scholarly journals Efficacy of urination in alleviating man’s urethral pain associated with flexible cystoscopy: a single-center randomized trial

BMC Urology ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Yingwei Xie ◽  
Wei Wang ◽  
Wei Yan ◽  
Dan Liu ◽  
Yuexin Liu
2015 ◽  
Vol 33 (2) ◽  
pp. 117-124 ◽  
Author(s):  
Carmelo Libetta ◽  
Pasquale Esposito ◽  
Marilena Gregorini ◽  
Elisa Margiotta ◽  
Claudia Martinelli ◽  
...  

2020 ◽  
Author(s):  
abhishek thakur ◽  
Aditya P Sharma ◽  
Sudheer K Devana ◽  
KALPESH PARMAR ◽  
ravimohan Mavuduru ◽  
...  

2019 ◽  
Vol 35 (4) ◽  
pp. 502-508 ◽  
Author(s):  
Lewandowski Pawel ◽  
Gralak-Lachowska Dagmara ◽  
Maciejewski Pawel ◽  
Ramotowski Bogumil ◽  
Budaj Andrzej ◽  
...  

Abstract Hemostatic devices used in the transradial approach (TRA) and transulnar approach (TUA) are limited. This study compared the efficacy and safety of hemostasis using the QuikClot Radial hemostatic pad (QC) vs. standard mechanical compression (SC) after coronary angiography (CAG). This prospective single-center randomized trial included CAG patients. The primary and secondary endpoints were efficacy (successful hemostasis) and safety (total artery occlusion [TAO], pseudoaneurysm, hematoma), respectively. A visual analog scale (VAS) evaluated patient pain during compression. In 2013–2017, 200 patients were randomized 2 × 2 into the: (1) TRA and TUA groups and (2) QC and SC groups. Successful hemostasis was achieved in 92 (92%) patients in the QC group and 100 (100%) patients in the SC group (p < 0.006). The TRA SC subgroup showed significantly better results than the TRA QC subgroup (100% vs. 90.0%; p < 0.03). Similar results were obtained in the TUA QC and TUA SC subgroups (95% vs. 100%; p = 0.5). The secondary endpoint was achieved in the QC and SC groups (8% vs. 9%; p = 0.8). Patients reported significantly less pain during QC application than during SC (VAS: 2.6 ± 2.6 vs. 3.4 ± 2.9; p < 0.03). In patients undergoing CAG with TRA or TUA, QC was associated with lower efficacy, less discomfort, and similar safety compared to SC.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Lei Wang ◽  
Zhibo Xiao ◽  
Zhendong Yue ◽  
Hongwei Zhao ◽  
Zhenhua Fan ◽  
...  

2016 ◽  
Vol 11 (9) ◽  
pp. 1045-1052 ◽  
Author(s):  
Claus Z Simonsen ◽  
Leif H Sørensen ◽  
Niels Juul ◽  
Søren P Johnsen ◽  
Albert J Yoo ◽  
...  

Rationale Endovascular therapy after acute ischemic stroke due to large vessel occlusion is now standard of care. There is equipoise as to what kind of anesthesia patients should receive during the procedure. Observational studies suggest that general anesthesia is associated with worse outcomes compared to conscious sedation. However, the findings may have been biased. Randomized clinical trials are needed to determine whether the choice of anesthesia may influence outcome. Aim and hypothesis The objective of GOLIATH (General or Local Anestesia in Intra Arterial Therapy) is to examine whether the choice of anesthetic regime during endovascular therapy for acute ischemic stroke influence patient outcome. Our hypothesis is that that conscious sedation is associated with less infarct growth and better functional outcome. Methods GOLIATH is an investigator-initiated, single-center, randomized study. Patients with acute ischemic stroke, scheduled for endovascular therapy, are randomized to receive either general anesthesia or conscious sedation. Study outcomes The primary outcome measure is infarct growth after 48–72 h (determined by serial diffusion-weighted magnetic resonance imaging). Secondary outcomes include 90-day modified Rankin Scale score, time parameters, blood pressure variables, use of vasopressors, procedural and anesthetic complications, success of revascularization, radiation dose, and amount of contrast media. Discussion Choice of anesthesia may influence outcome in acute ischemic stroke patients undergoing endovascular therapy. The results from this study may guide future decisions regarding the optimal anesthetic regime for endovascular therapy. In addition, this study may provide preliminary data for a multicenter randomized trial.


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