Adaptive Support Ventilation (ASV): Effect of Forced Weaning (FW) on Time till Extubation in Post-Cardiac Surgery Patients – A Randomized Controlled Trial.

Author(s):  
DA Dongelmans ◽  
DP Veelo ◽  
JM Binnekade ◽  
MB Vroom ◽  
MJ Schultz
2009 ◽  
Vol 108 (2) ◽  
pp. 565-571 ◽  
Author(s):  
Dave A. Dongelmans ◽  
Denise P. Veelo ◽  
Frederique Paulus ◽  
Bas A. J. M. de Mol ◽  
Johanna C. Korevaar ◽  
...  

2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Asishana A. Osho ◽  
Philicia Moonsamy ◽  
Breanna R. Ethridge ◽  
Gregory A. Leya ◽  
David A. D’Alessandro ◽  
...  

2008 ◽  
Vol 109 (1) ◽  
pp. 81-87 ◽  
Author(s):  
Pascale C. Gruber ◽  
Charles D. Gomersall ◽  
Patricia Leung ◽  
Gavin M. Joynt ◽  
Siu Keung Ng ◽  
...  

Background Adaptive-support ventilation (ASV) is a minute ventilation-controlled mode governed by a closed-loop algorithm. With ASV, tidal volume and respiratory rate are automatically adjusted to minimize work of breathing. Studies indicate that ventilation in ASV enables more rapid weaning. The authors conducted a randomized controlled trial to determine whether ventilation in ASV results in a shorter time to extubation than pressure-regulated volume-controlled ventilation with automode (PRVCa) after cardiac surgery. Methods Fifty patients were randomly assigned to ASV or PRVCa after elective coronary artery bypass grafting. Respiratory weaning progressed through three phases: phase 1 (controlled ventilation), phase 2 (assisted ventilation), and phase 3 (T-piece trial), followed by extubation. The primary outcome was duration of intubation (sum of phases 1-3). Secondary outcomes were duration of mechanical ventilation (sum of phases 1 and 2), number of arterial blood gas samples, and manual ventilator setting changes made before extubation. Results Forty-eight patients completed the study. The median duration of intubation was significantly shorter in the ASV group than in the PRVCa group (300 [205-365] vs. 540 [462-580] min; P < 0.05). This difference was due to a reduction in the duration of mechanical ventilation (165 [120-195] vs. 480 [360-510] min; P < 0.05). There were no significant differences between the ASV and PRVCa groups in the number of arterial blood gas samples taken or manual ventilator setting changes made. Conclusions ASV is associated with earlier extubation, without an increase in clinician intervention, when compared with PRVCa in patients undergoing uncomplicated cardiac surgery.


2021 ◽  
Author(s):  
Maryam Zahid ◽  
Ume Sughra ◽  
Sehrish Mumtaz ◽  
Mawara Hassan

BACKGROUND Malnutrition is the most common problem in congenital heart diseases patients. Nutrition based mobile applications play an important role in planning and tracking of diet for better nutritional status. OBJECTIVE To assess usefulness of the nutrition based mobile application among children post cardiac surgery. METHODS This was a single-center, double-blinded, randomized controlled trial that was conducted at a Tertiary Care Hospital, Rawalpindi. The study duration was 6 months from February 2021 till July 2021. Sample size was calculated to be 88. Intervention group caregivers were provided with a nutrition based mobile application by a dietitian, primary objective of the mobile application was to improve /maintain nutritional status of children. Caregiver’s of children were able to choose their nutritional goals. Nutritional intake was tracked, daily and monthly insight regarding nutrients intake was provided to the user. Usual care group was handed a pamphlet with diet instructions on discharge by a dietitian. RESULTS At the end of intervention preferred diet planning tool for 79% of the participant’s caregiver was mobile application. At 8th week 93% of the caregivers considered visual cues useful, 80% thought that the mobile application language was understandable, 79% thought nutritional goal setting was a useful feature in mobile application and 55% thought the recipes in the application were useful. CONCLUSIONS The study showed strength for the future of scalable modern technology for self-nutrition monitoring. The average income status and education level of the participant’s caregivers in our study was low to average. It represented a population that has been slow to adopt new technology but our participants showed interest in mobile application and used the technology after a brief training session. CLINICALTRIAL Study was registered on clinicaltrial.gov with trial identity number NCT04782635.


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