Evidence map›Paper›PMID 28540239›Full record

ReviewTranslational andrology and urology2017

The impact and management of sexual dysfunction secondary to pharmacological therapy of benign prostatic hyperplasia.

Jason Gandhi, Steven J Weissbart, Noel L Smith, Steven A Kaplan, Gautam Dagur, Anna Zumbo, Gargi Joshi, Sardar Ali Khan

Open access · hybridAbstract readReview
In one paragraph

Review in Translational andrology and urology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
5.2field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Drugs for benign prostatic hypertrophy.Australian prescriber · 2018
    Review
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Jason GandhiDepartment of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA.
Steven J WeissbartDepartment of Urology, Stony Brook University School of Medicine, Stony Brook, NY, USA.
Noel L SmithFoley Plaza Medical, New York, NY, USA.
Steven A KaplanDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Gautam DagurDepartment of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA.
Anna ZumboUniversity of Messina School of Medicine, Messina, Italy.
Gargi JoshiDepartment of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA.
Sardar Ali KhanDepartment of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA.
Stony Brook University · USFoley Hoag (United States) · USIcahn School of Medicine at Mount Sinai · USUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Benign prostatic hyperplasia (BPH) is one of the most common genitourinary complications in men over 50 years of age and typically presents with lower urinary tract symptoms (LUTS). Classes of medications include α1-adrenoceptor blockers, 5α-reductase inhibitors, and phosphodiesterase 5 inhibitors. Today, α1-adrenoceptor blockers and 5α-reductase inhibitors are often combined to give a synergistic effect. A review of the current literature identified several adverse sexual side effects, including erectile dysfunction (ED), decreased libido, orgasmic disorders, and ejaculatory disorders. We believe it is important to know the extent of these side effects, as the clinician and patient will need to decide the cost of improved voiding symptoms. The chief adverse effect is ejaculatory disorders, including the absence of ejaculation. Clinical consideration for BPH should include the elements of male sexual function, patients' age, and the characteristics and comprehensive effects of each group of drugs. Methodological bias in clinical studies, such as the subjective evaluation of the sexual side effect, makes it difficult to determine the ideal drug for treatment.

Indexed as

5α-reductase inhibitorsalpha1-adrenergic blockersBenign prostatic hyperplasia (BPH)ejaculatory disordersretrograde ejaculationsexual dysfunction

Identifiers

PMID28540239
PMCPMC5422692
OpenAlexW2604494199

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.