This study investigate the problems which patients experience after hospital discharge after TKA surgery during the first six weeks post-operative. We will use the outcome of this study to optimize the first six weeks after hospital discharge.Theā¦
ID
Source
Brief title
Condition
- Joint disorders
- Bone and joint therapeutic procedures
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The selected questionnaires focused on pain, rehabilitation, physical and
mental functioning, medication, quality of life and complications.
Secondary outcome
not applicable.
Background summary
Historically, the length of hospital stay after primary Total Hip Arthroplasty
(THA) and primary Total Knee Arthroplasty (TKA) exceeded several weeks, with a
subsequent period of bed rest during hospitalization. During the last decade,
there has been a continued interest in reducing the length of hospital stay to
a few days. Moreover rapid recovery protocols have been introduced worldwide
after elective primary THA and TKA. Various studies have shown these protocols
have reduced the length of hospital stay and the length of rehabilitation
following primary THA and TKA. Also a decrease in complication rate and
readmission rate have been described.
These rapid recovery protocols are based on analysis of clinical care
principles and pain management in combination with the revision of
organizational factors, allowing an optimized perioperative period that is safe
for the patient.
In Reinier de Graaf Hospital (RdGG), the introduction of the rapid recovery
protocol for primary THA and TKA started in 2009 and was introduced in several
phases. In February 2011 all phases of this rapid recovery protocol for primary
THA were introduced. The introduction of the rapid recovery protocol in our
hospital indeed yielded a shorter length of hospital stay without an increase
of complications, readmissions and reoperations after primary THA and TKA.
Most studies on rapid recovery focused on optimizing the postoperative phase
during hospital stay. However, little is known about the early postoperative
phase after discharge from the hospital. Studies on outcome after hospital
discharge mostly evaluate function after three to six month little is known of
the first 6 weeks after discharge.
The focus of this study will be on problems regarding pain, rehabilitation,
physical functioning, medication, quality of life and complications of patients
after TKA surgery with rapid recovery during the first 6 weeks after discharge
from the hospital.
Study objective
This study investigate the problems which patients experience after hospital
discharge after TKA surgery during the first six weeks post-operative. We will
use the outcome of this study to optimize the first six weeks after hospital
discharge.
The focus of this study will be on problems regarding pain, rehabilitation,
physical functioning, medication, quality of life and complications.
Study design
This a prospective, observational trail in which 30 patients are asked to
complete questionnaires on daily basis the first 6 weeks after primary TKA
surgery. We will call patients to remind and to motivate in the first 2 weeks 2
times and in the 3rd and 5th week one time by the research nurse. The completed
questionnaire will be returned to the surgeon at standard 6 weeks control.
Study burden and risks
Patients will be asked to complete questionnaires on daily basis. This will
take 5 minuts a day. During this 2 weeks the investigator / research nurse will
call two times a week to motivate to complete the questionnaires.
During the 3rd to 6th week patients will be asked daily basis. This will take 4
minutes a day. In the 3rd and 5th week the investigator / research nurse will
call to motivate.
Total effort for patients will be 3,5 hours during the six weeks.
There will be no risk for patients in this study.
Reinier de Graafweg 3-11
Delft 2625AD
NL
Reinier de Graafweg 3-11
Delft 2625AD
NL
Listed location countries
Age
Inclusion criteria
Patients aged 18 years and older
Primary total knee arthroplasty
Patients willing to participate
Speaking and writing Dutch language
Exclusion criteria
Patients unwilling to participate
mentally disabled patients
Patients with alcoholic and or drug abuse
insufficient command of the Dutch language
Patients participating in research in which a new prosthesis is studied
Design
Recruitment
metc-ldd@lumc.nl
metc-ldd@lumc.nl
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL45040.098.13 |