Hatzimouratidis K, Moysidis K, Bekos A,
  • Tsimtsiou Z, Ioannidis E, Hatzichristou D
  • 2nd Department of Urology, Papageorgiou General
    Hospital and
  • Center for Sexual and Reproductive Health,
  • Aristotle University of Thessaloniki, Greece

2
Study design
  • 100 consecutive patients non-responders to
    tadalafil or vardenafil
  • treated in a single center, basic work-up
  • drug expenses covered by patients

Treatment Phases
Study Phases
Screening
Phase I
Phase II
Phase III
Inappropriate use adequate instructions retrial 4
max doses on demand
New instructions Tadalafil gt2h before
sex Vardenafil fasted Retrial 4 max doses on
demand
Scheduled use Tadalafil 20mg / 48h Vardenafil
20mg OD
Demographics Sex-Med history IIEF
Q1 Were your erections rigid and last for
successful intercourse? YES NO Q2 Do you
want a new prescription? YES NO
Response definition
3
Results baseline characteristics (I)
4
Results baseline characteristics (II)
5
Results - Tadalafil group
Non-responders to tadalafil (n86)
Salvage 38 pts (44.2)
6
Results - Vardenafil group
Non-responders to vardenafil (n88)
Salvage 34 pts (38.7)
7
Conclusions
  • Timing of intercourse and food instructions may
    play a significant role in the response rate of
    ED patients under PDE5 inhibitors treatment
  • Continuous administration scheme may maximize
    efficacy
  • As much as 44 of so-called non-responders to
    tadalafil and vardenafil may be salvaged after
    new dosing instructions depending on
    pharmacokinetics of each drug despite current
    labeling information
  • Further research is needed on the appropriate
    dose and adverse events profile of the continuous
    administration of these new drugs
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