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10.21037/tau.2016.07.06

http://scihub22266oqcxt.onion/10.21037/tau.2016.07.06
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C5001985!5001985!27652216
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suck abstract from ncbi

pmid27652216      Transl+Androl+Urol 2016 ; 5 (4): 434-49
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  • The pathophysiology of acquired premature ejaculation #MMPMID27652216
  • McMahon CG; Jannini EA; Serefoglu EC; Hellstrom WJG
  • Transl Androl Urol 2016[Aug]; 5 (4): 434-49 PMID27652216show ga
  • The second Ad Hoc International Society for Sexual Medicine (ISSM) Committee for the Definition of Premature Ejaculation defined acquired premature ejaculation (PE) as a male sexual dysfunction characterized by a the development of a clinically significant and bothersome reduction in ejaculation latency time in men with previous normal ejaculatory experiences, often to about 3 minutes or less, the inability to delay ejaculation on all or nearly all vaginal penetrations, and the presence of negative personal consequences, such as distress, bother, frustration and/or the avoidance of sexual intimacy. The literature contains a diverse range of biological and psychological etiological theories. Acquired PE is commonly due to sexual performance anxiety, psychological or relationship problems, erectile dysfunction (ED), and occasionally prostatitis and hyperthyroidism, consistent with the predominant organic etiology of acquired PE, men with this complaint are usually older, have a higher mean BMI and a greater incidence of comorbid disease including hypertension, sexual desire disorder, diabetes mellitus, chronic prostatitis, and ED compared to lifelong, variable and subjective PE.
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