Purpose: The aim of this study was to evaluate the efficacy of a multimedia informed consent (IC) presentation on the understanding and satisfaction of patients who were scheduled to receive 120-W green-light high-performance system photoselective vaporization of the prostate (HPS-PVP).
Materials And Methods: A multimedia IC (M-IC) presentation for HPS-PVP was developed. Forty men with benign prostatic hyperplasia who were scheduled to undergo HPS-PVP were prospectively randomized to a conventional written IC group (W-IC group, n=20) or the M-IC group (n=20). The allocated IC was obtained by one certified urologist, followed by a 15-question test (maximum score, 15) to evaluate objective understanding, and questionnaires on subjective understanding (range, 0~10) and satisfaction (range, 0~10) using a visual analogue scale.
Results: Demographic characteristics, including age and the highest level of education, did not significantly differ between the two groups. No significant differences were found in scores reflecting the objective understanding of HPS-PVP (9.9±2.3 vs. 10.6±2.8, p=0.332) or in subjective understanding scores (7.5±2.1 vs. 8.6±1.7, p=0.122); however, the M-IC group showed higher satisfaction scores than the W-IC group (7.4±1.7 vs. 8.4±1.5, p=0.033). After adjusting for age and educational level, the M-IC group still had significantly higher satisfaction scores.
Conclusions: M-IC did not enhance the objective knowledge of patients regarding this surgical procedure. However, it improved the satisfaction of patients with the IC process itself.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853770 | PMC |
http://dx.doi.org/10.5534/wjmh.2016.34.1.47 | DOI Listing |
J Dent
December 2024
Department of Conservative Dentistry and Prosthodontics, Faculty of Dentistry, Complutense University of Madrid, Madrid, Spain; Department of Reconstructive Dentistry and Gerodontology, School of Dental Medicine, University of Bern, Bern, Switzerland.
Purpose: To assess the impact of involuntary interruptions (simulating tracking loss by moving the scanner out of its focal distance) and voluntary interruptions (pressing the scanner's turn-on button) on the accuracy of implant-supported full-arch scans using an intraoral scanner (TRIOS 5, version 22.1.10; 3Shape; Copenhagen, Denmark).
View Article and Find Full Text PDFPharmaceuticals (Basel)
June 2023
Faculty of Chemistry, 'Alexandru Ioan Cuza' University of Iasi, Bulevardul Carol I, nr. 11, 700506 Iasi, Romania.
In the search for innovative approaches to cancer chemotherapy, a chemical library of 49 cyanochalcones, , , and , was designed as dual inhibitors of human farnesyltransferase (FTIs) and tubulin polymerization (MTIs) (FTIs/MTIs), two important biological targets in oncology. This approach is innovative since the same molecule would be able to interfere with two different mitotic events of the cancer cells and prevent these cells from developing an emergency route and becoming resistant to anticancer agents. Compounds were synthesized by the Claisen-Schmidt condensation of aldehydes with -3-oxo-propanenitriles under classical magnetic stirring and under sonication.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2023
Department of Applied Chemistry, National Yang Ming Chiao Tung University, 1001 University Rood, Hsinchu 30010, Taiwan.
Terminal acceptor atoms and side-chain functionalization play a vital role in the construction of efficient nonfullerene small-molecule acceptors (NF-SMAs) for AM1.5G/indoor organic photovoltaic (OPV) applications. In this work, we report three dithienosilicon-bridged carbazole-based (DTSiC) ladder-type (A-DD'D-A) NF-SMAs for AM1.
View Article and Find Full Text PDFMolecules
December 2022
Department of Chemistry, University of Life Sciences, Akademicka 15, 20-950 Lublin, Poland.
Benzoxazole and naphthoxazole fused systems are found in many biologically active molecules. Novel benzoxazole and naphthoxazole analogs functionalized by the 2,4-dihydroxyphenyl moiety were designed, obtained and evaluated as a broad spectrum of biological potency compounds. Sulfinylbis[(2,4-dihydroxyphenyl)methanethione] or its analogs and 2-aminophenols or 1-amino-2-naphthol were used as starting reagents.
View Article and Find Full Text PDFFront Chem
September 2022
Chemistry Department, Faculty of Science, King Khalid University, Abha, Saudi Arabia.
The 7-quinolinyl-bearing triazole analogs were synthesized and further assessed for their inhibitory profile against α-amylase andα-glucosidase. The entire analogs showed a diverse range of activities having IC values between 0.80 ± 0.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!