Tadalafil, a Phosphodiesterase-5 Inhibitor, Improves Erectile Dysfunction in Patients With Liver Cirrhosis.

CLD, Chronic Liver Disease CTP, Child-Turcotte-Pugh ED, Erectile Dysfunction HE, Hepatic Encephalopathy HRQOL, Health-Related Quality of Life IIEF-15, International Index for Erectile Function MELD, Model for End-Stage Liver Disease MMSE, Mini-Mental State Examination PDE, Phosphodiesterase cirrhosis erectile dysfunction phosphodiesterase inhibitors tadalafil

Journal

Journal of clinical and experimental hepatology
ISSN: 0973-6883
Titre abrégé: J Clin Exp Hepatol
Pays: India
ID NLM: 101574137

Informations de publication

Date de publication:
Historique:
received: 12 12 2017
accepted: 11 07 2018
entrez: 31 7 2019
pubmed: 31 7 2019
medline: 31 7 2019
Statut: ppublish

Résumé

Erectile dysfunction(ED) is common in patients with chronic liver disease(CLD). Although it significantly worsens the quality of life, caregivers and researchers often neglect it. Evaluating the prevalence of ED in patients with CLD, associated factors, and response to therapy with tadalafil, a phosphodiesterase-5 inhibitor. A total of 60 males with Child-Pugh score between 5 and 10 and no overt hepatic encephalopathy were studied. ED was assessed based on the 15-question International Index of Erectile Function (IIEF) questionnaire. Patients were classified as ED+ if score was <25. Patients with ED were given 10 mg of tadalafil for 4 weeks. The mean age was 45.2 he 7.8 years. The mean Child-Turcotte-Pugh (CTP) score was 6.4 sc 1.7, and model for end-stage liver disease (MELD) score was 12.1 sc 4.5. Twenty-seven (45%) patients had compensated cirrhosis, and 45(75%) had alcohol as etiology. Twenty-five (42%) had an IIEF score <25, suggestive of ED. The IIEF score had significant correlation with the presence of ascites(r = -0.27, ED is common in patients with cirrhosis. Tadalafil administration significantly improves ED in these patients.

Sections du résumé

BACKGROUND BACKGROUND
Erectile dysfunction(ED) is common in patients with chronic liver disease(CLD). Although it significantly worsens the quality of life, caregivers and researchers often neglect it.
AIM OBJECTIVE
Evaluating the prevalence of ED in patients with CLD, associated factors, and response to therapy with tadalafil, a phosphodiesterase-5 inhibitor.
METHODS METHODS
A total of 60 males with Child-Pugh score between 5 and 10 and no overt hepatic encephalopathy were studied. ED was assessed based on the 15-question International Index of Erectile Function (IIEF) questionnaire. Patients were classified as ED+ if score was <25. Patients with ED were given 10 mg of tadalafil for 4 weeks.
RESULTS RESULTS
The mean age was 45.2 he 7.8 years. The mean Child-Turcotte-Pugh (CTP) score was 6.4 sc 1.7, and model for end-stage liver disease (MELD) score was 12.1 sc 4.5. Twenty-seven (45%) patients had compensated cirrhosis, and 45(75%) had alcohol as etiology. Twenty-five (42%) had an IIEF score <25, suggestive of ED. The IIEF score had significant correlation with the presence of ascites(r = -0.27,
CONCLUSION CONCLUSIONS
ED is common in patients with cirrhosis. Tadalafil administration significantly improves ED in these patients.

Identifiants

pubmed: 31360023
doi: 10.1016/j.jceh.2018.07.007
pii: S0973-6883(18)30637-6
pmc: PMC6637079
doi:

Types de publication

Journal Article

Langues

eng

Pagination

312-317

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Auteurs

Jitender Thakur (J)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Sahaj Rathi (S)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Sandeep Grover (S)

Department of Psychiatry, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Madhu Chopra (M)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Swastik Agrawal (S)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Sunil Taneja (S)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Ajay Duseja (A)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Anil Bhansali (A)

Department of Endocrinology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Yogesh K Chawla (YK)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Radha K Dhiman (RK)

Department of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Classifications MeSH