Redo Hip Surgery
Conditions
Brief summary
Several studies have demonstrated that goal-directed fluid therapy during high- risk-surgery reduces morbidity and length of hospital stay. This quality improvement is design to evaluate the implementation of an intraoperative goal-directed therapy, using a pulse contour analysis monitor to optimize the stroke volume, in patients undergoing redo-hip-surgery. The primary combined endpoints will be the incidence of postoperative complications and the secondary endpoints will be the decrease of hospital length of stay, length of ICU stay and hospital postoperative mortality. We amended another 130 patients getting crystalloid fluids in the hemodynamic optimization protocol.
Interventions
DEVICEStroke volume monitoring
Pulse contour stroke volume monitoring
Sponsors
Edwards Lifesciences
Charite University, Berlin, Germany
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* patients undergoing redo hip surgery * age above 18 years * signed informed consent
Exclusion criteria
* urgent or emergency surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative complications | 30days |
Secondary
| Measure | Time frame |
|---|---|
| length of hospital and ICU stay | 30days |
Countries
Germany
Outcome results
None listed