Complications of peripherally inserted central catheters in adult hospitalized patients and outpatients in the KTFIXPICC study: a randomized controlled trial evaluating a fixation device KT FIX Plusࣨsystem

Author(s):  
Audrey Fohlen ◽  
Anais R. Briant ◽  
Jean Jacques Dutheil ◽  
Vincent Le Pennec ◽  
Jean-Pierre Pelage ◽  
...  
Neonatology ◽  
2017 ◽  
Vol 112 (2) ◽  
pp. 150-158 ◽  
Author(s):  
Daniella W.E. Roofthooft ◽  
Sinno H.P. Simons ◽  
Richard A. van Lingen ◽  
Dick Tibboel ◽  
John N. van den Anker ◽  
...  

2020 ◽  
Vol 48 (9) ◽  
pp. 030006052094791
Author(s):  
Jia Li ◽  
Xue-fang Huang ◽  
Jie-lin Luo ◽  
Jiang-yun Zhang ◽  
Xiao-lin Liang ◽  
...  

Objective To evaluate the effects of a video-assisted education intervention on informed consent and patient education for peripherally inserted central catheters (PICCs). Methods We conducted a randomized controlled trial comparing the effects on informed consent of video-assisted patient education and traditional face-to-face discussion in a catheter outpatient ward of a cancer centre in Guangzhou, China, in 2018. Participants were 140 patients randomly allocated (1:1 ratio) to two groups: video-assisted or traditional intervention. General information, patient retention of PICC-related information, working time spent by nurses on the procedure, and patient and nurse satisfaction with the procedure were assessed. Results The time used for informed consent was significantly shorter in the experimental group (1.02 ± 0.24 minutes) than in the control group (6.87 ± 1.10 minutes). The time used for PICC-related education was significantly shorter in the experimental group (1.03 ± 0.28 minutes) than in the control group (5.11 ± 0.57 minutes). Nurses’ degree of satisfaction with the procedure was significantly higher in the experimental group (4.10 ± 0.57) than in the control group (2.60 ± 0.70). Conclusion The use of video-assisted informed consent and patient education in this cancer centre decreased nurses’ working time and improved nurses’ satisfaction. Clinical trial registration number: ChiCTR1800015664


Author(s):  
elham vahabi ◽  
somayeh ghafari ◽  
somayeh haghighat

Abstract Background There are evidences that periurethral cleaning by antiseptics before catheterization decreases the risk of urinary tract infections. The purpose of this study was to Comparing 10% povidone-iodine and chlorhexidine gluconate (CHG) effectiveness in periurethral cleaning before catheterization on bacteriuria and pyuria in hospitalized patients. Methods A randomized controlled trial was used, and subjects were randomly allocated to either the 10% povidone -iodine group or the 2% chlorhexidine gluconate group. Urine specimens for culture and Analyse were collected 3 times for each subject within 5 days. Results Overall, 216 urine samples were collected in 72 subjects .There were no significant difference in results of bacteriuria of two groups immediately, 72 hrs. and 5 days after catheterization (p>0.05). There was no significant difference between two groups regarding positive pyuria immediately after sampling (p>0.05). Although its amount was significantly higher 72 hrs and 5days after catheterization in 10% povidone-iodine group than 2% chlorhexidine gluconate (p<0.05). In order to evaluate average of micro-organism in different time intervals between two groups Mann– Whitney test was used. This test showed that there was no significant difference of number of time intervals (p>0.05). Conclusions The results of this study showed that using 2% chlorhexidine gluconate reduced the amount of bacteriuria in catheterazied patients compared to 10% povidone-iodine. However this difference was not significant. Therefore doing more studies with more number of samples in this field is suggested. Trial registration: Retrospectively registered. IRCT20170712035044N2 Key words: 10% povidone-iodine- 2% chlorhexidine gluconate - Bacteriuria- Periurethral cleansing


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