Abstract

The principal objective of this multicentre, non-comparative study was to determine the range of target blood propofol concentration settings required when 'Diprifusor' TCI systems are used to administer propofol for sedation in ventilated, adult, ICU patients. Following local ethics approval, data were obtained from 122 patients. Informed consent was obtained from patients or their next of kin. Three categories of ICU patients were studied: 57 post-cardiac surgery, 18 brain injured and 47 general ICU. Mean ages were 60.7, 41.1 and 60.7 years and mean APACHE II scores 9.2, 17.8 and 19 in the three groups respectively. The mean duration of sedation was 15 hours in the post-cardiac surgery patients, 47.6 hours in the brain injured group and 63.3 hours in the general ICU group. All post-cardiac surgery patients had received propofol by Diprifusor TCI for surgery and the same TCI system continued in use for sedation. Patients were excluded if they had received propofol by conventional modes of administration within 4 hours of the start of the study, had an established regimen of sedation with agents other than propofol for more than 24 hours, or a regional anaesthetic block persisting into the period of sedation. Depth of sedation was assessed with a modified Ramsay Score (UK Intensive Care Society National Guideline, 1999) and was also graded as light (L), desired level (D) or excessive (E). The 'Diprifusor' target blood propofol setting was titrated as required to obtain the depth of sedation desired in each patient. A desired level of sedation was obtained, after a mean time of 9.9 min, in all but one patient in whom sedation was 'excessive' throughout. For each patient, the time-weighted average target setting over the entire period of sedation, from the time when a desired level was first obtained, was calculated. Median, 10th and 90th percentile values are presented in Table ​Table11. Table 1 Time-weighted average Diprifusor target blood propofol settings (μg/ml)

Highlights

  • Intra-abdominal pressure (IAP) is an important parameter and prognostic indicator of the patient’s underlying physiologic status [1]

  • Several small studies have suggested that closed suction catheters offer benefits over open suction because disconnection from the ventilator circuit is not required [1], thereby maintaining ventilation, FIO2 and PEEP

  • Due to the prolonged stay of the critically ill under mechanical ventilation in intensive care unit (ICU) often stomatotracheal intubation should be replaced by tracheostomy

Read more

Summary

Introduction

Intra-abdominal pressure (IAP) is an important parameter and prognostic indicator of the patient’s underlying physiologic status [1]. The aim of this study was to assess the respiratory effects of sufentanil and remifentanil in postsurgical critically ill patients during spontaneous ventilation since the drugs show pharmacokinetic and pharmacodynamic properties which make them attractive for intensive care use. Preliminary evidence suggests that hU-II levels during cardiac surgery are increased in patients with myocardial dysfunction [2] It is not known, if hU-II plasma concentrations are related to pulmonary capillary wedge pressure (PCWP) as an estimate of left ventricular filling pressure. AAF in cardiac surgery postoperative period has been implicated as a complication that leads to longer ICU and hospital stay and to augmented costs It has not been associated with increased mortality rates. We aimed to investigate the effects of use of preoperative and early postoperative standard and immunonutrient products on immune system and acute inflammatory response in the patients undergoing gastrointestinal malignancy surgery.

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.